Crystallography Open Database

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7118720 CIFC428 H413 N84 O92P -128.125; 30.271; 35.821
69.22; 80.81; 88.35		28134Chandramouli, Nagula; Ferrand, Yann; Kauffmann, Brice; Huc, Ivan
Citric acid encapsulation by a double helical foldamer in competitive solvents.
Chemical communications (Cambridge, England), 2016, 52, 3939-3942
7118721 CIFC35 H46 Cu F6 N4 PP 1 21/c 18.96; 24.2; 17.53
90; 104.8; 90		3675Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118722 CIFC33 H43 Cl Cu F6 N3 PP 1 21 18.6259; 11.8633; 16.6506
90; 100.785; 90		1673.8Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118723 CIFC34 H43 Cu F6 N3 O PP 1 21 18.8683; 12.1402; 16.1427
90; 100.426; 90		1709.3Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118724 CIFC39 H54 Cu F6 N4 O PP 112.4078; 13.287; 14.052
96.92; 105.67; 107.141		2080.5Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118725 CIFC42 H38 Cu F6 N6 PP 1 21/n 114.8812; 17.179; 15.5446
90; 95.597; 90		3954.9Cheung, Pui Man; Berger, Robert F.; Zakharov, Lev N.; Gilbertson, John D.
Square planar Cu(i) stabilized by a pyridinediimine ligand.
Chemical communications (Cambridge, England), 2016, 52, 4156-4159
7118726 CIFC22 N9 Na O5P 1 21/n 132.313; 19.769; 3.7343
90; 98.59; 90		2358.7Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118727 CIFC27 H32 N9 Na O5P b c n13.908; 20.33; 10.298
90; 90; 90		2912Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118728 CIFC22 H16 N10 O3.75C 1 2/c 139.9667; 3.761; 35.3988
90; 122.88; 90		4468.59Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118729 CIFC22.88 H19 N10 O0.87P 42/n21.6792; 21.6792; 9.235
90; 90; 90		4340.34Lee, Gil Ryeong; Ohtsu, Hiroyoshi; Koo, Jinyoung; Yakiyama, Yumi; Park, Moon Jeong; Inoue, Daishi; Hashizume, Daisuke; Kawano, Masaki
Crystallinity-dependence of ionic conductivity in the ion pairs of a multi-interactive anion.
Chemical communications (Cambridge, England), 2016, 52, 3962-3965
7118730 CIFC17 H22 I2 N2 O3P 21 21 219.1833; 10.6603; 20.8558
90; 90; 90		2041.7Huang, Hai; Tang, Luning; Han, Xiaobo; He, Guangke; Xi, Yang; Zhu, Hongjun
Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides.
Chemical communications (Cambridge, England), 2016, 52, 4321-4324
7118731 CIFC15 H13 N O3 S2P 1 21/n 114.7831; 5.6288; 18.2621
90; 98.364; 90		1503.4Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118732 CIFC15 H13 N O3 S2C 1 2/c 113.7384; 9.1063; 24.1429
90; 100.747; 90		2967.44Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118733 CIFC15 H13 N O3 S2P -18.1399; 11.5584; 16.1506
96.721; 93.818; 104.724		1452.2Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118734 CIFC15 H13 N O3 S2P 1 21/c 111.4252; 6.9479; 19.4673
90; 102.898; 90		1506.35Swapna, Battini; Suresh, Kuthuru; Nangia, Ashwini
Color polymorphs of aldose reductase inhibitor epalrestat: configurational, conformational and synthon differences.
Chemical communications (Cambridge, England), 2016, 52, 4037-4040
7118735 CIFC66 H102 Cl4 Li N4 O4 W2C 1 2/c 123.7527; 12.0648; 25.9809
90; 113.065; 90		6850.2Ventura, K.; Prat, J. R.; Aguirre Quintana, L. M.; Goos, A.; Villagran, D.
Unprecedented W2(0) quadruply bonded complex supported by π-donor ligands.
Chemical communications (Cambridge, England), 2016, 52, 3974-3976
7118736 CIFC58 H88 K2 N4 O2 W2P -110.879; 13.364; 23.272
96.119; 99.34; 105.7		3173.4Ventura, K.; Prat, J. R.; Aguirre Quintana, L. M.; Goos, A.; Villagran, D.
Unprecedented W2(0) quadruply bonded complex supported by π-donor ligands.
Chemical communications (Cambridge, England), 2016, 52, 3974-3976
7118737 CIFC24 H44 Br F10 P2 Pd S2P -110.6334; 12.3442; 12.6391
102.884; 91.323; 90.704		1616.56Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118738 CIFC24 H46 F5 I P2 Pd SP 1 21/n 114.4952; 12.5053; 18.0453
90; 112.244; 90		3027.59Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118739 CIFC24 H46 Br F5 P2 Pd SP 1 21/c 19.3877; 12.7766; 26.0735
90; 108.762; 90		2961.2Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118740 CIFC12 H8 F10 S2P 1 21/n 112.1389; 8.7547; 13.5608
90; 100.44; 90		1417.3Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118741 CIFC24 H45 F11 P2 Pd S2P -110.779; 12.164; 12.241
80.079; 89.555; 88.284		1580.3Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118742 CIFC18 H18 B F20 O2 S4P -19.9552; 11.159; 13.6383
73.775; 71.961; 76.711		1366.1Berg, Claudia; Braun, Thomas; Laubenstein, Reik; Braun, Beatrice
Palladium-mediated borylation of pentafluorosulfanyl functionalized compounds: the crucial role of metal fluorido complexes.
Chemical communications (Cambridge, England), 2016, 52, 3931-3934
7118743 CIFC136 H191 Na6 O20P -117.7793; 18.0796; 22.8488
83.835; 84.664; 61.434		6405.9Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118744 CIFC200 H254 O24 Ti8C 1 2/c 142.023; 18.0435; 30.746
90; 95.407; 90		23209Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118745 CIFC140 H216 O23 Ti4P -114.496; 16.122; 17.367
77.94; 70.572; 63.959		3429.6Ryan, Jason D.; Gagnon, Kevin J.; Teat, Simon J.; McIntosh, Ruaraidh D.
Flexible macrocycles as versatile supports for catalytically active metal clusters.
Chemical communications (Cambridge, England), 2016, 52, 9071-9073
7118746 CIFC14 H14 F5 N OP -18.4914; 10.2896; 15.2108
89.626; 85.989; 89.673		1325.7Katayev, D.; Václavík, J; Brüning, F; Commare, B.; Togni, A.
Synthesis of quaternary α-perfluoroalkyl lactams via electrophilic perfluoroalkylation.
Chemical communications (Cambridge, England), 2016, 52, 4049-4052
7118747 CIFC10 H17 Br O2P 1 21 16.2235; 9.799; 9.2211
90; 97.094; 90		558.04Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118748 CIFC7 H11 Br O2P b c a13.176; 7.6455; 15.656
90; 90; 90		1577.1Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118749 CIFC14 H14 O2 SeP 1 21/n 16.1527; 26.213; 8.0982
90; 95.797; 90		1299.4Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118750 CIFC14 H14 Br2 O2 SeP -17.8195; 8.6185; 11.8731
84.638; 85.762; 75.567		770.45Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118751 CIFC11 H11 Br O4P 1 21/c 110.6207; 8.4724; 12.7806
90; 104.935; 90		1111.18Verma, Ajay; Jana, Sadhan; Durga Prasad, Ch; Yadav, Abhimanyu; Kumar, Sangit
Organoselenium and DMAP co-catalysis: regioselective synthesis of medium-sized halolactones and bromooxepanes from unactivated alkenes.
Chemical communications (Cambridge, England), 2016, 52, 4179-4182
7118752 CIFC11 H12 Br N O4P 1 21/n 15.4464; 8.716; 25.2572
90; 91.713; 90		1198.44Santra, Sourav Kumar; Banerjee, Arghya; Rajamanickam, Suresh; Khatun, Nilufa; Patel, Bhisma K.
Pd(II)/CuBr2 catalysed keto α-Csp3-H benzoxylation of N,N-dialkylamides directed by o-hydroxy groups.
Chemical communications (Cambridge, England), 2016, 52, 4501-4504
7118753 CIFC13 H16 Cl2 N4 O3P 1 21/n 16.9732; 15.0872; 14.2862
90; 95.411; 90		1496.3Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118754 CIFC49 H49 Cl N28 O29P 1 c 112.6037; 18.505; 14.088
90; 97.74; 90		3255.83Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118755 CIFC13 H15 Cl N4 O2P 1 21/a 17.4885; 10.5846; 17.5033
90; 98.615; 90		1371.71Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118756 CIFC42 H42 N24 O21.5P 1 21 112.6407; 15.8596; 12.6429
90; 102.853; 90		2471.1Sashuk, Volodymyr; Butkiewicz, Helena; Fiałkowski, Marcin; Danylyuk, Oksana
Triggering autocatalytic reaction by host-guest interactions.
Chemical communications (Cambridge, England), 2016, 52, 4191-4194
7118757 CIFC38 H41 N O2P 1 21 19.5705; 20.6075; 15.8172
90; 90.295; 90		3119.49Deng, Yu-Hua; Zhang, Xiang-Zhi; Yu, Ke-Yin; Yan, Xu; Du, Ji-Yuan; Huang, Hanmin; Fan, Chun-An
Bifunctional tertiary amine-squaramide catalyzed asymmetric catalytic 1,6-conjugate addition/aromatization of para-quinone methides with oxindoles.
Chemical communications (Cambridge, England), 2016, 52, 4183-4186
7118758 CIFC160 H112 Cu6 F18 Ge3 N32P m -321.2111; 21.2111; 21.2111
90; 90; 90		9543.1Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118759 CIFC160 H112 Cu6 F18 N32 Si3P m -321.1882; 21.1882; 21.1882
90; 90; 90		9512.2Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118760 CIFC160 H112 Cu6 F18 N32 Sn3P m -321.2379; 21.2379; 21.2379
90; 90; 90		9579.3Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118761 CIFC160 H112 Cu6 F18 N32 Ti3P m -321.2174; 21.2174; 21.2174
90; 90; 90		9551.6Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118762 CIFC160 H112 Cu6 F18 N32 Zr3P m -321.165; 21.165; 21.165
90; 90; 90		9481Lusi, Matteo; Fechine, Pierre B. A.; Chen, Kai-Jie; Perry, John J.; Zaworotko, Michael J.
A rare cationic building block that generates a new type of polyhedral network with "cross-linked" pto topology.
Chemical communications (Cambridge, England), 2016, 52, 4160-4162
7118763 CIFC75 H81 Cl9 N6 O8 S2P -112.1788; 13.6793; 24.891
89.173; 85.674; 65.484		3761.5Huang, Guobao; Valkonen, Arto; Rissanen, Kari; Jiang, Wei
endo-Functionalized molecular tubes: selective encapsulation of neutral molecules in non-polar media.
Chemical communications (Cambridge, England), 2016, 52, 9078-9081
7118764 CIFC9 H24 B10 N2 O SC 1 2 126.2252; 6.7734; 11.5919
90; 115.831; 90		1853.37de Bruin, Gerjan; Mock, Elliot D.; Hoogendoorn, Sascha; van den Nieuwendijk, Adrianus M. C. H.; Mazurek, Jaroslaw; van der Marel, Gijsbert A.; Florea, Bogdan I.; Overkleeft, Herman S.
Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.
Chemical communications (Cambridge, England), 2016, 52, 4064-4067
7118765 CIFC9 H26 B10 N2 O2 SP 21 21 216.7451; 11.1419; 26.4844
90; 90; 90		1990.39de Bruin, Gerjan; Mock, Elliot D.; Hoogendoorn, Sascha; van den Nieuwendijk, Adrianus M. C. H.; Mazurek, Jaroslaw; van der Marel, Gijsbert A.; Florea, Bogdan I.; Overkleeft, Herman S.
Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib.
Chemical communications (Cambridge, England), 2016, 52, 4064-4067
7118766 CIFC28 H47 N3 O6P 1 21 111.5615; 10.114; 12.3397
90; 100.223; 90		1420.01Zalewski, A. N.; Nathanael, J. G.; White, J. M.; Wille, U.
Oxidation of cholesterol and O-protected derivatives by the environmental pollutant NO2˙.
Chemical communications (Cambridge, England), 2016, 52, 4060-4063
7118767 CIFC28 H23 Cl N O P Pd SP 21 21 218.3737; 12.3461; 23.8575
90; 90; 90		2466.45Yang, Xiang-Yuan; Tay, Wee Shan; Li, Yongxin; Pullarkat, Sumod A.; Leung, Pak-Hing
The synthesis and efficient one-pot catalytic "self-breeding" of asymmetrical NC(sp(3))E-hybridised pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 4211-4214
7118768 CIFC28 H23 Cl N O2 P PdP 1 21 18.4079; 12.0255; 23.7756
90; 90.682; 90		2403.8Yang, Xiang-Yuan; Tay, Wee Shan; Li, Yongxin; Pullarkat, Sumod A.; Leung, Pak-Hing
The synthesis and efficient one-pot catalytic "self-breeding" of asymmetrical NC(sp(3))E-hybridised pincer complexes.
Chemical communications (Cambridge, England), 2016, 52, 4211-4214
7118769 CIFC27 H43 N3 O5P 1 21/c 111.0838; 50.0332; 10.6703
90; 107.01; 90		5658.4Angelici, G.; Bhattacharjee, N.; Roy, O.; Faure, S.; Didierjean, C.; Jouffret, L.; Jolibois, F.; Perrin, L.; Taillefumier, C.
Weak backbone CHO[double bond, length as m-dash]C and side chain tButBu London interactions help promote helix folding of achiral NtBu peptoids.
Chemical communications (Cambridge, England), 2016, 52, 4573-4576
7118770 CIFC37 H64 N5 O6P 1 21 111.149; 17.2409; 11.1991
90; 116.772; 90		1921.9Angelici, G.; Bhattacharjee, N.; Roy, O.; Faure, S.; Didierjean, C.; Jouffret, L.; Jolibois, F.; Perrin, L.; Taillefumier, C.
Weak backbone CHO[double bond, length as m-dash]C and side chain tButBu London interactions help promote helix folding of achiral NtBu peptoids.
Chemical communications (Cambridge, England), 2016, 52, 4573-4576
7118771 CIFC23 H26 N2 O3P 1 21/n 15.1957; 24.5851; 16.0276
90; 93.625; 90		2043.22Smith, Joshua J.; Best, Daniel; Lam, Hon Wai
Copper-catalyzed borylative coupling of vinylazaarenes and N-Boc imines.
Chemical communications (Cambridge, England), 2016, 52, 3770-3772
7118772 CIFC21 H24 N2 O3 SP 1 21/c 15.28349; 9.9736; 36.4673
90; 92.3374; 90		1920.06Smith, Joshua J.; Best, Daniel; Lam, Hon Wai
Copper-catalyzed borylative coupling of vinylazaarenes and N-Boc imines.
Chemical communications (Cambridge, England), 2016, 52, 3770-3772
7118773 CIFC28 H19 B NP -111.899; 13.11; 18.036
73.51; 89.05; 64.38		2414.2Huang, Huanan; Pan, Zexiong; Cui, Chunming
The synthesis of BN-embedded tetraphenes and their photophysical properties.
Chemical communications (Cambridge, England), 2016, 52, 4227-4230
7118774 CIFC36 H24 B NP -19.942; 16.9; 18.738
105.481; 92.118; 92.215		3028.2Huang, Huanan; Pan, Zexiong; Cui, Chunming
The synthesis of BN-embedded tetraphenes and their photophysical properties.
Chemical communications (Cambridge, England), 2016, 52, 4227-4230
7118775 CIFC8 H7 Au O2 SP b c a37.4027; 7.01569; 6.36593
90; 90; 90		1670.46Lavenn, Christophe; Guillou, Nathalie; Monge, Miguel; Podbevšek, Darjan; Ledoux, Gilles; Fateeva, Alexandra; Demessence, Aude
Shedding light on an ultra-bright photoluminescent lamellar gold thiolate coordination polymer [Au(p-SPhCO2Me)]n.
Chemical communications (Cambridge, England), 2016, 52, 9063-9066
7118776 CIFC16 H14 O4 S2P -15.9165; 7.6653; 17.819
79.997; 85.946; 75.915		771.57Lavenn, Christophe; Guillou, Nathalie; Monge, Miguel; Podbevšek, Darjan; Ledoux, Gilles; Fateeva, Alexandra; Demessence, Aude
Shedding light on an ultra-bright photoluminescent lamellar gold thiolate coordination polymer [Au(p-SPhCO2Me)]n.
Chemical communications (Cambridge, England), 2016, 52, 9063-9066
7118777 CIFC22 H34 N2 O7P 1 21 16.582; 10.854; 15.521
90; 94.787; 90		1105Wang, Siyuan; Taniguchi, Tohru; Monde, Kenji; Kawahata, Masatoshi; Yamaguchi, Kentaro; Otani, Yuko; Ohwada, Tomohiko
Hydrogen bonding to carbonyl oxygen of nitrogen-pyramidalized amide - detection of pyramidalization direction preference by vibrational circular dichroism spectroscopy.
