Crystallography Open Database

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7116144 CIFC20 H20 N2 O2 S2P 1 21/n 15.215; 23.832; 14.377
90; 95.528; 90
1778.5Joydeep Dhar; Durga Prasad Karothu; Satish Patil
Herringbone to cofacial solid state packing via H-bonding in diketopyrrolopyrrole (DPP) based molecular crystals: influence on charge transport
Chem.Commun., 2015, 51, 51
7116145 CIFC24 H24 N2 O2P 1 21/n 14.9724; 26.488; 14.65
90; 96.55; 90
1916.9Joydeep Dhar; Durga Prasad Karothu; Satish Patil
Herringbone to cofacial solid state packing via H-bonding in diketopyrrolopyrrole (DPP) based molecular crystals: influence on charge transport
Chem.Commun., 2015, 51, 51
7116146 CIFC30 H27 N O4P 1 21/c 116.322; 9.073; 16.857
90; 114.032; 90
2280S. Ito; Y. Tokimaru; K. Nozaki
Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons
Chem.Commun., 2015, 51, 221
7116147 CIFC38 H29 NP b c a8.784; 20.52; 29.114
90; 90; 90
5248S. Ito; Y. Tokimaru; K. Nozaki
Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons
Chem.Commun., 2015, 51, 221
7116148 CIFC42 H33 N O4P b c a9.666; 22.449; 29.445
90; 90; 90
6389S. Ito; Y. Tokimaru; K. Nozaki
Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons
Chem.Commun., 2015, 51, 221
7116149 CIFC29 H34 Br2 Cl Ir N2P 1 21/c 112.9409; 11.8975; 19.1295
90; 109.446; 90
2777.25Samantha K. Furfari; Matthew R. Gyton; Daniel Twycross; Marcus L. Cole
Air stable NHCs: a study of stereoelectronics and metallorganic catalytic activity
Chem.Commun., 2015, 51, 74
7116150 CIFC49 H62 Br2 Cl Ir N2P 1 21/c 110.6872; 21.9371; 19.3647
90; 99.668; 90
4475.5Samantha K. Furfari; Matthew R. Gyton; Daniel Twycross; Marcus L. Cole
Air stable NHCs: a study of stereoelectronics and metallorganic catalytic activity
Chem.Commun., 2015, 51, 74
7116151 CIFC34 H42 Br2 N2P -110.4613; 11.4351; 15.2078
77.02; 76.084; 70.612
1644.8Samantha K. Furfari; Matthew R. Gyton; Daniel Twycross; Marcus L. Cole
Air stable NHCs: a study of stereoelectronics and metallorganic catalytic activity
Chem.Commun., 2015, 51, 74
7116152 CIFC17 H48 Si4 Sn2C 1 2/c 129.6997; 6.4318; 16.6792
90; 115.646; 90
2872.2Michael Wagner; Michael Lutter; Bernhard Zobel; Wolf Hiller; Marc H. Prosenc; Klaus Jurkschat
[Me2C{SnCH(SiMe3)2}2]2. A mu-Me2C-bridged tetrastanna tetrahedrane
Chem.Commun., 2015, 51, 153
7116153 CIFC34 H88 Si8 Sn4P 1 21/c 113.1495; 22.2439; 19.4674
90; 103.119; 90
5545.5Michael Wagner; Michael Lutter; Bernhard Zobel; Wolf Hiller; Marc H. Prosenc; Klaus Jurkschat
[Me2C{SnCH(SiMe3)2}2]2. A mu-Me2C-bridged tetrastanna tetrahedrane
Chem.Commun., 2015, 51, 153
7116154 CIFC34 H88 O3 Si8 Sn4C 1 2/c 127.325; 13.2488; 16.5435
90; 109.718; 90
5638Michael Wagner; Michael Lutter; Bernhard Zobel; Wolf Hiller; Marc H. Prosenc; Klaus Jurkschat
[Me2C{SnCH(SiMe3)2}2]2. A mu-Me2C-bridged tetrastanna tetrahedrane
Chem.Commun., 2015, 51, 153
7116155 CIFC34 H25 Mg3 N2 O11.5P 1 21/c 111.5486; 11.3339; 23.0576
90; 90.649; 90
3017.83Zhao-Feng Wu; Bin Tan; Jin-Yun Wang; Cheng-Feng Du; Zhong-Hua Deng; Xiao-Ying Huang
Tunable photoluminescence and direct white-light emission in Mg-based coordination networks
Chem.Commun., 2015, 51, 157
7116156 CIFC38 H34 Mg3 N2 O13P 1 21/c 16.75674; 16.231; 16.3562
90; 97.495; 90
1778.44Zhao-Feng Wu; Bin Tan; Jin-Yun Wang; Cheng-Feng Du; Zhong-Hua Deng; Xiao-Ying Huang
Tunable photoluminescence and direct white-light emission in Mg-based coordination networks
Chem.Commun., 2015, 51, 157
7116157 CIFC37 H30 Mg3 N2 O11P 1 21/c 111.54; 12.0576; 22.8377
90; 92.783; 90
3174Zhao-Feng Wu; Bin Tan; Jin-Yun Wang; Cheng-Feng Du; Zhong-Hua Deng; Xiao-Ying Huang
Tunable photoluminescence and direct white-light emission in Mg-based coordination networks
Chem.Commun., 2015, 51, 157
7116158 CIFC15 H12 O2 SP b c a7.867; 13.181; 23.94
90; 90; 90
2482Yong Luo; Xiaolin Pan; Chen Chen; Liangqing Yao; Jie Wu
An unexpected reaction of 2-alkynylaryldiazonium tetrafluoroborate with sulfur dioxide
Chem.Commun., 2015, 51, 180
7116159 CIFC36 H84 N2 Si4 SmP b c a20.509; 16.0788; 26.515
90; 90; 90
8743.6Nicholas F. Chilton; Conrad A. P. Goodwin; David P. Mills; Richard E. P. Winpenny
The first near-linear bis(amide) f-block complex: a blueprint for a high temperature single molecule magnet
Chem.Commun., 2015, 51, 101
7116160 CIFC16 H15 N O3 SP 1 21/n 113.2128; 5.2286; 22.078
90; 90.021; 90
1525.2Xiang-Ying Tang; Yong-Sheng Zhang; Lv He; Yin Wei; Min Shi
Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles
Chem.Commun., 2015, 51, 133
7116161 CIFC21 H19 N O4 SP -18.1851; 11.3028; 11.9273
79.944; 72.676; 78.178
1023.4Xiang-Ying Tang; Yong-Sheng Zhang; Lv He; Yin Wei; Min Shi
Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles
Chem.Commun., 2015, 51, 133
7116162 CIFC23 H20 N2 O4 S2P n a 218.0251; 25.4919; 10.5814
90; 90; 90
2164.7Xiang-Ying Tang; Yong-Sheng Zhang; Lv He; Yin Wei; Min Shi
Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles
Chem.Commun., 2015, 51, 133
7116163 CIFC23 H22 N2 O4 S2P -110.559; 10.991; 11.719
63.538; 78.349; 71.093
1149.2Xiang-Ying Tang; Yong-Sheng Zhang; Lv He; Yin Wei; Min Shi
Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles
Chem.Commun., 2015, 51, 133
7116164 CIFC30 H23 N3 O8 SP 1 21/n 111.441; 15.055; 15.927
90; 97.324; 90
2721Xiang-Ying Tang; Yong-Sheng Zhang; Lv He; Yin Wei; Min Shi
Intramolecular annulation of aromatic rings with N-sulfonyl 1,2,3-triazoles: divergent synthesis of 3-methylene-2,3-dihydrobenzofurans and 3-methylene-2,3-dihydroindoles
Chem.Commun., 2015, 51, 133
7116165 CIFC35 H48 F Ir N2P 4/n :238.809; 38.809; 10.795
90; 90; 90
16259Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116166 CIFC34 H55.82 Cl0.18 F2 Ir2 N4P -110.057; 12.486; 14.296
101.386; 96.141; 90.28
1749.1Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116167 CIFC23 H36 F N2 RhP 1 21/c 110.995; 16.868; 11.682
90; 98.162; 90
2144.6Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116168 CIFC35 H49 F2 Ir N2P 1 21/c 120.4091; 16.5631; 20.0077
90; 104.828; 90
6538.1Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116169 CIFC35 H49 F2 N2 RhP 1 21/c 120.384; 16.53; 19.817
90; 104.41; 90
6467.2Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116170 CIFC17 H31 F2 Ir N2 OP 21 21 219.8551; 16.1164; 24.342
90; 90; 90
3866.2Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116171 CIFC18 H28 F3 Ir N2P n m a14.237; 14.568; 8.8236
90; 90; 90
1830.1Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116172 CIFC24 H36 F3 N2 RhP -110.015; 10.5165; 12.2179
80.696; 71.535; 71.882
1157.2Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116173 CIFC35 H48.67 F N2 O0.33 RhP 21 21 2113.3131; 20.0341; 38.159
90; 90; 90
10177.6Byron J. Truscott; Fady Nahra; Alexandra M. Z. Slawin; David B. Cordes; Steven P. Nolan
Fluoride, bifluoride and trifluoromethyl complexes of iridium(I) and rhodium(I)
Chem.Commun., 2015, 51, 62
7116174 CIFC316.5 H366 N93 O111 Pd12P -123.379; 27.15; 43.649
107.717; 92.383; 103.95
25415Sato, Sota; Takeuchi, Ryosuke; Yagi-Utsumi, Maho; Yamaguchi, Takumi; Yamaguchi, Yoshiki; Kato, Koichi; Fujita, Makoto
A self-assembled, π-stacked complex as a finely-tunable magnetic aligner for biomolecular NMR applications.
Chemical communications (Cambridge, England), 2015, 51, 2540-2543
7116175 CIFC16 H11 N O3P n a 2116.539; 6.2596; 11.472
90; 90; 90
1187.7Cagide, F.; Silva, T.; Reis, J.; Gaspar, A.; Borges, F.; Gomes, L. R.; Low, J. N.
Discovery of two new classes of potent monoamine oxidase-B inhibitors by tricky chemistry.
Chemical communications (Cambridge, England), 2015, 51, 2832
7116176 CIFC16 H11 N O3P 1 21/n 16.6795; 7.3003; 24.602
90; 94.306; 90
1196.27Cagide, F.; Silva, T.; Reis, J.; Gaspar, A.; Borges, F.; Gomes, L. R.; Low, J. N.
Discovery of two new classes of potent monoamine oxidase-B inhibitors by tricky chemistry.
Chemical communications (Cambridge, England), 2015, 51, 2832
7116177 CIFC48 H36 Cd3 N10 O18P 43 3 229.5955; 29.5955; 29.5955
90; 90; 90
25922.5Xu, Zhong-Xuan; Tan, Yan-Xi; Fu, Hong-Ru; Kang, Yao; Zhang, Jian
Integration of rigid and flexible organic parts for the construction of a homochiral metal-organic framework with high porosity.
Chemical communications (Cambridge, England), 2015, 51, 2565-2568
7116178 CIFC8 H16 N11 Ni5 O38 P S3 W9P 63/m32.897; 32.897; 13.939
90; 90; 120
13064Cao, Gao-Juan; Liu, Jing-Dong; Zhuang, Ting-Ting; Cai, Xiu-Hong; Zheng, Shou-Tian
A polyoxometalate-organic supramolecular nanotube with high chemical stability and proton-conducting properties.
Chemical communications (Cambridge, England), 2015, 51, 2048-2051
7116179 CIFC14 H8 Cl3 N OP 21 21 216.2868; 8.7137; 24.2013
90; 90; 90
1325.78Verma, Ajay; Patel, Saket; Meenakshi, ?; Kumar, Amit; Yadav, Abhimanyu; Kumar, Shailesh; Jana, Sadhan; Sharma, Shubham; Prasad, Ch Durga; Kumar, Sangit
Transition metal free intramolecular selective oxidative C(sp(3))-N coupling: synthesis of N-aryl-isoindolinones from 2-alkylbenzamides.
Chemical communications (Cambridge, England), 2014, 51, 1371-1374
7116180 CIFC15 H12 Br N OP 1 21/n 111.335; 8.635; 13.184
90; 94.87; 90
1285.8Verma, Ajay; Patel, Saket; Meenakshi, ?; Kumar, Amit; Yadav, Abhimanyu; Kumar, Shailesh; Jana, Sadhan; Sharma, Shubham; Prasad, Ch Durga; Kumar, Sangit
Transition metal free intramolecular selective oxidative C(sp(3))-N coupling: synthesis of N-aryl-isoindolinones from 2-alkylbenzamides.
Chemical communications (Cambridge, England), 2014, 51, 1371-1374
7116181 CIFC20 H15 N OP 1 21/c 111.4297; 5.9995; 21.003
90; 96.386; 90
1431.3Verma, Ajay; Patel, Saket; Meenakshi, ?; Kumar, Amit; Yadav, Abhimanyu; Kumar, Shailesh; Jana, Sadhan; Sharma, Shubham; Prasad, Ch Durga; Kumar, Sangit
Transition metal free intramolecular selective oxidative C(sp(3))-N coupling: synthesis of N-aryl-isoindolinones from 2-alkylbenzamides.
Chemical communications (Cambridge, England), 2014, 51, 1371-1374
7116182 CIFC21 H15 B Br F2 N OP b c a16.379; 10.494; 21.831
90; 90; 90
3752.3Yang, Zheng; Jiang, Bo; Hao, Wen-Juan; Zhou, Peng; Tu, Shu-Jiang; Li, Guigen
Synthesis of enaminones and their difluoroboron complexes through domino aryl migration.
Chemical communications (Cambridge, England), 2014, 51, 1267-1270
7116183 CIFC21 H16 Cl N OC 1 2/c 116.9201; 10.043; 19.7402
90; 98.841; 90
3314.6Yang, Zheng; Jiang, Bo; Hao, Wen-Juan; Zhou, Peng; Tu, Shu-Jiang; Li, Guigen
Synthesis of enaminones and their difluoroboron complexes through domino aryl migration.
Chemical communications (Cambridge, England), 2014, 51, 1267-1270
7116184 CIFC111 H110 F6 Mn2 N5 O10 P4 S2P 1 21/c 112.451; 27.816; 14.753
90; 105.155; 90
4931.8Pierri, Agustin E.; Huang, Po-Ju; Garcia, John V.; Stanfill, James G.; Chui, Megan; Wu, Guang; Zheng, Nanfeng; Ford, Peter C.
A photoCORM nanocarrier for CO release using NIR light.
Chemical communications (Cambridge, England), 2015, 51, 2072-2075
7116185 CIFC155 H112 Cd4 N12 O19C 1 2 128.95; 39.508; 10.2785
90; 95.737; 90
11697.2Qin, Ling; Zheng, Meng-Xi; Guo, Zi-Jian; Zheng, He-Gen; Xu, Yan
One non-interpenetrated chiral porous multifunctional metal-organic framework and its applications for sensing small solvent molecules and adsorption.
Chemical communications (Cambridge, England), 2015, 51, 2447-2449
7116186 CIFH52 Ir Na8 O50 W6P 1 21/n 110.7874; 11.7736; 17.9983
90; 93.574; 90
2281.46Adonin, Sergey A.; Izarova, Natalya V.; Besson, Claire; Abramov, Pavel A.; Santiago-Schübel, Beatrix; Kögerler, Paul; Fedin, Vladimir P.; Sokolov, Maxim N.
An Ir(IV)-containing polyoxometalate.
Chemical communications (Cambridge, England), 2014, 51, 1222-1225
7116187 CIFH54 Ir Na6 O50 W6P -18.9995; 11.2653; 12.4259
108.449; 106.127; 105.317
1058.86Adonin, Sergey A.; Izarova, Natalya V.; Besson, Claire; Abramov, Pavel A.; Santiago-Schübel, Beatrix; Kögerler, Paul; Fedin, Vladimir P.; Sokolov, Maxim N.
An Ir(IV)-containing polyoxometalate.
Chemical communications (Cambridge, England), 2014, 51, 1222-1225
7116188 CIFC40 H48 Dy2 N4 O20 Ru2P 1 21/n 18.096; 17.161; 17.146
90; 92.44; 90
2380Langley, Stuart K.; Wielechowski, Daniel P.; Vieru, Veacheslav; Chilton, Nicholas F.; Moubaraki, Boujemaa; Chibotaru, Liviu F.; Murray, Keith S.
The first 4d/4f single-molecule magnet containing a {Ru(III)2Dy(III)2} core.
Chemical communications (Cambridge, England), 2015, 51, 2044-2047
7116189 CIFC9 H21 Cl6 N2 O WP 1 21/c 111.225; 10.379; 16.136
90; 90.59; 90
1879.8Bortoluzzi, Marco; Marchetti, Fabio; Pampaloni, Guido; Zacchini, Stefano
A crystallographically characterized salt of self-generated N-protonated tetraethylurea.
Chemical communications (Cambridge, England), 2014, 51, 1323-1325
7116190 CIFC56 H62 N2 P3P 1 21/n 111.3859; 32.688; 13.0222
90; 96.019; 90
4819.9Hinz, Alexander; Schulz, Axel; Villinger, Alexander
P-P σ-bond activation by gold(I) coordination.
Chemical communications (Cambridge, England), 2014, 51, 1363-1366
7116191 CIFC63.5 H69.5 Au2 Cl2 N2 P3P -112.4677; 21.4096; 22.9115
75.619; 89.277; 82.235
5868.4Hinz, Alexander; Schulz, Axel; Villinger, Alexander
P-P σ-bond activation by gold(I) coordination.
Chemical communications (Cambridge, England), 2014, 51, 1363-1366
7116192 CIFC59 H65 Au Cl N2 P3C 1 2/c 119.8747; 12.2909; 44.936
90; 101.502; 90
10756.4Hinz, Alexander; Schulz, Axel; Villinger, Alexander
P-P σ-bond activation by gold(I) coordination.
Chemical communications (Cambridge, England), 2014, 51, 1363-1366
7116193 CIFC68 H74 Au Cl N2 P3P -111.4133; 11.8735; 24.862
97.632; 90.569; 114.933
3020Hinz, Alexander; Schulz, Axel; Villinger, Alexander
P-P σ-bond activation by gold(I) coordination.
Chemical communications (Cambridge, England), 2014, 51, 1363-1366
7116194 CIFC48 H61 Br0 Cl N3 Nb OP -111.3526; 19.7589; 20.1301
96.454; 102.126; 91.32
4381.7Obenhuber, A. H.; Gianetti, T. L.; Bergman, R. G.; Arnold, J.
Regioselective [2+2] and [4+2] cycloaddition reactivity in an asymmetric niobium(bisimido) moiety towards unsaturated organic molecules.
Chemical communications (Cambridge, England), 2014, 51, 1278-1281
7116195 CIFC29 H41 N2 Nb OP 1 21/n 111.126; 16.7319; 15.5707
90; 108.06; 90
2755.8Obenhuber, A. H.; Gianetti, T. L.; Bergman, R. G.; Arnold, J.
Regioselective [2+2] and [4+2] cycloaddition reactivity in an asymmetric niobium(bisimido) moiety towards unsaturated organic molecules.
Chemical communications (Cambridge, England), 2014, 51, 1278-1281
7116196 CIFC47 H60 N3 NbP -110.714; 11.714; 18.976
86.853; 76.422; 65.449
2103.3Obenhuber, A. H.; Gianetti, T. L.; Bergman, R. G.; Arnold, J.
Regioselective [2+2] and [4+2] cycloaddition reactivity in an asymmetric niobium(bisimido) moiety towards unsaturated organic molecules.
Chemical communications (Cambridge, England), 2014, 51, 1278-1281
7116197 CIFC39 H60 N3 NbC 1 c 112.5601; 35.993; 9.2081
90; 116.264; 90
3733Obenhuber, A. H.; Gianetti, T. L.; Bergman, R. G.; Arnold, J.
Regioselective [2+2] and [4+2] cycloaddition reactivity in an asymmetric niobium(bisimido) moiety towards unsaturated organic molecules.
Chemical communications (Cambridge, England), 2014, 51, 1278-1281
7116198 CIFC40 H60 N3 NbC 1 2/c 134.02; 13.276; 16.2477
90; 96.893; 90
7285.2Obenhuber, A. H.; Gianetti, T. L.; Bergman, R. G.; Arnold, J.
Regioselective [2+2] and [4+2] cycloaddition reactivity in an asymmetric niobium(bisimido) moiety towards unsaturated organic molecules.
Chemical communications (Cambridge, England), 2014, 51, 1278-1281
7116199 CIFC18 H20 B2 Cu2 N12P -19.0107; 9.2903; 15.7168
103.806; 91.307; 115.131
1145.14Wen, Tian; Zhang, De-Xiang; Liu, Juan; Zhang, Hai-Xia; Zhang, Jian
Facile synthesis of bimetal Au-Ag nanoparticles in a Cu(i) boron imidazolate framework with mechanochromic properties.
Chemical communications (Cambridge, England), 2014, 51, 1353-1355
7116200 CIFC21 H22 F7 N2 O3P n a 2126.437; 10.311; 9.126
90; 90; 90
2487.7Liu, Chunmei; Shi, Erbo; Xu, Feng; Luo, Qiang; Wang, Hongxiang; Chen, Jijun; Wan, Xiaobing
Combination of fluoroalkylation and Kornblum-DeLaMare reaction: a new strategy for the construction of (Z)-β-perfluoroalkyl enaminones.
Chemical communications (Cambridge, England), 2014, 51, 1214-1217
7116201 CIFC51 H62 Cl Li N2 O2 P2P -113.3879; 14.2429; 15.839
63.721; 84.21; 63.061
2395.4Ho, Samuel Y.-F.; So, Cheuk-Wai; Saffon-Merceron, Nathalie; Mézailles, Nicolas
Formation of a zwitterionic boronium species from the reaction of a stable carbenoid with borane: CO2 reduction.
Chemical communications (Cambridge, England), 2015, 51, 2107-2110
7116202 CIFC43 H44 B Cl N2 P2P 1 21/c 112.7251; 18.239; 16.632
90; 102.121; 90
3774.1Ho, Samuel Y.-F.; So, Cheuk-Wai; Saffon-Merceron, Nathalie; Mézailles, Nicolas
Formation of a zwitterionic boronium species from the reaction of a stable carbenoid with borane: CO2 reduction.
Chemical communications (Cambridge, England), 2015, 51, 2107-2110
7116203 CIFC23 H17 Cl N2 O SP 1 21 113.6665; 5.3783; 14.176
90; 115.422; 90
941.08Ni, Qijian; Song, Xiaoxiao; Xiong, Jiawen; Raabe, Gerhard; Enders, Dieter
Regio- and stereoselective synthesis of benzothiazolo-pyrimidinones via an NHC-catalyzed Mannich/lactamization domino reaction.
Chemical communications (Cambridge, England), 2014, 51, 1263-1266
7116204 CIFC28 H245 N7 Na12 O268 Se8 Sn7 W54P 1 21/c 133.9004; 36.2831; 28.2841
90; 110.239; 90
32642Chen, Wei-Chao; Qin, Chao; Li, Yang-Guang; Zang, Hong-Ying; Shao, Kui-Zhan; Su, Zhong-Min; Wang, En-Bo; Liu, Hong-Sheng
Assembly of tetrameric dimethyltin-functionalized selenotungstates: from nanoclusters to one-dimensional chains.
Chemical communications (Cambridge, England), 2015, 51, 2433-2436
7116205 CIFC48 H390 N8 Na10 O330 Se11 Sn16 W56P 1 21/n 122.382; 20.536; 42.014
90; 96.598; 90
19183Chen, Wei-Chao; Qin, Chao; Li, Yang-Guang; Zang, Hong-Ying; Shao, Kui-Zhan; Su, Zhong-Min; Wang, En-Bo; Liu, Hong-Sheng
Assembly of tetrameric dimethyltin-functionalized selenotungstates: from nanoclusters to one-dimensional chains.
Chemical communications (Cambridge, England), 2015, 51, 2433-2436
7116206 CIFC44 H47 B2 F8 N7 O3P -18.6769; 15.92; 17.935
115.794; 103.951; 90.302
2147.6Teng, Qiaoqiao; Huynh, Han Vinh
Controlled access to a heterometallic N-heterocyclic carbene helicate.
Chemical communications (Cambridge, England), 2014, 51, 1248-1251
7116207 CIFC29 H31 Au B F4 N7 O2P 1 21/n 113.924; 15.956; 14.787
90; 116.941; 90
2929Teng, Qiaoqiao; Huynh, Han Vinh
Controlled access to a heterometallic N-heterocyclic carbene helicate.
Chemical communications (Cambridge, England), 2014, 51, 1248-1251
7116208 CIFC82 H79 Au2 B2 F8 N14 O5P 1 21/c 123.26; 20.275; 8.2071
90; 94.156; 90
3860.3Teng, Qiaoqiao; Huynh, Han Vinh
Controlled access to a heterometallic N-heterocyclic carbene helicate.
Chemical communications (Cambridge, England), 2014, 51, 1248-1251
7116209 CIFC82.5 H74.5 Au2 B Cl0.5 Co F4 N14 O4P -115.0076; 16.2066; 17.9512
63.78; 82.005; 79.629
3844.1Teng, Qiaoqiao; Huynh, Han Vinh
Controlled access to a heterometallic N-heterocyclic carbene helicate.
Chemical communications (Cambridge, England), 2014, 51, 1248-1251
7116210 CIFC104 H264 N26 Nb36 O209 P3 Sb6P -113.5271; 15.379; 38.1915
95.015; 93.776; 93.571
7879Son, Jung-Ho; Casey, William H.
Reversible capping/uncapping of phosphorous-centered Keggin-type polyoxoniobate clusters.
Chemical communications (Cambridge, England), 2015, 51, 1436-1438
7116211 CIFC28 H84 N7 Nb14 O68 PP -113.429; 14.943; 25.521
77.02; 88.45; 82.922
4952Son, Jung-Ho; Casey, William H.
Reversible capping/uncapping of phosphorous-centered Keggin-type polyoxoniobate clusters.
Chemical communications (Cambridge, England), 2015, 51, 1436-1438
7116212 CIFC40 H52 N10 Nb12 O70 PP -113.479; 13.786; 16.904
70.1318; 69.2539; 74.0995
2720.2Son, Jung-Ho; Casey, William H.
Reversible capping/uncapping of phosphorous-centered Keggin-type polyoxoniobate clusters.
Chemical communications (Cambridge, England), 2015, 51, 1436-1438
7116213 CIFC16 H118 Cu4 N16 Nb12 O66 Sb2 SiI 41/a :225.645; 25.645; 16.21
90; 90; 90
10660.8Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116214 CIFC16 H118 Cu4 Ge N16 Nb12 O66 Sb2I 41/a :225.541; 25.541; 16.145
90; 90; 90
10532.1Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116215 CIFC16 H117 Cu4 N16 Nb12 O66 P Sb2I 41/a :225.61; 25.61; 16.186
90; 90; 90
10615.9Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116216 CIFC16 H117 As Cu4 N16 Nb12 O66 Sb2I 41/a :225.605; 25.605; 16.189
90; 90; 90
10613.8Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116217 CIFC36 H180 Cu9 Ge2 N36 Nb24 O97 Sb4P 1 21/n 114.893; 39.874; 19.332
90; 95.052; 90
11435.6Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116218 CIFC16 H76 Cu4 Ge N16 Nb12 O45 Sb2P -113.869; 14.621; 22.136
84.638; 80.632; 62.318
3921.1Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116219 CIFC16 H76 Cu4 N16 Nb12 O45 Sb2 SiP -113.9137; 14.473; 21.9355
84.819; 79.839; 61.342
3815.2Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116220 CIFC36 H180 Cu9 N36 Nb24 O97 Sb4 Si2P 1 21/n 114.745; 40.053; 19.158
90; 94.812; 90
11274.5Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116221 CIFC16 H117 Cu4 N16 Nb12 O66 Sb2 VI 41/a :225.702; 25.702; 16.236
90; 90; 90
10725.4Zhang, Zhe-Yu; Peng, Jun; Shi, Zhen-Yu; Zhou, Wan-Li; Khan, Shifa Ullah; Liu, Hong-Sheng
Antimony-dependent expansion for the Keggin heteropolyniobate family.
Chemical communications (Cambridge, England), 2015, 51, 3091-3093
7116222 CIFC138 H115 F96 N17 P16C 1 2/c 153.047; 13.8933; 23.3837
90; 107.888; 90
16400.6Sun, Junling; Frasconi, Marco; Liu, Zhichang; Barnes, Jonathan C.; Wang, Yuping; Chen, Dongyang; Stern, Charlotte L.; Fraser Stoddart, J.
Formation of ring-in-ring complexes between crown ethers and rigid TVBox(8+).
Chemical communications (Cambridge, England), 2015, 51, 1432-1435
7116223 CIFC104 H100 F48 N12 P8P 1 21/c 113.978; 16.44; 27.093
90; 102; 90
6090Sun, Junling; Frasconi, Marco; Liu, Zhichang; Barnes, Jonathan C.; Wang, Yuping; Chen, Dongyang; Stern, Charlotte L.; Fraser Stoddart, J.
Formation of ring-in-ring complexes between crown ethers and rigid TVBox(8+).
Chemical communications (Cambridge, England), 2015, 51, 1432-1435
7116224 CIFC108 H100 Cl4 F48 N16 P8P 1 21/n 113.8603; 16.2006; 27.9776
90; 102.962; 90
6122.2Sun, Junling; Frasconi, Marco; Liu, Zhichang; Barnes, Jonathan C.; Wang, Yuping; Chen, Dongyang; Stern, Charlotte L.; Fraser Stoddart, J.
Formation of ring-in-ring complexes between crown ethers and rigid TVBox(8+).
Chemical communications (Cambridge, England), 2015, 51, 1432-1435
7116225 CIFC22 H18 N2 O8 Re2P 1 21/n 115.5756; 7.6106; 19.6042
90; 100.084; 90
2288Massena, Casey J.; Riel, Asia Marie S.; Neuhaus, George F.; Decato, Daniel A.; Berryman, Orion B.
Solution and solid-phase halogen and C-H hydrogen bonding to perrhenate.
Chemical communications (Cambridge, England), 2015, 51, 1417-1420
7116226 CIFC22 H16 I2 N2 O8 Re2P 1 21/c 16.9841; 34.338; 11.4497
90; 99.704; 90
2706.6Massena, Casey J.; Riel, Asia Marie S.; Neuhaus, George F.; Decato, Daniel A.; Berryman, Orion B.
Solution and solid-phase halogen and C-H hydrogen bonding to perrhenate.
Chemical communications (Cambridge, England), 2015, 51, 1417-1420
7116227 CIFAl H5 Mg O10 P2P 1 21 15.0119; 7.769; 9.995
90; 102.595; 90
379.81Mu, Ying; Wang, Yanyan; Li, Yi; Li, Jiyang; Yu, Jihong
Organotemplate-free synthesis of an open-framework magnesium aluminophosphate with proton conduction properties.
Chemical communications (Cambridge, England), 2015, 51, 2149-2151
7116228 CIFC28 H23 N O2P 21 21 219.4323; 10.403; 21.195
90; 90; 90
2079.74Saha, Satyajit; Alamsetti, Santosh Kumar; Schneider, Christoph
Chiral Brønsted acid-catalyzed Friedel-Crafts alkylation of electron-rich arenes with in situ-generated ortho-quinone methides: highly enantioselective synthesis of diarylindolylmethanes and triarylmethanes.
Chemical communications (Cambridge, England), 2015, 51, 1461-1464
7116229 CIFC28 H26 Fe2 N2 O2 SP 1 21/c 17.1125; 11.3143; 29.525
90; 95.838; 90
2363.6Förster, Christoph; Veit, Philipp; Ksenofontov, Vadim; Heinze, Katja
Diferrocenyl tosyl hydrazone with an ultrastrong NHFe hydrogen bond as double click switch.
Chemical communications (Cambridge, England), 2015, 51, 1514-1516
7116230 CIFC12 H10 Co K N10R -3 m :H8.7151; 8.7151; 19.011
90; 90; 120
1250.5Zhang, Xi; Shao, Xiu-Dan; Li, Si-Chao; Cai, Ying; Yao, Ye-Feng; Xiong, Ren-Gen; Zhang, Wen
Dynamics of a caged imidazolium cation-toward understanding the order-disorder phase transition and the switchable dielectric constant.
