Crystallography Open Database

Result: there are 1946 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 56

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 2 | Next 1000 Right arrow | Last Right arrow Right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
7126611 CIFC52 H100 I2 Li2 Mo2 N4 O2 P4P 1 21/n 115.3229; 20.668; 20.2145
90; 101.531; 90		6272.6Tanabe, Yoshiaki; Sekiguchi, Yoshiya; Tanaka, Hiromasa; Konomi, Asuka; Yoshizawa, Kazunari; Kuriyama, Shogo; Nishibayashi, Yoshiaki
Preparation and reactivity of molybdenum complexes bearing pyrrole-based PNP-type pincer ligand.
Chemical communications (Cambridge, England), 2020, 56, 6933-6936
7126612 CIFC52 H100 K Mo2 N8 O2 P4P 21 21 2116.2771; 18.0042; 20.8139
90; 90; 90		6099.6Tanabe, Yoshiaki; Sekiguchi, Yoshiya; Tanaka, Hiromasa; Konomi, Asuka; Yoshizawa, Kazunari; Kuriyama, Shogo; Nishibayashi, Yoshiaki
Preparation and reactivity of molybdenum complexes bearing pyrrole-based PNP-type pincer ligand.
Chemical communications (Cambridge, England), 2020, 56, 6933-6936
7126613 CIFC50 H99 I2 Li2 Mo2 N4 O1.5 P4P -115.1684; 20.9015; 21.1912
84.099; 86.66; 69.37		6252.6Tanabe, Yoshiaki; Sekiguchi, Yoshiya; Tanaka, Hiromasa; Konomi, Asuka; Yoshizawa, Kazunari; Kuriyama, Shogo; Nishibayashi, Yoshiaki
Preparation and reactivity of molybdenum complexes bearing pyrrole-based PNP-type pincer ligand.
Chemical communications (Cambridge, England), 2020, 56, 6933-6936
7126614 CIFC24 H19 N OP 21 21 219.9107; 12.0632; 14.3759
90; 90; 90		1718.71Li, Sifeng; Wang, Zihao; Xiao, Haitao; Bian, Zhaoxiang; Wang, Jun Joelle
Enantioselective synthesis of indole derivatives by Rh/Pd relay catalysis and their anti-inflammatory evaluation.
Chemical communications (Cambridge, England), 2020, 56, 7573-7576
7126615 CIFC6 H9 N3 O2P 21 21 215.27; 7.44; 18.99
90; 90; 90		745Zapata, Fabiola; González, Lidia; Bastida, Adolfo; Bautista, Delia; Caballero, Antonio
Formation of self-assembled supramolecular polymers by anti-electrostatic anion-anion and halogen bonding interactions.
Chemical communications (Cambridge, England), 2020, 56, 7084-7087
7126616 CIFC13 H14 O3C 1 2/c 117.1906; 6.2367; 21.3876
90; 112.311; 90		2121.37Osberger, Thomas J.; Kidd, Sarah L.; King, Thomas A.; Spring, David R.
C(sp<sup>3</sup>)-H arylation to construct all-syn cyclobutane-based heterobicyclic systems: a novel fragment collection.
Chemical communications (Cambridge, England), 2020, 56, 7423-7426
7126617 CIFC25 H17 NP 1 21/c 18.3412; 20.3704; 10.3467
90; 95.383; 90		1750.29Adil, Laxmi Raman; Iyer, Parameswar Krishnan
Effects of incorporating regioisomers and flexible rotors to direct aggregation induced emission to achieve stimuli-responsive luminogens, security inks and chemical warfare agent sensors.
Chemical communications (Cambridge, England), 2020, 56, 7633-7636
7126618 CIFC25 H19 NP 1 21/n 15.7544; 11.1791; 28.221
90; 95.062; 90		1808.3Adil, Laxmi Raman; Iyer, Parameswar Krishnan
Effects of incorporating regioisomers and flexible rotors to direct aggregation induced emission to achieve stimuli-responsive luminogens, security inks and chemical warfare agent sensors.
Chemical communications (Cambridge, England), 2020, 56, 7633-7636
7126619 CIFC25 H17 NP 1 21/n 116.8722; 6.0689; 18.7149
90; 110.549; 90		1794.4Adil, Laxmi Raman; Iyer, Parameswar Krishnan
Effects of incorporating regioisomers and flexible rotors to direct aggregation induced emission to achieve stimuli-responsive luminogens, security inks and chemical warfare agent sensors.
Chemical communications (Cambridge, England), 2020, 56, 7633-7636
7126620 CIFC25 H17 NP 1 21/n 116.8262; 6.0687; 18.6754
90; 110.396; 90		1787.45Adil, Laxmi Raman; Iyer, Parameswar Krishnan
Effects of incorporating regioisomers and flexible rotors to direct aggregation induced emission to achieve stimuli-responsive luminogens, security inks and chemical warfare agent sensors.
Chemical communications (Cambridge, England), 2020, 56, 7633-7636
7126621 CIFC49 H65 Br N10 O7P 110.0071; 10.6965; 12.3292
90.333; 103.664; 108.641		1210.36Milbeo, Pierre; Simon, Matthieu; Didierjean, Claude; Wenger, Emmanuel; Aubert, Emmanuel; Martinez, Jean; Amblard, Muriel; Calmès, Monique; Legrand, Baptiste
A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas.
Chemical communications (Cambridge, England), 2020, 56, 7921-7924
7126622 CIFC81 H113 Br N19 O10P 4311.7593; 11.7593; 63.07
90; 90; 90		8721.4Milbeo, Pierre; Simon, Matthieu; Didierjean, Claude; Wenger, Emmanuel; Aubert, Emmanuel; Martinez, Jean; Amblard, Muriel; Calmès, Monique; Legrand, Baptiste
A bicyclic unit reversal to stabilize the 12/14-helix in mixed homochiral oligoureas.
Chemical communications (Cambridge, England), 2020, 56, 7921-7924
7126623 CIFC21 H25 B F N O3P -16.782; 9.955; 15.273
96.852; 91.313; 97.621		1014Su, Zhenni; Feng, Yunqiu; Zou, Rong; Qiu, Xianfan; Wang, Jian; Tao, Chuanzhou
Copper-catalyzed borylamidation of vinyl arenes with isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 7483-7486
7126624 CIFC27 H47 Au F6 N3 Sb Si3P 1 21/n 111.831; 21.434; 14.563
90; 98.575; 90		3652Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126625 CIFC21 H39 Au Cl Ge N3 Si2P 1 21/c 18.9235; 18.5223; 17.845
90; 101.332; 90		2892Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126626 CIFC33 H42 Au F6 N2 SbP 1 21/c 113.4432; 14.6762; 17.3789
90; 100.206; 90		3374.5Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126627 CIFC55 H75 Co O4 PP -112.132; 13.703; 17.467
112.033; 104.987; 92.737		2566Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126628 CIFC29 H51 Au F6 N3 Sb Si3P 1 21/c 122.214; 18.276; 18.686
90; 93.012; 90		7576Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126629 CIFC27 H46 Co N3 O Si3P -19.741; 17.157; 18.969
102.473; 91.56; 91.73		3092Parvin, Nasrina; Mishra, Bijoyananda; George, Anjana; Neralkar, Mahesh; Hossain, Jabed; Parameswaran, Pattiyil; Hotha, Srinivas; Khan, Shabana
N-Heterocyclic silylene/germylene ligands in Au(i) catalysis.
Chemical communications (Cambridge, England), 2020, 56, 7625-7628
7126630 CIFC50.5 H113 Ag21 Cl5 S12P 2 2 219.018; 19.679; 26.25
90; 90; 90		9824.2Chen, Tao; Yang, Sha; Song, Yongbo; Chai, Jinsong; Li, Qinzhen; Ma, Xiangyu; Li, Guang; Yu, Haizhu; Zhu, Manzhou
All-thiolate-stabilized Ag<sub>42</sub> nanocluster with a tetrahedral kernel and its transformation to an Ag<sub>61</sub> nanocluster with a bi-tetrahedral kernel.
Chemical communications (Cambridge, England), 2020, 56, 7605-7608
7126631 CIFC242 H444 Ag61 Cl5 S40P 21 21 2122.088; 39.696; 39.85
90; 90; 90		34941Chen, Tao; Yang, Sha; Song, Yongbo; Chai, Jinsong; Li, Qinzhen; Ma, Xiangyu; Li, Guang; Yu, Haizhu; Zhu, Manzhou
All-thiolate-stabilized Ag<sub>42</sub> nanocluster with a tetrahedral kernel and its transformation to an Ag<sub>61</sub> nanocluster with a bi-tetrahedral kernel.
Chemical communications (Cambridge, England), 2020, 56, 7605-7608
7126632 CIFC19 H15 N3 O2P -19.346; 12.963; 13.931
104.993; 99.436; 97.9		1579.3Liu, Lu; Li, Lei; Mao, Shukuan; Wang, Xin; Zhou, Ming-Dong; Zhao, Yu-Long; Wang, He
Synthesis of pyrazolo[1,5-c]quinazoline derivatives through the copper-catalyzed domino reaction of o-alkenyl aromatic isocyanides with diazo compounds.
Chemical communications (Cambridge, England), 2020, 56, 7665-7668
7126634 CIFC17 H39 Br F12 N6 P2P 21 21 217.9823; 13.9805; 24.662
90; 90; 90		2752.2Shircliff, Anthony D.; Burke, Benjamin P.; Davilla, Dustin J.; Burgess, Gwendolyn E.; Okorocha, Faith A.; Shrestha, Alina; Allbritton, Elisabeth M. A.; Nguyen, Phillip T.; Lamar, Rachael L.; Jones, Donald G.; Gorbet, Michael-Joseph; Allen, Michael B.; Eze, John I.; Fernandez, Andrea T.; Ramirez, Daniel; Archibald, Stephen J.; Prior, Timothy J.; Krause, Jeanette A.; Oliver, Allen G.; Hubin, Timothy J.
An ethylene cross-bridged pentaazamacrocycle and its Cu<sup>2+</sup> complex: constrained ligand topology and excellent kinetic stability.
Chemical communications (Cambridge, England), 2020, 56, 7519-7522
7126635 CIFC15 H33 Cl2 Cu N5 O1.79P 1 21/n 18.8067; 15.792; 14.03
90; 90.357; 90		1951.2Shircliff, Anthony D.; Burke, Benjamin P.; Davilla, Dustin J.; Burgess, Gwendolyn E.; Okorocha, Faith A.; Shrestha, Alina; Allbritton, Elisabeth M. A.; Nguyen, Phillip T.; Lamar, Rachael L.; Jones, Donald G.; Gorbet, Michael-Joseph; Allen, Michael B.; Eze, John I.; Fernandez, Andrea T.; Ramirez, Daniel; Archibald, Stephen J.; Prior, Timothy J.; Krause, Jeanette A.; Oliver, Allen G.; Hubin, Timothy J.
An ethylene cross-bridged pentaazamacrocycle and its Cu<sup>2+</sup> complex: constrained ligand topology and excellent kinetic stability.
Chemical communications (Cambridge, England), 2020, 56, 7519-7522
7126636 CIFC15.62 H35.5 I2 N5 O1.62C 1 2/c 116.5537; 18.04; 15.0137
90; 97.514; 90		4445Shircliff, Anthony D.; Burke, Benjamin P.; Davilla, Dustin J.; Burgess, Gwendolyn E.; Okorocha, Faith A.; Shrestha, Alina; Allbritton, Elisabeth M. A.; Nguyen, Phillip T.; Lamar, Rachael L.; Jones, Donald G.; Gorbet, Michael-Joseph; Allen, Michael B.; Eze, John I.; Fernandez, Andrea T.; Ramirez, Daniel; Archibald, Stephen J.; Prior, Timothy J.; Krause, Jeanette A.; Oliver, Allen G.; Hubin, Timothy J.
An ethylene cross-bridged pentaazamacrocycle and its Cu<sup>2+</sup> complex: constrained ligand topology and excellent kinetic stability.
Chemical communications (Cambridge, England), 2020, 56, 7519-7522
7126637 CIFC21 H15 F N2P -18.768; 9.173; 10.452
89.574; 84.573; 78.861		821.1Zhu, Zhongzhi; Lin, Hanze; Liang, Baihui; Huang, Junjie; Liang, Wanyi; Chen, Lu; Huang, Yubing; Chen, Xiuwen; Li, Yibiao
Copper-catalyzed [2+3]-annulation of N-H imines with vinyl azides: access to polyaryl 2H-imidazoles.
Chemical communications (Cambridge, England), 2020, 56, 5621-5624
7126638 CIFC60 H70 Au F6 N6 O6 PP -110.8241; 18.2147; 32.3647
102.209; 97.728; 104.498		5918.4Sen, Sajal; Perrin, Mark W.; Sedgwick, Adam C.; Dunsky, Evie Y.; Lynch, Vincent M.; He, Xiao-Peng; Sessler, Jonathan L.; Arambula, Jonathan F.
Toward multifunctional anticancer therapeutics: post-synthetic carbonate functionalisation of asymmetric Au(i) bis-N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2020, 56, 7877-7880
7126639 CIFC52 H60 Au F6 N4 O3 PP b c a16.4786; 22.1586; 27.4653
90; 90; 90		10028.8Sen, Sajal; Perrin, Mark W.; Sedgwick, Adam C.; Dunsky, Evie Y.; Lynch, Vincent M.; He, Xiao-Peng; Sessler, Jonathan L.; Arambula, Jonathan F.
Toward multifunctional anticancer therapeutics: post-synthetic carbonate functionalisation of asymmetric Au(i) bis-N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2020, 56, 7877-7880
7126640 CIFC50 H62 Au F6 N4 O3 PP 1 21/n 117.129; 14.925; 19.946
90; 107.13; 90		4873Sen, Sajal; Perrin, Mark W.; Sedgwick, Adam C.; Dunsky, Evie Y.; Lynch, Vincent M.; He, Xiao-Peng; Sessler, Jonathan L.; Arambula, Jonathan F.
Toward multifunctional anticancer therapeutics: post-synthetic carbonate functionalisation of asymmetric Au(i) bis-N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2020, 56, 7877-7880
7126641 CIFC18 H10 I N5P -18.547; 10.078; 10.245
92.009; 106.09; 100.898		829Zou, Long; Wang, Lei; Sun, Li; Xie, Xiaofei; Li, Pinhua
Photo-driven haloazidation cyclization of 1,5-enynes having cyano groups with TMSN<sub>3</sub> and NIS/NCS/NBS under metal-free conditions.
Chemical communications (Cambridge, England), 2020, 56, 7933-7936
7126642 CIFC71 H60 Cl6 Fe2 P4 Rh2P 1 21/c 113.1742; 26.8362; 18.2963
90; 90.747; 90		6468Barnett, Harrison J.; Hill, Anthony F.
Halogenation of A-frame μ-carbido complexes: a diamagnetic rhodium(ii) carbido complex.
Chemical communications (Cambridge, England), 2020, 56, 7738-7740
7126643 CIFC34.5 H28 Cl2 Fe P2 RhF d d d :213.1949; 31.055; 40.4621
90; 90; 90		16580.1Barnett, Harrison J.; Hill, Anthony F.
Halogenation of A-frame μ-carbido complexes: a diamagnetic rhodium(ii) carbido complex.
Chemical communications (Cambridge, England), 2020, 56, 7738-7740
7126644 CIFC26 H32 O6P -17.3978; 17.6152; 18.2995
98.202; 99.446; 90.544		2326.96Barnes, Timothy H.; Johnson, Kara F.; Gorden, John D.; Merner, Bradley L.
A macrocycle directed total synthesis of di-O-methylendiandrin A.
Chemical communications (Cambridge, England), 2020, 56, 8747-8749
7126645 CIFC61 H54 N4 O5 SC 1 2/c 141.915; 9.9907; 26.883
90; 116.974; 90		10032.9Denißen, Melanie; Hannen, Ricarda; Itskalov, Dana; Biesen, Lukas; Nirmalananthan-Budau, Nithiya; Hoffmann, Katrin; Reiss, Guido J.; Resch-Genger, Ute; Müller, Thomas J J
One-pot synthesis of a white-light emissive bichromophore operated by aggregation-induced dual emission (AIDE) and partial energy transfer.
Chemical communications (Cambridge, England), 2020, 56, 7407-7410
7126646 CIFC32 H32 Cl2 N2 O6P -110.6908; 11.1997; 14.8988
93.513; 110.671; 113.518		1487.3Dong, Kui; Jin, Xiao-Ling; Chen, Shihao; Wu, Li-Zhu; Liu, Qiang
Controllable synthesis of 2- and 3-aryl-benzomorpholines from 2-aminophenols and 4-vinylphenols.
Chemical communications (Cambridge, England), 2020, 56, 7941-7944
7126647 CIFC16 H16 Cl N O3P 1 21/c 18.5657; 9.2244; 19.2955
90; 100.946; 90		1496.87Dong, Kui; Jin, Xiao-Ling; Chen, Shihao; Wu, Li-Zhu; Liu, Qiang
Controllable synthesis of 2- and 3-aryl-benzomorpholines from 2-aminophenols and 4-vinylphenols.
Chemical communications (Cambridge, England), 2020, 56, 7941-7944
7126648 CIFC29 H46 B2 F8 N4 Ni O9 P4P -18.9718; 14.0281; 17.394
81.344; 82.327; 74.196		2072.54Hanf, Schirin; Grell, Toni; Waters, Jessica E.; García-Rodríguez, Raúl; Hey-Hawkins, Evamarie; Wright, Dominic S.
Facile synthesis of a nickel(0) phosphine complex at ambient temperature.
Chemical communications (Cambridge, England), 2020, 56, 7893-7896
7126649 CIFC64 H88 N36 Re4P 1 21/n 113.9432; 14.8675; 21.0174
90; 109.024; 90		4118.95Yanagisawa, Junichi; Hiraoka, Tomoaki; Kobayashi, Fumiya; Saito, Daisuke; Yoshida, Masaki; Kato, Masako; Takeiri, Fumitaka; Kobayashi, Genki; Ohba, Masaaki; Lindoy, Leonard F.; Ohtani, Ryo; Hayami, Shinya
Luminescent ionic liquid formed from a melted rhenium(v) cluster.
Chemical communications (Cambridge, England), 2020, 56, 7957-7960
7126650 CIFC64 H88 N36 Re4P 1 21/c 113.7177; 14.6965; 20.9142
90; 108.894; 90		3989.17Yanagisawa, Junichi; Hiraoka, Tomoaki; Kobayashi, Fumiya; Saito, Daisuke; Yoshida, Masaki; Kato, Masako; Takeiri, Fumitaka; Kobayashi, Genki; Ohba, Masaaki; Lindoy, Leonard F.; Ohtani, Ryo; Hayami, Shinya
Luminescent ionic liquid formed from a melted rhenium(v) cluster.
Chemical communications (Cambridge, England), 2020, 56, 7957-7960
7126651 CIFC64 H84 N36 O4 Re4P 1 21/c 114.0768; 14.8467; 20.953
90; 109.516; 90		4127.5Yanagisawa, Junichi; Hiraoka, Tomoaki; Kobayashi, Fumiya; Saito, Daisuke; Yoshida, Masaki; Kato, Masako; Takeiri, Fumitaka; Kobayashi, Genki; Ohba, Masaaki; Lindoy, Leonard F.; Ohtani, Ryo; Hayami, Shinya
Luminescent ionic liquid formed from a melted rhenium(v) cluster.
Chemical communications (Cambridge, England), 2020, 56, 7957-7960
7126652 CIFC7 H13 Cl F N O4 S2P 1 21/c 114.829; 5.526; 18.143
90; 127.47; 90		1180Li, Chen; Zheng, Yujie; Rakesh, K. P.; Qin, Hua-Li
But-3-ene-1,3-disulfonyl difluoride (BDF): a highly selective SuFEx clickable hub for the quick assembly of sultam-containing aliphatic sulfonyl fluorides.
Chemical communications (Cambridge, England), 2020, 56, 8075-8078
7126653 CIFC8 H16 F N O4 S2P 1 21/c 112.6609; 10.4865; 9.8417
90; 97.188; 90		1296.4Li, Chen; Zheng, Yujie; Rakesh, K. P.; Qin, Hua-Li
But-3-ene-1,3-disulfonyl difluoride (BDF): a highly selective SuFEx clickable hub for the quick assembly of sultam-containing aliphatic sulfonyl fluorides.
Chemical communications (Cambridge, England), 2020, 56, 8075-8078
7126654 CIFC12 H15 F N2 O5 S2P 1 21/c 114.0641; 9.2583; 12.1126
90; 102.973; 90		1536.9Li, Chen; Zheng, Yujie; Rakesh, K. P.; Qin, Hua-Li
But-3-ene-1,3-disulfonyl difluoride (BDF): a highly selective SuFEx clickable hub for the quick assembly of sultam-containing aliphatic sulfonyl fluorides.
Chemical communications (Cambridge, England), 2020, 56, 8075-8078
7126655 CIFC20 H36 F3 N3 O3 SP 1 21/n 111.5596; 16.1768; 12.4775
90; 95.002; 90		2324.4Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126656 CIFC20 H37 N3P 1 21/c 115.1826; 8.4655; 16.3019
90; 108.622; 90		1985.6Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126657 CIFC21 H35 F6 N3 O6 S2P 1 21/n 117.893; 8.3124; 19.3921
90; 107.751; 90		2746.94Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126658 CIFC9 H15 F3 N2 O3 SP n m a8.571; 6.972; 21.017
90; 90; 90		1255.9Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126659 CIFC36 H58 F12 N6 O12 S4P -18.2515; 15.1873; 20.33
81.547; 87.795; 80.681		2486.5Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126660 CIFC29 H46 F3 N3 O3 SP 21 21 217.4452; 18.8437; 21.3251
90; 90; 90		2991.8Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126661 CIFC20 H34 F3 N3 O3 SP 1 21/n 19.3281; 23.912; 11.1067
90; 111.055; 90		2312Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126662 CIFC21 H38 F3 N3 O3 SP 1 21/n 18.4819; 26.6123; 11.1305
90; 104.586; 90		2431.44Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126663 CIFC30 H45 F6 N3 O6 S2P 1 21/n 111.4405; 19.999; 16.0796
90; 107.195; 90		3514.6Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126664 CIFC28 H45 N3P -19.409; 10.8582; 13.6751
73.417; 88.835; 73.82		1283.31Mandal, Debdeep; Stein, Felix; Chandra, Shubhadeep; Neuman, Nicolás I; Sarkar, Pallavi; Das, Shubhajit; Kundu, Abhinanda; Sarkar, Arighna; Rawat, Hemant; Pati, Swapan K.; Chandrasekhar, Vadapalli; Sarkar, Biprajit; Jana, Anukul
Trisubstituted geminal diazaalkene derived transient 1,2-carbodications.
Chemical communications (Cambridge, England), 2020, 56, 8233-8236
7126665 CIFC39 H34 N2 O8 S2P -112.537; 13.807; 13.921
115.493; 98.531; 104.79		2009Tang, Bu-Zheng; Hao, Wen-Juan; Li, Jia-Zhuo; Zhu, Shan-Shan; Tu, Shu-Jiang; Jiang, Bo
Stereoselective synthesis of fully substituted ethylenes via an Ag-catalyzed 1,6-nucleophilic addition/annulation cascade.
Chemical communications (Cambridge, England), 2020, 56, 7749-7752
7126666 CIFC141 H119 B2 Cl9 F48 N2 O23P -120.123; 20.4221; 21.1299
81.209; 76.368; 72.895		8032.9Sakata, Yoko; Ogura, Takaya; Akine, Shigehisa
Efficient formation of [3]pseudorotaxane based on cooperative complexation of dibenzo-24-crown-8 with diphenylviologen axle.
Chemical communications (Cambridge, England), 2020, 56, 8735-8738
7126667 CIFC13 H14.5 N3.5 O4 SI b a 229.306; 9.4752; 11.4635
90; 90; 90		3183.2Mishra, Debashish; Borah, Arun Jyoti; Phukan, Pinakinee; Hazarika, Debojit; Phukan, Prodeep
Unprecedented 1,3-tert-butyl migration via the C-N single bond scission of isonitrile: an expedient metal-free route to N-sulfonyl amidines.
Chemical communications (Cambridge, England), 2020, 56, 8408-8411
7126668 CIFC12 H12 F4 I2 N2C 1 2/c 18.4114; 11.119; 17.6646
90; 103.661; 90		1605.37Arhangelskis, Mihails; Topić, Filip; Hindle, Poppy; Tran, Ricky; Morris, Andrew J.; Cinčić, Dominik; Friščić, Tomislav
Mechanochemical reactions of cocrystals: comparing theory with experiment in the making and breaking of halogen bonds in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 8293-8296
7126669 CIFC18 H12 F8 I4 N2P -17.5107; 12.8506; 13.4853
94.235; 102.514; 102.883		1228.41Arhangelskis, Mihails; Topić, Filip; Hindle, Poppy; Tran, Ricky; Morris, Andrew J.; Cinčić, Dominik; Friščić, Tomislav
Mechanochemical reactions of cocrystals: comparing theory with experiment in the making and breaking of halogen bonds in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 8293-8296
7126670 CIFC18 H24 F4 I2 N4P 21 21 216.5273; 17.4784; 19.2084
90; 90; 90		2191.4Arhangelskis, Mihails; Topić, Filip; Hindle, Poppy; Tran, Ricky; Morris, Andrew J.; Cinčić, Dominik; Friščić, Tomislav
Mechanochemical reactions of cocrystals: comparing theory with experiment in the making and breaking of halogen bonds in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 8293-8296
7126671 CIFC12 H12 F4 I2 N2P -16.7231; 14.097; 17.5147
76.882; 80.884; 78.615		1573.6Arhangelskis, Mihails; Topić, Filip; Hindle, Poppy; Tran, Ricky; Morris, Andrew J.; Cinčić, Dominik; Friščić, Tomislav
Mechanochemical reactions of cocrystals: comparing theory with experiment in the making and breaking of halogen bonds in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 8293-8296
7126672 CIFC18 H15 N3P -18.0685; 8.5074; 10.8878
93.111; 96.047; 91.869		741.55Bao, Wen; Gao, Zhu-Peng; Jin, Da-Ping; Xue, Cao-Gen; Liang, Huan; Lei, Ling-Sheng; Xu, Xue-Tao; Zhang, Kun; Wang, Shao-Hua
Direct synthesis of 2-substituted benzonitriles via alkylcyanation of arynes with N,N-disubstituted aminomalononitriles.
Chemical communications (Cambridge, England), 2020, 56, 7641-7644
7126673 CIFC17 H13 N3P 1 21/n 18.4918; 10.0409; 16.7446
90; 100.191; 90		1405.21Bao, Wen; Gao, Zhu-Peng; Jin, Da-Ping; Xue, Cao-Gen; Liang, Huan; Lei, Ling-Sheng; Xu, Xue-Tao; Zhang, Kun; Wang, Shao-Hua
Direct synthesis of 2-substituted benzonitriles via alkylcyanation of arynes with N,N-disubstituted aminomalononitriles.
Chemical communications (Cambridge, England), 2020, 56, 7641-7644
7126674 CIFC18 H15 N3P 1 21/c 18.271; 9.9844; 18.3806
90; 102.74; 90		1480.52Bao, Wen; Gao, Zhu-Peng; Jin, Da-Ping; Xue, Cao-Gen; Liang, Huan; Lei, Ling-Sheng; Xu, Xue-Tao; Zhang, Kun; Wang, Shao-Hua
Direct synthesis of 2-substituted benzonitriles via alkylcyanation of arynes with N,N-disubstituted aminomalononitriles.
Chemical communications (Cambridge, England), 2020, 56, 7641-7644
7126675 CIFC18 H15 N3 OP 1 21/c 19.278; 23.2807; 7.4089
90; 102.52; 90		1562.26Bao, Wen; Gao, Zhu-Peng; Jin, Da-Ping; Xue, Cao-Gen; Liang, Huan; Lei, Ling-Sheng; Xu, Xue-Tao; Zhang, Kun; Wang, Shao-Hua
Direct synthesis of 2-substituted benzonitriles via alkylcyanation of arynes with N,N-disubstituted aminomalononitriles.
Chemical communications (Cambridge, England), 2020, 56, 7641-7644
7126676 CIFC37 H73 Mo2P -19.4411; 9.816; 22.436
97.004; 91.791; 113.348		1887.5Ohki, Yasuhiro; Ishihara, Kodai; Yaoi, Moeko; Tada, Mizuki; Sameera, W. M. C.; Cramer, Roger E.
A dinuclear Mo<sub>2</sub>H<sub>8</sub> complex supported by bulky C<sub>5</sub>H<sub>2</sub><sup>t</sup>Bu<sub>3</sub> ligands.
Chemical communications (Cambridge, England), 2020, 56, 8035-8038
7126677 CIFC17 H29 Cl4 MoP 1 21/c 18.443; 26.099; 9.924
90; 113.425; 90		2006.6Ohki, Yasuhiro; Ishihara, Kodai; Yaoi, Moeko; Tada, Mizuki; Sameera, W. M. C.; Cramer, Roger E.
A dinuclear Mo<sub>2</sub>H<sub>8</sub> complex supported by bulky C<sub>5</sub>H<sub>2</sub><sup>t</sup>Bu<sub>3</sub> ligands.
Chemical communications (Cambridge, England), 2020, 56, 8035-8038
7126678 CIFC24 H43 K O6.5P 1 21/n 19.704; 15.687; 17.654
90; 97.336; 90		2665.4Ohki, Yasuhiro; Ishihara, Kodai; Yaoi, Moeko; Tada, Mizuki; Sameera, W. M. C.; Cramer, Roger E.
A dinuclear Mo<sub>2</sub>H<sub>8</sub> complex supported by bulky C<sub>5</sub>H<sub>2</sub><sup>t</sup>Bu<sub>3</sub> ligands.
Chemical communications (Cambridge, England), 2020, 56, 8035-8038
7126679 CIFC47 H78 K Mo2 O8P -110.038; 13.927; 18.546
99.992; 105.254; 94.41		2442.9Ohki, Yasuhiro; Ishihara, Kodai; Yaoi, Moeko; Tada, Mizuki; Sameera, W. M. C.; Cramer, Roger E.
A dinuclear Mo<sub>2</sub>H<sub>8</sub> complex supported by bulky C<sub>5</sub>H<sub>2</sub><sup>t</sup>Bu<sub>3</sub> ligands.
Chemical communications (Cambridge, England), 2020, 56, 8035-8038
7126680 CIFC40 H64 Mo2C 1 c 121.34; 19.875; 19.984
90; 119.218; 90		7397Ohki, Yasuhiro; Ishihara, Kodai; Yaoi, Moeko; Tada, Mizuki; Sameera, W. M. C.; Cramer, Roger E.
A dinuclear Mo<sub>2</sub>H<sub>8</sub> complex supported by bulky C<sub>5</sub>H<sub>2</sub><sup>t</sup>Bu<sub>3</sub> ligands.
Chemical communications (Cambridge, England), 2020, 56, 8035-8038
7126681 CIFC30 H26 O9 Si2P -19.1221; 10.3996; 24.2182
83.396; 80.039; 79.81		2218.7Delmas, Luke C.; White, Andrew J. P.; Pugh, David; Evans, Arwyn; Isbell, Mark Antonin; Heng, Jerry Y. Y.; Lickiss, Paul D.; Davies, Robert P.
Stable metal-organic frameworks with low water affinity built from methyl-siloxane linkers.
Chemical communications (Cambridge, England), 2020, 56, 7905-7908
7126682 CIFC25.5 H35.5 N3.5 O10 Si Zr1.5I b a m17.2986; 30.7451; 27.021
90; 90; 90		14371Delmas, Luke C.; White, Andrew J. P.; Pugh, David; Evans, Arwyn; Isbell, Mark Antonin; Heng, Jerry Y. Y.; Lickiss, Paul D.; Davies, Robert P.
Stable metal-organic frameworks with low water affinity built from methyl-siloxane linkers.
Chemical communications (Cambridge, England), 2020, 56, 7905-7908
7126683 CIFC24 H32 Hf1.5 N3 O9.5 SiI b a m17.2191; 30.6244; 27.1584
90; 90; 90		14321.3Delmas, Luke C.; White, Andrew J. P.; Pugh, David; Evans, Arwyn; Isbell, Mark Antonin; Heng, Jerry Y. Y.; Lickiss, Paul D.; Davies, Robert P.
Stable metal-organic frameworks with low water affinity built from methyl-siloxane linkers.
Chemical communications (Cambridge, England), 2020, 56, 7905-7908
7126684 CIFC25 H19 N O5 SP -19.2626; 10.0278; 12.623
77.431; 89.378; 73.685		1096.71Cheng, Bin; Zhang, Xinping; Li, Yuntong; Li, Hui; He, Yixuan; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of indolizines from pyridinium 1,4-zwitterionic thiolates and α-functionalized bromoalkanes via a stepwise [(5+1)-1] pathway.
Chemical communications (Cambridge, England), 2020, 56, 8396-8399
7126685 CIFC56 H66 CoC 1 2/c 117.579; 14.548; 17.555
90; 92.35; 90		4486Blundell, Toby J.; Taylor, Laurence J.; Valentine, Andrew J.; Lewis, William; Blake, Alexander J.; McMaster, Jonathan; Kays, Deborah L.
A transition metal-gallium cluster formed via insertion of "GaI".
Chemical communications (Cambridge, England), 2020, 56, 8139-8142
7126686 CIFC62 H66 D6 Ga2 I4P 1 21/n 112.2172; 30.7592; 16.4155
90; 109.962; 90		5798.18Blundell, Toby J.; Taylor, Laurence J.; Valentine, Andrew J.; Lewis, William; Blake, Alexander J.; McMaster, Jonathan; Kays, Deborah L.
A transition metal-gallium cluster formed via insertion of "GaI".
Chemical communications (Cambridge, England), 2020, 56, 8139-8142
7126687 CIFC56 H66 Ga IP 1 21/n 115.1817; 17.9327; 16.9613
90; 91.9796; 90		4614.94Blundell, Toby J.; Taylor, Laurence J.; Valentine, Andrew J.; Lewis, William; Blake, Alexander J.; McMaster, Jonathan; Kays, Deborah L.
A transition metal-gallium cluster formed via insertion of "GaI".
Chemical communications (Cambridge, England), 2020, 56, 8139-8142
7126688 CIFC28 H33 Co Ga3 I5P b c a16.6877; 17.7466; 24.3929
90; 90; 90		7224Blundell, Toby J.; Taylor, Laurence J.; Valentine, Andrew J.; Lewis, William; Blake, Alexander J.; McMaster, Jonathan; Kays, Deborah L.
A transition metal-gallium cluster formed via insertion of "GaI".
Chemical communications (Cambridge, England), 2020, 56, 8139-8142
7126689 CIFC32 H41 Co Ga4 I8 OP 1 21/c 120.1625; 13.8708; 17.0402
90; 101.025; 90		4677.7Blundell, Toby J.; Taylor, Laurence J.; Valentine, Andrew J.; Lewis, William; Blake, Alexander J.; McMaster, Jonathan; Kays, Deborah L.
A transition metal-gallium cluster formed via insertion of "GaI".
Chemical communications (Cambridge, England), 2020, 56, 8139-8142
7126690 CIFC52 H32 Cl2 Ir N3 O S2P -110.9146; 12.9032; 14.947
91.818; 106.55; 94.174		2009.4Lai, Po-Ni; Yoon, Sungwon; Teets, Thomas S.
Efficient near-infrared luminescence from bis-cyclometalated iridium(iii) complexes with rigid quinoline-derived ancillary ligands.
Chemical communications (Cambridge, England), 2020, 56, 8754-8757
7126691 CIFC52 H30 Ir N3 O2 S2P 1 21/c 111.6553; 17.7049; 21.3456
90; 98.312; 90		4358.5Lai, Po-Ni; Yoon, Sungwon; Teets, Thomas S.
Efficient near-infrared luminescence from bis-cyclometalated iridium(iii) complexes with rigid quinoline-derived ancillary ligands.
Chemical communications (Cambridge, England), 2020, 56, 8754-8757
7126692 CIFC18 H13 Br F3 N3P 1 21/n 123.678; 11.5222; 26.8116
90; 113.661; 90		6699.9Li, Deng-Yuan; Chen, Jia-Yan; Feng, Da-Fu; Chen, Shuang; Xu, Xian-Kuan; Dang, Li; Liu, Pei-Nian
Construction of multiple bonds via a domino reaction of trifluoroacetimidoyl nitriles with in situ generated bis-nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 8222-8225
7126693 CIFC40 H23 Li2 N5 O18 Zn2C 1 2/c 118.477; 17.976; 17.533
90; 117.21; 90		5179Sapianik, Aleksandr A.; Kovalenko, Konstantin A.; Samsonenko, Denis G.; Barsukova, Marina O.; Dybtsev, Danil N.; Fedin, Vladimir P.
Exceptionally effective benzene/cyclohexane separation using a nitro-decorated metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 8241-8244
7126694 CIFC12 H12 I N3 OP -14.1678; 10.6544; 14.6694
73.012; 84.892; 78.774		610.7Leggott, Abbie; Clarke, Justin E.; Chow, Shiao; Warriner, Stuart L.; O'Neill, Alex J; Nelson, Adam
Activity-directed expansion of a series of antibacterial agents.
Chemical communications (Cambridge, England), 2020, 56, 8047-8050
7126695 CIFC42 H49 Cl N2 P2C 1 2/c 123.6941; 10.0307; 15.1078
90; 93.655; 90		3583.34Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126696 CIFC35 H40 Cl3 In N2 P2P 1 21/c 110.2163; 32.6718; 10.7854
90; 108.952; 90		3404.9Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126697 CIFC35 H40 N2 P2C 1 2/c 115.26; 9.5382; 20.529
90; 94.766; 90		2977.7Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126698 CIFC35 H40 Cl3 Ga N2 P2P 1 21/n 110.22942; 18.88; 17.9216
90; 104.045; 90		3357.76Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126699 CIFC35 H40 Cl2 N2 P2 ZnP 1 21/n 110.1005; 18.2003; 18.2051
90; 96.883; 90		3322.56Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126700 CIFC41 H47 N2 O3 P2 RhP -114.0618; 16.9278; 19.7394
88.863; 89.772; 77.86		4592.69Kroll, Alexander; Steinert, Henning; Scharf, Lennart T.; Scherpf, Thorsten; Mallick, Bert; Gessner, Viktoria H.
A diamino-substituted carbodiphosphorane as strong C-donor and weak N-donor: isolation of monomeric trigonal-planar L·ZnCl<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8051-8054
7126701 CIFC36 H29 F12 N5 O2 Os P2P 21 21 219.2495; 10.7934; 35.831
90; 90; 90		3577.1Wang, Guanghui; Zhou, Zijun; Shen, Xiang; Ivlev, Sergei; Meggers, Eric
Asymmetric catalysis with a chiral-at-osmium complex.
Chemical communications (Cambridge, England), 2020, 56, 7714-7717
7126702 CIFC29 H23 F12 N5 O Os P2P 114.2056; 15.5349; 16.0807
70.816; 78.674; 76.497		3231.2Wang, Guanghui; Zhou, Zijun; Shen, Xiang; Ivlev, Sergei; Meggers, Eric
Asymmetric catalysis with a chiral-at-osmium complex.
Chemical communications (Cambridge, England), 2020, 56, 7714-7717
7126703 CIFC29 H27 Cl Fe2 N3 O2P 1 21/n 111.2073; 9.594; 11.9682
90; 98.963; 90		1271.1Sarkar, Tukki; Bhattacharyya, Arnab; Banerjee, Samya; Hussain, Akhtar
LMCT transition-based red-light photochemotherapy using a tumour-selective ferrocenyl iron(iii) coumarin conjugate.
Chemical communications (Cambridge, England), 2020, 56, 7981-7984
7126704 CIFC183 H285 Br6 Cl3 O20P 21 21 2124.6057; 25.5361; 29.3687
90; 90; 90		18453.3Nagata, Yuuya; Suzuki, Misaki; Shimada, Yasuo; Sengoku, Hiroki; Nishida, Shungo; Kakuta, Takahiro; Yamagishi, Tada-Aki; Suginome, Michinori; Ogoshi, Tomoki
Holding of planar chirality of pillar[5]arene by kinetic trapping using host-guest interactions with achiral guest solvents.
Chemical communications (Cambridge, England), 2020, 56, 8424-8427
7126705 CIFC86 H132 Cl2 O10P 21 21 2115.581; 22.162; 23.828
90; 90; 90		8228Nagata, Yuuya; Suzuki, Misaki; Shimada, Yasuo; Sengoku, Hiroki; Nishida, Shungo; Kakuta, Takahiro; Yamagishi, Tada-Aki; Suginome, Michinori; Ogoshi, Tomoki
Holding of planar chirality of pillar[5]arene by kinetic trapping using host-guest interactions with achiral guest solvents.
Chemical communications (Cambridge, England), 2020, 56, 8424-8427
7126706 CIFH8 O8 S16 Sn10F d -3 m :274.1412; 74.1412; 74.1412
90; 90; 90		407548Luo, Ming-Bu; Huang, Shan-Lin; Lai, Heng-Dong; Zhang, Jian; Lin, Qipu
Tin-oxychalcogenide supertetrahedral clusters maintained in a MTN zeolite-analog arrangement by coulombic interactions.
Chemical communications (Cambridge, England), 2020, 56, 8388-8391
7126707 CIFC12 H16 N6 O8P -19.3092; 9.8441; 10.1956
63.563; 71.551; 73.22		781.5Zhou, Bo; Zhao, Qihang; Tang, Longchang; Yan, Dongpeng
Tunable room temperature phosphorescence and energy transfer in ratiometric co-crystals.
Chemical communications (Cambridge, England), 2020, 56, 7698-7701
7126708 CIFC12 H16 N6 O8P -19.4813; 11.8746; 14.6779
72.186; 82.829; 81.819		1551.5Zhou, Bo; Zhao, Qihang; Tang, Longchang; Yan, Dongpeng
Tunable room temperature phosphorescence and energy transfer in ratiometric co-crystals.