Chemical communications (Cambridge, England), 2016, 52, 4018-4021
7118778 CIFC63 H66 B N2 O3 P2 RuP -112.4687; 15.731; 17.5343
67.02; 80.866; 70.636		2985.5Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118779 CIFC55 H49 B N2 O5 P2 RuP 4110.4711; 10.4711; 44.073
90; 90; 90		4832.3Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118780 CIFC40 H47 B N4 O2 ZnP -114.4273; 14.5211; 21.5927
100.551; 91.968; 102.418		4330.3Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118781 CIFC41 H47 B N4 O4 ZnP b c a15.0418; 21.3952; 28.2235
90; 90; 90		9083Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118782 CIFC34 H36 N4 ZnC 1 2/c 121.309; 10.0652; 29.168
90; 108.052; 90		5948Janes, Trevor; Osten, Kimberly M.; Pantaleo, Adam; Yan, Ellen; Yang, Yanxin; Song, Datong
Insertion of CO2 into the carbon-boron bond of a boronic ester ligand.
Chemical communications (Cambridge, England), 2016, 52, 4148-4151
7118783 CIFC30 H50 O4 Rh2 S2C 1 c 113.97; 25.545; 8.975
90; 97.362; 90		3176Nakai, Hidetaka; Matsuba, Kengo; Akimoto, Masataka; Nozaki, Tomonori; Matsumoto, Takahiro; Isobe, Kiyoshi; Irie, Masahiro; Ogo, Seiji
Photoinduced bending of rod-like millimetre-size crystals of a rhodium dithionite complex with n-pentyl moieties.
Chemical communications (Cambridge, England), 2016, 52, 4349-4352
7118784 CIFC9 H11 N O2 S2P 1 21/c 113.333; 5.705; 13.908
90; 91.316; 90		1057.6Javorskis, Tomas; Bagdžiūnas, Gintautas; Orentas, Edvinas
N-Tosyl-1,5,2,6-dithiadiazocane: a waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles.
Chemical communications (Cambridge, England), 2016, 52, 4325-4328
7118785 CIFC19 H17 N O2 S2P 1 21/n 19.92; 17.616; 10.628
90; 111.511; 90		1728Javorskis, Tomas; Bagdžiūnas, Gintautas; Orentas, Edvinas
N-Tosyl-1,5,2,6-dithiadiazocane: a waste-free electrophilic sulfur reagent for the efficient synthesis of medium-ring S,N-heterocycles.
Chemical communications (Cambridge, England), 2016, 52, 4325-4328
7118786 CIFC279 H156 Co18 N124 O83 W12P -119.1433; 20.6439; 27.4002
77.864; 80.791; 66.5		9673.2Chorazy, Szymon; Rams, Michał; Hoczek, Anna; Czarnecki, Bernard; Sieklucka, Barbara; Ohkoshi, Shin-Ichi; Podgajny, Robert
Structural anisotropy of cyanido-bridged {CoW} single-molecule magnets induced by bidentate ligands: towards the rational enhancement of an energy barrier.
Chemical communications (Cambridge, England), 2016, 52, 4772-4775
7118787 CIFC68 H86 N12 O17 Ti4P -4 21 c17.367; 17.367; 13.73
90; 90; 90		4141.1Su, Hu-Chao; Wu, Yin-Yin; Hou, Jin-Le; Zhang, Guang-Ling; Zhu, Qin-Yu; Dai, Jie
Dye molecule bonded titanium alkoxide: a possible new type of dye for sensitized solar cells.
Chemical communications (Cambridge, England), 2016, 52, 4072-4075
7118788 CIFC28 H35 F24 N13 P4C 1 2/c 123.2328; 9.5152; 20.7638
90; 112.516; 90		4240.2Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118789 CIFC28 H29 F12 N13 Ni2 P2P 1 21/c 115.613; 13.757; 16.854
90; 96.309; 90		3598.1Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118790 CIFC60 H64 Br F18 N28 Ni4 P3C 1 2/c 115.985; 30.833; 15.2616
90; 93.494; 90		7507.9Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118791 CIFC64 H80 Cl F18 N28 Ni4 O4 P3C 1 2/c 116.233; 31.342; 15.432
90; 95.632; 90		7814Altmann, Philipp J.; Pöthig, Alexander
Capsoplexes: encapsulating complexes via guest recognition.
Chemical communications (Cambridge, England), 2016, 52, 9089-9092
7118792 CIFC336 H312 N48 O38 Pd6I 4/m33.231; 33.231; 28.78
90; 90; 90		31782Roy, Bijan; Zangrando, Ennio; Mukherjee, Partha Sarathi
Self-assembly of a redox active water soluble Pd6L8 'molecular dice'.
Chemical communications (Cambridge, England), 2016, 52, 4489-4492
7118793 CIFC33 H26.5 Cu4 I4 N9 O3P 1 21/c 119.4538; 32.5779; 22.6155
90; 103.876; 90		13914.6Zhao, Chao-Wei; Ma, Jian-Ping; Liu, Qi-Kui; Wang, Xue-Ru; Liu, Yi; Yang, Jing; Yang, Jia-Shi; Dong, Yu-Bin
An in situ self-assembled Cu4I4-MOF-based mixed matrix membrane: a highly sensitive and selective naked-eye sensor for gaseous HCl.
Chemical communications (Cambridge, England), 2016, 52, 5238-5241
7118794 CIFC54 H54 B2 F4 N8 O5P 1 21/c 113.3756; 14.865; 24.544
90; 91.671; 90		4878Doulain, Pierre-Emmanuel; Goze, Christine; Bodio, Ewen; Richard, Philippe; Decréau, Richard A
BODIPY atropisomer interconversion, face discrimination, and superstructure appending.
Chemical communications (Cambridge, England), 2016, 52, 4474-4477
7118795 CIFC123 H116 B4 F16 Ir2 N22 O7 Zn3P 1 21/c 129.0096; 19.0252; 24.8069
90; 111.599; 90		12729.9Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118796 CIFC116 H98 B4 F17 Ir2 N25 O3 Zn3P 1 21/c 129.505; 19.1096; 24.976
90; 112.295; 90		13029.4Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118797 CIFC118 H104 B4 F16 Ir2 N24 O6 S Zn3P 1 21/c 129.347; 18.8722; 25.16
90; 112.374; 90		12886Li, Xuezhao; Wu, Jinguo; He, Cheng; Zhang, Rong; Duan, Chunying
Multicomponent self-assembly of a pentanuclear Ir-Zn heterometal-organic polyhedron for carbon dioxide fixation and sulfite sequestration.
Chemical communications (Cambridge, England), 2016, 52, 5104-5107
7118798 CIFC45 H48 Au3 F18 N12 O P3P -111.7938; 13.6822; 20.7195
76.314; 74.412; 83.443		3124.4Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118799 CIFC16 H20 Au F6 N2 O2 PP 21 21 217.3239; 13.6625; 21.1998
90; 90; 90		2121.31Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118800 CIFC20 H21 Au F6 N3 PP n m a15.7075; 6.8525; 20.3447
90; 90; 90		2189.81Xiao, Xin-Shan; Zou, Chao; Guan, Xiangguo; Yang, Chen; Lu, Wei; Che, Chi-Ming
Homoleptic gold(i) N-heterocyclic allenylidene complexes: excited-state properties and lyotropic chromonics.
Chemical communications (Cambridge, England), 2016, 52, 4983-4986
7118801 CIFC45 H44 Cl Ir N4 O S2P 1 21/c 118.999; 13.938; 18.33
90; 100.52; 90		4772.3Tian, Cheng; Gong, Lei; Meggers, Eric
Chiral-at-metal iridium complex for efficient enantioselective transfer hydrogenation of ketones.
Chemical communications (Cambridge, England), 2016, 52, 4207-4210
7118802 CIFC20 H14 O3P 1 21/n 110.307; 6.9664; 20.194
90; 92.558; 90		1448.5Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118803 CIFC19 H13 Br O3P n n a6.4553; 15.35; 15.588
90; 90; 90		1544.6Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118804 CIFC29 H18 Cl2 F2 O3C 1 2/c 122.6443; 6.8474; 30.763
90; 100.073; 90		4696.4Sezukuri, Kyohei; Suzuki, Mitsuharu; Hayashi, Hironobu; Kuzuhara, Daiki; Aratani, Naoki; Yamada, Hiroko
A laterally π-expanded fluorone dye as an efficient near infrared fluorophore.
Chemical communications (Cambridge, England), 2016, 52, 4872-4875
7118805 CIFC12 H12 N2 O3P 1 21/n 113.0764; 6.7268; 26.5912
90; 99.083; 90		2309.69Roy, Saikat; Goud, N. Rajesh; Matzger, Adam J.
Polymorphism in phenobarbital: discovery of a new polymorph and crystal structure of elusive form V.
Chemical communications (Cambridge, England), 2016, 52, 4389-4392
7118806 CIFC12 H12 N2 O3P 1 21/n 114.5744; 6.88; 22.9964
90; 93.987; 90		2300.31Roy, Saikat; Goud, N. Rajesh; Matzger, Adam J.
Polymorphism in phenobarbital: discovery of a new polymorph and crystal structure of elusive form V.
Chemical communications (Cambridge, England), 2016, 52, 4389-4392
7118807 CIFC30 H34 N2 O9P 21 21 219.09127; 10.54359; 30.6974
90; 90; 90		2942.49Yu, Kuan; Gao, Beiling; Liu, Zhaobo; Ding, Hanfeng
Enantioselective total synthesis and structural reassignment of (+)-alsmaphorazine E via a traceless chirality transfer strategy.
Chemical communications (Cambridge, England), 2016, 52, 4485-4488
7118808 CIFC21 H26 N2 O6P 1 n 17.323; 9.703; 13.3813
90; 93.357; 90		949.18Yu, Kuan; Gao, Beiling; Liu, Zhaobo; Ding, Hanfeng
Enantioselective total synthesis and structural reassignment of (+)-alsmaphorazine E via a traceless chirality transfer strategy.
Chemical communications (Cambridge, England), 2016, 52, 4485-4488
7118809 CIFC36 H40 Br2 Cl6 Fe N2 P2P 1 21/n 110.6315; 25.473; 14.959
90; 90.028; 90		4051.1Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118810 CIFC34 H38 Fe N4 P2P -19.2948; 12.9539; 13.7381
79.3091; 77.1334; 72.6186		1526.31Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118811 CIFC61.84 H70.97 Fe2 N4 P4P -113.1669; 21.8049; 22.842
109.42; 104.575; 105.963		5504.3Ghosh, Chandrani; Groy, Thomas L.; Bowman, Amanda C.; Trovitch, Ryan J.
Two-step C-H, C-P bond activation at an α-diimine iron dinitrogen complex.
Chemical communications (Cambridge, England), 2016, 52, 4553-4556
7118812 CIFC16 H19 BrC 1 2/c 118.281; 7.3569; 19.925
90; 104.092; 90		2599.1Su, Xiang; Sun, Yihua; Yao, Jiannian; Chen, Hui; Chen, Chao
Acid-promoted bicyclization of arylacetylenes to benzobicyclo[3.2.1]octanes through cationic rearrangements.
Chemical communications (Cambridge, England), 2016, 52, 4537-4540
7118813 CIFC26 H42 Fe N P3P 1 21/c 117.283; 19.422; 15.933
90; 92.103; 90		5344.6Lindley, Brian M.; Jacobs, Brian P.; MacMillan, Samantha N.; Wolczanski, Peter T.
Neutral Fe(iv) alkylidenes, including some that bind dinitrogen.
Chemical communications (Cambridge, England), 2016, 52, 3891-3894
7118814 CIFC30 H41 Fe N3 P2P 1 21/n 110.6131; 14.2296; 19.7148
90; 97.83; 90		2949.6Lindley, Brian M.; Jacobs, Brian P.; MacMillan, Samantha N.; Wolczanski, Peter T.
Neutral Fe(iv) alkylidenes, including some that bind dinitrogen.
Chemical communications (Cambridge, England), 2016, 52, 3891-3894
7118815 CIFC60 H54 Cl2 Cu4 N12 O35 W10C 1 2/m 120.0634; 17.3159; 15.642
90; 124.211; 90		4494Shi, Dongying; He, Cheng; Sun, Wenlong; Ming, Zheng; Meng, Changgong; Duan, Chunying
A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles.
Chemical communications (Cambridge, England), 2016, 52, 4714-4717
7118816 CIFC63 H53 Cl2 Cu4 N13 O33 W10C 1 2/m 120.0299; 17.2261; 15.8221
90; 125.919; 90		4421.1Shi, Dongying; He, Cheng; Sun, Wenlong; Ming, Zheng; Meng, Changgong; Duan, Chunying
A photosensitizing decatungstate-based MOF as heterogeneous photocatalyst for the selective C-H alkylation of aliphatic nitriles.
Chemical communications (Cambridge, England), 2016, 52, 4714-4717
7118817 CIFC21 H26 Cl3 N2 RhP n m a22.5211; 12.1599; 7.8427
90; 90; 90		2147.76Pitman, C. L.; Finster, O. N. L.; Miller, A. J. M.
Cyclopentadiene-mediated hydride transfer from rhodium complexes.
Chemical communications (Cambridge, England), 2016, 52, 9105-9108
7118818 CIFC18 H16 N2 O2I 41/a24.392; 24.392; 4.8236
90; 90; 90		2869.9Grzybowski, Marek; Deperasińska, Irena; Chotkowski, Maciej; Banasiewicz, Marzena; Makarewicz, Artur; Kozankiewicz, Bolesław; Gryko, Daniel T.
Dipyrrolonaphthyridinediones - structurally unique cross-conjugated dyes.
Chemical communications (Cambridge, England), 2016, 52, 5108-5111
7118819 CIFC25 H41 Fe N2 O4 P Si3P 1 21/n 111.1641; 16.6308; 17.5587
90; 94.787; 90		3248.72Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118820 CIFC53 H62 Fe2 N4 O18 P2 Si2 W2C 1 2/c 125.6547; 10.4018; 24.8836
90; 91.797; 90		6637.05Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118821 CIFC19 H25 Fe N2 O4 P SiP 21 21 2112.5723; 13.3184; 13.6939
90; 90; 90		2292.95Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118822 CIFC28.8 H30.2 Fe N3 O7.3P 1 21/c 116.0853; 28.696; 7.0062
90; 96.758; 90		3211.5Breit, Nora C.; Eisenhut, Carsten; Inoue, Shigeyoshi
Phosphinosilylenes as a novel ligand system for heterobimetallic complexes.
Chemical communications (Cambridge, England), 2016, 52, 5523-5526
7118823 CIFC26 H44 N5 O7P 21 21 2111.936; 16.0501; 16.5597
90; 90; 90		3172.4Metrano, A. J.; Abascal, N. C.; Mercado, B. Q.; Paulson, E. K.; Miller, S. J.
Structural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.
Chemical communications (Cambridge, England), 2016, 52, 4816-4819
7118824 CIFC27 H48 N6 O6P 21 21 2111.7899; 15.9908; 16.3363
90; 90; 90		3079.9Metrano, A. J.; Abascal, N. C.; Mercado, B. Q.; Paulson, E. K.; Miller, S. J.
Structural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.
Chemical communications (Cambridge, England), 2016, 52, 4816-4819
7118825 CIFC29 H30 N2 O4P 1 21/c 115.268; 11.6042; 15.6622
90; 115.596; 90		2502.6Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118826 CIFC31 H32 F N3 O3P 1 21/c 19.0977; 16.6165; 17.6
90; 96.066; 90		2645.7Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118827 CIFC31 H32 F N3 O3P 1 21/c 19.0851; 16.648; 17.522
90; 98.553; 90		2620.71Li, Zhenghua; Sharma, Nandini; Sharma, Upendra K.; Jacobs, Jeroen; Van Meervelt, Luc; Van der Eycken, Erik V.
Ligand-controlled product selectivity in palladium-catalyzed domino post-Ugi construction of (spiro)polyheterocycles.
Chemical communications (Cambridge, England), 2016, 52, 5516-5519
7118828 CIFC18 H18P 1 21/n 110.23; 4.7903; 14.674
90; 108.855; 90		680.5Lungerich, Dominik; Nizovtsev, Alexey V.; Heinemann, Frank W.; Hampel, Frank; Meyer, Karsten; Majetich, George; Schleyer, Paul V. R.; Jux, Norbert
[18]Annulene put into a new perspective.
Chemical communications (Cambridge, England), 2016, 52, 4710-4713
7118829 CIFC24 H12I 41/a c d21.6492; 21.6492; 14.6312
90; 90; 90		6857.47Lungerich, Dominik; Nizovtsev, Alexey V.; Heinemann, Frank W.; Hampel, Frank; Meyer, Karsten; Majetich, George; Schleyer, Paul V. R.; Jux, Norbert
[18]Annulene put into a new perspective.
Chemical communications (Cambridge, England), 2016, 52, 4710-4713
7118830 CIFC192 H240 B6.25 F25 Fe4 N38P 6340.6845; 40.6845; 34.133
90; 90; 120		48929Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118831 CIFC192 H240 B4 F16 N36 Ni4I 2 323.2474; 23.2474; 23.2474
90; 90; 90		12563.9Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118832 CIFC192 H240 B4 F16 Fe0.8 N36 Ni3.2I 2 323.2506; 23.2506; 23.2506
90; 90; 90		12569.1Zhang, Feng-Li; Chen, Jia-Qian; Qin, Long-Fang; Tian, Lei; Li, Zaijun; Ren, Xuehong; Gu, Zhi-Guo
Metal-center exchange of tetrahedral cages: single crystal to single crystal and spin-crossover properties.