Chemical communications (Cambridge, England), 2015, 51, 4568-4571
7116231 CIFC12 H10 Co K N10C 1 2/c 113.427; 8.7318; 15.083
90; 111.7; 90
1643Zhang, Xi; Shao, Xiu-Dan; Li, Si-Chao; Cai, Ying; Yao, Ye-Feng; Xiong, Ren-Gen; Zhang, Wen
Dynamics of a caged imidazolium cation-toward understanding the order-disorder phase transition and the switchable dielectric constant.
Chemical communications (Cambridge, England), 2015, 51, 4568-4571
7116232 CIFC39 H36 B2 N6 OP -110.9203; 12.3994; 13.6076
94.079; 99.826; 110.183
1687.1Fu, Yubin; Qiu, Feng; Zhang, Fan; Mai, Yiyong; Wang, Yingchao; Fu, Shibo; Tang, Ruizhi; Zhuang, Xiaodong; Feng, Xinliang
A dual-boron-cored luminogen capable of sensing and imaging.
Chemical communications (Cambridge, England), 2015, 51, 5298-5301
7116233 CIFC24 H23 N3 O4P 1 21 16.8289; 13.5136; 12.1421
90; 106.143; 90
1076.33Feng, Xian; Wang, Jian-Jun; Xun, Zhan; Zhang, Juan-Juan; Huang, Zhi-Bin; Shi, Da-Qing
Highly selective synthesis of functionalized polyhydroisoquinoline derivatives via a three-component domino reaction.
Chemical communications (Cambridge, England), 2015, 51, 1528-1531
7116234 CIFC25 H25 N3 O3P 1 21/c 118.9871; 18.0668; 12.546
90; 94.438; 90
4290.8Feng, Xian; Wang, Jian-Jun; Xun, Zhan; Zhang, Juan-Juan; Huang, Zhi-Bin; Shi, Da-Qing
Highly selective synthesis of functionalized polyhydroisoquinoline derivatives via a three-component domino reaction.
Chemical communications (Cambridge, England), 2015, 51, 1528-1531
7116235 CIFC105 H184 Cu27 N20 O104P 1 21/c 131.939; 18.8704; 32.73
90; 117.116; 90
17558Kühne, Irina A; Kostakis, George E.; Anson, Christopher E.; Powell, Annie K.
A magnetically highly frustrated Cu(II)27 coordination cluster containing a Cu18 folded-sheet motif.
Chemical communications (Cambridge, England), 2015, 51, 2702-2705
7116236 CIFC28 H30 I2 N2 OP -19.5036; 11.1664; 12.3553
87.908; 83.391; 82.468
1290.9Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116237 CIFC27 H26 I2 N2P 1 21/n 17.8813; 16.2049; 19.5829
90; 99.067; 90
2469.79Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116238 CIFC57 H52 N4 O8 S2P -18.2074; 16.4498; 19.3506
70.455; 86.37; 77.9
2407.2Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116239 CIFC37.5 H33.5 F6 N2.5 O8 S2P -112.8456; 13.7518; 21.796
75.143; 84.454; 87.583
3703.52Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116240 CIFC26 H26 F6 N2 O6 S2P 1 21/c 114.2532; 8.9518; 21.2552
90; 92.286; 90
2709.8Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116241 CIFC27.5 H29 F6 N2 O6.5 S2P -19.0232; 12.5214; 14.3223
101.78; 106.423; 101.248
1463.38Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116242 CIFC24 H26 I2 N2P 21 21 218.753; 13.2791; 19.75
90; 90; 90
2295.58Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116243 CIFC24 H26 Br2 N2P 21 21 227.6754; 10.0575; 14.6734
90; 90; 90
4084.3Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116244 CIFC24 H32 Br2 N2 O3P 21 21 2112.7303; 12.7933; 14.8125
90; 90; 90
2412.4Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116245 CIFC44 H44 F6 N4 O6 S2P b c a25.3083; 17.1165; 42.198
90; 90; 90
18280Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116246 CIFC44 H44 F6 N4 O6 S2P -110.9183; 13.1838; 15.8627
69.603; 77.874; 78.155
2070.59Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116247 CIFC39 H34 I2 N2 OP -113.5867; 14.1603; 19.3953
87.9609; 76.1122; 86.1412
3613.48Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116248 CIFC42 H34 I2 N2P b c a7.7728; 23.8635; 36.1252
90; 90; 90
6700.7Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116249 CIFC42 H44 Cl2 N4 O8P 42 21 213.3242; 13.3242; 24.3016
90; 90; 90
4314.4Reyes-Gutiérrez, Paul E; Jirásek, Michael; Severa, Lukáš; Novotná, Pavlína; Koval, Dušan; Sázelová, Petra; Vávra, Jan; Meyer, Andreas; Císařová, Ivana; Šaman, David; Pohl, Radek; Štěpánek, Petr; Slavíček, Petr; Coe, Benjamin J.; Hájek, Miroslav; Kašička, Václav; Urbanová, Marie; Teplý, Filip
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible region.
Chemical communications (Cambridge, England), 2015, 51, 1583-1586
7116250 CIFC9 H11 N O9 P S YP -16.778; 7.572; 13.356
90.423; 93.298; 102.31
668.5Zeng, Dai; Ren, Min; Bao, Song-Song; Feng, Jian-Shen; Li, Li; Zheng, Li-Min
pH-controlled polymorphism in a layered dysprosium phosphonate and its impact on the magnetization relaxation.
Chemical communications (Cambridge, England), 2015, 51, 2649-2652
7116251 CIFC10 H12 F4 I2 N2 O2P 1 21/c 18.6275; 12.005; 8.3466
90; 118.08; 90
762.7Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116252 CIFC8 H4 F8 I2 N2 OP -15.3515; 11.1482; 12.0159
85.076; 80.408; 84.424
701.72Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116253 CIFC12 H12 F8 I2 N2 O2P 1 21/c 19.3817; 12.862; 8.1127
90; 110.521; 90
916.82Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116254 CIFC20 H12 F24 I4 N2 O2P -112.3893; 12.6332; 13.1553
67.319; 75.273; 67.884
1745.6Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116255 CIFC8 H12 N2 O2P 1 21/c 13.8328; 10.291; 10.396
90; 98.77; 90
405.26Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116256 CIFC18 H16 N6P 1 21/c 15.1637; 16.705; 9.1021
90; 98.398; 90
776.7Aakeröy, Christer B; Wijethunga, Tharanga K.; Benton, Joshua; Desper, John
Stabilizing volatile liquid chemicals using co-crystallization.
Chemical communications (Cambridge, England), 2015, 51, 2425-2428
7116257 CIFC37 H50 N2 Ni O4P c a 2115.7155; 20.8328; 21.8429
90; 90; 90
7151.3Shi, Xincui; Sui, Aiguo; Wang, Yongxia; Li, Yuesheng; Geng, Yanhou; Wang, Fosong
Controlled synthesis of high molecular weight poly(3-hexylthiophene)s via Kumada catalyst transfer polycondensation with Ni(IPr)(acac)2 as the catalyst.
Chemical communications (Cambridge, England), 2015, 51, 2138-2140
7116258 CIFC18 H40 Cl N O10P n m a16.5769; 15.1415; 10.0908
90; 90; 90
2532.78Ji, Chengmin; Sun, Zhihua; Zhang, Shuquan; Zhao, Sangen; Chen, Tianliang; Tang, Yuanyuan; Luo, Junhua
A host-guest inclusion compound for reversible switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2015, 51, 2298-2300
7116259 CIFC18 H40 Cl N O10P 21 21 2110.031; 15.109; 16.199
90; 90; 90
2455Ji, Chengmin; Sun, Zhihua; Zhang, Shuquan; Zhao, Sangen; Chen, Tianliang; Tang, Yuanyuan; Luo, Junhua
A host-guest inclusion compound for reversible switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2015, 51, 2298-2300
7116260 CIFC6 H16 Cl N O4C m c m16.3536; 8.6485; 7.7268
90; 90; 90
1092.83Ji, Chengmin; Sun, Zhihua; Zhang, Shuquan; Zhao, Sangen; Chen, Tianliang; Tang, Yuanyuan; Luo, Junhua
A host-guest inclusion compound for reversible switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2015, 51, 2298-2300
7116261 CIFC6 H16 Cl N O4P n m a8.5346; 7.5928; 16.1352
90; 90; 90
1045.59Ji, Chengmin; Sun, Zhihua; Zhang, Shuquan; Zhao, Sangen; Chen, Tianliang; Tang, Yuanyuan; Luo, Junhua
A host-guest inclusion compound for reversible switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2015, 51, 2298-2300
7116262 CIFC6 H16 Cl N O4P m c n7.4714; 16.0278; 8.4874
90; 90; 90
1016.37Ji, Chengmin; Sun, Zhihua; Zhang, Shuquan; Zhao, Sangen; Chen, Tianliang; Tang, Yuanyuan; Luo, Junhua
A host-guest inclusion compound for reversible switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2015, 51, 2298-2300
7116263 CIFC62 H67 N5 O12P 1 21/c 121.1314; 15.228; 18.2607
90; 110.133; 90
5517Patil, Rahul S.; Kumari, Harshita; Barnes, Charles L.; Atwood, Jerry L.
Engineering supramolecular organic frameworks (SOFs) of C-alkylpyrogallol[4]arene with bipyridine-based spacers.
Chemical communications (Cambridge, England), 2015, 51, 2304-2307
7116264 CIFC73 H75 N5 O12P n a 2123.451; 16.433; 16.899
90; 90; 90
6512Patil, Rahul S.; Kumari, Harshita; Barnes, Charles L.; Atwood, Jerry L.
Engineering supramolecular organic frameworks (SOFs) of C-alkylpyrogallol[4]arene with bipyridine-based spacers.
Chemical communications (Cambridge, England), 2015, 51, 2304-2307
7116265 CIFC79 H64 N10 O12P 4/n c c :221.6686; 21.6686; 15.3857
90; 90; 90
7224Patil, Rahul S.; Kumari, Harshita; Barnes, Charles L.; Atwood, Jerry L.
Engineering supramolecular organic frameworks (SOFs) of C-alkylpyrogallol[4]arene with bipyridine-based spacers.
Chemical communications (Cambridge, England), 2015, 51, 2304-2307
7116266 CIFC85 H73 N9 O13C 1 2/c 120.8301; 12.6507; 29.0453
90; 107.332; 90
7306.4Patil, Rahul S.; Kumari, Harshita; Barnes, Charles L.; Atwood, Jerry L.
Engineering supramolecular organic frameworks (SOFs) of C-alkylpyrogallol[4]arene with bipyridine-based spacers.
Chemical communications (Cambridge, England), 2015, 51, 2304-2307
7116267 CIFC92 H80 B2 F48 O7 Zn2P -112.6592; 14.0662; 14.2052
77.951; 88.733; 85.817
2467.1Banh, Hung; Gemel, Christian; Seidel, Rüdiger W; Fischer, Roland A.
A solvated zinc analogue of the calomel-dication.
Chemical communications (Cambridge, England), 2015, 51, 2170-2172
7116268 CIFC76 H60 B2 F48 P4 ZnP 113.0001; 13.4282; 14.1449
102.57; 115.154; 91.67
2160.73Banh, Hung; Gemel, Christian; Seidel, Rüdiger W; Fischer, Roland A.
A solvated zinc analogue of the calomel-dication.
Chemical communications (Cambridge, England), 2015, 51, 2170-2172
7116269 CIFC110 H62 B2 Cl8 F48 N6 Zn2P 1 21/c 115.1012; 16.1231; 24.7275
90; 102.147; 90
5885.8Banh, Hung; Gemel, Christian; Seidel, Rüdiger W; Fischer, Roland A.
A solvated zinc analogue of the calomel-dication.
Chemical communications (Cambridge, England), 2015, 51, 2170-2172
7116270 CIFC14 H15 N OP -17.8602; 8.4121; 9.3329
102.282; 108.921; 93.927
564.05Wang, Bao-Juan; Xue, Ping; Gu, Peiming
Intramolecular Schmidt reaction of acyl chlorides with alkyl azides: preparation of pyrrolizine by intramolecular capture of intermediates with alkenes or alkynes.
Chemical communications (Cambridge, England), 2015, 51, 2277-2279
7116271 CIFC14 H14 Cl N OC 1 2/c 117.485; 10.6501; 13.4479
90; 97.808; 90
2481Wang, Bao-Juan; Xue, Ping; Gu, Peiming
Intramolecular Schmidt reaction of acyl chlorides with alkyl azides: preparation of pyrrolizine by intramolecular capture of intermediates with alkenes or alkynes.
Chemical communications (Cambridge, England), 2015, 51, 2277-2279
7116272 CIFC16 H30 Cl5 N4 SbC 1 c 115.3778; 27.5062; 17.4435
90; 102.004; 90
7217Wang, Ze-Ping; Wang, Jin-Yun; Li, Jian-Rong; Feng, Mei-Ling; Zou, Guo-Dong; Huang, Xiao-Ying
[Bmim]2SbCl5: a main group metal-containing ionic liquid exhibiting tunable photoluminescence and white-light emission.
Chemical communications (Cambridge, England), 2015, 51, 3094-3097
7116273 CIFC23 H16 F6 I2 O7 S2P 1 21/n 110.5549; 13.6694; 19.151
90; 94.31; 90
2755.3Dempsey Hyatt, I. F.; Nasrallah, Daniel J.; Maxwell, Michael A.; Hairston, A Christina F; Abdalhameed, Manahil M.; Croatt, Mitchell P.
Formation and in situ reactions of hypervalent iodonium alkynyl triflates to form cyanocarbenes.
Chemical communications (Cambridge, England), 2015, 51, 5287-5289
7116274 CIFC19 H9 N2 O10 Zn2P 42/n n m :217.7349; 17.7349; 28.1732
90; 90; 90
8861.2Sen, Susan; Neogi, Subhadip; Rissanen, Kari; Bharadwaj, Parimal K.
Solvent induced single-crystal to single-crystal structural transformation and concomitant transmetalation in a 3D cationic Zn(ii)-framework.
Chemical communications (Cambridge, England), 2015, 51, 3173-3176
7116275 CIFC19 H9 N2 O10 Zn2I 41/a m d :225.5552; 25.5552; 51.403
90; 90; 90
33570Sen, Susan; Neogi, Subhadip; Rissanen, Kari; Bharadwaj, Parimal K.
Solvent induced single-crystal to single-crystal structural transformation and concomitant transmetalation in a 3D cationic Zn(ii)-framework.
Chemical communications (Cambridge, England), 2015, 51, 3173-3176
7116276 CIFC19 H9 N2 O10 Zn2I 41/a m d :225.444; 25.444; 53.616
90; 90; 90
34711Sen, Susan; Neogi, Subhadip; Rissanen, Kari; Bharadwaj, Parimal K.
Solvent induced single-crystal to single-crystal structural transformation and concomitant transmetalation in a 3D cationic Zn(ii)-framework.
Chemical communications (Cambridge, England), 2015, 51, 3173-3176
7116277 CIFC19 H9 Cu2 N2 O10P 42/n n m :217.7179; 17.7179; 27.5566
90; 90; 90
8650.7Sen, Susan; Neogi, Subhadip; Rissanen, Kari; Bharadwaj, Parimal K.
Solvent induced single-crystal to single-crystal structural transformation and concomitant transmetalation in a 3D cationic Zn(ii)-framework.
Chemical communications (Cambridge, England), 2015, 51, 3173-3176
7116278 CIFC19 H9 Cu2 N2 O10I 41/a m d :225.4117; 25.4117; 52.162
90; 90; 90
33684Sen, Susan; Neogi, Subhadip; Rissanen, Kari; Bharadwaj, Parimal K.
Solvent induced single-crystal to single-crystal structural transformation and concomitant transmetalation in a 3D cationic Zn(ii)-framework.
Chemical communications (Cambridge, England), 2015, 51, 3173-3176
7116279 CIFC66 H62 B Cl6 Cu3 F4 P6P 1 21/n 112.4596; 27.6079; 20.0624
90; 104.466; 90
6682.34Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116280 CIFC80 H72 B Cl6 Cu3 F4 Mo2 O4 P8P 1 21/c 112.8855; 43.5442; 14.9499
90; 95.216; 90
8353.49Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116281 CIFC80 H72 As2 B Cl6 Cu3 F4 Mo2 O4 P6P 1 21/c 112.888; 43.5784; 15.0001
90; 95.152; 90
8390.6Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116282 CIFC74 H73 B Cl2 Cu3 F4 Fe P11P 1 21/c 112.5098; 25.2944; 27.8308
90; 97.692; 90
8727.2Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116283 CIFC76 H77 As5 B Cl6 Cu3 F4 Fe P6P 1 21/c 112.5858; 24.4849; 27.9362
90; 98.748; 90
8508.73Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116284 CIFC68 H64 B Cl2 Cu3 F4 N2 P6P -112.7414; 13.4211; 21.404
85.562; 72.949; 79.079
3435Fleischmann, Martin; Dütsch, Luis; Moussa, Mehdi Elsayed; Schindler, Andrea; Balázs, Gábor; Lescop, Christophe; Scheer, Manfred
Organometallic polyphosphorus and -arsenic ligands as linkers between pre-assembled linear Cu(I) fragments.
Chemical communications (Cambridge, England), 2015, 51, 2893
7116285 CIFC28 H19 N OP 1 21/n 19.9451; 10.9422; 18.8339
90; 90.772; 90
2049.3Huang, Ji-Rong; Qin, Liu; Zhu, Yu-Qin; Song, Qiang; Dong, Lin
Multi-site cyclization via initial C-H activation using a rhodium(iii) catalyst: rapid assembly of frameworks containing indoles and indolines.
Chemical communications (Cambridge, England), 2015, 51, 2844
7116286 CIFC26 H24 Cl3 N O2 SiP -19.6847; 10.6101; 12.7428
82.268; 87.114; 75.081
1253.58Huang, Ji-Rong; Qin, Liu; Zhu, Yu-Qin; Song, Qiang; Dong, Lin
Multi-site cyclization via initial C-H activation using a rhodium(iii) catalyst: rapid assembly of frameworks containing indoles and indolines.
Chemical communications (Cambridge, England), 2015, 51, 2844
7116287 CIFC10 H6 Al2 Cl10 N2P 1 21/c 17.1166; 11.566; 25.5436
90; 91.39; 90
2101.9Del Grosso, Alessandro; Ayuso Carrillo, Josue; Ingleson, Michael J.
Regioselective electrophilic borylation of haloarenes.
Chemical communications (Cambridge, England), 2015, 51, 2878
7116288 CIFC5 H3 Al B Cl8 NP 1 21/n 17.2646; 13.5445; 14.7907
90; 97.625; 90
1442.47Del Grosso, Alessandro; Ayuso Carrillo, Josue; Ingleson, Michael J.
Regioselective electrophilic borylation of haloarenes.
Chemical communications (Cambridge, England), 2015, 51, 2878
7116289 CIFC12 H15 B Br F O2P 1 21/c 113.8821; 7.6711; 12.4528
90; 92.002; 90
1325.3Del Grosso, Alessandro; Ayuso Carrillo, Josue; Ingleson, Michael J.
Regioselective electrophilic borylation of haloarenes.
Chemical communications (Cambridge, England), 2015, 51, 2878
7116290 CIFC12 H15 B Cl F O2P 1 21/c 113.8661; 7.502; 12.4291
90; 92.422; 90
1291.76Del Grosso, Alessandro; Ayuso Carrillo, Josue; Ingleson, Michael J.
Regioselective electrophilic borylation of haloarenes.
Chemical communications (Cambridge, England), 2015, 51, 2878
7116291 CIFC32 H32 N2 O4 S4P -14.6152; 11.558; 14.422
80.38; 88.11; 86.45
756.83Maini, Lucia; Gallino, Federico; Zambianchi, Massimo; Durso, Margherita; Gazzano, Massimo; Rubini, Katia; Gentili, Denis; Manet, Ilse; Muccini, Michele; Toffanin, Stefano; Cavallini, Massimiliano; Melucci, Manuela
Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials.
Chemical communications (Cambridge, England), 2015, 51, 2033-2035
7116292 CIFC13 H10 N O2 S2P -15.265; 5.473; 22.49
87.9; 87.4; 87.05
646.1Maini, Lucia; Gallino, Federico; Zambianchi, Massimo; Durso, Margherita; Gazzano, Massimo; Rubini, Katia; Gentili, Denis; Manet, Ilse; Muccini, Michele; Toffanin, Stefano; Cavallini, Massimiliano; Melucci, Manuela
Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials.
Chemical communications (Cambridge, England), 2015, 51, 2033-2035
7116293 CIFC28 H24 N2 O4 S4P -15.127; 5.526; 25.038
84.04; 89.75; 86.19
704Maini, Lucia; Gallino, Federico; Zambianchi, Massimo; Durso, Margherita; Gazzano, Massimo; Rubini, Katia; Gentili, Denis; Manet, Ilse; Muccini, Michele; Toffanin, Stefano; Cavallini, Massimiliano; Melucci, Manuela
Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials.
Chemical communications (Cambridge, England), 2015, 51, 2033-2035
7116294 CIFC30 H28 N2 O4 S4P -15.289; 5.474; 25.81
85.15; 84.36; 87.27
740.4Maini, Lucia; Gallino, Federico; Zambianchi, Massimo; Durso, Margherita; Gazzano, Massimo; Rubini, Katia; Gentili, Denis; Manet, Ilse; Muccini, Michele; Toffanin, Stefano; Cavallini, Massimiliano; Melucci, Manuela
Chemical design enables the control of conformational polymorphism in functional 2,3-thieno(bis)imide-ended materials.
Chemical communications (Cambridge, England), 2015, 51, 2033-2035
7116295 CIFC15 H13 N S2P b c a6.1546; 15.4938; 28.98
90; 90; 90
2763.48Xiao, Xiao; Feng, Minghao; Jiang, Xuefeng
Transition-metal-free persulfuration to construct unsymmetrical disulfides and mechanistic study of the sulfur redox process.
Chemical communications (Cambridge, England), 2015, 51, 4208-4211
7116296 CIFC14 H13 Br O2 S2P 1 21/n 110.1609; 14.3305; 10.5313
90; 94.541; 90
1528.7Xiao, Xiao; Feng, Minghao; Jiang, Xuefeng
Transition-metal-free persulfuration to construct unsymmetrical disulfides and mechanistic study of the sulfur redox process.
Chemical communications (Cambridge, England), 2015, 51, 4208-4211
7116297 CIFC14 H14 O2 S2P 1 21/c 115.245; 6.6576; 15.228
90; 118.268; 90
1361.2Xiao, Xiao; Feng, Minghao; Jiang, Xuefeng
Transition-metal-free persulfuration to construct unsymmetrical disulfides and mechanistic study of the sulfur redox process.
Chemical communications (Cambridge, England), 2015, 51, 4208-4211
7116298 CIFC32 H23 N3 O4P 1 21/c 127.8; 8.1692; 10.9466
90; 98.172; 90
2460.8Jia, Jinlong; Shi, Jingjing; Zhou, Jie; Liu, Xuelei; Song, Yanling; Xu, H. Eric; Yi, Wei
Rhodium(iii)-catalyzed C-H activation and intermolecular annulation with terminal alkynes: from indoles to carbazoles.
Chemical communications (Cambridge, England), 2015, 51, 2925
7116299 CIFC67 H54 B F24 P RuP -112.6963; 12.933; 19.631
85.538; 79.98; 85.472
3157.6Takano, Koichi; Ikeda, Yousuke; Kodama, Shintaro; Ishii, Youichi
Remote rearrangement of the metal center in a (η(6)-C6Me6)Ru(ii) complex.
Chemical communications (Cambridge, England), 2015, 51, 4981-4984
7116300 CIFC62 H52 B F24 P RuP -112.467; 14.291; 17.015
82.854; 79.193; 88.453
2955Takano, Koichi; Ikeda, Yousuke; Kodama, Shintaro; Ishii, Youichi
Remote rearrangement of the metal center in a (η(6)-C6Me6)Ru(ii) complex.
Chemical communications (Cambridge, England), 2015, 51, 4981-4984
7116301 CIFC27 H27 Br N2 O5 S2P b c a11.3613; 15.8902; 29.9856
90; 90; 90
5413.4Moriyama, Katsuhiko; Ishida, Kazuma; Togo, Hideo
Regioselective Csp(2)-H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Chemical communications (Cambridge, England), 2015, 51, 2273-2276
7116302 CIFC35 H35 Cl6 I N2 O5 S2P 1 21/n 118.254; 9.5783; 23.967
90; 97.187; 90
4157.5Moriyama, Katsuhiko; Ishida, Kazuma; Togo, Hideo
Regioselective Csp(2)-H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Chemical communications (Cambridge, England), 2015, 51, 2273-2276
7116303 CIFC22 H18 N2 O2 SP -19.9285; 10.1079; 10.4705
66.69; 76.007; 89.854
931.25Moriyama, Katsuhiko; Ishida, Kazuma; Togo, Hideo
Regioselective Csp(2)-H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Chemical communications (Cambridge, England), 2015, 51, 2273-2276
7116304 CIFC24 H22 N2 O3 SP -16.8453; 11.1232; 14.3467
95.864; 94.617; 106.163
1036.91Moriyama, Katsuhiko; Ishida, Kazuma; Togo, Hideo
Regioselective Csp(2)-H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Chemical communications (Cambridge, England), 2015, 51, 2273-2276
7116305 CIFC27 H30 N3 O5 S2P -19.5145; 11.3505; 12.4229
79.1933; 86.0059; 82.605
1305.4Moriyama, Katsuhiko; Ishida, Kazuma; Togo, Hideo
Regioselective Csp(2)-H dual functionalization of indoles using hypervalent iodine(iii): bromo-amination via 1,3-migration of imides on indolyl(phenyl)iodonium imides.
Chemical communications (Cambridge, England), 2015, 51, 2273-2276
7116306 CIFC25 H18 O3P 1 21/c 111.129; 10.015; 16.4841
90; 94.211; 90
1832.31Liang, Renxiao; Jiang, Huanfeng; Zhu, Shifa
An efficient route to highly strained cyclobutenes: indium-catalyzed reactions of enynals with alkynes.
Chemical communications (Cambridge, England), 2015, 51, 5530-5533
7116307 CIFC24 H24 O4P 21 21 218.814; 9.199; 24.64
90; 90; 90
1997.8Dethe, Dattatraya H.; Erande, Rohan D.; Mahapatra, Samarpita; Das, Saikat; B, Vijay Kumar
Protecting group free enantiospecific total syntheses of structurally diverse natural products of the tetrahydrocannabinoid family.
Chemical communications (Cambridge, England), 2015, 51, 2871
7116308 CIFC45 H77 Ca2 Cl4 N20 O18.5P 1 21/c 129.068; 15.5743; 28.894
90; 109.519; 90
12329Jiang, Xiaoqing; Yao, Xuyang; Huang, Xinghua; Wang, Qiaochun; Tian, He
A cucurbit[5]uril analogue from dimethylpropanediurea-formaldehyde condensation.
Chemical communications (Cambridge, England), 2015, 51, 2890
7116309 CIFC53 H86 Cl N22 O16.5P b c n28.753; 36.229; 14.8139
90; 90; 90
15432Jiang, Xiaoqing; Yao, Xuyang; Huang, Xinghua; Wang, Qiaochun; Tian, He
A cucurbit[5]uril analogue from dimethylpropanediurea-formaldehyde condensation.
Chemical communications (Cambridge, England), 2015, 51, 2890
7116310 CIFC43 H60 Cl3 N4 O6 SiP -19.7693; 11.7068; 21.0929
95.8445; 90.879; 93.088
2395.79Ng, Chun-Fai; Chow, Hak-Fun
A supramolecular ladder polymer prepared by hydrogen bonding-mediated self-assembly of a metallomacrocycle.
Chemical communications (Cambridge, England), 2015, 51, 2349-2352
7116311 CIFC22 H25 Br N2 O4P 1 21 110.417; 10; 11.057
90; 106.396; 90
1105Jia, Minqiang; Monari, Magda; Yang, Qing-Qing; Bandini, Marco
Enantioselective gold catalyzed dearomative [2+2]-cycloaddition between indoles and allenamides.