Chemical communications (Cambridge, England), 2020, 56, 7698-7701
7126709 CIFC25 H34 Cl N O Si2P -18.8523; 9.551; 16.927
81.918; 78.36; 64.955		1267.5Ji, Xiaoming; Wei, Feng; Wan, Bin; Cheng, Cang; Zhang, Yanghui
Palladium-catalyzed intermolecular C-H silylation initiated by aminopalladation.
Chemical communications (Cambridge, England), 2020, 56, 7801-7804
7126710 CIFC16 H12 O3P -15.865; 14.967; 14.978
72.081; 82.356; 84.576		1237.9An, Juzeng; Pedrazzani, Riccardo; Monari, Magda; Marin-Luna, Marta; Lopez, Carlos Silva; Bandini, Marco
Site-selective synthesis of 1,3-dioxin-3-ones via a gold(i) catalyzed cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 7734-7737
7126711 CIFC31.5 H43 Co OC 1 2/c 119.276; 15.481; 20.6
90; 101.414; 90		6026Grass, Amanda; Bellow, James A.; Morrison, Gregory; Zur Loye, Hans-Conrad; Lord, Richard L.; Groysman, Stanislav
One electron reduction transforms high-valent low-spin cobalt alkylidene into high-spin cobalt(ii) carbene radical.
Chemical communications (Cambridge, England), 2020, 56, 8416-8419
7126712 CIFC63 H86 Co2 O2P -112.0917; 13.2206; 18.3083
83.843; 74.551; 73.23		2699.6Grass, Amanda; Bellow, James A.; Morrison, Gregory; Zur Loye, Hans-Conrad; Lord, Richard L.; Groysman, Stanislav
One electron reduction transforms high-valent low-spin cobalt alkylidene into high-spin cobalt(ii) carbene radical.
Chemical communications (Cambridge, England), 2020, 56, 8416-8419
7126713 CIFC42 H48 Co NP b c n14.6058; 14.6784; 30.7441
90; 90; 90		6591.2Grass, Amanda; Bellow, James A.; Morrison, Gregory; Zur Loye, Hans-Conrad; Lord, Richard L.; Groysman, Stanislav
One electron reduction transforms high-valent low-spin cobalt alkylidene into high-spin cobalt(ii) carbene radical.
Chemical communications (Cambridge, England), 2020, 56, 8416-8419
7126714 CIFC72 H72 Co2 N8P -112.0255; 13.8796; 21.0959
98.389; 99.02; 113.189		3111.9Grass, Amanda; Bellow, James A.; Morrison, Gregory; Zur Loye, Hans-Conrad; Lord, Richard L.; Groysman, Stanislav
One electron reduction transforms high-valent low-spin cobalt alkylidene into high-spin cobalt(ii) carbene radical.
Chemical communications (Cambridge, England), 2020, 56, 8416-8419
7126715 CIFC40 H66 N4 O25P -110.9214; 10.9343; 20.6594
98.174; 90.822; 102.662		2380Kravets, Mykola; Sobczak, Grzegorz; Rad, Nazar; Misztalewska-Turkowicz, Iwona; Danylyuk, Oksana; Sashuk, Volodymyr
Visual discrimination of aromatic acid substitution patterns by supramolecular nanocooperativity.
Chemical communications (Cambridge, England), 2020, 56, 8595-8598
7126716 CIFC24 H20 N2 O4P -17.6587; 11.0602; 12.3929
87.763; 74.272; 87.728		1009.23Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126717 CIFC14 H16 B N2 O2.25P n m a26.6432; 6.8628; 7.9989
90; 90; 90		1462.57Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126718 CIFC118.5 H84 F48 Mg N8 O3.5P -19.3959; 15.9579; 19.8503
104.367; 101.254; 97.571		2776.5Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126719 CIFC36 H44 N2P -18.953; 11.442; 15.907
105.674; 90.147; 102.422		1529Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126720 CIFC288 H354 N16 O Zn2P -119.5182; 19.5876; 22.5521
99.467; 111.596; 95.906		7781Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126721 CIFC20 H26 B2 N2 O4P 1 21/c 113.6361; 11.8505; 13.0118
90; 92.2; 90		2101.1Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126722 CIFC27 H15 F12 N2C 1 2/c 126.32; 8.4133; 22.4036
90; 95.7836; 90		4935.8Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126723 CIFC129 H65 F48 N14.6 O0.5 ZnP -19.8387; 15.9659; 19.707
104.067; 102.217; 94.6532		2906Mulholland, Katie D.; Yoon, Sangbin; Rennie, Christopher C.; Sitch, Eleanor K.; McKay, Alasdair I.; Edkins, Katharina; Edkins, Robert M.
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C<sub>4h</sub> octaarylphthalocyanines.
Chemical communications (Cambridge, England), 2020, 56, 8452-8455
7126724 CIFC24 H26 N2 O4P -19.6454; 10.4111; 11.3573
75.236; 81.627; 67.452		1017.07Wu, Lingang; Hao, Yanan; Liu, Yuxiu; Song, Haibin; Wang, Qingmin
Visible-light-induced dearomative oxamination of indole derivatives and dearomative amidation of phenol derivatives.
Chemical communications (Cambridge, England), 2020, 56, 8436-8439
7126725 CIFC76 H44 Cu4 N4 O17I 4/m12.121; 12.121; 23.73
90; 90; 90		3486.4Taggart, Garrett A.; Lorzing, Gregory R.; Dworzak, Michael R.; Yap, Glenn P. A.; Bloch, Eric D.
Synthesis and characterization of low-nuclearity lantern-type porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 8924-8927
7126726 CIFC84 H56 Cr4 O19I 4/m12.989; 12.989; 23.881
90; 90; 90		4029.1Taggart, Garrett A.; Lorzing, Gregory R.; Dworzak, Michael R.; Yap, Glenn P. A.; Bloch, Eric D.
Synthesis and characterization of low-nuclearity lantern-type porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 8924-8927
7126727 CIFC90 H70 Cu4 N2 O19I 4/m12.859; 12.859; 23.9559
90; 90; 90		3961.2Taggart, Garrett A.; Lorzing, Gregory R.; Dworzak, Michael R.; Yap, Glenn P. A.; Bloch, Eric D.
Synthesis and characterization of low-nuclearity lantern-type porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 8924-8927
7126728 CIFC170 H112 Cl Mo8 O35C 1 2/m 112.8297; 26.2957; 27.2919
90; 101.794; 90		9013Taggart, Garrett A.; Lorzing, Gregory R.; Dworzak, Michael R.; Yap, Glenn P. A.; Bloch, Eric D.
Synthesis and characterization of low-nuclearity lantern-type porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 8924-8927
7126729 CIFC24 H16 F3 N O2P 1 21/n 115.0044; 8.2203; 19.4734
90; 108.91; 90		2272.2Yuan, Hairui; Du, Yuanbo; Liu, Fengting; Guo, Lirong; Sun, Qianyu; Feng, Lei; Gao, Hongyin
Tandem approach to NOBIN analogues from arylhydroxylamines and diaryliodonium salts via [3,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 8226-8229
7126730 CIFC23 H15 Br2 N O2P 21 21 218.9805; 11.7542; 18.4054
90; 90; 90		1942.85Yuan, Hairui; Du, Yuanbo; Liu, Fengting; Guo, Lirong; Sun, Qianyu; Feng, Lei; Gao, Hongyin
Tandem approach to NOBIN analogues from arylhydroxylamines and diaryliodonium salts via [3,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 8226-8229
7126731 CIFC216 H131.2 Ag24 O53.6I 1 2/a 134.285; 5.934; 39.22
90; 104.56; 90		7723Kim, Dongwook; Seong, Junmo; Han, Seungwan; Baek, Seung Bin; Lah, Myoung Soo
Pore space partition of a fragile Ag(i)-carboxylate framework via post-synthetic linker insertion.
Chemical communications (Cambridge, England), 2020, 56, 8615-8618
7126732 CIFC279.89 H171.11 Ag24 N12.78 O48I 1 2/a 133.95; 6.002; 39.546
90; 105.22; 90		7776Kim, Dongwook; Seong, Junmo; Han, Seungwan; Baek, Seung Bin; Lah, Myoung Soo
Pore space partition of a fragile Ag(i)-carboxylate framework via post-synthetic linker insertion.
Chemical communications (Cambridge, England), 2020, 56, 8615-8618
7126733 CIFC252.21 H144.14 Ag24 N6.04 O48I 1 2 134.592; 6.257; 35.505
90; 107.21; 90		7341Kim, Dongwook; Seong, Junmo; Han, Seungwan; Baek, Seung Bin; Lah, Myoung Soo
Pore space partition of a fragile Ag(i)-carboxylate framework via post-synthetic linker insertion.
Chemical communications (Cambridge, England), 2020, 56, 8615-8618
7126734 CIFC251.75 H143.83 Ag24 N17.87 O48P 1 21/c 134.512; 5.9589; 38.939
90; 104.48; 90		7754Kim, Dongwook; Seong, Junmo; Han, Seungwan; Baek, Seung Bin; Lah, Myoung Soo
Pore space partition of a fragile Ag(i)-carboxylate framework via post-synthetic linker insertion.
Chemical communications (Cambridge, England), 2020, 56, 8615-8618
7126735 CIFC42 H40 Fe N2 O P2C 1 2 115.4937; 9.734; 12.9942
90; 119.954; 90		1698Hatzis, Gregory P.; Thomas, Christine M.
Metal-ligand cooperativity across two sites of a square planar iron(ii) complex ligated by a tetradentate PNNP ligand.
Chemical communications (Cambridge, England), 2020, 56, 8611-8614
7126736 CIFC38 H38 B2 Fe N2 P2P -114.1841; 14.9374; 23.6074
104.204; 92.996; 105.812		4627.2Hatzis, Gregory P.; Thomas, Christine M.
Metal-ligand cooperativity across two sites of a square planar iron(ii) complex ligated by a tetradentate PNNP ligand.
Chemical communications (Cambridge, England), 2020, 56, 8611-8614
7126737 CIFC50 H58 B2 Fe N2 O4 P2P -111.7019; 14.3131; 19.1169
83.392; 73.967; 72.76		2937.2Hatzis, Gregory P.; Thomas, Christine M.
Metal-ligand cooperativity across two sites of a square planar iron(ii) complex ligated by a tetradentate PNNP ligand.
Chemical communications (Cambridge, England), 2020, 56, 8611-8614
7126738 CIFC47 H47 Fe N2 P3P 1 c 117.3592; 16.4666; 14.4482
90; 106.046; 90		3969.1Hatzis, Gregory P.; Thomas, Christine M.
Metal-ligand cooperativity across two sites of a square planar iron(ii) complex ligated by a tetradentate PNNP ligand.
Chemical communications (Cambridge, England), 2020, 56, 8611-8614
7126739 CIFBe4 Cs4 Li O24 P7P 2 2 2113.0892; 13.0889; 13.2528
90; 90; 90		2270.51Chen, Yi-Gang; Yang, Chunyu; Wang, Fang; Guo, Yao; Jiang, Xingxing; Zhang, Xian-Ming
M<sub>4</sub>LiBe<sub>4</sub>P<sub>7</sub>O<sub>24</sub> and M<sub>4</sub>Li(Li<sub>3</sub>P)P<sub>7</sub>O<sub>24</sub> (M = Cs, Rb): deep-ultraviolet nonlinear-optical phosphates with a tetrahedra-substituted paracelsian-like framework.
Chemical communications (Cambridge, England), 2020, 56, 8639-8642
7126740 CIFBe4 Li O24 P7 Rb4P 2 2 2112.8805; 12.9118; 12.9447
90; 90; 90		2152.84Chen, Yi-Gang; Yang, Chunyu; Wang, Fang; Guo, Yao; Jiang, Xingxing; Zhang, Xian-Ming
M<sub>4</sub>LiBe<sub>4</sub>P<sub>7</sub>O<sub>24</sub> and M<sub>4</sub>Li(Li<sub>3</sub>P)P<sub>7</sub>O<sub>24</sub> (M = Cs, Rb): deep-ultraviolet nonlinear-optical phosphates with a tetrahedra-substituted paracelsian-like framework.
Chemical communications (Cambridge, England), 2020, 56, 8639-8642
7126741 CIFC21 H28 Ag F6 N4 PP -110.4171; 10.7634; 11.4213
100.44; 108.085; 94.085		1185.99Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126742 CIFC14 H20 Ag F6 N4 PP -18.6651; 10.6439; 11.578
90.059; 109.119; 113.062		918Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126743 CIFC12 H14 Ag F6 N2 PP -18.4968; 9.1809; 10.9655
72.296; 71.948; 73.418		757.33Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126744 CIFC12 H15 Ag F6 N3 PP 1 21/n 17.8394; 14.2529; 14.6397
90; 100.629; 90		1607.69Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126745 CIFC14 H18 Ag F6 N2 PP 1 21/n 18.0602; 19.5517; 10.8483
90; 90.69; 90		1709.47Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126746 CIFC12.5 H16 Cl F6 I N3 PC 1 2/m 122.793; 10.3913; 8.4476
90; 91.168; 90		2000.4Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126747 CIFC16 H24 Ag Cl2 F6 N4 PP -17.7214; 10.584; 14.3078
109.04; 90.185; 90.561		1105.23Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126748 CIFC15 H22 Cl2 F6 I N4 PP 1 21/m 19.9904; 10.3032; 11.832
90; 114.588; 90		1107.47Ward, Jas S.; Fiorini, Giorgia; Frontera, Antonio; Rissanen, Kari
Asymmetric [N-I-N]<sup>+</sup> halonium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8428-8431
7126749 CIFC20 H10 Br F5 O SI 41/a :231.0847; 31.0847; 7.6891
90; 90; 90		7429.7Chu, Xue-Qiang; Xie, Ting; Wang, Ya-Wen; Li, Xiang-Rui; Rao, Weidong; Xu, Haiyan; Shen, Zhi-Liang
Synthesis of di(hetero)aryl sulfides by defluorinative sulfenylation of polyfluoroalkyl ketones with sodium sulfinates or arylsulfonyl chlorides.
Chemical communications (Cambridge, England), 2020, 56, 8699-8702
7126750 CIFC14 H13 F3 O3 SP 21 21 219.8802; 10.6122; 13.9723
90; 90; 90		1465Li, Maizhan; Zhou, Wei
Highly enantioselective [3+2] cycloadditions of terminal allenoates with β-trifluoromethyl α,β-enones.
Chemical communications (Cambridge, England), 2020, 56, 8842-8845
7126751 CIFC34 H34 N4 Si2P 1 21/c 110.379; 9.789; 14.974
90; 105.172; 90		1468.3Usui, Ryosuke; Sunada, Yusuke
Insertion of Ni(0) and Pd(0) precursors into the Si-Si bond of a disilane with two hypercoordinate silicon atoms.
Chemical communications (Cambridge, England), 2020, 56, 8464-8467
7126752 CIFC43 H50 N6 Ni Si2P 1 21/n 111.583; 14.712; 23.855
90; 98.977; 90		4015.3Usui, Ryosuke; Sunada, Yusuke
Insertion of Ni(0) and Pd(0) precursors into the Si-Si bond of a disilane with two hypercoordinate silicon atoms.
Chemical communications (Cambridge, England), 2020, 56, 8464-8467
7126753 CIFC44 H52 N6 Pd2 Si2C 1 2/c 120.04; 23.534; 12.734
90; 126.46; 90		4830Usui, Ryosuke; Sunada, Yusuke
Insertion of Ni(0) and Pd(0) precursors into the Si-Si bond of a disilane with two hypercoordinate silicon atoms.
Chemical communications (Cambridge, England), 2020, 56, 8464-8467
7126754 CIFC52 H66 N8 Ni Si2P b c a17.514; 11.9262; 23.97
90; 90; 90		5006.7Usui, Ryosuke; Sunada, Yusuke
Insertion of Ni(0) and Pd(0) precursors into the Si-Si bond of a disilane with two hypercoordinate silicon atoms.
Chemical communications (Cambridge, England), 2020, 56, 8464-8467
7126755 CIFC58 H42 Cl6 Cu N10 O14P -111.189; 11.495; 11.892
104.709; 98.483; 101.948		1414.6Fuku, Kentaro; Miyata, Momoka; Takaishi, Shinya; Yoshida, Takefumi; Yamashita, Masahiro; Hoshino, Norihisa; Akutagawa, Tomoyuki; Ohtsu, Hiroyoshi; Kawano, Masaki; Iguchi, Hiroaki
Emergence of electrical conductivity in a flexible coordination polymer by using chemical reduction.
Chemical communications (Cambridge, England), 2020, 56, 8619-8622
7126756 CIFC30 H25 B N2 OP 1 21/c 117.643; 8.5349; 15.3612
90; 95.447; 90		2302.66Zu, Weisai; Day, Craig; Wei, Lanfeng; Jia, Xin; Xu, Liang
Dual aminoquinolate diarylboron and nickel catalysed metallaphotoredox platform for carbon-oxygen bond construction.
Chemical communications (Cambridge, England), 2020, 56, 8273-8276
7126757 CIFC17 H15 Br2 Fe N2 P SP 1 21/n 114.9127; 8.7466; 14.9471
90; 96.386; 90		1937.53Xu, Man-Man; Jia, Tong-Tong; Li, Bingjie; Ma, Wang; Chen, Xiaoyuan; Zhao, Xueli; Zang, Shuang-Quan
Tuning the properties of atomically precise gold nanoclusters for biolabeling and drug delivery.
Chemical communications (Cambridge, England), 2020, 56, 8766-8769
7126758 CIFC178 H162 N8 Nd14 O82C 1 2/c 134; 21.258; 37.58
90; 104.305; 90		26320Shi, Dongliang; Yang, Xiaoping; Ma, Yanan; Niu, Mengyu; Jones, Richard A.
Construction of 14-metal lanthanide nanorings with NIR luminescence response to ions.
Chemical communications (Cambridge, England), 2020, 56, 8651-8654
7126759 CIFC178 H162 Gd14 N8 O82C 1 2/c 133.9; 21.086; 37.72
90; 104.641; 90		26087Shi, Dongliang; Yang, Xiaoping; Ma, Yanan; Niu, Mengyu; Jones, Richard A.
Construction of 14-metal lanthanide nanorings with NIR luminescence response to ions.
Chemical communications (Cambridge, England), 2020, 56, 8651-8654
7126760 CIFC36 H19 N7P 1 21/n 110.7471; 10.0653; 50.8287
90; 94.389; 90		5482.16Liang, Qingxin; Xu, Jingyi; Xue, Jie; Qiao, Juan
Near-infrared-II thermally activated delayed fluorescence organic light-emitting diodes.
Chemical communications (Cambridge, England), 2020, 56, 8988-8991
7126761 CIFC19 H20 O4P 31 2 112.8198; 12.8198; 27.9907
90; 90; 120		3983.89Sun, Siyuan; Nagorny, Pavel
Exploration of chiral diastereomeric spiroketal (SPIROL)-based phosphinite ligands in asymmetric hydrogenation of heterocycles.
Chemical communications (Cambridge, England), 2020, 56, 8432-8435
7126762 CIFC33 H47 N O Zn2P 1 21/c 115.9994; 13.4294; 15.3641
90; 108.019; 90		3139.3Li, Bin; Wölper, Christoph; Huse, Kevin; Schulz, Stephan
Intermediate snapshot on the insertion reaction of isocyanates into the Zn-Cp* bond of dizincocene Cp*<sub>2</sub>Zn<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8643-8646
7126763 CIFC25 H39 N O Zn2P 1 21/m 19.0241; 12.0224; 12.0743
90; 110.467; 90		1227.3Li, Bin; Wölper, Christoph; Huse, Kevin; Schulz, Stephan
Intermediate snapshot on the insertion reaction of isocyanates into the Zn-Cp* bond of dizincocene Cp*<sub>2</sub>Zn<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 8643-8646
7126764 CIFC38.5 H33 Cl5 Fe2 N4P n a 2125.661; 13.0847; 12.5254
90; 90; 90		4205.6Wang, Liang; Wang, Xiaowu; Hou, Hongbin; Zhu, Guangqian; Han, Zhenyu; Yang, Weiying; Chen, Xiao; Wang, Qinggang
An unsymmetrical binuclear iminopyridine-iron complex and its catalytic isoprene polymerization.
Chemical communications (Cambridge, England), 2020, 56, 8846-8849
7126765 CIFC40 H36 Cl4 Fe2 N4C 1 2/c 123.531; 13.955; 15.0761
90; 129.84; 90		3801.3Wang, Liang; Wang, Xiaowu; Hou, Hongbin; Zhu, Guangqian; Han, Zhenyu; Yang, Weiying; Chen, Xiao; Wang, Qinggang
An unsymmetrical binuclear iminopyridine-iron complex and its catalytic isoprene polymerization.
Chemical communications (Cambridge, England), 2020, 56, 8846-8849
7126766 CIFC15 H14 O3P 21 21 215.8696; 10.0626; 20.142
90; 90; 90		1189.66Niu, Jia-Pan; Nie, Jing; Li, Shen; Ma, Jun-An
Organocatalytic asymmetric synthesis of β,β-diaryl ketones via one-pot tandem dehydration/1,6-addition/decarboxylation transformation of β-keto acids and 4-hydroxybenzyl alcohols.
Chemical communications (Cambridge, England), 2020, 56, 8687-8690
7126767 CIFC21 H17 Cl O2P 21 21 215.339; 15.845; 23.929
90; 90; 90		2024Niu, Jia-Pan; Nie, Jing; Li, Shen; Ma, Jun-An
Organocatalytic asymmetric synthesis of β,β-diaryl ketones via one-pot tandem dehydration/1,6-addition/decarboxylation transformation of β-keto acids and 4-hydroxybenzyl alcohols.
Chemical communications (Cambridge, England), 2020, 56, 8687-8690
7126768 CIFC22 H17 Cl O4P 21 21 215.6683; 12.265; 32.881
90; 90; 90		2285.9Niu, Jia-Pan; Nie, Jing; Li, Shen; Ma, Jun-An
Organocatalytic asymmetric synthesis of β,β-diaryl ketones via one-pot tandem dehydration/1,6-addition/decarboxylation transformation of β-keto acids and 4-hydroxybenzyl alcohols.
Chemical communications (Cambridge, England), 2020, 56, 8687-8690
7126769 CIFC8 H5 Br F2 O SeP -16.062; 7.902; 10.845
105.988; 93.472; 92.468		497.5Guo, Rui-Li; Zhu, Xue-Qing; Zhang, Xing-Long; Wang, Yong-Qiang
Synthesis of difluoromethylselenoesters from aldehydes via a radical process.
Chemical communications (Cambridge, England), 2020, 56, 8976-8979
7126770 CIFC4.5 H3.25 F0.5 O0.75 S0.25 Se0.25P -18.167; 9.361; 12.114
97.388; 97.162; 106.374		868.5Guo, Rui-Li; Zhu, Xue-Qing; Zhang, Xing-Long; Wang, Yong-Qiang
Synthesis of difluoromethylselenoesters from aldehydes via a radical process.
Chemical communications (Cambridge, England), 2020, 56, 8976-8979
7126771 CIFC42 H60 B2 F8 N4 O4 ZnP 1 21/n 112.5375; 21.6425; 18.0088
90; 93.428; 90		4877.8Marinova, Maya; Bonnefont, Antoine; Achard, Thierry; Maisse-François, Aline; Bellemin-Laponnaz, Stéphane
Chiral stimuli-responsive metallo-supramolecular assembly induced by Cu<sup>II</sup>/Cu<sup>I</sup> redox change.
Chemical communications (Cambridge, England), 2020, 56, 8703-8706
7126772 CIFC43 H62 B2 Cl2 Cu F8 N4 O4P -111.9804; 14.2208; 14.3883
82.847; 81.601; 83.038		2392.89Marinova, Maya; Bonnefont, Antoine; Achard, Thierry; Maisse-François, Aline; Bellemin-Laponnaz, Stéphane
Chiral stimuli-responsive metallo-supramolecular assembly induced by Cu<sup>II</sup>/Cu<sup>I</sup> redox change.
Chemical communications (Cambridge, England), 2020, 56, 8703-8706
7126773 CIFC25 H28 Cl N2 O RhP b c a11.9749; 15.7608; 23.8262
90; 90; 90		4496.8Wang, Jinlei; Zheng, Guangfan; Li, Xingwei
Rhodium(iii)-catalyzed diamidation of olefins via amidorhodation and further amidation.
Chemical communications (Cambridge, England), 2020, 56, 7809-7812
7126774 CIFC28 H31 PP -19.0785; 10.6049; 13.1636
94.492; 96.629; 110.761		1167.39Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126775 CIFC49 H41 B F10 N PP -111.3195; 12.0466; 19.8048
78.274; 83.658; 79.969		2595.93Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126776 CIFC45 H46 B F10 PP 1 21/n 18.6994; 23.0965; 20.3461
90; 94.248; 90		4076.82Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126777 CIFC28 H31 PP 1 21/c 18.1976; 18.0312; 15.7056
90; 104.521; 90		2247.33Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126778 CIFC55 H44 B F10 O PP 1 21/c 112.0862; 17.6699; 21.1798
90; 99.967; 90		4454.93Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126779 CIFC48 H38 B F10 PP -112.0403; 13.4516; 13.5382
111.455; 95.241; 97.459		2000.43Chen, Chaohuang; Daniliuc, Constantin G.; Mück-Lichtenfeld, Christian; Kehr, Gerald; Erker, Gerhard
A rare olefin 1,1-carboboration reaction opens a synthetic pathway to an unusually structured frustrated Lewis pair.
Chemical communications (Cambridge, England), 2020, 56, 8806-8809
7126780 CIFC50 H48 F12 Mn N8 O4 P2P -18.585; 15.909; 37.26
97.656; 91.686; 95.702		5013.9Yang, Xinda; Zhang, Duoteng; Li, Jie; Ji, Wenhui; Yang, Naidi; Gu, Shunxin; Wu, Qiong; Jiang, Qin; Shi, Pengfei; Li, Lin
A mitochondrion-targeting Mn(ii)-terpyridine complex for two-photon photodynamic therapy.
Chemical communications (Cambridge, England), 2020, 56, 9032-9035
7126781 CIFC24 H60 O18 V6P a -316.3679; 16.3679; 16.3679
90; 90; 90		4385.09Meyer, Rachel L.; Love, Robert; Brennessel, William W.; Matson, Ellen M.
Mechanistic insights into polyoxometalate self-assembly in organic solvent: conversion of a cyclic polyoxovanadate-ethoxide to its Lindqvist congener.
Chemical communications (Cambridge, England), 2020, 56, 8607-8610
7126782 CIFC125 H130 O40 S10C 1 2/c 121.5402; 22.7876; 28.6846
90; 97.979; 90		13943.5Ruengsuk, Araya; Khamphaijun, Korawit; Pananusorn, Puttipong; Docker, Andrew; Tantirungrotechai, Jonggol; Sukwattanasinitt, Mongkol; Harding, David J.; Bunchuay, Thanthapatra
Pertosylated pillar[5]arene: self-template assisted synthesis and supramolecular polymer formation.
Chemical communications (Cambridge, England), 2020, 56, 8739-8742
7126783 CIFC135 H146 N2 O41 S10P -114.98554; 18.2946; 28.2056
103.655; 90.0967; 113.613		6844.65Ruengsuk, Araya; Khamphaijun, Korawit; Pananusorn, Puttipong; Docker, Andrew; Tantirungrotechai, Jonggol; Sukwattanasinitt, Mongkol; Harding, David J.; Bunchuay, Thanthapatra
Pertosylated pillar[5]arene: self-template assisted synthesis and supramolecular polymer formation.
Chemical communications (Cambridge, England), 2020, 56, 8739-8742
7126784 CIFC22 H25 N O6P 1 21/n 111.0462; 14.645; 13.553
90; 107.712; 90		2088.6Babu, Kaki Raveendra; Li, Yang; Xu, Wenbo; Tang, Yuhai; Zhang, Wenquan; Xu, Silong
Multicomponent benzannulation of allylic P-ylides with isocyanates or aldehydes for construction of anilines and biaryls.
Chemical communications (Cambridge, England), 2020, 56, 8865-8868
7126785 CIFC38 H42 Cl4 Co3 N4P 1 21/c 113.3704; 15.8172; 18.5339
90; 102.526; 90		3826.3Alexandropoulos, Dimitris I.; Vignesh, Kuduva R.; Xie, Haomiao; Dunbar, Kim R.
Quinoxaline radical-bridged transition metal complexes with very strong antiferromagnetic coupling.
Chemical communications (Cambridge, England), 2020, 56, 9122-9125
7126786 CIFC38 H42 Cl4 Co N4 Zn2P 1 21/c 113.302; 15.821; 18.6
90; 102.662; 90		3819Alexandropoulos, Dimitris I.; Vignesh, Kuduva R.; Xie, Haomiao; Dunbar, Kim R.
Quinoxaline radical-bridged transition metal complexes with very strong antiferromagnetic coupling.
Chemical communications (Cambridge, England), 2020, 56, 9122-9125
7126787 CIFC38 H42 Cl4 Co Fe2 N4P 1 21/c 113.44; 15.842; 18.607
90; 102.501; 90		3867.8Alexandropoulos, Dimitris I.; Vignesh, Kuduva R.; Xie, Haomiao; Dunbar, Kim R.
Quinoxaline radical-bridged transition metal complexes with very strong antiferromagnetic coupling.
Chemical communications (Cambridge, England), 2020, 56, 9122-9125
7126788 CIFC50 H68 N12 O3P -110.454; 11.2457; 22.6586
77.86; 79.348; 82.174		2546.2He, Ying-Chun; Yan, Yan-Mei; Tong, Hong-Bo; Ren, Zhen-Xing; Wang, Jun-Hong; Zhang, Yong-Bin; Chao, Jian-Bin; Wang, Meng-Liang
Benzenebistriazole-strapped calix[4]pyrrole: a neutral anion receptor with CH and NH donor groups that exhibits high sulfate binding affinity and selectivity in aqueous solutions.
Chemical communications (Cambridge, England), 2020, 56, 9364-9367
7126789 CIFC53 H80 N12 O5 SP 1 21/c 114.1432; 19.0048; 21.5747
90; 99.75; 90		5715.3He, Ying-Chun; Yan, Yan-Mei; Tong, Hong-Bo; Ren, Zhen-Xing; Wang, Jun-Hong; Zhang, Yong-Bin; Chao, Jian-Bin; Wang, Meng-Liang
Benzenebistriazole-strapped calix[4]pyrrole: a neutral anion receptor with CH and NH donor groups that exhibits high sulfate binding affinity and selectivity in aqueous solutions.
Chemical communications (Cambridge, England), 2020, 56, 9364-9367
7126790 CIFC104.5 H76.5 B4 F16 Fe2 N16 O6.5 S6P n a 2119.637; 27.707; 19.921
90; 90; 90		10839Howard-Smith, Kyle J; Craze, Alexander R.; Zenno, Hikaru; Yagyu, Junya; Hayami, Shinya; Li, Feng
A large dinuclear Fe(ii) triple helicate demonstrating a two-step spin crossover.
Chemical communications (Cambridge, England), 2020, 56, 8838-8841
7126791 CIFC102.22 H75.65 B4 F16 Fe2 N15 O6.25 S6P n a 2119.69; 27.779; 19.967
90; 90; 90		10921Howard-Smith, Kyle J; Craze, Alexander R.; Zenno, Hikaru; Yagyu, Junya; Hayami, Shinya; Li, Feng
A large dinuclear Fe(ii) triple helicate demonstrating a two-step spin crossover.
Chemical communications (Cambridge, England), 2020, 56, 8838-8841
7126792 CIFC101 H72.5 B4 F15.8 Fe2 N14.5 O6 S6P c c n20.127; 27.951; 19.854
90; 90; 90		11169Howard-Smith, Kyle J; Craze, Alexander R.; Zenno, Hikaru; Yagyu, Junya; Hayami, Shinya; Li, Feng
A large dinuclear Fe(ii) triple helicate demonstrating a two-step spin crossover.
Chemical communications (Cambridge, England), 2020, 56, 8838-8841
7126793 CIFC101.17 H72.75 B4 F16 Fe2 N14.58 O6 S6P n a 2119.772; 27.872; 20.025
90; 90; 90		11035Howard-Smith, Kyle J; Craze, Alexander R.; Zenno, Hikaru; Yagyu, Junya; Hayami, Shinya; Li, Feng
A large dinuclear Fe(ii) triple helicate demonstrating a two-step spin crossover.
Chemical communications (Cambridge, England), 2020, 56, 8838-8841
7126794 CIFC42 H42 B Cu N4 P2C 1 2/c 113.3593; 16.3964; 17.537
90; 108.015; 90		3653.1Lee, Kyounghoon; Lai, Po-Ni; Parveen, Riffat; Donahue, Courtney M.; Wymore, Mikayla M.; Massman, Blake A.; Vlaisavljevich, Bess; Teets, Thomas S.; Daly, Scott R.
Modifying the luminescent properties of a Cu(i) diphosphine complex using ligand-centered reactions in single crystals.
Chemical communications (Cambridge, England), 2020, 56, 9110-9113
7126795 CIFC30 H32 B Cl Cu N3 P2P 1 21/n 112.4036; 19.0304; 12.5089
90; 105.131; 90		2850.3Lee, Kyounghoon; Lai, Po-Ni; Parveen, Riffat; Donahue, Courtney M.; Wymore, Mikayla M.; Massman, Blake A.; Vlaisavljevich, Bess; Teets, Thomas S.; Daly, Scott R.
Modifying the luminescent properties of a Cu(i) diphosphine complex using ligand-centered reactions in single crystals.
Chemical communications (Cambridge, England), 2020, 56, 9110-9113
7126796 CIFC31 H36 B Cl Cu N3 O P2P 1 21/c 111.194; 21.08; 13.3883
90; 107.235; 90		3017.4Lee, Kyounghoon; Lai, Po-Ni; Parveen, Riffat; Donahue, Courtney M.; Wymore, Mikayla M.; Massman, Blake A.; Vlaisavljevich, Bess; Teets, Thomas S.; Daly, Scott R.
Modifying the luminescent properties of a Cu(i) diphosphine complex using ligand-centered reactions in single crystals.
Chemical communications (Cambridge, England), 2020, 56, 9110-9113
7126797 CIFC93 H78 N9 O19 Zn4P 3 2 125.6587; 25.6587; 10.1334
90; 90; 120		5777.7Tang, Haitong; Yang, Keke; Wang, Kun-Yu; Meng, Qi; Wu, Fan; Fang, Yu; Wu, Xiang; Li, Yougui; Zhang, WenCheng; Luo, Yunfei; Zhu, Chengfeng; Zhou, Hong-Cai
Engineering a homochiral metal-organic framework based on an amino acid for enantioselective separation.
Chemical communications (Cambridge, England), 2020, 56, 9016-9019
7126798 CIFC6 H6 N2 O2P 21 21 213.8712; 6.84; 23.77
90; 90; 90		629.4Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126799 CIFC9 H10 N2P 21 21 216.0018; 8.6564; 14.5956
90; 90; 90		758.3Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126800 CIFC10 H11 B F4 N2 SeP 1 21/n 112.1299; 6.2796; 16.088
90; 94.965; 90		1220.8Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126801 CIFC10 H12 N2 SeP 21 21 215.8033; 10.5327; 16.799
90; 90; 90		1026.8Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126802 CIFC12 H12 F6 N2 O6 S2P 1 21/c 16.8205; 12.3993; 21.2683
90; 90.48; 90		1798.58Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126803 CIFC18 H23 B Cl F4 N2 RhP 1 21/c 18.0887; 20.767; 11.8752
90; 106.634; 90		1911.3Appel, Sebastian; Brüggemann, Peter; Ganter, Christian
A tropylium annulated N-heterocyclic carbene.
Chemical communications (Cambridge, England), 2020, 56, 9020-9023
7126804 CIFC36 H52 Bi2 Cl10 N4P -110.4247; 14.2467; 15.6532
85.418; 85.632; 89.424		2310.6Dashitsyrenova, Dolgor D.; Adonin, Sergey A.; Gorokh, Igor D.; Kraevaya, Olga A.; Pavlova, Alina V.; Abramov, Pavel A.; Frolova, Lyubov A.; Sokolov, Maxim N.; Fedin, Vladimir P.; Troshin, Pavel A.
Memory devices based on novel alkyl viologen halobismuthate(iii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 9162-9165
7126805 CIFC40 H60 Bi2 Br10 N4P -111.8794; 12.036; 20.2002
92.755; 105.01; 104.72		2678.01Dashitsyrenova, Dolgor D.; Adonin, Sergey A.; Gorokh, Igor D.; Kraevaya, Olga A.; Pavlova, Alina V.; Abramov, Pavel A.; Frolova, Lyubov A.; Sokolov, Maxim N.; Fedin, Vladimir P.; Troshin, Pavel A.
Memory devices based on novel alkyl viologen halobismuthate(iii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 9162-9165
7126806 CIFC40 H59 Bi2 Cl10 N4P -111.2548; 11.3269; 11.4527
77.607; 69.581; 68.028		1262.94Dashitsyrenova, Dolgor D.; Adonin, Sergey A.; Gorokh, Igor D.; Kraevaya, Olga A.; Pavlova, Alina V.; Abramov, Pavel A.; Frolova, Lyubov A.; Sokolov, Maxim N.; Fedin, Vladimir P.; Troshin, Pavel A.
Memory devices based on novel alkyl viologen halobismuthate(iii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 9162-9165
7126807 CIFC36 H52 Bi2 Br10 N4P -110.4555; 11.4437; 12.2399
75.666; 67.787; 65.258		1224.38Dashitsyrenova, Dolgor D.; Adonin, Sergey A.; Gorokh, Igor D.; Kraevaya, Olga A.; Pavlova, Alina V.; Abramov, Pavel A.; Frolova, Lyubov A.; Sokolov, Maxim N.; Fedin, Vladimir P.; Troshin, Pavel A.
Memory devices based on novel alkyl viologen halobismuthate(iii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 9162-9165
7126808 CIFC102 H214 Ca10 N10 Si4R -3 :H46.5535; 46.5535; 18.2299
90; 90; 120		34215.2Martin, Johannes; Eyselein, Jonathan; Langer, Jens; Elsen, Holger; Harder, Sjoerd
Large decanuclear calcium and strontium hydride clusters.
Chemical communications (Cambridge, England), 2020, 56, 9178-9181
7126809 CIFC123 H238 N10 Si4 Sr10P -115.0995; 18.8526; 28.8886
100.413; 91.1677; 110.944		7521.3Martin, Johannes; Eyselein, Jonathan; Langer, Jens; Elsen, Holger; Harder, Sjoerd
Large decanuclear calcium and strontium hydride clusters.
Chemical communications (Cambridge, England), 2020, 56, 9178-9181
7126810 CIFC H Cl O SP -110.0045; 14.86; 16.494
76.859; 76.555; 72.955		2246.5Li, Fei; Shang, Yanbo; Niu, Chuang; Li, Chao; Huang, Xinmin; Xu, Guoyong; Xuan, Jun; Zhou, Hongping; Yang, Shangfeng
Potassium salt promoted regioselective three-component coupling synthesis of 1,4-asymmetrical [60]fullerene bisadducts with superior electron transport properties.
Chemical communications (Cambridge, England), 2020, 56, 9513-9516
7126811 CIFC22 H41 F6 Ir N3 O P3C 1 2/c 111.5628; 11.2503; 22.9994
90; 93.55; 90		2986.14Hu, Gongfang; Jiang, Jianbing Jimmy; Kelly, H. Ray; Matula, Adam J.; Wu, Yueshen; Romano, Neyen; Mercado, Brandon Q.; Wang, Hailiang; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Surprisingly big linker-dependence of activity and selectivity in CO<sub>2</sub> reduction by an iridium(i) pincer complex.
Chemical communications (Cambridge, England), 2020, 56, 9126-9129
7126812 CIFC22 H39 F6 Ir N O3 P3P 1 21/c 18.4834; 27.8076; 12.4613
90; 91.593; 90		2938.52Hu, Gongfang; Jiang, Jianbing Jimmy; Kelly, H. Ray; Matula, Adam J.; Wu, Yueshen; Romano, Neyen; Mercado, Brandon Q.; Wang, Hailiang; Batista, Victor S.; Crabtree, Robert H.; Brudvig, Gary W.
Surprisingly big linker-dependence of activity and selectivity in CO<sub>2</sub> reduction by an iridium(i) pincer complex.
Chemical communications (Cambridge, England), 2020, 56, 9126-9129
7126813 CIFC118 H214 N2 O28 Si16 Yb2P -116.342; 23.291; 24.187
113.031; 90.664; 100.204		8305Willauer, Aurélien R; Dabrowska, Anna M.; Scopelliti, Rosario; Mazzanti, Marinella
Structure and small molecule activation reactivity of a metallasilsesquioxane of divalent ytterbium.
Chemical communications (Cambridge, England), 2020, 56, 8936-8939
7126814 CIFC98 H188 O26 Si16 Yb2P 1 21/c 116.788; 30.084; 25.587
90; 90.57; 90		12922Willauer, Aurélien R; Dabrowska, Anna M.; Scopelliti, Rosario; Mazzanti, Marinella
Structure and small molecule activation reactivity of a metallasilsesquioxane of divalent ytterbium.
Chemical communications (Cambridge, England), 2020, 56, 8936-8939
7126815 CIFC21 H20 O2P b c a14.8226; 9.0342; 23.887
90; 90; 90		3198.7Li, Jian; Yang, Fang; Hu, Weiwei; Ren, Bo; Chen, Zi-Sheng; Ji, Kegong
Gold(i)-catalyzed tandem cyclization of cyclopropylidene-tethered propargylic alcohols: an approach to functionalized naphtho[2,3-c]pyrans.