Chemical communications (Cambridge, England), 2016, 52, 4796-4799
7118833 CIFC26 H25 N O5 S2P 1 21/c 113.9256; 10.3322; 17.0868
90; 94.647; 90		2450.4Undeela, Sridhar; Ravikumar, Gurram; Nanubolu, Jagadeesh Babu; Singarapu, Kiran Kumar; Menon, Rajeev S.
The facile synthesis of 1-benzoazepine derivatives via gold-catalyzed regioselective cycloisomerization reactions of N-(o-alkynylaryl)-N-vinyl sulfonamides.
Chemical communications (Cambridge, England), 2016, 52, 4824-4827
7118834 CIFC26 H24 Cl N O5 S2P -19.7246; 11.0418; 12.8181
70.832; 71.93; 88.331		1231.88Undeela, Sridhar; Ravikumar, Gurram; Nanubolu, Jagadeesh Babu; Singarapu, Kiran Kumar; Menon, Rajeev S.
The facile synthesis of 1-benzoazepine derivatives via gold-catalyzed regioselective cycloisomerization reactions of N-(o-alkynylaryl)-N-vinyl sulfonamides.
Chemical communications (Cambridge, England), 2016, 52, 4824-4827
7118835 CIFC36 H20 SP 1 21/c 123.8009; 3.8485; 26.3591
90; 113.997; 90		2205.75Oniwa, Kazuaki; Kikuchi, Hiromasa; Shimotani, Hidekazu; Ikeda, Susumu; Asao, Naoki; Yamamoto, Yoshinori; Tanigaki, Katsumi; Jin, Tienan
2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors.
Chemical communications (Cambridge, England), 2016, 52, 4800-4803
7118836 CIFC40 H22 S2P 1 21/c 122.725; 3.8289; 15.667
90; 109.481; 90		1285.2Oniwa, Kazuaki; Kikuchi, Hiromasa; Shimotani, Hidekazu; Ikeda, Susumu; Asao, Naoki; Yamamoto, Yoshinori; Tanigaki, Katsumi; Jin, Tienan
2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors.
Chemical communications (Cambridge, England), 2016, 52, 4800-4803
7118837 CIFC15 H9 Dy N2 O6.5C 1 2/c 113.666; 15.154; 15.228
90; 101.24; 90		3093.1Liu, Cai-Ming; Zhang, De-Qing; Zhu, Dao-Ben
A 3D MOF constructed from dysprosium(iii) oxalate and capping ligands: ferromagnetic coupling and field-induced two-step magnetic relaxation.
Chemical communications (Cambridge, England), 2016, 52, 4804-4807
7118838 CIFC38 H12 F10 N4P -16.799; 8.219; 13.376
82.308; 75.542; 83.754		715.1Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118839 CIFC41 H22 F10 N4 OP -19.9304; 12.231; 14.545
75.314; 82.512; 80.77		1679.3Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118840 CIFC46 H18 F10 N4P 1 21/n 110.144; 12.998; 25.579
90; 96.312; 90		3352.2Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118841 CIFC57 H36 N6 O4P -112.261; 13.38; 14.218
77.74; 81.518; 89.721		2253.5Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118842 CIFC62 H21 F15 N6 O3P 1 21/c 18.6387; 14.094; 42.764
90; 91.418; 90		5205Gadekar, Santosh C.; Reddy, Baddigam K.; Panchal, Santosh P.; Anand, Venkataramanarao G.
Metal assisted cyclomerization of benzodipyrrins into expanded norroles, aza-heptalene and acyclic dimers.
Chemical communications (Cambridge, England), 2016, 52, 4565-4568
7118843 CIFC86 H132 N16 O16P 1 21 114.1965; 21.9607; 16.3804
90; 111.904; 90		4738.2Bandyopadhyay, Anupam; Misra, Rajkumar; Gopi, Hosahudya N.
Structural features and molecular aggregations of designed triple-stranded β-sheets in single crystals.
Chemical communications (Cambridge, England), 2016, 52, 4938-4941
7118844 CIFC79 H134 N16 O16P 112.367; 13.818; 16.091
105.224; 97.197; 113.827		2342.2Bandyopadhyay, Anupam; Misra, Rajkumar; Gopi, Hosahudya N.
Structural features and molecular aggregations of designed triple-stranded β-sheets in single crystals.
Chemical communications (Cambridge, England), 2016, 52, 4938-4941
7118845 CIFC20 H26 B2 F2P 1 21/n 19.024; 15.783; 12.907
90; 96.65; 90		1825.9Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118846 CIFC21 H31 B2 F2 PP b c a8.463; 14.865; 32.625
90; 90; 90		4104.3Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118847 CIFC21 H31 B2 F2 O3 PP 1 21/c 110.3; 14.375; 15.204
90; 104.85; 90		2176Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118848 CIFC33 H44 B2 Cl2 F2 N4P -111.043; 11.083; 14.473
92.267; 92.359; 113.535		1619.6Arnold, Nicole; Braunschweig, Holger; Damme, Alexander; Dewhurst, Rian D.; Pentecost, Leanne; Radacki, Krzysztof; Stellwag-Konertz, Sascha; Thiess, Torsten; Trumpp, Alexandra; Vargas, Alfredo
New outcomes of Lewis base addition to diboranes(4): electronic effects override strong steric disincentives.
Chemical communications (Cambridge, England), 2016, 52, 4898-4901
7118849 CIFC32 H14 B2 Cl2 F15 N O2P -111.253; 11.41; 14.135
69.313; 74.449; 84.848		1635.7Zheng, Junhao; Fan, Xiaoting; Zhou, Benyu; Li, Zhen Hua; Wang, Huadong
Tautomerization of 2,6-lutidines in the presence of B(C6F5)3 using catecholborane as a precatalyst.
Chemical communications (Cambridge, England), 2016, 52, 4655-4658
7118850 CIFC25 H9 B F15 NP 1 21/c 17.69; 18.994; 15.963
90; 92.675; 90		2329Zheng, Junhao; Fan, Xiaoting; Zhou, Benyu; Li, Zhen Hua; Wang, Huadong
Tautomerization of 2,6-lutidines in the presence of B(C6F5)3 using catecholborane as a precatalyst.
Chemical communications (Cambridge, England), 2016, 52, 4655-4658
7118851 CIFC26 H27 Cl F N O8 SP 1 21/c 111.3397; 20.295; 13.45
90; 114.44; 90		2818Yang, Jieru; Zhou, Xiaofan; Zeng, Yu; Huang, Chaoqian; Xiao, Yuanjing; Zhang, Junliang
Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates.
Chemical communications (Cambridge, England), 2016, 52, 4922-4925
7118852 CIFC15 H10 N2 O2C 1 2/c 119.7366; 11.0069; 14.8933
90; 130.433; 90		2462.7Fan, Liwen; Wang, Tao; Tian, Ying; Xiong, Fei; Wu, Simei; Liang, Qingjin; Zhao, Junfeng
Copper-catalyzed oxidative coupling between quinazoline 3-oxides and unactivated aldehydes: an efficient approach to functionalized quinazolines.
Chemical communications (Cambridge, England), 2016, 52, 5375-5378
7118853 CIFC15 H10 N2 O3P 1 21/n 16.8611; 18.3584; 9.5657
90; 90.0894; 90		1204.88Fan, Liwen; Wang, Tao; Tian, Ying; Xiong, Fei; Wu, Simei; Liang, Qingjin; Zhao, Junfeng
Copper-catalyzed oxidative coupling between quinazoline 3-oxides and unactivated aldehydes: an efficient approach to functionalized quinazolines.
Chemical communications (Cambridge, England), 2016, 52, 5375-5378
7118854 CIFC19 H17 N O4P -18.9379; 10.7203; 11.0337
118.687; 110.073; 93.964		835.3Tiwari, Dipak Kumar; Phanindrudu, Mandalaparthi; Aravilli, Vinod Kumar; Sridhar, B.; Likhar, Pravin R.; Tiwari, Dharmendra Kumar
Magnetically recoverable Cu(0)/Fe3O4 catalyzed highly regioselective synthesis of 2,3,4-trisubstituted pyrroles from unactivated terminal alkynes and isocyanides.
Chemical communications (Cambridge, England), 2016, 52, 4675-4678
7118855 CIFC23 H21 K N5 O10 YbC 1 2/c 119.9224; 14.1721; 10.3924
90; 111.833; 90		2723.75Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118856 CIFC25 H29 Li N5 O12 YbP 1 21/c 110.5784; 17.3413; 16.6413
90; 104.996; 90		2948.8Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118857 CIFC25 H29 N5 Na O12 YbP 1 21/c 110.5784; 17.3413; 16.6413
90; 104.996; 90		2948.8Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118858 CIFC92 H84 N20 O40 Rb4 Yb4P -112.2689; 13.8207; 16.0314
89.063; 84.408; 88.521		2704.3Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118859 CIFC46 H42 N9 O17 Rb Yb2C 1 2/c 118.668; 17.357; 16.785
90; 102.458; 90		5311Chen, Wanmin; Tang, Xiaoliang; Dou, Wei; Ju, Zhenghua; Xu, Benhua; Xu, Wenxuan; Liu, Weisheng
K(+)-Induced in situ self-assembly of near-infrared luminescent membrane material armored with bigger Yb(iii) complex crystallites.
Chemical communications (Cambridge, England), 2016, 52, 5124-5127
7118860 CIFC232.5 H275.5 Cl8 Cu32 N67.5 O57R -3 :H23.108; 23.108; 56.327
90; 90; 120		26048Feng, Sisi; Jia, Fei; Lu, Liping; Li, Zhongping; Zhang, Shuo
An unusual 32-membered copper(ii) metallomacrocube based on a Cu4O3X cubic core: photocatalytic, electrocatalytic, and magnetic properties.
Chemical communications (Cambridge, England), 2016, 52, 4294-4297
7118861 CIFC50 H73 Br N3 Na O10P 21 21 2114.7059; 18.0236; 19.3772
90; 90; 90		5135.99Shi, Qiuyan; Li, Yu; Bo, Shaowei; Li, Xiaofei; Zhao, Peng; Liu, Qi; Yang, Zhigang; Cong, Hengjiang; Deng, Hexiang; Chen, Mingnan; Chen, Shizhen; Zhou, Xin; Ding, Hong; Jiang, Zhong-Xing
Discovery of a (19)F MRI sensitive salinomycin derivative with high cytotoxicity towards cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 5136-5139
7118862 CIFC50 H75 Br K N3 O11P 41 21 213.5526; 13.5526; 57.9362
90; 90; 90		10641.3Shi, Qiuyan; Li, Yu; Bo, Shaowei; Li, Xiaofei; Zhao, Peng; Liu, Qi; Yang, Zhigang; Cong, Hengjiang; Deng, Hexiang; Chen, Mingnan; Chen, Shizhen; Zhou, Xin; Ding, Hong; Jiang, Zhong-Xing
Discovery of a (19)F MRI sensitive salinomycin derivative with high cytotoxicity towards cancer cells.
Chemical communications (Cambridge, England), 2016, 52, 5136-5139
7118863 CIFC67 H58 Cl2 N2 P4 RuP -110.5042; 12.4115; 22.3482
75.394; 77.732; 86.444		2754.9Sugimoto, Kaho; Tanaka, Yuya; Fujii, Shintaro; Tada, Tomofumi; Kiguchi, Manabu; Akita, Munetaka
Organometallic molecular wires as versatile modules for energy-level alignment of the metal-molecule-metal junction.
Chemical communications (Cambridge, England), 2016, 52, 5796-5799
7118864 CIFC21 H30 Bi2 Br13 N3C 1 2/c 111.91371; 15.9042; 21.6218
90; 91.0689; 90		4096.14Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118865 CIFC18 H24 Bi2 Br11 N3P 1 21/c 19.5341; 21.4727; 35.055
90; 97.093; 90		7121.6Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118866 CIFC12 H14 Bi Br7 N2C m c m14.1671; 19.7299; 7.74397
90; 90; 90		2164.56Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118867 CIFC28 H36 Bi Br13 N4P n m a16.0606; 13.9864; 19.4745
90; 90; 90		4374.56Adonin, Sergey A.; Gorokh, Igor D.; Samsonenko, Denis G.; Sokolov, Maxim N.; Fedin, Vladimir P.
Bi(iii) polybromides: a new chapter in coordination chemistry of bismuth.
Chemical communications (Cambridge, England), 2016, 52, 5061-5063
7118868 CIFC92 H28 Cl8 F40 N8 O2P 1 21/n 117.2568; 14.4839; 18.3034
90; 96.454; 90		4545.9Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118869 CIFC70 H24 Cu2 F30 N6 O4 S2P 1 21/n 111.1752; 16.3892; 37.51
90; 93.375; 90		6858.1Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118870 CIFC83 H23 Cu2 F35 N10 O2P 1 21/c 115.2047; 23.71; 25.959
90; 103.577; 90		9096.8Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118871 CIFC92 H24 Cl8 Cu2 F40 N8 O2P 1 21/c 117.0506; 14.6158; 23.435
90; 129.005; 90		4538.4Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118872 CIFC94 H29 F40 N11 O2 Zn2P -113.133; 16.1932; 20.7009
81.317; 86.431; 83.348		4318.1Zhang, Kai; Savage, Mathew; Li, Xin; Jiang, Yu; Ishida, Masatoshi; Mitsuno, Koki; Karasawa, Satoru; Kato, Tatsuhisa; Zhu, Weihua; Yang, Sihai; Furuta, Hiroyuki; Xie, Yongshu
Rational syntheses of helical π-conjugated oligopyrrins with a bipyrrole linkage: geometry control of bis-copper(ii) coordination.
Chemical communications (Cambridge, England), 2016, 52, 5148-5151
7118873 CIFC140 H266 Ag19.4 Au5.6 N S18P -117.0545; 29.3289; 35.668
85.911; 89.317; 86.562		17762.8Li, Qi; Wang, Shuxin; Kirschbaum, Kristin; Lambright, Kelly J.; Das, Anindita; Jin, Rongchao
Heavily doped Au25-xAgx(SC6H11)18(-) nanoclusters: silver goes from the core to the surface.
Chemical communications (Cambridge, England), 2016, 52, 5194-5197
7118874 CIFC76 H66 B F24 Ir N O PP 1 21 113.5677; 13.0684; 20.6626
90; 105.603; 90		3528.6Yu, Yan-Bo; Cheng, Lei; Li, Yi-Pan; Fu, Yue; Zhu, Shou-Fei; Zhou, Qi-Lin
Enantioselective iridium-catalyzed hydrogenation of β,β-disubstituted nitroalkenes.
Chemical communications (Cambridge, England), 2016, 52, 4812-4815
7118875 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.4201; 13.4798; 12.0817
90; 102.537; 90		2769.37O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118876 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.4151; 13.4808; 12.079
90; 102.508; 90		2768.48O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118877 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.2129; 13.3158; 11.79
90; 102.848; 90		2634.65O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118878 CIFC30 H24 Au2 Cl2 P2C 1 2/c 117.0509; 13.1824; 11.579
90; 103.183; 90		2534.04O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118879 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.8213; 13.0052; 11.2967
90; 103.502; 90		2403O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118880 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.6333; 12.8767; 11.1124
90; 103.804; 90		2311.3O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118881 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.5181; 12.7957; 10.9986
90; 103.959; 90		2256.02O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118882 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.3552; 12.6807; 10.8457
90; 104.192; 90		2180.7O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118883 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.1848; 12.5654; 10.6996
90; 104.452; 90		2107.11O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118884 CIFC30 H24 Au2 Cl2 P2C 1 2/c 116.1185; 12.5191; 10.6485
90; 104.564; 90		2079.71O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118885 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.9507; 12.4062; 10.5188
90; 104.813; 90		2012.4O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118886 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.9198; 12.3906; 10.5027
90; 104.853; 90		2002.5O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118887 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.8861; 12.3656; 10.4819
90; 104.901; 90		1989.83O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118888 CIFC30 H24 Au2 Cl2 P2C 1 2/c 115.8107; 12.3314; 10.4704
90; 104.924; 90		1972.5O'Connor, Alice E; Mirzadeh, Nedaossadat; Bhargava, Suresh K.; Easun, Timothy L.; Schröder, Martin; Blake, Alexander J.
Aurophilicity under pressure: a combined crystallographic and in situ spectroscopic study.
Chemical communications (Cambridge, England), 2016, 52, 6769-6772
7118889 CIFC5 H6 F4P 1 21/c 110.115; 4.5875; 11.876
90; 90.026; 90		551.1Fang, Zeguo; Al-Maharik, Nawaf; Slawin, Alexandra M. Z.; Bühl, Michael; O'Hagan, David
Polar alicyclic rings: synthesis and structure of all cis-1,2,3,4-tetrafluorocyclopentane.
Chemical communications (Cambridge, England), 2016, 52, 5116-5119
7118890 CIFC18 H19 N O2P b c a9.5809; 13.6588; 22.8484
90; 90; 90		2990Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118891 CIFC28 H25 N O3P 1 21/n 17.7189; 9.7482; 29.5931
90; 94.235; 90		2220.66Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118892 CIFC18 H16 Br N OP -17.9573; 9.6303; 10.5963
68.147; 75.128; 69.312		697.7Nandi, Raj Kumar; Ratsch, Friederike; Beaud, Rodolphe; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Intermolecular dearomative C2-arylation of N-Ac indoles activated by FeCl3.