Chemical communications (Cambridge, England), 2015, 51, 2320-2323
7116312 CIFC15 H22 O2P 21 21 216.9058; 12.139; 15.599
90; 90; 90
1307.7Yinliang Guo; Qiang Liu; Yanxing Jia
Concise synthesis of the tricyclic skeleton of crotobarin and crotogoudin via a gold-catalyzed cycloisomerization reaction
Chem.Commun., 2015, 51, 889
7116314 CIFC20 H18 Br N O2P 1 21 19.6683; 5.72898; 16.9335
90; 104.603; 90
907.64Xiao-Hong Wei; Gang-Wei Wang; Shang-Dong Yang
Enantioselective synthesis of arylglycine derivatives by direct C-H oxidative cross-coupling
Chem.Commun., 2015, 51, 832
7116315 CIFC89 H116 Cl3 N11 Zn2P 113.469; 16.818; 19.323
105.183; 100.695; 100.481
4026Sk Asif Ikbal; Sanfaori Brahma; Sankar Prasad Rath
Step-wise induction, amplification and inversion of molecular chirality through the coordination of chiral diamines with Zn(II) bisporphyrin
Chem.Commun., 2015, 51, 895
7116316 CIFC368 H502 Cl8 N48 O3 Zn8P 1 2 124.876; 13.2663; 26.3877
90; 102.292; 90
8508.6Sk Asif Ikbal; Sanfaori Brahma; Sankar Prasad Rath
Step-wise induction, amplification and inversion of molecular chirality through the coordination of chiral diamines with Zn(II) bisporphyrin
Chem.Commun., 2015, 51, 895
7116317 CIFC15 H10 Au Cl2 NP -18.4554; 8.8766; 10.4398
70.37; 89.106; 65.222
662.86Mikhail Kondrashov; Sudarkodi Raman; Ola F. Wendt
Metal controlled regioselectivity in the cyclometallation of 2-(1-naphthyl)-pyridine
Chem.Commun., 2015, 51, 911
7116318 CIFC20 H15 Cl N2 PdP 1 21/c 112.553; 15.1519; 9.3199
90; 111.79; 90
1646Mikhail Kondrashov; Sudarkodi Raman; Ola F. Wendt
Metal controlled regioselectivity in the cyclometallation of 2-(1-naphthyl)-pyridine
Chem.Commun., 2015, 51, 911
7116319 CIFC40 H41 Cl2 N12 Ni O2.5C 1 2/c 117.941; 21.24; 13.616
90; 130.316; 90
3956Xiao-Meng Zhang; Chao-Wei Zhao; Jian-Ping Ma; Yang Yu; Qi-Kui Liu; Yu-Bin Dong
A Ni(II)-MOF: reversible guest adsorption and heterogeneous catalytic properties for silylcyanation of aromatic aldehydes
Chem.Commun., 2015, 51, 839
7116320 CIFC38 H32 Cl2 N12 NiC 1 2/c 118.101; 20.893; 13.626
90; 130.367; 90
3926Xiao-Meng Zhang; Chao-Wei Zhao; Jian-Ping Ma; Yang Yu; Qi-Kui Liu; Yu-Bin Dong
A Ni(II)-MOF: reversible guest adsorption and heterogeneous catalytic properties for silylcyanation of aromatic aldehydes
Chem.Commun., 2015, 51, 839
7116321 CIFC40 H41 Cl2 N12 Ni O2.5C 1 2/c 117.979; 21.364; 13.657
90; 130.835; 90
3969Xiao-Meng Zhang; Chao-Wei Zhao; Jian-Ping Ma; Yang Yu; Qi-Kui Liu; Yu-Bin Dong
A Ni(II)-MOF: reversible guest adsorption and heterogeneous catalytic properties for silylcyanation of aromatic aldehydes
Chem.Commun., 2015, 51, 839
7116322 CIFC38 H32 Cl2 I1.5 N12 NiC 1 2/c 118.421; 20.91; 13.545
90; 130.19; 90
3986Xiao-Meng Zhang; Chao-Wei Zhao; Jian-Ping Ma; Yang Yu; Qi-Kui Liu; Yu-Bin Dong
A Ni(II)-MOF: reversible guest adsorption and heterogeneous catalytic properties for silylcyanation of aromatic aldehydes
Chem.Commun., 2015, 51, 839
7116323 CIFC11 H7 N3 O2P n a 2111.9949; 20.6933; 3.7537
90; 90; 90
931.72Rajarshi Samanta; Rishikesh Narayan; Jonathan O. Bauer; Carsten Strohmann; Sonja Sievers; Andrey P. Antonchick
Oxidative regioselective amination of chromones exposes potent inhibitors of the hedgehog signaling pathway
Chem.Commun., 2015, 51, 925
7116324 CIFC22 H32 B10 N2 P2P 1 21/c 114.5505; 15.3833; 12.6324
90; 92.549; 90
2824.77Anika Kreienbrink; Menyhart B. Sarosi; Robert Kuhnert; Peter Wonneberger; Anna I. Arkhypchuk; Peter Lonnecke; Sascha Ott; Evamarie Hey-Hawkins
Carbaborane-based alkynylphosphanes and phospholes
Chem.Commun., 2015, 51, 836
7116325 CIFC22 H24 N2 O2 SP 4112.4405; 12.4405; 13.4141
90; 90; 90
2076.05Rumpa Pal; Govindappa Nagendra; M. Samarasimhareddy; Vommina V. Sureshbabu; Tayur N. Guru Row
Observation of a reversible isomorphous phase transition and an interplay of 'sigma-holes' and 'pi-holes' in Fmoc-Leu-psi[CH2-NCS]
Chem.Commun., 2015, 51, 933
7116326 CIFC22 H24 N2 O2 SP 4117.4665; 17.4665; 13.1291
90; 90; 90
4005.41Rumpa Pal; Govindappa Nagendra; M. Samarasimhareddy; Vommina V. Sureshbabu; Tayur N. Guru Row
Observation of a reversible isomorphous phase transition and an interplay of 'sigma-holes' and 'pi-holes' in Fmoc-Leu-psi[CH2-NCS]
Chem.Commun., 2015, 51, 933
7116327 CIFC22 H24 N2 O2 SP 1 21 14.9386; 15.0974; 13.3932
90; 97.286; 90
990.53Rumpa Pal; Govindappa Nagendra; M. Samarasimhareddy; Vommina V. Sureshbabu; Tayur N. Guru Row
Observation of a reversible isomorphous phase transition and an interplay of 'sigma-holes' and 'pi-holes' in Fmoc-Leu-psi[CH2-NCS]
Chem.Commun., 2015, 51, 933
7116328 CIFC21 H22 N2 O2 SP 1 21 14.9807; 15.9306; 12.0456
90; 99.174; 90
943.54Rumpa Pal; Govindappa Nagendra; M. Samarasimhareddy; Vommina V. Sureshbabu; Tayur N. Guru Row
Observation of a reversible isomorphous phase transition and an interplay of 'sigma-holes' and 'pi-holes' in Fmoc-Leu-psi[CH2-NCS]
Chem.Commun., 2015, 51, 933
7116329 CIFC19 H18 N2 O2 SP 1 21 14.969; 11.3897; 15.0388
90; 91.707; 90
850.75Rumpa Pal; Govindappa Nagendra; M. Samarasimhareddy; Vommina V. Sureshbabu; Tayur N. Guru Row
Observation of a reversible isomorphous phase transition and an interplay of 'sigma-holes' and 'pi-holes' in Fmoc-Leu-psi[CH2-NCS]
Chem.Commun., 2015, 51, 933
7116330 CIFC96 H136 N44 O4 Zn10P 21 21 219.5161; 30.1575; 45.9367
90; 90; 90
13183Qi Shi; Xiaozhen Kang; Fa-Nian Shi; Jinxiang Dong
Zn10(Im)20^.^4DBF: an unprecedented 10-nodal zeolitic topology with a 10-MR channel and 10 crystallographically independent Zn atoms
Chem.Commun., 2015, 51, 1131
7116331 CIFC42 H20 Cu3 N2 O15P m -3 m27.86; 27.86; 27.86
90; 90; 90
21624Ulrich Stoeck; Irena Senkovska; Volodymyr Bon; Simon Krause; Stefan Kaskel
Assembly of metal-organic polyhedra into highly porous frameworks for ethene delivery
Chem.Commun., 2015, 51, 1046
7116332 CIFC54 H28 Cu3 N2 O15P m -3 m33.97; 33.97; 33.97
90; 90; 90
39200Ulrich Stoeck; Irena Senkovska; Volodymyr Bon; Simon Krause; Stefan Kaskel
Assembly of metal-organic polyhedra into highly porous frameworks for ethene delivery
Chem.Commun., 2015, 51, 1046
7116333 CIFC13 H11 N O3P c a 2115.024; 21.464; 13.309
90; 90; 90
4291.8Raymond C. F. Jones; Alexander Chatterley; Romain Marty; W. Martin Owton; Mark R. J. Elsegood
Isoxazole to oxazole: a mild and unexpected transformation
Chem.Commun., 2015, 51, 1112
7116334 CIFC15 H15 N O3P n a 2112.93; 9.3159; 21.663
90; 90; 90
2609.4Raymond C. F. Jones; Alexander Chatterley; Romain Marty; W. Martin Owton; Mark R. J. Elsegood
Isoxazole to oxazole: a mild and unexpected transformation
Chem.Commun., 2015, 51, 1112
7116335 CIFC13 H13 N O4P 1 21/n 15.5001; 15.2463; 13.668
90; 97.7388; 90
1135.7Raymond C. F. Jones; Alexander Chatterley; Romain Marty; W. Martin Owton; Mark R. J. Elsegood
Isoxazole to oxazole: a mild and unexpected transformation
Chem.Commun., 2015, 51, 1112
7116336 CIFC15 H17 N O3 SP 1 21/c 19.7309; 7.3003; 20.4979
90; 91.2676; 90
1455.78Raymond C. F. Jones; Alexander Chatterley; Romain Marty; W. Martin Owton; Mark R. J. Elsegood
Isoxazole to oxazole: a mild and unexpected transformation
Chem.Commun., 2015, 51, 1112
7116337 CIFC26 H34 Br2 N2P -15.9858; 10.0355; 10.1711
93.862; 91.455; 96.575
605.25Pei-Qiang Huang; Qi-Wei Lang; Ai-E Wang; Jian-Feng Zheng
Direct reductive coupling of secondary amides: chemoselective formation of vicinal diamines and vicinal amino alcohols
Chem.Commun., 2015, 51, 1096
7116338 CIFC16 H13 N SP b c a5.7076; 20.718; 21.125
90; 90; 90
2498Yunfeng Liao; Yi Peng; Hongrui Qi; Guo-Jun Deng; Hang Gonga; Chao-Jun Li
Palladium-catalyzed benzothieno[2,3-b]indole formation via dehydrative-dehydrogenative double C-H sulfuration using sulfur powder, indoles and cyclohexanones
Chem.Commun., 2015, 51, 1031
7116339 CIFC52 H48 N2 O4P 1 21/n 120.5116; 5.1146; 21.4898
90; 116.49; 90
2017.8Monika Warzecha; Jesus Calvo-Castro; Alan R. Kennedy; Alisdair N. Macpherson; Kenneth Shankland; Norman Shankland; Andrew J. McLean; Callum J. McHugh
Detection of nitroaromatic vapours with diketopyrrolopyrrole thin films: exploring the role of structural order and morphology on thin film properties and fluorescence quenching efficiency
Chem.Commun., 2015, 51, 1143
7116340 CIFC18 H23 N O3P 21 21 219.976; 10.5599; 14.5715
90; 90; 90
1535Yu Yoshii; Takanori Otsu; Norihiko Hosokawa; Kiyosei Takasu; Kentaro Okano; Hidetoshi Tokuyama
Synthetic studies toward penitrem E: enantiocontrolled construction of B-E rings
Chem.Commun., 2015, 51, 1070
7116341 CIFC20 H23 N O6P 1 21/c 18.7052; 7.879; 27.3581
90; 93.841; 90
1872.23Zhi-Jun Jia; Constantin Gabriel Daniliuc; Andrey P. Antonchick; Herbert Waldmann
Phosphine-catalyzed dearomatizing [3+2] annulations of isoquinolinium methylides with allenes
Chem.Commun., 2015, 51, 1054
7116343 CIFC68 H110 Cl2 Ga2 N4 Na2 O3C 1 2/c 122.583; 14.5431; 22.793
90; 106.309; 90
7184.6Yanxia Zhao; Yanyan Liu; Zeyi Wang; Wenhua Xu; Bin Liu; Ji-Hu Su; Biao Wu; Xiao-Juan Yang
Gallium complexes with alpha-diimine and phenazine in various reduced states
Chem.Commun., 2015, 51, 1237
7116344 CIFC88 H128 Ga2 N6 O5P 1 21/c 111.056; 24.846; 15.591
90; 92.912; 90
4277Yanxia Zhao; Yanyan Liu; Zeyi Wang; Wenhua Xu; Bin Liu; Ji-Hu Su; Biao Wu; Xiao-Juan Yang
Gallium complexes with alpha-diimine and phenazine in various reduced states
Chem.Commun., 2015, 51, 1237
7116345 CIFC31 H21 N O2 SP -18.8667; 11.8588; 15.4264
112.252; 95.204; 94.286
1484.57Maxime Romain; Denis Tondelier; Bernard Geffroy; Anna Shirinskaya; Olivier Jeannin; Joelle Rault-Berthelot; Cyril Poriel
Spiro-configured phenyl acridine thioxanthene dioxide as a host for efficient PhOLEDs
Chem.Commun., 2015, 51, 1313
7116346 CIFC17 H15 Br OP 1 21/c 15.7276; 18.038; 13.687
90; 100.05; 90
1392.4Jing Chen; Chao Chen; Junjie Chen; Guohua Wang; Hongmei Qu
Cu-catalyzed intramolecular aryl-etherification reactions of alkoxyl alkynes with diaryliodonium salts via cleavage of a stable C-O bond
Chem.Commun., 2015, 51, 1356
7116347 CIFC22 H17 F N2 O4 S2P 1 21/c 19.0012; 11.6897; 19.0204
90; 92.744; 90
1999.06Bagineni Prasad; Raju Adepu; Atul Kumar Sharma; Manojit Pal
Creation of molecular complexities via a new Cu-catalyzed cascade reaction: a direct access to novel 2,2'-spirobiindole derivatives
Chem.Commun., 2015, 51, 1259
7116348 CIFC51 H51 Cl2 F6 Fe O P4P 1 21/n 112.7886; 17.372; 22.188
90; 92.649; 90
4924.1Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116349 CIFC50 H51 Fe O2 P3P 1 21/n 110.6741; 22.0513; 18.8153
90; 104.313; 90
4291.2Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116350 CIFC52 H53 Fe O P3P -110.9336; 13.3435; 16.5675
76.51; 77.792; 69.833
2183.44Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116351 CIFC52 H53 Fe O P3C 1 2/c 142.0668; 8.5013; 25.591
90; 111.301; 90
8526.7Ayham Tohme; Charles T. Hagen; Stephanie Essafi (nee Labouille); Arnaud Bondon; Thierry Roisnel; Duncan Carmichael; Frederic Paul
Easy and quantitative access to Fe(II) and Fe(III) di(aryl)alkynylphosphine oxides featuring [Fe(dppe)Cp*] endgroups: terminal P[double bond, length as m-dash]O functionality blocks the dimerisation of the Fe(III) derivatives
Chem.Commun., 2015, 51, 1316
7116352 CIFC29 H26 F6 N7 O3 P Ru SC 1 2/c 113.6846; 22.956; 20.732
90; 98.493; 90
6441.4Yue Zheng; Qianxiong Zhou; Wanhua Lei; Yuanjun Hou; Ke Li; Yongjie Chen; Baowen Zhang; Xuesong Wang
DNA photocleavage in anaerobic conditions by a Ru(II) complex: a new mechanism
Chem.Commun., 2015, 51, 428
7116353 CIFC33 H23.5 N O10.75 TbF d d 28.487; 34.829; 52.441
90; 90; 90
15501Zhiyong Guo; Xuezhi Song; Huaping Lei; Hailong Wang; Shengqun Su; Hui Xu; Guodong Qian; Hongjie Zhang; Banglin Chen
A ketone functionalized luminescent terbium metal-organic framework for sensing of small molecules
Chem.Commun., 2015, 51, 376
7116354 CIFC22 H20 N2 O2P b c n15.715; 12.1408; 9.9342
90; 90; 90
1895.4Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116355 CIFC20 H16 N2 O2P 43 21 27.0094; 7.0094; 32.787
90; 90; 90
1610.88Digambar Balaji Shinde; Sharath Kandambeth; Pradip Pachfule; Raya Rahul Kumar; Rahul Banerjee
Bifunctional covalent organic frameworks with two dimensional organocatalytic micropores
Chem.Commun., 2015, 51, 310
7116356 CIFC43 H60 Cl Cu4 N15 O28P 4/m n c13.3088; 13.3088; 20.4387
90; 90; 90
3620.2Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116357 CIFC61 H84 Cl Cu4 N20 O29.5I 4/m m m13.959; 13.959; 20.0475
90; 90; 90
3906.3Di-ming Chen; Wei Shi; Peng Cheng
A cage-based cationic body-centered tetragonal metal-organic framework: single-crystal to single-crystal transformation and selective uptake of organic dyes
Chem.Commun., 2015, 51, 370
7116358 CIFC29 H74 Ge N2 Si8P 1 21/n 112.106; 23.293; 16.666
90; 103.081; 90
4577.6Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116359 CIFC32 H64 Ge Si8P 1 21/c 113.326; 18.718; 18.391
90; 102.16; 90
4484.5Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116360 CIFC29 H69 Ge P Si8P b c a25.174; 14.054; 25.198
90; 90; 90
8915Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116361 CIFC37 H75 Ge P Si8P -19.809; 14.698; 20.257
105.37; 97.24; 109.32
2583.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116362 CIFC34 H66 Ge Si8P 1 21/n 113.204; 19.641; 18.411
90; 109.7; 90
4495.2Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116363 CIFC26 H60 Ge Si8P 1 21/n 19.642; 18.886; 22.043
90; 98.58; 90
3969.1Malgorzata Walewska; Judith Baumgartner; Christoph Marschner
Synthesis of vinyl germylenes
Chem.Commun., 2015, 51, 276
7116364 CIFC30 H28 Cl6 Fe2 N2 OP 1 21/c 110.588; 11.729; 26.02
90; 91.42; 90
3230.3Martin Brzozowski; Jose A. Forni; G. Paul Savage; Anastasios Polyzos
The direct alpha-C(sp3)-H functionalisation of N-aryl tetrahydroisoquinolinesvia an iron-catalysed aerobic nitro-Mannich reaction and continuous flow processing
Chem.Commun., 2015, 51, 334
7116365 CIFC15 H12 O3P 1 21/c 19.0155; 14.112; 9.6804
90; 90.552; 90
1231.5Saikat Khamarui; Rituparna Maiti; Dilip K. Maiti
General base-tuned unorthodox synthesis of amides and ketoesters with water
Chem.Commun., 2015, 51, 384
7116366 CIFC39 H32 Au2 F10 N2P -112.3529; 12.613; 12.95
99.282; 107.229; 100.92
1840.7Zhao Chen; Jing Zhang; Min Song; Jun Yin; Guang-AoYu; Sheng Hua Liu
A novel fluorene-based aggregation-induced emission (AIE)-active gold(I) complex with crystallization-induced emission enhancement (CIEE) and reversible mechanochromism characteristics
Chem.Commun., 2015, 51, 326
7116367 CIFC20 H16 N2P 1 21/c 118.16; 5.8576; 14.864
90; 109.694; 90
1488.7Rajeshwer Vanjari; Tirumaleswararao Guntreddi; Saurabh Kumar; Krishna Nand Singh
Sulphur promoted C(sp3)-C(sp2) cross dehydrogenative cyclisation of acetophenonehydrazones with aldehydes: efficient synthesis of 3,4,5-trisubstituted 1H-pyrazoles
Chem.Commun., 2015, 51, 366
7116368 CIFC62 H60P -14.9784; 11.3963; 19.9225
95.603; 92.746; 93.2
1121.54Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116369 CIFC86 H78P -19.7359; 16.193; 22.166
99.203; 101.335; 101.921
3278.4Gaole Dai; Jingjing Chang; Wenhua Zhang; Shiqiang Bai; Kuo-Wei Huang; Jianwei Xu; Chunyan Chi
Dianthraceno[a,e]pentalenes: synthesis, crystallographic structures and applications in organic field-effect transistors
Chem.Commun., 2015, 51, 503
7116370 CIFC15 H14 Cl N3 O5P -16.0904; 7.695; 16.3916
83.899; 82.995; 87.213
757.65Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116371 CIFC15 H15 N3 O2C 1 c 119.9626; 4.6037; 15.3349
90; 112.829; 90
1298.91Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116372 CIFC33 H13 B F15 N3 OP -111.777; 12.266; 12.551
76.4; 64.72; 64.59
1477.8Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116373 CIFC18 H21 B N3 O1.5P -19.0122; 11.123; 17.8748
72.078; 87.907; 79.532
1676.14Ming Liu; Martin Nieger; Andreas Schmidt
Mesomericbetaine - N-heterocyclic carbene interconversions of 1,2,4-triazolium-phenolates. Sulfur, selenium, and borane adduct formation
Chem.Commun., 2015, 51, 477
7116374 CIFC44 H60 B N O2P 1 21/c 118.442; 11.9605; 19.592
90; 116.965; 90
3851.7Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116375 CIFC52 H79 B2 NP 1 21/c 120.9432; 12.5599; 17.1099
90; 91.099; 90
4499.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116376 CIFC50 H65 B N2P 1 21/c 112.3306; 13.0545; 25.512
90; 90.626; 90
4106.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116377 CIFC52 H69 B N OP 1 21/n 110.6296; 23.2451; 18.409
90; 104.193; 90
4409.8Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116378 CIFC40 H52 B N O2P 1 21/n 110.1073; 16.6024; 20.2451
90; 94.273; 90
3387.79Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116379 CIFC39 H54 B N OP 1 21/c 117.347; 10.634; 19.7137
90; 112.174; 90
3367.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116380 CIFC37 H50 B N O2P 1 21/n 113.4374; 14.3288; 18.5873
90; 105.742; 90
3444.6Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116381 CIFC49 H70 B NP -110.9523; 12.2836; 18.2004
77.103; 81.075; 65.736
2170.4Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116382 CIFC52.5 H81 B N2P -110.318; 12.8163; 17.8056
83.969; 86.164; 85.117
2329.1Brandon R. Barnett; Curtis E. Moore; Arnold L. Rheingold; Joshua S. Figuero
Frustrated Lewis pair behavior of monomeric (boryl)iminomethanes accessed from isocyanide 1,1-hydroboration
Chem.Commun., 2015, 51, 541
7116383 CIFC34 H27 N O3 SP 1 21/c 16.1013; 15.039; 23.894
90; 90.877; 90
2192.2Seema Dhiman; S. S. V. Ramasastry
Synthesis of polysubstituted cyclopenta[b]indoles via relay gold(I)/Bronsted acid catalysis
Chem.Commun., 2015, 51, 557
7116384 CIFC21 H20 Cl2 O3P 21 21 2110.9383; 11.4949; 15.5104
90; 90; 90
1950.2Yuxiao Liu; Yongming Deng; Peter Y. Zavalij; Renhua Liu; Michael P. Doyle
An efficient route to highly enantioenrichedtetrahydroazulenes and beta-tetralones by desymmetrization reactions of delta,delta-diaryldiazoaceto-acetates
Chem.Commun., 2015, 51, 565
7116385 CIFC126 H108 Eu2 N18 O12P 21 21 226.0606; 28.4219; 23.3299
90; 90; 90
17280.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116386 CIFC138 H90 Eu2 F18 N18 O18 S6P -116.679; 20.3099; 24.4218
87.025; 70.961; 89.269
7809.7Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116387 CIFC44 H40 N6 O4P 1 21 110.3285; 17.8133; 10.5822
90; 100.506; 90
1914.3Chi-Tung Yeung; Wesley Ting Kwok Chan; Siu-Cheong Yan; Kwan-Leung Yu; King-Him Yim; Wing-Tak Wong; Ga-Lai Law
Lanthanide supramolecular helical diastereoselective breaking induced by point chirality: mixture or P-helix, M-helix
Chem.Commun., 2015, 51, 592
7116388 CIFC17 H17 N O3P 21 21 2110.2469; 10.4606; 13.5437
90; 90; 90
1451.7Zhao-Lin He; Chun-Jiang Wang
Ag(I)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines
Chem.Commun., 2015, 51, 534
7116389 CIFC98 H167 Ag12 N12 O0.5 P6 Si6P 1 21 115.889; 18.207; 23.994
90; 95.206; 90
6913Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116390 CIFC141 H250.8 Ag26 N16 P12 Si10P -117.285; 20.433; 29.512
95.465; 91.603; 90.317
10371Bahareh Khalili Najafabadi; John F. Corrigan
N-Heterocyclic carbene stabilized Ag-P nanoclusters
Chem.Commun., 2015, 51, 665
7116391 CIFC15.74 H19.56 N9.19 O Zn2P b c a15.504; 15.364; 18.127
90; 90; 90
4317.9Yichao Lin; Qiuju Zhang; Chongchong Zhao; Huailong Li; Chunlong Kong; Cai Shen; Liang Chen
An exceptionally stable functionalized metal-organic framework for lithium storage
Chem.Commun., 2015, 51, 697
7116392 CIFC30 H24 S2P 1 21/n 18.641; 10.6699; 25.373
90; 97.159; 90
2321.1Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116393 CIFC33 H29 Cl S2P -19.901; 11.029; 14.297
74.65; 76.568; 68.378
1383.7Sengodagounder Muthusamy; Manickasamy Sivaguru; Eringathodi Suresh
Indium(III) chloride catalyzed highly diastereoselective domino synthesis of indenodithiepines and indenodithiocines
Chem.Commun., 2015, 51, 707
7116394 CIFC39 H34 B N3P 21 21 218.621; 18.3501; 19.69
90; 90; 90
3114.9Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116395 CIFC25 H19 B F2 N2P 21 21 2110.9427; 12.7077; 14.9474
90; 90; 90
2078.5Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116396 CIFC27 H24 B F2 N3P -112.2723; 14.705; 14.7883
69.664; 67.961; 82.665
2319.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116397 CIFC37 H29 B N2P 1 21/n 110.9565; 19.2414; 13.7066
90; 95.002; 90
2878.6Xiaoqing Wang; Yanping Wu; Qingsong Liu; Zhenyu Li; Hui Yan; Chonglei Ji; Jicheng Duan; Zhipeng Liu
Aggregation-induced emission (AIE) of pyridyl-enamido-based organoboron luminophores
Chem.Commun., 2015, 51, 784
7116398 CIFC81 H19 NC m c 2115.499; 27.568; 9.7851
90; 90; 90
4180.9T. W. Chamberlain; M. A. Lebedeva; W. Abuajwa; M. Suyetin; W. Lewis; E. Bichoutskaia; M. Schroder; A.; N.; Khlobystov'
Switching intermolecular interactions by confinement in carbon nanotubes
Chem.Commun., 2015, 51, 648
7116399 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.682; 30.682; 23.596
90; 90; 120
19237Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116400 CIFC168 H192 Cl8 Fe4 N36 O32R 3 :H30.825; 30.825; 22.939
90; 90; 120
18876Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116401 CIFC211.17 H272.75 Cl8 Fe4 N47.58 O47P 119.6065; 19.7357; 20.2252
116.621; 115.561; 94.4565
5944.6Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116402 CIFC192 H234 Cl8 Fe4 N42 O44P 119.7723; 19.7731; 20.282
115.476; 116.397; 94.961
6022.1Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116403 CIFC174 H189 Cl20 Fe4 N39 O32R 3 :H31.4702; 31.4702; 22.296
90; 90; 120
19123Dong-Hong Ren; Dan Qiu; Chun-Yan Pang; Zaijun Li; Zhi-Guo Gu
Chiral tetrahedral iron(II) cages: diastereoselective subcomponent self-assembly, structure interconversion and spin-crossover properties
Chem.Commun., 2015, 51, 788
7116404 CIFC H B N O ZnP 43 21 28.67; 8.67; 12.722
90; 90; 90
956.3Chun-Yang Pan; Li-Juan Zhong; Feng-Hua Zhao; Hong-Mei Yang; Jian Zhou
Zn(1,3-DAP)[B4O7]: a rare chiral zeolitic framework constructed of four-connected [B4O9] clusters with a single-stranded helical channel
Chem.Commun., 2015, 51, 753
7116405 CIFC21 H19 Br N3 O3C 1 2 119.7543; 6.8067; 15.8605
90; 98.736; 90
2107.89Bao-Dong Cui; Yong You; Jian-Qiang Zhao; Jian Zuo; Zhi-Jun Wu; Xiao-Ying Xu; Xiao-Mei Zhang; Wei-Cheng Yuan
3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3'-disubstituted oxindole derivatives
Chem.Commun., 2015, 51, 757
7116406 CIFC10 H9 N O3P 1 21/c 19.3511; 11.4869; 8.4156
90; 102.475; 90
882.62Jingjing Shi; Jie Zhou; Yunnan Yan; Jinlong Jia; Xuelei Liu; Huacan Song; H. Eric Xu; Wei Yi
One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh(III)-catalyzed carbenoid insertion C-H activation/cyclization
Chem.Commun., 2015, 51, 668
7116407 CIFC52 H72 B2 Be N4P 1 21/n 112.855; 27.0697; 14.2004
90; 92.555; 90
4936.6T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116408 CIFC63 H86 B2 Be N6P 1 21 112.3713; 20.3783; 12.4856
90; 114.919; 90
2854.7T. Arnold; H. Braunschweig; W. C. Ewing; T. Kramer; J. Mies; J. K. Schuster
Beryllium bis(diazaborolyl): old neighbors finally shake hands
Chem.Commun., 2015, 51, 737
7116409 CIFC149 H248 B8 P8 Sn4P 1 21/c 114.0885; 26.577; 20.0509
90; 95.273; 90
7475.89Keith Izod; Casey M. Dixon; Ross W. Harrington; Michael R. Probert
Impact of a rigid backbone on the structure of an agostically-stabilised dialkylstannylene: isolation of an unusual bridged stannyl-stannylene
Chem.Commun., 2015, 51, 679
7116410 CIFC37 H38 N4 Ni O6P 1 21 18.2226; 39.325; 10.4346
90; 91.494; 90
3372.9Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116411 CIFC36 H34 N4 Ni O5P 1 21/n 111.0249; 18.09; 15.8569
90; 91.288; 90
3161.7Tingting Li; Shengbin Zhou; Jiang Wang; Jose Luis Acena; Vadim A. Soloshonok; Hong Liu
Asymmetric synthesis of alpha-(1-oxoisoindolin-3-yl)glycine: synthetic and mechanistic challenges
Chem.Commun., 2015, 51, 1624
7116412 CIFC24 H20 B Cl2 F2 N3 O SP 1 21/n 19.5908; 10.9141; 22.863
90; 99.059; 90
2363.3Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116413 CIFC27 H26 B F2 N3 O2 SP 1 21/n 114.5722; 16.046; 22.1206
90; 107.66; 90
4928.61Hui Liu; Hua Lu; Zhikuan Zhou; Soji Shimizu; Zhifang Li; Nagao Kobayashi; Zhen Shen
Asymmetric core-expanded aza-BODIPY analogues: facile synthesis and optical properties
Chem.Commun., 2015, 51, 1713
7116414 CIFC17 H14 F6 O2 S2P 1 21/c 19.9685; 10.863; 15.8102
90; 98.901; 90
1691.4Ryuhei Kodama; Kimio Sumaru; Kana Morishita; Toshiyuki Kanamori; Kengo Hyodo; Takashi Kamitanaka; Masakazu Morimoto; Satoshi Yokojima; Shinichiro Nakamura; Kingo Uchida
A diarylethene as the SO2 gas generator upon UV irradiation
Chem.Commun., 2015, 51, 1736
7116415 CIFC26 H27 O3 PP 1 21/c 118.332; 6.1364; 20.639
90; 107.621; 90
2212.8Yuzhen Gao; Xueqin Li; Jian Xu; Yile Wu; Weizhu Chen; Guo Tang; Yufen Zhao
Mn(OAc)3-mediated phosphonation-lactonization of alkenoic acids: synthesis of phosphono-gamma-butyrolactones
Chem.Commun., 2015, 51, 1605
7116416 CIFC H Cl SP -111.7098; 12.2432; 19.742
75.953; 72.973; 75.614
2576.9Ru-Qiang Lu; Yi-Nyu Zhou; Xiao-Yun Yan; Ke Shi; Yu-Qing Zheng; Ming Luo; Xin-Chang Wang; Jian Pei; Haiping Xia; Laura Zoppi; Kim K. Baldridge; Jay S. Siegel; Xiao-Yu Cao
Thiophene-fused bowl-shaped polycyclic aromatics with a dibenzo[a,g]corannulene core for organic field-effect transistors
Chem.Commun., 2015, 51, 1681
7116417 CIFC26 H17 NP 1 21/c 113.6965; 7.3314; 18.6691
90; 103.364; 90
1823.89Iyyanar Karthikeyan; Dhanarajan Arunprasath; Govindasamy Sekar
An efficient synthesis of pyrido[1,2-a]indoles through aza-Nazarov type cyclization
Chem.Commun., 2015, 51, 1701
7116418 CIFC27 H16 O4 ZnI b a m36.006; 6.013; 31.426
90; 90; 90
6803.9Xun-Gao Liu; Hui Wang; Bin Chen; Yang Zou; Zhi-Guo Gu; Zujin Zhao; Liang Shen
A luminescent metal-organic framework constructed using a tetraphenylethene-based ligand for sensing volatile organic compounds
Chem.Commun., 2015, 51, 1677
7116419 CIFC11 H13 B Cl2 N2P 1 21/n 17.839; 16.0342; 9.5567
90; 96.056; 90
1194.5Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deisshurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116420 CIFC13 H17 B Cl2 N2C 1 c 115.0371; 7.5273; 13.1615
90; 108.431; 90
1413.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116421 CIFC25 H25 B N2P 1 21/n 110.68; 14.1175; 13.6179
90; 93.975; 90
2048.3Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116422 CIFC27 H29 B N2P 1 21/n 111.205; 13.058; 16.087
90; 106.498; 90
2256.9Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116423 CIFC37 H55 B N2 P2 PtP -115.9324; 15.9875; 16.3672
63.872; 87.926; 79.834
3680.2Holger Braunschweig; Christina Claes; Alexander Damme; Andrea Deissenberger; Rian D. Dewhurst; Christian Horl; Thomas Kramer
A facile and selective route to remarkably inert monocyclic NHC-stabilized boriranes
Chem.Commun., 2015, 51, 1627
7116424 CIFC40.67 H53.33 N5 O4.17 RhR -3 :H34.6494; 34.6494; 16.6624
90; 90; 120
17324.5Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116425 CIFC109 H134 N15 O7 Rh3P 1 21/n 121.7612; 21.6015; 23.3468
90; 90.011; 90
10974.7Eva Jurgens; Barbara Wucher; Frank Rominger; Karl W. Tornroos; Doris Kunz
Selective rearrangement of terminal epoxides into methylketones catalysed by a nucleophilic rhodium-NHC-pincer complex
Chem.Commun., 2015, 51, 1897
7116426 CIFC39 H39 Ir N2 O2 S2P b c a13.4876; 18.3802; 27.8072
90; 90; 90
6893.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116427 CIFC60 H65 Cl2 Ir N2 O2 S2P -112.8835; 14.7285; 16.0114
103.949; 93.493; 103.298
2847.71Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116428 CIFC31.25 H24 Ir N2 O2.25 S2P -118.4383; 18.6855; 19.9281
107.775; 99.052; 117.763
5407.5Ming Li; Baozhan Zheng; Daibing Luo; Huiqin Sun; Ning Wang; Yan Huang; Jun Dai; Dan Xiao; Shi-Jian Su; Zhiyun Lu
Small molecular neutral microcrystalline iridium(III) complexes as promising molecular oxygen sensors
Chem.Commun., 2015, 51, 1926
7116429 CIFC58 H58 N10 O18 S4P -17.8554; 13.428; 14.296
74.64; 83.39; 82.18
1435.6Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116430 CIFC58 H74 N10 O26 S4P -110.5682; 12.4098; 13.8043
70.117; 82.636; 85.85
1687.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116431 CIFC58 H61 N10 O19.5 S4P -112.2027; 13.5862; 19.851
72.658; 78.079; 72.902
2977Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116432 CIFC65 H68 N11 O18.5 S4P -114.085; 16.457; 16.585
80.08; 66.96; 72.44
3366.4Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116433 CIFC65 H69 N11 O19 S4P -113.9; 16.237; 16.444
79.98; 66.84; 73.12
3257.7Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116434 CIFC62 H69 N10 O21.5 S4P -114.166; 16.38; 18.029
103.04; 109.53; 98.05
3733.8Han-Yuan Gong; Feng Tang; Brett M. Rambo; Rui Cao; Jun-Feng Xiang; Jonathan L. Sessler
Aromatic sulfonate anion-induced pseudorotaxanes: environmentally benign synthesis, selectivity, and structural characterization
Chem.Commun., 2015, 51, 1795
7116435 CIFC96 H144 Br4 N8 O22P 1 21/c 110.8583; 18.3496; 22.4335
90; 91.834; 90
4467.5Wei Zhang; Yi Li; Jing-Hua Sun; Cai-Ping Tan; Liang-Nian Ji; Zong-Wan Mao
Supramolecular self-assembled nanoparticles for chemo-photodynamic dual therapy against cisplatin resistant cancer cells
Chem.Commun., 2015, 51, 1807
7116436 CIFC56 H42C 1 2/c 123.491; 10.5581; 16.883
90; 99.21; 90
4133.3Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116437 CIFC74 H80 O SP -114.3679; 14.8455; 16.0061
75.95; 83.391; 83.523
3277.2Guoying Zhang; Yinjun Xie; Zhengkun Wang; Yang Liu; Hanmin Huang
Diboron as a reductant for nickel-catalyzed reductive coupling: rational design and mechanistic studies
Chem.Commun., 2015, 51, 1850
7116438 CIFC132 H120 N24P 21 21 2123.855; 26.655; 27.082
90; 90; 90
17220Huimin Ding; Yihui Yang; Bijian Li; Feng Pan; Guozhu Zhu; Matthias Zeller; Daqiang Yuan; Cheng Wang
Targeted synthesis of a large triazine-based [4+6] organic molecular cage: structure, porosity and gas separation
Chem.Commun., 2015, 51, 1976
7116439 CIFC65 H90 F6 N8 Na O10 P Rh4P 1 21/c 116.7562; 16.3493; 27.6506
90; 91.707; 90
7571.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116440 CIFC65 H92 B F4 N8 Na O11 Rh4P 1 21/c 116.662; 16.4372; 27.4724
90; 94.94; 90
7496.1Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116441 CIFC66 H87 N12 Na O12 Rh4P b c a22.6289; 21.7265; 29.7275
90; 90; 90
14615.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116442 CIFC62 H97.5 Ca N10.5 O22 Rh4P -111.3211; 18.6735; 18.7302
89.602; 75.171; 87.676
3824.6Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116443 CIFC62 H83 La N12 O19 Rh4P 21 21 218.7826; 19.9113; 10.6111
90; 90; 90
3968.4Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116444 CIFC62 H83 Eu N12 O19 Rh4P 21 21 218.4641; 19.8783; 10.5405
90; 90; 90
3868.7Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116445 CIFC66 H86 Dy N13 O20 Rh4P 1 21/c 113.9749; 18.7743; 28.0431
90; 93.975; 90
7339.9Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116446 CIFC66 H86 Er N13 O20 Rh4P 1 21/c 113.8619; 18.8672; 28.1155
90; 93.687; 90
7338Ayana Kashima; Mika Sakate; Hiromi Ota; Akira Fuyuhiro; Yukinari Sunatsuki; Takayoshi Suzuki
Thyminate(2-)-bridged cyclic tetranuclear rhodium(III) complexes formed by a template of a sodium, calcium or lanthanoid ion
Chem.Commun., 2015, 51, 1889
7116447 CIFC57 H48 B Cl2 F24 Ir N P SP 41 21 212.9489; 12.9489; 70.484
90; 90; 90
11818.3Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer
Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines
Chem.Commun., 2015, 51, 1941
7116448 CIFC12 H21 B N PP 21 21 2110.793; 11.0539; 11.3385
90; 90; 90
1352.7Areli Flores-Gaspar; Silvia Orgue; Arnald Grabulosa; Antoni Riera; Xavier Verdaguer
Borane as an efficient directing group. Stereoselective 1,2-addition of organometallic reagents to borane P-stereogenic N-phosphanylimines
Chem.Commun., 2015, 51, 1941
7116449 CIFC34 H34 N2 O4 S4A b a 228.621; 26.533; 9.756
90; 90; 90
7409Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116450 CIFC36 H38 N2 O4 S4P -19.597; 13.9714; 14.765
105.066; 107.053; 97.126
1784.1Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116451 CIFC18 H19 N O2 S2P 1 21/c 19.6224; 14.3505; 13.0206
90; 102.158; 90
1757.6Yu Jiang; Xiang-Ying Tang; Min Shi
A Rh-catalyzed 1,2-sulfur migration/aza-Diels-Alder cascade initiated by aza-vinyl carbenoids from sulfur-tethered N-sulfonyl-1,2,3-triazoles
Chem.Commun., 2015, 51, 2122
7116453 CIFC20 H17 N3 O3P 1 21 15.3666; 14.0877; 11.0289
90; 94.065; 90
831.72Daniel Hack; Pankaj Chauhan; Kristina Deckers; Yusuke Mizutani; Gerhard Raabe; Dieter Enders
Combining silver- and organocatalysis: an enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles
Chem.Commun., 2015, 51, 2266
7116454 CIFC15 H18 O4P 1 21/c 18.5618; 8.4049; 18.442
90; 93.163; 90
1325.1Fiene Horeischi; Claudia Guttroff; Bernd Plietker
The enantioselective total synthesis of (+)-clusianone
Chem.Commun., 2015, 51, 2259
7116455 CIFC16 H17 IP 1 21/n 110.6651; 14.1041; 17.531
90; 101.441; 90
2584.6Stephen J. Murray; Hasim Ibrahim
Asymmetric Kita spirolactonisation catalysed by anti-dimethanoanthracene-based iodoarenes
Chem.Commun., 2015, 51, 2376
7116456 CIFC26 H27 N3 O8P 21 21 2110.6406; 11.0802; 21.8683
90; 90; 90
2578.27Pankaj Chauhan; Suruchi Mahajan; Gerhard Raabe; Dieter Enders
Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters
Chem.Commun., 2015, 51, 2270
7116457 CIFC229 H308 Cl3 Eu2 N20 O16P -119.854; 24.158; 25.212
99.59; 106.63; 106.33
10710Guifen Lu; Sen Yan; Mengying Shi; Wenhan Yu; Jing Li; Weihua Zhu; Zhongping Ou; Karl M. Kadish
A new class of rare earth tetrapyrrole sandwich complexes containing corrole and phthalocyanine macrocycles: synthesis, physicochemical characterization and X-ray analysis
Chem.Commun., 2015, 51, 2411
7116458 CIFC21 H18 N2P b c a15.517; 8.4691; 23.518
90; 90; 90
3090.6Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116459 CIFC25 H34 N2 SiP -17.7419; 14.8215; 21.0488
75.571; 80.3817; 85.172
2303.92Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116460 CIFC24 H27 Cl4 N2 RhP 1 21/c 126.7294; 8.902; 20.8098
90; 90.4289; 90
4951.5Yang, Xiao-Fei; Hu, Xu-Hong; Feng, Chao; Loh, Teck-Peng
Rhodium(iii)-catalyzed C7-position C-H alkenylation and alkynylation of indolines.