Chemical communications (Cambridge, England), 2020, 56, 9154-9157
7126816 CIFC204 H162 Cu12 N12 O48R -3 :H21.265; 21.265; 69.25
90; 90; 120		27119Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126817 CIFC828 H612 Mo36 N36 O180R -3 :H26.357; 26.357; 56.276
90; 90; 120		33857Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126818 CIFC242 H146 Mo12 N16 O54C 1 2/c 159.221; 23.4873; 41.898
90; 125.318; 90		47552Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126819 CIFC240 H120 Br12 Cr12 N12 O60C 1 2/c 142.1022; 27.7671; 37.031
90; 104.565; 90		41900Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126820 CIFC384 H216 Cu12 N24 O60R -3 :H35.9602; 35.9602; 36.207
90; 90; 120		40548Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126821 CIFC240 H132 Cu12 N12 O60P 1 21/c 120.2176; 22.8067; 40.8077
90; 100.344; 90		18510.5Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126822 CIFC312 H180 Mo12 N12 O48P 1 21/c 119.686; 27.191; 39.897
90; 93.427; 90		21318Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126823 CIFC260 H140 Br12 Cu12 N18 O54P 1 21/n 126.9417; 26.9492; 35.287
90; 90.249; 90		25620Rowland, Casey A.; Lorzing, Gregory R.; Bhattacharjee, Rameswar; Caratzoulas, Stavros; Yap, Glenn P. A.; Bloch, Eric D.
Design and synthesis of aryl-functionalized carbazole-based porous coordination cages.
Chemical communications (Cambridge, England), 2020, 56, 9352-9355
7126824 CIFC28 H32 N10 O14 Zn3P 1 21/n 17.3787; 15.3471; 14.9299
90; 96.703; 90		1679.1Liu, Jiao; Zhao, Ying; Dang, Li-Long; Yang, Guoping; Ma, Lu-Fang; Li, Dong-Sheng; Wang, Yaoyu
Highly stable 3D porous HMOF with enhanced catalysis and fine color regulation by the combination of d- and p-ions when compared with those of its monometallic MOFs.
Chemical communications (Cambridge, England), 2020, 56, 8758-8761
7126825 CIFC18 H11 N8 O10 Pb2P -17.0192; 12.1615; 14.3322
66.712; 85.198; 89.169		1119.6Liu, Jiao; Zhao, Ying; Dang, Li-Long; Yang, Guoping; Ma, Lu-Fang; Li, Dong-Sheng; Wang, Yaoyu
Highly stable 3D porous HMOF with enhanced catalysis and fine color regulation by the combination of d- and p-ions when compared with those of its monometallic MOFs.
Chemical communications (Cambridge, England), 2020, 56, 8758-8761
7126826 CIFC9 H5 N4 O5 Pb Zn0.5C 1 2/c 120.796; 22.171; 6.8392
90; 105.035; 90		3045.4Liu, Jiao; Zhao, Ying; Dang, Li-Long; Yang, Guoping; Ma, Lu-Fang; Li, Dong-Sheng; Wang, Yaoyu
Highly stable 3D porous HMOF with enhanced catalysis and fine color regulation by the combination of d- and p-ions when compared with those of its monometallic MOFs.
Chemical communications (Cambridge, England), 2020, 56, 8758-8761
7126827 CIFC15 H4 N4 O5P 1 21/n 17.8806; 8.6623; 19.524
90; 95.543; 90		1326.56Niazi, Muhammad Rizwan; Hamzehpoor, Ehsan; Ghamari, Pegah; Perepichka, Igor F.; Perepichka, Dmitrii F.
Nitroaromatics as n-type organic semiconductors for field effect transistors.
Chemical communications (Cambridge, England), 2020, 56, 6432-6435
7126828 CIFC22 H13 F O S2P 1 21/c 111.3658; 12.2954; 12.4661
90; 102.113; 90		1703.3Sundaravelu, Nallappan; Sekar, Govindasamy
Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 8826-8829
7126829 CIFC23 H16 O S2P 1 21/c 111.1152; 12.7185; 12.9078
90; 103.703; 90		1772.82Sundaravelu, Nallappan; Sekar, Govindasamy
Cu-Catalyzed one-pot synthesis of thiochromeno-quinolinone and thiochromeno-thioflavone via oxidative double hetero Michael addition using in situ generated nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 8826-8829
7126830 CIFC43 H66 Au2 N21 O4 P4 Ru2P 1 21/n 113.359; 13.2038; 17.1923
90; 108.975; 90		2867.8Scalambra, Franco; Sierra-Martin, Benjamin; Serrano-Ruiz, Manuel; Fernandez-Barbero, Antonio; Romerosa, Antonio
First exfoliated Ru-Ru-Au organometallic polymer with layered structure.
Chemical communications (Cambridge, England), 2020, 56, 9441-9444
7126831 CIFC37 H41 N5 O3P 1 21/c 19.236; 14.416; 25.771
90; 95.167; 90		3417.4Behera, Kanhu Charan; Bag, Bamaprasad
Selective DCP detection with xanthene derivatives by carbonyl phosphorylation.
Chemical communications (Cambridge, England), 2020, 56, 9308-9311
7126832 CIFC35 H35 N3 O5C 1 c 116.2392; 12.0245; 17.25
90; 110.696; 90		3151Behera, Kanhu Charan; Bag, Bamaprasad
Selective DCP detection with xanthene derivatives by carbonyl phosphorylation.
Chemical communications (Cambridge, England), 2020, 56, 9308-9311
7126833 CIFC74 H85 N10 O6P 1 21/c 19.309; 14.055; 25.6
90; 95.731; 90		3332.7Behera, Kanhu Charan; Bag, Bamaprasad
Selective DCP detection with xanthene derivatives by carbonyl phosphorylation.
Chemical communications (Cambridge, England), 2020, 56, 9308-9311
7126834 CIFC16 H15 N SP 1 21/n 112.2588; 7.5269; 13.4609
90; 93.275; 90		1240.02Kirkeby, Emily K.; Roberts, Andrew G.
Design, synthesis and characterization of structurally dynamic cyclic N,S-acetals.
Chemical communications (Cambridge, England), 2020, 56, 9118-9121
7126835 CIFC17 H17 N O SP 1 21/c 118.2786; 5.5078; 13.668
90; 95.902; 90		1368.73Kirkeby, Emily K.; Roberts, Andrew G.
Design, synthesis and characterization of structurally dynamic cyclic N,S-acetals.
Chemical communications (Cambridge, England), 2020, 56, 9118-9121
7126836 CIFC17 H16 N2 O3 SP -17.2999; 8.7882; 12.8272
70.781; 74.659; 80.397		746.48Kirkeby, Emily K.; Roberts, Andrew G.
Design, synthesis and characterization of structurally dynamic cyclic N,S-acetals.
Chemical communications (Cambridge, England), 2020, 56, 9118-9121
7126837 CIFC19 H19 N O4P -17.7313; 8.231; 13.2902
81.614; 79.942; 89.931		823.58Tathe, Akash G.; Chintawar, Chetan C.; Bhoyare, Vivek W.; Patil, Nitin T.
Ligand-enabled gold-catalyzed 1,2-heteroarylation of alkenes.
Chemical communications (Cambridge, England), 2020, 56, 9304-9307
7126838 CIFC14.36 H8.72 Cl0.73 N O2C 1 2/c 115.4081; 18.0628; 8.5341
90; 97.705; 90		2353.71Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126839 CIFC28 H16 N2 O4I 41/a :215.938; 15.938; 15.9529
90; 90; 90		4052.4Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126840 CIFC15.25 H9.25 N O2C 1 2/c 115.512; 17.987; 8.5142
90; 97.05; 90		2357.6Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126841 CIFC28 H16 N2 O4I 41/a :215.9394; 15.9394; 15.9489
90; 90; 90		4052Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126842 CIFC14.46 H8.9 Cl0.46 N O2C 1 2/c 115.442; 18.01; 8.5151
90; 97.36; 90		2348.6Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126843 CIFC14.93 H9.9 N O2C 1 2/c 115.564; 18.062; 8.5078
90; 96.99; 90		2373.9Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126844 CIFC16.25 H10.62 N O2C 1 2/c 115.4912; 18.1068; 8.5193
90; 97.128; 90		2371.16Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126845 CIFC14 H10 N O3C 1 2/m 111.0304; 11.821; 9.3939
90; 115.468; 90		1105.85Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126846 CIFC28 H16 N2 O4I 41/a :215.926; 15.926; 15.916
90; 90; 90		4036.9Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126847 CIFC15.75 H12.1 N O2C 1 2/c 115.45; 17.951; 8.5315
90; 97.51; 90		2345.9Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126848 CIFC15.5 H11 N O2C 1 2/c 115.487; 17.983; 8.5171
90; 97.19; 90		2353.4Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126849 CIFC14.86 H8 N O2.21C 1 2/c 115.5901; 18.1053; 8.5158
90; 97.025; 90		2385.65Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126850 CIFC15.5 H11.3 N O2C 1 2/c 115.496; 17.8919; 8.5454
90; 97.664; 90		2348.07Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126851 CIFC28 H16 N2 O4I 41/a :215.926; 15.926; 15.926
90; 90; 90		4039.4Yakiyama, Yumi; Fujinaka, Takahisa; Nishimura, Mio; Seki, Ryotaro; Sakurai, Hidehiro
Control by one drop of solvent: selective preparation of guest release/trap-triggered interconvertible molecular crystals.
Chemical communications (Cambridge, England), 2020, 56, 9687-9690
7126852 CIFC21 H19 N3 O2P n a 2112.4892; 7.3635; 18.9497
90; 90; 90		1742.7Wen, Chunxia; Zhong, Ronglin; Qin, Zengxin; Zhao, Mengfei; Li, Jizhen
Regioselective remote C5 cyanoalkoxylation and cyanoalkylation of 8-aminoquinolines with azobisisobutyronitrile.
Chemical communications (Cambridge, England), 2020, 56, 9529-9532
7126853 CIFC17 H12 F6 N2 O SP 21 21 217.1213; 9.6599; 24.5371
90; 90; 90		1687.93Kosobokov, Mikhail D.; Zubkov, Mikhail O.; Levin, Vitalij V.; Kokorekin, Vladimir A.; Dilman, Alexander D.
Fluoroalkyl sulfides as photoredox-active coupling reagents for alkene difunctionalization.
Chemical communications (Cambridge, England), 2020, 56, 9453-9456
7126854 CIFC56 H52 Cl2 O4 Pd Se2P -18.2319; 10.9599; 14.1131
101.732; 100.174; 97.026		1210.44Meena, Neha; Sharma, Shobha; Bhatt, Ramprasad; Shinde, Vikki N.; Sunda, Anurag Prakash; Bhuvanesh, Nattamai; Kumar, Anil; Joshi, Hemant
A selenium-coordinated palladium(ii) trans-dichloride molecular rotor as a catalyst for site-selective annulation of 2-arylimidazo[1,2-a]pyridines.
Chemical communications (Cambridge, England), 2020, 56, 10223-10226
7126855 CIFC28 H19 F N2P 1 21/n 111.805; 7.031; 24.4855
90; 103.258; 90		1978.15Meena, Neha; Sharma, Shobha; Bhatt, Ramprasad; Shinde, Vikki N.; Sunda, Anurag Prakash; Bhuvanesh, Nattamai; Kumar, Anil; Joshi, Hemant
A selenium-coordinated palladium(ii) trans-dichloride molecular rotor as a catalyst for site-selective annulation of 2-arylimidazo[1,2-a]pyridines.
Chemical communications (Cambridge, England), 2020, 56, 10223-10226
7126856 CIFC92 H80 N8 O4 S32C 1 2 146.8847; 4.9361; 11.2909
90; 99.121; 90		2579.99Short, Jonathan I.; Blundell, Toby J.; Krivickas, Sara J.; Yang, Songjie; Wallis, John D.; Akutsu, Hiroki; Nakazawa, Yasuhiro; Martin, Lee
Chiral molecular conductor with an insulator-metal transition close to room temperature.
Chemical communications (Cambridge, England), 2020, 56, 9497-9500
7126857 CIFC46 H40 N4 O2 S16P 123.723; 4.857; 11.6968
89.841; 81.637; 87.168		1331.8Short, Jonathan I.; Blundell, Toby J.; Krivickas, Sara J.; Yang, Songjie; Wallis, John D.; Akutsu, Hiroki; Nakazawa, Yasuhiro; Martin, Lee
Chiral molecular conductor with an insulator-metal transition close to room temperature.
Chemical communications (Cambridge, England), 2020, 56, 9497-9500
7126858 CIFC5 H2 Cu N3 OP b c m8.056; 10.787; 6.0093
90; 90; 90		522.2García-Valdivia, Antonio A; Romero, Francisco J.; Cepeda, Javier; Morales, Diego P.; Casati, Nicola; Mota, Antonio J.; Zotti, Linda A.; Palacios, Juan J.; Choquesillo-Lazarte, Duane; F Salmerón, José; Rivadeneyra, Almudena; Rodríguez-Diéguez, Antonio
Rational design of an unusual 2D-MOF based on Cu(i) and 4-hydroxypyrimidine-5-carbonitrile as linker with conductive capabilities: a theoretical approach based on high-pressure XRD.
Chemical communications (Cambridge, England), 2020, 56, 9473-9476
7126859 CIFC5 H2 Cu N3 OP b c m8.0286; 10.776; 5.88
90; 90; 90		508.7García-Valdivia, Antonio A; Romero, Francisco J.; Cepeda, Javier; Morales, Diego P.; Casati, Nicola; Mota, Antonio J.; Zotti, Linda A.; Palacios, Juan J.; Choquesillo-Lazarte, Duane; F Salmerón, José; Rivadeneyra, Almudena; Rodríguez-Diéguez, Antonio
Rational design of an unusual 2D-MOF based on Cu(i) and 4-hydroxypyrimidine-5-carbonitrile as linker with conductive capabilities: a theoretical approach based on high-pressure XRD.
Chemical communications (Cambridge, England), 2020, 56, 9473-9476
7126860 CIFC5 H2 Cu N3 OP b c m7.9702; 10.714; 5.6247
90; 90; 90		480.3García-Valdivia, Antonio A; Romero, Francisco J.; Cepeda, Javier; Morales, Diego P.; Casati, Nicola; Mota, Antonio J.; Zotti, Linda A.; Palacios, Juan J.; Choquesillo-Lazarte, Duane; F Salmerón, José; Rivadeneyra, Almudena; Rodríguez-Diéguez, Antonio
Rational design of an unusual 2D-MOF based on Cu(i) and 4-hydroxypyrimidine-5-carbonitrile as linker with conductive capabilities: a theoretical approach based on high-pressure XRD.
Chemical communications (Cambridge, England), 2020, 56, 9473-9476
7126861 CIFC5 H2 Cu N3 OP b c m7.9478; 10.61; 5.5058
90; 90; 90		464.3García-Valdivia, Antonio A; Romero, Francisco J.; Cepeda, Javier; Morales, Diego P.; Casati, Nicola; Mota, Antonio J.; Zotti, Linda A.; Palacios, Juan J.; Choquesillo-Lazarte, Duane; F Salmerón, José; Rivadeneyra, Almudena; Rodríguez-Diéguez, Antonio
Rational design of an unusual 2D-MOF based on Cu(i) and 4-hydroxypyrimidine-5-carbonitrile as linker with conductive capabilities: a theoretical approach based on high-pressure XRD.
Chemical communications (Cambridge, England), 2020, 56, 9473-9476
7126862 CIFC16 H20 Cl N2 O5P 3211.309; 11.309; 11.3065
90; 90; 120		1252.3Zhang, Shilong; Liu, Yungen; Xing, Fangrong; Che, Chi-Ming
Direct preparation of unprotected aminimides (R<sub>3</sub>N<sup>+</sup>-NH<sup>-</sup>) from natural aliphatic tertiary alkaloids (R<sub>3</sub>N) by [Mn(TDCPP)Cl]-catalysed N-amination reaction.
Chemical communications (Cambridge, England), 2020, 56, 9102-9105
7126863 CIFC19 H29 Cl N2 O6P 21 21 217.2666; 14.444; 19.5127
90; 90; 90		2048Zhang, Shilong; Liu, Yungen; Xing, Fangrong; Che, Chi-Ming
Direct preparation of unprotected aminimides (R<sub>3</sub>N<sup>+</sup>-NH<sup>-</sup>) from natural aliphatic tertiary alkaloids (R<sub>3</sub>N) by [Mn(TDCPP)Cl]-catalysed N-amination reaction.
Chemical communications (Cambridge, England), 2020, 56, 9102-9105
7126864 CIFC58 H36 Cl8 Mn N5P b c a12.6724; 19.811; 20.784
90; 90; 90		5217.9Zhang, Shilong; Liu, Yungen; Xing, Fangrong; Che, Chi-Ming
Direct preparation of unprotected aminimides (R<sub>3</sub>N<sup>+</sup>-NH<sup>-</sup>) from natural aliphatic tertiary alkaloids (R<sub>3</sub>N) by [Mn(TDCPP)Cl]-catalysed N-amination reaction.
Chemical communications (Cambridge, England), 2020, 56, 9102-9105
7126865 CIFC13 H10 Br N3P 1 21/n 113.7045; 4.1406; 20.539
90; 95.208; 90		1160.67Zhang, Chunyan; Zhao, Haowen; Li, Zehua; Liang, Zuyu; Qi, Shuo; Cai, Mingyu; Zhang, Sheng; Jia, Xiaofei; Zhang, Guoying; Hu, Mao-Lin
Rapid access to 3-aminoindazoles from nitriles with hydrazines: a strategy to overcome the basicity barrier imparted by hydrazines.
Chemical communications (Cambridge, England), 2020, 56, 9521-9524
7126866 CIFC15 H12 O3P 1 21/n 114.261; 5.3923; 16.6024
90; 112.37; 90		1180.64Ma, Ben; Tang, Zhiqiong; Zhang, Junliang; Liu, Lu
Copper-catalysed ortho-selective C-H bond functionalization of phenols and naphthols with α-aryl-α-diazoesters.
Chemical communications (Cambridge, England), 2020, 56, 9485-9488
7126867 CIFC73 H133 F8 N O29 Tb6P n m a36.191; 23.761; 15.011
90; 90; 90		12908Ling, Bo-Kai; Li, Junhao; Zhai, Yuan-Qi; Hsu, Hung-Kai; Chan, Yi-Tsu; Chen, Wei-Peng; Han, Tian; Zheng, Yan-Zhen
Terbium-fluorido cluster: an energy cage for photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 9130-9133
7126868 CIFC72 H170 Ag7 Cu7 O24 P12 S24P 1 21/n 113.0789; 23.272; 22.9115
90; 98.181; 90		6902.7Zhong, Yu-Jie; Liao, Jian-Hong; Chiu, Tzu-Hao; Wu, Ying-Yann; Kahlal, Samia; Saillard, Jean-Yves; Liu, C. W.
Hydride-encapsulated bimetallic clusters supported by 1,1-dithiolates.
Chemical communications (Cambridge, England), 2020, 56, 9300-9303
7126869 CIFC36 H85 Ag3 Cu4 O12 P6 S12P 1 21/n 113.1365; 23.3343; 22.8775
90; 98.1499; 90		6941.8Zhong, Yu-Jie; Liao, Jian-Hong; Chiu, Tzu-Hao; Wu, Ying-Yann; Kahlal, Samia; Saillard, Jean-Yves; Liu, C. W.
Hydride-encapsulated bimetallic clusters supported by 1,1-dithiolates.
Chemical communications (Cambridge, England), 2020, 56, 9300-9303
7126870 CIFC18 H33 Cl Co N7 O6C 1 c 117.659; 11.39; 12.836
90; 115.338; 90		2333Shin, Bongki; Park, Younwoo; Jeong, Donghyun; Cho, Jaeheung
Nucleophilic reactivity of a mononuclear cobalt(iii)-bis(tert-butylperoxo) complex.
Chemical communications (Cambridge, England), 2020, 56, 9449-9452
7126871 CIFC21 H36 Cl Co N6 O6 SP b c a9.177; 17.401; 33.72
90; 90; 90		5385Shin, Bongki; Park, Younwoo; Jeong, Donghyun; Cho, Jaeheung
Nucleophilic reactivity of a mononuclear cobalt(iii)-bis(tert-butylperoxo) complex.
Chemical communications (Cambridge, England), 2020, 56, 9449-9452
7126872 CIFC50 H72 B Co N4 O5P 1 21/c 112.353; 23.359; 16.581
90; 92.432; 90		4780Shin, Bongki; Park, Younwoo; Jeong, Donghyun; Cho, Jaeheung
Nucleophilic reactivity of a mononuclear cobalt(iii)-bis(tert-butylperoxo) complex.
Chemical communications (Cambridge, England), 2020, 56, 9449-9452
7126873 CIFC59 H54 Cl4 N4 O7P -17.3092; 18.6978; 20.9767
114.686; 94.742; 99.943		2527.02Harada, Mei; Tanioka, Masaru; Muranaka, Atsuya; Aoyama, Tetsuya; Kamino, Shinichiro; Uchiyama, Masanobu
A remarkably air-stable quinodimethane radical cation.
Chemical communications (Cambridge, England), 2020, 56, 9565-9568
7126875 CIFC20 H18 O3P 1 21/c 17.3935; 25.0493; 8.8978
90; 111.188; 90		1536.5Zhang, Ling; Shi, Qiu; Cao, Tongxiang; Zhu, Shifa
Catalytic regio- and stereoselective intermolecular [5+2] cycloaddition via conjugative activation of oxidopyrylium.
Chemical communications (Cambridge, England), 2020, 56, 9533-9536
7126876 CIFC23 H19 N O3P 1 21 14.9097; 20.9012; 16.8201
90; 96.123; 90		1716.2Zhang, Ling; Shi, Qiu; Cao, Tongxiang; Zhu, Shifa
Catalytic regio- and stereoselective intermolecular [5+2] cycloaddition via conjugative activation of oxidopyrylium.
Chemical communications (Cambridge, England), 2020, 56, 9533-9536
7126877 CIFC23 H20 O3P b c a6.8575; 17.6675; 29.0079
90; 90; 90		3514.4Zhang, Ling; Shi, Qiu; Cao, Tongxiang; Zhu, Shifa
Catalytic regio- and stereoselective intermolecular [5+2] cycloaddition via conjugative activation of oxidopyrylium.
Chemical communications (Cambridge, England), 2020, 56, 9533-9536
7126878 CIFC22 H26 O3P 1 21 17.7307; 5.8517; 20.5811
90; 92.53; 90		930.13Han, Xu; Retailleau, Pascal; Gandon, Vincent; Voituriez, Arnaud
Enantioselective gold(i)-catalyzed cyclization/intermolecular nucleophilic additions of 1,5-enyne derivatives.
Chemical communications (Cambridge, England), 2020, 56, 9457-9460
7126879 CIFC66 H56 Cl3 N O4 P4 RuP 1 21 111.6796; 19.9722; 13.188
90; 104.793; 90		2974.36Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126880 CIFC66 H56 Cl3 N O4 Os P4P 1 21 111.624; 19.9252; 13.1753
90; 104.818; 90		2950.05Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126881 CIFC16 H12 F3 N O3 SP n a 2113.891; 16.245; 6.9806
90; 90; 90		1575.24Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126882 CIFC67 H56 Br Cl3 F3 N O3 Os P4 SP -113.0222; 14.4045; 19.6691
79.101; 71.46; 85.621		3434.4Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126883 CIFC70 H66 F6 N O8.5 P4 Ru S2P 1 21/n 122.978; 16.4419; 36.9317
90; 104; 90		13538.4Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126884 CIFC69 H62 F6 N O7.5 Os P4 S2P 1 21/n 123.062; 16.4101; 36.9903
90; 104.016; 90		13582.2Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126885 CIFC35 H28 Cl N5 O5 RuP 1 21/c 19.9119; 14.4815; 21.9881
90; 97.114; 90		3131.86Yeung, Chi-Fung; Chung, Lai-Hon; Tse, Sheung-Ying; Shek, Hau-Lam; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Conventional and unconventional alkyne activations by Ru and Os for unprecedented dimetalated quinolizinium complexes.
Chemical communications (Cambridge, England), 2020, 56, 8908-8911
7126886 CIFC35 H42 Cl6 N3 P RuP b c a16.093; 20.363; 23.088
90; 90; 90		7566Dutta, Moumita; Das, Kanu; Prathapa, Siriyara Jagannatha; Srivastava, Hemant Kumar; Kumar, Akshai
Selective and high yield transformation of glycerol to lactic acid using NNN pincer ruthenium catalysts.
Chemical communications (Cambridge, England), 2020, 56, 9886-9889
7126887 CIFC55 H43 Cl F6 N5 P3 RuP 1 21/n 19.9974; 38.806; 13.9459
90; 92.722; 90		5404.3Dutta, Moumita; Das, Kanu; Prathapa, Siriyara Jagannatha; Srivastava, Hemant Kumar; Kumar, Akshai
Selective and high yield transformation of glycerol to lactic acid using NNN pincer ruthenium catalysts.
Chemical communications (Cambridge, England), 2020, 56, 9886-9889
7126888 CIFC20 H16 Br N O2 SP 1 21 17.4286; 7.2641; 17.1612
90; 96.473; 90		920.15Blay, Gonzalo; Castilla, Alvaro; Sanz, David; Sanz-Marco, Amparo; Vila, Carlos; Muñoz, M Carmen; Pedro, José R
Enantioselective zinc-mediated conjugate alkynylation of saccharin-derived 1-aza-butadienes.
Chemical communications (Cambridge, England), 2020, 56, 9461-9464
7126889 CIFC18 H12 F2 N2 O2 SnC 1 2/c 113.442; 9.42; 13.5862
90; 108.526; 90		1631.2Ki, Wooseok; Ngo, Kathleen; Ghosh, Phalguni; Averkiev, Boris; Reeves, Gordan T.; Ailes, Isaiah; Pemberton, Barry C.; Zhu, Kun; Li, Jing
Blue-shifted aggregation-induced enhancement of a Sn(iv) fluoride complex: the role of fluorine in luminescence enhancement.
Chemical communications (Cambridge, England), 2020, 56, 9648-9650
7126890 CIFC41 H64 Co2 F6 N7 O6 P2 S2C 1 2/c 120.5654; 12.3627; 20.3762
90; 108.773; 90		4904.9Spentzos, Ariana Z.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Unusual cyanide and methyl binding modes at a dicobalt macrocycle following acetonitrile C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 9675-9678
7126891 CIFC97 H150 Co4 F8 N14 O6 P4 S2C 1 m 122.62; 21.11; 12.65
90; 115.833; 90		5436.8Spentzos, Ariana Z.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Unusual cyanide and methyl binding modes at a dicobalt macrocycle following acetonitrile C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 9675-9678
7126892 CIFC48 H75 Co2 F4 N6 O3 P SP 1 21/n 111.1401; 18.761; 26.561
90; 90.032; 90		5551.2Spentzos, Ariana Z.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Unusual cyanide and methyl binding modes at a dicobalt macrocycle following acetonitrile C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 9675-9678
7126893 CIFC136 H134 B2 Co4 F48 N14 P2C 2 2 2110.4664; 35.353; 39.212
90; 90; 90		14509.2Spentzos, Ariana Z.; Gau, Michael R.; Carroll, Patrick J.; Tomson, Neil C.
Unusual cyanide and methyl binding modes at a dicobalt macrocycle following acetonitrile C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 9675-9678
7126894 CIFCs2 O15 Pu Si6C m c 217.2502; 16.1726; 13.4121
90; 90; 90		1572.63Pace, Kristen A.; Klepov, Vladislav V.; Christian, Matthew S.; Morrison, Gregory; Deason, Travis K.; Kutahyali Aslani, Ceren; Besmann, Theodore M.; Diprete, David P.; Amoroso, Jake W.; Zur Loye, Hans-Conrad
Targeting complex plutonium oxides by combining crystal chemical reasoning with density-functional theory calculations: the quaternary plutonium oxide Cs<sub>2</sub>PuSi<sub>6</sub>O<sub>15</sub>.
Chemical communications (Cambridge, England), 2020, 56, 9501-9504
7126895 CIFCe Cs2 O15 Si6C m c 217.2565; 16.2451; 13.4354
90; 90; 90		1583.8Pace, Kristen A.; Klepov, Vladislav V.; Christian, Matthew S.; Morrison, Gregory; Deason, Travis K.; Kutahyali Aslani, Ceren; Besmann, Theodore M.; Diprete, David P.; Amoroso, Jake W.; Zur Loye, Hans-Conrad
Targeting complex plutonium oxides by combining crystal chemical reasoning with density-functional theory calculations: the quaternary plutonium oxide Cs<sub>2</sub>PuSi<sub>6</sub>O<sub>15</sub>.
Chemical communications (Cambridge, England), 2020, 56, 9501-9504
7126896 CIFC17 H17 Cl O6P 21 21 2111.6345; 12.0011; 23.8695
90; 90; 90		3332.82Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126897 CIFC21 H19 F N6 O2P b c a13.1669; 15.4955; 18.8598
90; 90; 90		3847.92Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126898 CIFC22 H24 Cl F N4 O3P -18.811; 9.661; 12.4893
93.66; 97.586; 101.871		1026.74Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126899 CIFC21 H22 Cl2 F N5 OC 1 2 115.2412; 10.1051; 14.0138
90; 100.491; 90		2122.24Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126900 CIFC18 H20 N2 O6P 1 21/c 18.8259; 15.2013; 12.9474
90; 93.777; 90		1733.32Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126901 CIFC22 H18 N4 O SP -111.812; 12.3827; 14.7603
80.868; 81.207; 65.701		1933.49Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126902 CIFC22 H17 Cl N2P -18.6846; 10.3809; 10.5107
113.566; 97.751; 96.767		845.09Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126903 CIFC17 H18 N2 O6P 1 21/c 110.6219; 10.4085; 14.78
90; 94.879; 90		1628.13Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126904 CIFC12 H17 N O2P 1 21/c 125.3104; 27.6509; 19.1485
90; 96.126; 90		13324.7Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126905 CIFC13 H12 F2 N6 OP b c a12.9345; 6.0221; 34.8527
90; 90; 90		2714.78Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126906 CIFC27 H36 N2 O4P 21 21 218.3221; 13.3053; 22.7527
90; 90; 90		2519.36Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126907 CIFC21 H26 N2 O7P 1 21/c 113.7626; 10.7276; 14.7835
90; 104.3; 90		2115Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126908 CIFC17 H26 N3 O2P 21 21 2110.1427; 10.6044; 14.5141
90; 90; 90		1561.1Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126909 CIFC4 H11 Cl N5P 1 21/c 17.9234; 13.8743; 7.9286
90; 114.547; 90		792.83Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126910 CIFC17 H14 F3 N3 O2 SP -15.064; 10.0139; 16.4073
89.882; 85.865; 80.538		818.524Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126911 CIFC9 H8 O4P 1 21/c 111.2582; 6.5471; 11.26
90; 95.949; 90		825.49Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126912 CIFC19 H16 Cl N O4P -19.2173; 9.606; 10.8436
69.959; 87.197; 69.501		842.09Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126913 CIFC8 H9 N O2P 1 21/n 17.0895; 9.2112; 11.5966
90; 97.89; 90		750.122Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126914 CIFC15 H21 N3 O3 SP 1 21/n 110.6352; 14.3296; 10.8995
90; 106.623; 90		1591.64Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126915 CIFC18 H19 Cl2 N O4P 1 21/c 112.0936; 12.0624; 13.4258
90; 116.167; 90		1757.8Ou, Xiao; Li, Xizhen; Rong, Haowei; Yu, Lian; Lu, Ming
A general method for cultivating single crystals from melt microdroplets.
Chemical communications (Cambridge, England), 2020, 56, 9950-9953
7126916 CIFC14 H17 Cl2 N O2 SP 1 21 111.9152; 7.6328; 16.9893
90; 93.025; 90		1542.96Craig, Donald; Spreadbury, Samuel R. J.; White, Andrew J. P.
Synthesis and hetero-Diels-Alder reactions of enantiomerically pure dihydro-1<i>H</i>-azepines.
Chemical communications (Cambridge, England), 2020, 56, 9803-9806
7126917 CIFC29 H29 Br N2 O6 SP 1 21 18.2726; 8.1657; 20.9582
90; 94.621; 90		1411.16Craig, Donald; Spreadbury, Samuel R. J.; White, Andrew J. P.
Synthesis and hetero-Diels-Alder reactions of enantiomerically pure dihydro-1<i>H</i>-azepines.
Chemical communications (Cambridge, England), 2020, 56, 9803-9806
7126918 CIFC22 H21 Cl N4 O4 SP 21 21 2111.8791; 12.8935; 14.4464
90; 90; 90		2212.66Craig, Donald; Spreadbury, Samuel R. J.; White, Andrew J. P.
Synthesis and hetero-Diels-Alder reactions of enantiomerically pure dihydro-1<i>H</i>-azepines.
Chemical communications (Cambridge, England), 2020, 56, 9803-9806
7126919 CIFC44 H44 Cl N7 O8 SP 1 21 113.9352; 23.768; 13.9594
90; 113.163; 90		4250.8Craig, Donald; Spreadbury, Samuel R. J.; White, Andrew J. P.
Synthesis and hetero-Diels-Alder reactions of enantiomerically pure dihydro-1<i>H</i>-azepines.
Chemical communications (Cambridge, England), 2020, 56, 9803-9806
7126920 CIFC18 H14 O10 P2 W2P 1 21/c 125.4396; 10.82292; 18.9442
90; 111.485; 90		4853.47Wang, Min; Yang, Tingting; Tian, Rongqiang; Wei, Donghui; Duan, Zheng; Mathey, François
The chemistry of phosphirane-substituted phosphinidene complexes.
Chemical communications (Cambridge, England), 2020, 56, 9707-9710
7126921 CIFC10 H8 O5 P WP 41 21 215.924; 15.924; 9.853
90; 90; 90		2498.5Wang, Min; Yang, Tingting; Tian, Rongqiang; Wei, Donghui; Duan, Zheng; Mathey, François
The chemistry of phosphirane-substituted phosphinidene complexes.
Chemical communications (Cambridge, England), 2020, 56, 9707-9710
7126922 CIFC22 H20 O10 P2 W2P 1 21/n 110.8615; 14.1665; 17.7114
90; 90.165; 90		2725.23Wang, Min; Yang, Tingting; Tian, Rongqiang; Wei, Donghui; Duan, Zheng; Mathey, François
The chemistry of phosphirane-substituted phosphinidene complexes.
Chemical communications (Cambridge, England), 2020, 56, 9707-9710
7126923 CIFC32 H40 Mo2 O8 P4P -112.1297; 17.3992; 18.9772
87.053; 85.059; 74.342		3840.5Wang, Min; Yang, Tingting; Tian, Rongqiang; Wei, Donghui; Duan, Zheng; Mathey, François
The chemistry of phosphirane-substituted phosphinidene complexes.
Chemical communications (Cambridge, England), 2020, 56, 9707-9710
7126924 CIFC35 H41 F3 I2 N4P -110.694; 14.115; 14.216
108.316; 109.057; 101.581		1812.1Torita, Koki; Haraguchi, Ryosuke; Morita, Yoshitsugu; Kemmochi, Satoshi; Komatsu, Teruyuki; Fukuzawa, Shin-Ichi
Lewis acid-base synergistic catalysis of cationic halogen-bonding-donors with nucleophilic counter anions.
Chemical communications (Cambridge, England), 2020, 56, 9715-9718
7126925 CIFC38 H42 Cl6 Cu2 F6 N6 O8 S3P -112.9903; 14.2793; 15.5742
74.072; 66.275; 86.862		2538.12Mangue, Jordan; Gondre, Clément; Pécaut, Jacques; Duboc, Carole; Ménage, Stéphane; Torelli, Stéphane
Controlled O<sub>2</sub> reduction at a mixed-valent (II,I) Cu<sub>2</sub>S core.
Chemical communications (Cambridge, England), 2020, 56, 9636-9639
7126926 CIFC16 H22 B Br2 N6 O WP 1 21/c 18.123; 14.145; 18.726
90; 100.18; 90		2117.7Thomas, Simon; Gable, Robert W.; Young, Charles G.
Synthesis and characterisation of fifteen-electron dihalo(carbonyl)tungsten(iii) complexes, Tp*WX<sub>2</sub>(CO) (X = Br, I).
Chemical communications (Cambridge, England), 2020, 56, 10349-10352
7126927 CIFC16 H22 B I2 N6 O WP 1 21/c 18.1399; 14.223; 19.364
90; 99.627; 90		2210.3Thomas, Simon; Gable, Robert W.; Young, Charles G.
Synthesis and characterisation of fifteen-electron dihalo(carbonyl)tungsten(iii) complexes, Tp*WX<sub>2</sub>(CO) (X = Br, I).
Chemical communications (Cambridge, England), 2020, 56, 10349-10352
7126928 CIFC12 H24 Co N10 Na OP m m n :28.4803; 12.4172; 9.5901
90; 90; 90		1009.85Xu, Wei-Jian; Zeng, Ying; Yuan, Wei; Zhang, Wei-Xiong; Chen, Xiao-Ming
A large room-temperature entropy change in a new hybrid ferroelastic with an unconventional bond-switching mechanism.
Chemical communications (Cambridge, England), 2020, 56, 10054-10057
7126929 CIFC12 H24 Co N10 Na OP 1 21/c 18.3357; 12.4689; 18.5938
90; 90.564; 90		1932.49Xu, Wei-Jian; Zeng, Ying; Yuan, Wei; Zhang, Wei-Xiong; Chen, Xiao-Ming
A large room-temperature entropy change in a new hybrid ferroelastic with an unconventional bond-switching mechanism.
Chemical communications (Cambridge, England), 2020, 56, 10054-10057
7126930 CIFC49 H39 F6 N6 O2 P RuP -113.6054; 13.9682; 15.6806
66.457; 65.954; 81.255		2494.6Ballester, Francisco J.; Ortega, Enrique; Bautista, Delia; Santana, M. Dolores; Ruiz, José
Ru(ii) photosensitizers competent for hypoxic cancers via green light activation.
Chemical communications (Cambridge, England), 2020, 56, 10301-10304
7126931 CIFC18 H12 Cu N2 O4P 1 21/c 110.111; 11.154; 15.896
90; 104.51; 90		1735.5Kamakura, Yoshinobu; Hikawa, Arata; Yoshikawa, Hirofumi; Kosaka, Wataru; Miyasaka, Hitoshi; Tanaka, Daisuke
Coordination distortion induced water adsorption in hydrophobic flexible metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 9106-9109
7126932 CIFC21 H16 N2 O2 SP 1 21/c 110.334; 10.31; 17.381
90; 104.83; 90		1790.1Ansari, Mohd Yeshab; Swarnkar, Sumedha; Kumar, Atul
Stereoselective aminosulfonylation of alkynes: an approach to access (Z)-β-amino vinylsulfones.
Chemical communications (Cambridge, England), 2020, 56, 9561-9564
7126933 CIFC15 H37 Cl4 Cr2 O4 SiP 1 21 16.5229; 20.072; 10.299
90; 104.225; 90		1307.1Murai, Masahito; Taniguchi, Ryuji; Kurogi, Takashi; Shunsuke, Moritani; Takai, Kazuhiko
Cyclization of 5-alkynones with chromium alkylidene equivalents generated in situ from gem-dichromiomethanes.
Chemical communications (Cambridge, England), 2020, 56, 9711-9714
7126934 CIFC15 H9.5 Br3 Dy O10 S3P -19.9121; 10.6798; 12.7892
78.919; 72.796; 85.035		1268.53Benmansour, Samia; Hernández-Paredes, Antonio; Mondal, Arpan; López Martínez, Gustavo; Canet-Ferrer, Josep; Konar, Sanjit; Gómez-García, Carlos J
Slow relaxation of the magnetization, reversible solvent exchange and luminescence in 2D anilato-based frameworks.
Chemical communications (Cambridge, England), 2020, 56, 9862-9865
7126935 CIFC18 H21 Br3 Dy N3 O9P 1 21/n 110.0215; 13.4454; 19.4727
90; 95.859; 90		2610.1Benmansour, Samia; Hernández-Paredes, Antonio; Mondal, Arpan; López Martínez, Gustavo; Canet-Ferrer, Josep; Konar, Sanjit; Gómez-García, Carlos J
Slow relaxation of the magnetization, reversible solvent exchange and luminescence in 2D anilato-based frameworks.
Chemical communications (Cambridge, England), 2020, 56, 9862-9865
7126936 CIFC9 H10 Br3 O12 YbP -19.0568; 10.2351; 10.916
65.763; 70.612; 80.712		870Benmansour, Samia; Hernández-Paredes, Antonio; Mondal, Arpan; López Martínez, Gustavo; Canet-Ferrer, Josep; Konar, Sanjit; Gómez-García, Carlos J
Slow relaxation of the magnetization, reversible solvent exchange and luminescence in 2D anilato-based frameworks.
Chemical communications (Cambridge, England), 2020, 56, 9862-9865
7126937 CIFC26 H12 F10 S2 SnP 1 21 18.2617; 14.3435; 10.6028
90; 98.182; 90		1243.66Ramirez Y Medina, Isabel-Maria; Rohdenburg, Markus; Lork, Enno; Staubitz, Anne
Aggregation induced emission - emissive stannoles in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 9775-9778
7126938 CIFC28 H20 F6 S2 SnP 1 2/c 111.5212; 12.1354; 9.7135
90; 104.176; 90		1316.73Ramirez Y Medina, Isabel-Maria; Rohdenburg, Markus; Lork, Enno; Staubitz, Anne
Aggregation induced emission - emissive stannoles in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 9775-9778
7126939 CIFC38 H44 Br2 N2 S2 SnI 1 2/c 118.204; 9.6686; 22.537
90; 112.803; 90		3656.7Ramirez Y Medina, Isabel-Maria; Rohdenburg, Markus; Lork, Enno; Staubitz, Anne
Aggregation induced emission - emissive stannoles in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 9775-9778
7126940 CIFC30 H18 F12 S2 SnP 1 21/c 19.5906; 19.6935; 16.2093
90; 95.607; 90		3046.8Ramirez Y Medina, Isabel-Maria; Rohdenburg, Markus; Lork, Enno; Staubitz, Anne
Aggregation induced emission - emissive stannoles in the solid state.