Chemical communications (Cambridge, England), 2016, 52, 5328-5331
7118893 CIFC33 H75 Cl N4 Pu Si3P 1 21/n 113.0136; 15.5458; 20.433
90; 90.546; 90		4133.5Brown, Jessie L.; Gaunt, Andrew J.; King, David M.; Liddle, Stephen T.; Reilly, Sean D.; Scott, Brian L.; Wooles, Ashley J.
Neptunium and plutonium complexes with a sterically encumbered triamidoamine (TREN) scaffold.
Chemical communications (Cambridge, England), 2016, 52, 5428-5431
7118894 CIFC33 H75 Cl N4 Np Si3P 1 21/n 112.9845; 15.6008; 20.4035
90; 90.648; 90		4132.8Brown, Jessie L.; Gaunt, Andrew J.; King, David M.; Liddle, Stephen T.; Reilly, Sean D.; Scott, Brian L.; Wooles, Ashley J.
Neptunium and plutonium complexes with a sterically encumbered triamidoamine (TREN) scaffold.
Chemical communications (Cambridge, England), 2016, 52, 5428-5431
7118897 CIFC61 H95 N8 O12P 21 21 222.4; 29.9961; 9.5945
90; 90; 90		6446.7Yoon, Eunyoung; Gong, Jintaek; Jung, Yoonchul; Lee, Wonchul; Driver, Russell W.; Lee, Hee-Seung
Unambiguous characterization of anisotropic foldamer packing in a foldecture with an elongated hexagonal plate shape.
Chemical communications (Cambridge, England), 2016, 52, 5250-5253
7118898 CIFC12 H96 K3 Mo16 N O74 S16C 1 2/m 120.6782; 11.2433; 23.3822
90; 108.634; 90		5151.2Zang, Hongying; Surman, Andrew; Long, Deliang; Cronin, Leroy; Miras, Haralampos N.
Exploiting the equilibrium dynamics in the self-assembly of inorganic macrocycles based upon polyoxothiometalate building blocks.
Chemical communications (Cambridge, England), 2016, 52, 9109-9112
7118899 CIFC12 H90 Mo12 N2 O52 S12C 1 2/c 138.31; 17.3787; 12.5611
90; 91.431; 90		8360.3Zang, Hongying; Surman, Andrew; Long, Deliang; Cronin, Leroy; Miras, Haralampos N.
Exploiting the equilibrium dynamics in the self-assembly of inorganic macrocycles based upon polyoxothiometalate building blocks.
Chemical communications (Cambridge, England), 2016, 52, 9109-9112
7118900 CIFC14 H22 Cl2 I6 N4 PtP -19.1654; 9.1839; 10.0995
113.841; 100.43; 108.001		692.27Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118901 CIFC14 H22 Cl2 I6 N4 PtP -19.1564; 9.1703; 10.0589
113.561; 100.692; 107.883		689.26Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118902 CIFC14 H22 Cl2 I6 N4 PtP -19.1806; 9.3566; 10.3153
114.93; 99.18; 108.364		717.25Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118903 CIFC8 H14 Cl2 I6 N4 PtP -19.2555; 9.6136; 15.3533
81.5317; 75.7689; 65.7138		1205.36Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118904 CIFC16 H28 Cl7 I9 N8 Pt2P -19.2558; 9.3667; 15.2697
75.799; 81.826; 65.21		1163.95Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118905 CIFC6 H12 Br2 N4 PtP 1 21/c 15.7573; 11.8165; 9.2197
90; 108.047; 90		596.37Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118906 CIFC8 H14 Br2 I6 N4 PtP -19.28; 9.8201; 15.7209
81.037; 75.8368; 65.7179		1263.74Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118907 CIFC12 H22 Cl2 I6 N4 PtP -18.2473; 8.7723; 11.3779
104.013; 98.93; 116.223		683.18Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118908 CIFC12 H18 Cl2 I6 N4 PtP 1 21/c 19.9496; 9.35436; 14.6232
90; 103.295; 90		1324.54Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118909 CIFC14 H22 Cl2 I6 N4 PtP -19.129; 9.1612; 10.0487
100.776; 113.593; 107.793		685.71Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118910 CIFC14 H22 Cl2 I6 N4 PtP -19.1465; 9.1681; 10.068
113.589; 100.676; 107.808		689.34Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118911 CIFC14 H22 Cl2 I6 N4 PtP -19.168; 9.1918; 10.109
113.897; 100.373; 107.948		693.9Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118912 CIFC14 H22 Cl2 I6 N4 PtP -19.1724; 9.2419; 10.1625
114.172; 100.036; 108.096		700.48Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118913 CIFC14 H22 Cl2 I6 N4 PtP -19.1743; 9.2939; 10.2287
114.48; 99.652; 108.236		707.88Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118914 CIFC14 H22 Cl2 I6 N4 PtP -19.158; 9.3355; 10.2955
114.801; 99.221; 108.383		713.2Ivanov, Daniil M.; Novikov, Alexander S.; Ananyev, Ivan V.; Kirina, Yulia V.; Kukushkin, Vadim Yu
Halogen bonding between metal centers and halocarbons.
Chemical communications (Cambridge, England), 2016, 52, 5565-5568
7118915 CIFC145 H161 Co24 N9 O101P -4 21 m27.646; 27.646; 17.306
90; 90; 90		13227Liang, Guang-Ming; Ni, Qing-Ling; Zou, Hua-Hong; Gui, Liu-Cheng; Wang, Xiu-Jian
Rare double spin canting antiferromagnetic behaviours in a [Co24] cluster.
Chemical communications (Cambridge, England), 2016, 52, 5293-5296
7118916 CIFC38 H36 Cu2 P2P -110.0317; 12.1017; 13.3609
97.647; 94.311; 95.342		1594.3Molteni, Roberto; Bertermann, Rüdiger; Edkins, Katharina; Steffen, Andreas
An unexpected transmetalation intermediate: isolation and structural characterization of a solely CH3 bridged di-copper(i) complex.
Chemical communications (Cambridge, England), 2016, 52, 5019-5022
7118917 CIFC16 H13 F3 N2 OP -15.4475; 12.1951; 12.2971
114.682; 98.556; 98.672		713.13Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118918 CIFC17 H18 N2 O5 S2P -19.2208; 9.2881; 11.3189
92.755; 107.193; 106.506		878.64Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118919 CIFC18 H16 B F2 N OP b c a13.5204; 12.9163; 17.273
90; 90; 90		3016.4Tomakinian, Terry; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Synthesis of benzofuro[3,2-b]indoline amines via deamination-interrupted Fischer indolization and their unexpected reactivity towards nucleophiles.
Chemical communications (Cambridge, England), 2016, 52, 5443-5446
7118920 CIFC17.09 H116.4 Br N O38P m m a21.0329; 12.5972; 12.0333
90; 90; 90		3188.3Muromachi, Sanehiro; Udachin, Konstantin A.; Alavi, Saman; Ohmura, Ryo; Ripmeester, John A.
Selective occupancy of methane by cage symmetry in TBAB ionic clathrate hydrate.
Chemical communications (Cambridge, England), 2016, 52, 5621-5624
7118921 CIFC22 H16 O3P n a 2111.353; 16.909; 8.235
90; 90; 90		1580.9Mao, Wenbin; Zhu, Chen
Synthesis of highly substituted γ-hydroxybutenolides through the annulation of keto acids with alkynes and subsequent hydroxyl transposition.
Chemical communications (Cambridge, England), 2016, 52, 5269-5272
7118922 CIFC34.5 H25 Cl N2 O2C 1 2/c 115.3088; 17.993; 19.4932
90; 92.57; 90		5364Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118923 CIFC36 H24 N2C 1 2/c 114.0547; 19.251; 18.41
90; 90.832; 90		4980.6Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118924 CIFC42 H26 N2P 1 21/n 111.4684; 18.005; 13.845
90; 92.989; 90		2854.9Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118925 CIFC33 H24 N2P 1 21/n 113.67; 10.7087; 16.477
90; 98.766; 90		2383.9Wang, Huan; Zhang, Zhiyun; Zhou, Haitao; Wang, Tonghai; Su, Jianhua; Tong, Xiaofeng; Tian, He
Cu-catalyzed C-H amination/Ullmann N-arylation domino reaction: a straightforward synthesis of 9,14-diaryl-9,14-dihydrodibenzo[a,c]phenazine.
Chemical communications (Cambridge, England), 2016, 52, 5459-5462
7118926 CIFC20 H19 N O3 SP -17.326; 10.134; 12.489
80.774; 82.54; 77.77		890Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118927 CIFC23 H25 N O3 SP 1 21 113.598; 5.7831; 14.8716
90; 111.469; 90		1088.34Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118928 CIFC27 H29 N O3 S2P 1 21/c 112.8698; 13.262; 15.0271
90; 92.583; 90		2562.2Huang, Hai; Tang, Luning; Liu, Qi; Xi, Yang; He, Guangke; Zhu, Hongjun
Formation of α-chalcogenyl acrylamides through unprecedented chalcogen-mediated metal-free oxyfunctionalization of ynamides with DMSO as an oxidant.
Chemical communications (Cambridge, England), 2016, 52, 5605-5608
7118929 CIFC4 H6 N8 O0 ZnI -4 3 m17.1168; 17.1168; 17.1168
90; 90; 90		5014.96Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118930 CIFC4 H6 N8 O0 ZnI -4 3 m17.0293; 17.0293; 17.0293
90; 90; 90		4938.4Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118931 CIFC18 H45 N15 O8 S2 Zn2P 21 21 2115.7886; 15.9425; 16.3286
90; 90; 90		4110.1Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118932 CIFC24 H52 B3 F12 N48 O8 Zn7I -4 3 d22.3819; 22.3819; 22.3819
90; 90; 90		11212.2Tang, Yu-Huan; Wang, Fei; Liu, Jin-Xiu; Zhang, Jian
Diverse tetrahedral tetrazolate frameworks with N-rich surface.
Chemical communications (Cambridge, England), 2016, 52, 5625-5628
7118933 CIFC11 H15 N4 O2P 1 21/c 16.211; 40.769; 9.646
90; 96.104; 90		2428.7Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118934 CIFC21 H19 Co F12 N4 O6P -114.967; 15.106; 15.938
69.812; 62.763; 66.38		2877.1Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118935 CIFC31 H23 Co2 F24 N4 O10P 1 21/n 112.6019; 20.7451; 17.6713
90; 104.665; 90		4469.3Wang, Jian; Li, Jia-Nan; Zhang, Shao-Liang; Zhao, Xin-Hua; Shao, Dong; Wang, Xin-Yi
Syntheses and magnetic properties of a pyrimidyl-substituted nitronyl nitroxide radical and its cobalt(ii) complexes.
Chemical communications (Cambridge, England), 2016, 52, 5033-5036
7118936 CIFC36 H40 B N O2P -19.7416; 10.1024; 16.6
92.408; 106.474; 105.593		1496.5Jiang, Han-Chun; Tang, Xiang-Ying; Shi, Min
Copper-catalyzed regio- and enantioselective aminoboration of alkylidenecyclopropanes: the synthesis of cyclopropane-containing β-aminoalkylboranes.
Chemical communications (Cambridge, England), 2016, 52, 5273-5276
7118937 CIFC30 H36 B N O2P -110.5305; 11.491; 13.29
68.577; 71.096; 63.363		1313.1Jiang, Han-Chun; Tang, Xiang-Ying; Shi, Min
Copper-catalyzed regio- and enantioselective aminoboration of alkylidenecyclopropanes: the synthesis of cyclopropane-containing β-aminoalkylboranes.
Chemical communications (Cambridge, England), 2016, 52, 5273-5276
7118938 CIFC18 H48 Li3 N6 P7P -311.3403; 11.3403; 15.1182
90; 90; 120		1683.76Bhattacharyya, Koyel X.; Dreyfuss, Sébastien; Saffon-Merceron, Nathalie; Mézailles, Nicolas
P4 functionalization by hydrides: direct synthesis of P-H bonds.
Chemical communications (Cambridge, England), 2016, 52, 5179-5182
7118939 CIFC50 H32 O2P 1 21/c 18.8161; 13.0764; 29.5577
90; 94.937; 90		3394.9Pozo, Iago; Cobas, Agustín; Peña, Diego; Guitián, Enrique; Pérez, Dolores
1,7-Naphthodiyne: a new platform for the synthesis of novel, sterically congested PAHs.
Chemical communications (Cambridge, England), 2016, 52, 5534-5537
7118940 CIFC39 H25 Cl3P 1 21/c 114.0105; 13.0164; 16.1008
90; 102.591; 90		2865.63Pozo, Iago; Cobas, Agustín; Peña, Diego; Guitián, Enrique; Pérez, Dolores
1,7-Naphthodiyne: a new platform for the synthesis of novel, sterically congested PAHs.
Chemical communications (Cambridge, England), 2016, 52, 5534-5537
7118941 CIFC27 H43 Li N4P 1 21/c 116.526; 9.874; 18.038
90; 115.24; 90		2662.4Finkelmeier, Nils; Visscher, Arne; Wandtke, Sebastian; Herbst-Irmer, Regine; Stalke, Dietmar
CH3-deprotonation of 9-methylanthracene under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 5440-5442
7118942 CIFC69 H98 Li2 N8P 1 21/n 19.486; 34.841; 19.391
90; 93.77; 90		6394.9Finkelmeier, Nils; Visscher, Arne; Wandtke, Sebastian; Herbst-Irmer, Regine; Stalke, Dietmar
CH3-deprotonation of 9-methylanthracene under mild conditions.
Chemical communications (Cambridge, England), 2016, 52, 5440-5442
7118943 CIFC16 H14 N2 OP 21 21 216.4272; 11.7684; 18.3674
90; 90; 90		1389.27Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118944 CIFC16 H14 N2 OP 1 21 19.0535; 7.4148; 10.4203
90; 104.406; 90		677.52Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118945 CIFC16 H16 N2 OP 1 21 16.9841; 12.5978; 15.735
90; 97.885; 90		1371.3Laugeois, Maxime; Ponra, Sudipta; Ratovelomanana-Vidal, Virginie; Michelet, Véronique; Vitale, Maxime R.
Asymmetric preparation of polysubstituted cyclopentanes by synergistic Pd(0)/amine catalyzed formal [3+2] cycloadditions of vinyl cyclopropanes with enals.
Chemical communications (Cambridge, England), 2016, 52, 5332-5335
7118946 CIFC20 H15 N O3P 1 21/c 116.698; 5.9368; 15.65
90; 97.783; 90		1537.1Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118947 CIFC20 H14 Cl N O3P -16.977; 8.8337; 14.5708
93.367; 102.682; 108.417		823.26Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118948 CIFC19 H12 Cl N O2P 1 21/c 116.024; 15.055; 6.3189
90; 101.11; 90		1495.8Rathore, Kuldeep Singh; Lad, Bapurao Sudam; Chennamsetti, Haribabu; Katukojvala, Sreenivas
An unprecedented benzannulation of oxindoles with enalcarbenoids: a regioselective approach to functionalized carbazoles.
Chemical communications (Cambridge, England), 2016, 52, 5812-5815
7118949 CIFC113 H38 N2 O2 S2C 1 2/c 121.845; 16.43; 20.014
90; 107.937; 90		6834.2Li, Shu-Hui; Li, Zong-Jun; Nakagawa, Takafumi; Jeon, Il; Ju, Zheng; Matsuo, Yutaka; Gao, Xiang
Multifunctionalization of C70 at the two polar regions with a high regioselectivity via oxazolination and benzylation reactions.