Chemical communications (Cambridge, England), 2015, 51, 2532-2535
7116461 CIFC16 H11 B F2 N2 OP -16.9566; 8.3315; 23.1202
95.844; 90.57; 96.433
1324.35Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116462 CIFC17 H13 B F2 N2 OP -17.0915; 10.1014; 10.3857
86.948; 70.988; 86.697
701.75Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116463 CIFC29 H22 B F2 N3 OP 1 21/n 118.0013; 6.9212; 20.263
90; 116.034; 90
2268.42Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116464 CIFC22 H15 B F2 N2 OP -17.1054; 11.1114; 11.9627
96.493; 106.301; 105.521
855.17Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116465 CIFC34 H24 B F2 N3 OP 1 2/n 114.9332; 11.3243; 17.9422
90; 94.526; 90
3024.71Liao, Chia-Wei; Rao M, Rajeswara; Sun, Shih-Sheng
Structural diversity of new solid-state luminophores based on quinoxaline-β-ketoiminate boron difluoride complexes with remarkable fluorescence switching properties.
Chemical communications (Cambridge, England), 2015, 51, 2656-2659
7116466 CIFC20 H15 N OP b c a13.099; 9.359; 24.26
90; 90; 90
2974Yan, Rulong; Li, Xiaoni; Yang, Xiaodong; Kang, Xing; Xiang, Likui; Huang, Guosheng
A novel one-pot method for the synthesis of substituted furopyridines: iodine-mediated oxidation of enaminones by tandem metal-free cyclization.
Chemical communications (Cambridge, England), 2015, 51, 2573-2576
7116467 CIFC20 H14 I N OP 1 21/c 17.4452; 19.3722; 11.2423
90; 91.073; 90
1621.19Yan, Rulong; Li, Xiaoni; Yang, Xiaodong; Kang, Xing; Xiang, Likui; Huang, Guosheng
A novel one-pot method for the synthesis of substituted furopyridines: iodine-mediated oxidation of enaminones by tandem metal-free cyclization.
Chemical communications (Cambridge, England), 2015, 51, 2573-2576
7116468 CIFC64 H80 F12 N3 O15 P3P 1 21 111.316; 24.717; 14.0638
90; 100.065; 90
3873.1Wang, Qi; Cheng, Ming; Xiong, Shuhan; Hu, Xiao-Yu; Jiang, Juli; Wang, Leyong; Pan, Yi
P[double bond, length as m-dash]O functional group-containing cryptands: from supramolecular complexes to poly[2]pseudorotaxanes.
Chemical communications (Cambridge, England), 2015, 51, 2667-2670
7116469 CIFC62 H73 F12 N2 O13 P3P 1 21/n 117.2062; 23.6008; 18.4826
90; 90.615; 90
7505Wang, Qi; Cheng, Ming; Xiong, Shuhan; Hu, Xiao-Yu; Jiang, Juli; Wang, Leyong; Pan, Yi
P[double bond, length as m-dash]O functional group-containing cryptands: from supramolecular complexes to poly[2]pseudorotaxanes.
Chemical communications (Cambridge, England), 2015, 51, 2667-2670
7116470 CIFC25 H26 O2P 1 21/n 112.4084; 6.0932; 26.1861
90; 96.043; 90
1968.85Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116471 CIFC24 H23 Cl O2P 1 21/n 112.4763; 6.01195; 26.1383
90; 97.18; 90
1945.18Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116472 CIFC28 H25 N O2P 1 21/c 19.89753; 24.4163; 9.00094
90; 93.3654; 90
2171.43Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116473 CIFC26 H20 OP 1 21/n 19.3875; 10.893; 18.522
90; 95.417; 90
1885.56Khan, Imtiaz; Chidipudi, Suresh Reddy; Lam, Hon Wai
Synthesis of spiroindanes by palladium-catalyzed oxidative annulation of non- or weakly activated 1,3-dienes involving C-H functionalization.
Chemical communications (Cambridge, England), 2015, 51, 2613-2616
7116476 CIFC25 H35 Cl Ir N3P -18.5409; 11.3926; 13.7162
69.634; 87.763; 71.53
1182.94He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116477 CIFC25 H36 B Cl F4 Ir N3C 1 2/c 122.1698; 20.5501; 14.5843
90; 110.936; 90
6205.8He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116478 CIFC33 H47 Cl2 Ir2 N3P 1 21/c 18.7044; 21.9069; 19.1631
90; 115.407; 90
3300.7He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116479 CIFC50 H68 Ir2 N6P -112.2904; 13.329; 19.4944
86.542; 72.6; 62.575
2693.6He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116480 CIFC25 H35 F6 Ir N3 PP -110.275; 10.7121; 13.6503
105.834; 110.036; 97.403
1316.23He, Fan; Braunstein, Pierre; Wesolek, Marcel; Danopoulos, Andreas A.
Imine-functionalised protic NHC complexes of Ir: direct formation by C-H activation.
Chemical communications (Cambridge, England), 2015, 51, 2814
7116481 CIFC22 H43 N P2P 1 21/c 113.7199; 12.3613; 28.1443
90; 96.935; 90
4738.2Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116482 CIFC36 H68 Li2 N2 P4P 21 21 2124.1538; 13.7672; 12.0771
90; 90; 90
4016Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116483 CIFC22 H42 Br N Ni P2P 21 21 2111.4257; 14.471; 15.0601
90; 90; 90
2490.06Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116484 CIFC50 H90 Hg N2 Ni2 P4P -113.9339; 16.4179; 24.9947
108.376; 96.539; 97.87
5299.7Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116485 CIFC18 H35 N Ni P2P b c a13.2113; 14.5597; 21.1415
90; 90; 90
4066.6Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116486 CIFC22 H43 N Ni P2P 21 21 2111.0422; 14.7303; 14.7768
90; 90; 90
2403.52Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116487 CIFC19 H35 N Ni O2 P2P b c a15.7937; 13.5622; 20.653
90; 90; 90
4423.82Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116488 CIFC23 H45 N Ni P2P 21 21 2111.4225; 14.6398; 14.939
90; 90; 90
2498.15Kreye, Markus; Freytag, Matthias; Jones, Peter G.; Williard, Paul G.; Bernskoetter, Wesley H.; Walter, Marc D.
Homolytic H2 cleavage by a mercury-bridged Ni(i) pincer complex [{(PNP)Ni}2{μ-Hg}].
Chemical communications (Cambridge, England), 2015, 51, 2946
7116489 CIFC22 H33 Cl2 Cr N5 O19P 1 21/n 115.236; 14.7664; 16.0081
90; 118.237; 90
3172.9de Sousa, David P.; Bigelow, Jennifer O.; Sundberg, Jonas; Que, Lawrence; McKenzie, Christine J.
Caught! Crystal trapping of a side-on peroxo bound to Cr(iv).
Chemical communications (Cambridge, England), 2015, 51, 2802
7116490 CIFC24 H28 Cl2 Cr N5 O11P 1 21/c 116.3004; 12.4635; 13.5694
90; 91.647; 90
2755.6de Sousa, David P.; Bigelow, Jennifer O.; Sundberg, Jonas; Que, Lawrence; McKenzie, Christine J.
Caught! Crystal trapping of a side-on peroxo bound to Cr(iv).
Chemical communications (Cambridge, England), 2015, 51, 2802
7116491 CIFC29 H23 N O4P -17.8653; 12.7093; 12.7665
105.75; 100.5; 105.51
1137.98Selvaraju, Subhashini; Niradha Sachinthani, K. A.; Hopson, RaiAnna A; McFarland, Frederick M.; Guo, Song; Rheingold, Arnold L.; Nelson, Toby L.
Eumelanin-inspired core derived from vanillin: a new building block for organic semiconductors.
Chemical communications (Cambridge, England), 2015, 51, 2957
7116492 CIFC168 H96 N9 O53 Zn17R 3 2 :H23.2738; 23.2738; 33.9318
90; 90; 120
15917.4Hu, Jin-Song; Zhang, Lei; Qin, Ling; Zheng, He-Gen; Zhang, Xiang-Biao
A rare three-coordinated zinc cluster-organic framework with two types of secondary building units.
Chemical communications (Cambridge, England), 2015, 51, 2899
7116493 CIFC54 H65 N5 O10 Os3 P2P 1 21/c 112.4416; 15.7773; 28.046
90; 102.532; 90
5374.1Lipeng Wu; Qiang Liu; Anke Spannenberg; alf Jackstell; Matthias Beller
Highly regioselective osmium-catalyzed hydroformylation
Chem.Commun., 2015, 51, 3080
7116494 CIFC60 H50 N2 O10F d d 220.642; 78.16; 8.624
90; 90; 90
13914Zhichao Hu; Guangxi Huang; William P. Lustig; Fangming Wang; Hao Wang; Simon J. Teat; Debasis Banerjee; Deqing Zhang; Jing Li
Achieving exceptionally high luminescence quantum efficiency by immobilizing an AIE molecular chromophore into a metal-organic framework
Chem.Commun., 2015, 51, 3045
7116495 CIFC54 H32 O8 Zn2C 1 2/c 136.929; 31.08; 11.8533
90; 99.228; 90
13429Zhichao Hu; Guangxi Huang; William P. Lustig; Fangming Wang; Hao Wang; Simon J. Teat; Debasis Banerjee; Deqing Zhang; Jing Li
Achieving exceptionally high luminescence quantum efficiency by immobilizing an AIE molecular chromophore into a metal-organic framework
Chem.Commun., 2015, 51, 3045
7116496 CIFC49 H77 Li2 N3 O4P -111.302; 12.6719; 17.2731
91.27; 103.597; 99.07
2369.89Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116497 CIFC61 H95 Li2 N3 O6P -110.8651; 14.5756; 20.5112
102.51; 100.746; 106.653
2928.9Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116498 CIFC74 H106 Li4 N6 O2C 1 2/c 131.4483; 18.8909; 26.5581
90; 94.384; 90
15731.7Andreas A. Danopoulos; Pierre Braunstein; Elixabete Rezabal; Gilles Frison
Unprecedented directed lateral lithiations of tertiary carbons on NHC platforms
Chem.Commun., 2015, 51, 3049
7116499 CIFC18 H20 F12 N4 Ni PC m c m10.3657; 13.2968; 16.2518
90; 90; 90
2240Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116500 CIFC53 H76 F12 N8 Ni2P 1 21/n 110.2621; 19.5073; 13.473
90; 96.154; 90
2681.6Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116501 CIFC28 H40 F12 N4 Ni O PP b c a14.2479; 14.493; 30.515
90; 90; 90
6301.2Fengzhi Tang; Nigam P. Rath; Liviu M. Mirica
Stable bis(trifluoromethyl)nickel(III) complexes
Chem.Commun., 2015, 51, 3113
7116502 CIFC70 H90 N2 O8 Si4 Ti2P -110.0526; 11.8019; 14.793
74.19; 89.42; 75.231
1629.5Christian Godemann; Laura Dura; Dirk Hollmann; Kathleen Grabow; Ursula Bentrup; Haijun Jiao; Axel Schulz; Angelika Bruckner; Torsten Beweries
Highly selective visible light-induced Ti-O bond splitting in an ansa-titanocene dihydroxido complex
Chem.Commun., 2015, 51, 3065
7116503 CIFC25 H36 Cl3 Ir N2P -19.516; 9.914; 14.152
95.215; 95.676; 105.908
1267.9Y. Gothe; T. Marzo; L. Messori; N. Metzler-Nolte
Cytotoxic activity and protein binding through an unusual oxidative mechanism by an iridium(I)-NHC complex
Chem.Commun., 2015, 51, 3151
7116504 CIFC22 H18P 1 21/c 111.2196; 12.1534; 11.867
90; 112.497; 90
1495Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Preparation of phenanthrenes from ortho-amino-biphenyls and alkynes via base-promoted homolytic aromatic substitution
Chem.Commun., 2015, 51, 3121
7116505 CIFC21 H15 ClP 1 21/c 111.2081; 12.3535; 11.9376
90; 113.383; 90
1517.12Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Preparation of phenanthrenes from ortho-amino-biphenyls and alkynes via base-promoted homolytic aromatic substitution
Chem.Commun., 2015, 51, 3121
7116506 CIFC29 H24 Br2 O2P -18.9872; 9.0894; 15.463
79.651; 77.966; 77.931
1195.8Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116507 CIFC37 H26 OP -19.9865; 10.56; 13.7281
86.2498; 84.3378; 64.127
1295.86Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116508 CIFC29 H25 Br O2P 1 21/n 18.4379; 16.1157; 16.807
90; 101.44; 90
2240.06Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116509 CIFC41 H26 OC 1 2/c 141.059; 10.4431; 13.0847
90; 98.557; 90
5548Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116510 CIFC29 H25 Br O2P 1 21/c 18.4457; 15.2032; 17.4327
90; 92.8463; 90
2235.63Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116511 CIFC29 H26 O2P 1 21/n 18.4797; 16.5725; 15.9445
90; 103.454; 90
2179.2Katsutoshi Arai; Yoichi Kobayashi; Jiro Abe
Rational molecular designs for drastic acceleration of the color-fading speed of photochromic naphthopyrans
Chem.Commun., 2015, 51, 3057
7116513 CIFC16 H15 Cl2 N O2 SP -18.2507; 9.1868; 10.7811
92.8871; 100.081; 91.7403
802.9Steven J. Mansfield; Craig D. Campbell; Michael W. Jones; Edward A. Anderson
A robust and modular synthesis of ynamides
Chem.Commun., 2015, 51, 3316
7116514 CIFC5 H5 Cl2 N O2P 21 c n5.8679; 10.425; 11.8622
90; 90; 90
725.64Steven J. Mansfield; Craig D. Campbell; Michael W. Jones; Edward A. Anderson
A robust and modular synthesis of ynamides
Chem.Commun., 2015, 51, 3316
7116515 CIFC21 H40 N O2 SP -15.8562; 8.0977; 23.1501
84.648; 86.401; 84.429
1086.27Stefanie-Ann Alexander; Emma M. Rouse; Jonathan M. White; Nicole Tse; Caroline Kyi; Carl H. Schiesser
Controlling biofilms on cultural materials: the role of 3-(dodecane-1-thiyl)-4-(hydroxymethyl)-2,2,5,5-tetramethyl-1-pyrrolinoxyl
Chem.Commun., 2015, 51, 3355
7116516 CIFC64 H88 N O16P -112.306; 12.532; 25.592
95.097; 99.985; 107.517
3665Shilu Wang; Yiliang Wang; Zhenxia Chen; Yuejian Lin; Linhong Weng; Kang Han; Jian Li; Xueshun Jia; Chunju Li
The marriage of endo-cavity and exo-wall complexation provides a facile strategy for supramolecular polymerization
Chem.Commun., 2015, 51, 3434
7116524 CIFC28 H19 N OP 21 21 218.519; 9.631; 24.207
90; 90; 90
1986.1Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116525 CIFC79 H51 Cl9 N4P -18.6479; 12.683; 16.619
111.32; 92.12; 99.49
1665.5Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116526 CIFC41 H28 F6 N5 P RuP -112.308; 13.017; 13.044
111.17; 111.32; 98.55
1718.5Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116527 CIFC28 H17 NP -13.8489; 17.796; 25.127
86.217; 89.836; 85.622
1712.3Yan-Qin He; Yu-Wu Zhong
The synthesis of 2- and 2,7-functionalized pyrene derivatives through Ru(II)-catalyzed C-H activation
Chem.Commun., 2015, 51, 3411
7116528 CIFC16 H111 Cu4 Dy2 K2 N16 O101.5 Si2 W22C 1 m 120.5847; 13.4613; 22.9069
90; 101.973; 90
6209.3Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116529 CIFC26 H126 Cu6 Er2 N24 O97 Si2 W22F d d 243.425; 43.548; 25.625
90; 90; 90
48459Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116530 CIFC16 H77 Cu Er N12 O85 Si2 W22P 1 21/c 119.142; 24.362; 21.693
90; 99.006; 90
9992Fei-Yan Yi; Wei Zhu; Song Dang; Jian-Ping Li; Dai Wu; Yun-hui Li; Zhong-Ming Sun
Polyoxometalates-based heterometallic organic-inorganic hybrid materials for rapid adsorption and selective separation of methylene blue from aqueous solutions
Chem.Commun., 2015, 51, 3336
7116531 CIFC40 H34 As2 Br N O2 PdP 1 21/n 112.2363; 15.6103; 19.0632
90; 105.412; 90
3510.36Thomas O. Ronson; Jonathan R. Carney; Adrian C. Whitwood; Richard J.K. Taylor; Ian J. S. Fairlamb
AsCat and FurCat: new Pd catalysts for selective room-temperature Stille cross-couplings of benzyl chlorides with organostannanes
Chem.Commun., 2015, 51, 3466
7116532 CIFC17 H18 F6 O5 S2P 1 21/c 19.8939; 13.25; 15.9721
90; 102.881; 90
2041.16Benito Alcaide; Pedro Almendros; Israel Fernandez; Carlos Lazaro-Milla
Unveiling the uncatalyzed reaction of alkynes with 1,2-dipoles for the room temperature synthesis of cyclobutenes
Chem.Commun., 2015, 51, 3395
7116533 CIFC15 H15 Br F N O2 SP 1 21/c 111.571; 5.2088; 26.139
90; 93.278; 90
1572.8Jorge Saavedra-Olavarria; Gean C. Arteaga; Jhon J. Lopez; Edwin G. Perez
Copper-catalyzed intermolecular and regioselective aminofluorination of styrenes: facile access to beta-fluoro-N-protected phenethylamines
Chem.Commun., 2015, 51, 3379
7116534 CIFC38 H38 O2P -19.6115; 12.5777; 14.3804
110.013; 107.49; 99.474
1486.96Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116535 CIFC38 H38 O2P -19.3559; 9.9674; 16.4761
99.935; 101.993; 96.7
1461.72Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116536 CIFC38 H38 O2P -15.5707; 8.2832; 15.9643
92.864; 96.899; 93.15
729.02Yao Xiong; Xilong Yan; Yawen Ma; Yang Li; Guohui Yin; Ligong Chen
Regulating the piezofluorochromism of 9,10-bis(butoxystyryl)anthracenes by isomerization of butyl groups
Chem.Commun., 2015, 51, 3403
7116537 CIFC28 H50 N3 O6 ReP 1 21/c 111.2427; 25.9864; 11.3945
90; 106.509; 90
3191.75Mirza Cokoja; Iulius I. E. Markovits; Michael H. Anthofer; Saner Poplata; Alexander Pothig; Danny S. Morris; Peter A. Tasker; Wolfgang A. Herrmann; Fritz E. Kuhn; Jason B. Love
Catalytic epoxidation by perrhenate through the formation of organic-phase supramolecular ion pairs
Chem.Commun., 2015, 51, 3399
7116539 CIFC29 H21P 1 21/c 113.911; 9.1555; 16.101
90; 99.76; 90
2021Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116540 CIFC37 H30 O2C 1 2/c 118.733; 8.5251; 17.406
90; 95.92; 90
2764.9Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116541 CIFC64 H46P -111.3462; 14.6342; 27.3605
101.652; 99.918; 92.534
4368.2Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116542 CIFC32 H23P 1 21/c 114.154; 9.1925; 17.307
90; 100.42; 90
2214.7Luigi R. Nassimbeni; Nikoletta B. Bathori; Leena Desiree Patel; Hong Su; Edwin Weber
Separation of xylenes by enclathration
Chem.Commun., 2015, 51, 3627
7116543 CIFC20 H19 B N2 O9C 1 2/c 116.8086; 10.0372; 24.1763
90; 90.321; 90
4078.75Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116544 CIFC11 H19 B Cl N5 O8P 1 21/n 114.3477; 6.9395; 17.098
90; 94.14; 90
1697.9Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116545 CIFC21 H31 B N6 O9P 1 21/c 119.2489; 7.1031; 20.6727
90; 115.222; 90
2557.04Shinya Adachi; Armand B. Cognetta; Micah J. Niphakis; Zhi He; Adam Zajdlik; Jeffrey D. St. Denis; Conor C. G. Scully; Benjamin F. Cravatt; Andrei K. Yudin
Facile synthesis of borofragments and their evaluation in activity-based protein profiling
Chem.Commun., 2015, 51, 3608
7116546 CIFC144 H132 K N2 Nb2 O4I 2 346.878; 46.878; 46.878
90; 90; 90
103017Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116547 CIFC149 H144 Cl5 K3 Nb2 O4P -116.7009; 17.9962; 24.535
92.288; 100.453; 114.629
6536.7Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116548 CIFC151 H140 N2 Nb2 O4P b c a24.645; 25.8062; 37.2338
90; 90; 90
23680.5Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116549 CIFC165 H156 Cl6 Nb2 O4P 1 2/c 118.1297; 15.6334; 26.09
90; 93.396; 90
7381.7Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116550 CIFC92 H94 Cl2 Nb O4P 1 21/n 115.8132; 14.3842; 17.9838
90; 111.412; 90
3808.3Keith Searles; Patrick J. Carroll; Chun-Hsing Chen; Maren Pink; Daniel J. Mindiola
Niobium-nitrides derived from nitrogen splitting
Chem.Commun., 2015, 51, 3526
7116551 CIFC19 H16 Br O4P 1 21 15.8959; 11.7317; 12.73
90; 96.833; 90
874.27Jun-Bing Lin; Shi-Ming Xu; Ji-Kang Xie; Hong-Yu Li; Peng-Fei Xu
An organocatalytic Michael-cyclization cascade of 4-oxa-alpha,beta-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral gamma-lactols and trisubstituted gamma-lactones
Chem.Commun., 2015, 51, 3596
7116552 CIFC19 H18 O4P 1 21 15.6167; 25.0791; 11.3191
90; 90.779; 90
1594.28Jun-Bing Lin; Shi-Ming Xu; Ji-Kang Xie; Hong-Yu Li; Peng-Fei Xu
An organocatalytic Michael-cyclization cascade of 4-oxa-alpha,beta-unsaturated carboxylic acids with aldehydes: facile synthesis of chiral gamma-lactols and trisubstituted gamma-lactones
Chem.Commun., 2015, 51, 3596
7116553 CIFC43 H34 O1.5C 1 2/c 127.2227; 16.4194; 6.9476
90; 101.779; 90
3040Arun Naibi Lakshminarayana; Jingjing Chang; Jie Luo; Bin Zheng; Kuo-Wei Huang; Chunyan Chi
Bisindeno-annulated pentacenes with exceptionally high photo-stability and ordered molecular packing: simple synthesis by a regio-selective Scholl reaction
Chem.Commun., 2015, 51, 3604
7116554 CIFC59 H70 O5P -14.6842; 14.8758; 17.803
107.779; 94.984; 91.886
1174.5Arun Naibi Lakshminarayana; Jingjing Chang; Jie Luo; Bin Zheng; Kuo-Wei Huang; Chunyan Chi
Bisindeno-annulated pentacenes with exceptionally high photo-stability and ordered molecular packing: simple synthesis by a regio-selective Scholl reaction
Chem.Commun., 2015, 51, 3604
7116555 CIFC36 H37 N O26 Zn6P 21 21 218.0822; 20.8183; 30.8295
90; 90; 90
5187.3Cui-Lan Chang; Xiao-Yue Qi; Jiang-Wei Zhang; Ya-Ming Qiu; Xian-Jiang Li; Xin Wang; Yu Bai; Jun-Liang Sun; Hu-Wei Liu
Facile synthesis of magnetic homochiral metal-organic frameworks for 'enantioselective fishing'
Chem.Commun., 2015, 51, 3566
7116557 CIFC216 H184 Cu24 N8 O144I 4/m28.096; 28.096; 40.947
90; 90; 90
32323Hyehyun Kim; Minhak Oh; Dongwook Kim; Jeongin Park; Junmo Seong; Sang Kyu Kwak; Myoung Soo Lah
Single crystalline hollow metal-organic frameworks: a metal-organic polyhedron single crystal as a sacrificial template
Chem.Commun., 2015, 51, 3678
7116558 CIFC26 H35 B2 F8 Fe N5 O6P -17.7688; 8.5125; 24.4247
82.716; 85.057; 84.926
1591.34Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter
Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization
Chem.Commun., 2015, 51, 3616
7116559 CIFC27 H21 Fe N9 Ni O2C 1 2/c 117.3572; 15.1852; 10.1318
90; 91.117; 90
2669.96Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter
Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization
Chem.Commun., 2015, 51, 3616
7116560 CIFC23 H21 Cl2 Fe N5 O2P 1 21/c 18.6132; 13.1321; 22.5986
90; 108.557; 90
2423.22Arun Kumar Bar; Celine Pichon; Nayanmoni Gogoi; Carine Duhayon; S. Ramasesha; Jean-Pascal Sutter
Single-ion magnet behaviour of heptacoordinated Fe(II) complexes: on the importance of supramolecular organization
Chem.Commun., 2015, 51, 3616
7116561 CIFC26 H31 N O5P b c n29.508; 8.3721; 19.678
90; 90; 90
4861.3Qiao-Hui Deng; Jia-Rong Chen; Qiang Wei; Quan-Qing Zhao; Liang-Qiu Lu; Wen-Jing Xiao
Visible-light-induced photocatalytic oxytrifluoromethylation of N-allylamides for the synthesis of CF3-containing oxazolines and benzoxazines
Chem.Commun., 2015, 51, 3537
7116570 CIFC67 H74 N2 O8 S2P -115.302; 15.3895; 15.4431
71.988; 60.74; 87.419
2992.4Erik Gabrielsson; Haining Tian; Susanna K. Eriksson; Jiajia Gao; Hong Chen; Fusheng Li; Johan Oscarsson; Junliang Sun; Hakan Rensmo; Lars Kloo; Anders Hagfeldt; Licheng Sun
Dipicolinic acid: a strong anchoring group with tunable redox and spectral behavior for stable dye-sensitized solar cells