Chemical communications (Cambridge, England), 2020, 56, 9775-9778
7126941 CIFC29 H37 N3 O6P 1 21 19.8916; 10.1278; 14.6801
90; 98.829; 90		1453.23Sadamitsu, Yuta; Saito, Kodai; Yamada, Tohru
Stereoselective amination via vinyl-silver intermediates derived from silver-catalyzed carboxylative cyclization of propargylamine.
Chemical communications (Cambridge, England), 2020, 56, 9517-9520
7126942 CIFC26 H39 N3 O7P -19.6147; 12.4662; 12.8127
92.315; 106.443; 104.289		1417.26Sadamitsu, Yuta; Saito, Kodai; Yamada, Tohru
Stereoselective amination via vinyl-silver intermediates derived from silver-catalyzed carboxylative cyclization of propargylamine.
Chemical communications (Cambridge, England), 2020, 56, 9517-9520
7126943 CIFC3 H21 B2 N3 O12P 1 n 110.6478; 3.6669; 18.5931
90; 90.737; 90		725.9Deng, Yalan; Wang, Lei; Ge, Yuwei; Huang, Ling; Gao, Daojiang; Bi, Jian; Zou, Guohong
(NH<sub>4</sub>)<sub>3</sub>[B(OH)<sub>3</sub>]<sub>2</sub>(COOH)<sub>3</sub>: a graphite-like UV nonlinear optical material with a large birefringence <i>via</i> structural optimization.
Chemical communications (Cambridge, England), 2020, 56, 9982-9985
7126944 CIFC13 H15 Br O3P 1 21 111.8308; 4.88; 12.3237
90; 111.046; 90		664.04Zhang, Yu-Long; Zhao, Zhen-Ni; Li, Wang-Lai; Li, Jing-Jie; Kalita, Subarna Jyoti; Schneider, Uwe; Huang, Yi-Yong
Catalytic asymmetric aldehyde prenylation and application in the total synthesis of (-)-rosiridol and (-)-bifurcadiol.
Chemical communications (Cambridge, England), 2020, 56, 10030-10033
7126945 CIFC15 H12 Cl N5 O6 PtP -16.5658; 10.3732; 13.065
77.632; 86.382; 89.238		867.45Norton, Amie E.; Abdolmaleki, Mahmood Karimi; Liang, Jiamin; Sharma, Malvika; Golsby, Robert; Zoller, Ann; Krause, Jeanette A.; Connick, William B.; Chatterjee, Sayandev
Phase transformation induced mechanochromism in a platinum salt: a tale of two polymorphs.
Chemical communications (Cambridge, England), 2020, 56, 10175-10178
7126946 CIFC15 H12 Cl N5 O6 PtP -19.0638; 9.7744; 10.3917
68.652; 84.693; 89.76		853.359Norton, Amie E.; Abdolmaleki, Mahmood Karimi; Liang, Jiamin; Sharma, Malvika; Golsby, Robert; Zoller, Ann; Krause, Jeanette A.; Connick, William B.; Chatterjee, Sayandev
Phase transformation induced mechanochromism in a platinum salt: a tale of two polymorphs.
Chemical communications (Cambridge, England), 2020, 56, 10175-10178
7126947 CIFC31 H23 Cl2 F12 Fe N7 P2P m n a11.5092; 10.5574; 35.527
90; 90; 90		4316.8Fujisaki, Hiroto; Ishizuka, Tomoya; Shimoyama, Yoshihiro; Kotani, Hiroaki; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Selective catalytic 2e<sup>-</sup>-oxidation of organic substrates by an Fe<sup>II</sup> complex having an N-heterocyclic carbene ligand in water.
Chemical communications (Cambridge, England), 2020, 56, 9783-9786
7126948 CIFC33 H36 Cl4 Fe N6 O14P -112.005; 14.781; 23.238
85.501; 87.116; 73.751		3945Fujisaki, Hiroto; Ishizuka, Tomoya; Shimoyama, Yoshihiro; Kotani, Hiroaki; Shiota, Yoshihito; Yoshizawa, Kazunari; Kojima, Takahiko
Selective catalytic 2e<sup>-</sup>-oxidation of organic substrates by an Fe<sup>II</sup> complex having an N-heterocyclic carbene ligand in water.
Chemical communications (Cambridge, England), 2020, 56, 9783-9786
7126949 CIFC93.64 H148.93 K2 N2 Ni3 O8 P2 Si4C 1 2/c 128.067; 20.574; 18.052
90; 97.215; 90		10342Shoshani, Manar M.; Agapie, Theodor
Ligand architecture for triangular metal complexes: a high oxidation state Ni<sub>3</sub> cluster with proximal metal arrangement.
Chemical communications (Cambridge, England), 2020, 56, 11279-11282
7126950 CIFC112.83 H176.5 Fe N2 Ni3 O7.47 P2 Si2.94P 1 21/c 125.101; 30.772; 18.538
90; 100.85; 90		14063Shoshani, Manar M.; Agapie, Theodor
Ligand architecture for triangular metal complexes: a high oxidation state Ni<sub>3</sub> cluster with proximal metal arrangement.
Chemical communications (Cambridge, England), 2020, 56, 11279-11282
7126951 CIFC25 H25 N O8P n a 2111.712; 11.717; 17.423
90; 90; 90		2390.9Yu, Yang; Wang, Xin-Yu; Peng, Ju-Yin; Liu, Tao; Zhao, Yu-Long
Copper-catalyzed cascade cyclization reaction of 3-aminocyclobutenones with electron-deficient internal alkynes: synthesis of fully substituted indoles.
Chemical communications (Cambridge, England), 2020, 56, 9815-9818
7126952 CIFC50 H82 B2 F8 N4 Ni O10P 21 21 2111.548; 22.1219; 22.729
90; 90; 90		5806.4Yang, Wei; Lin, Xiaobin; Zhang, Yongyan; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Nickel(II)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles.
Chemical communications (Cambridge, England), 2020, 56, 10002-10005
7126953 CIFC26 H27 N3 O3 SC 1 2 167.83; 8.284; 8.771
90; 90.65; 90		4928Yang, Wei; Lin, Xiaobin; Zhang, Yongyan; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Nickel(II)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles.
Chemical communications (Cambridge, England), 2020, 56, 10002-10005
7126954 CIFC26 H27 N3 O2 SP 1 21 112.795; 7.636; 13.0428
90; 114.686; 90		1157.86Yang, Wei; Lin, Xiaobin; Zhang, Yongyan; Cao, Weidi; Liu, Xiaohua; Feng, Xiaoming
Nickel(II)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles.
Chemical communications (Cambridge, England), 2020, 56, 10002-10005
7126955 CIFC24 H22 O2P 21 21 216.8735; 8.7567; 31.8081
90; 90; 90		1914.5Hu, Jiadong; Gao, Yu-Qi; Xu, Dongyang; Chen, Le; Wen, Wen; Hou, Yi; Chen, Lu; Xie, Weiqing
Highly enantioselective addition of aliphatic aldehydes to 2-hydroxychalcone enabled by cooperative organocatalysts.
Chemical communications (Cambridge, England), 2020, 56, 10018-10021
7126956 CIFC179 H209 Cl3 N12 O52P 1 21/c 123.5752; 33.8217; 22.6177
90; 101.29; 90		17685.3Wan, Kang; Gao, Shi-Chang; Fang, Xu; Xu, Meng-Yu; Yang, Yong; Xue, Min
Oxacalix[4]arene-bridged pillar[5]arene dimers: syntheses, planar chirality and construction of chiral rotaxanes.
Chemical communications (Cambridge, England), 2020, 56, 10155-10158
7126957 CIFC132 H158 Cl6 N4 O28P -114.4932; 21.9303; 24.2711
85.199; 74.81; 83.34		7383.1Wan, Kang; Gao, Shi-Chang; Fang, Xu; Xu, Meng-Yu; Yang, Yong; Xue, Min
Oxacalix[4]arene-bridged pillar[5]arene dimers: syntheses, planar chirality and construction of chiral rotaxanes.
Chemical communications (Cambridge, England), 2020, 56, 10155-10158
7126958 CIFC54 H66 N4 O15 S2P -110.1378; 10.9386; 23.3534
87.576; 85.907; 86.452		2576.31Li, Haidong; Duwald, Romain; Pascal, Simon; Voci, Silvia; Besnard, Céline; Bosson, Johann; Bouffier, Laurent; Lacour, Jérôme; Sojic, Neso
Near-infrared electrochemiluminescence in water through regioselective sulfonation of diaza [4] and [6]helicene dyes.
Chemical communications (Cambridge, England), 2020, 56, 9771-9774
7126959 CIFC10 As4 Br10 Cl4 F26 O8 S4P -18.8126; 11.9355; 12.5355
68.761; 74.151; 75.96		1166.97Rupf, Susanne Margot; Pröhm, Patrick; Malischewski, Moritz
The [2+2] cycloaddition product of perhalogenated cyclopentadienyl cations: structural characterization of salts of the [C<sub>10</sub>Cl<sub>10</sub>]<sup>2+</sup> and [C<sub>10</sub>Br<sub>10</sub>]<sup>2+</sup> dications.
Chemical communications (Cambridge, England), 2020, 56, 9834-9837
7126960 CIFC5 Cl6P -18.2289; 10.3003; 12.507
97.189; 107.491; 111.379		908.04Rupf, Susanne Margot; Pröhm, Patrick; Malischewski, Moritz
The [2+2] cycloaddition product of perhalogenated cyclopentadienyl cations: structural characterization of salts of the [C<sub>10</sub>Cl<sub>10</sub>]<sup>2+</sup> and [C<sub>10</sub>Br<sub>10</sub>]<sup>2+</sup> dications.
Chemical communications (Cambridge, England), 2020, 56, 9834-9837
7126961 CIFC7 H3 Br6 NP n m a8.5108; 7.1691; 21.9711
90; 90; 90		1340.56Rupf, Susanne Margot; Pröhm, Patrick; Malischewski, Moritz
The [2+2] cycloaddition product of perhalogenated cyclopentadienyl cations: structural characterization of salts of the [C<sub>10</sub>Cl<sub>10</sub>]<sup>2+</sup> and [C<sub>10</sub>Br<sub>10</sub>]<sup>2+</sup> dications.
Chemical communications (Cambridge, England), 2020, 56, 9834-9837
7126962 CIFC10 Cl12 F34 O4 S2 Sb6P 1 21/n 19.8021; 19.9917; 12.0793
90; 97.406; 90		2347.32Rupf, Susanne Margot; Pröhm, Patrick; Malischewski, Moritz
The [2+2] cycloaddition product of perhalogenated cyclopentadienyl cations: structural characterization of salts of the [C<sub>10</sub>Cl<sub>10</sub>]<sup>2+</sup> and [C<sub>10</sub>Br<sub>10</sub>]<sup>2+</sup> dications.
Chemical communications (Cambridge, England), 2020, 56, 9834-9837
7126963 CIFC54 H57 N5 O21 Zn4P 21 21 2116.4452; 18.9661; 19.6218
90; 90; 90		6120.07Dodson, Ryan A.; Kalenak, Andre P.; Du Bois, Derek R.; Gill-Ljunghammer, Sasha L; Matzger, Adam J.
N,N-Diethyl-3-methylbenzamide (DEET) acts as a metal-organic framework synthesis solvent with phase-directing capabilities.
Chemical communications (Cambridge, England), 2020, 56, 9966-9969
7126964 CIFC19 H19 F3 O7 SP 1 21/n 111.1889; 15.6583; 11.3387
90; 103.564; 90		1931.1Zhang, Da-Wei; Fan, Hui-Lan; Zhang, Wenzhao; Li, Cheng-Ji; Luo, Sanzhong; Qin, Hong-Bo
Collective enantioselective total synthesis of (+)-sinensilactam A, (+)-lingzhilactone B and (-)-lingzhiol: divergent reactivity of styrene.
Chemical communications (Cambridge, England), 2020, 56, 10066-10069
7126965 CIFC22 H25 N O8P 1 21/n 118.9306; 11.0428; 21.1989
90; 114.695; 90		4026.3Zhang, Da-Wei; Fan, Hui-Lan; Zhang, Wenzhao; Li, Cheng-Ji; Luo, Sanzhong; Qin, Hong-Bo
Collective enantioselective total synthesis of (+)-sinensilactam A, (+)-lingzhilactone B and (-)-lingzhiol: divergent reactivity of styrene.
Chemical communications (Cambridge, England), 2020, 56, 10066-10069
7126966 CIFC29 H24 N4 OP -110.6093; 11.4966; 12.6556
63.223; 69.002; 62.815		1203.04Maeda, Takeshi; Liess, Andreas; Kudzus, Astrid; Krause, Ana-Maria; Stolte, Matthias; Amitani, Hitoshi; Yagi, Shigeyuki; Fujiwara, Hideki; Würthner, Frank
Hydrogen bond-rigidified planar squaraine dye and its electronic and organic semiconductor properties.
Chemical communications (Cambridge, England), 2020, 56, 9890-9893
7126967 CIFC29 H22 F2 N4 OP -110.041; 11.3867; 11.654
85.675; 81.578; 68.373		1225Maeda, Takeshi; Liess, Andreas; Kudzus, Astrid; Krause, Ana-Maria; Stolte, Matthias; Amitani, Hitoshi; Yagi, Shigeyuki; Fujiwara, Hideki; Würthner, Frank
Hydrogen bond-rigidified planar squaraine dye and its electronic and organic semiconductor properties.
Chemical communications (Cambridge, England), 2020, 56, 9890-9893
7126968 CIFC31 H20 Br4 SiP -111.1507; 11.5156; 11.6809
74.098; 80.106; 83.183		1416.99Nesmelov, Andrei; Lee, David; Bejger, Christopher; Kocherga, Margaret; Lyles, Zachary; Greenier, Madeline K.; Vitallo, Ashley Ariel; Kaouk, Ghallia; Jones, Daniel S.; Schmedake, Thomas A.
Accessing new microporous polyspirobifluorenes via a C/Si switch.
Chemical communications (Cambridge, England), 2020, 56, 9846-9849
7126969 CIFC24 H12 Br4 SiP b c a10.3068; 14.7409; 28.6394
90; 90; 90		4351.23Nesmelov, Andrei; Lee, David; Bejger, Christopher; Kocherga, Margaret; Lyles, Zachary; Greenier, Madeline K.; Vitallo, Ashley Ariel; Kaouk, Ghallia; Jones, Daniel S.; Schmedake, Thomas A.
Accessing new microporous polyspirobifluorenes via a C/Si switch.
Chemical communications (Cambridge, England), 2020, 56, 9846-9849
7126970 CIFC17 H34 B2 Cl2 N4P 21 21 219.1674; 10.6202; 22.2091
90; 90; 90		2162.3Fırıncı, Erkan; Fırıncı, Rukiye; Sevinçek, Resul; Aygün, Muhittin; Şahin, Yüksel
Neutral cyclic sp<sup>2</sup>-sp<sup>3</sup> and sp<sup>3</sup>-sp<sup>3</sup> diboranes from <i>N</i>,<i>N</i>'-dicyclohexylcarbodiimide insertion into 1,2-dichlorodiboranes(4).
Chemical communications (Cambridge, England), 2020, 56, 9807-9810
7126971 CIFC33 H48 B2 Cl2 N2P 1 21/n 110.335; 22.822; 13.912
90; 102.15; 90		3207.9Fırıncı, Erkan; Fırıncı, Rukiye; Sevinçek, Resul; Aygün, Muhittin; Şahin, Yüksel
Neutral cyclic sp<sup>2</sup>-sp<sup>3</sup> and sp<sup>3</sup>-sp<sup>3</sup> diboranes from <i>N</i>,<i>N</i>'-dicyclohexylcarbodiimide insertion into 1,2-dichlorodiboranes(4).
Chemical communications (Cambridge, England), 2020, 56, 9807-9810
7126972 CIFC30 H56 B2 Cl2 N6I 41 c d17.638; 17.638; 24.541
90; 90; 90		7634.7Fırıncı, Erkan; Fırıncı, Rukiye; Sevinçek, Resul; Aygün, Muhittin; Şahin, Yüksel
Neutral cyclic sp<sup>2</sup>-sp<sup>3</sup> and sp<sup>3</sup>-sp<sup>3</sup> diboranes from <i>N</i>,<i>N</i>'-dicyclohexylcarbodiimide insertion into 1,2-dichlorodiboranes(4).
Chemical communications (Cambridge, England), 2020, 56, 9807-9810
7126973 CIFC40 H30 Ca F6 N8 O8C 1 2/c 127.4699; 9.5594; 18.4011
90; 129.344; 90		3736.9Trautnitz, Markus F. K.; Haas, Tobias; Schubert, Hartmut; Seitz, Michael
Unexpected discovery of calcium cryptates with exceptional stability.
Chemical communications (Cambridge, England), 2020, 56, 9874-9877
7126974 CIFC38 H30 Ca F6 N8 O10 S2C 1 2/c 127.2841; 9.7632; 17.9917
90; 127.373; 90		3808.7Trautnitz, Markus F. K.; Haas, Tobias; Schubert, Hartmut; Seitz, Michael
Unexpected discovery of calcium cryptates with exceptional stability.
Chemical communications (Cambridge, England), 2020, 56, 9874-9877
7126975 CIFC63 H84 O10 S6C 1 2/c 120.246; 15.263; 21.6226
90; 114.172; 90		6095.9Shin, Mingyeong; Seo, Sujin; Park, In-Hyeok; Lee, Eunji; Habata, Yoichi; Lee, Shim Sung
Metallosupramolecules of pillar[5]-bis-trithiacrown including a mercury(ii) iodide ion-triplet complex.
Chemical communications (Cambridge, England), 2020, 56, 10135-10138
7126976 CIFC59 H74 Cl6 Hg O10 S6C 1 c 111.9926; 27.2154; 20.3121
90; 93.071; 90		6620Shin, Mingyeong; Seo, Sujin; Park, In-Hyeok; Lee, Eunji; Habata, Yoichi; Lee, Shim Sung
Metallosupramolecules of pillar[5]-bis-trithiacrown including a mercury(ii) iodide ion-triplet complex.
Chemical communications (Cambridge, England), 2020, 56, 10135-10138
7126977 CIFC59 H73.5 Br6 Cl0.5 Hg3 N O10 S6P 1 c 115.5878; 20.0801; 24.7383
90; 94.682; 90		7717.4Shin, Mingyeong; Seo, Sujin; Park, In-Hyeok; Lee, Eunji; Habata, Yoichi; Lee, Shim Sung
Metallosupramolecules of pillar[5]-bis-trithiacrown including a mercury(ii) iodide ion-triplet complex.
Chemical communications (Cambridge, England), 2020, 56, 10135-10138
7126978 CIFC57 H70 Hg I2 O10 S6P 1 21/c 120.1865; 15.1666; 22.7025
90; 120.148; 90		6010.4Shin, Mingyeong; Seo, Sujin; Park, In-Hyeok; Lee, Eunji; Habata, Yoichi; Lee, Shim Sung
Metallosupramolecules of pillar[5]-bis-trithiacrown including a mercury(ii) iodide ion-triplet complex.
Chemical communications (Cambridge, England), 2020, 56, 10135-10138
7126979 CIFC8 H10 Br N O4 Pb SP 6510.1079; 10.1079; 21.838
90; 90; 120		1932.3Song, Xueling; Peng, Chengdong; Xu, Xiaoxiang; Yin, Jinlin; Fei, Honghan
Efficient, broadband self-trapped white-light emission from haloplumbate-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 10078-10081
7126980 CIFC8 H10 Cl N O4 Pb SP 6110.0345; 10.0345; 21.669
90; 90; 120		1889.6Song, Xueling; Peng, Chengdong; Xu, Xiaoxiang; Yin, Jinlin; Fei, Honghan
Efficient, broadband self-trapped white-light emission from haloplumbate-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 10078-10081
7126981 CIFC43 H62.5 Cl Li N11.5 O7P -19.721; 14.384; 17.153
88.5; 86.85; 77.08		2334Hong, Kyeong-Im; Kim, Hyeongcheol; Kim, Younghun; Choi, Moon-Gun; Jang, Woo-Dong
Strapped calix[4]pyrrole as a lithium salts selective receptor through separated ion-pair binding.
Chemical communications (Cambridge, England), 2020, 56, 10541-10544
7126982 CIFH129 La9 O240 Si3 W44F m -3 c37.5612; 37.5612; 37.5612
90; 90; 90		52993Liu, Jin-Hua; Lin, Li-Dan; Wang, Guo-Qiang; Li, Ling-Yun; Sun, Yan-Qiong; Li, Xin-Xiong; Zheng, Shou-Tian
All-inorganic open frameworks based on gigantic four-shell Ln@W<sub>8</sub>@Ln<sub>8</sub>@(SiW<sub>12</sub>)<sub>6</sub> clusters.
Chemical communications (Cambridge, England), 2020, 56, 10305-10308
7126983 CIFC30 H12 Eu3 N12 O19F m -3 m27.6237; 27.6237; 27.6237
90; 90; 90		21078.8Cao, Wenqian; Xia, Tifeng; Cui, Yuanjing; Yu, Yang; Qian, Guodong
Lanthanide metal-organic frameworks with nitrogen functional sites for the highly selective and sensitive detection of NADPH.
Chemical communications (Cambridge, England), 2020, 56, 10851-10854
7126984 CIFC42 H40 N2 O16 Zr3F m m m20.717; 31.9589; 34.5056
90; 90; 90		22846Zhang, Xiurong; Fan, Weidong; Fu, Mingyue; Jiang, Weifeng; Lu, Kebin; Wang, Yutong; Sun, Daofeng
Optimizing zirconium metal-organic frameworks through steric tuning for efficient removal of Cr<sub>2</sub>O<sub>7</sub><sup>2</sup>.
Chemical communications (Cambridge, England), 2020, 56, 10513-10516
7126985 CIFC18 H22 O5C 1 2/c 131.452; 5.5892; 19.232
90; 90.16; 90		3380.8Zhang, Jiayong; Hao, Jiahang; Huang, Zhiqiang; Han, Jie; He, Zhengjie
P<sup>III</sup>-Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles.
Chemical communications (Cambridge, England), 2020, 56, 10251-10254
7126986 CIFC23 H21 N O9P -19.4995; 9.5604; 12.684
97.84; 105.01; 103.9		1055.5Zhang, Jiayong; Hao, Jiahang; Huang, Zhiqiang; Han, Jie; He, Zhengjie
P<sup>III</sup>-Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles.
Chemical communications (Cambridge, England), 2020, 56, 10251-10254
7126987 CIFC23 H25 N O6 SP -18.7393; 9.8405; 28.488
80.848; 87.645; 69.047		2258.48Zhang, Jiayong; Hao, Jiahang; Huang, Zhiqiang; Han, Jie; He, Zhengjie
P<sup>III</sup>-Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles.
Chemical communications (Cambridge, England), 2020, 56, 10251-10254
7126988 CIFC21 H N5 O SP -16.0259; 12.569; 12.93
115.34; 93.96; 100.21		859.4Zhang, Jiayong; Hao, Jiahang; Huang, Zhiqiang; Han, Jie; He, Zhengjie
P<sup>III</sup>-Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles.
Chemical communications (Cambridge, England), 2020, 56, 10251-10254
7126989 CIFC164 H124 Cu4 F24 N12 P12 Pd2P -116.1306; 16.6998; 18.3422
74.727; 77.311; 65.227		4294Moutier, F.; Khalil, A. M.; Baudron, S. A.; Lescop, C.
Gleaned snapshots on the road to coordination polymers: heterometallic architectures based on Cu(I) metallaclips and 2,2'-bis-dipyrrin metalloligands.
Chemical communications (Cambridge, England), 2020, 56, 10501-10504
7126990 CIFC228 H160 Cl0 Cu4 F24 N24 Ni4 P12P -118.207; 26.995; 28.766
73.564; 86.988; 72.007		12888Moutier, F.; Khalil, A. M.; Baudron, S. A.; Lescop, C.
Gleaned snapshots on the road to coordination polymers: heterometallic architectures based on Cu(I) metallaclips and 2,2'-bis-dipyrrin metalloligands.
Chemical communications (Cambridge, England), 2020, 56, 10501-10504
7126991 CIFC112 H76 Cl0 Cu2 F0 N14 Ni2 P4P -116.697; 18.05; 24.093
94.584; 96.139; 112.996		6587Moutier, F.; Khalil, A. M.; Baudron, S. A.; Lescop, C.
Gleaned snapshots on the road to coordination polymers: heterometallic architectures based on Cu(I) metallaclips and 2,2'-bis-dipyrrin metalloligands.
Chemical communications (Cambridge, England), 2020, 56, 10501-10504
7126992 CIFC32 H18 N6 PdP -19.9898; 12.0743; 12.2286
117.238; 103.019; 98.413		1223.64Moutier, F.; Khalil, A. M.; Baudron, S. A.; Lescop, C.
Gleaned snapshots on the road to coordination polymers: heterometallic architectures based on Cu(I) metallaclips and 2,2'-bis-dipyrrin metalloligands.
Chemical communications (Cambridge, England), 2020, 56, 10501-10504
7126993 CIFC28 H30 N2 O6P 21 21 218.5125; 16.338; 17.8809
90; 90; 90		2486.83Cai, Liu; Liu, Xiangshuai; Wang, Jie; Chen, Li; Li, Xin; Cheng, Jin-Pei
Enantioselective and regioselective aza-Friedel-Crafts reaction of electron-rich phenols with isatin-derived ketimines.
Chemical communications (Cambridge, England), 2020, 56, 10361-10364
7126994 CIFC32 H31 F12 N8 O P2 RuP -115.546; 15.7344; 16.911
99.814; 116.882; 96.323		3552.1Park, Sungho V.; Fry, Charles G.; Bill, Eckhard; Berry, John F.
A metastable Ru<sup>III</sup> azido complex with metallo-Staudinger reactivity.
Chemical communications (Cambridge, England), 2020, 56, 10738-10741
7126995 CIFC38 H43 F12 N5 O3 P2 RuP -112.725; 12.889; 15.603
113.141; 91.774; 117.69		2010.7Park, Sungho V.; Fry, Charles G.; Bill, Eckhard; Berry, John F.
A metastable Ru<sup>III</sup> azido complex with metallo-Staudinger reactivity.
Chemical communications (Cambridge, England), 2020, 56, 10738-10741
7126996 CIFC35 H37 Cl6.39 N5 O2 Ru SbP n m a23.348; 13.355; 12.292
90; 90; 90		3833Park, Sungho V.; Fry, Charles G.; Bill, Eckhard; Berry, John F.
A metastable Ru<sup>III</sup> azido complex with metallo-Staudinger reactivity.
Chemical communications (Cambridge, England), 2020, 56, 10738-10741
7126997 CIFC30.5 H28 F4.65 N5 O4.18 P2 RuP -111.39; 16.353; 20.162
99.44; 94.919; 109.589		3450Park, Sungho V.; Fry, Charles G.; Bill, Eckhard; Berry, John F.
A metastable Ru<sup>III</sup> azido complex with metallo-Staudinger reactivity.
Chemical communications (Cambridge, England), 2020, 56, 10738-10741
7126998 CIFC32 H31 Cl F6 N5 O P RuP m c 2110.366; 8.964; 17.126
90; 90; 90		1591.4Park, Sungho V.; Fry, Charles G.; Bill, Eckhard; Berry, John F.
A metastable Ru<sup>III</sup> azido complex with metallo-Staudinger reactivity.
Chemical communications (Cambridge, England), 2020, 56, 10738-10741
7126999 CIFC32 H28 O12 ZrP 1 c 117.0775; 5.63423; 16.986
90; 114.885; 90		1482.62Crosland, James M.; Corlett, Emily K.; Scapens, Dave; Guillou, Nathalie; Brown, Steven P.; Walton, Richard I.
Isolated zirconium centres captured from aqueous solution: the structure of zirconium mandelate revealed from NMR crystallography.
Chemical communications (Cambridge, England), 2020, 56, 10159-10162
7127000 CIFC14 H18 N4 S2P 21 21 216.8868; 14.8106; 15.0914
90; 90; 90		1539.3Bhunia, Supriya; Dolai, Anirban; Samanta, Subhas
Robust bi-directional photoswitching of thiomethyl substituted arylazopyrazoles under visible light.
Chemical communications (Cambridge, England), 2020, 56, 10247-10250
7127001 CIFC13 H16 N4 SP -16.9549; 8.8714; 11.149
80.68; 89.072; 84.658		675.9Bhunia, Supriya; Dolai, Anirban; Samanta, Subhas
Robust bi-directional photoswitching of thiomethyl substituted arylazopyrazoles under visible light.
Chemical communications (Cambridge, England), 2020, 56, 10247-10250
7127002 CIFC15 H11 F2 N3 O2P -17.793; 9.718; 10.297
99.54; 107.52; 109.15		671.5Zhang, Dong; Fang, Zheng; Cai, Jinlin; Liu, Chengkou; He, Wei; Duan, Jindian; Qin, Ning; Yang, Zhao; Guo, Kai
The copper(ii)-catalyzed and oxidant-promoted regioselective C-2 difluoromethylation of indoles and pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 8119-8122
7127003 CIFC12 H18 B2 Co F8 N6P 1 21/n 15.8051; 17.7416; 22.026
90; 90.256; 90		2268.5Saber, Mohamed R.; Singh, Mukesh K.; Dunbar, Kim R.
Geometrical control of the magnetic anisotropy in six coordinate cobalt complexes.
Chemical communications (Cambridge, England), 2020, 56, 8492-8495
7127004 CIFC76 H70 Cl7 N8 O6P 1 21/c 123.7142; 24.8126; 26.7983
90; 108.122; 90		14986.2Wong, Kevin Kei Gwan; Hoyas Pérez, Nadia; White, Andrew J. P.; Lewis, James E. M.
Self-assembly of a porous metallo-[5]rotaxane.
Chemical communications (Cambridge, England), 2020, 56, 10453-10456
7127005 CIFC56 H60 D12 N8 O15P -110.2036; 14.4428; 19.7614
79.654; 84.51; 75.81		2773.37Butera, Roberto; Shrinidhi, Annadka; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
Fourfold symmetric MCR's <i>via</i> the tetraisocyanide 1,3-diisocyano-2,2-bis(isocyanomethyl)propane.
Chemical communications (Cambridge, England), 2020, 56, 10662-10665
7127006 CIFC9 H8 N4P 42/n :28.3584; 8.3584; 6.7005
90; 90; 90		468.12Butera, Roberto; Shrinidhi, Annadka; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
Fourfold symmetric MCR's <i>via</i> the tetraisocyanide 1,3-diisocyano-2,2-bis(isocyanomethyl)propane.
Chemical communications (Cambridge, England), 2020, 56, 10662-10665
7127007 CIFC73 H96 F4 N8 O8I 41/a :215.6151; 15.6151; 33.2923
90; 90; 90		8117.71Butera, Roberto; Shrinidhi, Annadka; Kurpiewska, Katarzyna; Kalinowska-Tłuścik, Justyna; Dömling, Alexander
Fourfold symmetric MCR's <i>via</i> the tetraisocyanide 1,3-diisocyano-2,2-bis(isocyanomethyl)propane.
Chemical communications (Cambridge, England), 2020, 56, 10662-10665
7127008 CIFC47 H69 Fe Ge2 N4 P5P -112.9054; 13.5536; 17.432
98.83; 110.41; 92.274		2809.5Yadav, Ravi; Goswami, Bhupendra; Simler, Thomas; Schoo, Christoph; Reichl, Stephan; Scheer, Manfred; Roesky, Peter W.
A bis(germylene) functionalized metal-coordinated polyphosphide and its isomerization.
Chemical communications (Cambridge, England), 2020, 56, 10207-10210
7127009 CIFC54 H77 Fe Ge2 N4 P5P -112.1225; 14.174; 16.7654
84.679; 79.665; 83.291		2807Yadav, Ravi; Goswami, Bhupendra; Simler, Thomas; Schoo, Christoph; Reichl, Stephan; Scheer, Manfred; Roesky, Peter W.
A bis(germylene) functionalized metal-coordinated polyphosphide and its isomerization.
Chemical communications (Cambridge, England), 2020, 56, 10207-10210
7127010 CIFC43 H70 Fe N6 O P3 SnP 1 21/c 111.8994; 16.0639; 24.3083
90; 104.102; 90		4506.5Dorantes, Michael J.; Moore, James T.; Bill, Eckhard; Mienert, Bernd; Lu, Connie C.
Bimetallic iron-tin catalyst for N<sub>2</sub> to NH<sub>3</sub> and a silyldiazenido model intermediate.
Chemical communications (Cambridge, England), 2020, 56, 11030-11033
7127011 CIFC55 H92 Li N4 O4 P3 SnP 6313.6945; 13.6945; 18.3276
90; 90; 120		2976.7Dorantes, Michael J.; Moore, James T.; Bill, Eckhard; Mienert, Bernd; Lu, Connie C.
Bimetallic iron-tin catalyst for N<sub>2</sub> to NH<sub>3</sub> and a silyldiazenido model intermediate.
Chemical communications (Cambridge, England), 2020, 56, 11030-11033
7127012 CIFC43 H68 Fe K N6 O P3 SnP c a 2119.5107; 10.8907; 21.8866
90; 90; 90		4650.6Dorantes, Michael J.; Moore, James T.; Bill, Eckhard; Mienert, Bernd; Lu, Connie C.
Bimetallic iron-tin catalyst for N<sub>2</sub> to NH<sub>3</sub> and a silyldiazenido model intermediate.
Chemical communications (Cambridge, England), 2020, 56, 11030-11033
7127013 CIFC88 H148 Fe2 N12 O P6 Si2 Sn2P 1 21/c 111.4678; 21.538; 19.703
90; 96.834; 90		4831.9Dorantes, Michael J.; Moore, James T.; Bill, Eckhard; Mienert, Bernd; Lu, Connie C.
Bimetallic iron-tin catalyst for N<sub>2</sub> to NH<sub>3</sub> and a silyldiazenido model intermediate.
Chemical communications (Cambridge, England), 2020, 56, 11030-11033
7127014 CIFC16 H14 O SP 1 21/n 14.7107; 10.021; 27.643
90; 94.105; 90		1301.6Sangeetha, Subramani; Sekar, Govindasamy
Copper-catalyzed double C-S bond formation for the synthesis of 2-acyldihydrobenzo[<i>b</i>]thiophenes and 2-acylbenzo[<i>b</i>]thiophenes.
Chemical communications (Cambridge, England), 2020, 56, 10906-10909
7127015 CIFC14 H10 O2 S2P 1 21/n 113.9604; 5.9708; 16.2069
90; 113.622; 90		1237.73Sangeetha, Subramani; Sekar, Govindasamy
Copper-catalyzed double C-S bond formation for the synthesis of 2-acyldihydrobenzo[<i>b</i>]thiophenes and 2-acylbenzo[<i>b</i>]thiophenes.
Chemical communications (Cambridge, England), 2020, 56, 10906-10909
7127016 CIFC7 H13 Ni1.5 S4P b c n16.0517; 12.69; 11.0788
90; 90; 90		2256.71Pieri, Cyril; Bhattacharjee, Anirban; Barrozo, Alexandre; Faure, Bruno; Giorgi, Michel; Fize, Jennifer; Réglier, Marius; Field, Martin; Orio, Maylis; Artero, Vincent; Hardré, Renaud
Hydrogen evolution reaction mediated by an all-sulfur trinuclear nickel complex.
Chemical communications (Cambridge, England), 2020, 56, 11106-11109
7127017 CIFC66 H56 Cl2 N6 O10P 21 21 2110.4684; 12.28; 45.879
90; 90; 90		5897.8Mei, Ming-Shun; Wang, Yu-Hui; Hu, Qing; Li, Qing-Hua; Shi, Da-Yu; Gao, Dingding; Ge, Guangbo; Lin, Guo-Qiang; Tian, Ping
Enantioselective [3+2] annulation of isatin-derived MBH-carbonates and 3-nitroindoles enabled by a bifunctional DMAP-thiourea.
Chemical communications (Cambridge, England), 2020, 56, 10718-10721
7127018 CIFC36 H29 Br N4 O4 SP 21 21 2110.4627; 10.6763; 29.015
90; 90; 90		3241.1Wei, Shiqiang; Bao, Xiaoze; Wang, Wenyao; Nawaz, Shah; Dai, Qimin; Qu, Jingping; Wang, Baomin
Enantioselective construction of dispirotriheterocycles featuring a 4-aminopyrazolone motif through a cascade Michael/cyclization process.
Chemical communications (Cambridge, England), 2020, 56, 10690-10693
7127019 CIFC2 H5 F6 N2 SbP 1 21/c 17.7291; 9.3482; 10.1754
90; 97.481; 90		728.95Cantin, Thomas; Morgenstern, Yvonne; Mingot, Agnès; Kornath, Andreas; Thibaudeau, Sébastien
Evidence and exploitation of dicationic ammonium-nitrilium superelectrophiles: direct synthesis of unsaturated piperidinones.
Chemical communications (Cambridge, England), 2020, 56, 11110-11113
7127020 CIFC2 H7 F13 N2 Sb2P b c a14.8174; 10.5692; 15.649
90; 90; 90		2450.8Cantin, Thomas; Morgenstern, Yvonne; Mingot, Agnès; Kornath, Andreas; Thibaudeau, Sébastien
Evidence and exploitation of dicationic ammonium-nitrilium superelectrophiles: direct synthesis of unsaturated piperidinones.
Chemical communications (Cambridge, England), 2020, 56, 11110-11113
7127021 CIFC119 H44 N4 Ni S2 Sc4P -114.5681; 14.6511; 19.9842
83.154; 84.459; 61.176		3706.5Nie, Mingzhe; Meng, Haibing; Zhao, Chong; Lu, Yuxi; Zhang, Jie; Feng, Lai; Wang, Chunru; Wang, Taishan
Crystallographic evidence and spin activation for the Russian-doll-type metallofullerene Sc<sub>4</sub>C<sub>2</sub>@C<sub>80</sub>.
Chemical communications (Cambridge, England), 2020, 56, 10879-10882
7127022 CIFC18 H14 Br2 O4P -16.5732; 12.3258; 22.4447
105.598; 93.439; 93.704		1742.17Li, Mingrui; Sun, Yiming; Xie, Yuxing; Yu, Yang; Huang, Fei; Huang, He
Copper-catalyzed carbene insertion and ester migration for the synthesis of polysubstituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 11050-11053
7127023 CIFC25 H21 N O2P -17.8574; 10.1476; 13.2472
73.398; 88.834; 80.053		996.53Li, Mingrui; Sun, Yiming; Xie, Yuxing; Yu, Yang; Huang, Fei; Huang, He
Copper-catalyzed carbene insertion and ester migration for the synthesis of polysubstituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 11050-11053
7127024 CIFC49 H99 K3 N3 O18 Pb11 RuC 1 2/c 145.648; 14.2377; 25.141
90; 93.2134; 90		16314Li, Ai-Min; Wang, Yi; Zavalij, Peter Y.; Chen, Fu; Muñoz-Castro, Alvaro; Eichhorn, Bryan W.
[Cp*RuPb<sub>11</sub>]<sup>3-</sup> and [Cu@Cp*RuPb<sub>11</sub>]<sup>2-</sup>: centered and non-centered transition-metal substituted zintl icosahedra.
Chemical communications (Cambridge, England), 2020, 56, 10859-10862
7127025 CIFC89 H150 Cu2 K4 O24 Pb22 Ru2P -113.18; 13.185; 20.7259
92.8432; 104.274; 102.191		3392.1Li, Ai-Min; Wang, Yi; Zavalij, Peter Y.; Chen, Fu; Muñoz-Castro, Alvaro; Eichhorn, Bryan W.
[Cp*RuPb<sub>11</sub>]<sup>3-</sup> and [Cu@Cp*RuPb<sub>11</sub>]<sup>2-</sup>: centered and non-centered transition-metal substituted zintl icosahedra.
Chemical communications (Cambridge, England), 2020, 56, 10859-10862
7127026 CIFC30 H22 N2 O6 S2P 1 21/c 19.9499; 9.6309; 27.2708
90; 93.901; 90		2607.21Takeda, Takashi; Akutagawa, Tomoyuki
Conformation change significantly affected the optical and electronic properties of arylsulfonamide-substituted anthraquinones.
Chemical communications (Cambridge, England), 2020, 56, 10564-10567
7127027 CIFC32 H28 Cl6 N2 O6 S2C 1 2/c 152.9762; 15.1879; 13.2
90; 102.745; 90		10359Takeda, Takashi; Akutagawa, Tomoyuki
Conformation change significantly affected the optical and electronic properties of arylsulfonamide-substituted anthraquinones.
Chemical communications (Cambridge, England), 2020, 56, 10564-10567
7127028 CIFC16 H15 FP 1 21/c 114.697; 5.79; 14.578
90; 104.759; 90		1199.6Gu, Yichao; Sun, Xueliang; Wan, Bin; Lu, Zhuoer; Zhang, Yanghui
C(sp<sup>3</sup>)-H activation-enabled cross-coupling of two aryl halides: an approach to 9,10-dihydrophenanthrenes.