Chemical communications (Cambridge, England), 2016, 52, 5710-5713
7118957 CIFC76 H68 Cl8 Fe2 N4 O4 P4 PtC 1 2/c 129.1376; 15.0037; 18.0317
90; 109.95; 90		7409.9Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118958 CIFC224 H188 Cl32 Fe6 N12 O12 P12 Pt4P -121.3085; 22.6838; 31.6313
90.2849; 90.4102; 117.182		13599.8Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118959 CIFC237 H201 Br8 Cl63 Fe6 N12 O12 P12 Pt4P -121.4683; 23.594; 32.9537
88.034; 89.129; 65.458		15174.9Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118960 CIFC61 H58 Cl2 N3 O4 P3 PtP -111.7999; 12.6886; 19.4168
83.953; 73.888; 87.375		2777.02Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118961 CIFC36 H30 Fe N2 O2 P2P 1 21/c 113.7346; 11.888; 9.9583
90; 104.743; 90		1572.4Masaki Ito; Masato Iseki; Masumi Itazaki; Hiroshi Nakazawa
Tetrahedral cage complex with planar vertices: selective synthesis of Pt4L6 cage complexes involving hydrogen bonds driven by halide binding
Chem.Commun., 2016, 52, 7205
7118962 CIFC7 H3 Cl F2 OP 1 21/n 13.8289; 14.522; 12.2527
90; 95.836; 90		677.76Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118963 CIFC7 H3 Cl F2 OP -17.4814; 8.5648; 10.7372
100.231; 95.404; 91.365		673.48Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118964 CIFC7 H3 Cl F2 OP 1 21/c 17.4388; 15.7661; 11.8282
90; 93.597; 90		1384.49Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118965 CIFC7 H4 Cl F OP n a 2113.8205; 12.5452; 3.8197
90; 90; 90		662.26Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118966 CIFC7 H5 Cl OP 1 21/n 17.4704; 3.9581; 22.3439
90; 93.566; 90		659.4Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118967 CIFC7 H3 Cl F2 OP -16.859; 7.2006; 8.0365
94.613; 104.275; 115.906		337.85Dhananjay Dey; Subhrajyoti Bhandary; Abhishek Sirohiwal; Venkatesha R. Hathwar; Deepak Chopra
'Conformational lock' via unusual intramolecular C-F^...^O[double bond, length as m-dash]C and C-H^...^Cl-C parallel dipoles observed in in situ cryocrystallized liquids
Chem.Commun., 2016, 52, 7225
7118968 CIFC20 H37 Gd Mn2 N8 O44 P4P 1 21/c 112.3; 19.75; 24.63
90; 95.3; 90		5958Javier Arinez-Soriano; Jorge Albalad; Christian Vila-Parrondo; Javier Perez-Carvajal; Sabina Rodriguez-Hermida; Aurelio Cabeza; Jordi Juanhuix; Inhar Imaz; Daniel Maspoch
Single-crystal and humidity-controlled powder diffraction study of the breathing effect in a metal-organic framework upon water adsorption/desorption
Chem.Commun., 2016, 52, 7229
7118969 CIFC20 H37 Gd Mn2 N8 O28 P4C 1 2/c 126.09; 14.51; 12.2
90; 110.19; 90		4335Javier Arinez-Soriano; Jorge Albalad; Christian Vila-Parrondo; Javier Perez-Carvajal; Sabina Rodriguez-Hermida; Aurelio Cabeza; Jordi Juanhuix; Inhar Imaz; Daniel Maspoch
Single-crystal and humidity-controlled powder diffraction study of the breathing effect in a metal-organic framework upon water adsorption/desorption
Chem.Commun., 2016, 52, 7229
7118970 CIFC30 H40 O4 SP 1 21 113.5064; 5.8689; 17.8643
90; 102.617; 90		1381.87Congde Huo; Yajun Wang; Yong Yuan; Fengjuan Chen; Jing Tang
Auto-oxidative hydroxysulfenylation of alkenes
Chem.Commun., 2016, 52, 7233
7118971 CIFC12 H9 F5 N2 O2 SP 1 21/c 111.8093; 10.6449; 10.6262
90; 91.185; 90		1335.52V. V. Khutorianskyi; M. Sonawane; M. Posta; B. Klepetarova; P. Beier
Oxidative nucleophilic aromatic amination of nitrobenzenes
Chem.Commun., 2016, 52, 7237
7118972 CIFC51 H23 Cu6 N3 O33C 1 2/c 132.27; 18.631; 23.512
90; 117.225; 90		12570Mingxing Zhang; Bin Li; Yunzhi Li; Qian Wang; Wenwei Zhang; Banglin Chen; Shuhua Li; Yi Pan; Xiaozeng You; Junfeng Bai
Finely tuning MOFs towards high performance in C2H2 storage: synthesis and properties of a new MOF-505 analogue with an inserted amide functional group
Chem.Commun., 2016, 52, 7241
7118973 CIFC26 H28 N2 O6 SP n a 2119.8378; 9.3737; 13.4463
90; 90; 90		2500.4Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118974 CIFC26 H27 F3 N2 O4 SP -19.9556; 14.589; 18.274
81.682; 76.959; 88.485		2558.4Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118975 CIFC28 H26 N2 O4 SP n a 2112.3454; 8.661; 22.8626
90; 90; 90		2444.5Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118976 CIFC30 H27 N3 O8 SP 1 21/n 114.3817; 10.8082; 19.0025
90; 109.283; 90		2788Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118977 CIFC26 H25 N3 O5 SP -19.3636; 10.8898; 12.521
99.75; 95.533; 107.818		1182.9Peng-Long Zhu; Xiang-Ying Tang; Min Shi
Intramolecular cyclizations of cyclopropenes with indole
Chem.Commun., 2016, 52, 7245
7118980 CIFC19 H36 B10 Cl2 N PP 1 21/c 19.8778; 19.2098; 16.2304
90; 101.765; 90		3015Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118981 CIFC19 H36 B10 N PP n m a17.159; 13.438; 11.014
90; 90; 90		2539.6Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118982 CIFC23 H42 B10 N O4 PP -110.3092; 10.9189; 16.0645
80.327; 73.798; 74.727		1666.41Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118983 CIFC38 H72 B20 N2 P2 SP -110.177; 10.4214; 25.2588
101.476; 99.642; 90.279		2586.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118984 CIFC38 H72 B20 N2 P2 SeP -110.2136; 10.4144; 25.274
101.61; 99.7572; 90.6407		2592.4Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118985 CIFC27 H56 B10 N3 P Si2P b c a18.683; 13.262; 31.5134
90; 90; 90		7808.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118986 CIFC19 H37 B10 Cl N PP n m a17.4405; 13.6893; 10.8979
90; 90; 90		2601.85Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118987 CIFC25 H55 B10 N2 P Si2P 1 21/c 117.4404; 12.4044; 18.5294
90; 115.893; 90		3606.2Tek Long Chan; Zuowei Xie
The synthesis, structure and reactivity of an imine-stabilized carboranylphosphorus(I) compound
Chem.Commun., 2016, 52, 7280
7118988 CIFC31 H24 Au Cl2 O PP b c a13.4335; 9.7044; 42.1106
90; 90; 90		5489.71Eric Omar Asomoza-Solis; Jonathan Rojas-Ocampo; Ruben Alfredo Toscano; Susana Porcel
Arenediazonium salts as electrophiles for the oxidative addition of gold(I)
Chem.Commun., 2016, 52, 7295
7118989 CIFC24 H19 Au Cl2 N O2 PP 1 21/n 19.36; 16.371; 16.662
90; 95.597; 90		2541Eric Omar Asomoza-Solis; Jonathan Rojas-Ocampo; Ruben Alfredo Toscano; Susana Porcel
Arenediazonium salts as electrophiles for the oxidative addition of gold(I)
Chem.Commun., 2016, 52, 7295
7118990 CIFC105 H143 K2 N12 O37 PP -116.775; 19.152; 20.418
93.782; 113.688; 106.847		5623.4Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118991 CIFC98 H128 K N16 O28 PP -114.99; 16.27; 25.088
99.668; 100.824; 105.587		5632Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118992 CIFC116 H174 N17 O27 PP -114.782; 19.415; 21.552
85.538; 85.989; 89.867		6151.4Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118993 CIFC360 H490 K8 N48 O133 S4P 1 21/c 116.6867; 19.4; 32.767
90; 112.755; 90		9781.8Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118994 CIFC97 H132 K2 N13 O35 SP 1 21/c 118.0761; 21.11; 32.803
90; 122.13; 90		10600.1Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118995 CIFC50 H75 Cl N10 O14C 1 c 120.611; 31.842; 8.872
90; 104.307; 90		5642Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118996 CIFC51 H78 Cl N9 O14P 1 21/c 118.572; 34.162; 8.774
90; 94.732; 90		5548Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118997 CIFC51 H68 I2 N10 O10P -112.275; 13.0629; 19.863
71.072; 78.86; 70.582		2828.3Liguo Ji; Zaiwen Yang; Yanxia Zhao; Meng Sun; Liping Cao; Xiao-Juan Yang; Yao-Yu Wang; Biao Wu
Sandwich phosphate complexes of macrocyclic tris(urea) ligands and their rotation around the anion
Chem.Commun., 2016, 52, 7310
7118998 CIFC29 H21 P SeP -19.4639; 10.1522; 14.1214
77.6074; 86.1247; 71.6074		1257.47Massimo Rigo; Manuela Weber; Christian Muller
Expanding the phosphorus-carbon analogy: formation of an unprecedented 5-phosphasemibullvalene derivative
Chem.Commun., 2016, 52, 7090
7118999 CIFC18 H9 B O3C 1 2/c 117.055; 10.409; 7.301
90; 111.071; 90		1209.4Yuichi Kitamoto; Takatsugu Suzuki; Yasuo Miyata; Hiroshi Kita; Kenji Funaki; Shuichi Oi
The first synthesis and X-ray crystallographic analysis of an oxygen-bridged planarized triphenylborane
Chem.Commun., 2016, 52, 7098
7119000 CIFC37 H33 N5 NiP 1 21/a 17.0843; 25.1223; 8.2327
90; 103.844; 90		1422.65Ryo Nozawa; Keitaro Yamamoto; Ichiro Hisaki; Ji-Young Shin; Hiroshi Shinokubo
Ni^II^ tetrahydronorcorroles: antiaromatic porphyrinoids with saturated pyrrole units
Chem.Commun., 2016, 52, 7106
7119001 CIFC14 H15 N O3P 1 21/c 114.579; 9.8759; 9.0753
90; 102.459; 90		1275.9Nicole S. Y. Loy; Subin Choi; Sunggak Kim; Cheol-Min Park
The synthesis of pyrroles and oxazoles based on gold alpha-imino carbene complexes
Chem.Commun., 2016, 52, 7336
7119002 CIFC14 H15 N3 O5I 1 2/a 130.509; 14.5498; 33.049
90; 91.858; 90		14663Nicole S. Y. Loy; Subin Choi; Sunggak Kim; Cheol-Min Park
The synthesis of pyrroles and oxazoles based on gold alpha-imino carbene complexes
Chem.Commun., 2016, 52, 7336
7119003 CIFC44 H65 B Br Cl9 F N2 PP 1 21/c 124.7264; 9.6603; 23.4725
90; 109.127; 90		5297.2Shubhanchi Nigam; Benjamin P. Burke; Laura H. Davies; Juozas Domarkas; Jennifer F. Wallis; Paul G. Waddell; Jennifer S. Waby; David M. Benoit; Anne-Marie Seymour; Christopher Cawthorne; Lee J. Higham; Stephen J. Archibald
Structurally optimised BODIPY derivatives for imaging of mitochondrial dysfunction in cancer and heart cells
Chem.Commun., 2016, 52, 7114
7119004 CIFC25 H28 Br N3 O3P 1 21 110.064; 8.502; 13.718
90; 100.284; 90		1154.9Jakob Blom; Tore Kiilerich Johansen; Frank Jensen; Karl Anker Jorgensen
Dynamic resolution of 2-cyclohexylidene acetaldehydes through organocatalytic dienamine [4+2] cycloaddition
Chem.Commun., 2016, 52, 7153
7119005 CIFC30 H27 N3 O4P 1 21 112.983; 10.976; 16.961
90; 99.955; 90		2380.6Jakob Blom; Tore Kiilerich Johansen; Frank Jensen; Karl Anker Jorgensen
Dynamic resolution of 2-cyclohexylidene acetaldehydes through organocatalytic dienamine [4+2] cycloaddition
Chem.Commun., 2016, 52, 7153
7119006 CIFC26 H24 N2 O6P 1 21/c 115.361; 4.955; 14.843
90; 98.245; 90		1118.1Kazuto Nakamura; Nobuhiro Yasuda; Hiromitsu Maeda
Dimension-controlled assemblies of modified bipyrroles stabilized by electron-withdrawing moieties
Chem.Commun., 2016, 52, 7157
7119007 CIFC30 H32 N2 O9P -17.9706; 10.519; 17.44
87.803; 86.847; 78.375		1429.5Kazuto Nakamura; Nobuhiro Yasuda; Hiromitsu Maeda
Dimension-controlled assemblies of modified bipyrroles stabilized by electron-withdrawing moieties
Chem.Commun., 2016, 52, 7157
7119008 CIFC40 H112 I3 N8 Nd O10 P4P -113.7969; 14.7646; 20.728
92.826; 108.606; 114.956		3544Sandeep K. Gupta; Thayalan Rajeshkumar; Gopalan Rajaraman; Ramaswamy Murugavel
An unprecedented zero field neodymium(III) single-ion magnet based on a phosphonic diamide
Chem.Commun., 2016, 52, 7168
7119009 CIFC54 H38 Cd N8 O4P -18.8932; 11.8369; 15.1942
72.926; 88.754; 88.696		1528.4Jian-Cheng Wang; Jian-Ping Ma; Qi-Kui Liu; Yu-Hong Hu; Yu-Bin Dong
Cd(II)-MOF-IM: post-synthesis functionalization of a Cd(II)-MOF as a triphase transfer catalyst
Chem.Commun., 2016, 52, 6989
7119010 CIFC22 H24 Co N4 O7 SP 1 21 111.479; 8.356; 12.079
90; 104.039; 90		1124Jian-Shen Feng; Min Ren; Zhong-Sheng Cai; Kun Fan; Song-Song Bao; Li-Min Zheng
Enantiopure phosphonic acids as chiral inducers: homochiral crystallization of cobalt coordination polymers showing field-induced slow magnetization relaxation
Chem.Commun., 2016, 52, 6877
7119011 CIFC22 H24 Co N4 O7 SP 1 21 111.495; 8.412; 12.098
90; 103.45; 90		1137.7Jian-Shen Feng; Min Ren; Zhong-Sheng Cai; Kun Fan; Song-Song Bao; Li-Min Zheng
Enantiopure phosphonic acids as chiral inducers: homochiral crystallization of cobalt coordination polymers showing field-induced slow magnetization relaxation
Chem.Commun., 2016, 52, 6877
7119012 CIFC55 H31 N3C c m 2113.9705; 34.3796; 8.1479
90; 90; 90		3913.4Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119013 CIFC61 H41 Cl4 N3 O4 ZnP 1 21/n 115.3452; 16.8828; 18.9071
90; 94.356; 90		4884.1Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119014 CIFC55 H31 N3P 21 2 218.9558; 11.4826; 21.7545
90; 90; 90		2237.1Helena Isla; Monika Srebro-Hooper; Marion Jean; Nicolas Vanthuyne; Thierry Roisnel; Jamie L. Lunkley; Gilles Muller; J. A. Gareth Williams; Jochen Autschbach; Jeanne Crassous
Conformational changes and chiroptical switching of enantiopure bis-helicenic terpyridine upon Zn^2+^ binding
Chem.Commun., 2016, 52, 5932
7119015 CIFC27 H18 Ag7 F15 N6 O10P -18.7316; 15.311; 16.873
72.77; 82.43; 86.08		2134.7Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119016 CIFC82 H96 Ag22 F48 O48.5 S16P 1 21/n 120.7; 23.694; 31.929
90; 92.38; 90		15647Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119017 CIFC128 H150 Ag34 F72 O74 S24P 1 21/c 126.341; 13.125; 36.552
90; 105.85; 90		12157Xin He; Hai-Xia Liu; Liang Zhao
Integration of acetylenic carbon clusters and silver clusters: template synthesis and stability enhancement
Chem.Commun., 2016, 52, 5682
7119018 CIFC15 H7 N4 O7 Zn2C m c m10.267; 32.086; 6.955
90; 90; 90		2291Yingli Hu; Meili Ding; Xiao-Qin Liu; Lin-Bing Sun; Hai-Long Jiang
Rational synthesis of an exceptionally stable Zn(II) metal-organic framework for the highly selective and sensitive detection of picric acid
Chem.Commun., 2016, 52, 5734
7119019 CIFC62 H89 Cl N4 O2 P2P 1 21/n 112.974; 31.717; 15.286
90; 95.96; 90		6256Yuzhong Wang; Hunter P. Hickox; Yaoming Xie; Pingrong Wei; Dongtao Cui; Melody R. Walter; Henry F. Schaefer III; Gregory H. Robinson
Protonation of carbene-stabilized diphosphorus: complexation of HP2+
Chem.Commun., 2016, 52, 5746
7119020 CIFC76 H76 O8P -111.4425; 11.4934; 13.0446
74.006; 71.922; 78.818		1556.65Bo Gao; Li-Li Tan; Nan Song; Ke Li; Ying-Wei Yang
A high-yield synthesis of [m]biphenyl-extended pillar[n]arenes for an efficient selective inclusion of toluene and m-xylene in the solid state
Chem.Commun., 2016, 52, 5804
7119021 CIFC78 H80 O8P -111.3535; 11.5292; 13.4501
70.421; 73.067; 78.916		1578.1Bo Gao; Li-Li Tan; Nan Song; Ke Li; Ying-Wei Yang
A high-yield synthesis of [m]biphenyl-extended pillar[n]arenes for an efficient selective inclusion of toluene and m-xylene in the solid state
Chem.Commun., 2016, 52, 5804
7119022 CIFC4 H6 N4 O3 S2P 1 21/n 14.7306; 21.6655; 8.1069
90; 103.803; 90		806.89Sounak Sarkar; Mysore S. Pavan; Suryanarayan Cherukuvada; Tayur N. Guru Row
Acetazolamide polymorphism: a case of hybridization induced polymorphism?