Chem.Commun., 2015, 51, 3858
7116572 CIFC16 H14.5 Cl2 Co N5.5 OP -19.611; 13.18; 15.861
75.031; 76.859; 89.895
1886.7Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116573 CIFC16 H14.5 Br2 Co N5.5 OP -19.832; 13.304; 15.925
105.24; 103.61; 90.386
1948.1Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116574 CIFC15 H13 Cl2 Co N5 SP -18.479; 9.071; 13.536
77.03; 80.74; 67.56
934.4Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116575 CIFC15 H13 Br2 Co N5 SP -18.441; 9.015; 13.725
77.19; 80.64; 68.94
946.4Shefali Vaidya; Apoorva Upadhyay; Saurabh Kumar Singh; Tulika Gupta; Subrata Tewary; Stuart K. Langley; James P. S. Walsh; Keith S. Murray; Gopalan Rajaraman; Maheswaran Shanmugam
A synthetic strategy for switching the single ion anisotropy in tetrahedral Co(II) complexes
Chem.Commun., 2015, 51, 3739
7116576 CIFC26 H34 B4 Mo2 O6 Ru2C 1 2/c 117.5892; 15.9899; 11.2183
90; 102.022; 90
3085.94Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116577 CIFC22 H36 B4 Mo2 O2P 43 21 29.0041; 9.0041; 31.3056
90; 90; 90
2538.06Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116578 CIFC25 H34 B3 Cl Mo2 O5 WP 1 21/n 19.0059; 18.5886; 17.7675
90; 99.389; 90
2934.6Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116579 CIFC30 H31 B Mo2 O10 Ru2P c c n17.2668; 30.7845; 12.5659
90; 90; 90
6679.4Bijan Mondal; Bijnaneswar Mondal; Koushik Pal; Babu Varghese; Sundargopal Ghosh
An electron-poor di-molybdenum triple-decker with a puckered [B4Ru2] bridging ring is an oblato-closo cluster
Chem.Commun., 2015, 51, 3828
7116580 CIFC12 H36 Be N2 Si4P 1 21/n 19.8756; 16.6972; 14.5875
90; 109.492; 90
2267.55D. Naglav; A. Neumann; D. Blaser; C. Wolper; R. Haack; G. Jansen; S. Schulz
Bonding situation in Be[N(SiMe3)2]2 - an experimental and computational study
Chem.Commun., 2015, 51, 3889
7116581 CIFC83 H31 Cl2.5 F6 N6P -110.3923; 18.707; 18.841
61.769; 75.03; 74.372
3070.6Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116582 CIFC86 H36 Cl12 F6 N6 O6C 1 2/c 137.189; 25.4108; 19.26
90; 107.552; 90
17353.4Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116583 CIFC162 H48 S4P -116.8833; 18.4991; 23.1447
100.718; 96.6104; 91.6599
7046Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116584 CIFC74 H35 Cl N6P -110.6327; 14.0819; 19.8579
109.255; 90.5719; 109.406
2623.52Takashi Kubo; Shogo Miyazaki; Takuya Kodama; Mitsuya Aoba; Yasukazu Hirao; Hiroyuki Kurata
A facile synthesis of trinaphtho[3.3.3]propellane and its pi-extension and the formation of a two-dimensional honeycomb molecular assembly
Chem.Commun., 2015, 51, 3801
7116585 CIFC70 H132 As4 Ge8 K3 N8 O18 VP -111.9985; 16.7415; 25.3291
80.709; 88.755; 69.258
4692.3Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen
[V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms
Chem.Commun., 2015, 51, 3866
7116586 CIFC63 H124 As6 Ge8 K3 N8 Nb O18P -116.1475; 16.7769; 18.0373
89.184; 80.452; 79.42
4736.1Stefan Mitzinger; Lies Broeckaert; Werner Massa; Florian Weigend; Stefanie Dehnen
[V@Ge8As4]^3-^ and [Nb@Ge8As6]^3-^: encapsulation of electron-poor transition metal atoms
Chem.Commun., 2015, 51, 3866
7116587 CIFC28 H39 N2 O6 P WP 1 21/c 110.9216; 23.5529; 14.5767
90; 126.717; 90
3005.7Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116588 CIFC22 H29 N2 O5 P WP -110.9909; 11.0605; 12.874
108.084; 95.194; 118.186
1257.68Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116589 CIFC22 H31 N2 O6 P WP 1 21/c 19.5748; 27.7242; 10.5851
90; 115.34; 90
2539.5Jose Manuel Villalba Franco; Takahiro Sasamori; Gregor Schnakenburg; Arturo Espinosa Ferao; Rainer Streubel
Going for strain: synthesis of the first 3-imino-azaphosphiridine complexes and their conversion into oxaphosphirane complex valence isomers
Chem.Commun., 2015, 51, 3878
7116590 CIFC31 H24 Br N O6P 1 21 19.4993; 18.9341; 15.0393
90; 97.203; 90
2683.63Haipeng Hu; Yangbin Liu; Jing Guo; Lili Lin; Yali Xu; Xiaohua Liu; Xiaoming Feng
Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(III)-complex catalyzed inverse-electron-demand hetero-Diels-Alder reaction
Chem.Commun., 2015, 51, 3835
7116599 CIFC24 H20 Cl N4 O8 RuP 1 21 110.0833; 9.8576; 12.7262
90; 95.327; 90
1259.48Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita
Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer'
Chem.Commun., 2015, 51, 4105
7116600 CIFC30 H20 Cl N4 O8 RuP 21 21 217.6696; 11.321; 32.206
90; 90; 90
2796.4Javier J. Concepcion; Diane K. Zhong; David J. Szalda; James T. Muckerman; Etsuko Fujita
Mechanism of water oxidation by [Ru(bda)(L)2]: the return of the 'blue dimer'
Chem.Commun., 2015, 51, 4105
7116601 CIFC36 H50 Eu2 N8 O34 ZnC 1 2/c 117.0712; 16.981; 20.3832
90; 108.073; 90
5617.3Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116602 CIFC36 H50 N8 O34 Tb2 ZnC 1 2/c 117.0778; 16.9284; 20.3385
90; 108.115; 90
5588.4Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116603 CIFC36 H34 I2 N6 O21 Tb2 ZnC 1 2/c 117.2316; 16.7585; 21.2567
90; 106.996; 90
5870.3Peng-Fei Shi; Huan-Cheng Hu; Zhan-Yun Zhang; Gang Xiong; Bin Zhao
Heterometal-organic frameworks as highly sensitive and highly selective luminescent probes to detect I^-^ ions in aqueous solutions
Chem.Commun., 2015, 51, 3985
7116604 CIFC21 H21 As O3 S2P 1 21/n 111.687; 14.366; 12.127
90; 106.254; 90
1954.7Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank
Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics
Chem.Commun., 2015, 51, 4109
7116605 CIFC23 H24 As Br O SP 1 21/n 111.17; 13.6075; 14.4757
90; 91.738; 90
2199.23Nikhil Lalwani; Yu-Su Chen; Gemma Brooke; Neil A. Cross; David W. Allen; Alan Reynolds; Jesus Ojeda; Graham J. Tizzard; Simon J. Coles; Neil Bricklebank
Triphenylarsonium-functionalised gold nanoparticles: potential nanocarriers for intracellular therapeutics
Chem.Commun., 2015, 51, 4109
7116606 CIFC116 Cl4 Fe N7 O72 Si2 W18C 1 2/c 135.5945; 14.4862; 38.2599
90; 113.9; 90
18036.3Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116607 CIFC124 Cl12 Co N7 O70 Si2 W18P -114.6616; 18.7039; 19.0694
106.86; 92.59; 98.25
4931.97Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116608 CIFC114 Mn N7 O74 Si2 W18C 1 2/c 135.6567; 14.4553; 38.3421
90; 113.89; 90
18069.4Rinta Sato; Kosuke Suzuki; Takuo Minato; Masahiro Shinoe; Kazuya Yamaguchi; Noritaka Mizuno
Field-induced slow magnetic relaxation of octahedrally coordinated mononuclear Fe(III)-, Co(II)-, and Mn(III)-containing polyoxometalates
Chem.Commun., 2015, 51, 4081
7116609 CIFC42 H36 N6 O7 Zn4P -3 c 114.5525; 14.5525; 24.7573
90; 90; 120
4540.56D. Prochowicz; K. Sokolowski; I. Justyniak; A. Kornowicz; D. Fairen-Jimenez; T. Friscic; J. Lewinski
A mechanochemical strategy for IRMOF assembly based on pre-designed oxo-zinc precursors
Chem.Commun., 2015, 51, 4032
7116610 CIFC14 H22 F N2 O5 PP 1 21 17.71; 12.999; 17.692
90; 92.506; 90
1771.4Inmaculada Serrano; David Monge; Eleuterio Alvarez; Rosario Fernandez; Jose M. Lassaletta
Asymmetric organocatalytic synthesis of quaternary alpha-hydroxy phosphonates: en route to alpha-aryl phosphaisoserines
Chem.Commun., 2015, 51, 4077
7116614 CIFC34 H25 B TeP -111.3756; 12.5651; 19.3584
82.926; 75.15; 77.945
2608.5Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116615 CIFC34 H10 B F15 TeP -112.4545; 13.2182; 20.2994
74.416; 73.514; 81.701
3078.2Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116616 CIFC34 H15 B F10 TeP -111.3615; 11.5042; 13.1803
77.723; 66.878; 69.212
1475.82Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116617 CIFC68 H30 B2 F20 Te2C 1 2/c 139.238; 21.195; 20.08
90; 108.82; 90
15807Fu An Tsao; Alan. J. Lough; Douglas W. Stephan
Intramolecular 1,1-carboboration versus intermolecular FLP addition in reactions of boranes and bis(phenylethynyl)telluroether
Chem.Commun., 2015, 51, 4287
7116618 CIFC17 H20 Cl Li N2 O3P 21 21 217.7015; 12.0371; 18.2095
90; 90; 90
1688.09Krzysztof Ziach; Janusz Jurczak
Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines
Chem.Commun., 2015, 51, 4306
7116619 CIFC37 H40 Cl2 Li2 N4 O14P 1 n 17.6122; 18.1368; 14.751
90; 96.894; 90
2021.81Krzysztof Ziach; Janusz Jurczak
Mirror symmetry breaking upon spontaneous crystallization from a dynamic combinatorial library of macrocyclic imines
Chem.Commun., 2015, 51, 4306
7116620 CIFC39 H52 Cl3 O3P -19.807; 13.8699; 16.6745
109.657; 95.088; 107.141
1996.1Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh
Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene
Chem.Commun., 2015, 51, 4227
7116621 CIFC78 H92 O6P -113.323; 16.3491; 17.448
72.532; 84.273; 89.557
3606.2Shafali Arora; Shivali Sharma; Venus S. Mithu; Chang Hee-Lee; Kamaljit Singh
Selective functionalization of methylene bridges of calix[6]arenes. Isolation and identification of stable conformers of methyl ether of p-tert-butylcalix[6]arene
Chem.Commun., 2015, 51, 4227
7116622 CIFC55 H55 Cl3 N8P -110.6574; 14.7322; 17.013
66.539; 80.163; 80.329
2399.5Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116623 CIFC48 H42 N4 O6P -3 c 113.5006; 13.5006; 29.691
90; 90; 120
4686.6Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116624 CIFC56 H56 Cl6 N8 O3P 1 21/c 117.6515; 27.369; 11.1516
90; 102.653; 90
5256.5Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116625 CIFC33 H36 N4 O6P 1 21/n 17.2035; 18.776; 21.734
90; 91.764; 90
2938.2Koushik Acharyya; Partha Sarathi Mukherjee
Shape and size directed self-selection in organic cage formation
Chem.Commun., 2015, 51, 4241
7116626 CIFC30 H46 Ge2 N4 Se3P 1 21/c 116.736; 11.336; 18.978
90; 106.354; 90
3454.8Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran
Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity
Chem.Commun., 2015, 51, 4310
7116627 CIFC30 H46 Ge2 N4 S3P 1 21/c 116.4; 11.364; 18.733
90; 106.005; 90
3355.9Surendar Karwasara; Dhirendra Yadav; Chandan Kumar Jha; Gopalan Rajaraman; Selvarajan Nagendran
Single-step conversion of silathiogermylene to germaacid anhydrides: unusual reactivity
Chem.Commun., 2015, 51, 4310
7116628 CIFC26 H27 Cl2 Cu N5 O3P -110.671; 11.025; 11.868
89.45; 77.812; 79.52
1341.4Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116629 CIFC20 H13 Cl Cu F3 N3 O4 SP 1 21/c 17.59; 20.098; 13.487
90; 94.218; 90
2051.8Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116630 CIFC28 H29 Cl2 Cu N5 O2P -110.758; 10.951; 12.045
87.424; 78.339; 79.489
1366.4Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116631 CIFC26 H27 Cl2 Cu N5 O2 SP -110.634; 10.982; 11.926
89.311; 77.918; 79.929
1340.5Weiwei Fang; Cong Liu; Jiangbo Chen; Zhengwei Lu; Zhi-Ming Li; Xiaoling Bao; Tao Tu
The electronic effects of ligands on metal-coordination geometry: a key role in the visual discrimination of dimethylaminopyridine and its application towards chemo-switch
Chem.Commun., 2015, 51, 4267
7116632 CIFC16 H8 N4P 1 21/c 14.6304; 14.479; 8.886
90; 90.402; 90
595.7Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116633 CIFC16 H7 Cl N4P 1 21/n 13.8176; 18.9603; 8.7979
90; 95.327; 90
634.07Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116634 CIFC16 H6 Cl2 N4P 1 21/n 13.8194; 19.4986; 8.9236
90; 99.974; 90
654.52Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116635 CIFC16 H4 Cl2 N4P -14.7573; 7.941; 8.892
92.898; 100.56; 94.347
328.6Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116636 CIFC16 H4 Cl4 N4P -15.8383; 6.0989; 10.5832
82.636; 76.077; 82.498
360.8Shuaijun Yang; Danqing Liu; Xiaomin Xu; Qian Miao
Molecular packing and n-channel thin film transistors of chlorinated cyclobuta[1,2-b:3,4-b']diquinoxalines
Chem.Commun., 2015, 51, 4275
7116637 CIFC46 H50 Cl6 Ir2 N4P -17.991; 9.776; 15.449
100.26; 102.15; 103.55
1113.7Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116638 CIFC254 H220 F18 Ir6 N24 O21 S6P 1 21/n 127.189; 30.491; 29.069
90; 100.26; 90
23713Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116639 CIFC256 H208 Ir6 N26 O4I -4 2 d46.154; 46.154; 49.592
90; 90; 90
105640Nem Singh; Jae-Ho Jo; Young Ho Song; Hyunuk Kim; Dongwook Kim; Myoung Soo Lah; Ki-Whan Chi
Coordination-driven self-assembly of an iridium-cornered prismatic cage and encapsulation of three heteroguests in its large cavity
Chem.Commun., 2015, 51, 4492
7116640 CIFC17 H14 O4P 1 21/n 17.761; 9.02; 21.077
90; 97.965; 90
1461.2Juan Du; Xiuli Zhang; Xi Sun; Lei Wang
Copper-catalyzed direct alpha-ketoesterification of propiophenones with acetophenones via C(sp^3^)-H oxidative cross-coupling
Chem.Commun., 2015, 51, 4372
7116641 CIFC32 H22 N2P 1 21/n 114.6334; 8.9414; 17.7375
90; 105.381; 90
2237.7Wei Huang; Lu Sun; Zhiwen Zheng; Jianhua Su; He Tian
Colour-tunable fluorescence of single molecules based on the vibration induced emission of phenazine
Chem.Commun., 2015, 51, 4462
7116642 CIFC16 H23 B F4 Fe N6P 1 21/n 113.0808; 10.6982; 14.0524
90; 96.336; 90
1954.5Dong Shao; Shao-Liang Zhang; Xin-Hua Zhao; Xin-Yi Wang
Spin canting, metamagnetism, and single-chain magnetic behaviour in a cyano-bridged homospin iron(II) compound
Chem.Commun., 2015, 51, 4360
7116643 CIFC42 H36 B3 N3 O6P 17.3418; 15.788; 31.0079
83.135; 87.475; 89.797
3564.96Xiao-Ye Wang; Fang-Dong Zhuang; Xin-Chang Wang; Xiao-Yu Cao; Jie-Yu Wang; Jian Pei
Synthesis, structure and properties of C3-symmetric heterosuperbenzene with three BN units
Chem.Commun., 2015, 51, 4368
7116644 CIFC232.5 H188 F52.5 N20.5 O P16.75 Pd4 Ru2P -123.8865; 25.4288; 31.7818
96.15; 107.106; 113.591
16341.8Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves
Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes
Chem.Commun., 2015, 51, 4465
7116645 CIFC63 H45 F7.5 N11 O2 P1.25 RuC 1 2/c 131.584; 16.937; 26.449
90; 105.27; 90
13649Jiajia Yang; Mohan Bhadbhade; William A. Donald; Hasti Iranmanesh; Evan G. Moore; Hong Yan; Jonathon E. Beves
Self-assembled supramolecular cages containing ruthenium(II) polypyridyl complexes
Chem.Commun., 2015, 51, 4465
7116646 CIFC15 H18 I N O2P 1 21/n 19.3649; 15.0028; 11.1821
90; 92.996; 90
1568.93H.Q. Nimal Gunaratne; Peter Nockemann; Kenneth R. Seddon
Pro-fragrant ionic liquids with stable hemiacetal motifs: water-triggered release of fragrances
Chem.Commun., 2015, 51, 4455
7116647 CIFC24 H23 Cl O8P -19.2814; 11.711; 12.1339
113.081; 96.35; 102.204
1158.1Hong Lu; Jin-Yu Liu; Chen-Guang Li; Jun-Bing Lin; Yong-Min Liang; Peng-Fei Xu
A new chiral C1-symmetric NHC-catalyzed addition to alpha-aryl substituted alpha,beta-disubstituted enals: enantioselective synthesis of fully functionalized dihydropyranones
Chem.Commun., 2015, 51, 4473
7116648 CIFC14 H14 Br2 N2C 2 2 217.3088; 31.966; 12.46
90; 90; 90
2911.1Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima
Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands
Chem.Commun., 2015, 51, 4380
7116649 CIFC72 H76 Br2 Ir2 N4P 1 21 114.4388; 14.3302; 14.9599
90; 94.1029; 90
3087.43Yusuke Kita; Kosuke Higashida; Kenta Yamaji; Atsuhiro Iimuro; Kazushi Mashima
Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands
Chem.Commun., 2015, 51, 4380
7116650 CIFC30 H23 Br N2 O3 SP 1 21/c 115.2526; 8.7689; 19.1451
90; 90.857; 90
2560.3Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang
Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon
Chem.Commun., 2015, 51, 4507
7116651 CIFC29 H24 N2 O2 SP 1 21/c 113.7344; 11.3573; 15.3726
90; 95.591; 90
2386.5Yuanhao Wang; Xiaoqiang Lei; Yefeng Tang
Rh(II)-catalyzed cycloadditions of 1-tosyl 1,2,3-triazoles with 2H-azirines: switchable reactivity of Rh-azavinylcarbene as [2C]- or aza-[3C]-synthon
Chem.Commun., 2015, 51, 4507
7116652 CIFC20 H23 N O6 S2P 1 21 19.1418; 9.388; 12.6939
90; 110.69; 90
1019.17Chao Song; Wen Yang; Nannan Zhou; Rui Qian; Yajun Zhang; Kaiyan Lou; Rui Wang; Wei Wang
Fluorescent theranostic agents for Hg2+ detection and detoxification treatment
Chem.Commun., 2015, 51, 4443
7116653 CIFC98 H126 O6P -110.3348; 19.1818; 22.503
80.708; 78.639; 78.993
4257.4Liang Han; Yuewei Zhang; Weiping Chen; Xiao Cheng; Kaiqing Ye; Jingying Zhang; Yue Wang
Assembly of twisted luminescent architectures based on acenaphtho[1,2-k]fluoranthene derivatives
Chem.Commun., 2015, 51, 4477
7116654 CIFC74 H66 B F27 Ir N6 O6P -114.2926; 17.57617; 30.9787
96.4495; 91.4551; 106.009
7420.04Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116655 CIFC71 H58 B Cl2 F26 Ir N6 O4P 1 21/n 119.5682; 18.7483; 20.39
90; 104.772; 90
7233.2Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116656 CIFC77 H70 B F26 Ir N6 O6P 1 21/c 120.7249; 22.1162; 18.7709
90; 116.331; 90
7711.1Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116657 CIFC71 H63 B F27 Ir N6 O6P -114.3353; 17.5209; 30.9758
95.9306; 91.1596; 106.158
7423Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116658 CIFC67 H63 B F24 Ir N7 O6P 1 21/c 113.782; 20.0926; 25.2535
90; 91.1355; 90
6991.73Simone A. Hauser; Ivan Prokes; Adrian B. Chaplin
Low-coordinate iridium NHC complexes derived from selective and reversible C-H bond activation of fluoroarenes
Chem.Commun., 2015, 51, 4425
7116659 CIFC15 H22 B F N2P -17.486; 9.564; 10.597
75.8; 76.99; 75.35
700.8Masahito Murai; Tetsuya Omura; Yoichiro Kuninobu; Kazuhiko Takai
Rhenium-catalysed dehydrogenative borylation of primary and secondary C(sp^3^)-H bonds adjacent to a nitrogen atom
Chem.Commun., 2015, 51, 4583
7116660 CIFC46 H79 Fe9 N2 O50P 32 2 118.927; 18.927; 24.693
90; 90; 120
7661Jiong-Peng Zhao; Song-De Han; Xue Jiang; Jian Xu; Ze Chang; Xian-He Bu
A three dimensional magnetically frustrated metal-organic framework via the vertices augmentation of underlying net
Chem.Commun., 2015, 51, 4627
7116661 CIFC H N OP 21 21 2110.5611; 15.5632; 22.4083
90; 90; 90
3683.1Pei-Qiang Huang; Su-Yu Huang; Long-Hui Gao; Zhong-Yi Mao; Zong Chang; Ai-E Wang
Enantioselective total synthesis of (+)-methoxystemofoline and (+)-isomethoxystemofoline
Chem.Commun., 2015, 51, 4576
7116662 CIFC70 H110 Li2 O2 Pb2 Si4P -112.2658; 16.7325; 20.375
99.254; 107.15; 107.882
3654.6Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura
A reversible two-electron redox system involving a divalent lead species
Chem.Commun., 2015, 51, 4674
7116663 CIFC36 H56 Li2 O2 Pb Si2P -112.4117; 12.4449; 13.7628
82.874; 67.352; 75.447
1898.1Masaichi Saito; Marisa Nakada; Takuya Kuwabara; Mao Minoura
A reversible two-electron redox system involving a divalent lead species
Chem.Commun., 2015, 51, 4674
7116664 CIFC16 H17 N O2 SP 1 21/n 114.3451; 5.6024; 19.171
90; 110.01; 90
1447.7Xiang-Wei Liu; Jiang-Ling Shi; Jiang-Bo Wei; Chao Yang; Jia-Xuan Yan; Kun Peng; Le Dai; Chen-Guang Li; Bi-Qin Wang; Zhang-Jie Shi
Diversified syntheses of multifunctionalized thiazole derivatives via regioselective and programmed C-H activation
Chem.Commun., 2015, 51, 4599
7116665 CIFFe1.172 H Li0.828 O SP 4/n m m :13.7038; 3.7038; 8.8852
90; 90; 90
121.888U. Pachmayr; D. Johrendt
[(Li0.8Fe0.2)OH]FeS and the ferromagnetic superconductors [(Li0.8Fe0.2)OH]Fe(S1-xSex) (0 < x ? 1)
Chem.Commun., 2015, 51, 4689
7116666 CIFC148 H96 Mn6 N20 O18P 1 21/c 127.159; 13.925; 41.043
90; 112.375; 90
14353L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi
Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds
Chem.Commun., 2015, 51, 4631
7116667 CIFC49 H62 N6 O3P 1 21/n 114.623; 16.641; 18.326
90; 101.777; 90
4365.6L. A. Barrios; J. Salinas-Uber; O. Roubeau; S. J. Teat; G. Aromi
Molecular self-recognition: a chiral [Mn(II)6] wheel via donor-acceptor pi^...^pi contacts and H-bonds
Chem.Commun., 2015, 51, 4631
7116668 CIFC72 H96 O Si4P 21 21 2113.7114; 19.2562; 25.0769
90; 90; 90
6621Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116669 CIFC72 H98 O2 Si4P 1 21/c 113.426; 18.425; 28.086
90; 94.327; 90
6928Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116670 CIFC67.2 H91.2 N1.6 O2.4 Si3.2P 1 21/c 113.31; 29.8304; 19.4965
90; 93.59; 90
7725.8Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116671 CIFC72 H96 O Si4P 1 21/c 119.768; 21.986; 16.67
90; 111.807; 90
6727Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116672 CIFC72 H98 O2 Si4P -113.171; 14.918; 17.544
85.743; 79.779; 84.496
3371Takashi Matsuno; Yutaro Koyama; Satoru Hiroto; Jatish Kumar; Tsuyoshi Kawai; Hiroshi Shinokubo
Isolation of a 1,4-diketone intermediate in oxidative dimerization of 2-hydroxyanthracene and its conversion to oxahelicene
Chem.Commun., 2015, 51, 4607
7116688 CIFC29 H28 Cl2 N P Ru SP 1 21/n 112.6476; 11.7959; 18.6459
90; 102.933; 90
2711.21Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin
Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides.
Chemical communications (Cambridge, England), 2015, 51, 3450-3453
7116689 CIFC15 H12 N O P SC 1 2/c 110.4363; 13.1058; 20.7087
90; 96.816; 90
2812.44Zhang, Hui-Jun; Lin, Weidong; Wu, Zhengjian; Ruan, Wenqing; Wen, Ting-Bin
Silver-mediated direct phosphorylation of benzothiazoles and thiazoles with diarylphosphine oxides.