Chemical communications (Cambridge, England), 2020, 56, 10942-10945
7127029 CIFC42 H56 Br1.08 Cl4.92 Fe2 N2 O12P 1 21/n 110.8043; 20.7436; 12.2725
90; 101.419; 90		2696.1Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127030 CIFC48 H70 Br1.08 Cl4.92 Fe2 N2 O15P 1 21/c 120.2837; 21.7936; 14.4042
90; 108.042; 90		6054.4Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127031 CIFC42 H56 Br2.12 Cl3.88 Fe2 N2 O12P 1 21/n 110.8837; 20.7386; 12.3417
90; 101.41; 90		2730.6Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127032 CIFC42 H56 Br3.88 Cl2.12 Fe2 N2 O12P 1 21/n 110.9142; 20.5604; 12.3173
90; 101.617; 90		2707.4Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127033 CIFC48 H70 Br2.12 Cl3.88 Fe2 N2 O15P 1 21/c 120.3278; 21.7798; 14.4219
90; 107.935; 90		6074.8Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127034 CIFC48 H70 Br3.91 Cl2.09 Fe2 N2 O15P 1 21/c 120.4745; 21.8256; 14.444
90; 107.895; 90		6142.3Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127035 CIFC42 H56 Br0.48 Cl5.52 Fe2 N2 O12P 1 21/n 110.7693; 20.6834; 12.2409
90; 101.308; 90		2673.7Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127036 CIFC48 H70 Br0.6 Cl5.4 Fe2 N2 O15P 1 21/c 120.2076; 21.8087; 14.3967
90; 108.08; 90		6031.4Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127037 CIFC42 H56 Cl5.66 F0.34 Fe2 N2 O12P 1 21/n 110.7147; 20.7638; 12.2126
90; 101.108; 90		2666.13Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127038 CIFC48 H70 Cl5.66 F0.34 Fe2 N2 O15P 1 21/c 120.1787; 21.8982; 14.4
90; 108; 90		6051.6Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127039 CIFC42 H56 Cl4.55 F1.45 Fe2 N2 O12P 1 21/n 110.5632; 21.1362; 12.2412
90; 100.998; 90		2682.8Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127040 CIFC42 H56 Cl3.49 F2.51 Fe2 N2 O12P 1 21/n 110.4272; 21.1795; 12.1426
90; 101.168; 90		2630.83Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127041 CIFC48 H70 Cl4.16 F1.84 Fe2 N2 O15P 1 21/c 119.8524; 21.9805; 14.2863
90; 107.662; 90		5940.2Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127042 CIFC48 H70 Cl4.55 F1.45 Fe2 N2 O15P 1 21/c 119.8773; 21.9737; 14.2912
90; 107.608; 90		5949.6Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127043 CIFC42 H56 Cl4.16 F1.84 Fe2 N2 O12P 1 21/n 110.4941; 21.164; 12.1914
90; 101.118; 90		2656.9Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127044 CIFC48 H70 Cl5.31 F0.69 Fe2 N2 O15P 1 21/c 120.1163; 21.8555; 14.3929
90; 108.051; 90		6016.4Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127045 CIFC48 H70 Cl4.98 F1.02 Fe2 N2 O15P 1 21/c 120.0262; 21.8928; 14.3496
90; 107.832; 90		5989Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127046 CIFC48 H70 Cl3.49 F2.51 Fe2 N2 O15P 1 21/c 119.6602; 22.2123; 14.2016
90; 107.21; 90		5924.1Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127047 CIFC42 H56 Cl4.98 F1.02 Fe2 N2 O12P 1 21/n 110.6203; 20.9025; 12.2015
90; 101.021; 90		2658.67Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127048 CIFC42 H56 Cl5.31 F0.69 Fe2 N2 O12P 1 21/n 110.6805; 20.8987; 12.2445
90; 101.108; 90		2681.9Sekine, Yoshihiro; Chen, Jian; Eguchi, Naoki; Miyasaka, Hitoshi
Fine tuning of intra-lattice electron transfers through site doping in tetraoxolene-bridged iron honeycomb layers.
Chemical communications (Cambridge, England), 2020, 56, 10867-10870
7127049 CIFC18 H18 N2 O3P -17.6107; 9.6669; 11.6421
74.194; 82.375; 75.798		796.96Vaishanv, Narendra Kumar; Chandrasekharan, Sanoop P.; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Substrate-controlled, PBu<sub>3</sub>-catalyzed annulation of phenacylmalononitriles with allenoates enables tunable access to cyclopentenes.
Chemical communications (Cambridge, England), 2020, 56, 11054-11057
7127050 CIFC17 H15 Br N2 O3C 1 2/c 124.827; 6.5559; 21.173
90; 107.267; 90		3290.9Vaishanv, Narendra Kumar; Chandrasekharan, Sanoop P.; Zaheer, Mohd Khalid; Kant, Ruchir; Mohanan, Kishor
Substrate-controlled, PBu<sub>3</sub>-catalyzed annulation of phenacylmalononitriles with allenoates enables tunable access to cyclopentenes.
Chemical communications (Cambridge, England), 2020, 56, 11054-11057
7127051 CIFC68 H56 Fe2 N8 O8 S8P -113.268; 15.98; 18.693
67.82; 76.64; 81.97		3564.7Zappe, Lisa; Schönfeld, Sophie; Hörner, Gerald; Zenere, Katrina A.; Leong, Chanel F.; Kepert, Cameron J.; D'Alessandro, Deanna M; Weber, Birgit; Neville, Suzanne M.
Spin crossover modulation in a coordination polymer with the redox-active bis-pyridyltetrathiafulvalene (py<sub>2</sub>TTF) ligand.
Chemical communications (Cambridge, England), 2020, 56, 10469-10472
7127052 CIFC3 H8 Cl2 Cu0.5 NC 1 2/c 114.5625; 14.5977; 5.9349
90; 107.284; 90		1204.66Gautier, Romain; Clérac, Rodolphe; Paris, Michael; Massuyeau, Florian
Role of specific distorted metal complexes in exciton self-trapping for hybrid metal halides.
Chemical communications (Cambridge, England), 2020, 56, 10139-10142
7127053 CIFC3 H8 Cd0.5 Cl2 NC 1 2/c 115.2462; 15.1744; 5.7267
90; 105.733; 90		1275.25Gautier, Romain; Clérac, Rodolphe; Paris, Michael; Massuyeau, Florian
Role of specific distorted metal complexes in exciton self-trapping for hybrid metal halides.
Chemical communications (Cambridge, England), 2020, 56, 10139-10142
7127054 CIFC27 H19 N O3P 1 21/c 19.7392; 11.0547; 19.1794
90; 101.876; 90		2020.73Wang, Ding; Ma, Zhishuang; Wang, Nana; Li, Chenyu; Wang, Tao; Liang, Yong; Zhang, Zunting
Synthesis of 7-hydroxy-6H-naphtho[2,3-c]coumarin via a TsOH-mediated tandem reaction.
Chemical communications (Cambridge, England), 2020, 56, 10369-10372
7127055 CIFC47 H57 N3 O4P 1 21/c 120.6141; 16.28811; 24.27716
90; 96.8619; 90		8093.03Picci, Giacomo; Kubicki, Maciej; Garau, Alessandra; Lippolis, Vito; Mocci, Rita; Porcheddu, Andrea; Quesada, Roberto; Ricci, Pier Carlo; Scorciapino, M. Andrea; Caltagirone, Claudia
Simple squaramide receptors for highly efficient anion binding in aqueous media and transmembrane transport.
Chemical communications (Cambridge, England), 2020, 56, 11066-11069
7127056 CIFC22 H16 N4 O3P 1 21/n 112.60987; 10.80108; 13.03058
90; 102.317; 90		1733.92Picci, Giacomo; Kubicki, Maciej; Garau, Alessandra; Lippolis, Vito; Mocci, Rita; Porcheddu, Andrea; Quesada, Roberto; Ricci, Pier Carlo; Scorciapino, M. Andrea; Caltagirone, Claudia
Simple squaramide receptors for highly efficient anion binding in aqueous media and transmembrane transport.
Chemical communications (Cambridge, England), 2020, 56, 11066-11069
7127057 CIFC36 H50 Cl N5 O2I 1 2/a 133.3689; 22.8121; 38.3244
90; 107.4; 90		27838.1Picci, Giacomo; Kubicki, Maciej; Garau, Alessandra; Lippolis, Vito; Mocci, Rita; Porcheddu, Andrea; Quesada, Roberto; Ricci, Pier Carlo; Scorciapino, M. Andrea; Caltagirone, Claudia
Simple squaramide receptors for highly efficient anion binding in aqueous media and transmembrane transport.
Chemical communications (Cambridge, England), 2020, 56, 11066-11069
7127058 CIFC20 H22 Fe N O5 SC 1 c 118.1583; 17.6762; 8.0886
90; 128.002; 90		2045.8Kobayashi, Fumiya; Akiyoshi, Ryohei; Kosumi, Daisuke; Nakamura, Masaaki; Lindoy, Leonard F.; Hayami, Shinya
Solvent vapor-induced polarity and ferroelectricity switching.
Chemical communications (Cambridge, England), 2020, 56, 10509-10512
7127059 CIFC25.5 H23.5 Fe N2.5 O4P 1 21/n 19.3501; 19.938; 12.331
90; 111.89; 90		2133Kobayashi, Fumiya; Akiyoshi, Ryohei; Kosumi, Daisuke; Nakamura, Masaaki; Lindoy, Leonard F.; Hayami, Shinya
Solvent vapor-induced polarity and ferroelectricity switching.
Chemical communications (Cambridge, England), 2020, 56, 10509-10512
7127060 CIFC26 H23 N3P -19.038; 10.7196; 10.8654
97.184; 94.287; 111.2		965.509Yang, Yurong; Zhang, Kaixin; Yang, Jian; Zhu, Guoxun; Chen, Weijie; Zhang, Chao; Zhou, Zhi; Yi, Wei
Ru(II)-Catalyzed and acidity-controlled tunable [5+1]/[5+2] annulation for building ring-fused quinazolines and 1,3-benzodiazepines.
Chemical communications (Cambridge, England), 2020, 56, 11315-11318
7127061 CIFC26 H23 N3P 1 21/c 114.8745; 9.2268; 14.352
90; 101.721; 90		1928.65Yang, Yurong; Zhang, Kaixin; Yang, Jian; Zhu, Guoxun; Chen, Weijie; Zhang, Chao; Zhou, Zhi; Yi, Wei
Ru(II)-Catalyzed and acidity-controlled tunable [5+1]/[5+2] annulation for building ring-fused quinazolines and 1,3-benzodiazepines.
Chemical communications (Cambridge, England), 2020, 56, 11315-11318
7127062 CIFC27 H27 N O2 SP -17.1857; 17.0238; 19.6063
113.132; 90.973; 96.562		2186.09Andrés Castán, José María; Dalinot, Clément; Dayneko, Sergey; Abad Galan, Laura; Simón Marqués, Pablo; Alévêque, Olivier; Allain, Magali; Maury, Olivier; Favereau, Ludovic; Blanchard, Philippe; Welch, Gregory C.; Cabanetos, Clément
Synthesis, characterization and use of benzothioxanthene imide based dimers.
Chemical communications (Cambridge, England), 2020, 56, 10131-10134
7127063 CIFC47 H37 Cl3 N2 O8 S2P -110.6018; 13.9495; 15.1107
85.675; 86.516; 74.883		2149.3Andrés Castán, José María; Dalinot, Clément; Dayneko, Sergey; Abad Galan, Laura; Simón Marqués, Pablo; Alévêque, Olivier; Allain, Magali; Maury, Olivier; Favereau, Ludovic; Blanchard, Philippe; Welch, Gregory C.; Cabanetos, Clément
Synthesis, characterization and use of benzothioxanthene imide based dimers.
Chemical communications (Cambridge, England), 2020, 56, 10131-10134
7127064 CIFC48 H38 Cl6 N2 O4 S2P -19.3061; 13.3044; 18.0105
83.284; 87.291; 83.287		2198.16Andrés Castán, José María; Dalinot, Clément; Dayneko, Sergey; Abad Galan, Laura; Simón Marqués, Pablo; Alévêque, Olivier; Allain, Magali; Maury, Olivier; Favereau, Ludovic; Blanchard, Philippe; Welch, Gregory C.; Cabanetos, Clément
Synthesis, characterization and use of benzothioxanthene imide based dimers.
Chemical communications (Cambridge, England), 2020, 56, 10131-10134
7127065 CIFC176 H172 N6 O12 S6R -3 :H45.615; 45.615; 12.3835
90; 90; 120		22314.6Andrés Castán, José María; Dalinot, Clément; Dayneko, Sergey; Abad Galan, Laura; Simón Marqués, Pablo; Alévêque, Olivier; Allain, Magali; Maury, Olivier; Favereau, Ludovic; Blanchard, Philippe; Welch, Gregory C.; Cabanetos, Clément
Synthesis, characterization and use of benzothioxanthene imide based dimers.
Chemical communications (Cambridge, England), 2020, 56, 10131-10134
7127066 CIFC97 H152 N2 O Si7P 1 21/c 113.0001; 28.8076; 26.4244
90; 93.4546; 90		9878Poitiers, Nadine E.; Huch, Volker; Zimmer, Michael; Scheschkewitz, David
Nickel-assisted complete cleavage of CO by a silylene/siliconoid hybrid under formation of an Si[double bond, length as m-dash]C enol ether bridge.
Chemical communications (Cambridge, England), 2020, 56, 10898-10901
7127067 CIFC42 H34 F12 N2 O6 P2 Re2 Ru2P -19.5337; 10.9943; 11.1572
99.017; 103.077; 102.808		1084.12Hernández-Valdés, Daniel; Wettstein, Lionel; Fernández-Terán, Ricardo; Probst, Benjamin; Fox, Thomas; Spingler, Bernhard; Nadeem, Qaisar; Alberto, Roger
Dynamic dimer-monomer equilibrium in a cycloruthenated complex of [Re(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2020, 56, 10658-10661
7127068 CIFC25 H18 F6 N O7 Re RuP 1 21/n 110.5504; 17.4219; 14.6483
90; 102.806; 90		2625.5Hernández-Valdés, Daniel; Wettstein, Lionel; Fernández-Terán, Ricardo; Probst, Benjamin; Fox, Thomas; Spingler, Bernhard; Nadeem, Qaisar; Alberto, Roger
Dynamic dimer-monomer equilibrium in a cycloruthenated complex of [Re(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2020, 56, 10658-10661
7127069 CIFC25 H18 F6 N O7 Re RuP 1 21/n 112.5216; 12.3888; 16.6363
90; 102.256; 90		2521.93Hernández-Valdés, Daniel; Wettstein, Lionel; Fernández-Terán, Ricardo; Probst, Benjamin; Fox, Thomas; Spingler, Bernhard; Nadeem, Qaisar; Alberto, Roger
Dynamic dimer-monomer equilibrium in a cycloruthenated complex of [Re(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)<sub>2</sub>]<sup/>.
Chemical communications (Cambridge, England), 2020, 56, 10658-10661
7127070 CIFC19 H15 Br Cl N O4P 1 21/n 112.4479; 10.9895; 14.072
90; 104.748; 90		1861.57Liang, Hao; He, Xiaobo; Zhang, Yaqi; Chen, Bin; Ouyang, Jia-Sheng; Li, Yongsu; Pan, Bendu; Subba Reddy, Chitreddy V.; Chan, Wesley Ting Kwok; Qiu, Liqin
Copper-catalyzed (4+1) and (3+2) cyclizations of iodonium ylides with alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11429-11432
7127071 CIFC11.368 H7.579 N0.842P 1 21/c 113.1152; 9.7918; 33.822
90; 91.189; 90		4342.5Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127072 CIFC10.8 H7 Cl0.4 N0.8P 1 21 113.3538; 10.7542; 15.7395
90; 96.853; 90		2244.2Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127073 CIFC10.67 H6.48 F1.14 N0.76P 1 21/n 115.7886; 10.8211; 28.7265
90; 90.484; 90		4907.7Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127074 CIFC30 H31 Cl N3 RhC 1 2/c 130.7434; 9.7093; 22.2459
90; 126.426; 90		5343Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127075 CIFC9.23 H9.54 Cl0.62 N0.62 Rh0.31P 1 21/n 115.6342; 7.2912; 25.8878
90; 98.679; 90		2917.21Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127076 CIFC11.11 H7.11 N0.89 S0.44P -19.8941; 13.9468; 16.4764
102.279; 99.94; 97.712		2153.46Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127077 CIFC10.67 H7.05 Cl0.05 F0.57 N0.76 O0.05P 1 21/n 115.7038; 10.8165; 28.0637
90; 90.879; 90		4766.34Xu, Fen; Song, Yuan-Yuan; Zhu, Wen-Jing; Liu, Chun-Sen; Lu, Ya-Zhou; Du, Miao
Rhodium-catalyzed multiple C-H activation/highly <i>meta</i>-selective C-H amination between amidines and alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11227-11230
7127078 CIFF I O3 ZnP 1 21/n 15.0197; 5.2136; 12.4572
90; 95.943; 90		324.26Cao, Liling; Luo, Min; Lin, Chensheng; Zhou, Yuqiao; Zhao, Dan; Yan, Tao; Ye, Ning
From centrosymmetric to noncentrosymmetric: intriguing structure evolution in d<sup>10</sup>-transition metal iodate fluorides.
Chemical communications (Cambridge, England), 2020, 56, 10734-10737
7127079 CIFCd F I O3P 21 21 215.5051; 5.7913; 10.9326
90; 90; 90		348.55Cao, Liling; Luo, Min; Lin, Chensheng; Zhou, Yuqiao; Zhao, Dan; Yan, Tao; Ye, Ning
From centrosymmetric to noncentrosymmetric: intriguing structure evolution in d<sup>10</sup>-transition metal iodate fluorides.
Chemical communications (Cambridge, England), 2020, 56, 10734-10737
7127080 CIFC32 H31 Cl N2 O4 SP 1 21 18.29029; 20.9516; 8.39594
90; 97.0201; 90		1447.4Lu, Dongming; Wu, Jia-Hong; Pan, Jianke; Chen, Xue; Ren, Xiaoyu; Wang, Tianli
Asymmetric synthesis of benzothiazolopyrimidines with high catalytic efficiency and stereoselectivity under bifunctional phosphonium salt systems.
Chemical communications (Cambridge, England), 2020, 56, 11231-11234
7127081 CIFC23 H18 N2 O3P 1 21/n 19.7282; 14.5036; 13.5002
90; 108.564; 90		1805.7Yuan, Shuo; Yue, Ya-Le; Zhang, Dan-Qing; Zhang, Jing-Ya; Yu, Bin; Liu, Hong-Min
Synthesis of new tetracyclic benzodiazepine-fused isoindolinones using recyclable mesoporous silica nanoparticles.
Chemical communications (Cambridge, England), 2020, 56, 11461-11464
7127082 CIFC15 H18 F0.5 N3 O6 PP 1 21 111.2111; 6.05545; 13.6909
90; 112.986; 90		855.65Wu, Wei; Wang, Yan; Guo, Jing; Cai, Liu; Chen, Yuan; Huang, Yanmin; Peng, Yungui
Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids.
Chemical communications (Cambridge, England), 2020, 56, 11235-11238
7127083 CIFC16 H18 Br N3 O4P 1 21 17.32373; 15.62333; 8.2508
90; 112.635; 90		871.35Wu, Wei; Wang, Yan; Guo, Jing; Cai, Liu; Chen, Yuan; Huang, Yanmin; Peng, Yungui
Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids.
Chemical communications (Cambridge, England), 2020, 56, 11235-11238
7127084 CIFC18 H16 N2 O7P 21 21 217.4818; 10.0714; 23.347
90; 90; 90		1759.25Wang, Hai-Xia; Li, Wen-Peng; Zhang, Mi-Mi; Xie, Ming-Sheng; Qu, Gui-Rong; Guo, Hai-Ming
Synthesis of chiral pyrimidine-substituted diester D-A cyclopropanes <i>via</i> asymmetric cyclopropanation of phenyliodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 11649-11652
7127085 CIFC28 H31 N O4 SP 1 21 111.8701; 9.35538; 12.279
90; 117.558; 90		1208.87Qian, Hui; Sun, Song; Zhao, Wanxiang; Sun, Jianwei
An efficient [3+2] annulation for the asymmetric synthesis of densely-functionalized pyrrolidinones and γ-butenolides.
Chemical communications (Cambridge, England), 2020, 56, 11295-11298
7127086 CIFC21 H35 N OP 1 21/n 19.9088; 20.8368; 19.7657
90; 98.387; 90		4037.3Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127087 CIFC43 H69 I Mg N2P 1 21/c 110.8072; 18.5224; 21.5987
90; 104.313; 90		4189.32Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127088 CIFC37 H57 I Mg N2P b c a16.7941; 19.6395; 21.899
90; 90; 90		7222.9Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127089 CIFC86 H138 Mg2 N4P -111.0072; 16.9342; 21.7042
91.446; 95.022; 97.171		3995.9Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127090 CIFC46.79 H77.58 Mg N2P -110.1571; 10.6195; 21.6789
97.526; 99.465; 105.672		2182.57Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127091 CIFC43 H70 N2P 1 21/n 111.9665; 23.6431; 15.0792
90; 112.986; 90		3927.54Rösch, Bastian; Gentner, Thomas Xaver; Eyselein, Jonathan; Friedrich, Alexander; Langer, Jens; Harder, Sjoerd
Mg-Mg bond polarization induced by a superbulky β-diketiminate ligand.
Chemical communications (Cambridge, England), 2020, 56, 11402-11405
7127092 CIFC31 H21 N OP -110.6271; 10.757; 11.7417
66.929; 70.116; 62.767		1076.6Xu, Ting; Lin, Na; Hao, Wen-Juan; Zhang, Jie; Li, Meng-Fan; Tu, Shu-Jiang; Jiang, Bo
Synthesis of polycyclic indoles <i>via</i> organocatalytic bicyclization of α-alkynylnaphthalen-2-ols with nitrones.
Chemical communications (Cambridge, England), 2020, 56, 11406-11409
7127093 CIFC8 H12 O5 Pt S4 VC 1 2/c 127.225; 8.3989; 15.7502
90; 122.16; 90		3048.9Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127094 CIFC29 H22 Cl2 O5 Pt S4 VP -111.7092; 11.7557; 12.2506
71.254; 75.235; 88.198		1541.8Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127095 CIFC50 H75 Nd O8 Pt S4 VP b c a20.6526; 21.3478; 25.5068
90; 90; 90		11245.6Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127096 CIFC80.5 H95 Nd O8 Pt S4 VP -116.7686; 22.4235; 22.4927
81.342; 72.858; 83.434		7967.7Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127097 CIFC80.5 H95 Ce O8 Pt S4 VP -116.9219; 22.5655; 22.5881
81.471; 83.275; 72.952		8130.3Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127098 CIFC58.32 H86.96 Ce O8.22 Pt S4 Si0.44 VP 1 21/n 115.9088; 23.5478; 17.7553
90; 93.81; 90		6636.74Beach, Stephanie A.; Guillet, Jesse L.; Lagueux, Sydney P.; Perfetti, Mauro; Livesay, Brooke N.; Shores, Matthew P.; Bacon, Jeffrey W.; Rheingold, Arnold L.; Arnold, Polly L.; Doerrer, Linda H.
Heterotrimetallic {LnOVPt} complexes with antiferromagnetic Ln-V coupling and magnetic memory.
Chemical communications (Cambridge, England), 2020, 56, 11062-11065
7127099 CIFC19 H17 N O3P 1 21/c 110.7539; 15.7753; 10.6322
90; 118.742; 90		1581.48Kwak, Se Hun; Daugulis, Olafs
N-Iminopyridinium ylide-directed, cobalt-catalysed coupling of sp<sup>2</sup> C-H bonds with alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11070-11073
7127100 CIFC23 H26 Co I N2 O2P 1 21/c 18.4964; 31.85; 8.5016
90; 112.618; 90		2123.7Kwak, Se Hun; Daugulis, Olafs
N-Iminopyridinium ylide-directed, cobalt-catalysed coupling of sp<sup>2</sup> C-H bonds with alkynes.
Chemical communications (Cambridge, England), 2020, 56, 11070-11073
7127101 CIFC168 H198 F4 N6 O6 S4P 1 21/c 112.984; 33.1749; 18.489
90; 108.557; 90		7549.9Ding, Kui; Shan, Tong; Xu, Jinqiu; Li, Mengyang; Wang, Yan; Zhang, Yi; Xie, Ziyi; Ma, Zaifei; Liu, Feng; Zhong, Hongliang
A perylene diimide-containing acceptor enables high fill factor in organic solar cells.
Chemical communications (Cambridge, England), 2020, 56, 11433-11436
7127102 CIFC25 H40 N2 O8P 1 21 110.65993; 11.44033; 11.66689
90; 113.252; 90		1307.25Xiang, Junhong; Zhang, Xuemei; Wang, Dehong; Li, Jiaxin; Li, Qiuying; Wang, Qin; Ding, Yahui; Chen, Tianyang; Sun, Yuanjun; Bao, Shiqi; Chen, Jing; Li, Dongmei; Wang, Liang; Chen, Yue
Chemical modification of ovatodiolide revealed a promising amino-prodrug with improved pharmacokinetic profile.
Chemical communications (Cambridge, England), 2020, 56, 11018-11021
7127103 CIFC25 H36 N2 O4P 1 21 113.93601; 13.66097; 14.35128
90; 92.6127; 90		2729.35Xiang, Junhong; Zhang, Xuemei; Wang, Dehong; Li, Jiaxin; Li, Qiuying; Wang, Qin; Ding, Yahui; Chen, Tianyang; Sun, Yuanjun; Bao, Shiqi; Chen, Jing; Li, Dongmei; Wang, Liang; Chen, Yue
Chemical modification of ovatodiolide revealed a promising amino-prodrug with improved pharmacokinetic profile.
Chemical communications (Cambridge, England), 2020, 56, 11018-11021
7127104 CIFC65 H88 N6 UP n a 2123.3078; 14.5446; 17.1713
90; 90; 90		5821.1Raghavan, Adharsh; Anderson, Nickolas H.; Tatebe, Caleb J.; Stanley, Dalton A.; Zeller, Matthias; Bart, Suzanne C.
Insight into geometric preferences in uranium(VI) mixed tris(imido) systems.
Chemical communications (Cambridge, England), 2020, 56, 11138-11141
7127105 CIFC57 H70 N6 UP 1 21/n 114.6346; 21.6509; 15.5875
90; 90.829; 90		4938.4Raghavan, Adharsh; Anderson, Nickolas H.; Tatebe, Caleb J.; Stanley, Dalton A.; Zeller, Matthias; Bart, Suzanne C.
Insight into geometric preferences in uranium(VI) mixed tris(imido) systems.
Chemical communications (Cambridge, England), 2020, 56, 11138-11141
7127106 CIFC65 H86 N6 O UP 1 21/c 111.3843; 23.5278; 22.0095
90; 100.311; 90		5800Raghavan, Adharsh; Anderson, Nickolas H.; Tatebe, Caleb J.; Stanley, Dalton A.; Zeller, Matthias; Bart, Suzanne C.
Insight into geometric preferences in uranium(VI) mixed tris(imido) systems.
Chemical communications (Cambridge, England), 2020, 56, 11138-11141
7127107 CIFC12 H10 F N3 Pt S0.5P -16.768; 13.774; 13.88
87.61; 85.88; 87.59		1288.5Li, Jun; Ma, Yun; Liu, Suyi; Mao, Zhu; Chi, Zhenguo; Qian, Peng-Cheng; Wong, Wai-Yeung
Soft salts based on platinum(II) complexes with high emission quantum efficiencies in the near infrared region for <i>in vivo</i> imaging.
Chemical communications (Cambridge, England), 2020, 56, 11681-11684
7127108 CIFC25 H24 O4 S2P 1 21/c 110.917; 7.526; 28.688
90; 100.154; 90		2320.1Fei, Weihong; Xu, Ping; Hou, Jie; Yao, Weijun
Phosphine catalyzed [3+2] cyclization/Michael addition of allenoate with CS<sub>2</sub> to form 2-thineyl vinyl sulfide.
Chemical communications (Cambridge, England), 2020, 56, 11669-11672
7127109 CIFC74 H66 N3 O14 P4 YbP c c n15.9815; 16.5996; 26.6002
90; 90; 90		7056.7Borah, Aditya; Dey, Sourav; Gupta, Sandeep K.; Walawalkar, Mrinalini G.; Rajaraman, Gopalan; Murugavel, Ramaswamy
Enhancing the barrier height for Yb(III) single-ion magnets by modulating axial ligand fields.
Chemical communications (Cambridge, England), 2020, 56, 11879-11882
7127110 CIFC152 H126 F18 O27 P8 S6 Yb2P -113.6979; 14.633; 19.8834
94.599; 108.159; 90.614		3772.09Borah, Aditya; Dey, Sourav; Gupta, Sandeep K.; Walawalkar, Mrinalini G.; Rajaraman, Gopalan; Murugavel, Ramaswamy
Enhancing the barrier height for Yb(III) single-ion magnets by modulating axial ligand fields.
Chemical communications (Cambridge, England), 2020, 56, 11879-11882
7127111 CIFC74 H66 Br0.47 Cl0.62 I3.91 O5 P4 YbP -113.9941; 15.4903; 17.781
89.738; 84.044; 80.588		3781.72Borah, Aditya; Dey, Sourav; Gupta, Sandeep K.; Walawalkar, Mrinalini G.; Rajaraman, Gopalan; Murugavel, Ramaswamy
Enhancing the barrier height for Yb(III) single-ion magnets by modulating axial ligand fields.
Chemical communications (Cambridge, England), 2020, 56, 11879-11882
7127112 CIFC36 H26 N4 O2P -13.7895; 10.0133; 18.8245
84.216; 84.817; 79.331		696.5O'Connor, Helen M; Coletta, Marco; Etcheverry-Berríos, Alvaro; Nichol, Gary S.; Brechin, Euan K.; Lusby, Paul J.
Kinetic selection of Pd<sub>4</sub>L<sub>2</sub> metallocyclic and Pd<sub>6</sub>L<sub>3</sub> trigonal prismatic assemblies.
Chemical communications (Cambridge, England), 2020, 56, 11799-11802
7127113 CIFC116 H144 F24 N16 O30 Pd4 S8P 1 21/c 111.208; 21.44; 29.333
90; 93.016; 90		7038.9O'Connor, Helen M; Coletta, Marco; Etcheverry-Berríos, Alvaro; Nichol, Gary S.; Brechin, Euan K.; Lusby, Paul J.
Kinetic selection of Pd<sub>4</sub>L<sub>2</sub> metallocyclic and Pd<sub>6</sub>L<sub>3</sub> trigonal prismatic assemblies.
Chemical communications (Cambridge, England), 2020, 56, 11799-11802
7127114 CIFC552 H418 F72 N24 O72 P24 Pd12 S24C m c 2118.6651; 51.156; 74.909
90; 90; 90		71525O'Connor, Helen M; Coletta, Marco; Etcheverry-Berríos, Alvaro; Nichol, Gary S.; Brechin, Euan K.; Lusby, Paul J.
Kinetic selection of Pd<sub>4</sub>L<sub>2</sub> metallocyclic and Pd<sub>6</sub>L<sub>3</sub> trigonal prismatic assemblies.
Chemical communications (Cambridge, England), 2020, 56, 11799-11802
7127115 CIFCu3 F N O10 Pb Se2R 3 m :H6.6973; 6.6973; 18.5548
90; 90; 120		720.753Zhang, Mengsi; Zhao, Zhiying; Zhang, Wanwan; Li, Jinyang; Huang, Xiaoying; He, Zhangzhen
Pb(OF)Cu<sub>3</sub>(SeO<sub>3</sub>)<sub>2</sub>(NO<sub>3</sub>): a selenite fluoride nitrate with a breathing kagomé lattice.
Chemical communications (Cambridge, England), 2020, 56, 11965-11968
7127116 CIFC27 H26 Br3 N3P 1 21/c 18.2431; 26.7192; 12.0799
90; 100.315; 90		2617.6B S, Anju; Bhattacharjee, Rameswar; Gupta, Shourya; Ahammad, Soniya; Datta, Ayan; Kundu, Subrata
Deoxygenation of nitrosoarene by N-heterocyclic carbene (NHC): an elusive Breslow-type intermediate bridging carbene and nitrene.
Chemical communications (Cambridge, England), 2020, 56, 12166-12169
7127117 CIFC17 H15 N O3P 21 21 218.5318; 9.341; 18.0021
90; 90; 90		1434.69Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127118 CIFC20 H21 N O2P 1 21 17.8485; 12.7347; 9.0832
90; 90.438; 90		907.82Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127119 CIFC18 H19 N O3P 21 21 217.87176; 12.32287; 16.6389
90; 90; 90		1614.02Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127120 CIFC17 H17 N O3P 1 21 17.3742; 8.5904; 12.0878
90; 101.002; 90		751.656Li, Yan; Cheng, Xiu-Fen; Fei, Fan; Wu, Tian-Rui; Bian, Kang-Jie; Zhou, Xin; Wang, Xi-Sheng
Palladium(II)-catalyzed asymmetric C-H carbonylation to diverse isoquinoline derivatives bearing all-carbon quaternary stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 11605-11608
7127121 CIFC70 H58C 1 2/c 128.3914; 12.6728; 15.826
90; 98.238; 90		5635.4Sharma, Himanshu; Sharma, Priyank Kumar; Das, Soumyajit
Revisiting indeno[2,1-<i>c</i>]fluorene synthesis while exploring the fully conjugated <i>s</i>-indaceno[2,1-<i>c</i>:6,5-<i>c</i>']difluorene.
Chemical communications (Cambridge, England), 2020, 56, 11319-11322
7127122 CIFC23 H26 B10P 1 21/n 112.0902; 10.2573; 17.8407
90; 91.309; 90		2211.9Feuerstein, Wolfram; Breher, Frank
Synthetic access to a phosphorescent non-palindromic pincer complex of palladium by a double oxidative addition - comproportionation sequence.
Chemical communications (Cambridge, England), 2020, 56, 12589-12592
7127123 CIFC22 H16 N2 NiP 1 21/n 19.282; 12.71; 14.038
90; 90.89; 90		1655.9Feuerstein, Wolfram; Breher, Frank
Synthetic access to a phosphorescent non-palindromic pincer complex of palladium by a double oxidative addition - comproportionation sequence.
Chemical communications (Cambridge, England), 2020, 56, 12589-12592
7127124 CIFC58 H42 Co4 N6 O18P 110.298; 10.352; 17.615
105.643; 103.514; 90.658		1753Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127125 CIFC26 H14 Co2 N2 O8C 1 c 114.3091; 14.5181; 17.5565
90; 104.706; 90		3527.7Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127126 CIFC13 H7 Co N O4P 1 21/c 110.696; 13.078; 12.46
90; 108.79; 90		1650Gao, Yajun; Zhang, Mingxing; Chen, Cong; Zhang, Yong; Gu, Yuming; Wang, Qian; Zhang, Wenwei; Pan, Yi; Ma, Jing; Bai, Junfeng
A low symmetry cluster meets a low symmetry ligand to sharply boost MOF thermal stability.
Chemical communications (Cambridge, England), 2020, 56, 11985-11988
7127127 CIFC28 H56 I6 O7 Sm2C 1 2/c 112.8008; 12.0522; 28.7469
90; 98.444; 90		4386.9Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127128 CIFH68 I8 O41 Sm6P n n m12.8578; 14.8418; 14.8987
90; 90; 90		2843.16Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127129 CIFC37.6 H99.4 I8 N2 O29 Sm6P 1 21/n 114.2715; 22.8583; 14.2693
90; 90.739; 90		4654.6Marks, Walker R.; Baumgardner, Douglas F.; Reinheimer, Eric W.; Gilbertson, John D.
Complete denitrification of nitrate and nitrite to N<sub>2</sub> gas by samarium(II) iodide.
Chemical communications (Cambridge, England), 2020, 56, 11441-11444
7127130 CIFC15 H18 N2 OP -110.3988; 11.976; 12.1316
86.151; 70.363; 65.045		1285.2Niu, Kaikai; Song, Lingyun; Hao, Yanke; Liu, Yuxiu; Wang, Qingmin
Electrochemical decarboxylative C3 alkylation of quinoxalin-2(1<i>H</i>)-ones with <i>N</i>-hydroxyphthalimide esters.
Chemical communications (Cambridge, England), 2020, 56, 11673-11676
7127131 CIFC94 H150 N4 Si16P -19.8911; 16.0352; 19.2371
88.17; 76.903; 73.041		2840.61Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127132 CIFC52 H34 O4 Si2P 1 21/c 114.4193; 15.3229; 18.272
90; 93.967; 90		4027.4Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127133 CIFC90 H158 N4 Si18C 1 2/c 143.6057; 8.5663; 33.257
90; 101.568; 90		12170.5Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127134 CIFC230 H308 N8 Si36P -122.1092; 22.318; 29.0414
74.547; 79.773; 71.053		12998.3Mateos-Martín, Javier; Carini, Marco; Melle-Franco, Manuel; Mateo-Alonso, Aurelio
Increasing and dispersing strain in pyrene-fused azaacenes.
Chemical communications (Cambridge, England), 2020, 56, 11457-11460
7127135 CIFC54 H76 I4 O9 Sm2P 21 21 2116.1373; 17.5042; 21.114
90; 90; 90		5964.1Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127136 CIFC38 H30 I2 N5 O SmP 1 21/c 111.6323; 12.3012; 24.5249
90; 91.769; 90		3507.6Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127137 CIFC55 H47 I2 N8 O SmP -115.8733; 16.1883; 19.8595
90; 103.03; 90		4971.74Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127138 CIFC33 H29 I2 N4 O SmP 1 21/c 19.2854; 15.4014; 24.686
90; 100.528; 90		3470.9Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127139 CIFC25 H18 N2 OC 1 2/c 117.8482; 18.0365; 12.5808
90; 117.094; 90		3605.6Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127140 CIFC18 H15 N OP 1 21/c 18.1307; 14.6655; 11.5353
90; 95.749; 90		1368.56Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127141 CIFC41 H31 I2 N6 O SmP -111.4446; 11.9484; 14.6103
78.322; 81.909; 84.338		1931.97Jaoul, Arnaud; Yang, Yan; Casaretto, Nicolas; Clavaguéra, Carine; Maron, Laurent; Nocton, Grégory
Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 11875-11878
7127142 CIFC14 H14 Br F3 O3P 21 21 218.1811; 17.8856; 21.2028
90; 90; 90		3102.5Murata, Ryuichi; Matsumoto, Akira; Asano, Keisuke; Matsubara, Seijiro
Desymmetrization of gem-diols via water-assisted organocatalytic enantio- and diastereoselective cycloetherification.
Chemical communications (Cambridge, England), 2020, 56, 12335-12338
7127143 CIFC14 H12 Br F3 O2P 21 21 216.382; 14.0024; 15.777
90; 90; 90		1409.9Murata, Ryuichi; Matsumoto, Akira; Asano, Keisuke; Matsubara, Seijiro
Desymmetrization of gem-diols via water-assisted organocatalytic enantio- and diastereoselective cycloetherification.
Chemical communications (Cambridge, England), 2020, 56, 12335-12338
7127144 CIFC20 H21 N OP 1 21/c 110.162; 19.1; 8.941
90; 109.78; 90		1633Zhang, Xiao-Wen; Zhang, Hui; Wang, Hu-Chong; Zhu, Ming-Hui; Cong, Hengjiang; Liu, Wen-Bo
Pd-catalyzed arylation/aza-Michael addition cascade to C2-spiroindolines and azabicyclo[3.2.2]nonanones.
Chemical communications (Cambridge, England), 2020, 56, 12013-12016
7127145 CIFC27 H27 N OC 1 c 113.7872; 16.2182; 9.4765
90; 96.759; 90		2104.25Zhang, Xiao-Wen; Zhang, Hui; Wang, Hu-Chong; Zhu, Ming-Hui; Cong, Hengjiang; Liu, Wen-Bo
Pd-catalyzed arylation/aza-Michael addition cascade to C2-spiroindolines and azabicyclo[3.2.2]nonanones.
Chemical communications (Cambridge, England), 2020, 56, 12013-12016
7127146 CIFC21 H30 Cl O PP -15.7668; 11.743; 28.998
95.169; 90.067; 102.805		1906.7Shintani, Ryo; Ohzono, Ayase; Shirota, Kentaro
Phosphinative cyclopropanation of allyl phosphates with lithium phosphides.
Chemical communications (Cambridge, England), 2020, 56, 11851-11854
7127147 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4617; 4.2206; 19.5436
90; 90.441; 90		945.4Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127148 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4724; 4.2238; 19.5467
90; 90.445; 90		947.15Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127149 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.538; 4.2653; 19.7023
90; 90.478; 90		969.58Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127150 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.4918; 4.232; 19.5567
90; 90.451; 90		951.08Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127151 CIFC24 H29 B O4P 21 21 216.48035; 17.3087; 19.7454
90; 90; 90		2214.77Sun, Xiao; Gu, Peiming; Qin, Jiao; Su, Yan
Rhodium-catalysed diastereo- and enantio-selective cyclopropanation of α-boryl styrenes.
Chemical communications (Cambridge, England), 2020, 56, 12379-12382
7127152 CIFC46 H16 Cl16 F12 N2 O4 ZnP -18.9829; 15.1174; 20.8813
97.411; 94.728; 90.909		2801.4Kimura, Shun; Kimura, Shojiro; Nishihara, Hiroshi; Kusamoto, Tetsuro
Excimer emission and magnetoluminescence of radical-based zinc(II) complexes doped in host crystals.
Chemical communications (Cambridge, England), 2020, 56, 11195-11198
7127153 CIFC16 H10 B2 F12P 1 21/n 17.556; 8.4678; 13.593
90; 96.564; 90		864.02Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127154 CIFC32 H50 B2 O2 Si4F d d 218.4614; 34.6525; 11.8617
90; 90; 90		7588.3Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127155 CIFC25 H26 B F9 O Si2P 21 21 2110.9779; 13.7265; 18.8688
90; 90; 90		2843.3Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127156 CIFC34 H28 B2 F12 N2P -18.7742; 9.5777; 11.1573
98.124; 99.074; 113.422		827.78Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127157 CIFC35 H34 B F6 NP 1 21/c 110.311; 14.3855; 21.2243
90; 103.129; 90		3065.89Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127158 CIFC48 H54 B2 F12 Si4P -113.3784; 14.431; 16.3141
65.319; 66.05; 78.62		2614Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127159 CIFC44 H50 B2 F12 S2 Si4P n m a13.3555; 31.172; 11.7335
90; 90; 90		4884.9Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127160 CIFC31 H32 B F6 NP 1 21/c 18.7063; 17.2992; 18.1817
90; 93.565; 90		2733.1Škoch, Karel; Daniliuc, Constantin G.; Kehr, Gerald; Erker, Gerhard
Using the FpXylBH<sub>2</sub>•SMe<sub>2</sub> reagent for the regioselective synthesis of cyclic bis(alkenyl)boranes.