Chem.Commun., 2016, 52, 5820
7119023 CIFC28 H27 N O6P 1 21/c 112.3361; 16.8521; 12.0571
90; 112.1; 90		2322.38Ying Xie; Xun Chen; Xin Liu; Shi-Jian Su; Jianzhang Li; Wei Zeng
Rh(III)-catalyzed relay carbenoid functionalization of aromatic C-H bonds: access to pi-conjugated fused heteroarenes
Chem.Commun., 2016, 52, 5856
7119024 CIFC61.4 H43.6 Cl4 N2 O6.2P 6329.44; 29.44; 11.679
90; 90; 120		8766Midori Nagamoto; Daisuke Yamauchi; Takahiro Nishimura
Iridium-catalyzed asymmetric [3+2] annulation of aromatic ketimines with alkynes via C-H activation: unexpected inversion of the enantioselectivity induced by protic acids
Chem.Commun., 2016, 52, 5876
7119025 CIFC11 H10 N2 S2P -19.2746; 10.8353; 11.1364
91.652; 103.923; 90.151		1085.75M. S. C. Pedras; Q. H. To
Unveiling the first indole-fused thiazepine: structure, synthesis and biosynthesis of cyclonasturlexin, a remarkable cruciferous phytoalexin
Chem.Commun., 2016, 52, 5880
7119031 CIFC34.5 H23 Au2 Cl N2P 21 21 2113.3962; 19.3637; 22.587
90; 90; 90		5859.1Jin, Mingoo; Seki, Tomohiro; Ito, Hajime
Luminescent mechanochromism of a chiral complex: distinct crystal structures and color changes of racemic and homochiral gold( <scp>i</scp> ) isocyanide complexes with a binaphthyl moiety
Chem. Commun., 2016, 52, 8083-8086
7119032 CIFC34.25 H22.5 Au2 Cl0.5 N2P b c n13.0435; 18.7272; 23.6159
90; 90; 90		5768.6Jin, Mingoo; Seki, Tomohiro; Ito, Hajime
Luminescent mechanochromism of a chiral complex: distinct crystal structures and color changes of racemic and homochiral gold( <scp>i</scp> ) isocyanide complexes with a binaphthyl moiety
Chem. Commun., 2016, 52, 8083-8086
7119034 CIFC20 H57 B2 Li N2 P2 SnC m c m18.985; 10.8911; 14.8749
90; 90; 90		3075.6Maria Fernandez-Millan; Lucy K. Allen; Raul Garcia-Rodriguez; Andrew D. Bond; Marta E. G. Mosquera; Dominic S. Wright
Formation of a unique 'unsupported' hydridic stannate(II)
Chem.Commun., 2016, 52, 5993
7119035 CIFC216 H228 F96 N72 Sb16 Zn8P a -340.8424; 40.8424; 40.8424
90; 90; 90		68129Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119036 CIFC232 H240 Cd8 F48 N72 O48 S16P a -341.313; 41.313; 41.313
90; 90; 90		70512Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119037 CIFC240 H240 F39 Mn8 N84 P6.5P n -3 n :226.6801; 26.6801; 26.6801
90; 90; 90		18991.6Jing Yang; Xiao-Yong Chang; Kiu-Chor Sham; Shek-Man Yiu; Hoi-Lun Kwong; Chi-Ming Che
M8L12 cubic cages with all facial delta or facial lamda configuration: effects of surface anions on the occupancy of the cage and anion exchange
Chem.Commun., 2016, 52, 5981
7119038 CIFC20 H35 N3 O6P 21 21 219.1953; 15.9688; 16.377
90; 90; 90		2404.8Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119039 CIFC29 H49 N5 O8P 21 21 219.7107; 17.8054; 18.6925
90; 90; 90		3232Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119040 CIFC31 H52 Cl3 N5 O8P 21 21 219.5052; 17.583; 23.471
90; 90; 90		3922.7Mihye Lee; Jihyun Shim; Philjae Kang; Moon-Gun Choi; Soo Hyuk Choi
Stabilization of 11/9-helical alpha/beta-peptide foldamers in protic solvents
Chem.Commun., 2016, 52, 5950
7119041 CIFC26 H25 N O SP -18.28; 11.804; 12.324
64.811; 88.065; 80.753		1075Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi
Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation
Chem.Commun., 2016, 52, 5953
7119042 CIFC35 H42 O4 S3C 1 c 18.5603; 22.813; 17.3998
90; 94.2688; 90		3388.5Jia-Jia Zhao; Man Tang; Hong-Hao Zhang; Meng-Meng Xu; Feng Shi
Bronsted acid-catalyzed chemodivergent reactions of ortho-mercaptobenzyl alcohols with 3-alkyl-2-vinylindoles and styrenes: [5+2] cyclization versus hydroxysulfenylation
Chem.Commun., 2016, 52, 5953
7119043 CIFC20 H14 F4 N2 O2P -111.228; 12.46; 12.943
77.35; 89.67; 86.39		1763.2Yingle Liu; Ke Zhang; Yangen Huang; Shen Pan; Xiao-Qiang Liu; Yi Yang; Yan Jiang; Xiu-Hua Xu
Synthesis of 3-fluoroalkenyl-3-trifluoromethyl-2-oxindoles by the reaction of indoline-2,3-diones with difluoromethylene phosphabetaine
Chem.Commun., 2016, 52, 5969
7119044 CIFC14 H8 Fe N6 O2 PtC 1 2/c 115.667; 15.136; 7.3104
90; 110.57; 90		1623Tomoyuki Haraguchi; Kazuya Otsubo; Osami Sakata; Shogo Kawaguchi; Akihiko Fujiwara; Hiroshi Kitagawa
A three-dimensional accordion-like metal∓organic framework: synthesis and unconventional oriented growth on a surface
Chem.Commun., 2016, 52, 6017
7119045 CIFC23 H17 N O4 SP 1 21 18.33; 12.431; 9.528
90; 93.09; 90		985.2Zhuang Song; Yizhou Wu; Tao Xin; Chao Jin; Xiaoan Wen; Hongbin Sun; Qing-Long Xu
The Rh(II)-catalyzed formal N-S bond insertion reaction of aryldiazoacetates into N-phenyl-sulfenyl phthalimide
Chem.Commun., 2016, 52, 6079
7119046 CIFC467 Ag120 B4 Cl4 F64 N10 O45 S24 Si8C 1 2/m 143.889; 31.033; 26.186
90; 123.512; 90		29737Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak
Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors
Chem.Commun., 2016, 52, 6119
7119047 CIFC198 Ag46 B2 F8 N2 O14 S6P 1 21/n 119.8433; 28.203; 23.1207
90; 97.808; 90		12819.3Zi-Yi Chen; Dennis Y. S. Tam; Thomas C. W. Mak
Ethynide-stabilized high-nuclearity silver(I) sulfido molecular clusters assembled using organic sulfide precursors
Chem.Commun., 2016, 52, 6119
7119048 CIFC62.5 H75 Cl3 F5 N5 O WP 1 21/c 111.2444; 26.1267; 20.6154
90; 94.991; 90		6033.4Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119049 CIFC40.5 H58 Cl F6 N5 O6 S2 WP -111.7112; 20.3641; 21.9201
103.305; 97.459; 100.855		4913.7Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119050 CIFC55 H76 Cl2 N4 WP -110.5591; 13.627; 21.2326
86.879; 81.476; 88.576		3016.47Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119051 CIFC58.5 H79 Cl8 N5 WP 1 21/c 121.6865; 18.8737; 16.1005
90; 106.667; 90		6313.1Dominik A. Imbrich; Wolfgang Frey; Stefan Naumann; Michael R. Buchmeiser
Application of imidazolinium salts and N-heterocyclic olefins for the synthesis of anionic and neutral tungsten imido alkylidene complexes
Chem.Commun., 2016, 52, 6099
7119052 CIFC124 H90 F40 N12P -116.634; 18.391; 18.849
88.309; 76.986; 82.645		5571.9Won-Young Cha; Takanori Soya; Takayuki Tanaka; Hirotaka Mori; Yongseok Hong; Sangsu Lee; Kyu Hyung Park; Atsuhiro Osuka; Dongho Kim
Multifaceted [36]octaphyrin(1.1.1.1.1.1.1.1): deprotonation-induced switching among nonaromatic, Mobius aromatic, and Huckel antiaromatic species
Chem.Commun., 2016, 52, 6076
7119053 CIFC182 H256 N2 O16 P8 Ru4P 1 21/c 116.1117; 26.6027; 21.6003
90; 100.029; 90		9116.7Daniel Fink; Bernhard Weibert; Rainer F. Winter
Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism
Chem.Commun., 2016, 52, 6103
7119054 CIFC148 H234 Cl16 N2 O16 P8 Ru4P -111.6168; 16.816; 23.594
94.41; 99.289; 107.587		4297.1Daniel Fink; Bernhard Weibert; Rainer F. Winter
Redox-active tetraruthenium metallacycles: reversible release of up to eight electrons resulting in strong electrochromism
Chem.Commun., 2016, 52, 6103
7119055 CIFC72 H64 Cl4 N2 P2 Ru2P 110.3736; 13.2432; 13.7718
99.178; 107.636; 97.263		1748.99Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119056 CIFC40 H42 N2 O RuP 1 21/c 19.121; 15.475; 21.72
90; 92.615; 90		3062.5Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119057 CIFC56 H73 K N2 O8 RuP 1 21/c 111.8733; 24.8708; 17.2324
90; 95.965; 90		5061.1Demyan E. Prokopchuk; Alan J. Lough; Rafael E. Rodriguez-Lugo; Robert H. Morris; Hansjorg Grutzmacher
Insights into metal-ligand hydrogen transfer: a square-planar ruthenate complex supported by a tetradentate amino-amido-diolefin ligand
Chem.Commun., 2016, 52, 6138
7119058 CIFC35 H39 Br N2 O9P 21 21 2112.919; 15.875; 17.332
90; 90; 90		3554.6Bo-Liang Zhao; Da-Ming Du
Organocatalytic cascade Michael/Michael reaction for the asymmetric synthesis of spirooxindoles containing five contiguous stereocenters
Chem.Commun., 2016, 52, 6162
7119059 CIFC30 H27.5 F6 N2.5 O6 S2P 1 21 111.6454; 12.5993; 21.7275
90; 104.608; 90		3084.9Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour
Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering
Chem.Commun., 2016, 52, 6257
7119060 CIFC28 H29 I2 N3 O2P 21 21 217.9386; 17.6476; 19.6814
90; 90; 90		2757.31Jaroslav Sebestik; Filip Teply; Ivana Cisarova; Jan Vavra; Dusan Koval; Petr Bour
Intense chirality induction in nitrile solvents by a helquat dye monitored by near resonance Raman scattering
Chem.Commun., 2016, 52, 6257
7119061 CIFC41 H38 Dy F9 N14 O9 S3P b c a20.8179; 19.5864; 24.4923
90; 90; 90		9986.7Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong
Lanthanoid single-ion magnets with the LnN10 coordination geometry
Chem.Commun., 2016, 52, 6261
7119062 CIFC41 H38 Er F9 N14 O9 S3P b c a20.69; 19.5456; 24.427
90; 90; 90		9878.2Zhong-Xia Jiang; Jun-Liang Liu; Yan-Cong Chen; Jiang Liu; Jian-Hua Jia; Ming-Liang Tong
Lanthanoid single-ion magnets with the LnN10 coordination geometry
Chem.Commun., 2016, 52, 6261
7119064 CIFC40 H40 Cl4 Cu4 N2 P2P 1 21/c 111.1272; 13.525; 13.4866
90; 104.147; 90		1968.11Xu-Lin Chen; Rongmin Yu; Xiao-Yuan Wu; Dong Liang; Ji-Hui Jia; Can-Zhong Lu
A strongly greenish-blue-emitting Cu4Cl4 cluster with an efficient spin-orbit coupling (SOC): fast phosphorescence versus thermally activated delayed fluorescence
Chem.Commun., 2016, 52, 6288
7119065 CIFC22 H18 N2 O3 SP 1 21/n 19.4353; 17.316; 11.6428
90; 92.321; 90		1900.7Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119066 CIFC23 H18 N2 O3 S2P 1 21/c 118.929; 12.43; 8.472
90; 91.235; 90		1992.9Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119067 CIFC29 H36 Au F6 N3 O4 S2P 32 2 111.4418; 11.4418; 23.88
90; 90; 120		2707.4Ming Chen; Ning Sun; Haoyi Chen; Yuanhong Liu
Dioxazoles, a new mild nitrene transfer reagent in gold catalysis: highly efficient synthesis of functionalized oxazoles
Chem.Commun., 2016, 52, 6324
7119068 CIFC94.45 H106.45 N6 P2P -112.2213; 16.2437; 22.0973
97.7; 93.029; 106.714		4144.2Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119069 CIFC56.95 H58.95 Au Cl N2 P2P -110.94; 11.9932; 21.421
87.907; 76.158; 65.57		2478.4Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119070 CIFC51 H53 Au1.33 Cl1.33 N2 P2P -111.168; 12.029; 18.686
94.538; 94.411; 114.833		2254.1Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119071 CIFC51 H53 Au1.44 Cl1.44 N2 P2P -111.243; 12.0524; 18.7795
94.113; 94.288; 114.879		2287.1Alexander Hinz; Axel Schulz; Alexander Villinger
On the behaviour of biradicaloid [P(mu-NTer)]2 towards Lewis acids and bases
Chem.Commun., 2016, 52, 6328
7119072 CIFC25 H14 F N O4P 1 21/c 19.7639; 19.413; 10.4751
90; 105.633; 90		1912.1Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119073 CIFC26 H17 N O5P 21 21 2111.2312; 16.239; 22.524
90; 90; 90		4108Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119074 CIFC25 H13 F2 N O4P 1 21/c 110.033; 19.091; 10.544
90; 107.453; 90		1926.6Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119075 CIFC25 H13 Cl F N O4P -19.9815; 10.7217; 10.8522
66.536; 86.529; 76.874		1036.9Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119076 CIFC20 H12 F N O5P -111.727; 12.81; 12.935
103.837; 115.433; 91.903		1683.3Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119077 CIFC21 H14 Cl N O5C 1 2/c 122.142; 15.2704; 12.2599
90; 115.973; 90		3726.6Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119078 CIFC30 H21 N3 O5P 1 21/c 112.8577; 14.7678; 16.2529
90; 112.154; 90		2858.3Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119079 CIFC25 H17 Cl N2 O5P 1 21/n 111.783; 13.245; 15.8627
90; 94.265; 90		2468.8Rong-Guo Shi; Xiao-Hua Wang; Ruzhang Liu; Chao-Guo Yan
Two-carbon ring expansion of isatin: a convenient construction of a dibenzo[b,d]azepinone scaffold
Chem.Commun., 2016, 52, 6280
7119080 CIFC27 H39 Cl Cu NP 1 21/c 115.9209; 19.4144; 16.2447
90; 103.631; 90		4879.72Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119081 CIFC27.5 H40 Cl Cu I NP -111.1918; 11.9685; 20.7901
101.52; 94.798; 94.419		2706.59Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119082 CIFC27 H39 Br Cu NP 1 21/c 116.0878; 19.4137; 16.2912
90; 103.54; 90		4946.71Alexander S. Romanov; Dawei Di; Le Yang; Julio Fernandez-Cestau; Ciaran R. Becker; Charlotte E. James; Bonan Zhu; Mikko Linnolahti; Dan Credgington; Manfred Bochmann
Highly photoluminescent copper carbene complexes based on prompt rather than delayed fluorescence
Chem.Commun., 2016, 52, 6379
7119083 CIFC18 H14 FeP 1 21/c 113.4447; 19.4178; 9.8391
90; 91.496; 90		2567.8Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno
Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes
Chem.Commun., 2016, 52, 6419
7119084 CIFC19 H16 Fe OP 41 21 27.8273; 7.8273; 47.227
90; 90; 90		2893.4Antonio Urbano; Gloria Hernandez-Torres; Ana M. del Hoyo; Alicia Martinez-Carrion; M. Carmen Carreno
Mild access to planar-chiral ortho-condensed aromatic ferrocenes via gold(I)-catalyzed cycloisomerization of ortho-alkynylaryl ferrocenes
Chem.Commun., 2016, 52, 6419
7119085 CIFC122 H74 B2 F48 Pd4P -113.2706; 15.2693; 16.3133
101.437; 110.526; 102.271		2887.5Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119086 CIFC128 H78 B2 Cl2 F48 Pd4P -114.2381; 15.6226; 28.2509
81.3277; 79.8346; 77.6849		6001.1Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119087 CIFC153 H106 B2 Cl2 F48 Pd4P 1 21 118.5114; 21.0181; 19.5326
90; 111.452; 90		7073.2Kohei Masai; Katsunori Shirato; Koji Yamamoto; Yuki Kurashige; Tetsuro Murahashi
A mechanistic insight into metal-cluster pi-envelopment: a dual binding mode involving bent and planar ligand-conformers
Chem.Commun., 2016, 52, 6427
7119088 CIFC27 H21 Au B Cl F4 N PP 1 21/c 110.394; 16.6422; 15.389
90; 108.771; 90		2520.39Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119089 CIFC27 H20 Au B Cl2 F4 N PP -19.3558; 11.4552; 13.9422
86.4666; 70.5144; 67.9291		1301.94Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119090 CIFC26.5 H38.5 Au Cl6.5 F3 PP 1 21/c 112.1272; 14.5748; 18.6371
90; 96.632; 90		3272.09Long Huang; Frank Rominger; Matthias Rudolph; A. Stephen K. Hashmi
A general access to organogold(III) complexes by oxidative addition of diazonium salts
Chem.Commun., 2016, 52, 6435
7119091 CIFC12 H28.5 B10 Br N2.5P 1 21/c 17.6257; 25.7293; 10.2076
90; 92.279; 90		2001.19Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119092 CIFC11 H27 B9 N2P 1 21/c 115.6541; 13.7503; 18.375
90; 115.101; 90		3581.7Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119093 CIFC31 H55 B9 N4 Rh2P b c a11.9249; 23.7834; 25.2349
90; 90; 90		7157Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119094 CIFC32 H58 B9 N3 O Rh2P -111.1781; 12.5631; 14.8258
111.322; 92.917; 105.326		1845.32Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119095 CIFC29 H54 B9 N2 O0.5 Rh2P -110.7898; 11.4212; 14.8764
71.73; 83.274; 69.415		1629.6Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119096 CIFC19 H38 B10 Cl N2 RhP 1 21/c 112.3894; 15.3629; 13.6908
90; 93.441; 90		2601.17Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119097 CIFC19 H37 B10 N2 RhP 1 21/c 117.2832; 10.5283; 14.1775
90; 113.02; 90		2374.34Jordan Holmes; Christopher M. Pask; Mark A. Fox; Charlotte E. Willans