Chemical communications (Cambridge, England), 2015, 51, 3450-3453
7116702 CIFC27 H22 N4 O8 ZnP 1 21/c 111.361; 15.532; 16.269
90; 94.661; 90
2861.3Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee
A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis
Chem.Commun., 2015, 51, 4872
7116703 CIFC23 H14 N2 O5 ZnC 1 2/c 129.971; 16.271; 15.804
90; 115.749; 90
6942Bappaditya Gole; Udishnu Sanyal; Partha Sarathi Mukherjee
A smart approach to achieve an exceptionally high loading of metal nanoparticles supported by functionalized extended frameworks for efficient catalysis
Chem.Commun., 2015, 51, 4872
7116706 CIFC25 H24 N2 OP -19.491; 9.5574; 10.9648
91.766; 93.926; 97.631
982.69Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls
Copper catalysed amidation of aryl halides through chelation assistance
Chem.Commun., 2015, 51, 4834
7116707 CIFC19 H20 N2 O SP 1 21/c 116.8737; 9.68667; 10.28958
90; 96.9165; 90
1669.59Subban Kathiravan; Shishir Ghosh; Graeme Hogarth; Ian A. Nicholls
Copper catalysed amidation of aryl halides through chelation assistance
Chem.Commun., 2015, 51, 4834
7116708 CIFC23 H40 Cl Ir N2P 1 21/n 111.8497; 12.2144; 16.718
90; 91.591; 90
2418.8Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116709 CIFC15 H28 Cl Cu N2P 1 21/c 16.043; 18.944; 15.635
90; 100.45; 90
1760.2Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116710 CIFC30.5 H57 Cl5 N4 Pd2P -18.6743; 15.139; 15.947
86.794; 85.946; 80.765
2059.7Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116711 CIFC15 H28 Au Cl N2P 1 21/n 111.3202; 12.8913; 12.5373
90; 90.2151; 90
1829.6Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116712 CIFC31 H56 Au F3 N4 O3 SP 1 21/c 113.2941; 9.5096; 14.5324
90; 93.61; 90
1833.56Yannick D. Bidal; Mathieu Lesieur; Mohand Melaimi; David B. Cordes; Alexandra M. Z. Slawin; Guy Bertrand; Catherine S. J. Cazin
A simple access to transition metal cyclopropenylidene complexes
Chem.Commun., 2015, 51, 4778
7116713 CIFC6 H6 Fe Na3 O17C 1 2/c 117.4212; 12.5545; 14.9217
90; 101.047; 90
3203.1Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116714 CIFC6 H10 Cr Na3 O17C 1 2/c 117.2551; 12.4639; 15.1228
90; 100.454; 90
3198.4Qingchun Ge; Tai-Shung Chung
Oxalic acid complexes: promising draw solutes for forward osmosis (FO) in protein enrichment
Chem.Commun., 2015, 51, 4854
7116715 CIFC24 H18P n a 217.4869; 19.718; 11.2222
90; 90; 90
1656.7Lingzhi Li; Ming Chen; Haoke Zhang; Han Nie; Jing Zhi Sun; Anjun Qin; Ben Zhong Tang
Influence of the number and substitution position of phenyl groups on the aggregation-enhanced emission of benzene-cored luminogens
Chem.Commun., 2015, 51, 4830
7116716 CIFC20 H25 NP 21 21 2110.529; 11.655; 12.596
90; 90; 90
1545.7Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116717 CIFC26 H29 N SP 1 21/c 17.535; 14.973; 18.844
90; 95.77; 90
2115.2Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116718 CIFC20 H25 N SP 1 21/n 18.104; 8.358; 24.688
90; 96.2; 90
1662.4Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116719 CIFC20 H25 N SP 1 21/n 17.812; 11.736; 18.668
90; 96.49; 90
1700.5Mirja Enders; Christian J. Friedmann; Philipp N. Plessow; Angela Bihlmeier; Martin Nieger; Wim Klopper; Stefan Brase
Unprecedented pseudo-ortho and ortho metallation of [2.2]paracyclophanes ‒ a methyl group matters
Chem.Commun., 2015, 51, 4793
7116720 CIFC32 H28 O4P 1 21/n 110.2761; 15.204; 15.2549
90; 96.857; 90
2366.34Murat Cakici; Zhi-Gang Gu; Martin Nieger; Jochen Burck; Lars Heinke; Stefan Brase
Planar-chiral building blocks for metal-organic frameworks
Chem.Commun., 2015, 51, 4796
7116729 CIFC48.93 H35.72 Cu2 N2 O8.93P -110.7482; 12.23; 16.366
95.11; 96.968; 102.936
2066.2Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116730 CIFC48 H32 Cu2 N2 O8P -110.4745; 11.6064; 17.037
97.583; 104.918; 90.081
1982.5Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116731 CIFC48 H32 Cu2 N2 O8P -110.6065; 11.6485; 17.4513
80.612; 75.215; 89.821
2055.1Yuichi Takasaki; Satoshi Takamizawa
Reversible crystal deformation of a single-crystal host of copper(II) 1-naphthoate-pyrazine through crystal phase transition induced by methanol vapor sorption
Chem.Commun., 2015, 51, 5024
7116732 CIFC36 H24 Co3 N13 Na O15.25P 6313.1191; 13.1191; 16.014
90; 90; 120
2386.92Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116733 CIFC36 H27 Co3 N13 Na O15P 6313.1177; 13.1177; 16.005
90; 90; 120
2385.07Ru-Xin Yao; Xin Cui; Jun Wang; Xian-Ming Zhang
A homochiral magnet based on D3 symmetric [(NaO3)Co3] clusters: from spontaneous resolution to absolute chiral induction
Chem.Commun., 2015, 51, 5108
7116734 CIFC6 H5 B K N3P -19.5267; 9.9704; 10.1727
81.041; 68.165; 83.636
884.51Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116735 CIFC28 H36 B4 K4 N12 O2P 1 21/c 17.5693; 25.062; 22.116
90; 94.3; 90
4183.6Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116736 CIFC9 B F5 K N3P 1 21/c 111.894; 12.782; 7.5458
90; 103.98; 90
1113.2Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116737 CIFC6 H5 B K N3P -19.5044; 9.976; 10.1345
81.033; 68.217; 83.514
879.8Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116738 CIFC9 H8 B2 K2 N6 OP 1 21/n 19.8586; 13.1307; 12.1811
90; 93.991; 90
1573.02Johannes Landmann; Jan A. P. Sprenger; Rudiger Bertermann; Nikolai Ignatiev; Vera Bernhardt-Pitchougina; Eduard Bernhardt; Helge Willner; Maik Finze
Convenient access to the tricyanoborate dianion B(CN)3^2-^ and selected reactions as a boron-centred nucleophile
Chem.Commun., 2015, 51, 4989
7116739 CIFC26.5 H36.5 Br2 Fe N3.5 O1.5P 1 21 115.777; 10.03; 17.685
90; 100.09; 90
2755.3Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang
Iron-catalyzed asymmetric hydrosilylation of ketones
Chem.Commun., 2015, 51, 5073
7116740 CIFC47 H45 Br2 Fe N3 OP 433.2315; 33.2315; 18.2906
90; 90; 90
20198.9Ziqing Zuo; Lei Zhang; Xuebing Leng; Zheng Huang
Iron-catalyzed asymmetric hydrosilylation of ketones
Chem.Commun., 2015, 51, 5073
7116741 CIFC2 H10 B10 N2 Na2 O17C 1 2/c 121.9507; 6.4172; 11.0598
90; 103.407; 90
1515.45Jun-Hua Wang; Qi Wei; Jian-Wen Cheng; Huan He; Bai-Feng Yang; Guo-Yu Yang
Na2B10O17^.^H2en: a three-dimensional open-framework layered borate co-templated by inorganic cations and organic amines
Chem.Commun., 2015, 51, 5066
7116742 CIFC32 H33 Fe N4 O9.5P 1 21 18.4996; 14.4218; 26.0595
90; 97.616; 90
3166.2R. Gautam; E. A. Akam; A. V. Astashkin; J. J. Loughrey; E. Tomat
Sirtuin inhibitor sirtinol is an intracellular iron chelator
Chem.Commun., 2015, 51, 5104
7116743 CIFC69 H118 N12 Na7I -4 2 d32.759; 32.759; 29.376
90; 90; 90
31525Andreas Stascha
A pyrazolate-stabilized sodium hydride complex
Chem.Commun., 2015, 51, 5056
7116744 CIFC12.17 H20.33 N2 NaP 1 21/c 115.184; 19.831; 26.107
90; 100.11; 90
7739Andreas Stascha
A pyrazolate-stabilized sodium hydride complex
Chem.Commun., 2015, 51, 5056
7116745 CIFC56 H38 Cu2 N3 O11P -116.1748; 17.1245; 17.3765
61.699; 79.187; 79.168
4135.1Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116746 CIFC150.55 H187.34 Cu4 N5.82 O34.04P 1 21/c 118.2648; 27.0741; 16.6959
90; 110.078; 90
7754.4Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116747 CIFC136.45 H149.05 Cu4 N16.15 O34.15C 1 2/c 122.7256; 27.998; 23.4326
90; 91.88; 90
14901.5Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116748 CIFC108 H84 Cu4 N4 O24.61 S4P -114.935; 16.106; 16.995
105.989; 109.453; 104.285
3437Valentina Brega; Matthias Zeller; Yufan He; H. Peter Lu; Jeremy K. Klosterman
Multi-responsive metal-organic lantern cages in solution
Chem.Commun., 2015, 51, 5077
7116749 CIFC21 H44 Li N5P b c a10.5102; 18.8729; 23.8796
90; 90; 90
4736.7Stuart D. Robertson; Alan R. Kennedy; John J. Liggat; Robert E. Mulvey
Facile synthesis of a genuinely alkane-soluble but isolable lithium hydride transfer reagent
Chem.Commun., 2015, 51, 5452
7116750 CIFC30 H31 B O2 ZrP b c a10.3097; 15.5055; 32.3133
90; 90; 90
5165.51Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116751 CIFC20 H21 B O2 TeP b c a8.2167; 20.788; 22.069
90; 90; 90
3769.6Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116752 CIFC20 H14 TeP -15.7439; 11.1587; 12.0325
80.1921; 87.5978; 79.981
748.3Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116753 CIFC28 H34 B2 O4 TeP 1 21/n 110.6313; 21.4729; 13.1595
90; 113.042; 90
2764.4Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116754 CIFC28 H34 B2 O4 TeP -17.0792; 12.1454; 16.953
75.2698; 82.0304; 80.2126
1382.2Gang He; Benjamin D. Wiltshire; Paul Choi; Aliaksandr Savin; Shuai Sun; Arash Mohammadpour; Michael J. Ferguson; Robert McDonald; Samira Farsinezhad; Alex Brown; Karthik Shankar; Eric Rivard
Phosphorescence within benzotellurophenes and color tunable tellurophenes under ambient conditions
Chem.Commun., 2015, 51, 5444
7116755 CIFC18 H18 B Cu F5 N4 O3I 1 2/a 115.4006; 9.5362; 28.09
90; 90.988; 90
4124.8Cameron M. Moore; Nathaniel K. Szymczak
Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding
Chem.Commun., 2015, 51, 5490
7116756 CIFC18 H18 Cu F N4 O3P 1 21/n 18.793; 14.8014; 13.3814
90; 93.525; 90
1738.28Cameron M. Moore; Nathaniel K. Szymczak
Redox-induced fluoride ligand dissociation stabilized by intramolecular hydrogen bonding
Chem.Commun., 2015, 51, 5490
7116757 CIFC15 H11 N O3P b c a9.89; 7.3; 32.941
90; 90; 90
2378.2Soumitra Agasti; Upendra Sharma; Togati Naveen; Debabrata Maiti
Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C-H olefination of phenols
Chem.Commun., 2015, 51, 5375
7116758 CIFC34 H36 B2 F15 Li O6P 1 21/n 112.4374; 19.273; 15.5445
90; 93.373; 90
3719.7Junhao Zheng; Yuwen Wang; Zhen Hua Li; Huadong Wang
Application of a nucleophilic boryl complex in the frustrated Lewis pair: activation of H-H, B-H and C[double bond, length as m-dash]C bonds with B(C6F5)3 and boryl-borate lithium
Chem.Commun., 2015, 51, 5505
7116759 CIFC23 H23 N3 O7P 1 21 18.223; 20.352; 14.3
90; 105.02; 90
2311.4Audrey Dumoulin; Claudia Lalli; Pascal Retailleau; Geraldine Masson
Catalytic, highly enantioselective, direct amination of enecarbamates
Chem.Commun., 2015, 51, 5383
7116760 CIFC25 H48 B11 Li N2 O3P n m a15.1947; 12.6157; 16.666
90; 90; 90
3194.74Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo
Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion
Chem.Commun., 2015, 51, 5359
7116761 CIFC34.93 H66.85 B11 Li2 N2 O5.48P n n 215.9089; 26.7369; 10.561
90; 90; 90
4492.2Matthew J. Asay; Steven P. Fisher; Sarah E. Lee; Fook S. Tham; Dan Borchardt; Vincent Lavallo
Synthesis of unsymmetrical N-carboranyl NHCs: directing effect of the carborane anion
Chem.Commun., 2015, 51, 5359
7116762 CIFC13 H19 N O3 SP 21 21 2111.3743; 14.0235; 18.6496
90; 90; 90
2974.75Pablo Barrio; Elsa Rodriguez; Kodai Saito; Santos Fustero; Takahiko Akiyama
Gamma-Silylboronates in the chiral Bronsted acid-catalysed allylboration of aldehydes
Chem.Commun., 2015, 51, 5246
7116763 CIFC37 H51 F3 Mn N7 O4 SP -113.1912; 13.5415; 23.494
93.278; 103.037; 104.963
3920.1Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116764 CIFC48 H74 K Mn N7 O4P 1 21/c 123.141; 9.7932; 22.661
90; 105.914; 90
4938.7Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116765 CIFC40 H59 Mn N7 O2P 1 21/c 19.7762; 9.2337; 42.2828
90; 90.193; 90
3816.9Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116766 CIFC42 H59 F6 Mn N7 O7 S2P 21 21 2110.6932; 16.2784; 27.67
90; 90; 90
4816.5Yun Ji Park; Ellen M. Matson; Mark J. Nilges; Alison R. Fout
Exploring Mn-O bonding in the context of an electronically flexible secondary coordination sphere: synthesis of a Mn(III)-oxo
Chem.Commun., 2015, 51, 5310
7116767 CIFC8 H26 Fe3 N6 Se4C 2 2 219.1399; 18.122; 11.5436
90; 90; 90
1912Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir
Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes
Chem.Commun., 2015, 51, 5355
7116768 CIFC6 H18 Fe3 N4 Se4P 1 21/c 19.0393; 10.6303; 16.641
90; 102.652; 90
1560.2Joshua T. Greenfield; Chongin Pak; Saeed Kamali; Kathleen Lee; Kirill Kovnir
Control over connectivity and magnetism of tetrahedral FeSe2 chains through coordination Fe-amine complexes
Chem.Commun., 2015, 51, 5355
7116769 CIFC21 H21 I N O3P -111.5839; 15.7615; 32.762
91.604; 91.02; 101.055
5866.7K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode
Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR
Chem.Commun., 2015, 51, 5257
7116770 CIFC44.5 H36 Cl N4 O3P 42/n :236.726; 36.726; 5.6924
90; 90; 90
7678K. Ackermann; A. Giannoulis; D. B. Cordes; A. M. Z. Slawin; B. E. Bode
Assessing dimerisation degree and cooperativity in a biomimetic small-molecule model by pulsed EPR
Chem.Commun., 2015, 51, 5257
7116771 CIFC14 H30 N2 O23 U2P -16.2109; 9.997; 11.3778
97.9088; 93.7875; 104.294
674.38M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116772 CIFC16 H34 N2 O24 U2P -16.3074; 10.0063; 11.992
94.6846; 98.8324; 104.503
718.32M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116773 CIFC22 H30 N2 O22 U2P -16.7978; 9.8815; 11.7825
100.662; 99.5051; 91.0417
766.15M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116774 CIFC60 H96 N12 Na4 O94 U6P -119.987; 20.5879; 21.1208
68.467; 64.419; 67.96
7044.4M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116775 CIFC36 H27 Mg3 Na5 O81 U9P 63/m17.4123; 17.4123; 17.8443
90; 90; 120
4685.4M. Basile; D. K. Unruh; K. Gojdas; E. Flores; L. Streicher; T. Z. Forbes
Chemical controls on uranyl citrate speciation and the self-assembly of nanoscale macrocycles and sandwich complexes in aqueous solutions
Chem.Commun., 2015, 51, 5306
7116776 CIFC66 H55 N2 Np O7 P5P 1 21/n 113.61157; 16.5891; 26.4952
90; 91.6657; 90
5980.19Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan
Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI)
Chem.Commun., 2015, 51, 5402
7116777 CIFC67 H57 Cl2 N2 O7 P5 UP 1 21/n 19.7808; 23.697; 26.1815
90; 95.334; 90
6042Sean D. Woodall; Adam N. Swinburne; Nidhu lal Banik; Andrew Kerridge; Poppy Di Pietro; Christian Adam; Peter Kaden; Louise S. Natrajan
Neptunyl(VI) centred visible LMCT emission directly observable in the presence of uranyl(VI)
Chem.Commun., 2015, 51, 5402
7116778 CIFC23 H47 B Fe O2 P2P n m a13.8799; 16.5053; 11.7284
90; 90; 90
2686.9Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116779 CIFC17 H35 B Fe O8 P2P 1 21/c 110.5518; 14.372; 16.31
90; 108.637; 90
2343.7Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116780 CIFC23 H24 B F18 Fe O8 P3P 1 21/n 110.7235; 18.0733; 18.7761
90; 100.2; 90
3581.5Thomas J. Mazzacano; Neal P. Mankad
Thermal C-H borylation using a CO-free iron boryl complex
Chem.Commun., 2015, 51, 5379
7116781 CIFC24 H36 N5 O Re S4P -111.5743; 11.7501; 12.5007
86.489; 86.743; 60.987
1483.23Yan, Yong; Mague, Joel T.; Donahue, James P.; Sproules, Stephen
Unprecedented Spin Localisation in a Paramagnetic Dirhenium Complex with Multiple Metal Bonds
Chem.Commun., 2015, 51, 5482
7116782 CIFC17 H20 O4P 1 21/n 18.3539; 11.145; 16.1987
90; 101.731; 90
1476.67M. Presset; B. Michelet; R. Guillot; C. Bour; S. Bezzenine-Lafollee; V. Gandon
Gallium(III)- and calcium(II)-catalyzed Meyer-Schuster rearrangements followed by intramolecular aldol condensation or endo-Michael addition
Chem.Commun., 2015, 51, 5318
7116783 CIFC26 H29 F12 N7 O2 P2 PdP 1 21/c 117.4973; 9.579; 20.1652
90; 98.859; 90
3339.5Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116784 CIFC14 H15 F6 N4 O P PdP 1 21/m 112.097; 6.8619; 21.461
90; 91.882; 90
1780.5Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116785 CIFC14 H15 F6 N4 O Pd SbP 1 21 113.0668; 6.8152; 21.0073
90; 90.568; 90
1870.7Michael R. Chapman; Christopher M. Pask; Alireza Ariafard; Charlotte E. Willans
sigma-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)-H bond
Chem.Commun., 2015, 51, 5513
7116786 CIFC13 H13 N OP 21 21 215.018; 11.717; 18.072
90; 90; 90
1062.6Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116787 CIFC13 H13 N OP 1 21/c 19.4905; 4.937; 21.8359
90; 95.103; 90
1019.06Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116788 CIFC13 H13 N OP 1 21/n 110.5236; 7.17; 13.5856
90; 93.912; 90
1022.7Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116789 CIFC13 H13 N OP 1 21/c 14.918; 17.5881; 11.975
90; 97.432; 90
1027.12Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116790 CIFC13 H13 N OP 1 21/n 19.3763; 6.5586; 16.7932
90; 102.558; 90
1008Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116791 CIFC13 H13 N OP 1 21/n 112.7256; 5.4479; 14.793
90; 103.039; 90
999.12Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116792 CIFC13 H13 N OP b c a14.6822; 6.6231; 20.97
90; 90; 90
2039.2Robert M. Edkins; Elliott Hayden; Jonathan W. Steed; Katharina Fucke
Conserved hydrogen bonding in tetrahydrocarbazolone derivatives: influence of solution-state assembly on crystal form nucleation
Chem.Commun., 2015, 51, 5314
7116793 CIFC50 H61 Cu N4 O2P 1 21/c 119.5203; 11.1949; 20.5166
90; 99.303; 90
4424.5Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz
IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand
Chem.Commun., 2015, 51, 5271
7116794 CIFC50 H62 B Cu F4 N4 O2P -110.373; 18.414; 26.739
96.931; 91.874; 102.56
4940Vincent Cesar; Valentina Mallardo; Adela Nano; Georges Dahm; Noel Lugan; Guy Lavigne; Stephane Bellemin-Laponnaz
IMes-acac: hybrid combination of diaminocarbene and acetylacetonato sub-units into a new anionic ambidentate NHC ligand
Chem.Commun., 2015, 51, 5271
7116795 CIFC13 H31 Cl Cu N4 O6P n a 2117.0837; 12.5402; 9.2795
90; 90; 90
1988Athina Anastasaki; Vasiliki Nikolaou; Francesca Brandford-Adams; Gabit Nurumbetov; Qiang Zhang; Guy J. Clarkson; David J. Fox; Paul Wilson; Kristian Kempe; David M. Haddleton
Photo-induced living radical polymerization of acrylates utilizing a discrete copper(II)-formate complex
Chem.Commun., 2015, 51, 5626
7116796 CIFC18 H14 Cu2 N0 O10I m m a18.8261; 22.1934; 10.0062
90; 90; 90
4180.7Hui-Min Wen; Bin Li; Hailong Wang; Chuande Wu; Khalid Alfooty; Rajamani Krishna; Banglin Chen
A microporous metal-organic framework with rare lvt topology for highly selective C2H2/C2H4 separation at room temperature
Chem.Commun., 2015, 51, 5610
7116797 CIFC35 H41 Cu5 N40 O0F d d d16.18; 43.077; 45.485
90; 90; 90
31702B. X. Dong; S. Y. Zhang; W. L. Liu; Y. C. Wu; J. Ge; L. Song; Y. L. Teng
Gas storage and separation in a water-stable [Cu^I^5BTT3]^4-^ anion framework comprising a giant multi-prismatic nanoscale cage
Chem.Commun., 2015, 51, 5691
7116798 CIFC36 H51 N O2 ZrP 1 21 110.82; 11.235; 15.074
90; 110.637; 90
1714.9Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116799 CIFC42 H57 N O2 ZrP 3225.473; 25.473; 15.017
90; 90; 120
8439Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116800 CIFC50 H57 N O2 Si ZrP 21 21 2110.4723; 20.7272; 21.2971
90; 90; 90
4622.8Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116801 CIFC51 H57 N O2 ZrP 21 21 219.9279; 20.7319; 20.8378
90; 90; 90
4288.9Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116802 CIFC53 H61 N O2 ZrP 1 21 110.0708; 16.4364; 29.62
90; 91.34; 90
4901.6Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116803 CIFC56 H59 N O2 ZrP 1 21 112.3987; 10.2035; 35.906
90; 91.315; 90
4541.3Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116804 CIFC50 H55 N O2 ZrP 1 21 19.9153; 39.191; 10.9485
90; 93.596; 90
4246.1Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116805 CIFC49 H51 N O2 ZrP 1 21 110.249; 10.086; 20.139
90; 102.78; 90
2030.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116806 CIFC51 H55 N O2 ZrP 21 21 2110.4071; 20.0669; 20.1804
90; 90; 90
4214.4Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116807 CIFC53 H59 N O2 ZrP 21 21 2110.5049; 20.1449; 20.7934
90; 90; 90
4400.3Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116808 CIFC61 H59 N O2 ZrP 21 21 219.9859; 10.2631; 46.379
90; 90; 90
4753.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116809 CIFC44 H43 N O2 ZrC 1 2/c 129.258; 24.694; 23.148
90; 117.297; 90
14862Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116810 CIFC72 H87 N5 O4 Zr2P -112.0652; 13.096; 23.377
100.831; 93.008; 111.473
3346.2Xiaoguang Zhou; Bing Wei; Xiu-Li Sun; Yong Tang; Zuowei Xie
Asymmetric hydroamination catalyzed by a new chiral zirconium system: reaction scope and mechanism
Chem.Commun., 2015, 51, 5751
7116811 CIFC42 H34 O12 Zn3P 32 2 118.1019; 18.1019; 24.668
90; 90; 120
7000.2Hongmin Su; Fuxing Sun; Jiangtao Jia; Hongming He; Aifei Wang; Guangshan Zhu
A highly porous medical metal-organic framework constructed from bioactive curcumin
Chem.Commun., 2015, 51, 5774
7116812 CIFC13 H14 N2 O7P 21 21 215.0946; 14.4569; 18.2887
90; 90; 90
1347E.-K. Kim; R. Krishnamurthy
Synthesis of orotidine by intramolecular nucleosidation
Chem.Commun., 2015, 51, 5618
7116813 CIFC16 H29 N O7P 21 21 216.1806; 14.641; 20.36
90; 90; 90
1842.4Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116814 CIFC17 H31 N O7P 21 21 216.3376; 15.4586; 20.0153
90; 90; 90
1960.9Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116815 CIFC24 H31 N O7P 21 21 217.6206; 11.4755; 26.5274
90; 90; 90
2319.8Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116816 CIFC20 H29 N O7P 1 21 114.4045; 6.2322; 23.4872
90; 103.762; 90
2048Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116817 CIFC24 H31 N O7P 1 21 113.74; 6.188; 15.056
90; 113.998; 90
1169.5Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116818 CIFC20 H29 N O7P 1 21 114.634; 6.2305; 11.855
90; 102.86; 90
1053.8Nikoletta B. Bathori; Luigi R. Nassimbeni; Jacco van de Streek
One hydrogen bond does not a separation make, or does it? Resolution of amines by diacetoneketogulonic acid
Chem.Commun., 2015, 51, 5664
7116819 CIFC32 H24 B2 N2P 1 21/n 19.938; 15.052; 16.599
90; 94.82; 90
2474.2Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116820 CIFC24 H18 B2 N2 SP -19.492; 10.356; 10.494
76.69; 80.05; 77.48
971.7Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116821 CIFC28 H25 B N2P n a 2111.268; 23.152; 8.5403
90; 90; 90
2228Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116822 CIFC20 H17 B N2P -110.344; 17.825; 18.052
94.99; 98.18; 90.06
3281.8Cong Ma; Jianying Zhang; Jianfeng Li; Chunming Cui
Multiple C-H borylation of phenylhydrazones to boron-nitrogen analogues of benzopentalene
Chem.Commun., 2015, 51, 5732
7116823 CIFC30 H38 N2 O5 S2P 1 21 113.0848; 13.5713; 16.2698
90; 94.205; 90
2881.38Yi Li; Marcel Hartmann; Constantin Gabriel Daniliuc; Armido Studer
Radical aminooxygenation of alkenes with N-fluoro-benzenesulfonimide (NFSI) and TEMPONa
Chem.Commun., 2015, 51, 5706
7116824 CIFC35 H47 I N2 ZnP n a m13.0009; 24.7338; 10.817
90; 90; 90
3478.33Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116825 CIFC36 H46 Fe N2 O2 ZnP b c a20.9493; 14.21072; 22.37442
90; 90; 90
6660.97Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116826 CIFC58 H82 Hg N4 Zn2P 1 21/n 112.784; 17.3101; 13.0055
90; 101.117; 90
2824.01Matthew P. Blake; Nikolas Kaltsoyannis; Philip Mountford
Synthesis, molecular and electronic structure, and reactions of a Zn-Hg-Zn bonded complex
Chem.Commun., 2015, 51, 5743
7116827 CIFC39 H45 Br6 N3 O3C 1 2/c 134.3269; 16.0953; 17.3532
90; 115.959; 90
8620.3Ryohei Yamakado; Shin-ichi Matsuoka; Masato Suzuki; Daisuke Takeuchi; Hyuma Masu; Isao Azumaya; Koji Takagi
Diastereoselective cyclization of an aminobenzoic acid derivative and chiroptical properties of triple-stranded helical bis(phenylethynyl)benzene
Chem.Commun., 2015, 51, 5710
7116830 CIFC18 H13 N3 OP 1 21/c 18.3217; 9.5453; 17.1799
90; 100.577; 90
1341.47Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116831 CIFC12 H9 N3 OC 1 2/c 111.477; 8.789; 19.955
90; 103.778; 90
1955Sreekumar Pankajakshan; Zhi Guang Chng; Rakesh Ganguly; Teck Peng Loh
Copper-catalyzed aerobic carboxygenation and N-arylation of [1,2,3]triazolo[1,5-a]pyridines towards pyridinium triazolinone ylides
Chem.Commun., 2015, 51, 5929
7116832 CIFC26 H23 NP 1 21/n 115.205; 7.3621; 18.007
90; 96.56; 90
2002.5Jia Zheng; Liangbin Huang; Zun Li; Wanqing Wu; Jianxiao Li; Huanfeng Jiang
Synthesis of 3-bromosubstituted pyrroles via palladium-catalyzed intermolecular oxidative cyclization of bromoalkynes with N-allylamines
Chem.Commun., 2015, 51, 5894
7116833 CIFC30 H22 O2P -111.7482; 13.7728; 15.9289
102.716; 104.883; 113.218