Chemical communications (Cambridge, England), 2020, 56, 12178-12181
7127161 CIFC23 H13 N SP 1 21/c 121.4278; 4.9469; 15.5164
90; 107.158; 90		1571.56Jana, Arijit; Chakraborty, Papri; Dar, Wakeel Ahmed; Chandra, Sourov; Khatun, Esma; Kannan, M. P.; Ras, Robin H. A.; Pradeep, Thalappil
Dual emitting Ag<sub>35</sub> nanocluster protected by 2-pyrene imine thiol.
Chemical communications (Cambridge, England), 2020, 56, 12550-12553
7127162 CIFC52 H30 Mn N8 O4F d d d :217.6218; 36.0338; 50.356
90; 90; 90		31975Setter, Caitlin J.; Price, Michael B.; Conte, Luke; Schmitt, Wolfgang; Batten, Stuart R.; Richardson, Christopher; Hill, Matthew R.; Babarao, Ravichandar; Macreadie, Lauren K.
Mixed donor, phenanthroline photoactive MOFs with favourable CO<sub>2</sub> selectivity.
Chemical communications (Cambridge, England), 2020, 56, 13377-13380
7127163 CIFC54 H32 N8 O8 Zn2P n a 218.403; 24.858; 33.616
90; 90; 90		7022Setter, Caitlin J.; Price, Michael B.; Conte, Luke; Schmitt, Wolfgang; Batten, Stuart R.; Richardson, Christopher; Hill, Matthew R.; Babarao, Ravichandar; Macreadie, Lauren K.
Mixed donor, phenanthroline photoactive MOFs with favourable CO<sub>2</sub> selectivity.
Chemical communications (Cambridge, England), 2020, 56, 13377-13380
7127164 CIFC78 H79 B Cl2 Dy N5 O2 Si2P -114.3753; 22.1443; 23.4355
100.425; 103.832; 100.857		6911.6Canaj, Angelos B.; Dey, Sourav; Wilson, Claire; Céspedes, Oscar; Rajaraman, Gopalan; Murrie, Mark
Engineering macrocyclic high performance pentagonal bipyramidal Dy(iii) single-ion magnets.
Chemical communications (Cambridge, England), 2020, 56, 12037-12040
7127165 CIFC8 H11 N3 O4P -17.6321; 10.9503; 12.4367
92.39; 95.911; 100.137		1015.8Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127166 CIFC21 H27 N6 O14 YbP -18.8524; 10.434; 15.937
87.131; 87.135; 88.571		1468Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127167 CIFC12 H20 N4 O10P 1 21/c 111.8129; 10.3804; 6.9487
90; 100.27; 90		838.42Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127168 CIFC2.25 H2.25 Ho0.25 N0.5 O2.5P 1 21/n 19.6712; 11.3857; 12.687
90; 96.475; 90		1388.1Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127169 CIFC24 H28 Ho N8 O18C 1 c 112.0981; 17.5518; 18.316
90; 98.538; 90		3846.2Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127170 CIFC24 H28 Lu N8 O18C 1 c 112.038; 17.562; 18.345
90; 98.384; 90		3837Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127171 CIFC27 H48 N4 O19 TmP -111.897; 12.988; 14.598
63.692; 79.555; 74.701		1945Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127172 CIFC8 H7 Er N2 O10.5C 1 2 114.67; 11.5086; 9.198
90; 121.404; 90		1325.4Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127173 CIFC16 H14 Ho2 N4 O20P 1 21/n 110.023; 17.357; 14.354
90; 99.312; 90		2464.2Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127174 CIFC28 H35 Lu N10 O18C 1 c 112.0002; 17.5085; 18.066
90; 98.6189; 90		3752.9Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127175 CIFC24 H28 N8 O18 TmC 1 c 112.0526; 17.5649; 18.317
90; 98.558; 90		3834.6Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127176 CIFC27 H48 N4 O19 YbP -111.6122; 12.8415; 14.4646
64.182; 80.639; 75.308		1874.77Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127177 CIFC5.09 H6.36 N1.82 O3.27 Y0.18C 1 c 112.0684; 17.5403; 18.0493
90; 98.685; 90		3776.93Prodius, Denis; Klocke, Matthew; Smetana, Volodymyr; Alammar, Tarek; Perez Garcia, Marilu; Windus, Theresa L.; Nlebedim, Ikenna C.; Mudring, Anja-Verena
Rationally designed rare earth separation by selective oxalate solubilization.
Chemical communications (Cambridge, England), 2020, 56, 11386-11389
7127178 CIFC19 H35 Cl2 N2 Ni Rh S2P n a 2122.125; 8.337; 12.839
90; 90; 90		2368.2Ogo, Seiji; Ando, Tatsuya; Minh, Le Tu Thi; Mori, Yuki; Matsumoto, Takahiro; Yatabe, Takeshi; Yoon, Ki-Seok; Sato, Yukio; Hibino, Takashi; Kaneko, Kenji
A NiRhS fuel cell catalyst - lessons from hydrogenase.
Chemical communications (Cambridge, England), 2020, 56, 11787-11790
7127179 CIFC19 H36 Cl N2 Ni Rh S2P b c a15.669; 14.306; 20.014
90; 90; 90		4486Ogo, Seiji; Ando, Tatsuya; Minh, Le Tu Thi; Mori, Yuki; Matsumoto, Takahiro; Yatabe, Takeshi; Yoon, Ki-Seok; Sato, Yukio; Hibino, Takashi; Kaneko, Kenji
A NiRhS fuel cell catalyst - lessons from hydrogenase.
Chemical communications (Cambridge, England), 2020, 56, 11787-11790
7127180 CIFC17 H24 B PP 21 21 216.6359; 7.5137; 34.018
90; 90; 90		1696.1Wang, Cuiying; Yue, Chang-Duo; Yuan, Jia; Zheng, Jia-Lian; Zhang, Ying; Yu, Hong; Chen, Jian; Meng, Sixuan; Yu, Yang; Yu, Guang-Ao; Che, Chi-Ming
Synthesis of P-chiral phosphine compounds by palladium-catalyzed C-P coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 11775-11778
7127181 CIFC20 H28 B PP 21 21 2111.2902; 12.3392; 13.6341
90; 90; 90		1899.4Wang, Cuiying; Yue, Chang-Duo; Yuan, Jia; Zheng, Jia-Lian; Zhang, Ying; Yu, Hong; Chen, Jian; Meng, Sixuan; Yu, Yang; Yu, Guang-Ao; Che, Chi-Ming
Synthesis of P-chiral phosphine compounds by palladium-catalyzed C-P coupling reactions.
Chemical communications (Cambridge, England), 2020, 56, 11775-11778
7127182 CIFC17 H14 S2P 1 21/c 114.9903; 5.9477; 16.5251
90; 110.467; 90		1380.34Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127183 CIFC14 H11 N O S2P 1 21 19.5155; 4.8412; 13.9736
90; 96.436; 90		639.66Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127184 CIFC21 H20 S2P 1 21/n 116.4219; 7.1899; 16.4782
90; 118.374; 90		1711.87Ielo, Laura; Pillari, Veronica; Gajic, Natalie; Holzer, Wolfgang; Pace, Vittorio
Straightforward chemoselective access to unsymmetrical dithioacetals through a thiosulfonate homologation-nucleophilic substitution sequence.
Chemical communications (Cambridge, England), 2020, 56, 12395-12398
7127185 CIFC214 H282 Au10 O22 S2P 21 21 219.6562; 28.6975; 21.2232
90; 90; 90		11971.7Xu, Man-Man; Jia, Tong-Tong; Li, Bingjie; Ma, Wang; Chen, Xiaoyuan; Zhao, Xueli; Zang, Shuang-Quan
Tuning the properties of atomically precise gold nanoclusters for biolabeling and drug delivery.
Chemical communications (Cambridge, England), 2020, 56, 8766-8769
7127186 CIFC53 H59 Cl11 N8 O8 Pd2P 1 21/n 112.18; 15.906; 33.211
90; 93.15; 90		6424Scattolin, Thomas; Bortolamiol, Enrica; Palazzolo, Stefano; Caligiuri, Isabella; Perin, Tiziana; Canzonieri, Vincenzo; Demitri, Nicola; Rizzolio, Flavio; Cavallo, Luigi; Dereli, Busra; Mane, Manoj V.; Nolan, Steven P.; Visentin, Fabiano
The anticancer activity of an air-stable Pd(I)-NHC (NHC = N-heterocyclic carbene) dimer.
Chemical communications (Cambridge, England), 2020, 56, 12238-12241
7127187 CIFC22 H21 N O5 S2P 21 21 218.71695; 13.36161; 17.6913
90; 90; 90		2060.55Yang, Lei; Zhao, Jian-Qiang; You, Yong; Wang, Zhen-Hua; Yuan, Wei-Cheng
Organocatalytic enantioselective tandem sulfa-Michael/aldol reaction to access dihydrothiopyran-fused benzosulfolane skeletons bearing three contiguous stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 12363-12366
7127188 CIFC15 H12 O3 S2P 21 21 217.8266; 13.136; 13.1894
90; 90; 90		1356.01Yang, Lei; Zhao, Jian-Qiang; You, Yong; Wang, Zhen-Hua; Yuan, Wei-Cheng
Organocatalytic enantioselective tandem sulfa-Michael/aldol reaction to access dihydrothiopyran-fused benzosulfolane skeletons bearing three contiguous stereocenters.
Chemical communications (Cambridge, England), 2020, 56, 12363-12366
7127189 CIFC119.5 H108 Cl4 P8 Rh4 S2P -116.3139; 19.5375; 22.4893
71.332; 72.996; 79.948		6468.1Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127190 CIFC15 H10 Br Cl I N O2P 1 21/n 15.0083; 9.7548; 31.964
90; 92.576; 90		1560.02Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127191 CIFC58 H53 Cl5 O5 P4 Rh2 SP 1 21/c 112.7306; 15.6417; 30.6406
90; 92.455; 90		6095.81Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127192 CIFC61.5 H56 Cl2 P4 Rh2 SeP -116.2884; 20.0388; 22.3244
70.671; 75.071; 80.2		6615Barnett, Harrison J.; Hill, Anthony F.
Dimetalla-heterocyclic carbenes: the interconversion of chalcocarbonyl and carbido ligands.
Chemical communications (Cambridge, England), 2020, 56, 12593-12596
7127193 CIFC19 H16 O3P 1 21/c 17.034; 16.0025; 13.2355
90; 100.358; 90		1465.53Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127194 CIFC19 H18 O2P 1 21/n 114.4303; 7.16982; 14.45517
90; 90.2129; 90		1495.56Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127195 CIFC10.29 H9.14 O1.14P 1 21/n 113.6891; 7.0857; 14.1959
90; 91.491; 90		1376.49Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127196 CIFC10.86 H10.29 O1.14P b c a7.2898; 15.8113; 25.4414
90; 90; 90		2932.41Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127197 CIFC38 H32 O6P 1 21/c 120.5228; 8.2219; 17.4215
90; 96.111; 90		2922.94Gao, Bingjian; Zou, Suchen; Yang, Guoqing; Ding, Yongzheng; Huang, Hanmin
Carbonylative cycloaddition between two different alkenes enabled by reactive directing groups: expedited construction of bridged polycyclic skeletons.
Chemical communications (Cambridge, England), 2020, 56, 12198-12201
7127198 CIFC23 H18 Br Cl3 N2 OP -18.405; 10.003; 15.623
71.488; 78.914; 66.772		1141.2Zhao, Peng; Yu, Xiao-Xiao; Zhou, You; Huang, Chun; Wu, Yan-Dong; Zhu, Yan-Ping; Wu, An-Xin
Arylacetylenes as two-carbon synthons: synthesis of eight-membered rings via C[triple bond, length as m-dash]C bond cleavage.
Chemical communications (Cambridge, England), 2020, 56, 12554-12557
7127199 CIFC22 H18 N2 OC 1 2/c 113.602; 13.685; 19.401
90; 99.361; 90		3563.3Zhao, Peng; Yu, Xiao-Xiao; Zhou, You; Huang, Chun; Wu, Yan-Dong; Zhu, Yan-Ping; Wu, An-Xin
Arylacetylenes as two-carbon synthons: synthesis of eight-membered rings via C[triple bond, length as m-dash]C bond cleavage.
Chemical communications (Cambridge, England), 2020, 56, 12554-12557
7127200 CIFC49 H63 B F6 N3 O P2 RhI 1 2/a 128.3648; 12.213; 32.5843
90; 111.394; 90		10510MacNeil, Connor S.; Hsiang, Shou-Jen; Hayes, Paul G.
Reversible dehydrogenation of a primary aryl borane.
Chemical communications (Cambridge, England), 2020, 56, 12323-12326
7127201 CIFC44 H63 B N3 O P2 RhP -114.5167; 18.5067; 19.7008
65.627; 88.777; 77.349		4689.8MacNeil, Connor S.; Hsiang, Shou-Jen; Hayes, Paul G.
Reversible dehydrogenation of a primary aryl borane.
Chemical communications (Cambridge, England), 2020, 56, 12323-12326
7127202 CIFC27 H24 N2 O2 SP 1 21/n 18.1661; 25.3026; 10.7553
90; 96.512; 90		2207.96Tan, Heng; Khan, Ruhima; Xu, Dandan; Zhou, Yongyun; Zhang, Xuexin; Shi, Guangrui; Fan, Baomin
Cobalt-catalyzed ring-opening addition of azabenzonorbornadienes via C(sp<sup>3</sup>)-H bond activation of 8-methylquinoline.
Chemical communications (Cambridge, England), 2020, 56, 12570-12573
7127203 CIFC279 H381 O48P 1 21/c 121.609; 49.509; 28.125
90; 111.398; 90		28015Shimoyama, Daisuke; Sekiya, Ryo; Haino, Takeharu
Absorption of chemicals in amorphous trisresorcinarene.
Chemical communications (Cambridge, England), 2020, 56, 12582-12585
7127204 CIFC15 H8 Cl F N2 O4P 1 21 14.3265; 13.4831; 12.3293
90; 93.614; 90		717.79Peng, Qiupeng; Guo, Donghui; Zhang, Bei; Liu, Lala; Wang, Jian
Benzotetramisole catalyzed kinetic resolution of 2H-azirines.
Chemical communications (Cambridge, England), 2020, 56, 12427-12430
7127205 CIFC70 H76 N4 O8 S2C 1 2/c 133.803; 13.242; 13.405
90; 108.746; 90		5682Ohtsuka, Nobuhiko; Nakano, Masahiro; Nakagawa, Sae; Shahiduzzaman, Md; Karakawa, Makoto; Taima, Tetsuya; Minoura, Mao
Naphthalene diimide-incorporated helical thienoacene: a helical molecule with high electron mobility, good solubility, and thermally stable solid phase.
Chemical communications (Cambridge, England), 2020, 56, 12343-12346
7127206 CIFC27 H26 Br N OP 21 21 219.6932; 10.7179; 21.842
90; 90; 90		2269.2Zhang, Yu; Li, Yuan; Zhou, Wei; Zhang, Mengru; Zhang, Qian; Jia, Ran; Zhao, Jinbo
Assembly of polysubstituted chiral cyclopropylamines via highly enantioselective Cu-catalyzed three-component cyclopropene alkenylamination.
Chemical communications (Cambridge, England), 2020, 56, 12250-12253
7127207 CIFC51 H33 N3 O13 Zn4P -4 21 m17.2; 17.2; 17.2
90; 90; 90		5088.4Fishburn, Mitchell G.; Skelton, Dayne R.; Telfer, Shane G.; Wagner, Pawel; Richardson, Christopher
Second-order programming the synthesis of metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 12355-12358
7127208 CIFC35 H30 N4 O8P -110.5406; 10.8847; 13.6301
94.515; 101.132; 96.424		1516.65Fishburn, Mitchell G.; Skelton, Dayne R.; Telfer, Shane G.; Wagner, Pawel; Richardson, Christopher
Second-order programming the synthesis of metal-organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 12355-12358
7127209 CIFC10.5 H6 Cl2 N5 O3 ReC 1 2/c 116.06; 13.0072; 13.9753
90; 99.72; 90		2877.5Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127210 CIFC7 H5 N5P 1 21/c 17.2794; 9.3608; 10.4528
90; 96.97; 90		707Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127211 CIFC36 H38 Cl2 N6 O6 Re2C 1 2/c 117.9274; 12.2202; 17.9025
90; 103.284; 90		3817.1Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127212 CIFC22 H17 Cl Fe N3 O3 ReP 1 21/c 112.9074; 12.0184; 14.9765
90; 113.981; 90		2122.71Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127213 CIFC18 H13 Cl N3 O3 ReP 1 21/n 19.0781; 10.9568; 22.08
90; 92.87; 90		2193.5Schnierle, Marc; Blickle, Svenja; Filippou, Vasileios; Ringenberg, Mark R.
Tetrazine metallation boosts rate and regioselectivity of inverse electron demand Diels-Alder (iEDDA) addition of dienophiles.
Chemical communications (Cambridge, England), 2020, 56, 12033-12036
7127214 CIFC21 H20 O4P c a 2110.5308; 18.5025; 8.737
90; 90; 90		1702.4Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127215 CIFC19 H17 N O4P 1 21/c 115.6331; 8.0735; 12.5699
90; 92.556; 90		1584.92Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127216 CIFC22 H16 O4P -14.857; 13.6775; 14.0943
114.792; 97.894; 91.103		838.88Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127217 CIFC24 H18 O4P 1 21/c 111.2786; 10.8706; 15.3317
90; 97.475; 90		1863.77Dai, Qing-Song; Tao, Ying-Mao; Zhang, Xiang; Leng, Hai-Jun; Huang, Hua; Xiang, Peng; Li, Qing-Zhu; Wang, Qi-Wei; Li, Jun-Long
Palladium-catalysed cyclisation of vinylethylene carbonates and anhydrides: a new approach to diverse medium-sized bislactones.
Chemical communications (Cambridge, England), 2020, 56, 12439-12442
7127218 CIFC6 Cl Cu3 K4 N6 O6P -3 m 111.1833; 11.1833; 3.6304
90; 90; 120		393.21Kang, Kaijin; Liang, Fei; Meng, Xianghe; Tang, Jian; Zeng, Tixian; Xia, Mingjun; Lin, Zheshuai; Yin, Wenlong; Bin, Kang
K<sub>4</sub>Cu<sub>3</sub>(C<sub>3</sub>N<sub>3</sub>O<sub>3</sub>)<sub>2</sub>X (X = Cl, Br): strong anisotropic layered semiconductors containing mixed p-p and d-p conjugated π-bonds.
Chemical communications (Cambridge, England), 2020, 56, 12534-12537
7127219 CIFC6 Br Cu3 K4 N6 O6P -3 m 111.2089; 11.2089; 3.7195
90; 90; 120		404.71Kang, Kaijin; Liang, Fei; Meng, Xianghe; Tang, Jian; Zeng, Tixian; Xia, Mingjun; Lin, Zheshuai; Yin, Wenlong; Bin, Kang
K<sub>4</sub>Cu<sub>3</sub>(C<sub>3</sub>N<sub>3</sub>O<sub>3</sub>)<sub>2</sub>X (X = Cl, Br): strong anisotropic layered semiconductors containing mixed p-p and d-p conjugated π-bonds.
Chemical communications (Cambridge, England), 2020, 56, 12534-12537
7127220 CIFC16 H22 F3 N O2 SnP 1 21 111.7115; 12.6744; 12.5355
90; 103.528; 90		1809.1Delany, Pascal K.; Mortimer, Claire L.; Hodgson, David M.
Electrophile dependent mechanisms in the asymmetric trapping of α-lithio-<i>N</i>-(<i>tert</i>-butoxythiocarbonyl)azetidine.
Chemical communications (Cambridge, England), 2020, 56, 12174-12177
7127221 CIFC19 H21 N3 O2P 1 21/c 18.5708; 17.0112; 12.3358
90; 106.285; 90		1726.4Semenova, Evgeniya; Lahtigui, Ouidad; Scott, Sarah K.; Albritton, Matthew; Abboud, Khalil A.; Ghiviriga, Ion; Roitberg, Adrian E.; Grenning, Alexander J.
Selective ring-rearrangement or ring-closing metathesis of bicyclo[3.2.1]octenes.
Chemical communications (Cambridge, England), 2020, 56, 11779-11782
7127222 CIFC19 H25 N O6P 1 21 110.9242; 7.1718; 12.651
90; 105.167; 90		956.6Pei, Jun-Ping; Lv, Xue-Jiao; Peng, Chen-Jun; Liu, Yan-Kai
Asymmetric organocatalytic multicomponent reactions for efficient construction of bicyclic compounds bearing bisacetal and isoxazolidine moieties.
Chemical communications (Cambridge, England), 2020, 56, 12765-12768
7127223 CIFC17 H21 N O7P 21 21 216.921; 10.91; 24.068
90; 90; 90		1817Zhao, Can; Khan, Ijaz; Zhang, Yong Jian
Enantioselective total synthesis of furofuran lignans <i>via</i> Pd-catalyzed asymmetric allylic cycloadditon of vinylethylene carbonates with 2-nitroacrylates.
Chemical communications (Cambridge, England), 2020, 56, 12431-12434
7127224 CIFC13 H12 O5P 21 21 216.6885; 7.1093; 24.188
90; 90; 90		1150.15Zhao, Can; Khan, Ijaz; Zhang, Yong Jian
Enantioselective total synthesis of furofuran lignans <i>via</i> Pd-catalyzed asymmetric allylic cycloadditon of vinylethylene carbonates with 2-nitroacrylates.
Chemical communications (Cambridge, England), 2020, 56, 12431-12434
7127225 CIFC25 H22 N2 O8P 1 21/n 18.1947; 22.1997; 12.9203
90; 102.07; 90		2298.5Wang, Kai; Jiang, Chenghao; Zhang, Zhenming; Han, Chunyu; Wang, Xuewei; Li, Yaping; Chen, Kaiting; Zhao, Junfeng
Cut and sew: benzofuran-ring-opening enabled cyclopentenone ring formation.
Chemical communications (Cambridge, England), 2020, 56, 12817-12820
7127226 CIFC336 H304 Br82.4 Co8 N48 O34I -4 2 m24.552; 24.552; 17.693
90; 90; 90		10665Rabelo, Renato; Toma, Luminita; Moliner, Nicolás; Julve, Miguel; Lloret, Francesc; Pasán, Jorge; Ruiz-Pérez, Catalina; Ruiz-García, Rafael; Cano, Joan
Electroswitching of the single-molecule magnet behaviour in an octahedral spin crossover cobalt(ii) complex with a redox-active pyridinediimine ligand.
Chemical communications (Cambridge, England), 2020, 56, 12242-12245
7127227 CIFC42 H38 Cl2 Co N6 O12P 4319.3426; 19.3426; 43.5392
90; 90; 90		16289.6Rabelo, Renato; Toma, Luminita; Moliner, Nicolás; Julve, Miguel; Lloret, Francesc; Pasán, Jorge; Ruiz-Pérez, Catalina; Ruiz-García, Rafael; Cano, Joan
Electroswitching of the single-molecule magnet behaviour in an octahedral spin crossover cobalt(ii) complex with a redox-active pyridinediimine ligand.
Chemical communications (Cambridge, England), 2020, 56, 12242-12245
7127228 CIFC27 H19 N3 O2P 1 21/n 110.329; 19.409; 10.902
90; 98.698; 90		2160.4Singh, Sangh Priya; Tripathi, Shashank; Yadav, Anamika; Kant, Ruchir; Srivastava, Hemant Kumar; Srivastava, Ajay Kumar
Synthesis of β- and γ-lactam fused dihydropyrazinones from Ugi adducts <i>via</i> a sequential ring construction strategy.
Chemical communications (Cambridge, England), 2020, 56, 12789-12792
7127229 CIFC26 H19 F N2 O2P 21 21 219.0888; 10.564; 21.463
90; 90; 90		2060.8Singh, Sangh Priya; Tripathi, Shashank; Yadav, Anamika; Kant, Ruchir; Srivastava, Hemant Kumar; Srivastava, Ajay Kumar
Synthesis of β- and γ-lactam fused dihydropyrazinones from Ugi adducts <i>via</i> a sequential ring construction strategy.
Chemical communications (Cambridge, England), 2020, 56, 12789-12792
7127230 CIFC66 H35 N6 O0.5 Tb0.5C 1 2/m 122.7366; 17.3024; 22.0606
90; 90.923; 90		8677.5Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127231 CIFC69 H62 Cl8 N12 Sb TbP -113.1037; 15.3447; 18.9271
108.883; 104.223; 91.574		3466.69Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127232 CIFC72 H36 N6 Tb0.5C 1 2/c 124.8514; 15.5073; 27.2445
90; 118.812; 90		9199.7Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127233 CIFC67 H37 N6 Tb0.5C 1 2/m 122.811; 17.4164; 22.0814
90; 90.987; 90		8771.32Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127234 CIFC84 H96 N13 TbP 1 21/n 114.9131; 23.0259; 21.9427
90; 104.777; 90		7285.6Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127235 CIFC64 H30 B0.5 F2 N6 Tb0.5P 1 21/m 115.1885; 21.4887; 19.099
90; 104.999; 90		6021.2Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127236 CIFC162 H90 F6 N18 P Tb1.5C m c 2126.9958; 42.7901; 23.1133
90; 90; 90		26699.4Iwami, Hikaru; Xing, Junfei; Nakanishi, Ryo; Horii, Yoji; Katoh, Keiichi; Breedlove, Brian K.; Kawachi, Kazuhiko; Kasama, Yasuhiko; Kwon, Eunsang; Yamashita, Masahiro
Cocrystals of Li<sup>+</sup> encapsulated fullerenes and Tb(iii) double-decker single molecule magnet in a quasi-kagome lattice.
Chemical communications (Cambridge, England), 2020, 56, 12785-12788
7127237 CIFC19 H13 F6 N3 O4P 1 21/n 110.5749; 11.9556; 15.5244
90; 94.202; 90		1957.46Su, Hai-Yan; Zhu, Xiao-Lei; Huang, Yangen; Xu, Xiu-Hua; Qing, Feng-Ling
Copper-catalyzed chemoselective C-H functionalization of quinoxalin-2(1<i>H</i>)-ones with hexafluoroisopropanol.
Chemical communications (Cambridge, England), 2020, 56, 12805-12808
7127238 CIFC16 H20 B10P -17.2684; 10.407; 12.7741
74.227; 81.33; 86.111		918.89Lee, Sunhee; Shin, Jisu; Ko, Doo-Hyun; Han, Won-Sik
A new type of carborane-based electron-accepting material.
Chemical communications (Cambridge, England), 2020, 56, 12741-12744
7127239 CIFC9 H15 B10P 1 21/n 110.7957; 9.7951; 13.7818
90; 112.281; 90		1348.5Lee, Sunhee; Shin, Jisu; Ko, Doo-Hyun; Han, Won-Sik
A new type of carborane-based electron-accepting material.
Chemical communications (Cambridge, England), 2020, 56, 12741-12744
7127240 CIFC23 H17 Br Cl0 N2 O3P 21 21 217.7448; 15.656; 18.122
90; 90; 90		2197.3Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127241 CIFC27 H25 Br N2 O4P 1 21/n 19.4091; 11.5174; 22.8668
90; 91.996; 90		2476.53Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127242 CIFC27 H25 Br N2 O4P 1 21/c 113.2371; 16.5924; 11.5023
90; 106.316; 90		2424.57Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127243 CIFC27 H27 Br N2 O4C 1 2/c 121.8518; 10.5122; 22.7425
90; 108.208; 90		4962.6Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127244 CIFC28 H27 Br N2 O4P 1 21/c 110.957; 22.742; 11.167
90; 110.062; 90		2613.8Zhang, Dong; Dong, Shunxi; He, Qianwen; Luo, Yao; Liu, Yun; Liu, Xiaohua; Feng, Xiaoming
Enantioselective dicarbofunctionalization of (<i>E</i>)-alkenyloxindoles with pyridinium salts by chiral Lewis acid/photo relay catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12757-12760
7127245 CIFC43 H53 N O6P 1 21/n 112.9369; 17.1825; 17.9062
90; 102.098; 90		3891.9Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127246 CIFC43 H53 N O6P 1 21/n 113.1917; 16.8403; 18.4369
90; 106.313; 90		3930.9Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127247 CIFC41 H46 O6P 1 21/c 118.1214; 12.6174; 16.0888
90; 103.99; 90		3569.5Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127248 CIFC41 H47 N O5P n a 219.4753; 19.0877; 39.5036
90; 90; 90		7144.7Tlustý, Martin; Spálovská, Dita; Kohout, Michal; Eigner, Václav; Lhoták, Pavel
Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes.
Chemical communications (Cambridge, England), 2020, 56, 12773-12776
7127249 CIFC94 H64 F10 N4C 1 2/c 124.2592; 14.9349; 21.0144
90; 90.863; 90		7612.8Murugavel, M.; Adinarayana, B.; Das, Mainak; Peruncheralathan, S.; Palepu, Narasinga Rao; Srinivasan, A.
PtCl<sub>2</sub> mediated peripheral transformation of carbatriphyrin(3.1.1) into a <i>meso</i>-fused β-β' dimer and its monomer analogue.
Chemical communications (Cambridge, England), 2020, 56, 12809-12812
7127250 CIFC3.36 H2.21 F0.36 N0.14 O0.07P -110.4374; 13.2672; 16.3284
71.893; 73.259; 69.076		1967.1Murugavel, M.; Adinarayana, B.; Das, Mainak; Peruncheralathan, S.; Palepu, Narasinga Rao; Srinivasan, A.
PtCl<sub>2</sub> mediated peripheral transformation of carbatriphyrin(3.1.1) into a <i>meso</i>-fused β-β' dimer and its monomer analogue.
Chemical communications (Cambridge, England), 2020, 56, 12809-12812
7127251 CIFC16 H9 F4 N OP 1 21/c 126.225; 5.008; 10.261
90; 93.42; 90		1345.2Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127252 CIFC16 H9 F4 N OP 1 21/c 126.224; 5.008; 10.26
90; 93.41; 90		1345.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127253 CIFC16 H9 F4 N OP 1 21/c 126.225; 5.007; 10.259
90; 93.37; 90		1344.8Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127254 CIFC16 H9 F4 N OP 1 21/c 126.232; 5.008; 10.264
90; 93.43; 90		1346Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127255 CIFC16 H9 F4 N OP 1 21/c 126.2128; 5.0027; 10.2514
90; 93.435; 90		1341.9Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127256 CIFC16 H9 F4 N OP 1 21/c 126.233; 5.007; 10.266
90; 93.36; 90		1346.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127257 CIFC16 H9 F4 N OP 1 21/c 126.219; 5.009; 10.26
90; 93.4; 90		1345.1Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127258 CIFC16 H9 F4 N OP 1 21/c 126.23; 5.008; 10.263
90; 93.46; 90		1345.7Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127259 CIFC16 H9 F4 N OP 1 21/c 126.226; 5.007; 10.264
90; 93.46; 90		1345.3Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127260 CIFC16 H9 F4 N OP 1 21/c 126.229; 5.008; 10.259
90; 93.39; 90		1345.2Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127261 CIFC16 H9 F4 N OP 1 21/c 126.223; 5.007; 10.266
90; 93.45; 90		1345.5Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127262 CIFC16 H9 F4 N OP 1 21/c 126.23; 5.008; 10.263
90; 93.49; 90		1345.6Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127263 CIFC16 H9 F4 N OP 1 21/c 126.231; 5.008; 10.259
90; 93.42; 90		1345.3Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127264 CIFC16 H9 F4 N OP 1 21/c 126.231; 5.008; 10.262
90; 93.44; 90		1345.6Bhandary, Subhrajyoti; Thompson, Amy J.; McMurtrie, John C.; Clegg, Jack K.; Ghosh, Peuli; Mangalampalli, S. R. N. Kiran; Takamizawa, Satoshi; Chopra, Deepak
The mechanism of bending in a plastically flexible crystal.
Chemical communications (Cambridge, England), 2020, 56, 12841-12844
7127265 CIFC104 H106 N4 O77 Zn14P 1 21/n 122.1643; 16.4288; 23.8287
90; 93.08; 90		8664.3Li, Chuan-Ping; Long, Wei-Wei; Lei, Zhen; Guo, Ling; Xie, Ming-Jun; Lü, Jian; Zhu, Xian-Dong
Anionic metal-organic framework as a unique turn-on fluorescent chemical sensor for ultra-sensitive detection of antibiotics.
Chemical communications (Cambridge, England), 2020, 56, 12403-12406
7127266 CIFC34 H64 N4 Si4 YbP 1 21/c 115.5992; 11.4432; 23.1873
90; 94.693; 90		4125.2Lapshin, Ivan V.; Cherkasov, Anton V.; Asachenko, Andrey F.; Trifonov, Alexander A.
Ln(II) amido complexes coordinated by ring-expanded N-heterocyclic carbenes - promising catalysts for olefin hydrophosphination.
Chemical communications (Cambridge, England), 2020, 56, 12913-12916
7127267 CIFC34 H64 N4 Si4 SmP 1 21/c 115.5699; 11.47; 23.5397
90; 94.58; 90		4190.45Lapshin, Ivan V.; Cherkasov, Anton V.; Asachenko, Andrey F.; Trifonov, Alexander A.
Ln(II) amido complexes coordinated by ring-expanded N-heterocyclic carbenes - promising catalysts for olefin hydrophosphination.
Chemical communications (Cambridge, England), 2020, 56, 12913-12916
7127268 CIFC33 H28 F2 N2 O4P c a 2126.9151; 13.9396; 7.31714
90; 90; 90		2745.29Shi, Wei-Yu; Ding, Ya-Nan; Liu, Ce; Zheng, Nian; Gou, Xue-Ya; Li, Ming; Zhang, Zhe; Liu, Hong-Chao; Niu, Zhi-Jie; Liang, Yong-Min
Three-component ruthenium-catalyzed remote C-H functionalization of 8-aminoquinoline amides.
Chemical communications (Cambridge, England), 2020, 56, 12729-12732
7127269 CIFC6 N12 O16P 1 21/c 19.6672; 9.6302; 9.0564
90; 101.776; 90		825.38Mohammad, Khaja; Thaltiri, Vikranth; Kommu, Nagarjuna; Vargeese, Anuj A.
Octanitropyrazolopyrazole: a gem-trinitromethyl based green high-density energetic oxidizer.
Chemical communications (Cambridge, England), 2020, 56, 12945-12948
7127270 CIFC21 H16 O3P b c a8.8744; 11.4021; 60.208
90; 90; 90		6092.3Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127271 CIFC24 H20 O3P 1 21/n 113.017; 10.8103; 13.8173
90; 110.376; 90		1822.68Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127272 CIFC19 H20 O3P 1 21 18.6683; 8.386; 11.3586
90; 110.379; 90		774Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127273 CIFC21 H16 O3P 1 21 19.6092; 8.1201; 10.9799
90; 116.426; 90		767.22Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127274 CIFC22 H18 O3P 1 21/c 115.8736; 9.6592; 10.7426
90; 93.45; 90		1644.14Yasui, Takeshi; Kikuchi, Tomohiro; Yamamoto, Yoshihiko
Rhodium-catalyzed cycloisomerization of ester-tethered 1,6-diynes with cyclopropanol moiety leading to tetralone/exocyclic diene hybrid molecules.
Chemical communications (Cambridge, England), 2020, 56, 12865-12868
7127275 CIFC9.75 H7.75C m c e20.155; 4.7512; 26.999
90; 90; 90		2585.4Jiménez, Vicente G; Mayorga-Burrezo, Paula; Blanco, Victor; Lloveras, Vega; Gómez-García, Carlos J; Šolomek, Tomáš; Cuerva, Juan M.; Veciana, Jaume; Campaña, Araceli G
Dibenzocycloheptatriene as end-group of Thiele and tetrabenzo-Chichibabin hydrocarbons.
Chemical communications (Cambridge, England), 2020, 56, 12813-12816
7127276 CIFC59 H40 Cl2 O2P -110.9191; 14.2474; 15.1184
87.56; 70.753; 71.905		2106Jiménez, Vicente G; Mayorga-Burrezo, Paula; Blanco, Victor; Lloveras, Vega; Gómez-García, Carlos J; Šolomek, Tomáš; Cuerva, Juan M.; Veciana, Jaume; Campaña, Araceli G
Dibenzocycloheptatriene as end-group of Thiele and tetrabenzo-Chichibabin hydrocarbons.
Chemical communications (Cambridge, England), 2020, 56, 12813-12816
7127277 CIFC48 H42 Cl2 O4 P4 Pd2P -111.8642; 13.1675; 17.343
68.772; 78.937; 63.277		2254.4Oka, Sayaka; Shigehiro, Yuma; Kataoka, Yasutaka; Ura, Yasuyuki
Secondary phosphine oxide-triggered selective oxygenation of a benzyl ligand on palladium.
Chemical communications (Cambridge, England), 2020, 56, 12977-12980
7127278 CIFC42 H44 Cl2 O2.67 P2 Pd2P -110.05; 13.715; 23.78
78.415; 81.104; 86.079		3170Oka, Sayaka; Shigehiro, Yuma; Kataoka, Yasutaka; Ura, Yasuyuki
Secondary phosphine oxide-triggered selective oxygenation of a benzyl ligand on palladium.
Chemical communications (Cambridge, England), 2020, 56, 12977-12980
7127279 CIFC28 H37 Cl2 Mn N7 O9P 1 21 18.8444; 14.0029; 13.7453
90; 99.99; 90		1676.5Xu, Daqian; Sun, Qiangsheng; Lin, Jin; Sun, Wei
Ligand regulation for manganese-catalyzed enantioselective epoxidation of olefins without acid.
Chemical communications (Cambridge, England), 2020, 56, 13101-13104
7127280 CIFC103 H63 Cl9 O2P -115.3787; 16.0584; 16.3664
85.569; 82.256; 71.671		3799.1Pozo, Iago; Peña, Diego; Guitián, Enrique; Pérez, Dolores
2,6,10-Triphenylenotriyne: a star-shaped trisaryne.
Chemical communications (Cambridge, England), 2020, 56, 12853-12856
7127281 CIFC15 H22 B10 S2C m c 2120.2845; 11.9988; 8.454
90; 90; 90		2057.62Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127282 CIFC15 H20 B10 F2 S2C m c 2119.7267; 12.6094; 8.409
90; 90; 90		2091.67Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127283 CIFC5 H18 B10 S2P n m a8.4713; 13.2354; 12.3156
90; 90; 90		1380.84Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127284 CIFC15 H20 B10 Cl2 S2C m c 2121.136; 12.146; 8.5666
90; 90; 90		2199.2Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127285 CIFC20 H24 B10 S2C 1 2/c 125.878; 11.6738; 20.3229
90; 128.273; 90		4819.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127286 CIFC15 H22 B10 Se2C m c 2119.6577; 12.2928; 8.5569
90; 90; 90		2067.8Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127287 CIFC15 H20 B10 Br2 S2P b c a17.4444; 11.2142; 23.4319
90; 90; 90		4583.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127288 CIFC15 H22 B10 O2 S2C m c 2119.5554; 12.2522; 8.6766
90; 90; 90		2078.9Chen, Yu; Quan, Yangjian; Xie, Zuowei
8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)-H disulfenylation of <i>o</i>-carboranes.
Chemical communications (Cambridge, England), 2020, 56, 12997-13000
7127289 CIFC79 H39 B2 F40 SbP 1 21/c 116.5682; 15.2566; 28.2917
90; 90.006; 90		7151.4Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127290 CIFC25 H21 F9 N4 O9.5 S3 SbP -19.101; 13.275; 13.8328
81.615; 86.39; 84.352		1643.32Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127291 CIFC61 H64 B F20 N4 SbP 1 2/n 119.218; 8.3161; 20.922
90; 111.897; 90		3102.5Zhou, Jiliang; Kim, Hyehwang; Liu, Liu Leo; Cao, Levy L.; Stephan, Douglas W.
An arene-stabilized η<sup>5</sup>-pentamethylcyclopentadienyl antimony dication acts as a source of Sb<sup>+</sup> or Sb<sup>3+</sup> cations.
Chemical communications (Cambridge, England), 2020, 56, 12953-12956
7127292 CIFC20 H21 N O2 SP 16.0451; 8.3029; 9.2867
107.436; 107.421; 90.517		421.8Tao, Mengna; Li, Wenbo; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization of norbornene and norbornadiene.
Chemical communications (Cambridge, England), 2020, 56, 13125-13128
7127293 CIFC15 H16 O3P 21 21 216.0733; 11.523; 17.1932
90; 90; 90		1203.23Tao, Mengna; Li, Wenbo; Zhang, Junliang
Pd/Xiang-Phos-catalyzed enantioselective intermolecular carboheterofunctionalization of norbornene and norbornadiene.
Chemical communications (Cambridge, England), 2020, 56, 13125-13128
7127294 CIFC35 H35 F6 N5 O11 Ru S2P 110.011; 13.646; 16.369
66.564; 72.663; 78.969		1951.7Hirahara, Masanari; Goto, Hiroki; Yagi, Masayuki; Umemura, Yasushi
A multi-stimuli responsive ruthenium complex for catalytic water oxidation.
Chemical communications (Cambridge, England), 2020, 56, 12825-12828
7127295 CIFC35 H35 F6 N5 O11 Ru S2P -111.5955; 13.3944; 13.4286
94.6542; 108.322; 99.0418		1936.28Hirahara, Masanari; Goto, Hiroki; Yagi, Masayuki; Umemura, Yasushi
A multi-stimuli responsive ruthenium complex for catalytic water oxidation.
Chemical communications (Cambridge, England), 2020, 56, 12825-12828
7127296 CIFC58 H50 N7 O3 P2 ReP -113.556; 13.655; 16.754
71.32; 88.136; 61.543		2556Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127297 CIFC55 H43 N5 O5 P2 ReP -113.437; 13.848; 16.639
71.036; 89.469; 61.39		2530.3Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127298 CIFC62 H56 N7 O2 P2 ReP -113.6167; 14.0119; 15.9593
109.223; 90.428; 106.99		2731.5Sasaki, Kenta; Yamate, Hitomi; Yoshino, Haruka; Miura, Hiroki; Shimoda, Yuushi; Miyata, Kiyoshi; Onda, Ken; Ohtani, Ryo; Ohba, Masaaki
Vapor switching of the luminescence mechanism in a Re(V) complex.