Tethered N-heterocyclic carbene-carboranes: unique ligands that exhibit unprecedented and versatile coordination modes at rhodium
Chem.Commun., 2016, 52, 6443
7119098 CIFC27 H38 O3P 1 21 15.8458; 12.3784; 16.7657
90; 98.058; 90		1201.22Qiqiao Lin; Yuanzhen Li; Deb Kumar Das; Guoxiang Zhang; Zhifei Zhao; Shuang Yang; Xinqiang Fang
N-Heterocyclic carbene-catalyzed desymmetrization of functionalized 1,4-dienes via Stetter Reaction
Chem.Commun., 2016, 52, 6459
7119099 CIFC384 H288 Cu4.8 N288 Zn43.2I a -3 d34.4885; 34.4885; 34.4885
90; 90; 90		41022.6Xiao-Wei Zhu; Xiao-Ping Zhou; Dan Li
Exceptionally water stable heterometallic gyroidal MOFs: tuning the porosity and hydrophobicity by doping metal ions
Chem.Commun., 2016, 52, 6513
7119102 CIFC47 H82 O5 Si4P -111.8267; 13.4665; 18.3608
106.876; 92.299; 109.501		2607.2Jian Zhang; Hong Kang; Jacob Martin; Shouhai Zhang; Sylvie Thomas; Tim C. Merkel; Jianyong Jin
The enhancement of chain rigidity and gas transport performance of polymers of intrinsic microporosity via intramolecular locking of the spiro-carbon
Chem.Commun., 2016, 52, 6553
7119103 CIFC16 H28 O3P 21 21 216.67202; 12.80551; 18.3291
90; 90; 90		1566.01Yajun Ren; Marc Presset; Jeremy Godemert; Nicolas Vanthuyne; Jean-Valere Naubron; Michel Giorgi; Jean Rodriguez; Yoann Coquerel
A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone
Chem.Commun., 2016, 52, 6565
7119114 CIFC17 H16 F3 N O4 SP -19.3925; 9.5682; 10.9216
73.528; 66.26; 85.458		860.9Zhi-Wei Yang; Qi Zhang; Yuan-Ye Jiang; Lei Li; Bin Xiao; Yao Fu
Palladium-catalyzed directing group-assisted C8-triflation of naphthalenes
Chem.Commun., 2016, 52, 6709
7119115 CIFC45 H68 O3 S Sm2P 1 21/c 110.7989; 23.324; 18.592
90; 106.381; 90		4492.7Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119116 CIFC45 H68 O2 S2 Sm2P 1 21/n 118.588; 23.602; 21.654
90; 107.26; 90		9072Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119117 CIFC44 H68 O4 S Sm2P 1 21/c 117.824; 16.299; 16.056
90; 108.56; 90		4421.9Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119118 CIFC50 H70 N2 O4 S Sm2P 1 21/n 116.952; 13.879; 20.819
90; 90.81; 90		4897.7Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119119 CIFC68 H86 O4 Sm2P -110.561; 10.7; 15.035
110.25; 97.77; 98.73		1542.9Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119120 CIFC44 H66 N2 O8 Re2 Sm2P b c a16.207; 14; 21.465
90; 90; 90		4870.4Christoph Schoo; Svetlana V. Klementyeva; Michael T. Gamer; Sergey N. Konchenko; Peter W. Roesky
Samarocene oxide: from an undesired decomposition product to a new reagent
Chem.Commun., 2016, 52, 6654
7119121 CIFC34 H25 B OP -19.7747; 11.2285; 12.079
86.4386; 70.8147; 85.0255		1246.59Sam Yruegas; Dayna C. Patterson; Caleb D. Martin
Oxygen insertion into boroles as a route to 1,2-oxaborines
Chem.Commun., 2016, 52, 6658
7119122 CIFC40 H29 B OP -110.5923; 11.7946; 12.5909
91.8608; 94.7506; 113.478		1434.13Sam Yruegas; Dayna C. Patterson; Caleb D. Martin
Oxygen insertion into boroles as a route to 1,2-oxaborines
Chem.Commun., 2016, 52, 6658
7119123 CIFC12 H11 Cl N2 O5 SP -19.5347; 10.4694; 15.6057
92.938; 107.085; 116.622		1300.34Cory M. Widdifield; Harry Robson; Paul Hodgkinson
Furosemide's one little hydrogen atom: NMR crystallography structure verification of powdered molecular organics
Chem.Commun., 2016, 52, 6685
7119124 CIFC31 H20 N2 OP 1 21/n 115.6295; 11.7772; 23.646
90; 100.375; 90		4281.4Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119125 CIFC35 H22 N2 OP 1 21 110.417; 7.846; 15.614
90; 109.024; 90		1206.5Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119126 CIFC31 H20 N2 O3P 1 21/n 110.4123; 10.6141; 22.372
90; 101.14; 90		2425.9Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119127 CIFC31 H19.46 Cl0.08 N2 OP 1 21/n 115.6018; 11.8059; 23.666
90; 100.492; 90		4286.2Katsuya Mutoh; Yoichi Kobayashi; Yasukazu Hirao; Takashi Kubo; Jiro Abe
Stealth fast photoswitching of negative photochromic naphthalene-bridged phenoxyl-imidazolyl radical complexes
Chem.Commun., 2016, 52, 6797
7119128 CIFC24 H21 N O4 SP 1 21/c 110.284; 26.1213; 15.8601
90; 102.69; 90		4156.4Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang
Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides
Chem.Commun., 2016, 52, 6801
7119129 CIFC30 H25 N O4 SP -112.2963; 13.8393; 16.8203
71.704; 82.18; 66.12		2484.87Hongxu Liu; Yanyan Yang; Jie Wu; Xiao-Na Wang; Junbiao Chang
Regioselective synthesis of 3,4-disubstituted isocoumarins through the Pd-catalyzed annulation of 2-iodoaromatic acids with ynamides
Chem.Commun., 2016, 52, 6801
7119130 CIFC40 H32 Cl4 P2 PdP 1 21/c 19.8924; 19.0871; 19.8273
90; 100.618; 90		3679.63Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119131 CIFC41 H32 Cl8 P2 PtP 1 21 19.9582; 21.3845; 10.1108
90; 103.135; 90		2096.78Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119132 CIFC82 H68 Au2 Cl4 O P4P -112.7889; 16.392; 19.0982
93.515; 96.512; 112.335		3655.6Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119133 CIFC40 H32 Au2 Cl4 P2P 1 21/n 112.6409; 16.973; 18.0808
90; 104.661; 90		3753Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119134 CIFC39.5 H31 Au2 Cl3 P2C 1 2 134.8; 9.8414; 10.8355
90; 96.507; 90		3687Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119135 CIFC39.5 H31 Au2 Cl3 P2C 1 2 134.8079; 9.8397; 10.8227
90; 96.441; 90		3683.4Avassaya Vanitcha; Cecilia Damelincourt; Geoffrey Gontard; Nicolas Vanthuyne; Virginie Mouries-Mansuy; Louis Fensterbank
Bis-phosphine allene ligand: coordination chemistry and preliminary applications in catalysis
Chem.Commun., 2016, 52, 6785
7119136 CIFC38 H62 Li4 N2 O4P -18.7871; 9.5833; 13.1959
104.353; 93.696; 116.282		945.63Quentin Dufrois; Laure Vendier; Michel Etienne
alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives
Chem.Commun., 2016, 52, 6781
7119137 CIFC33 H49 Li2 O3P -18.5802; 9.438; 20.2265
80.998; 82.494; 70.198		1516.79Quentin Dufrois; Laure Vendier; Michel Etienne
alpha-CC agostic structures and aggregation diversity in cyclopropyllithium derivatives
Chem.Commun., 2016, 52, 6781
7119138 CIFC39 H32 B2 F12 N2 S2P 1 2/c 117.8505; 8.3333; 13.1813
90; 104.671; 90		1896.84Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene
Chem.Commun., 2016, 52, 6885
7119139 CIFC39 H34 B2 F12 N2 O S2P 1 21/c 19.7143; 32.9243; 11.9342
90; 96.4166; 90		3793.08Kazuki Takase; Kengo Hyodo; Masakazu Morimoto; Yuko Kojima; Hiroyuki Mayama; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
Photoinduced reversible formation of a superhydrophilic surface by crystal growth of diarylethene
Chem.Commun., 2016, 52, 6885
7119140 CIFC20 H23 N O3P 21 21 218.6053; 11.6403; 17.468
90; 90; 90		1749.7Yuan-Ming Sun; Peng Gu; Yu-Ning Gao; Qin Xu; Min Shi
Gold(I) catalyzed tandem cyclization of propargylic esters to 4-acyloxy-1,2-dihydroquinolines
Chem.Commun., 2016, 52, 6942
7119141 CIFC21 H29 F6 Ir N O PP 21 21 217.0929; 15.6774; 20.8647
90; 90; 90		2320.12Ross A. Arthurs; Peter N. Horton; Simon J. Coles; Christopher J. Richards
Metallocene to metallocene conversion. Synthesis of an oxazoline-substituted pentamethyliridocenium cation from a ferrocenyloxazoline
Chem.Commun., 2016, 52, 7024
7119142 CIFC14 H8 F2 N4P 1 21/c 14.375; 20.1126; 13.1678
90; 98.317; 90		1146.48Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119143 CIFC14 H9 N3 OP c a 2121.401; 4.7059; 10.6453
90; 90; 90		1072.1Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119144 CIFC16 H14 N4P 1 21/n 15.9753; 15.9285; 13.447
90; 90.062; 90		1279.9Erchang Shang; Junzhi Zhang; Jinyi Bai; Zhan Wang; Xiang Li; Bing Zhu; Xiaoguang Lei
Syntheses of [1,2,4]triazolo[1,5-a]benzazoles enabled by the transition-metal-free oxidative N-N bond formation
Chem.Commun., 2016, 52, 7028
7119145 CIFC38 H42 F10 P2 Pt ZnP 1 21/n 110.9506; 19.9969; 17.6775
90; 96.054; 90		3849.4Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley
Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand
Chem.Commun., 2016, 52, 7039
7119146 CIFC51 H42 F10 N2 Pt ZnP 1 21/c 112.995; 16.7483; 21.185
90; 106.136; 90		4429.1Allegra L. Liberman-Martin; Daniel S. Levine; Micah S. Ziegler; Robert G. Bergman; T. Don Tilley
Lewis acid-base interactions between platinum(II) diaryl complexes and bis(perfluorophenyl)zinc: strongly accelerated reductive elimination induced by a Z-type ligand
Chem.Commun., 2016, 52, 7039
7119147 CIFC56 H40 BP 1 21/c 114.436; 9.801; 28.668
90; 100.42; 90		3989Holger Braunschweig; Ivo Krummenacher; Lisa Mailander; Leanne Pentecost; Alfredo Vargas
Formation of a stable radical by oxidation of a tetraorganoborate
Chem.Commun., 2016, 52, 7005
7119148 CIFC40.17 H62.43 Na2 O28P 1 21 16.6058; 24.886; 14.6272
90; 102.224; 90		2350.08Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119149 CIFC21 H34 Na O13.5P 1 21 16.6503; 24.44; 14.717
90; 101.39; 90		2344.9Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119150 CIFC20.45 H30.90 Na O14.46P 1 21 16.6481; 24.625; 14.756
90; 102.798; 90		2355.7Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119151 CIFC20.29 H30.59 Na O14P 1 21 16.6239; 24.772; 14.6783
90; 102.43; 90		2352.1Guo-Hong Ning; Kazuki Matsumura; Yasuhide Inokuma; Makoto Fujita
A saccharide-based crystalline sponge for hydrophilic guests
Chem.Commun., 2016, 52, 7013
7119152 CIFC2 H6 CdP 42/m n m7.195; 7.195; 4.118
90; 90; 90		213.2Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119153 CIFC2 H6 CdP 1 21/n 17.483; 7.711; 7.734
90; 115.85; 90		401.6Hanke, Felix; Hindley, Sarah; Jones, Anthony C.; Steiner, Alexander
The solid state structures of the high and low temperature phases of dimethylcadmium
Chemical Communications, 2016, 52, 10144
7119160 CIFC13 H16 N2 O7P 1 21/c 112.554; 8.8499; 12.6253
90; 103.988; 90		1361.1Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119161 CIFC7 H8 O6P 1 21/n 13.6803; 27.724; 9.3579
90; 94.397; 90		952Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119162 CIFC15 H13 N3 O4 SP -17.8557; 10.1043; 10.4713
80.602; 68.952; 69.742		727.01Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119163 CIFC15 H13 N3 O4 SP -112.6899; 14.6928; 20.5097
84.866; 74.669; 84.683		3663.7Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119164 CIFC46 H43 N9 O13 S3P -17.0374; 12.917; 25.467
84.077; 89.174; 83.327		2287Lynne H. Thomas; Craig Wales; Chick C. Wilson
Selective preparation of elusive and alternative single component polymorphic solid forms through multi-component crystallisation routes
Chem.Commun., 2016, 52, 7372
7119165 CIFC16 H15 N OP b c a9.0171; 11.0071; 23.9483
90; 90; 90		2376.9Vijay K. Srirambhatla; Rui Guo; Sarah L. Price; Alastair J. Florence
Isomorphous template induced crystallisation: a robust method for the targeted crystallisation of computationally predicted metastable polymorphs
Chem.Commun., 2016, 52, 7384
7119166 CIFC26 H16 S2P 1 21/n 115.113; 7.708; 16.178
90; 94; 90		1880Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119167 CIFC26 H16 S2C 1 2/c 117.08; 11.919; 19.8
90; 104.04; 90		3910.4Haichao Liu; Liang Yao; Bao Li; Xiankai Chen; Yu Gao; Shitong Zhang; Weijun Li; Ping Lu; Bing Yang; Yuguang Ma
Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime
Chem.Commun., 2016, 52, 7356
7119168 CIFC22 H23 N3 O4P 1 21/n 110.9129; 7.8194; 22.428
90; 97.304; 90		1898.3Haiyan Yu; Wang Ren; Hongguang Lu; Yanan Liang; Qiusheng Wang
Synthesis and piezochromic luminescence study of a coumarin hydrozone compound
Chem.Commun., 2016, 52, 7387
7119169 CIFC21 H11 F26 N O2P -112.37; 12.834; 18.49
98.783; 91.487; 104.872		2797.3Yohei Haketa; Ryota Takasago; Hiromitsu Maeda
beta-Perfluoroalkyl-substituted pyrrole as an anion-responsive pi-electronic system through a single NH moiety
Chem.Commun., 2016, 52, 7364
7119170 CIFC132 H108 Cd4 N20 O12C 1 2/c 131.093; 34.507; 24.271
90; 128.646; 90		20339Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119171 CIFC70 H56 B Cd2 F4 N10 O8I b a m12.5188; 15.3848; 42.5644
90; 90; 90		8197.9Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119172 CIFC105 H69 Cd3 F9 N15 O24 Re3R 3 c :H18.6042; 18.6042; 51.5285
90; 90; 120		15445.4Thirumurugan Prakasam; Rana A. Bilbeisi; Matteo Lusi; John-Carl Olsen; Carlos Platas-Iglesias; Ali Trabolsi
Post-synthetic modifications of cadmium-based knots and links
Chem.Commun., 2016, 52, 7398
7119173 CIFC64 H60 F3 N12 O52 P W12 Zn2P 4/n :219.5965; 19.5965; 16.078
90; 90; 90		6174.32Jian-Zhen Liao; Chen Wu; Xiao-Yuan Wu; Shui-Quan Deng; Can-Zhong Lu
Exceptional photosensitivity of a polyoxometalate-based charge-transfer hybrid material
Chem.Commun., 2016, 52, 7394
7119174 CIFC18 H16 O4P 1 21/c 111.891; 16.2219; 15.2941
90; 93.262; 90		2945.4Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119175 CIFC19 H18 O4P 1 21/n 15.7294; 16.4971; 16.9275
90; 96.391; 90		1590Rajkumar Lalji Sahani; Rai-Shung Liu
Gold-catalyzed [4+3] and [4+4]-annulation reactions of t-butyl propiolate derivatives with epoxides and oxetanes for the construction of 1,4-dioxepane and 1,5-dioxocane cores
Chem.Commun., 2016, 52, 7482
7119176 CIFMn1.5 N O13 V4P 1 2/m 18.2011; 3.5207; 9.9129
90; 110.987; 90		267.234Martin K. Dufficy; Lan Luo; Peter S. Fedkiw; Paul A. Maggard
Vacancy-induced manganese vanadates and their potential application to Li-ion batteries
Chem.Commun., 2016, 52, 7509
7119177 CIFC12 H8 Co3 K O20I -4 2 d13.0691; 13.0691; 30.157
90; 90; 90		5150.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119178 CIFC12 H8 Co3 K O18I -4 2 d13.0005; 13.0005; 30.2002
90; 90; 90		5104.2Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119179 CIFC12 H8 Co3 K O18I -4 2 d12.8201; 12.8201; 30.2685
90; 90; 90		4974.8Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119180 CIFC12 H8 Co3 K O18I -4 2 d12.6111; 12.6111; 30.2999
90; 90; 90		4818.9Jack Binns; Konstantin V. Kamenev; Katie E. R. Marriott; Garry J. McIntyre; Stephen A. Moggach; Mark Murrie; Simon Parsons
A non-topological mechanism for negative linear compressibility
Chem.Commun., 2016, 52, 7486
7119181 CIFC21 H20 O4P 21 21 215.9638; 7.4011; 40.7678
90; 90; 90		1799.44Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119182 CIFC39 H38 N O P SP 21 21 218.966; 10.6824; 34.6972
90; 90; 90		3323.2Wei Zhou; Peng Chen; Mengna Tao; Xiao Su; Qingjie Zhao; Junliang Zhang
Enantioselective intermolecular cross Rauhut-Currier reactions of activated alkenes with acrolein
Chem.Commun., 2016, 52, 7612
7119183 CIFC16 H21 B Fe O2P 1 21/n 112.7414; 7.5452; 15.8499
90; 104.524; 90		1475.06Anis Tlili; Arnaud Voituriez; Angela Marinetti; Pierre Thuery; Thibault Cantat
Synergistic effects in ambiphilic phosphino-borane catalysts for the hydroboration of CO2
Chem.Commun., 2016, 52, 7553
7119350 CIFC6 Cl8 N10 O8P 1 21/c 16.1067; 13.7465; 12.4167
90; 96.024; 90		1036.57Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119351 CIFC4 H2 Cl2 N10 O8P 1 21/c 110.3037; 9.6323; 14.3934
90; 107.927; 90		1359.17Srinivas, Dharavath; Mitchell, Lauren A.; Parrish, Damon A.; Shreeve, Jean'ne M.