2134.1Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116834 CIFC30 H22 O2P -110.448; 12.7886; 16.6149
84.832; 71.771; 84.18
2093.72Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116835 CIFC42 H30 O2P 1 21/c 110.5584; 9.542; 29.2511
90; 91.525; 90
2945.95Shohei Eda; Fumiaki Eguchi; Hiroshi Haneda; Toshiyuki Hamura
A new synthetic route to substituted tetracenes and pentacenes via stereoselective [4+2] cycloadditions of 1,4-dihydro-1,4-epoxynaphthalene and isobenzofuran
Chem.Commun., 2015, 51, 5963
7116836 CIFC43 H38 Cl2 Li N8 O2 ScP -112.0145; 13.1895; 14.9239
64.581; 70.692; 88.526
1997Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116837 CIFC37 H21 N8 ScP -18.976; 15.873; 19.618
83.59; 86.358; 83.85
2758Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116838 CIFC45 H37 N8 O0.75 ScP b c m16.1402; 21.4116; 21.6902
90; 90; 90
7495.9Rachel H. Platel; Thiago Teixeira Tasso; Wen Zhou; Taniyuki Furuyama; Nagao Kobayashi; Daniel B. Leznoff
Metallophthalocyanin-ocenes: scandium phthalocyanines with an eta^5^-bound Cp ring
Chem.Commun., 2015, 51, 5986
7116839 CIFC32 H26 N4 Ni S2P b c a18.0049; 9.0457; 32.7494
90; 90; 90
5333.8Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116840 CIFC32 H26 N4 Ni S2P -19.7891; 11.7331; 12.5712
104.486; 99.689; 102.531
1326.3Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116841 CIFC32 H24 N4 Ni S2P -19.9075; 12.3331; 12.436
64.149; 69.893; 79.482
1283.19Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116842 CIFC33 H27 Cl3 N4 S2P -18.9232; 12.3869; 14.6782
75.749; 75.097; 86.521
1519.57Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116843 CIFC64 H48 N8 S4 Zn2P 1 21/n 115.1355; 14.9332; 24.9048
90; 106.399; 90
5400Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116844 CIFC205 H172 N24 O4 S12 Zn6P -113.3649; 18.2896; 18.8109
96.448; 99.538; 94.693
4482.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116845 CIFC34 H26 N4 Ni O4P -19.2124; 11.1476; 14.7168
86.166; 76.5; 70.682
1386.77Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116846 CIFC34 H24 N4 Ni O4C 1 2/c 134.4732; 9.868; 7.9143
90; 100.724; 90
2645.28Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116847 CIFC34 H26 N4 O4P 1 2/c 120.8248; 7.2192; 19.4469
90; 105.825; 90
2812.81Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116848 CIFC68 H48 N8 O8 Zn2C 1 2/c 123.8065; 16.6644; 42.744
90; 100.563; 90
16670.1Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116849 CIFC105 H75 Cl9 N12 O12 Zn3C 1 2/c 118.1355; 21.5289; 25.5659
90; 100.008; 90
9830Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116850 CIFC136 H96 N16 O16 Zn4I 2 2 215.3648; 19.7305; 23.6393
90; 90; 90
7166.4Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116851 CIFC136 H96 N16 O16 Zn4I 2 2 215.337; 19.7279; 23.6518
90; 90; 90
7156.2Stephane A. Baudron; Herve Ruffin; Mir Wais Hosseini
On Zn(II) 2,2'-bisdipyrrin circular helicates
Chem.Commun., 2015, 51, 5906
7116852 CIFC36 H15 As B F15 OP 1 21/n 113.134; 16.309; 14.601
90; 96.167; 90
3109.5Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116853 CIFC36 H15 B F15 O SbP 1 21/n 112.248; 17.312; 15.058
90; 95.34; 90
3179Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116854 CIFC30 H19 B F15 N2 O SbP -19.814; 10.784; 16.68
84.08; 87.26; 77.49
1713.6Ralf Kather; Tomas Svoboda; Maren Wehrhahn; Elena Rychagova; Enno Lork; Libor Dostal; Sergey Ketkov; Jens Beckmann
Lewis-acid induced disaggregation of dimeric arylantimony oxides
Chem.Commun., 2015, 51, 5932
7116855 CIFC25 H24 N2 O2 S3P 1 21/n 111.461; 12.938; 15.619
90; 93.48; 90
2311.8Chuan Liu; Qin Yin; Li-Xin Dai; Shu-Li You
Synthesis of pyrroloindolines and furoindolines via cascade dearomatization of indole derivatives with carbenium ion
Chem.Commun., 2015, 51, 5971
7116856 CIFC93 H97 Al N10 O2 UP 1 21/c 121.6483; 15.4318; 24.4807
90; 98.594; 90
8086.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116857 CIFC74 H88 Al N9 O3 UP 1 21/n 112.5004; 40.0423; 14.2199
90; 105.173; 90
6869.57Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116858 CIFC124 H124 Li2 N18 O4 U2P -111.963; 14.243; 17.926
99.705; 90.311; 114.231
2736Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116859 CIFC84.47 H84.47 Li0.87 N16.49 O2 UC 1 c 114.2782; 24.4176; 22.8717
90; 90.634; 90
7973.5Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116860 CIFC62 H62 B0 N12 Na O2 UC 1 c 114.427; 24.602; 23.182
90; 90.881; 90
8227Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116861 CIFC77 H76 K N15 O2 UP 21 21 2113.693; 21.7419; 24.2382
90; 90; 90
7216Markus Zegke; Gary S. Nichol; Polly L. Arnold; Jason B. Love
Catalytic one-electron reduction of uranyl(VI) to Group 1 uranyl(V) complexes via Al(III) coordination
Chem.Commun., 2015, 51, 5876
7116862 CIFC18 H11.33 Co O6.67P -3 1 c16.789; 16.789; 15.144
90; 90; 120
3696.8Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116863 CIFC18 H11.33 Co O6.67R -3 c :H17.431; 17.431; 48.043
90; 90; 120
12641.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116864 CIFC18 H11.33 Co O6.67P -3 1 c16.7639; 16.7639; 14.9592
90; 90; 120
3640.7Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116865 CIFC18 H11.33 Co O6.67P -3 1 c16.7335; 16.7335; 14.9637
90; 90; 120
3628.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116866 CIFC18 H11.33 Co O6.67R -3 c :H17.2813; 17.2813; 47.354
90; 90; 120
12247.3Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116867 CIFC18 H11.33 Co O6.67R -3 c :H17.3321; 17.3321; 47.616
90; 90; 120
12387.6Min Chen; Hui Zhao; Chun-Sen Liu; Xi Wang; Heng-Zhen Shi; Miao Du
Template-directed construction of conformational supramolecular isomers for bilayer porous metal-organic frameworks with distinct gas sorption behaviors
Chem.Commun., 2015, 51, 6014
7116870 CIFC54 H52P 21 21 2113.2582; 14.2403; 42.561
90; 90; 90
8035.5K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116871 CIFC42 H42 Cl2P 1 21/c 115.5669; 11.5716; 18.0171
90; 96.615; 90
3223.9K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116872 CIFC20 H8 Cl2 F6P -18.5128; 11.4844; 13.1495
97.59; 96.803; 103.045
1226.68K. W. J. Heard; J. J. Morrison; L. Weston; C. H. Lo; L. Pirvu; J. Raftery; M. S. Little; J. J. W. McDouall; S. G. Yeates; P. Quayle
An orthogonal C-H borylation - cross-coupling strategy for the preparation of tetrasubstituted 'A2B2'-chrysene derivatives with tuneable photophysical properties
Chem.Commun., 2015, 51, 6115
7116873 CIFC34 H45 Fe N2P -110.1306; 11.1529; 13.6025
93.475; 92.686; 101.503
1500.52Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116874 CIFC54 H74 Fe2 N4 P4P 1 21/n 114.4521; 12.9461; 14.8567
90; 105.421; 90
2679.6Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116875 CIFC43 H69 Fe K0.5 N2 O4 P2P 1 21/c 113.2205; 18.4486; 18.4434
90; 90.303; 90
4498.28Shenglai Yao; Tibor Szilvasi; Nils Lindenmaier; Yun Xiong; Shigeyoshi Inoue; Mario Adelhardt; Jorg Sutter; Karsten Meyer; Matthias Driess
Reductive cleavage of P4 by iron(I) centres: synthesis and structural characterisation of Fe2(P2)2 complexes with two bridging P22- ligands
Chem.Commun., 2015, 51, 6153
7116876 CIFC19 H18 Cl O2P 43 21 211.6351; 11.6351; 48.952
90; 90; 90
6626.9Yang Yang; Jinpeng Li; Biao Du; Changchun Yuan; Bo Liu; Song Qin
An entry to vinylcyclopropane through palladium-catalyzed intramolecular cyclopropanation of alkenes with unstabilized allylic tosylhydrazones
Chem.Commun., 2015, 51, 6179
7116877 CIFC19 H17 Br N2 O3P 21 21 215.613; 16.048; 18.9931
90; 90; 90
1710.8Srimanta Manna; Rishikesh Narayan; Christopher Golz; Carsten Strohmann; Andrey P. Antonchick
Regioselective annulation of nitrosopyridine with alkynes: straightforward synthesis of N-oxide-imidazopyridines
Chem.Commun., 2015, 51, 6119
7116878 CIFC56 H72 S8 Si4C 1 2/c 143.196; 6.377; 24.5113
90; 115.408; 90
6099Kengo Asai; Aiko Fukazawa; Shigehiro Yamaguchi
A cyclic octithiophene containing beta,beta'-linkages
Chem.Commun., 2015, 51, 6096
7116879 CIFC46 H45 B F15 P3 PdP 1 21/n 19.7351; 29.7778; 16.3484
90; 104.943; 90
4579Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116880 CIFC33 H53 Cl P2 PdP 1 21/c 112.3466; 11.6819; 23.5089
90; 91.4208; 90
3389.7Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116881 CIFC36 H61 P3 PdC 1 2/c 128.976; 14.6255; 31.853
90; 106.946; 90
12913Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116882 CIFC54 H61 B F15 P3 PdP 1 21/c 114.7706; 13.9199; 28.5994
90; 93.208; 90
5871Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116883 CIFC60 H58 B F24 P3 PdP 1 21/n 113.1862; 12.7167; 37.1231
90; 94.967; 90
6201.6Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116884 CIFC68 H74 B F24 P3 PdP -113.7002; 17.7228; 18.52
65.531; 74.7; 88.259
3931.8Peng Cui; Cezar C. Comanescu; Vlad M. Iluc
Frustrated Lewis pair-like reactions of nucleophilic palladium carbenes with B(C6F5)3
Chem.Commun., 2015, 51, 6206
7116885 CIFC29 H46 O5 SiP -110.3975; 11.144; 13.6268
113.777; 91.585; 102.55
1398.6Hideki Abe; Yuri Horii; Megumi Hagiwara; Toyoharu Kobayashi; Hisanaka Ito
Stereoselective synthesis of a highly oxygenated decahydrocyclopenta[g]chromene derivative: the common tricyclic framework of leucosceptrine and leucosesterterpenone
Chem.Commun., 2015, 51, 6108
7116886 CIFC74 H127 Cl3 Mg3 O11P -114.3956; 15.2219; 18.5435
88.65; 74.452; 85.197
3900.96Baofei Pan; Junjie Zhang; Jinhua Huang; John T. Vaughey; Lu Zhang; Sang-Don Han; Anthony K. Burrell; Zhengcheng Zhang; Chen Liao
A Lewis acid-free and phenolate-based magnesium electrolyte for rechargeable magnesium batteries
Chem.Commun., 2015, 51, 6214
7116887 CIFC16 H12 Cl N O3P -110.3981; 10.4368; 15.4169
78.123; 81.589; 61.978
1442.9Wen-Zhen Zhang; Tian Xia; Xu-Tong Yang; Xiao-Bing Lu
Synthesis of oxazolidine-2,4-diones by a tandem phosphorus-mediated carboxylative condensation-cyclization reaction using atmospheric carbon dioxide
Chem.Commun., 2015, 51, 6175
7116888 CIFC28 H20 O2P -110.5146; 11.1198; 18.1537
73.905; 80.721; 89.893
2010.6Jing Wang; Dekun Qin; Jingbo Lan; Yangyang Cheng; Shuai Zhang; Qiang Guo; Jie Wu; Di Wu; Jingsong You
Rh-catalysed direct cyclisation of 1,4-naphthoquinone and 9,10-phenanthraquinone with alkyne: facile access to 1,8-dioxapyrenes and 1,12-dioxaperylenes as orange and red-emitting luminophores
Chem.Commun., 2015, 51, 6337
7116889 CIFC29 H31 N O3P 1 21/c 113.186; 14.909; 12.985
90; 110.29; 90
2394.3Kai Zhang; Hang Wang; Jingfeng Zheng; Lei Yu; Hanfeng Ding
Hypervalent iodine mediated alkene difunctionalization of vinylphenols: diastereoselective synthesis of substituted indoles and indolizines
Chem.Commun., 2015, 51, 6399
7116890 CIFC29 H23 Br N2 SP -19.2263; 11.3952; 12.1843
99.988; 101.997; 95.944
1221.01Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116891 CIFC29 H24 N2 SP 1 21/n 18.6586; 22.4244; 12.0588
90; 100.455; 90
2302.51Ying Zhang; Jun-Hao Wang; Ji Zheng; Dan Li
A Br-substituted phenanthroimidazole derivative with aggregation induced emission from intermolecular halogen-hydrogen interactions
Chem.Commun., 2015, 51, 6350
7116892 CIFC28 H28 Cl N O9P -111.5552; 11.6532; 11.9655
77.69; 68.849; 63.172
1338.48Marie Cordier; Aurelie Dos Santos; Laurent El Kaim; Noisette Narboni
Passerini/Tsuji-Trost strategies towards achieving lactams and cyclopentane derivatives
Chem.Commun., 2015, 51, 6411
7116893 CIFC19 H20 I N OP 1 21/c 110.6819; 9.4115; 17.492
90; 92.723; 90
1756.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116894 CIFC16 H26 Al O4 TiP -19.6563; 9.8287; 10.6494
64.408; 74.407; 73.803
862.5Renhong Sun; Jun Liu; Shuang Yang; Ming Chen; Ning Sun; Haoyi Chen; Xin Xie; Xu You; Shi Li; Yuanhong Liu
Cp2TiCl2-catalyzed cis-hydroalumination of propargylic amines with Red-Al: stereoselective synthesis of Z-configured allylic amines
Chem.Commun., 2015, 51, 6426
7116895 CIFC18 H16 O3 S3P -14.5264; 13.238; 14.614
85.804; 82.143; 84.097
861.3Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116896 CIFC22 H27 N O4 SC 1 2/c 131.687; 6.2286; 23.0782
90; 106.427; 90
4368.9Hai-Bin Yang; Yu-Chao Yuan; Yin Wei; Min Shi
Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes
Chem.Commun., 2015, 51, 6430
7116897 CIFC212.07 H84 Cl4 O66.07 Ru11.36P -116.3234; 16.3914; 18.3063
64.293; 83.74; 83.301
4373.8Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116898 CIFC97 H40 O25 Ru3P 1 21/c 122.538; 34.0435; 18.4298
90; 92.787; 90
14124Chia-Hsiang Chen; Amineh Aghabali; Catalina Suarez; Marilyn M. Olmstead; Alan L. Balch; Luis Echegoyen
Synthesis and characterization of bis-triruthenium cluster derivatives of an all equatorial [60]fullerene tetramalonate
Chem.Commun., 2015, 51, 6489
7116899 CIFC37 H25 N2 O4 ZnP -19.8824; 11.548; 15.648
89.784; 76.441; 75.603
1678.7Suresh Sanda; Srinivasulu Parshamoni; Soumava Biswas; Sanjit Konar
Highly selective detection of palladium and picric acid by a luminescent MOF: a dual functional fluorescent sensor
Chem.Commun., 2015, 51, 6576
7116900 CIFC31 H39 Cl2 N3 NiP 21 21 2113.6222; 14.2676; 15.7854
90; 90; 90
3068Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116901 CIFC32 H39 Br2 Cl2 N3 NiP 1 21/n 19.787; 26.3927; 13.7739
90; 108.906; 90
3365.9Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116902 CIFC39 H47 Cl N3 Ni O2P -19.7349; 12.3308; 15.6197
87.49; 75.776; 85.562
1811.45Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116903 CIFC39 H47 Br N3 Ni O2P -19.8908; 12.3807; 15.5767
86.987; 75.727; 85.167
1841Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116904 CIFC37 H49 Br N3 Ni O1.5P -19.7274; 14.232; 14.9719
111.974; 99.695; 101.376
1816.3Blake R. Reed; Sebastian A. Stoian; Richard L. Lord; Stanislav Groysman
The aldimine effect in bis(imino)pyridine complexes: non-planar nickel(I) complexes of a bis(aldimino)pyridine ligand
Chem.Commun., 2015, 51, 6496
7116905 CIFC44 H44 Cu5 N6 O14P 1 21/n 16.2137; 16.2226; 22.6452
90; 91.2531; 90
2282.1Christian Plenk; Jasmin Krause; Martin Beck; Eva Rentschler
Rational linkage of magnetic molecules using click chemistry
Chem.Commun., 2015, 51, 6524
7116906 CIFC23 H17 F3 O SP -19.4049; 10.3048; 10.563
79.807; 74.337; 82.314
966.1Dao-Qian Chen; Pin Gao; Ping-Xin Zhou; Xian-Rong Song; Yi-Feng Qiu; Xue-Yuan Liu; Yong-Min Liang
Regioselective access to CF3S-substituted dihydrofurans from homopropargylic alcohols with trifluoromethanesulfenamide
Chem.Commun., 2015, 51, 6637
7116907 CIFC64 H82 N8 S8P -4 3 n22.6217; 22.6217; 22.6217
90; 90; 90
11576.5Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116908 CIFC80 H114 N8 S8P -112.7956; 17.1258; 18.8008
112.281; 91.994; 94.129
3793.8Yunus Zorlu; Ufuk Kumru; Umit Isci; Burcin Divrik; Erwann Jeanneau; Florian Albrieux; Yavuz Dede; Vefa Ahsen; Fabienne Dumoulin
1,4,8,11,15,18,22,25-Alkylsulfanyl phthalocyanines: effect of macrocycle distortion on spectroscopic and packing properties
Chem.Commun., 2015, 51, 6580
7116909 CIFC12 H9 N3 O2P b c a11.5359; 15.7377; 23.975
90; 90; 90
4352.6Cheng Xu; Feng-Cheng Jia; Qun Cai; Deng-Kui Li; Zhi-Wen Zhou; An-Xin Wu
Intramolecular decarboxylative coupling as the key step in copper-catalyzed domino reaction: facile access to 2-(1,3,4-oxadiazol-2-yl)aniline derivatives
Chem.Commun., 2015, 51, 6629
7116910 CIFC25 H19 N OP c a 2113.273; 18.584; 7.3811
90; 90; 90
1820.7Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116911 CIFC24 H32 Cl NP 21 21 217.0083; 8.9587; 32.914
90; 90; 90
2066.5Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116912 CIFC20 H20 F3 N OP -110.018; 10.446; 35.11
83.334; 86.119; 76.252
3542Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116913 CIFC21 H31 Cl N O2P -17.085; 12.661; 12.767
94.479; 93.887; 100.786
1117.6Liangwei Zhang; Xiangdong Li; Yuanhong Liu; Dayong Zhang
Palladium-catalyzed highly efficient synthesis of functionalized indolizines via cross-coupling/cycloisomerization cascade
Chem.Commun., 2015, 51, 6633
7116914 CIFC22 H19 N2P 1 21/n 19.7108; 11.3687; 14.8851
90; 97.059; 90
1630.85Likui Xiang; Yanning Niu; Xiaobo Pang; Xiaodong Yang; Rulong Yan
I2-catalyzed synthesis of substituted imidazoles from vinyl azides and benzylamines
Chem.Commun., 2015, 51, 6598
7116915 CIFC12 H14 Br N OP b c a8.8904; 13.0832; 19.2524
90; 90; 90
2239.3Rahul Kisan Kawade; Deepak B. Huple; Rong-Jing Lin; Rai-Shung Liu
Cu-catalyzed oxidative Povarov reactions between N-alkyl N-methylanilines and saturated oxa- and thiacycles
Chem.Commun., 2015, 51, 6625
7116916 CIFC16 H14 Co2 O7P -18.893; 16.495; 19.797
101.28; 102.13; 103.697
2664.8Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116917 CIFC16 H14 Co2 O7P -19.074; 12.983; 16.699
110.879; 96.205; 98.023
1793.4Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116918 CIFC23 H17 Co2 N O11C 1 2/c 139.343; 8.101; 16.72
90; 110.966; 90
4976Pierangelo Gobbo; Tommaso Romagnoli; Stephanie M. Barbon; Jacquelyn T. Price; Jennifer Keir; Joe B. Gilroy; Mark S. Workentin
Expanding the scope of strained-alkyne chemistry: a protection-deprotection strategy via the formation of a dicobalt-hexacarbonyl complex
Chem.Commun., 2015, 51, 6647
7116919 CIFC28 H17 OP b c n11.6165; 12.7592; 12.4644
90; 90; 90
1847.44Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116920 CIFC58.5 H37.5 Cl7.5 O2P -111.5782; 14.3354; 16.4867
96.3005; 101.787; 113.704
2395.88Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116921 CIFC52 H41 OP 1 21/n 110.6594; 21.7535; 16.0991
90; 100.123; 90
3674.93Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116922 CIFC57 H46 Cl15 OP 1 21/c 113.966; 19.591; 21.6636
90; 109.308; 90
5593.9Tatsuya Aotake; Mitsuharu Suzuki; Naoki Aratani; Junpei Yuasa; Daiki Kuzuhara; Hironobu Hayashi; Haruyuki Nakano; Tsuyoshi Kawai; Jishan Wu; Hiroko Yamada
9,9'-Anthryl-anthroxyl radicals: strategic stabilization of highly reactive phenoxyl radicals
Chem.Commun., 2015, 51, 6734
7116923 CIFC21 H22 N2 O4 SP 1 21/c 113.153; 17.8912; 9.1269
90; 109.86; 90
2020Xin-Hua Hao; Pin Gao; Xian-Rong Song; Yi-Feng Qiu; Dong-Po Jin; Xue-Yuan Liu; Yong-Min Liang
Metal-free nitro-carbocyclization of 1,6-enynes with tBuONO and TEMPO
Chem.Commun., 2015, 51, 6839
7116924 CIFC45 H40 Ag0 Cl7 F0 N5 O11 P0 Sb U Zn0P -110.3488; 15.1997; 16.7191
89.696; 77.054; 84.978
2552.93Christina M. Davis; Kei Ohkubo; I-Ting Ho; Zhan Zhang; Masatoshi Ishida; Yuanyuan Fang; Vincent M. Lynch; Karl M. Kadish; Jonathan L. Sessler; Shunichi Fukuzumi
Near-infrared-induced electron transfer of an uranyl macrocyclic complex without energy transfer to dioxygen
Chem.Commun., 2015, 51, 6757
7116925 CIFC32 H31 B Fe N7 SP 1 21/n 19.3767; 16.0545; 19.6816
90; 96.784; 90
2942.1M. Sallmann; B. Braun; C. Limberg
Dioxygenation of cysteamine to hypotaurine at a tris(pyrazolyl)borate iron(II) unit - cysteamine dioxygenase mimicking?
Chem.Commun., 2015, 51, 6785
7116926 CIFC36 H52 Eu2 N8 O22P -113.2205; 13.9973; 14.9
99.68; 91.009; 117.103
2405.6Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116927 CIFC33 H47 N7 O22 Tb2P -113.009; 13.7701; 15.0439
99.513; 90.402; 116.522
2368.1Yin-Ling Hou; Hang Xu; Rui-Rui Cheng; Bin Zhao
Controlled lanthanide-organic framework nanospheres as reversible and sensitive luminescent sensors for practical applications
Chem.Commun., 2015, 51, 6769
7116928 CIFC19 H19 F3 N2P b c a10.9173; 8.53033; 34.7268
90; 90; 90
3234.04Kazuki Isa; Maki Minakawa; Motoi Kawatsura
Palladium-catalyzed amination of 2,3,3-trifluoroallyl esters: synthesis of trifluoromethylenamines via an intramolecular fluorine shift and CF3 group construction
Chem.Commun., 2015, 51, 6761
7116929 CIFC55 H77 Ge N O4 SiP -111.9476; 13.7236; 16.2518
81.454; 83.839; 80.731
2591.21Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116930 CIFC50 H66 Ge N O3 SiP -110.074; 14.516; 18.777
109.23; 96.79; 97.99
2527.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116931 CIFC45 H55 Ge N O3 SiP 1 21/n 110.7047; 21.7462; 17.079
90; 92.615; 90
3971.6Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116932 CIFC45 H55 N O3 SiP 1 21/n 112.369; 21.768; 14.724
90; 96.32; 90
3940.3Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116933 CIFC53 H70 Li N O5 SiP 1 21/c 111.531; 24.287; 17.056
90; 98.37; 90
4725.7Terrance J. Hadlington; Benedikt Schwarze; Ekaterina I. Izgorodina; Cameron Jones
Two-coordinate hydrido-germylenes
Chem.Commun., 2015, 51, 6854
7116934 CIFC32 H26 N2 O2P 1 21/c 118.889; 7.1199; 18.6541
90; 104.646; 90
2427.2Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116935 CIFC42 H30 N2P -111.0719; 11.9763; 12.7664
95.06; 92.632; 117.362
1490.4Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116936 CIFC30.3 H25.6 Cl0.6 N4 O2 RhP -19.6401; 11.069; 12.562
82.69; 77.98; 83.72
1295.6Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116937 CIFC30 H21 Cl N2P -18.8053; 11.2771; 12.0975
67.401; 89.113; 83.151
1100.51Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116938 CIFC32 H26 N2 OP 1 21/c 19.9489; 17.1959; 14.4905
90; 109.121; 90
2342.3Ting Li; Zhen Wang; Mingliang Zhang; Hui-Jun Zhang; Ting-Bin Wen
Rh/Cu-catalyzed multiple C-H, C-C, and C-N bond cleavage: facile synthesis of pyrido[2,1-a]indoles from 1-(pyridin-2-yl)-1H-indoles and gamma-substituted propargyl alcohols
Chem.Commun., 2015, 51, 6777
7116939 CIFC72 H60 Ag O4 P4 ReR 3 :H14.2192; 14.2192; 51.1145
90; 90; 120
8950F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116940 CIFC72 H60 Ag2 O8 P4 Re2P -112.1764; 12.4966; 13.2647
89.938; 62.745; 68.528
1635.6F. Deiser; F. Kraus; H. Schmidbaur
Bis(triphenylphosphine)silver(I) perrhenate, a cyclic dimer
Chem.Commun., 2015, 51, 6746
7116941 CIFC28.84 H42.57 N O6 S SiP 1 21/c 115.627; 13.4083; 15.769
90; 110.208; 90
3100.7Urszula K. Klimczak; Bartosz K. Zambron
Effective 1,5-stereocontrol in Pd(0)/InI promoted reactions of chiral N-Ts-4-vinylazetidin-2-ones with aldehydes. An efficient entry into nonracemic semi-protected (3Z)-2,6-anti-enediols
Chem.Commun., 2015, 51, 6796
7116942 CIFC22 H12 K N9 O1.94P 42/n :220.9259; 20.9259; 9.6322
90; 90; 90
4217.9Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116943 CIFC22 K N9 O2P 1 2/a 120.904; 15.931; 9.711
90; 104.65; 90
3129Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116944 CIFC22 K N9 O6P 1 2/a 120.656; 15.978; 16.801
90; 100.68; 90
5449Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116945 CIFC22 K N9 O8.5P 1 2/n 124.131; 19.458; 16.672
90; 122.52; 90
6601Yumi Yakiyama; Gil Ryeong Lee; Sung Yeon Kim; Yoshitaka Matsushita; Yasushi Morita; Moon Jeong Park; Masaki Kawano
Formation of a nanometer-thick water layer at high humidity on a dynamic crystalline material composed of multi-interactive molecules
Chem.Commun., 2015, 51, 6828
7116946 CIFC10 H9 N OP b c a15.005; 12.061; 18.219
90; 90; 90
3297.2Yanli Xu; Weigao Hu; Xiaodong Tang; Jinwu Zhao; Wanqing Wu; Huanfeng Jiang
Palladium-catalyzed Csp2-H carbonylation of aromatic oximes: selective access to benzo[d][1,2]oxazin-1-ones and 3-methyleneisoindolin-1-ones
Chem.Commun., 2015, 51, 6843
7116947 CIFC10 H18 B16 Cu O5P m -3 n28.973; 28.973; 28.973
90; 90; 90
24321Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116948 CIFC12 H30 B24P 1 21/c 111.9932; 19.6594; 12.4615
90; 118.684; 90
2577.6Clingerman, Daniel J.; Morris, William; Mondloch, Joseph E.; Kennedy, Robert D.; Sarjeant, Amy A.; Stern, Charlotte; Hupp, Joseph T.; Farha, Omar K.; Mirkin, Chad A.
Stabilization of a highly porous metal-organic framework utilizing a carborane-based linker.
Chemical communications (Cambridge, England), 2015, 51, 6521-6523
7116949 CIFC75 H63 Mn3 N12 O12P -112.281; 12.919; 30.425
94.65; 93.93; 92.4
4794.5Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116950 CIFC77 H69 Cl5.25 Mn5.5 N13 O16.5P 1 21/m 112.338; 33.33; 25.857
90; 97.45; 90
10543Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116951 CIFC37.5 H33 Cl Mn2 N6 O7.5P 1 21/m 112.355; 33.452; 12.952
90; 97.63; 90
5306Bloch, Witold M.; Burgun, Alexandre; Doonan, Christian J.; Sumby, Christopher J.
Probing post-synthetic metallation in metal-organic frameworks: insights from X-ray crystallography.
Chemical communications (Cambridge, England), 2015, 51, 5486-5489
7116952 CIFC21 H22 N4 O4P 21 21 215.9906; 15.7335; 21.9353
90; 90; 90
2067.5Bag, Subhendu Sekhar; Jana, Subhashis; Yashmeen, Afsana; De, Suranjan
Triazolo-β-aza-ε-amino acid and its aromatic analogue as novel scaffolds for β-turn peptidomimetics.