Chemical communications (Cambridge, England), 2020, 56, 12961-12964
7127299 CIFC19 H13 N3 O2 PtP 1 21/c 111.0034; 12.6502; 23.9841
90; 98.435; 90		3302.36Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127300 CIFC21 H17 N3 O2 PtR -3 :H30.2541; 30.2541; 10.0134
90; 90; 120		7937.4Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127301 CIFC19 H14.33 N3 O2.67 PtR -3 :H30.4714; 30.4714; 10.0419
90; 90; 120		8074.79Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127302 CIFC19 H13 N3 O2 PtR -3 :H30.402; 30.402; 10.0404
90; 90; 120		8036.9Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127303 CIFC21 H17 N3 O2 PtR -3 :H30.2896; 30.2896; 10.057
90; 90; 120		7990.72Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127304 CIFC39 H52 Cl0.33 Co N2.33 P3P -19.4001; 10.1799; 19.692
96.945; 98.651; 92.505		1845.6Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127305 CIFC37 H48 Cl Co N P3P b c a11.1139; 17.2203; 36.7506
90; 90; 90		7033.5Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127306 CIFC39 H52 Cl Co N P3P b c a18.5652; 15.3844; 25.5535
90; 90; 90		7298.4Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127307 CIFC37 H48 Cl2 Co N P3P 1 21/c 118.0756; 12.9004; 16.8278
90; 112.241; 90		3632Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127308 CIFC25 H39 Cl Co P3P 1 21/n 110.5437; 16.2502; 15.7679
90; 98.878; 90		2669.26Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127309 CIFC71 H63 B Co F24 N2 P3P 1 21/n 112.5472; 41.432; 13.4271
90; 92.586; 90		6973Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127310 CIFC74 H98 Co2 N4 P6P -111.285; 15.184; 21.077
89.329; 89.127; 75.629		3498Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127311 CIFC39 H52 Cl2 Co N P3P 4115.4027; 15.4027; 32.0302
90; 90; 90		7598.9Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127312 CIFC39 H52 Cl Co N P3P -19.751; 12.142; 17.953
72.006; 76.941; 71.219		1895Wang, Fang; Cannon, Austin T.; Bhattacharya, Moumita; Baumgarten, Robert; VanderLinden, Ryan T.; Saouma, Caroline T.
Hydrogenation and electrocatalytic reduction of carbon dioxide to formate with a single Co catalyst.
Chemical communications (Cambridge, England), 2020, 56, 12142-12145
7127313 CIFC25 H24 O9P b c a22.085; 9.856; 22.387
90; 90; 90		4873Manna, Sabyasachi; Someswara Ashwathappa, Puneeth Kumar; Prabhu, Kandikere Ramaiah
Visible light-mediated ipso-annulation of activated alkynes: access to 3-alkylated spiro[4,5]-trienones, thiaspiro[4,5]-trienones and azaspiro[4,5]-trienones.
Chemical communications (Cambridge, England), 2020, 56, 13165-13168
7127314 CIFC19 H13 N3 O2 PtP 1 21/c 111.0034; 12.6502; 23.9841
90; 98.435; 90		3302.36Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127315 CIFC21 H17 N3 O2 PtR -3 :H30.2541; 30.2541; 10.0134
90; 90; 120		7937.4Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127316 CIFC19 H14.33 N3 O2.67 PtR -3 :H30.4714; 30.4714; 10.0419
90; 90; 120		8074.79Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127317 CIFC19 H13 N3 O2 PtR -3 :H30.402; 30.402; 10.0404
90; 90; 120		8036.9Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127318 CIFC21 H17 N3 O2 PtR -3 :H30.2896; 30.2896; 10.057
90; 90; 120		7990.72Kimura, Mari; Yoshida, Masaki; Fujii, Sho; Miura, Atsushi; Ueno, Kosei; Shigeta, Yasuhiro; Kobayashi, Atsushi; Kato, Masako
Liquid-liquid interface-promoted formation of a porous molecular crystal based on a luminescent platinum(II) complex.
Chemical communications (Cambridge, England), 2020, 56, 12989-12992
7127319 CIFC34 H34 Cl4 O10P b c a10.519; 14.5588; 22.7509
90; 90; 90		3484.2Joshi, Saurabh; Yip, Yong Jie; Türel, Tankut; Verma, Sandeep; Valiyaveettil, Suresh
Cu-tetracatechol metallopolymer catalyst for three component click reactions and β-borylation of α,β-unsaturated carbonyl compounds.
Chemical communications (Cambridge, England), 2020, 56, 13044-13047
7127320 CIFC30 H25 F N2 O5P -110.0079; 11.0103; 13.8154
68.117; 74.662; 67.141		1288.86Lv, Yunhe; Pu, Weiya; Wang, Xiaoxing
Ligand-free copper-catalyzed regio- and stereoselective 1,1-alkylmonofluoroalkylation of terminal alkynes.
Chemical communications (Cambridge, England), 2020, 56, 12933-12936
7127321 CIFC30 H22 N2 O5P 1 21 18.8477; 14.2309; 9.6371
90; 95.549; 90		1207.73Yuan, Xi; Wu, Xudong; Peng, Fei; Yang, Haijun; Zhu, Changjin; Fu, Hua
Organocatalytic asymmetric synthesis of arylindolyl indolin-3-ones with both axial and central chirality.
Chemical communications (Cambridge, England), 2020, 56, 12648-12651
7127322 CIFC20 H20 F6 Fe N2 O7 S5C 1 2/c 124.4848; 11.4726; 20.4806
90; 108.738; 90		5448.2Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127323 CIFC40 H42 F6 Fe N3 O8.5 S5P -110.277; 14.2819; 15.9309
88; 71.475; 89.017		2215.7Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127324 CIFC33 H29 F6 Fe N3 O7 S5P -113.0248; 13.4754; 21.3868
86.09; 76.878; 81.685		3614.8Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127325 CIFC35 H31 F6 Fe N3 O7 S5P b c a14.2635; 17.4695; 30.1975
90; 90; 90		7524.5Chan, Siu-Chung; Yeung, Chi-Fung; Shek, Hau-Lam; Ng, Sze-Wing; Tse, Sheung-Ying; Tse, Man-Kit; Yiu, Shek-Man; Wong, Chun-Yuen
Iron(ii)-induced cycloisomerization of alkynes via"non-vinylidene" pathways for iron(ii)-indolizine and -indolizinone complexes.
Chemical communications (Cambridge, England), 2020, 56, 12644-12647
7127326 CIFC42 H44 Co N6 O10P 1 21/n 110.2874; 19.8376; 11.0367
90; 111.416; 90		2096.8Koyama, Shohei; Tanabe, Tappei; Takaishi, Shinya; Yamashita, Masahiro; Iguchi, Hiroaki
Preliminary chemical reduction for synthesizing a stable porous molecular conductor with neutral metal nodes.
Chemical communications (Cambridge, England), 2020, 56, 13109-13112
7127327 CIFC42 H44 Co N6 O10 Rb0.5P 64 2 219.8453; 19.8453; 9.5591
90; 90; 120		3260.3Koyama, Shohei; Tanabe, Tappei; Takaishi, Shinya; Yamashita, Masahiro; Iguchi, Hiroaki
Preliminary chemical reduction for synthesizing a stable porous molecular conductor with neutral metal nodes.
Chemical communications (Cambridge, England), 2020, 56, 13109-13112
7127328 CIFC74 H75 Au5 Cl2 P3 Ru2 S0P -113.98; 16.129; 17.64
112.192; 90.973; 92.718		3676.1Sun, Yongnan; Yang, Dan; Zhang, Yuying; Hu, Weigang; Cheng, Xinglian; Liu, Xu; Chen, Mingyang; Zhu, Yan
Ligand-protected Au<sub>4</sub>Ru<sub>2</sub> and Au<sub>5</sub>Ru<sub>2</sub> nanoclusters: distinct structures and implications for site-cooperation catalysis.
Chemical communications (Cambridge, England), 2020, 56, 12833-12836
7127329 CIFC23 H34 OP 1 21 16.689; 10.95; 13.04
90; 94.67; 90		951.9Bettoni, Léo; Gaillard, Sylvain; Renaud, Jean-Luc
A phosphine-free iron complex-catalyzed synthesis of cycloalkanes <i>via</i> the borrowing hydrogen strategy.
Chemical communications (Cambridge, England), 2020, 56, 12909-12912
7127330 CIFC25 H26 O2 SP 1 21/c 110.361; 22.362; 10.254
90; 113.65; 90		2176.2Parameshwar, Matam; Singam, Maneesh Kumar Reddy; Nagireddy, Attunuri; Nanubolu, Jagadeesh Babu; Reddy, Maddi Sridhar
Regioselective benzannulation of allylic sulfur ylides with ynones: a rapid access to substituted thioanisoles.
Chemical communications (Cambridge, England), 2020, 56, 13457-13460
7127331 CIFC6 F1.87 La0.09 O0.8 S0.36P -115.184; 15.6113; 47.3346
99.304; 91.333; 110.381		10341Zhang, Yuan; Zhou, Yanyan; Gao, Ting; Yan, Pengfei; Li, Hongfeng
Metal-directed synthesis of quadruple-stranded helical Eu(III) molecular switch: a significant improvement in photocyclization quantum yield.
Chemical communications (Cambridge, England), 2020, 56, 13213-13216
7127332 CIFC54 H54 N4 O15 Zn4C 1 2/m 122.3686; 25.4298; 17.1469
90; 101.016; 90		9573.9Xi, Fu-Gui; Sun, Wei; Dong, Zhi-Yun; Yang, Ning-Ning; Gong, Teng; Gao, En-Qing
An in situ approach to functionalize metal-organic frameworks with tertiary aliphatic amino groups.
Chemical communications (Cambridge, England), 2020, 56, 13177-13180
7127333 CIFC9.6 H21.12 Eu O18 S3P 1 21/n 18.9194; 8.8509; 25.242
90; 90.154; 90		1992.7Ruaysap, Makabodee; Kennedy, Stuart R.; Mayhan, Collin M.; Kelley, Steven P.; Kumari, Harshita; Deakyne, Carol A.; Atwood, Jerry L.
Novel keto-enol tautomerism in 1,3,5-trihydroxybenzene systems.
Chemical communications (Cambridge, England), 2020, 56, 12985-12988
7127334 CIFC9.6 H19.5 O18 S3 SmP 1 21/n 18.9342; 8.8762; 25.291
90; 90.34; 90		2005.6Ruaysap, Makabodee; Kennedy, Stuart R.; Mayhan, Collin M.; Kelley, Steven P.; Kumari, Harshita; Deakyne, Carol A.; Atwood, Jerry L.
Novel keto-enol tautomerism in 1,3,5-trihydroxybenzene systems.
Chemical communications (Cambridge, England), 2020, 56, 12985-12988
7127335 CIFC16 H18 Br N O4P 1 21 110.42782; 7.6985; 11.51764
90; 106.53; 90		886.41Mato, Raquel; Reyes, Efraim; Carrillo, Luisa; Uria, Uxue; Prieto, Liher; Manzano, Ruben; Vicario, Jose L.
Catalytic enantioselective domino Michael/transannular aldol reaction under bifunctional catalysis.
Chemical communications (Cambridge, England), 2020, 56, 13149-13152
7127336 CIFC18 H21 N O4P 21 21 219.19139; 11.21187; 15.13619
90; 90; 90		1559.82Mato, Raquel; Reyes, Efraim; Carrillo, Luisa; Uria, Uxue; Prieto, Liher; Manzano, Ruben; Vicario, Jose L.
Catalytic enantioselective domino Michael/transannular aldol reaction under bifunctional catalysis.
Chemical communications (Cambridge, England), 2020, 56, 13149-13152
7127337 CIFC29 H22 Br N O SP 1 21 110.663; 9.0225; 12.3447
90; 90.216; 90		1187.6Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127338 CIFC29 H23 N O2P 21 21 217.1433; 16.4271; 18.919
90; 90; 90		2220.03Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127339 CIFC29 H23 N O SP 1 21 19.7976; 8.723; 14.089
90; 110.142; 90		1130.5Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127340 CIFC58 H46 N2 O2 S2P 21 21 2110.0966; 16.0127; 27.6462
90; 90; 90		4469.7Chang, Fenzhen; Shen, Bin; Wang, Sijing; Lin, Lili; Feng, Xiaoming
Lewis acid catalysed asymmetric cascade reaction of cyclopropyl ketones: concise synthesis of pyrrolobenzothiazoles.
Chemical communications (Cambridge, England), 2020, 56, 13429-13432
7127341 CIFC22 H23 Eu N4 O14P 1 21/c 116.3413; 10.2541; 15.7957
90; 91.96; 90		2645.26Fu, Ting; Wei, Yong-Li; Zhang, Chong; Li, Lin-Ke; Liu, Xiao-Fei; Li, Hai-Yang; Zang, Shuang-Quan
A viologen-based multifunctional Eu-MOF: photo/electro-modulated chromism and luminescence.
Chemical communications (Cambridge, England), 2020, 56, 13093-13096
7127342 CIFC34.5 H38 Cl Ir N2 O5.5P -17.7989; 9.4618; 24.171
95.058; 94.646; 112.464		1629.1Nguyen, Huong T. H.; Do, Loi H.
Organoiridium-quinone conjugates for facile hydrogen peroxide generation.
Chemical communications (Cambridge, England), 2020, 56, 13381-13384
7127343 CIFC54 H74 As4 Fe2 N4P -113.2431; 13.9354; 16.0383
89.203; 87.031; 67.239		2725.6Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127344 CIFC54 H74 As4 Fe2 N4P -113.2706; 14.0867; 15.8705
89.309; 86.365; 67.8		2741.13Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127345 CIFC101.5 H120 As8 Fe4 N8P -113.60288; 14.75365; 26.0325
82.1763; 76.4461; 78.1144		4948.88Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127346 CIFC83 H92 As8 Fe4 N8C 1 2/c 124.8828; 12.9874; 26.3513
90; 103.716; 90		8272.9Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127347 CIFC58 H82 As3.78 Fe2 N4P 1 21/n 114.2884; 13.6019; 15.3559
90; 103.879; 90		2897.28Spitzer, Fabian; Balázs, Gábor; Graßl, Christian; Scheer, Manfred
Iron β-diiminate complexes with As<sub>2</sub>-, As<sub>4</sub>- and As<sub>8</sub>-ligands.
Chemical communications (Cambridge, England), 2020, 56, 13209-13212
7127348 CIFC19 H14 N2 OP -16.1633; 10.2878; 11.0233
88.901; 81.769; 81.501		684.15Chakraborty, Soumi; Das, Arpan; Ahmed, Jasimuddin; Barman, Sayani; Mandal, Swadhin K.
Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO<sub>2</sub> functionalization.
Chemical communications (Cambridge, England), 2020, 56, 13788-13791
7127349 CIFC40 H36 Cl Cr N4 O5P -19.8879; 16.9397; 20.5976
83.383; 76.246; 89.429		3328.3Chakraborty, Soumi; Das, Arpan; Ahmed, Jasimuddin; Barman, Sayani; Mandal, Swadhin K.
Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO<sub>2</sub> functionalization.
Chemical communications (Cambridge, England), 2020, 56, 13788-13791
7127350 CIFC48 H84 Co Li N3 O6P 1 21 110.8897; 21.2774; 11.9691
90; 113.656; 90		2540.26Das, Chinmoy; Rasamsetty, Amaleswari; Tripathi, Shalini; Shanmugam, Maheswaran
Magnetization relaxation dynamics of a rare coordinatively unsaturated Co(II) complex: experimental and theoretical insights.
Chemical communications (Cambridge, England), 2020, 56, 13397-13400
7127351 CIFC39 H46 Cu N2 PP -110.0805; 10.9216; 16.5042
73.491; 88.101; 84.877		1735.11Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127352 CIFC106 H122 Cu2 N6 P2 S2P -116.7653; 16.7976; 17.4582
99.123; 103.295; 92.374		4708.68Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127353 CIFC68 H76 Cu2 N4 P2P -111.3727; 11.3954; 22.6857
90.164; 91.091; 101.25		2882.91Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127354 CIFC40 H50 Cu N2 PP -112.8035; 16.6298; 17.6961
104.81; 90.293; 95.555		3623.82Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127355 CIFC33 H36 Cu N2 PP 1 21/c 112.9476; 19.6806; 13.1443
90; 119.072; 90		2927.4Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127356 CIFC47 H56 Cu N2 P S2P 1 21/c 110.7063; 12.6577; 32.3409
90; 98.799; 90		4331.17Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127357 CIFC44 H57 Cu N3 O PP 1 21/n 112.5486; 18.9533; 17.66
90; 106.233; 90		4032.76Horsley Downie, Thomas M.; Hall, Jonathan W.; Collier Finn, Thomas P.; Liptrot, David J.; Lowe, John P.; Mahon, Mary F.; McMullin, Claire L.; Whittlesey, Michael K.
The first ring-expanded NHC-copper(i) phosphides as catalysts in the highly selective hydrophosphination of isocyanates.
Chemical communications (Cambridge, England), 2020, 56, 13359-13362
7127358 CIFC22 H36 Ca Cl2 N6 O6P -17.968; 12.17; 15.304
87.17; 86.3; 74.76		1428.1Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127359 CIFC22 H36 Ca Cl2 N6 O6P 1 21 111.9243; 8.0669; 15.4348
90; 92.338; 90		1483.47Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127360 CIFC22 H36 Ca Cl2 N6 O6P 21 21 217.9303; 15.1768; 23.7226
90; 90; 90		2855.17Song, Lixing; Robeyns, Koen; Tumanov, Nikolay; Wouters, Johan; Leyssens, Tom
Combining API in a dual-drug ternary cocrystal approach.
Chemical communications (Cambridge, England), 2020, 56, 13229-13232
7127361 CIFC23 H22 O4 S2P -18.8162; 9.9355; 12.7903
88.965; 85.831; 70.437		1052.86Wang, Yu; Tang, Kongshuang; Liu, Zhaohong; Ning, Yongquan
Disulfonation of terminal alkynes for 1,2-bisulfonylethenes.
Chemical communications (Cambridge, England), 2020, 56, 13141-13144
7127362 CIFC26 H23 Br F3 N O5P 1 21 18.78349; 25.2447; 11.5445
90; 92.4781; 90		2557.44Zhang, Xia-Yan; You, Yong; Wang, Zhen-Hua; Zhao, Jian-Qiang; Yuan, Wei-Cheng
Organocatalytic asymmetric tandem α-functionalization/1,3-proton shift reaction of benzylidene succinimides with β-trifluoromethyl enones.
Chemical communications (Cambridge, England), 2020, 56, 13449-13452
7127363 CIFC91 H10 Br O4 S4 YP 1 21/c 111.2309; 22.0675; 20.7788
90; 98.817; 90		5088.9Shen, Wangqiang; Yang, Le; Li, Bo; Jin, Peng; Yu, Bing; Cong, Hailin; Akasaka, Takeshi; Lu, Xing
Metal-encapsulation induces a highly regioselective Bingel-Hirsch reaction of the labile Y@<i>C</i><sub>s</sub>(6)-C<sub>82</sub>.
Chemical communications (Cambridge, England), 2020, 56, 14357-14360
7127364 CIFC24 H22 Br2 N2 O2P 1 21/n 16.0728; 24.305; 15.0006
90; 98.929; 90		2187.2Silvestri, A. P.; Oakdale, J. S.
Intermolecular cyclotrimerization of haloketoalkynes and internal alkynes: facile access to arenes and phthalides.
Chemical communications (Cambridge, England), 2020, 56, 13417-13420
7127365 CIFC12 H11 Br2 N O4P -18.5662; 8.5847; 9.5341
96.065; 102.093; 95.978		675.95Silvestri, A. P.; Oakdale, J. S.
Intermolecular cyclotrimerization of haloketoalkynes and internal alkynes: facile access to arenes and phthalides.
Chemical communications (Cambridge, England), 2020, 56, 13417-13420
7127366 CIFC47 H46 Cl N5 O5 P2 PtP 1 21 114.809; 9.7032; 18.6573
90; 113.307; 90		2462.2Leitão, Maria Inês P S; Gonzalez, Carmen; Francescato, Giulia; Filipiak, Zuzanna; Petronilho, Ana
On the reactivity of mRNA Cap0: C-H oxidative addition of 7-methylguanosine to Pt<sup>0</sup> and base pairing studies.
Chemical communications (Cambridge, England), 2020, 56, 13365-13368
7127367 CIFC46 H40 Co F18 N10 P3C 1 2/c 115.05; 15.46; 22.031
90; 108.853; 90		4851Mansoor, Iram F.; Wozniak, Derek I.; Wu, Yilei; Lipke, Mark C.
A delocalized cobaltoviologen with seven reversibly accessible redox states and highly tunable electrochromic behaviour.
Chemical communications (Cambridge, England), 2020, 56, 13864-13867
7127368 CIFC44 H37 Co F24 N9 P4P 1 21/c 112.9089; 31.053; 25.429
90; 90.106; 90		10193.5Mansoor, Iram F.; Wozniak, Derek I.; Wu, Yilei; Lipke, Mark C.
A delocalized cobaltoviologen with seven reversibly accessible redox states and highly tunable electrochromic behaviour.
Chemical communications (Cambridge, England), 2020, 56, 13864-13867
7127369 CIFC15 H19 Br2 N3 ZnP 1 21/n 113.6806; 9.1444; 14.0282
90; 100.311; 90		1726.6Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127370 CIFC17 H25 Br2 N3 ZnP 1 21/n 112.8681; 11.5859; 14.3384
90; 103.984; 90		2074.34Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127371 CIFC24 H39 B Br N5 ZnP -110.8931; 11.4206; 12.3188
83.305; 63.943; 73.559		1320.41Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127372 CIFC25 H38 B Br2 N3 ZnP 1 21/c 115.0468; 11.2801; 16.7588
90; 103.198; 90		2769.3Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127373 CIFC23 H34 B Br2 N3 ZnP -113.0034; 13.5104; 15.0119
86.957; 87.514; 73.838		2528.4Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127374 CIFC25 H40 B Br F3 N5 O3 S ZnP -111.9524; 11.9577; 12.1827
107.294; 93.865; 110.961		1522.69Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127375 CIFC29 H44 B Br2 N5 ZnP -110.661; 11.8149; 13.2704
105.494; 99.734; 101.5		1534.07Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127376 CIFC24 H60 F12 O4 P6 ZnP -112.419; 12.4357; 30.319
89.995; 90.007; 119.911		4058.7Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127377 CIFC28 H45 B Br2 N5 ZnC 1 2/c 112.0353; 24.2453; 21.535
90; 92.423; 90		6278.3Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127378 CIFC26 H44 B Br Cl2 F6 N5 P ZnC 1 2/c 127.6433; 15.2931; 18.2871
90; 119.684; 90		6716.4Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127379 CIFC55.41 H91.23 B2 Br4 N8 O2.04 Zn2P -115.0988; 20.3399; 21.5241
87.7923; 84.8814; 71.6768		6249.7Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127380 CIFC17 H23 Br2 N3 ZnP 1 21/n 117.2348; 11.4411; 20.0805
90; 92.729; 90		3955.1Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127381 CIFC28 H46 B Br F3 N5 O4 S ZnP -111.5579; 12.4732; 14.2722
106.92; 101.436; 113.029		1693.95Kiernicki, John J.; Norwine, Emily E.; Lovasz, Myles A.; Zeller, Matthias; Szymczak, Nathaniel K.
Mobility of Lewis acids within the secondary coordination sphere: toward a model for cooperative substrate binding.
Chemical communications (Cambridge, England), 2020, 56, 13105-13108
7127382 CIFC19 H16 N2P b c a17.2098; 7.3662; 22.672
90; 90; 90		2874.1Jiang, Bo; Jia, Jingwen; Sun, Yufei; Wang, Yichun; Zeng, Jing; Bu, Xiubin; Shi, Liangliang; Sun, Xiaoying; Yang, Xiaobo
γ-Carboline synthesis enabled by Rh(iii)-catalysed regioselective C-H annulation.
Chemical communications (Cambridge, England), 2020, 56, 13389-13392
7127383 CIFC22 H28 Cl N2 O RhP 1 21/c 118.1856; 7.4674; 16.226
90; 111.448; 90		2050.89Jiang, Bo; Jia, Jingwen; Sun, Yufei; Wang, Yichun; Zeng, Jing; Bu, Xiubin; Shi, Liangliang; Sun, Xiaoying; Yang, Xiaobo
γ-Carboline synthesis enabled by Rh(iii)-catalysed regioselective C-H annulation.
Chemical communications (Cambridge, England), 2020, 56, 13389-13392
7127384 CIFC27.72 H73.15 Cl0.28 Li6 N6 OC 1 2/c 137.719; 9.9975; 27.5561
90; 129.915; 90		7970.1Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127385 CIFC11.89 H31.67 Cl0.11 Li3 N3C 1 2/c 119.9942; 11.0399; 17.1245
90; 110.506; 90		3540.44Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127386 CIFC16 H32 Cl2 Li2 O4P 1 21/n 19.4887; 11.075; 9.7615
90; 95.203; 90		1021.6Knauer, Lena; Strohmann, Carsten
The structure-defining incorporation of chloride in methyllithium dimers.
Chemical communications (Cambridge, England), 2020, 56, 13543-13546
7127387 CIFC54 H32 O8P n n n :23.7618; 24.323; 41.416
90; 90; 90		3789.5Suzuki, Yuto; Tohnai, Norimitsu; Saeki, Akinori; Hisaki, Ichiro
Hydrogen-bonded organic frameworks of twisted polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2020, 56, 13369-13372
7127388 CIFC54 H32 O8I 41/a c d :247.5006; 47.5006; 7.417
90; 90; 90		16735Suzuki, Yuto; Tohnai, Norimitsu; Saeki, Akinori; Hisaki, Ichiro
Hydrogen-bonded organic frameworks of twisted polycyclic aromatic hydrocarbon.
Chemical communications (Cambridge, England), 2020, 56, 13369-13372
7127389 CIFC23 H20 O2P 1 21/n 15.97592; 22.3752; 13.3264
90; 97.3628; 90		1767.21Gu, Jia-Yi; Zhang, Wei; Jackson, Seth R.; He, Yan-Hong; Guan, Zhi
Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation.
Chemical communications (Cambridge, England), 2020, 56, 13441-13444
7127390 CIFC23 H20 O2P 1 21/n 16.11677; 21.9208; 13.21139
90; 96.7434; 90		1759.19Gu, Jia-Yi; Zhang, Wei; Jackson, Seth R.; He, Yan-Hong; Guan, Zhi
Photoinduced umpolung addition of carbonyl compounds with α,β-unsaturated esters enables the polysubstituted γ-lactone formation.
Chemical communications (Cambridge, England), 2020, 56, 13441-13444
7127391 CIFC17 H40 Cu N3 Si2P -18.858; 9.6854; 14.7645
104.257; 103.276; 101.697		1148.85Boysen, Nils; Misimi, Bujamin; Muriqi, Arbresha; Wree, Jan-Lucas; Hasselmann, Tim; Rogalla, Detlef; Haeger, Tobias; Theirich, Detlef; Nolan, Michael; Riedl, Thomas; Devi, Anjana
A carbene stabilized precursor for the spatial atomic layer deposition of copper thin films.
Chemical communications (Cambridge, England), 2020, 56, 13752-13755
7127392 CIFCs4 H62 K7 Na5 Nb23 O108 V5P 1 21/c 114.9822; 25.2721; 31.619
90; 93.655; 90		11947.6Zhen, Ni; Dong, Jing; Lin, Zhengguo; Li, Xiaoxia; Chi, Yingnan; Hu, Changwen
Self-assembly of polyoxovanadate-capped polyoxoniobates and their catalytic decontamination of sulfur mustard simulants.
Chemical communications (Cambridge, England), 2020, 56, 13967-13970
7127393 CIFCs4 H74 K8 Na5 Nb23 O115 V6P 1 21/m 115.9678; 23.5105; 16.2976
90; 104.33; 90		5927.9Zhen, Ni; Dong, Jing; Lin, Zhengguo; Li, Xiaoxia; Chi, Yingnan; Hu, Changwen
Self-assembly of polyoxovanadate-capped polyoxoniobates and their catalytic decontamination of sulfur mustard simulants.
Chemical communications (Cambridge, England), 2020, 56, 13967-13970
7127394 CIFC26 H27 Al Cl2 F6 N2 O3P 21 21 219.0833; 13.9679; 20.8666
90; 90; 90		2647.4Hador, Rami; Lipstman, Sophia; Rescigno, Raffaella; Venditto, Vincenzo; Kol, Moshe
Aluminium complexes of salanol ligands: coordination chemistry and stereoselective lactide polymerization.
Chemical communications (Cambridge, England), 2020, 56, 13528-13531
7127395 CIFC56 H59 Al N2 O3P 110.2589; 10.8028; 11.3273
100.728; 97.616; 109.85		1133.8Hador, Rami; Lipstman, Sophia; Rescigno, Raffaella; Venditto, Vincenzo; Kol, Moshe
Aluminium complexes of salanol ligands: coordination chemistry and stereoselective lactide polymerization.
Chemical communications (Cambridge, England), 2020, 56, 13528-13531
7127396 CIFC45 H56 Au B2 O2 P2P -111.1923; 13.0857; 15.6457
84.3144; 74.4558; 68.8762		2059.29Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127397 CIFC53 H81 Au B2 K O8.5 P2P 1 21/n 112.4601; 27.1704; 16.4408
90; 94.0898; 90		5551.8Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127398 CIFC48 H69.47 Au B2 K O7.53 P2P -111.5721; 13.3494; 17.4347
77.4593; 77.1738; 68.9764		2423.17Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127399 CIFC36 H45 Au B2 O P2P b c a19.5549; 17.1275; 19.6848
90; 90; 90		6592.96Taylor, Jordan W.; Harman, W. Hill
H<sub>2</sub> evolution from H<sub>2</sub>O via O-H oxidative addition across a 9,10-diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 13804-13807
7127400 CIFC5 H20 N10 S5P 1 21/c 110.5332; 21.0945; 8.1916
90; 94.7245; 90		1813.93Liu, Ziwei; Wu, Long-Fei; Bond, Andrew D.; Sutherland, John D.
Photoredox chemistry in the synthesis of 2-aminoazoles implicated in prebiotic nucleic acid synthesis.
Chemical communications (Cambridge, England), 2020, 56, 13563-13566
7127401 CIFC6 H16 Bi Cl5 N2 S2P 1 21/c 112.1998; 7.4008; 21.8754
90; 123.518; 90		1646.66Liu, Yu-Ting; He, Lei; Shi, Ping-Ping; Ye, Qiong; Fu, Da-Wei
A one-dimensional switchable dielectric material with Pd uptake function: [(CH<sub>2</sub>)<sub>3</sub>NH<sub>2</sub>S]<sub>2</sub>BiCl<sub>5</sub>.
Chemical communications (Cambridge, England), 2020, 56, 13764-13767
7127402 CIFC6 H16 Bi Cl5 N2 S2P 1 21/c 112.232; 7.5245; 22.0936
90; 123.339; 90		1698.84Liu, Yu-Ting; He, Lei; Shi, Ping-Ping; Ye, Qiong; Fu, Da-Wei
A one-dimensional switchable dielectric material with Pd uptake function: [(CH<sub>2</sub>)<sub>3</sub>NH<sub>2</sub>S]<sub>2</sub>BiCl<sub>5</sub>.
Chemical communications (Cambridge, England), 2020, 56, 13764-13767
7127403 CIFC15 H12 O3 SP -110.049; 10.24; 13.391
76.934; 77.667; 71.574		1258.3Chen, Xiang-Long; Tang, Bo-Cheng; He, Cai; Ma, Jin-Tian; Zhuang, Shi-Yi; Wu, Yan-Dong; Wu, An-Xin
Rongalite as a sulfone source: a novel copper-catalyzed sulfur dioxide anion incorporation process.
Chemical communications (Cambridge, England), 2020, 56, 13653-13656
7127404 CIFC68 H57 N9 O4 SP -18.9409; 16.6725; 20.1342
100.612; 93.221; 90.152		2945.1Feng, Xin; Chen, Yating; Lei, Yunxiang; Zhou, Yunbing; Gao, Wenxia; Liu, Miaochang; Huang, Xiaobo; Wu, Huayue
Multifunctional properties of a star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide fluorescent molecule containing multiple flexible chains.
Chemical communications (Cambridge, England), 2020, 56, 13638-13641
7127405 CIFC68 H57 N9 O4 SP -18.967; 16.6; 20.124
79.369; 86.581; 89.896		2938.7Feng, Xin; Chen, Yating; Lei, Yunxiang; Zhou, Yunbing; Gao, Wenxia; Liu, Miaochang; Huang, Xiaobo; Wu, Huayue
Multifunctional properties of a star-shaped triphenylamine-benzene-1,3,5-tricarbohydrazide fluorescent molecule containing multiple flexible chains.
Chemical communications (Cambridge, England), 2020, 56, 13638-13641
7127406 CIFC18 H54 Cl Ge N3 Si6R 3 c :H17.85648; 17.85648; 16.97342
90; 90; 120		4686.96Barrett, A. N.; Sanderson, H. J.; Mahon, M. F.; Webster, R. L.
Hydrophosphination using [GeCl{N(SiMe<sub>3</sub>)<sub>2</sub>}<sub>3</sub>] as a pre-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 13623-13626
7127407 CIFC31 H19 N3 O2P -15.1443; 14.4148; 14.9692
92.88; 93.257; 90.232		1106.8Tang, Lele; Zan, Jie; Peng, Hao; Yan, Xi; Tao, Ye; Tian, Dan; Yang, Qingqing; Li, Huanhuan; Chen, Qiushui; Huang, Wei; Chen, Runfeng
X-ray excited ultralong room-temperature phosphorescence for organic afterglow scintillators.
Chemical communications (Cambridge, England), 2020, 56, 13559-13562
7127408 CIFC60 H72 K3 Mo6 O16.5 P3C 1 2 143.5147; 7.94643; 20.3986
90; 100.944; 90		6925.3Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127409 CIFC35 H61 Li O6 P4 TaP 1 21/n 111.8625; 21.7618; 16.0909
90; 94.017; 90		4143.65Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127410 CIFC46 H69 N2 O4 P4 TaP b c a19.8677; 17.9409; 27.8048
90; 90; 90		9910.9Riedlberger, Felix; Seidl, Michael; Scheer, Manfred
The reaction behavior of [Cp<sub>2</sub>Mo<sub>2</sub>(CO)<sub>4</sub>(μ,η<sup>2:2</sup>-P<sub>2</sub>)] and [Cp''Ta(CO)<sub>2</sub>(η<sup>4</sup>-P<sub>4</sub>)] towards hydroxide and tert-butyl nucleophiles.
Chemical communications (Cambridge, England), 2020, 56, 13836-13839
7127411 CIFC23 H23 Cl2 N O6P 3112.3959; 12.3959; 13.34104
90; 90; 120		1775.32Xu, Huacheng; Nazli, Adila; Zou, Cheng; Wang, Zhi-Peng; He, Yun
Bench-stable imine surrogates for the one-pot and catalytic asymmetric synthesis of α-amino esters/ketones.
Chemical communications (Cambridge, England), 2020, 56, 14243-14246
7127412 CIFC28 H16 N2 S2P 1 21 13.9035; 44.025; 6.0394
90; 95.692; 90		1032.8Deng, Jian; Wan, Yuejuan; Cai, Chang; Gu, Cheng; Ma, Yuguang
Organic single crystals of cyano-substituted <i>p</i>-phenylene vinylene derivatives as transistors with low surface trap density.
Chemical communications (Cambridge, England), 2020, 56, 13776-13779
7127413 CIFC10 H6 N SP -13.938; 5.87; 18.06
80.84; 87.25; 86.08		410.9Deng, Jian; Wan, Yuejuan; Cai, Chang; Gu, Cheng; Ma, Yuguang
Organic single crystals of cyano-substituted <i>p</i>-phenylene vinylene derivatives as transistors with low surface trap density.
Chemical communications (Cambridge, England), 2020, 56, 13776-13779
7127414 CIFC23 H20 Br N3 O4 SC 1 2 118.6217; 9.3855; 14.7978
90; 101.185; 90		2537.1Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127415 CIFC22 H25 N3 O6 SP 1 21 111.6772; 6.3645; 15.4108
90; 93.913; 90		1142.65Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127416 CIFC22 H25 N3 O6 SP 1 21 111.6772; 6.3645; 15.4108
90; 93.913; 90		1142.65Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127417 CIFC23 H20 Br N3 O4 SC 1 2 118.6217; 9.3855; 14.7978
90; 101.185; 90		2537.1Liu, Hui; Yan, Yingkun; Zhang, Jiayan; Liu, Min; Cheng, Shaobing; Wang, Zhouyu; Zhang, Xiaomei
Enantioselective dearomative [3+2] annulation of 5-amino-isoxazoles with quinone monoimines.
Chemical communications (Cambridge, England), 2020, 56, 13591-13594
7127418 CIFC18 H13 N5P n a 2118.6944; 5.0904; 15.1667
90; 90; 90		1443.29Zhang, Chunyan; Liang, Zuyu; Jia, Xiaofei; Wang, Maorong; Zhang, Guoying; Hu, Mao-Lin
A practical base mediated synthesis of 1,2,4-triazoles enabled by a deamination annulation strategy.
Chemical communications (Cambridge, England), 2020, 56, 14215-14218
7127419 CIFC6 H18 Br7 Cs N2 Pb2P c a 218.2772; 8.0905; 35.589
90; 90; 90		2383.3Fu, Dongying; Wu, Shichao; Xin, Jianli; Zhang, Xinyuan; Han, Gaoyi; Zhang, Xian-Ming
Polar CsPbBr<sub>3</sub>-based Dion-Jacobson hybrid for promising UV photodetection.
Chemical communications (Cambridge, England), 2020, 56, 14381-14384
7127420 CIFC75 H49 Gd3 N8 O37P -114.3007; 17.1091; 18.9641
88.689; 83.151; 70.462		4340.9Li, Pei-Xin; Xie, Zhi-Xin; Jin, Ai-Ping; Li, Jing; Guo, Guo-Cong
A new photochromic Gd-MOF with photoswitchable bluish-white to greenish-yellow emission based on electron transfer.
Chemical communications (Cambridge, England), 2020, 56, 14689-14692
7127421 CIFC18 H16 N2 O6P 1 21/n 18.0723; 17.6758; 11.6674
90; 93.046; 90		1662.4Li, Pei-Xin; Xie, Zhi-Xin; Jin, Ai-Ping; Li, Jing; Guo, Guo-Cong
A new photochromic Gd-MOF with photoswitchable bluish-white to greenish-yellow emission based on electron transfer.
Chemical communications (Cambridge, England), 2020, 56, 14689-14692
7127422 CIFC25 H42 Cl2 Ge N2 P2 PdP 1 21/c 111.496; 18.413; 14.671
90; 106.665; 90		2975.06Cabeza, Javier A.; García-Álvarez, Pablo; Laglera-Gándara, Carlos J; Pérez-Carreño, Enrique
A Z-type PGeP pincer germylene ligand in a T-shaped palladium(0) complex.
Chemical communications (Cambridge, England), 2020, 56, 14095-14097
7127423 CIFC37 H52 Ge N2 P2 Pd S2P 1 21/n 117.5001; 12.1142; 18.945
90; 114.67; 90		3649.75Cabeza, Javier A.; García-Álvarez, Pablo; Laglera-Gándara, Carlos J; Pérez-Carreño, Enrique
A Z-type PGeP pincer germylene ligand in a T-shaped palladium(0) complex.
Chemical communications (Cambridge, England), 2020, 56, 14095-14097
7127424 CIFC41.5 H37 Cl15 K N O6P -111.603; 13.398; 19.749
90.788; 105.517; 113.557		2686.3Mayorga-Burrezo, Paula; Sporer, Christian; de Sousa, J. Alejandro; Capra, Nicola; Wurst, Klaus; Crivillers, Núria; Veciana, Jaume; Rovira, Concepció
Electrocatalytic oxidative Z/E isomerization of a stilbene favoured by the presence of an electroactive persistent radical.
Chemical communications (Cambridge, England), 2020, 56, 14211-14214
7127425 CIFC32 H20 F2 N OP -19.0495; 11.3463; 13.2051
84.652; 76.728; 75.775		1278.2Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127426 CIFC27 H21 Cl N2 O3P 1 21/n 113.51; 9.6529; 17.2677
90; 95.515; 90		2241.5Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127427 CIFC32 H23 N2 OP 1 21/n 110.6041; 18.1154; 13.0961
90; 104.601; 90		2434.5Gao, Yuan; Zhang, Mengfan; Wang, Chaoyu; Yang, Zhen; Huang, Xianqiang; Feng, Ruokun; Qi, Chenze
Cobalt(ii)-catalyzed hydroarylation of 1,3-diynes and internal alkynes with picolinamides promoted by alcohol.
Chemical communications (Cambridge, England), 2020, 56, 14231-14234
7127428 CIFC31 H26 N2 O5 SP -19.9502; 11.9913; 14.0968
113.915; 96.434; 93.254		1518.19Fang, Qing-Yun; Zhao, Li-Ming
A [4+3] annulation of benzofuran-derived azadienes and α-bromohydroxamates for the synthesis of benzofuran-fused 1,4-diazepinones.
Chemical communications (Cambridge, England), 2020, 56, 14079-14082
7127429 CIFC22 H36 Cl2 Co2 N10 O8P 6520.399; 20.399; 14.7613
90; 90; 120		5319.5Dolui, Dependu; Mir, Ab Qayoom; Dutta, Arnab
Probing the peripheral role of amines in photo- and electrocatalytic H<sub>2</sub> production by molecular cobalt complexes.
