Crystallography Open Database

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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

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