From FOX-7 to H-FOX to insensitive energetic materials with hypergolic properties
Chemical Communications, 2016, 52, 7668-7671
7119352 CIFC47 H43 Ag3 F6 N12 O7 S2P -112.88; 13.13; 15.88
99.38; 90.29; 101.76		2592Hui; Guo; Xin; He; Chong-Qing; Wan; Liang; Zhao
A stepwise bulk-to-cluster-to-particle transformation toward the efficient synthesis of alkynyl-protected silver nanoclusters
Chem.Commun., 2016, 52, 7723
7119353 CIFC24 H27 Br O5P 1 21 111.882; 6.1817; 15.84
90; 108.485; 90		1103.4Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119354 CIFC43 H44 N3 O5 RhP 21 21 2112.6831; 13.3648; 25.5629
90; 90; 90		4333.1Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119355 CIFC24 H27 Br O5P 21 21 216.202; 12.159; 30.276
90; 90; 90		2283.12Liangliang; Song; Lei; Gong; Eric; Meggers
Asymmetric dual catalysis via fragmentation of a single rhodium precursor complex
Chem.Commun., 2016, 52, 7699
7119356 CIFC12 H8 I2 N O3C 1 2/c 117.6; 4.372; 34.3
90; 97.444; 90		2617Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119357 CIFC24 H16 Cl4 N2 O6P -13.795; 14.7; 21.4
80.7; 89.35; 89.09		1178Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119358 CIFC11 H8 Br2 N OP -14.183; 8.769; 15.366
94.1; 95.78; 99.68		550.5Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119359 CIFC9 H6 Cl2 N O3P -13.777; 10.382; 13.45
68.43; 85.15; 80.26		483.3Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119360 CIFC9 H6 I2 N O3C 1 2/c 127.78; 4.706; 17.566
90; 96.051; 90		2284Subhankar; Saha; Gautam; R.; Desiraju
Using structural modularity in cocrystals to engineer properties: elasticity
Chem.Commun., 2016, 52, 7676
7119361 CIFC91.75 H99.7 Cl12.48 N14.43 O4.45 Pd6 S0.48P 1 21/c 119.6264; 52.3974; 14.3627
90; 90.6803; 90		14769.2Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119362 CIFC43 H52 Cl8 N6 O4 Pd3P 1 21/c 119.5796; 52.142; 14.2469
90; 91.162; 90		14541.9Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119363 CIFC94.65 H105.36 Cl12 N16.29 O3.82 Pd6 S0.41P 1 21/c 119.5493; 51.784; 14.2759
90; 90.7569; 90		14450.8Shohei; Tashiro; Hirotaka; Yonezawa; Ryou; Kubota; Tsutomu; Umeki; Mitsuhiko; Shionoya
Non-covalent immobilisation of p-toluenesulfonic acid in a porous molecular crystal for size-specific acid-catalysed reactions
Chem.Commun., 2016, 52, 7657
7119373 CIFC13 H17 N3 O3 S2P b c a10.4816; 12.7531; 22.3603
90; 90; 90		2989Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119374 CIFC32 H62 N4 O5 S3P -15.7565; 10.7037; 31.057
87.126; 85.544; 86.192		1901.7Celia; Ruiz-Palomero; Stuart; R.; Kennedy; M.; Laura; Soriano; Christopher; D.; Jones; Miguel; Valcarcel; Jonathan; W.; Steed
Pharmaceutical crystallization with nanocellulose organogels
Chem.Commun., 2016, 52, 7782
7119375 CIFC20 H15 N O3P 21 21 215.5517; 11.006; 24.121
90; 90; 90		1473.8Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119376 CIFC25 H19 N O2C 1 2/c 137.27; 7.992; 12.774
90; 91.797; 90		3803Chun-Wei; Kuo; Ashok; Konala; Lyu; Lin; Ting-Ta; Chiang; Chia-Yu; Huang; Tang-Hao; Yang; Veerababurao; Kavala; Ching-Fa; Yao
Synthesis of benzo[a]carbazole derivatives from 3-ethylindoles by exploiting the dual character of benzoquinone as an oxidizing agent and dienophile
Chem.Commun., 2016, 52, 7870
7119377 CIFC20 H15 Cl N2 O2P 21 21 217.174; 14.3271; 17.4194
90; 90; 90		1790.4Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119378 CIFC21 H18 Cl N O4P 21 21 217.1668; 12.4455; 21.2096
90; 90; 90		1891.78Zhu, Gongming; Yang, Junxian; Bao, Guangjun; Zhang, Ming; Li, Jing; Li, Yiping; Sun, Wangsheng; Hong, Liang; Wang, Rui
Catalyst-controlled switch of regioselectivity in the asymmetric allylic alkylation of oxazolones with MBHCs
Chemical Communications, 2016, 52, 7882-7885
7119379 CIFC62 H58 Gd2 N8 O20 Zn2P 1 21/c 113.8176; 14.3073; 16.9982
90; 95.502; 90		3344.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119380 CIFC62 H58 Dy2 N8 O20 Zn2P 1 21/c 113.75033; 14.3147; 16.9418
90; 95.2801; 90		3320.54Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119381 CIFC62 H58 N8 O20 Y2 Zn2P 1 21/c 113.7448; 14.3133; 16.9268
90; 95.068; 90		3317Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119382 CIFC62 H58 Eu2 N8 O20 Zn2P 1 21/c 113.8125; 14.3087; 16.9783
90; 95.498; 90		3340.14Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119383 CIFC23 H18 N2P 1 21/c 110.0681; 9.7551; 17.5082
90; 94.291; 90		1714.8Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119384 CIFC29 H24 N2 O2P -19.9468; 10.285; 11.5735
75.327; 82.383; 81.347		1126.82Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119385 CIFC23 H20 N2 O3P 1 21/n 18.8491; 10.6531; 20.9154
90; 96.794; 90		1957.9Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119386 CIFC25 H22 N2I 1 2/a 118.3322; 10.0821; 20.0451
90; 90.573; 90		3704.7Griffiths, Kieran; Kumar, Prashant; Akien, Geoffrey R.; Chilton, Nicholas F.; Abdul-Sada, Alaa; Tizzard, Graham J.; Coles, Simon J.; Kostakis, George E.
Tetranuclear Zn/4f coordination clusters as highly efficient catalysts for Friedel-Crafts alkylation
Chemical Communications, 2016, 52, 7866-7869
7119387 CIFC96 H92 N12 O32 Zr6F m -3 m29.983; 29.983; 29.983
90; 90; 90		26954Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119388 CIFC96 H80 O32 Zr6F m -3 m29.941; 29.941; 29.941
90; 90; 90		26841Naeem, Ayesha; Ting, Valeska P.; Hintermair, Ulrich; Tian, Mi; Telford, Richard; Halim, Saaiba; Nowell, Harriott; Hołyńska, Małgorzata; Teat, Simon J.; Scowen, Ian J.; Nayak, Sanjit
Mixed-linker approach in designing porous zirconium-based metal‒organic frameworks with high hydrogen storage capacity
Chemical Communications, 2016, 52, 7826-7829
7119389 CIFC36 H36 Cl6 Ge3 N4P 1 21/c 19.4771; 16.9192; 25.2949
90; 92.298; 90		4052.6Swamy, V. S. V. S. N.; Yadav, Sandeep; Pal, Shiv; Das, Tamal; Vanka, Kumar; Sen, Sakya S.
Facile access to a Ge(II) dication stabilized by isocyanides
Chemical Communications, 2016, 52, 7890-7892
7119440 CIFC29 H36 Br F3 N O3 PP 1 21/n 19.477; 15.308; 21.114
90; 102.525; 90		2990Ryosuke; Saijo; Hidemitsu; Uno; Shigeki; Mori; Masami; Kawase
Synthesis and structures of stable phosphorus zwitterions derived from mesoionic 4_trifluoroacetyl-1,3-oxazolium-5-olates
Chem.Commun., 2016, 52, 8006
7119441 CIFC39 H31 N O3 SP 4/n c c25.9455; 25.9455; 24.2457
90; 90; 90		16321.5Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119442 CIFC60 H45 N O3 SP 4/n c c26.7747; 26.7747; 24.0725
90; 90; 90		17257.2Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119443 CIFC62.5 H45 N O3 SP 4/n c c27.3864; 27.3864; 24.2386
90; 90; 90		18179.3Tetsuya; Hasegawa; Kei; Ohkubo; Ichiro; Hisaki; Mikiji; Miyata; Norimitsu; Tohnai; Shunichi; Fukuzumi
Photoinduced electron transfer in porous organic salt crystals impregnated with fullerenes
Chem.Commun., 2016, 52, 7928
7119446 CIFC26 H28 F12 N6 P2 RuC 1 2/c 120.6432; 12.1018; 12.8802
90; 110.019; 90		3023.3Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119447 CIFC30 H32 F12 N6 P2 RuC 1 2 125.132; 9.8199; 17.2577
90; 131.012; 90		3213.8Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119448 CIFC24 H32 F12 N6 P2 RuP 31 2 110.2422; 10.2422; 24.9887
90; 90; 120		2270.18Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119449 CIFC25 H29 Cl F12 Fe N5 P2P 1 21 110.1753; 16.8389; 9.2498
90; 112.218; 90		1467.2Yanay; Popowski; Israel; Goldberg; Moshe; Kol
The stereoselectivity of bipyrrolidine-based sequential polydentate ligands around Ru(II)
Chem.Commun., 2016, 52, 7932
7119450 CIFC60 H74 B2 F8 N10 O20 Ru3P 1 21/n 114.515; 14.999; 15.692
90; 96.15; 90		3397Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119451 CIFC60 H82 B F4 N10 O32 Ru3 S2P -115.229; 17.001; 17.204
65.62; 84.91; 71.63		3845.9Yuta; Tsubonouchi; Shu; Lin; Alexander; R.; Parent; Gary; W.; Brudvig; Ken; Sakai
Light-induced water oxidation catalyzed by an oxido-bridged triruthenium complex with a Ru-O-Ru-O-Ru motif
Chem.Commun., 2016, 52, 8018
7119454 CIFC36 H26 Cd N2 O4P 41 21 214.5436; 14.5436; 29.1864
90; 90; 90		6173.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119455 CIFC36 H25 Cd N2 O4P 43 21 214.573; 14.573; 28.941
90; 90; 90		6146Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119456 CIFC36 H26 Cd N2 O4P 43 21 214.523; 14.523; 29.1177
90; 90; 90		6141.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119457 CIFC36 H24 Cd N2 O4P 43 21 214.3555; 14.3555; 29.4087
90; 90; 90		6060.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119458 CIFC36 H26 Cd N2 O4P 41 21 214.5029; 14.5029; 29.2053
90; 90; 90		6142.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119459 CIFC36 H24 Cd N2 O4P 41 21 214.3664; 14.3664; 29.399
90; 90; 90		6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119460 CIFC36 H26 Cd N2 O4P 43 21 214.5318; 14.5318; 29.1429
90; 90; 90		6154.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119461 CIFC36 H26 Cd N2 O4P 41 21 214.5128; 14.5128; 29.194
90; 90; 90		6148.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119462 CIFC36 H26 Cd N2 O4P 43 21 214.4791; 14.4791; 29.069
90; 90; 90		6094.2Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119463 CIFC36 H26 Cd N2 O4P 43 21 214.4739; 14.4739; 29.0695
90; 90; 90		6089.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119464 CIFC36 H26 Cd N2 O4P 43 21 214.4958; 14.4958; 29.0361
90; 90; 90		6101.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119465 CIFC36 H26 Cd N2 O4P 43 21 214.5294; 14.5294; 29.1842
90; 90; 90		6160.9Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119466 CIFC36 H26 Cd N2 O4P 41 21 214.4838; 14.4838; 29.2182
90; 90; 90		6129.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119467 CIFC36 H26 Cd N2 O4P 41 21 214.4458; 14.4458; 29.3447
90; 90; 90		6123.7Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119468 CIFC36 H26 Cd N2 O4P 41 21 214.4171; 14.4171; 29.1929
90; 90; 90		6067.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119469 CIFC36 H26 Cd N2 O4P 41 21 214.5097; 14.5097; 28.8452
90; 90; 90		6072.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119470 CIFC36 H26 Cd N2 O4P 41 21 214.5222; 14.5222; 29.245
90; 90; 90		6167.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119471 CIFC36 H26 Cd N2 O4P 41 21 214.5387; 14.5387; 29.246
90; 90; 90		6181.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119472 CIFC36 H26 Cd N2 O4P 43 21 214.5486; 14.5486; 29.1966
90; 90; 90		6179.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119473 CIFC36 H26 Cd N2 O4P 43 21 214.486; 14.486; 28.911
90; 90; 90		6066.8Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119474 CIFC36 H26 Cd N2 O4P 41 21 214.4896; 14.4896; 29.1167
90; 90; 90		6113Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119475 CIFC36 H26 Cd N2 O4P 43 21 214.4789; 14.4789; 29.007
90; 90; 90		6081Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119476 CIFC36 H26 Cd N2 O4P 41 21 214.5067; 14.5067; 28.888
90; 90; 90		6079.3Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119477 CIFC36 H26 Cd N2 O4P 41 21 214.4975; 14.4975; 29.1189
90; 90; 90		6120.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119478 CIFC36 H26 Cd N2 O4P 43 21 214.5803; 14.5803; 29.181
90; 90; 90		6203.4Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119479 CIFC36 H26 Cd N2 O4P 41 21 214.5474; 14.5474; 29.2215
90; 90; 90		6184.1Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119480 CIFC36 H26 Cd N2 O4P 43 21 214.5616; 14.5616; 29.153
90; 90; 90		6181.6Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119481 CIFC36 H25 Cd N2 O4P 41 21 214.4906; 14.4906; 29.1148
90; 90; 90		6113.5Hu, Fei-Long; Wang, Hui-Fang; Guo, Dong; Zhang, Hui; Lang, Jian-Ping; Beves, Jonathon E.
Controlled formation of chiral networks and their reversible chiroptical switching behaviour by UV/microwave irradiation
Chemical Communications, 2016, 52, 7990-7993
7119482 CIFC72 H40 In2 O16R -3 :H44.874; 44.874; 42.074
90; 90; 120		73373Panpan; Yu; Qipeng; Li; Yue; Hu; Nannan; Liu; Lijie; Zhang; Kongzhao; Su; Jinjie; Qian; Shaoming; Huang; Maochun; Hong
Cuboctahedron-based indium-organic frameworks for gas sorption and selective cation exchange
Chem.Commun., 2016, 52, 7978
7119483 CIFC25 H16 O3C 1 2/c 125.507; 8.1552; 16.661
90; 92.869; 90		3461.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974
7119484 CIFC27 H22 O4P -19.173; 10.382; 12.748
104.062; 94.66; 116.023		1033.4Hikaru; Yanai; Nobuyuki; Ishii; Takashi; Matsumoto
Synthesis of 1,2,3,4-tetrasubstituted naphthalenes through a cascade reaction triggered by silyl acetal activation
Chem.Commun., 2016, 52, 7974

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