Chemical communications (Cambridge, England), 2020, 56, 14841-14844
7127430 CIFC36 H30 Li2 N5 O13C 1 2/c 123.699; 16.6746; 10.1581
90; 101.153; 90		3938.4Nath, Karabi; Bin Rahaman, Abdulla; Moi, Rajib; Maity, Kartik; Biradha, Kumar
Porous Li-MOF as a solid-state electrolyte: exploration of lithium ion conductivity through bio-inspired ionic channels.
Chemical communications (Cambridge, England), 2020, 56, 14873-14876
7127431 CIFC34 H38 Li2 N2 O12C 1 2/c 121.9; 16.99; 9.436
90; 109.177; 90		3316Nath, Karabi; Bin Rahaman, Abdulla; Moi, Rajib; Maity, Kartik; Biradha, Kumar
Porous Li-MOF as a solid-state electrolyte: exploration of lithium ion conductivity through bio-inspired ionic channels.
Chemical communications (Cambridge, England), 2020, 56, 14873-14876
7127434 CIFC53 H47 B Ir N3 O0.25P 1 21/c 122.2922; 13.8681; 14.6786
90; 107.043; 90		4338.6Pham, Pierce; Hilty, Christian
Tunable iridium catalyst designs with bidentate N-heterocyclic carbene ligands for SABRE hyperpolarization of sterically hindered substrates.
Chemical communications (Cambridge, England), 2020, 56, 15466-15469
7127451 CIFAl12 O67.44 P12P 21 21 215.0698; 17.9944; 5.03671
90; 90; 90		1365.81Komura, Kenichi; Aoki, Hisakazu; Tanaka, Kentaro; Ikeda, Takuji
GAM-3: a zeolite formed from AlPO<sub>4</sub>-5 <i>via</i> multistep structural changes.
Chemical communications (Cambridge, England), 2020, 56, 14901-14904
7127452 CIFC4 H9 Al3 N O12.75 P3P 21 21 216.7631; 17.4946; 4.97975
90; 90; 90		1460.38Komura, Kenichi; Aoki, Hisakazu; Tanaka, Kentaro; Ikeda, Takuji
GAM-3: a zeolite formed from AlPO<sub>4</sub>-5 <i>via</i> multistep structural changes.
Chemical communications (Cambridge, England), 2020, 56, 14901-14904
7127455 CIFC19 H14 N2 O3P -17.5891; 10.1094; 20.3877
95.642; 97.677; 104.552		1486.17Marques, Carolina S.; Cruz, Hugo; Lawrence, Simon E.; Gago, Sandra; Prates Ramalho, João P; Morgado, Jorge; Branco, Luís C; Burke, Anthony J.
Ambipolar pentacyclic diamides with interesting electrochemical and optoelectronic properties.
Chemical communications (Cambridge, England), 2020, 56, 14893-14896
7127456 CIFC30 H35 B O3 SeP -110.574; 10.8402; 12.7623
70.58; 82.1; 86.46		1366.3Mizoguchi, Haruki; Seriu, Masaya; Sakakura, Akira
Synthesis of functionalized cyclopropylboronic esters based on a 1,2-metallate rearrangement of cyclopropenylboronate.
Chemical communications (Cambridge, England), 2020, 56, 15545-15548
7127461 CIFC80 H86 N4 O4 Pt2P 1 21 121.7528; 51.3282; 22.4375
90; 113.392; 90		22993.2Inoue, Ryo; Kondo, Riki; Morisaki, Yasuhiro
Experimental and theoretical studies on circularly polarized phosphorescence of a [2.2]paracyclophane-based platinum(ii) complex.
Chemical communications (Cambridge, England), 2020, 56, 15438-15441
7127462 CIFC33 H37 N O5P 1 21 110.2748; 14.2248; 10.9525
90; 115.5; 90		1444.84Xiang, Min; Li, Chen-Yi; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
Organocatalytic and enantioselective [4+2] cyclization between hydroxymaleimides and <i>ortho</i>-hydroxyphenyl <i>para</i>-quinone methide-selective preparation of chiral hemiketals.
Chemical communications (Cambridge, England), 2020, 56, 14825-14828
7127463 CIFC34 H38 Cl3 N O5P -110.538; 12.9179; 13.0658
98.879; 105.364; 95.484		1677Xiang, Min; Li, Chen-Yi; Song, Xiang-Jia; Zou, Ying; Huang, Zhi-Cheng; Li, Xia; Tian, Fang; Wang, Li-Xin
Organocatalytic and enantioselective [4+2] cyclization between hydroxymaleimides and <i>ortho</i>-hydroxyphenyl <i>para</i>-quinone methide-selective preparation of chiral hemiketals.
Chemical communications (Cambridge, England), 2020, 56, 14825-14828
7127464 CIFC16 H11 N O2P -16.0435; 7.958; 13.3572
75.36; 83.114; 77.584		605.55Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127465 CIFC17 H13 N O2P 1 21/c 115.5206; 10.7027; 7.9095
90; 90.741; 90		1313.76Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127466 CIFC15 H11 N O3 SP c a 2116.21; 5.463; 30.5412
90; 90; 90		2704.6Wang, Ali; Xie, Xin; Zhang, Chunli; Liu, Yuanhong
Gold/Lewis acid catalyzed oxidative cyclization involving activation of nitriles.
Chemical communications (Cambridge, England), 2020, 56, 15581-15584
7127467 CIFC24 H132 Cs7.5 Dy4 K0.5 O180 P8 W32P -112.757; 14.616; 24.915
73.84; 86.54; 79.7		4389.8Wang, Wenyan; Izarova, Natalya V.; van Leusen, Jan; Kögerler, Paul
Polyoxometalates with separate lacuna sites.
Chemical communications (Cambridge, England), 2020, 56, 14857-14860
7127468 CIFC24 H128 Cs7.5 K0.5 O178 P8 W32 Y4P -112.902; 14.649; 24.956
73.56; 86.69; 79.61		4449.6Wang, Wenyan; Izarova, Natalya V.; van Leusen, Jan; Kögerler, Paul
Polyoxometalates with separate lacuna sites.
Chemical communications (Cambridge, England), 2020, 56, 14857-14860
7127469 CIFC30 H51 Al N3 Ni P3P 1 21/n 111.29; 17.502; 16.876
90; 96.935; 90		3310Lai, Qingheng; Cosio, Mario N.; Ozerov, Oleg V.
Ni complexes of an alane/tris(phosphine) ligand built around a strongly Lewis acidic tris(<i>N</i>-pyrrolyl)aluminum.
Chemical communications (Cambridge, England), 2020, 56, 14845-14848
7127470 CIFC24 H21 B F2 N2 O2 SP 21 21 218.7927; 13.0246; 19.6787
90; 90; 90		2253.63Lv, Fan; Guo, Xing; Wu, Hao; Li, Heng; Tang, Bing; Yu, Changjiang; Hao, Erhong; Jiao, Lijuan
Direct sulfonylation of BODIPY dyes with sodium sulfinates through oxidative radical hydrogen substitution at the α-position.
Chemical communications (Cambridge, England), 2020, 56, 15577-15580
7127472 CIFC17 H19 N O3P 1 21/n 110.7764; 8.4814; 15.9946
90; 97.431; 90		1449.61Mayakrishnan, Sivakalai; Tamizmani, Masilamani; Maheswari, Naryanan Uma
Harnessing hypervalent iodonium ylides as carbene precursors: C-H activation of N-methoxybenzamides with a Rh(iii)-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 15462-15465
7127473 CIFC31 H27 N O4P -19.9039; 11.0962; 11.7769
87.0152; 68.9253; 88.648		1206.01Mayakrishnan, Sivakalai; Tamizmani, Masilamani; Maheswari, Naryanan Uma
Harnessing hypervalent iodonium ylides as carbene precursors: C-H activation of N-methoxybenzamides with a Rh(iii)-catalyst.
Chemical communications (Cambridge, England), 2020, 56, 15462-15465
7127475 CIFC88.19 H116.39 La Na3 O13.05P 21 21 228.4265; 27.2114; 10.4341
90; 90; 90		8071Deng, Min; Schley, Nathan D.; Ung, Gaël
High circularly polarized luminescence brightness from analogues of Shibasaki's lanthanide complexes.
Chemical communications (Cambridge, England), 2020, 56, 14813-14816
7127476 CIFC80 H120 K La N4 O6 P4P -114.168; 18.79; 19.86
105.16; 97.23; 104.28		4842Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127477 CIFC130 H192 K2 La2 N4 O14 P4P -113.3178; 25.2864; 25.5213
116.117; 98.326; 99.911		7361.7Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127478 CIFC71 H109 K La N4 O6 P3P -112.75; 15.9812; 21.2031
105.285; 94.133; 109.532		3866.2Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127479 CIFC134 H204 K2 La2 N4 O13 P6P -114.0506; 14.3744; 18.1614
99.417; 90.617; 91.294		3617.3Watt, Fabian A.; McCabe, Karl N.; Schoch, Roland; Maron, Laurent; Hohloch, Stephan
A transient lanthanum phosphinidene complex.
Chemical communications (Cambridge, England), 2020, 56, 15410-15413
7127480 CIFC112 H72.53 Cd3 Cl1.47 N24 O0.53C m c e47.491; 18.5114; 27.2738
90; 90; 90		23977Huang, Qing; Niu, Qian; Ma, Na-Na; Dong, Long-Zhang; Li, Shun-Li; Li, Dong-Sheng; Cai, Yue-Peng; Lan, Ya-Qian
Axial Cl/Br atom-mediated CO<sub>2</sub> electroreduction performance in a stable porphyrin-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 14817-14820
7127481 CIFC112 H74.8 Br1.2 Cd3 N24 O0.8C m c e47.7736; 18.5513; 27.2877
90; 90; 90		24184.1Huang, Qing; Niu, Qian; Ma, Na-Na; Dong, Long-Zhang; Li, Shun-Li; Li, Dong-Sheng; Cai, Yue-Peng; Lan, Ya-Qian
Axial Cl/Br atom-mediated CO<sub>2</sub> electroreduction performance in a stable porphyrin-based metal-organic framework.
Chemical communications (Cambridge, England), 2020, 56, 14817-14820
7127482 CIFC17 H18 F6 N3 PP 1 21/c 16.352; 8.2274; 33.0348
90; 91.298; 90		1725.97OwYong, Tze Cin; Ding, Siyang; Wu, Na; Fellowes, Thomas; Chen, Sijie; White, Jonathan M.; Wong, Wallace W. H.; Hong, Yuning
Optimising molecular rotors to AIE fluorophores for mitochondria uptake and retention.
Chemical communications (Cambridge, England), 2020, 56, 14853-14856
7127483 CIFC23 H22 F6 N3 PC 1 2/c 130.1428; 6.1951; 23.4009
90; 93.329; 90		4362.46OwYong, Tze Cin; Ding, Siyang; Wu, Na; Fellowes, Thomas; Chen, Sijie; White, Jonathan M.; Wong, Wallace W. H.; Hong, Yuning
Optimising molecular rotors to AIE fluorophores for mitochondria uptake and retention.
Chemical communications (Cambridge, England), 2020, 56, 14853-14856
7127484 CIFC70 H56P 1 21/n 18.80384; 9.18711; 30.3074
90; 96.5951; 90		2435.1Kitamura, Kei; Kudo, Ryoji; Sugiyama, Haruki; Uekusa, Hidehiro; Hamura, Toshiyuki
Isoacenofuran: a novel quinoidal building block for efficient access to high-ordered polyacene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 14988-14991
7127485 CIFC25 H16 O2P 1 21/c 18.30435; 23.1463; 9.755
90; 108.672; 90		1776.37Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127486 CIFC53 H34 B F4 N OP 1 21/n 116.353; 13.2053; 20.2472
90; 100.35; 90		4301.2Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127487 CIFC53.5 H34 B0.5 Cl F2 O2P 42/n :219.1081; 19.1081; 24.3996
90; 90; 90		8908.8Chen, Xingyu; Yan, Lipeng; Liu, Yanhong; Yang, Yudong; You, Jingsong
Switchable cascade C-H annulation to polycyclic pyryliums and pyridiniums: discovering mitochondria-targeting fluorescent probes.
Chemical communications (Cambridge, England), 2020, 56, 15080-15083
7127488 CIFC23 H18 Cl N3 OP b c a18.3148; 7.58; 27.7096
90; 90; 90		3846.82Cui, Yixin; Bai, Dachang; Liu, Bingxian; Chang, Junbiao; Li, Xingwei
Rh(iii)-Catalyzed acylation of heteroarenes with cyclobutenones via C-H/C-C bond activation.
Chemical communications (Cambridge, England), 2020, 56, 15631-15634
7127489 CIFC34 H64 Si6C 1 2/c 113.861; 13.3307; 20.858
90; 98.406; 90		3812.7Ishida, Shintaro; Sugawara, Shohei; Honda, Shunya; Iwamoto, Takeaki
Naphtho- and anthra-disilacyclobutadienes.
Chemical communications (Cambridge, England), 2020, 56, 15072-15075
7127490 CIFC45 H74 Si6P -112.95; 13.4087; 14.2041
92.261; 101.164; 100.116		2375.2Ishida, Shintaro; Sugawara, Shohei; Honda, Shunya; Iwamoto, Takeaki
Naphtho- and anthra-disilacyclobutadienes.
Chemical communications (Cambridge, England), 2020, 56, 15072-15075
7127494 CIFCl Mn7 Rb6 Se44 Yb23R -3 m :H19.844; 19.844; 19.496
90; 90; 120		6649Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127495 CIFCl Er23 Mn7 Rb6 Se44R -3 m :H19.948; 19.948; 19.5948
90; 90; 120		6752.6Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127496 CIFCl Ho23 Mn7 Rb6 Se44R -3 m :H20.0423; 20.0423; 19.6668
90; 90; 120		6841.6Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127497 CIFCl Mn7 Rb6 Se44 Tm23R -3 m :H19.9137; 19.9137; 19.547
90; 90; 120		6713Chen, Hong; Liu, Peng-Fei; Lin, Hua; Wu, Xin-Tao
A new type of novel salt-inclusion chalcogenide with ultralow thermal conductivity.
Chemical communications (Cambridge, England), 2020, 56, 15149-15152
7127498 CIFC38 H35 N O5P -110.5434; 12.209; 12.9764
89.428; 77.02; 75.639		1574.99Kumar, Krishna; Singh, Bhuvnesh; Singh, Ravi P.
A silver-catalyzed stereoselective domino cycloisomerization-vinylogous aldol reaction of <i>ortho</i>-alkynylbenzaldehydes with 3-alkylidene oxindoles: an entry to functionalized isochromenes.
Chemical communications (Cambridge, England), 2020, 56, 15153-15156
7127499 CIFC37 H33 N O4P 1 21/n 115.1432; 12.4911; 16.2178
90; 104.238; 90		2973.4Kumar, Krishna; Singh, Bhuvnesh; Singh, Ravi P.
A silver-catalyzed stereoselective domino cycloisomerization-vinylogous aldol reaction of <i>ortho</i>-alkynylbenzaldehydes with 3-alkylidene oxindoles: an entry to functionalized isochromenes.
Chemical communications (Cambridge, England), 2020, 56, 15153-15156
7127500 CIFC36 H56 Bi N P2 PtP 1 21/c 118.0184; 12.0638; 19.2753
90; 115.96; 90		3767.1Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127501 CIFC30 H51 Bi Cl N P2 PtP 1 21/n 112.278; 14.7178; 18.1372
90; 91.378; 90		3276.5Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127502 CIFC31 H53 Bi Cl3 N P2 PtP 1 21/c 112.8505; 13.1916; 21.3892
90; 94.966; 90		3612.3Shimada, Shigeru; Wang, Xiang-Bo; Tanaka, Masato
Oxidative addition of Bi-C bonds to Pt(0): reaction of Pt(PEt<sub>3</sub>)<sub>3</sub> with cyclic organobismuth compounds.
Chemical communications (Cambridge, England), 2020, 56, 15216-15219
7127504 CIFC38 H16 F12 I6P -15.9321; 11.9878; 14.8586
73.9545; 80.1893; 84.8797		999.63Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127505 CIFC34 H8 F16 I4 N4P -16.0619; 11.9613; 12.6449
88.7995; 79.8911; 88.7903		902.3Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127506 CIFC38 H16 F12 I6P -15.9617; 12.0425; 14.9758
73.9375; 80.8173; 85.0271		1018.93Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127507 CIFC54 H24 F16 I4 N4P -16.0053; 11.9473; 18.8788
71.556; 89.199; 83.434		1276.14Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127508 CIFC22 H8 F8 I4P -15.9541; 9.6644; 11.8639
67.331; 85.205; 80.816		621.68Vainauskas, Jogirdas; Topić, Filip; Bushuyev, Oleksandr S.; Barrett, Christoper J.; Friščić, Tomislav
Halogen bonding to the azulene π-system: cocrystal design of pleochroism.
Chemical communications (Cambridge, England), 2020, 56, 15145-15148
7127509 CIFC30 H36 Co N1.5 O1.5 Se1.5P -116.0226; 17.1096; 23.7566
93.645; 98.841; 94.484		6396.6Sarkar, Prasenjit; Konch, Tukhar Jyoti; Kamilya, Tapas; Raidongia, Kalyan; Acharya, Somobrata; Mukherjee, Chandan
The range of antiferromagnetic coupling governs the conductivity: semiconducting behavior and ammonia gas sensing property of diamagnetic hexaradical-containing tetranuclear Co<sup>III</sup><sub>4</sub> cluster and its nonradical congener.
Chemical communications (Cambridge, England), 2020, 56, 15220-15223
7127510 CIFC126 H150 Co4 N6 O6 Se6P -117.1932; 19.1994; 21.9119
98.522; 101.989; 110.296		6442Sarkar, Prasenjit; Konch, Tukhar Jyoti; Kamilya, Tapas; Raidongia, Kalyan; Acharya, Somobrata; Mukherjee, Chandan
The range of antiferromagnetic coupling governs the conductivity: semiconducting behavior and ammonia gas sensing property of diamagnetic hexaradical-containing tetranuclear Co<sup>III</sup><sub>4</sub> cluster and its nonradical congener.
Chemical communications (Cambridge, England), 2020, 56, 15220-15223
7127511 CIFC58 H38 O4P -111.14; 13.27; 16.669
98.91; 90.453; 99.668		2398.4Chang, Hao; Liu, Haoliang; Dmitrieva, Evgenia; Chen, Qiang; Ma, Ji; He, Piao; Liu, Pengcai; Popov, Alexey A.; Cao, Xiao-Yu; Wang, Xiao-Ye; Zou, Yingping; Narita, Akimitsu; Müllen, Klaus; Peng, Hongjian; Hu, Yunbin
Furan-containing double tetraoxa[7]helicene and its radical cation.
Chemical communications (Cambridge, England), 2020, 56, 15181-15184
7127515 CIFC47 H48 O6P -18.5959; 18.7821; 27.0537
108.997; 95.076; 94.172		4089.7Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127516 CIFC41 H36 O6P -18.662; 11.8573; 17.3792
96.695; 99.325; 108.28		1645.59Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127517 CIFC19 H18 O3P 1 21/n 19.1429; 10.3536; 16.2762
90; 105.372; 90		1485.6Yao, Liangliang; Fang, Bo; Hu, Qiong; Lei, Yu; Bao, Li; Hu, Yimin
Phenanthrenes/dihydrophenanthrenes: the selectivity controlled by different benzynes and allenes.
Chemical communications (Cambridge, England), 2020, 56, 15185-15188
7127520 CIFC60 H57 Cu4 Mo12 N16 O50 P3C 1 2/m 124.841; 18.316; 10.897
90; 105.586; 90		4776Li, Shaobin; Tan, Xiaoguo; Yue, Ming; Zhang, Li; Chai, Dongfeng; Wang, Wendi; Pan, Hong; Fan, Linlin; Zhao, Chunyan
A polyoxometalate-encapsulated nanocage cluster organic framework built from {Cu<sub>4</sub>P<sub>2</sub>} units and its efficient bifunctional electrochemical performance.
Chemical communications (Cambridge, England), 2020, 56, 15177-15180
7127535 CIFC59 H48 Cl2 N2 O6 S2P 1 21/n 18.3459; 31.8448; 18.0413
90; 92.018; 90		4791.9De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127536 CIFC29 H21 N O3 SC 1 2/c 117.1953; 11.2998; 23.4679
90; 99.631; 90		4495.63De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127537 CIFC29 H21 N O2 SP -18.5406; 10.0271; 13.9349
89.172; 79.068; 66.547		1072.43De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127538 CIFC30 H23 N O4 SP 1 21/c 112.6739; 16.317; 12.1213
90; 109.725; 90		2359.6De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127539 CIFC64 H58 N2 O10 S2P -18.748; 14.05; 22.585
97.243; 100.218; 97.968		2673De, Sukanya; Jash, Moumita; Chowdhury, Chinmay
Palladium(ii) catalysed cascade strategy for the synthesis of dibenzo[5,6:7,8]cycloocta[1,2-b]indol-10-ols/-10(15H)-ones: easy access to 1,3,5,7-cyclooctatetraenes (COTs).
Chemical communications (Cambridge, England), 2020, 56, 15659-15662
7127590 CIFC17 H17 B Cl F N2 O2P 1 21/c 18.4212; 14.1413; 13.5406
90; 101.611; 90		1579.5Ohtani, Shunsuke; Takeda, Yusuke; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki
Facile strategy for obtaining luminescent polymorphs based on the chirality of a boron-fused azomethine complex.
Chemical communications (Cambridge, England), 2020, 56, 15305-15308
7127591 CIFC17 H17 B Cl F N2 O2P 3212.8397; 12.8397; 8.5551
90; 90; 120		1221.4Ohtani, Shunsuke; Takeda, Yusuke; Gon, Masayuki; Tanaka, Kazuo; Chujo, Yoshiki
Facile strategy for obtaining luminescent polymorphs based on the chirality of a boron-fused azomethine complex.
Chemical communications (Cambridge, England), 2020, 56, 15305-15308
7127599 CIFC33 H24P -16.9996; 10.3778; 17.063
91.762; 99.022; 105.266		1177.6Wu, Li-Jun; Yang, Liang-Feng; Lv, Gui-Fen; Li, Jin-Heng
Divergent functionalization of terminal alkynes enabled alkynylative [5+1] benzannulation of 3-acetoxy-1,4-enynes.
Chemical communications (Cambridge, England), 2020, 56, 15329-15332
7127600 CIFC90.88 H116.1 Cl0.6 Ir0.6 Mn3 N12 O20.02P 1 21/m 112.364; 33.5; 12.912
90; 97.29; 90		5305Perlata, Ricardo A.; Huxley, Michael T.; Shi, Zhaolin; Zhang, Yue-Biao; Sumby, Christopher J.; Doonan, Christian J.
A metal-organic framework supported iridium catalyst for the gas phase hydrogenation of ethylene.
Chemical communications (Cambridge, England), 2020, 56, 15313-15316
7127601 CIFC22 H17 N O SeP 21 21 215.5032; 14.7847; 21.373
90; 90; 90		1739Liu, Xiang; Wang, Yajun; Song, Dan; Wang, Yuhan; Cao, Hua
Electrochemical regioselective selenylation/oxidation of N-alkylisoquinolinium salts via double C(sp<sup>2</sup>)-H bond functionalization.
Chemical communications (Cambridge, England), 2020, 56, 15325-15328
7127602 CIFB3 F2 O4 RbP 1 21/c 14.698; 17.77; 7.328
90; 118.95; 90		535.3Lu, Zixiu; Zhang, Fangfang; Tudi, Abudukadi; Yang, Zhihua; Pan, Shilie
RbB<sub>3</sub>O<sub>4</sub>F<sub>2</sub>: a rubidium fluorooxoborate with an unprecedented [B<sub>3</sub>O<sub>5</sub>F<sub>2</sub>]<sup>3-</sup> functionalized unit and a large birefringence.
Chemical communications (Cambridge, England), 2020, 56, 15333-15336
7127604 CIFC34 H20 SP 1 21/c 110.7856; 24.1392; 9.3144
90; 94.959; 90		2416Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127605 CIFC36 H26 O2P -110.417; 11.3442; 12.577
108.867; 105.293; 99.814		1302.26Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127606 CIFC30 H18 S2P 1 21/c 111.7855; 9.5702; 19.7443
90; 96.996; 90		2210.4Manikandan, Palani; Karunakaran, Jayachandran; Varathan, Elumalai; Schreckenbach, Georg; Mohanakrishnan, Arasambattu K.
Diels-Alder reaction of tetraarylcyclopentadienones with benzo[b]thiophene S,S-dioxides: an unprecedented de-oxygenation vs. sulfur dioxide extrusion.
Chemical communications (Cambridge, England), 2020, 56, 15317-15320
7127647 CIFC20 H20 Br N O2P -19.6343; 19.0413; 19.4763
83.018; 89.376; 82.19		3513.47Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127648 CIFC27 H19 Br Cl3 N O2P 1 21/m 112.6799; 6.6733; 15.0742
90; 109.16; 90		1204.87Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127649 CIFC25 H28 N2 O3P n a 2110.1266; 21.0008; 10.2483
90; 90; 90		2179.47Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127650 CIFC22 H16 Br N O SP 1 21/m 18.5848; 6.8902; 15.8079
90; 98.98; 90		923.59Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127651 CIFC22 H16 Br N O SeP c c n30.762; 10.8014; 11.0953
90; 90; 90		3686.7Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127652 CIFC23 H18 Br Cl2 N O2P -18.7249; 9.7643; 13.4767
90.141; 106.286; 112.456		1010.68Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127653 CIFC31 H40 N2 O4P c c n20.58; 24.0995; 11.4414
90; 90; 90		5674.6Göbel, Dominik; Rusch, Pascal; Duvinage, Daniel; Bigall, Nadja C.; Nachtsheim, Boris J.
Emission color-tunable oxazol(in)yl-substituted excited-state intramolecular proton transfer (ESIPT)-based luminophores.
Chemical communications (Cambridge, England), 2020, 56, 15430-15433
7127688 CIFC22 H36 N4 O6 S2P 1 21/n 19.7754; 12.5427; 22.3714
90; 96.082; 90		2727.52Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127689 CIFC16 H0 N11 O6 S2P 1 21/n 19.6616; 12.3127; 22.5851
90; 97.458; 90		2664Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127690 CIFC22 H44 N4 O10 S2P 1 21/c 111.2723; 18.109; 14.821
90; 110.51; 90		2833.6Wang, Yijie; Zhang, Minghui; Yang, Qianqian; Yin, Jianbo; Liu, Di; Shang, Yanxue; Kang, Zixi; Wang, Rongming; Sun, Daofeng; Jiang, Jianzhuang
Single-crystal-to-single-crystal transformation and proton conductivity of three hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2020, 56, 15529-15532
7127718 CIFC24 H28 Cl O PP 1 21/c 111.7689; 15.1355; 13.096
90; 111.37; 90		2172.38Niu, Yuan; Qi, Zhichao; Lou, Qinxin; Bai, Pengbo; Yang, Shangdong
Copper-catalyzed arylation of polycyclic aromatic hydrocarbons by the P[double bond, length as m-dash]O group.
Chemical communications (Cambridge, England), 2020, 56, 14721-14724
7127719 CIFC6 H16 Cl2 N12 OC m c 2116.7812; 12.2467; 6.9816
90; 90; 90		1434.82Liu, Lehui; Hu, Chun-Li; Bai, Zhiyong; Yuan, Feifei; Huang, Yisheng; Zhang, Lizhen; Lin, Zhoubin
2(C<sub>3</sub>H<sub>7</sub>N<sub>6</sub>)<sup>+</sup>·2Cl<sup>-</sup>·H<sub>2</sub>O: an ultraviolet nonlinear optical crystal with large birefrigence and strong second-harmonic generation.
Chemical communications (Cambridge, England), 2020, 56, 14657-14660
7127720 CIFC23 H18 Au O P S3P -112.027; 12.23; 33.79
83.652; 86.895; 62.035		4362.9Roesch, Saskia; Fermi, Valentina; Rominger, Frank; Herold-Mende, Christel; Romero-Nieto, Carlos
Gold(i) complexes based on six-membered phosphorus heterocycles as bio-active molecules against brain cancer.
Chemical communications (Cambridge, England), 2020, 56, 14593-14596
7127721 CIFC21 H13 Au N P S2P 1 21/c 112.7527; 18.7996; 16.53
90; 108.271; 90		3763.2Roesch, Saskia; Fermi, Valentina; Rominger, Frank; Herold-Mende, Christel; Romero-Nieto, Carlos
Gold(i) complexes based on six-membered phosphorus heterocycles as bio-active molecules against brain cancer.
Chemical communications (Cambridge, England), 2020, 56, 14593-14596
7127722 CIFC122 H118 Ag3 B2 N13 O7 P6 W2P 1 21/n 115.377; 30.6356; 28.8107
90; 98.31; 90		13429.7Manzano, Richard A.; Hill, Anthony F.; Georgelin, Rosemary L.
Tetrel and pnictogen functionalised propargylidynes.
Chemical communications (Cambridge, England), 2020, 56, 14597-14600
7127723 CIFC33 H37 B2 Cl2 N6 O2 P WP 1 21/c 114.6458; 13.04801; 19.07
90; 102.382; 90		3559.48Manzano, Richard A.; Hill, Anthony F.; Georgelin, Rosemary L.
Tetrel and pnictogen functionalised propargylidynes.
Chemical communications (Cambridge, England), 2020, 56, 14597-14600
7127724 CIFC16 H21 N O5 SC 1 2/c 119.9401; 5.3894; 32.9348
90; 101.506; 90		3468.2Zhang, Chun; Huang, Jiapian; Ye, Shengqing; Tang, Jie; Wu, Jie
A metal-free reaction of sulfur dioxide, cyclopropanols and electron-deficient olefins.
Chemical communications (Cambridge, England), 2020, 56, 13852-13855
7127725 CIFC106 H146 O20 Ti4P 1 21/c 114.6214; 28.2561; 14.335
90; 93.955; 90		5908.3Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127726 CIFC104 H136 N4 O22 Ti4P -114.2318; 14.6532; 18.081
103.02; 102.821; 107.509		3328.9Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127727 CIFC136 H174 N6 O26 Ti6P 1 21/n 118.742; 15.6878; 24.515
90; 106.32; 90		6917.5Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127728 CIFC137 H169 O26 Ti6P 1 21/n 118.124; 15.607; 25.066
90; 105.645; 90		6827.5Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127729 CIFC128 H188 N8 O26 Ti4P -114.4277; 14.608; 17.6599
82.875; 72.447; 75.012		3423.7Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127730 CIFC144 H172 Br4 N8 O20 Ti4C 1 2/c 126.9642; 24.087; 23.819
90; 94.28; 90		15427Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127731 CIFC95 H150 O27.52 Ti6P -115.419; 19.356; 20.165
84.214; 70.821; 86.94		5654Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127732 CIFC128 H164 O30 Ti6P 1 21/n 117.654; 15.3326; 24.8024
90; 105.996; 90		6453.6Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127733 CIFC151 H225 O34 Ti6P 1 21/n 121.3911; 25.7936; 33.0748
90; 99.423; 90		18002.9Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127734 CIFC130 H164 Br12 O46 Ti10P -114.966; 15.4941; 20.8678
98.6889; 110.598; 100.033		4340.33Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127735 CIFC196 H158 F60 O46 Ti10P -117.6619; 18.0164; 21.2467
68.017; 69.349; 61.753		5393.7Yang, Xin-Xue; Yu, Wei-Dong; Yi, Xiao-Yi; Li, Lei-Jiao; Liu, Chao
Monocarboxylate-driven structural growth in Calix[n]arene-polyoxotitanate hybrid systems: utility in hydrogen production from water.
Chemical communications (Cambridge, England), 2020, 56, 14035-14038
7127736 CIFC91 H130 N6 Ni P8 Si2P 1 21/c 123.6231; 13.3113; 30.4842
90; 105.741; 90		9226.4Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127737 CIFC85 H118 N6 Ni P8 Si2P 1 21/c 117.4813; 22.9979; 22.0196
90; 97.889; 90		8768.8Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127738 CIFC56 H76 N4 Ni P4 SiP b c a17.4645; 15.4359; 42.649
90; 90; 90		11497.3Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127739 CIFC85 H116 N6 Ni2 P8 Si2P 1 21/c 123.3638; 16.0951; 27.7549
90; 107.229; 90		9968.7Ziegler, Christoph G. P.; Taube, Clemens; Kelly, John A.; Hierlmeier, Gabriele; Uttendorfer, Maria; Weigand, Jan J.; Wolf, Robert
An unusual Ni<sub>2</sub>Si<sub>2</sub>P<sub>8</sub> cluster formed by complexation and thermolysis.
Chemical communications (Cambridge, England), 2020, 56, 14071-14074
7127740 CIFC39.5 H49 Al Cl4 N2 O2P -19.1488; 17.223; 25.5541
74.736; 86.924; 89.597		3878.81Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127741 CIFC52 H63 Al Cl6 N2 O6P -113.562; 13.8874; 15.489
99.761; 94.142; 108.246		2705.8Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127742 CIFC135 H175 Al3 N6 O15C 2 2 2122.6444; 30.8757; 21.0423
90; 90; 90		14712Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127743 CIFC137 H179 Al3 N6 O15C 2 2 2122.7869; 30.5983; 21.2437
90; 90; 90		14812Popowski, Yanay; Moreno, Juan J.; Nichols, Asa W.; Hooe, Shelby L.; Bouchey, Caitlin J.; Rath, Nigam P.; Machan, Charles W.; Tolman, William B.
Mechanistic insight into initiation and regioselectivity in the copolymerization of epoxides and anhydrides by Al complexes.
Chemical communications (Cambridge, England), 2020, 56, 14027-14030
7127744 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5103; 4.2412; 19.5894
90; 90.446; 90		956.28Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127745 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5218; 4.2497; 19.6222
90; 90.458; 90		960.75Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127746 CIFC5 H6 Cu2 I2 N2P 1 21/n 111.5363; 4.2584; 19.6624
90; 90.49; 90		965.9Wu, Ting; Jiang, Shenlong; Samanta, Pabitra Narayan; Xie, Yangbin; Li, Jipeng; Wang, Xiaoling; Devashis, Majumdar; Gu, Xiangwei; Wang, Yusong; Huang, Wei; Zhang, Qun; Leszczynski, Jerzy; Wu, Dayu
Negative thermal quenching of photoluminescence in a copper-organic framework emitter.
Chemical communications (Cambridge, England), 2020, 56, 12057-12060
7127747 CIFC120 H100 Cu4 N8 O28P -119.294; 19.413; 23.421
72.2; 86.15; 65.93		7610Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127748 CIFC168 H124 Cu4 N12 O28P -116.005; 17.777; 20.441
104.91; 109.45; 104.86		4912Schneider, Matthew L.; Linder-Patton, Oliver M; Bloch, Witold M.
A covalent deprotection strategy for assembling supramolecular coordination polymers from metal-organic cages.
Chemical communications (Cambridge, England), 2020, 56, 12969-12972
7127749 CIFC18 H14 K2 N2 O11 S2P -15.6244; 6.1097; 15.9088
89.883; 81.215; 76.999		526.121Ke, Hua; Hu, Fen; Meng, Lingyi; Chen, Qi-Hua; Lai, Qian-Sheng; Li, Ze-Chen; Huang, Ze-Long; Liao, Jian-Zhen; Qiu, Jian-Ding; Lu, Can-Zhong
Ultrastable radical-doped coordination compounds with antimicrobial activity against antibiotic-resistant bacteria.
Chemical communications (Cambridge, England), 2020, 56, 14353-14356
7127750 CIFC18 H16 Ca N2 O12 S2P 1 21/n 18.8177; 28.7454; 8.9688
90; 108.766; 90		2152.46Ke, Hua; Hu, Fen; Meng, Lingyi; Chen, Qi-Hua; Lai, Qian-Sheng; Li, Ze-Chen; Huang, Ze-Long; Liao, Jian-Zhen; Qiu, Jian-Ding; Lu, Can-Zhong
Ultrastable radical-doped coordination compounds with antimicrobial activity against antibiotic-resistant bacteria.
Chemical communications (Cambridge, England), 2020, 56, 14353-14356
7127751 CIFC160 H184 B4 Cl4 N24 O8 Pt4 ZnP -112.1513; 17.9898; 19.21888
77.5748; 80.99; 89.3233		4051.17Rubbiani, Riccardo; Wu, Wenyu; Naik, Anu; Larocca, Michele; Schneider, Lukas; Padrutt, Roxane; Babu, Vipin; König, Christiane; Hinger, Doris; Maake, Caroline; Ferrari, Stefano; Gasser, Gilles; Spingler, Bernhard
Studying the cellular distribution of highly phototoxic platinated metalloporphyrins using isotope labelling.
Chemical communications (Cambridge, England), 2020, 56, 14373-14376
7127752 CIFC64 H92 F12 K2 N16 O16 P2P 1 21/n 114.5377; 16.9875; 31.4097
90; 92.689; 90		7748.4Xiao, Tangxin; Zhong, Weiwei; Yang, Weiwei; Qi, Lijie; Gao, Yan; Sue, Andrew C.-H.; Li, Zheng-Yi; Sun, Xiao-Qiang; Lin, Chen; Wang, Leyong
Reversible hydrogen-bonded polymerization regulated by allosteric metal templation.
Chemical communications (Cambridge, England), 2020, 56, 14385-14388
7127753 CIFC24 H19 ClP c a 2110.8825; 21.5798; 8.2395
90; 90; 90		1935Xue, Ze-Jian; Li, Meng-Yao; Zhu, Bin-Bin; He, Zhi-Tao; Feng, Chen-Guo; Lin, Guo-Qiang
Stereoselective synthesis of conjugated trienes <i>via</i> 1,4-palladium migration/Heck sequence.
Chemical communications (Cambridge, England), 2020, 56, 14420-14422
7127754 CIFC24 H38 F3 Fe N3 O6 SP -19.1103; 9.944; 15.5023
77.338; 89.422; 88.622		1369.8Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127755 CIFC27 H44 F3 Fe N5 O5 SP -110.8333; 12.2736; 13.012
79.726; 74.064; 81.746		1628.8Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127756 CIFC52 H88 Cl2 Fe2 N6 O10P 1 21/n 112.832; 15.977; 30.509
90; 98.773; 90		6182Sánchez-Eguía, Brenda N; Serrano-Plana, Joan; Company, Anna; Costas, Miquel
Catalytic O<sub>2</sub> activation with synthetic models of α-ketoglutarate dependent oxygenases.
Chemical communications (Cambridge, England), 2020, 56, 14369-14372
7127757 CIFC25.5 H17 F6 N5 O0.5 P PtP 1 21/c 16.8545; 39.3855; 17.3529
90; 98.991; 90		4627.2He, Lei; Meng, Zhenyu; Guo, Qianqian; Wu, Xiangyang; Teulade-Fichou, Marie-Paule; Yeow, Edwin Kok Lee; Shao, Fangwei
Fluorogenic Pt complexes distinguish the quantity and folding behavior of RNA G-quadruplexes between live cancerous and healthy cells.
Chemical communications (Cambridge, England), 2020, 56, 14459-14462
7127758 CIFC25 H25 B F2 O4P -17.813; 9.3837; 16.3462
101.355; 97.002; 104.391		1119.53Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127759 CIFC31 H26 O2P -19.6358; 10.2626; 12.5875
75.48; 73.81; 83.749		1156.19Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127760 CIFC31 H25 B F2 O2C 1 2/c 124.5441; 12.1699; 20.6663
90; 123.726; 90		5134.1Yan, Cai-Xin; Lin, Qian-Qian; Li, Sha; Wu, Cheng-Juan; Li, Yan-An; Fan, Jian-Zhong; Ma, Jian-Ping; Geng, Yan; Dong, Yu-Bin
Synthesis of fulvene-containing boron complexes with aggregation-induced emission and mechanochromic luminescence.
Chemical communications (Cambridge, England), 2020, 56, 14435-14438
7127761 CIFC316 H437 Ag51 Cl7 F12 P2 Pt2 S28 Sb2P -125.6867; 30.3229; 37.02
107.289; 99.777; 110.352		24582Liu, Ying; Wang, Shuxin; Kang, Xi; Yin, Bing; Jin, Shan; Chen, Shuang; Zhu, Manzhou
Heterogeneous metal alloy engineering: embryonic growth of M<sub>13</sub> icosahedra in Ag-based alloy superatomic nanoclusters.
Chemical communications (Cambridge, England), 2020, 56, 14203-14206
7127762 CIFC280 H406 Ag48 Au3 Cl7 F12 S28 Sb2C 1 2/c 141.694; 29.9362; 62.1774
90; 108.961; 90		73396.4Liu, Ying; Wang, Shuxin; Kang, Xi; Yin, Bing; Jin, Shan; Chen, Shuang; Zhu, Manzhou
Heterogeneous metal alloy engineering: embryonic growth of M<sub>13</sub> icosahedra in Ag-based alloy superatomic nanoclusters.
Chemical communications (Cambridge, England), 2020, 56, 14203-14206
7127763 CIFC52 H52 N4 Si2P -110.2134; 14.0734; 16.2616
100.776; 93.428; 109.092		2151.38Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127764 CIFC24 H22 N2 SiP -19.8911; 10.3035; 10.8066
82.034; 64.483; 87.683		984.09Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127765 CIFC52 H50 Cl2 Li2 N6 Si2P 18.9867; 11.6858; 12.4491
77.799; 74.843; 78.754		1219.77Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338
7127766 CIFC48.7 H45.4 Cl1.4 F12 Li2 N4 P2 Si2P 1 21/n 110.5712; 18.1992; 27.2894
90; 100.784; 90		5157.42Espinosa-Jalapa, Noel Angel; Berg, Nele; Seidl, Michael; Shenderovich, Ilya G.; Gschwind, Ruth M.; Bauer, Jonathan O.
Complexation behaviour of LiCl and LiPF<sub>6</sub>- model studies in the solid-state and in solution using a bidentate picolyl-based ligand.
Chemical communications (Cambridge, England), 2020, 56, 13335-13338

Blue left arrow Blue left arrow First | Blue left arrow Previous 1000 | of 2 | Next 1000 Right arrow | Last Right arrow Right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.