Chemical communications (Cambridge, England), 2015, 51, 5242-5245
7116961 CIFC42 H46 N4 O13 S3P 21 21 218.6884; 19.6749; 25.149
90; 90; 90
4299.1Zhiyuan Hu; Rory L. Arrowsmith; James A. Tyson; Vincenzo Mirabello; Haobo Ge; Ian M. Eggleston; Stanley W. Botchway; G. Dan Pantos; Sofia I. Pascu
A fluorescent Arg-Gly-Asp (RGD) peptide-naphthalenediimide (NDI) conjugate for imaging integrin alpha-v-beta3in vitro
Chem.Commun., 2015, 51, 6901
7116963 CIFC120 H76 O36 S12 Zr6F m -3 m32.7165; 32.7165; 32.7165
90; 90; 90
35018.7Bo Gui; Ka-Kit Yee; Yan-Lung Wong; Shek-Man Yiu; Matthias Zeller; Cheng Wang; Zhengta Xu
Tackling poison and leach: catalysis by dangling thiol-palladium functions within a porous metal-organic solid
Chem.Commun., 2015, 51, 6917
7116964 CIFC72 H80 Cl2 N4 Ni2P 1 21/n 116.1963; 12.2535; 16.3252
90; 94.689; 90
3229.1Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116965 CIFC64.5 H63 Cl N2 Ni PP -111.2339; 13.5323; 19.012
72.179; 88.564; 84.99
2741Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116966 CIFC38 H46 Al Br2 N2 NiP b c n13.7598; 18.9444; 14.2281
90; 90; 90
3708.9Wei Gao; Lan Xin; Zhiqiang Hao; Guodong Li; Ji-Hu Su; Lijing Zhou; Ying Mu
The ligand redox behavior and role in 1,2-bis[(2,6-diisopropylphenyl)imino]-acenaphthene nickel-TMA(MAO) systems for ethylene polymerization
Chem.Commun., 2015, 51, 7004
7116967 CIFC18 H10 O2P 21 21 215.2561; 9.121; 24.027
90; 90; 90
1151.9Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116968 CIFC54 H32P 1 21/c 19.2045; 16.8399; 22.397
90; 90.064; 90
3471.6Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116969 CIFC78 H81.4P -17.6054; 18.7609; 21.2252
72.252; 84.027; 87.9
2868.66Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116970 CIFC66.15 H56.83 Cl0.45P 1 21/c 19.3755; 26.1158; 20.0039
90; 101.625; 90
4797.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116971 CIFC62 H36P -110.1459; 14.0677; 15.4819
66.782; 77.518; 85.704
1982.63Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116972 CIFC68 H54 Cl4C 1 2/c 147.051; 9.3095; 27.9099
90; 125.063; 90
10006.5Ruth Dorel; Carlos Manzano; Maricarmen Grisoli; We-Hyo Soe; Christian Joachim; Antonio M. Echavarren
Tetrabenzocircumpyrene: a nanographene fragment with an embedded peripentacene core
Chem.Commun., 2015, 51, 6932
7116973 CIFC44 H56 O6 S2P -19.2441; 9.4374; 11.5116
81.533; 81.481; 87.419
982.09Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116974 CIFC43 H54 O5 S2P 1 21/a 113.3707; 18.8446; 16.9728
90; 107.545; 90
4077.62Michal Hucko; Hana Dvorakova; Vaclav Eigner; Pavel Lhotak
2,14-Dithiacalix[4]arene and its homooxa analogues: synthesis and dynamic NMR study of conformational behaviour
Chem.Commun., 2015, 51, 7051
7116975 CIFC32 H30 N OI 41/a :227.745; 27.745; 6.4943
90; 90; 90
4999Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116976 CIFC30 H40 Cl2.08 N2 O3P -19.7572; 11.9316; 13.8051
89.961; 102.504; 110.06
1469.11Subham Bhattacharjee; Santanu Bhattacharya
Role of synergistic pi-pi stacking and X-H^...^Cl (X = C, N, O) H-bonding interactions in gelation and gel phase crystallization
Chem.Commun., 2015, 51, 7019
7116977 CIFC17 H16 N2 O3 SC 1 2/c 126.8782; 8.2244; 19.4674
90; 132.644; 90
3165.5Jisu Jeong; Donggun Lee; Sukbok Chang
Copper-catalyzed oxygen atom transfer of N-oxides leading to a facile deoxygenation procedure applicable to both heterocyclic and amine N-oxides
Chem.Commun., 2015, 51, 7035
7116978 CIFC18 H14 F3 N3 O3P 1 21/n 111.296; 13.615; 11.516
90; 105.89; 90
1703Devalina Ray; T. Manikandan; Arup Roy; Krishna N. Tripathi; Ravi P. Singh
Ligand-promoted intramolecular dehydrogenative cross-coupling using a Cu catalyst: direct access to polycyclic heteroarenes
Chem.Commun., 2015, 51, 7065
7116981 CIFC39 H29 N O3 P2P 21 21 2111.279; 16.1962; 17.5843
90; 90; 90
3212.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116982 CIFC39 H29 N O4 P2P 21 21 2111.281; 16.1001; 17.7437
90; 90; 90
3222.7G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116983 CIFC40 H31 N O4 P2P 21 21 2111.1755; 15.95; 18.117
90; 90; 90
3229.3G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116984 CIFC40 H30 Cl N O4 P2P -19.9475; 13.0705; 14.9853
106.24; 94.143; 110.585
1719.37G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116985 CIFC42 H32 Br Cl6 N O4 P2P -111.5145; 13.3968; 14.6374
86.833; 75.632; 87.59
2183G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116986 CIFC39 H33 N O4 P2P 21 21 2111.335; 17.7472; 16.1457
90; 90; 90
3247.9G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116987 CIFC39 H33 N O4 P2P 21 21 2111.3101; 17.7378; 16.0426
90; 90; 90
3218.4G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116988 CIFC39 H33 Cl N O4 P2P -19.7782; 12.6735; 15.218
72.422; 88.076; 69.077
1673.42G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116989 CIFC39 H33 N O4 P2P 21 21 2111.326; 15.94; 17.593
90; 90; 90
3176.2G. Gangadhararao; R. N. Prasad Tulichala; K. C. Kumara Swamy
Spontaneous resolution upon crystallization of allenyl-bis-phosphine oxides
Chem.Commun., 2015, 51, 7168
7116990 CIFC28 H19 N3P 1 21/c 115.3114; 12.9392; 10.8302
90; 102.639; 90
2093.7Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116991 CIFC17 H10 Mn N3 O4P 1 21/c 111.7689; 10.7605; 13.511
90; 107.25; 90
1634.1Lijun Shi; Xiang Zhong; Houde She; Ziqiang Lei; Fuwei Li
Manganese catalyzed C-H functionalization of indoles with alkynes to synthesize bis/trisubstituted indolylalkenes and carbazoles: the acid is the key to control selectivity
Chem.Commun., 2015, 51, 7136
7116992 CIFC12 H22 B10P 21 21 219.009; 12.9189; 14.1739
90; 90; 90
1649.65Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116993 CIFC13 H24 B10 O2P 1 21/c 17.3151; 13.218; 19.6674
90; 93.078; 90
1898.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116994 CIFC12 H22 B10 OC 1 2/c 124.2272; 13.0711; 23.5734
90; 108.334; 90
7086.2Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116995 CIFC10 H20 B10P b c a24.322; 8.2628; 15.382
90; 90; 90
3091.3Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116996 CIFC13 H24 B10 O2P 1 21/n 17.0474; 19.9445; 13.4339
90; 94.295; 90
1882.92Ke Cao; Yawen Huang; Junxiao Yang; Ji Wu
Palladium catalyzed selective mono-arylation of o-carboranes via B-H activation
Chem.Commun., 2015, 51, 7257
7116997 CIFC70 H66 Cl4 N6 O4P -110.963; 10.985; 15.643
94.45; 104.45; 119.51
1542Chenhao Zhang; Ke Shi; Kang Cai; Jiajun Xie; Ting Lei; Qifan Yan; Jie-Yu Wang; Jian Pei; Dahui Zhao
Cyano- and chloro-substituted coronene diimides as solution-processable electron-transporting semiconductors
Chem.Commun., 2015, 51, 7144
7116998 CIFC36 H36 As Cl2 N SiP -18.8947; 12.7255; 15.2825
78.686; 73.993; 70.48
1556.81Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7116999 CIFC38 H40 Br2 N Sb SiP -110.1762; 11.2391; 15.5145
95.865; 95.903; 100.813
1720.21Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117000 CIFC44 H52 Br2 N Sb SiP 1 21/c 110.104; 17.041; 23.615
90; 101.92; 90
3978.4Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117001 CIFC38 H40 Bi Br2 N SiP -110.1646; 11.259; 15.5011
95.931; 96.15; 100.498
1720.51Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117002 CIFC44 H52 Bi Br2 N SiP 1 21/c 110.13; 17.182; 23.696
90; 102.26; 90
4030.3Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117003 CIFC51 H42 Bi Br2 N SiP -110.3779; 12.172; 18.3157
82.925; 88.322; 66.682
2108Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117004 CIFC82 H90 B Bi2 N3 SiP -113.6508; 14.2481; 20.2258
97.059; 95.917; 112.943
3545.8Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117005 CIFC63.5 H73.5 As B N3 SiP -112.3574; 12.667; 19.7946
99.963; 104.228; 100.574
2874Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117006 CIFC65.25 H80 As B N3 SiP -112.4034; 13.37; 20.102
77.434; 77.587; 65.731
2936.5Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117007 CIFC98 H128 N2 Sb2 Si2P -112.6918; 13.6933; 14.0983
72.74; 77.066; 67.955
2151.2Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117008 CIFC52 H72 B2 Bi2 N4P -110.501; 12.7973; 21.8679
88.502; 76.645; 67.584
2636.9Deepak Dange; Amelia Davey; Joseph A. B. Abdalla; Simon Aldridge; Cameron Jones
Utilisation of a lithium boryl as a reducing agent in low oxidation state group 15 chemistry: synthesis and characterisation of an amido-distibene and a boryl-dibismuthene
Chem.Commun., 2015, 51, 7128
7117018 CIFC27 H36 Br2 F6 In N2 SbP -19.5651; 10.502; 18.1036
94.315; 95.583; 115.957
1613.18Bastien Michelet; Jean-Remy Colard-Itte; Guillaume Thiery; Regis Guillot; Christophe Bour; Vincent Gandon
Dibromoindium(III) cations as a pi-Lewis acid: characterization of [IPr^.^InBr2][SbF6] and its catalytic activity towards alkynes and alkenes
Chem.Commun., 2015, 51, 7401
7117019 CIFC36 H24 Co3 Mn3 N17 Na O19R -317.343; 17.343; 31.6652
90; 90; 120
8248.2Jiang Liu; Mei Qu; Rodolphe Clerac; Xian Ming Zhang
A two-dimensional honeycomb coordination network based on fused triacontanuclear heterometallic {Co12Mn18} wheels
Chem.Commun., 2015, 51, 7356
7117020 CIFGd2 H8 O7C m c m16.583; 12.975; 7.3106
90; 90; 90
1573Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117021 CIFGd H3 O3P 63/m6.2993; 6.2993; 3.6057
90; 90; 120
123.91Yan Yang; Qian-Chong Zhang; Yin-Yin Pan; La-Sheng Long; Lan-Sun Zheng
Magnetocaloric effect and thermal conductivity of Gd(OH)3 and Gd2O(OH)4(H2O)2
Chem.Commun., 2015, 51, 7317
7117022 CIFC8 H10 N14 O4P -15.4207; 6.797; 10.53
82.822; 77.868; 71.33
358.65Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117023 CIFC8 H10 N14 O4P 1 21/c 16.2903; 7.2315; 15.5555
90; 92.037; 90
707.15Jiaheng Zhang; Damon A. Parrish; Jean'ne M. Shreeve
Curious cases of 3,6-dinitropyrazolo[4,3-c]pyrazole-based energetic cocrystals with high nitrogen content: an alternative to salt formation
Chem.Commun., 2015, 51, 7337
7117024 CIFC54 H40 Cd Cl2 N12 O10P 43 21 215.8664; 15.8664; 21.7986
90; 90; 90
5487.6Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117025 CIFC56 H46 Cd Cl2 N12 O11P 43 21 215.8983; 15.8983; 21.6675
90; 90; 90
5476.59Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117026 CIFC54 H41.2 Cd Cl2 N12 O10P 41 21 215.90821; 15.90821; 21.6184
90; 90; 90
5470.99Fan Yang; Qi-Kui Liu; Dan Wu; An-Yan Li; Yu-Bin Dong
p-Benzoquinone adsorption-separation, sensing and its photoinduced transformation within a robust Cd(II)-MOF in a SC-SC fashion
Chem.Commun., 2015, 51, 7443
7117027 CIFC24 H20 N9 P SnP -110.756; 11.0605; 12.354
91.668; 108.414; 116.545
1222.1Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117028 CIFC24 H20 Ge N9 PP -17.7712; 11.4711; 14.2003
93.278; 99.357; 100.865
1221.59Benjamin Peerless; Theo Keane; Anthony J. H. M. Meijer; Peter Portius
Homoleptic low-valent polyazides of group 14 elements
Chem.Commun., 2015, 51, 7435
7117029 CIFC16 H17 O3 PP 1 21 15.826; 17.749; 14.404
90; 93.154; 90
1487.2Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117030 CIFC16 H17 O3 PP 1 21 15.8589; 17.826; 14.463
90; 93.258; 90
1508.1Junli Hou; Yang Chen; Dongmei Ma; Burghard Cordes; Jingyun Wang; Xin Wang; Fritz E. Kuhn; Hao Guo; Mingdong Zhou
Methyltrioxorhenium-catalyzed highly selective dihydroxylation of 1,2-allenylic diphenyl phosphine oxides
Chem.Commun., 2015, 51, 7439
7117031 CIFC27 H19 B F2 N2 SP -110.1096; 12.4472; 18.3814
95.587; 95.919; 96.9
2269.9Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117032 CIFC66 H66 B2 F4 N8 O S2C 1 2 129.997; 8.4716; 12.7084
90; 112.788; 90
2977.4Xiaoqing Wang; Qingsong Liu; Hui Yan; Zhipeng Liu; Mingguang Yao; Qingfu Zhang; Shuwen Gong; Weijiang He
Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: intra- and inter-molecular effects induced by hydrostatic compression
Chem.Commun., 2015, 51, 7497
7117033 CIFC9.66667 H13 Br N4.33333 PP -110.1735; 12.6747; 16.2901
83.778; 72.596; 73.177
1918.05Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117034 CIFC21 H20 Br N4 PP 1 21/c 112.2417; 4.8288; 33.91
90; 98.281; 90
1983.6Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117035 CIFC10 H12 F3 N4 O3 P SP -18.2477; 8.4833; 10.7821
97.866; 104.396; 93.252
720.59Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117036 CIFC49 H48 B N4 O PP -111.0003; 13.6439; 14.0585
77.876; 79.118; 87.493
2025.82Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117037 CIFC46 H42 B Cl2 N4 PP -111.012; 13.4813; 13.8114
78.513; 77.138; 87.889
1958.84Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117038 CIFC20 H24 Au Cl F6 N8 O6 P2 S2C 1 2/c 120.7657; 14.6302; 13.2427
90; 123.628; 90
3349.9Justin F. Binder; Ala'aeddeen Swidan; Martin Tang; Jennifer H. Nguyen; Charles L. B. Macdonald
Remarkably stable chelating bis-N-heterocyclic carbene adducts of phosphorus(I) cations
Chem.Commun., 2015, 51, 7741
7117039 CIFC88 H0.5 Cl12 Co14 N48 O4P -117.9278; 18.574; 28.0345
74.801; 87.6211; 61.281
7861.1Fu-Ping Huang; Peng-Fei Yao; Hai-Ye Li; Qing Yu; He-Dong Bian; Hong Liang
An intuitional hierarchical assembly of cluster-organic frameworks with a thickness of 1.97 nm from a discrete Co14 cluster
Chem.Commun., 2015, 51, 7598
7117040 CIFC31.33 H26 Cl2 Co4.67 N16 O3.33P -323.2046; 23.2046; 17.2439
90; 90; 120
8041.1Fu-Ping Huang; Peng-Fei Yao; Hai-Ye Li; Qing Yu; He-Dong Bian; Hong Liang
An intuitional hierarchical assembly of cluster-organic frameworks with a thickness of 1.97 nm from a discrete Co14 cluster
Chem.Commun., 2015, 51, 7598
7117041 CIFC29 H16 B F10 N O2P -111.0372; 11.6357; 11.866
111.316; 103.831; 100.243
1318.13Lu Wang; Kai Wang; Houyu Zhang; Chuanjun Jiao; Bo Zou; Kaiqi Ye; Hongyu Zhang; Yue Wang
The facile realization of RGB luminescence based on one yellow emissive four-coordinate organoboron material
Chem.Commun., 2015, 51, 7701
7117042 CIFC29 H16 B F10 N O2P -110.4884; 11.0467; 11.5358
95.268; 98.354; 99.426
1295.34Lu Wang; Kai Wang; Houyu Zhang; Chuanjun Jiao; Bo Zou; Kaiqi Ye; Hongyu Zhang; Yue Wang
The facile realization of RGB luminescence based on one yellow emissive four-coordinate organoboron material
Chem.Commun., 2015, 51, 7701
7117043 CIFC26 H28 N2 O3P 1 21/c 17.2482; 12.373; 24.27
90; 97.43; 90
2158.3Timothy K. Beng; Hironori Takeuchi; Manuel Weber; Richmond Sarpong
Stereocontrolled synthesis of vicinally functionalized piperidines by nucleophilic beta-addition of alkyllithiums to alpha-aryl substituted piperidine enecarbamates
Chem.Commun., 2015, 51, 7653
7117044 CIFC27 H30 N2 O3P -17.215; 12.5739; 13.1379
70.358; 86.908; 85.384
1118.43Timothy K. Beng; Hironori Takeuchi; Manuel Weber; Richmond Sarpong
Stereocontrolled synthesis of vicinally functionalized piperidines by nucleophilic beta-addition of alkyllithiums to alpha-aryl substituted piperidine enecarbamates
Chem.Commun., 2015, 51, 7653
7117045 CIFC36 H32 SiP 1 21/c 114.0394; 10.71244; 18.6534
90; 107.182; 90
2680.2Shunsuke Sueki; Yoichiro Kuninobu
Rhodium-catalysed synthesis of multi-substituted silylindenes from aryl alkynes and hydrosilanes via C-H bond activation
Chem.Commun., 2015, 51, 7685
7117046 CIFC39 H35 B Fe N6 O3P b c a11.861; 22.463; 25.58
90; 90; 90
6815Debobrata Sheet; Shrabanti Bhattacharya; Tapan Kanti Paine
Dioxygen activation and two consecutive oxidative decarboxylations of phenylpyruvate by nonheme iron(II) complexes: functional models of hydroxymandelate synthase (HMS) and CloR
Chem.Commun., 2015, 51, 7681
7117047 CIFC48 H67 N O2 ZrP 21 21 2111.2139; 17.371; 23.2242
90; 90; 90
4524Qiu Sun; Yaorong Wang; Dan Yuan; Yingming Yao; Qi Shen
Zirconium catalysed intermolecular hydroamination reactions of secondary amines with alkynes
Chem.Commun., 2015, 51, 7633
7117048 CIFC19 H18 Mn N9 S5C 1 2/c 111.928; 13.662; 17.417
90; 105.321; 90
2737.4Dariusz Matoga; Marcin Oszajca; Marcin Molenda
Ground to conduct: mechanochemical synthesis of a metal-organic framework with high proton conductivity
Chem.Commun., 2015, 51, 7637
7117049 CIFC14 H8 Mn N6 O4 S2P 1 21/c 19.723; 14.061; 7.1516
90; 97.92; 90
968.4Dariusz Matoga; Marcin Oszajca; Marcin Molenda
Ground to conduct: mechanochemical synthesis of a metal-organic framework with high proton conductivity
Chem.Commun., 2015, 51, 7637
7117050 CIFC28 H28 N4 O S8P 1 21/n 18.8402; 14.927; 23.777
90; 96.92; 90
3114.7Anup Rana; Sangsu Lee; Dongho Kim; Pradeepta K. Panda
Beta-Octakis(methylthio)porphycenes: synthesis, characterisation and third order nonlinear optical studies
Chem.Commun., 2015, 51, 7705
7117051 CIFC14 H16 N2 O2 S4P 1 21/c 14.918; 8.5807; 19.8851
90; 97.072; 90
832.76Anup Rana; Sangsu Lee; Dongho Kim; Pradeepta K. Panda
Beta-Octakis(methylthio)porphycenes: synthesis, characterisation and third order nonlinear optical studies
Chem.Commun., 2015, 51, 7705
7117052 CIFC18 H18 Cl2 Co N4P -111.574; 15.2041; 19.9081
90.06; 103.277; 110.696
3176.6Sharon Lai-Fung Chan; Tsz Lung Lam; Chen Yang; Siu-Cheong Yan; Nga Man Cheng
A robust and efficient cobalt molecular catalyst for CO2 reduction
Chem.Commun., 2015, 51, 7799
7117053 CIFC18 H18 Fe SiP 21 21 219.6741; 10.9465; 29.0292
90; 90; 90
3074.1Takanori Shibata; Tsubasa Shizuno; Tomoya Sasaki
Enantioselective synthesis of planar-chiral benzosiloloferrocenes by Rh-catalyzed intramolecular C-H silylation
Chem.Commun., 2015, 51, 7802
7117054 CIFC22 H26P 1 21/c 112.4844; 8.092; 17.7356
90; 92.499; 90
1790.01Takashi Otani; Kanako Ueki; Kinryo Cho; Kan Kanai; Kotaro Tateno; Takao Saito
Construction of dibenzo-fused seven- to nine-membered carbocycles via Bronsted acid-promoted intramolecular Friedel-Crafts-type alkenylation
Chem.Commun., 2015, 51, 7895
7117055 CIFC21 H24P 1 21/n 15.881; 16.344; 17.969
90; 95.555; 90
1719Takashi Otani; Kanako Ueki; Kinryo Cho; Kan Kanai; Kotaro Tateno; Takao Saito
Construction of dibenzo-fused seven- to nine-membered carbocycles via Bronsted acid-promoted intramolecular Friedel-Crafts-type alkenylation
Chem.Commun., 2015, 51, 7895
7117056 CIFC74 H48 Cl8 F8 N4 O18 Ru4P -110.641; 14.224; 15.449
91.028; 110.013; 109.772
2043.8Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117057 CIFC74 H48 Cl8 F8 N4 O18 Ru4P -19.994; 14.265; 14.433
82.602; 79.222; 82.472
1992.4Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117058 CIFC70 H40 F8 N4 O18 Ru4P -110.551; 13.573; 30.865
80.126; 79.263; 74.635
4152.6Hiroki Fukunaga; Takafumi Yoshino; Hajime Sagayama; Jun-ichi Yamaura; Taka-hisa Arima; Wataru Kosaka; Hitoshi Miyasaka
A charge-disproportionate ordered state with delta = 0.75 in a chemically sensitive donor/acceptor D^delta^+2A^2delta-^ layered framework
Chem.Commun., 2015, 51, 7795
7117059 CIFC102 H108 Co2 N18 Ni4 O24 Tb2P 1 21/c 116.8968; 22.282; 19.3332
90; 106.728; 90
6970.8Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117060 CIFC120 H134 Dy2 N34 Ni4 O20 W2P -116.712; 20.624; 20.852
87.814; 89.178; 74.215
6910.9Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117061 CIFC120 H134 N34 Ni4 O20 Tb2 W2P -116.7341; 20.6199; 20.8979
87.881; 89.214; 74.309
6937.4Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117062 CIFC120 H134 N34 Ni4 O20 W2 Y2P -116.71; 20.663; 20.852
87.797; 89.185; 74.158
6921.1Sebastien Dhers; Jean-Pierre Costes; Philippe Guionneau; Carley Paulsen; Laure Vendier; Jean-Pascal Sutter
On the importance of ferromagnetic exchange between transition metals in field-free SMMs: examples of ring-shaped hetero-trimetallic [(LnNi2){W(CN)8}]2 compounds
Chem.Commun., 2015, 51, 7875
7117066 CIFC23 H18 N2 O SP 1 21/c 116.26; 8.0578; 16.7298
90; 118.216; 90
1931.47Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117067 CIFC22 H15 Cl N2 O SP 1 21/n 112.0459; 10.3781; 15.4051
90; 107.395; 90
1837.78Xiaohan Ye; Jeffrey L. Petersen; Xiaodong Shi
Nickel-catalyzed directed sulfenylation of sp2 and sp3 C-H bonds
Chem.Commun., 2015, 51, 7863
7117068 CIFC32 H47 Au N2 SP -19.6005; 11.3245; 15.2126
74.9336; 82.8296; 77.8418
1556.94Kazunori Miyamoto; Masaya Hirobe; Masanobu Uchiyama; Masahito Ochiai
Stereoselective synthesis and reaction of gold(I) (Z)-enethiolates
Chem.Commun., 2015, 51, 7962
7117069 CIFC8 H6 F3 I O6 SP -15.4618; 9.7781; 11.8765
98.2; 93.463; 91.657
626.19Akira Yoshimura; Khiem C. Nguyen; Scott C. Klasen; Akio Saito; Victor N. Nemykin; Viktor V. Zhdankin
Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent
Chem.Commun., 2015, 51, 7835
7117071 CIFC40 H50 Cl2 Cu N2 O2C 1 2 113.608; 10.347; 14.528
90; 117.341; 90
1817.1Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117072 CIFC36 H42 Cl2 Cu N2 O2P 1 21 113.8568; 15.8847; 15.2073
90; 96.046; 90
3328.68Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117073 CIFC32 H34 Cl2 Cu N2C 1 2/c 125.878; 10.4574; 10.7037
90; 102.636; 90
2826.44Koichi Tanaka; Tomoharu Iwashita; Erika Yoshida; Tomomi Ishikawa; Shinya Otuka; Zofia Urbanczyk-Lipkowska; Hiroki Takahashi
Solvent-dependent strong asymmetric amplification in the catalytic enantioselective Henry reaction using the trans-N,N'-bis-biphenyl-4-ylmethyl-cyclohexane-1,2-diamine-CuCl2 complex
Chem.Commun., 2015, 51, 7907
7117074 CIFC21 H45 Cu3 I6 N3P 2 21 218.52016; 31.2866; 13.2813
90; 90; 90
3540.35Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117075 CIFC18 H42 Cu3 I6 N3P 2 21 218.5342; 31.3102; 13.3245
90; 90; 90
3560.4Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117076 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.5719; 13.4018; 31.305
90; 90; 90
3596.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117077 CIFC21 H45 Cu3 I6 N3P 2 21 218.6; 31.212; 13.5728
90; 90; 90
3643.3Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117078 CIFC21 H45 Cu2.99 I6 N3P 2 21 218.6034; 13.5945; 31.256
90; 90; 90
3655.7Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117079 CIFC21 H45 Cu3.01 I6 N3P 2 21 218.6312; 13.6767; 31.2048
90; 90; 90
3683.6Shi-Li Li; Fu-Qiang Zhang; Xian-Ming Zhang
An organic-ligand-free thermochromic luminescent cuprous iodide trinuclear cluster: evidence for cluster centered emission and configuration distortion with temperature
Chem.Commun., 2015, 51, 8062
7117080 CIFC44 H32 Cd2 Cl2 N4 O8P -18.9041; 17.9362; 18.9879
100.842; 102.263; 103.409
2791.2Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117081 CIFC44 H32 Br2 Cd2 N4 O8P -19.0867; 18.0356; 18.8207
102.462; 103.387; 100.625
2839.4Cheng Chen; Li-Xuan Cai; Bin Tan; Ya-Jun Zhang; Xiao-Dong Yang; Jie Zhang
Ammonia detection by using flexible Lewis acidic sites in luminescent porous frameworks constructed from a bipyridinium derivative
Chem.Commun., 2015, 51, 8189
7117082 CIFC20 H17 N O2 SP 1 21 15.7758; 20.087; 7.3139
90; 92.951; 90
847.42Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117083 CIFC20 H17 N O2 SP 1 21 15.7825; 20.098; 7.311
90; 92.824; 90
848.6Li Lin; Yuhong Yang; Mei Wang; Luhao Lai; Yarong Guo; Rui Wang
Oxidative N-heterocyclic carbene catalyzed stereoselective annulation of simple aldehydes and 5-alkenyl thiazolones
Chem.Commun., 2015, 51, 8134
7117084 CIFC25 H21 Cl3 N2 SiP 1 21/c 110.681; 19.442; 11.152
90; 101.368; 90
2270.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117085 CIFC26 H24 N2 SiP 1 21/a 114.1331; 7.8144; 18.4958
90; 102.186; 90
1996.68Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117086 CIFC36 H28 N2 O0.5 SiC 1 2/c 121.767; 12.983; 19.854
90; 108.48; 90
5321.4Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117087 CIFC73 H58 Cl2 N4 Si2P 32 2 113.156; 13.156; 28.415
90; 90; 120
4259.2Takayuki Tanaka; Atsuhiro Osuka
Tetracoordinate silicon complexes of 1,2-bis(indol-2-yl)benzene as blue-emitting dyes in the solid state
Chem.Commun., 2015, 51, 8123
7117088 CIFC22 H22 Cu4 N2 O18 S2F d d 224.748; 32.354; 21.712
90; 90; 90
17385Xing; Meng,ab; Shu-Yan Song; Xue-Zhi Song; Min Zhu; Shu-Na Zhao; Lan-Lan Wu; Hong-Jie Zhang
A tetranuclear copper cluster-based MOF with sulfonate-carboxylate ligands exhibiting high proton conduction properties
Chem.Commun., 2015, 51, 8150
7117089 CIFC40 H38 Cl2 Fe2 N2 O2P 1 21/n 110.271; 20.397; 17.702
90; 105.15; 90
3579.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117090 CIFC42 H43 Fe2 N2 O2.5P 1 21/c 116.505; 14.661; 17.918
90; 111.59; 90
4031.6Fabio Marchetti; Stefano Zacchini; Valerio Zanotti
Carbon monoxide-isocyanide coupling promoted by acetylide addition to a diiron complex
Chem.Commun., 2015, 51, 8101
7117097 CIFC20 H19 BrP 1 n 16.0119; 15.806; 8.3765
90; 98.292; 90
787.65Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117098 CIFC21 H22 OP 1 21/c 117.781; 15.3478; 6.0728
90; 99.114; 90
1636.34Xin-Xing Wu; Yi Shen; Wen-Long Chen; Si Chen; Xin-Hua Hao; Yu Xia; Peng-Fei Xu; Yong-Min Liang
Palladium-catalyzed ring opening of norbornene: efficient synthesis of methylenecyclopentane derivatives
Chem.Commun., 2015, 51, 8031
7117099 CIFC2 H11 Cl2 N3 O2 PtP -17.103; 9.028; 13.105
90.17; 94.67; 90.44
837.5Giorgio Pelosi; Mauro Ravera; Elisabetta Gabano; Federico Fregonese; Domenico Osella
Unprecedented one-pot synthesis of an unsymmetrical cisplatin-based Pt(IV)-acetamidato complex
Chem.Commun., 2015, 51, 8051
7117100 CIFC15 H21 N O4P 21 21 2110.9624; 11.2771; 12.2022
90; 90; 90
1508.49Alejandra Millan-Ortiz; German Lopez-Valdez; Fernando Cortez-Guzman; Luis D. Miranda
A novel carbamoyl radical based dearomatizing spiroacylation process
Chem.Commun., 2015, 51, 8345
7117101 CIFC15 H14 Br NP b c a19.318; 7.18486; 19.6634
90; 90; 90
2729.22Johannes F. Franz; Wolfgang B. Kraus; Kirsten Zeitler
No photocatalyst required ‒ versatile, visible light mediated transformations with polyhalomethanes
Chem.Commun., 2015, 51, 8280
7117102 CIFC76 H28 F10 O2I 41/a28.7283; 28.7283; 12.1809
90; 90; 90
10053.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117103 CIFC46 H20 Cl6 F10 O4P 1 21/c 110.3234; 15.5838; 13.5017
90; 102.531; 90
2120.4Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117104 CIFC82 H9 F5 O2C 1 2/c 126.962; 13.616; 24.071
90; 97.746; 90
8756Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117105 CIFC78.25 H24 F10 O4.75P -115.928; 19.014; 20.624
101.456; 110.099; 108.543
5218.1Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117106 CIFC32 H10 F10 O4P 1 21/c 114.649; 10.269; 8.425
90; 99.012; 90
1251.7Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117107 CIFC106 H26 F10 O4P 1 21/c 127.439; 9.7293; 23.787
90; 97.272; 90
6299.2Baddigam Kiran Reddy; Santosh C. Gadekar; Venkataramanarao G. Anand
Non-covalent composites of antiaromatic isophlorin-fullerene
Chem.Commun., 2015, 51, 8276
7117108 CIFC8 H14 Cr Mn N O12P -3 1 c8.2865; 8.2865; 13.88
90; 90; 120
825.4Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117109 CIFC7 H12 Cr Mn N O12P -3 1 c8.2708; 8.2708; 14.088
90; 90; 120
834.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117110 CIFC8 H14 Al Mn N O12P -3 1 c8.2179; 8.2179; 13.646
90; 90; 120
798.1Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117111 CIFC8 H14 Cr Mg N O12P -3 1 c8.1565; 8.1565; 13.705
90; 90; 120
789.6Jiong-Peng Zhao; Song-De Han; Xue Jiang; Sui-Jun Liu; Ran Zhao; Ze Chang; Xian-He Bu
A heterometallic strategy to achieve a large magnetocaloric effect in polymeric 3d complexes
Chem.Commun., 2015, 51, 8288
7117112 CIFC34 H53 Cu N2 O S SiC 1 2/c 128.986; 12.887; 19.067
90; 92.619; 90
7115Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117113 CIFC34 H53 Cu N2 O Se SiC 1 2/c 129.597; 12.842; 19.184
90; 93.196; 90
7280Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117114 CIFC30 H45 Cu N2 Si TeP 1 21/n 19.789; 21.443; 15.58
90; 100.673; 90
3214Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117115 CIFC58 H80 Cl8 Cu2 Hg N4 S2P 1 21/n 113.026; 16.803; 16.264
90; 106.93; 90
3405.5Mahmood Azizpoor Fard; Florian Weigend; John F. Corrigan
Simple but effective: thermally stable Cu-ESiMe3via NHC ligation
Chem.Commun., 2015, 51, 8361
7117116 CIFC26 H15 N O4 S ZnP -17.9902; 11.043; 13.43
105.463; 102.922; 107.508
1028Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117117 CIFC36 H24 N4 O4 S ZnP b c a18.379; 10.6606; 31.736
90; 90; 90
6218.1Zhi-Qiang Shi; Zi-Jian Guo; He-Gen Zheng
Two luminescent Zn(II) metal-organic frameworks for exceptionally selective detection of picric acid explosives
Chem.Commun., 2015, 51, 8300
7117118 CIFC48 H47 Co N3 O8P -112.848; 14.185; 15.785
114.87; 97.126; 109.338
2343.4Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117119 CIFC60 H65 Co N4 O11P -110.6129; 14.9365; 18.7658
108.987; 92.348; 106.134
2673.7Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117120 CIFC72 H64 Co3 N4 O14C 1 2/c 126.758; 10.635; 29.565
90; 116.906; 90
7503Chuan-Lei Zhang; Yan-Le Li; Ting Wang; Ze-Min Ju; He-Gen Zheng; Jing Ma
Three different metal-organic frameworks derived from a one-pot crystallization and their controllable synthesis
Chem.Commun., 2015, 51, 8338
7117121 CIFC46 H25 Cl3 F10 N6 O2P 4113.62; 13.62; 22.0245
90; 90; 90
4085.64Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117122 CIFC44 H28 Cl3 F10 N5 O2P -111.084; 13.9124; 15.6917
95.169; 107.245; 111.916
2088.2Rafal Orlowski; Olena Vakuliuk; Maria Pia Gullo; Oksana Danylyuk; Barbara Ventura; Beata Koszarna; Anna Tarnowska; Nina Jaworska; Andrea Barbieri; Daniel T. Gryko
Self-assembling corroles
Chem.Commun., 2015, 51, 8284
7117123 CIFC30 H8 F10 N4P -15.996; 7.348; 13.198
87.325; 86.01; 71.49
549.9Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117124 CIFC30 H8 F10 N4 OP 1 21/c 128.021; 11.565; 7.319
90; 95.576; 90
2360.6Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117125 CIFC31 H10 F10 N4P 16.1461; 7.3648; 14.031
76.834; 82.082; 72.763
588.95Santosh C. Gadekar; Baddigam Kiran Reddy; Venkataramanarao G. Anand
Metal assisted cyclodimerization of doubly N-confused dipyrrins into planar aza-heptalenes
Chem.Commun., 2015, 51, 8342
7117126 CIFC40 H72 Mo2 N32 O11 Zn4P c a 2114.7778; 14.8566; 31.0576
90; 90; 90
6818.6N. Bridonneau; J. Long; J.-L. Cantin; J. von Bardeleben; S. Pillet; E.-E. Bendeif; D. Aravena; E. Ruiz; V. Marvaud
First evidence of light-induced spin transition in molybdenum(IV)
Chem.Commun., 2015, 51, 8229
7117127 CIFC34 H42 N4 O11 SP 1 21/n 18.6053; 18.642; 12.19
90; 98.319; 90
1934.9M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117128 CIFC28 H28 N4 O10P 21 21 219.942; 14.412; 18.805
90; 90; 90
2694.5M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117129 CIFC28 H28 N4 O10P 21 21 219.9943; 14.47; 18.796
90; 90; 90
2718.2M. Pandeeswar; Harshavardhan Khare; Suryanarayanarao Ramakumar; T. Govindaraju
Crystallographic insight-guided nanoarchitectonics and conductivity modulation of an n-type organic semiconductor through peptide conjugation
Chem.Commun., 2015, 51, 8315
7117130 CIFC27 H21 Br O5P 1 21/n 18.0879; 27.2026; 10.7134
90; 93.374; 90
2352.99Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117131 CIFC16 H13 F O2C 1 2/c 125.8977; 8.7711; 11.9279
90; 111.181; 90
2526.4Jieru Yang; Ao Mao; Zhenting Yue; Wenxuan Zhu; Xuewei Luo; Chuwei Zhu; Yuanjing Xiao; Junliang Zhang
A simple base-mediated synthesis of diverse functionalized ring-fluorinated 4H-pyrans via double direct C-F substitutions
Chem.Commun., 2015, 51, 8326
7117133 CIFC20 H16 Cl3 F2 N O Pt SP 1 21 15.897; 13.924; 12.852
90; 96.001; 90
1049.5Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117134 CIFC20 H18 F2 N P PtC 1 2/c 123.9938; 12.5106; 12.1687
90; 107.325; 90
3487.04Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117135 CIFC29 H36 Cl2 F2 N P PtP b c a14.9738; 15.8809; 24.6498
90; 90; 90
5861.7Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117136 CIFC29.5 H36.5 Cl3.5 F2 N P PtP 1 21/c 142.5003; 8.95573; 15.7762
90; 92.949; 90
5996.8Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117137 CIFC29 H36 Cl2 F2 N P PtP n a 2117.9634; 13.9987; 11.0698
90; 90; 90
2783.66Paul A. Shaw; Jessica M. Phillips; Christopher P. Newman; Guy J. Clarkson; Jonathan P. Rourke
Intramolecular transcyclometallation: the exchange of an aryl-Pt bond for an alkyl-Pt bond via an agostic intermediate
Chem.Commun., 2015, 51, 8365
7117138 CIFC82 H20 Cl4P b c a17.0287; 18.1277; 29.437
90; 90; 90
9086.9Ran Tao; Tomokazu Umeyama; Tomohiro Higashino; Tomoyuki Koganezawa; Hiroshi Imahori
A single cis-2 regioisomer of ethylene-tethered indene dimer-fullerene adduct as an electron-acceptor in polymer solar cells
Chem.Commun., 2015, 51, 8233
7117139 CIFC44 H71 B2 F8 N4 Ni O6.5P 1 21 116.4359; 15.6364; 19.2398
90; 92.863; 90
4938.4Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117140 CIFC55 H92 B2 F8 N4 Ni O8I 1 2 116.452; 8.8684; 22.2394
90; 110.682; 90
3035.68Yulong Zhang; Na Yang; Xiaohua Liu; Jing Guo; Xiying Zhang; Lili Lin; Changwei Hu; Xiaoming Feng
Reversal of enantioselective Friedel-Crafts C3-alkylation of pyrrole by slightly tuning the amide units of N,N'-dioxide ligands
Chem.Commun., 2015, 51, 8432
7117141 CIFC32 H24 B F15 Si2P -113.8787; 14.2041; 19.8693
101.859; 98.658; 117.694
3254.49Christina Eller; Gerald Kehr; Constantin G. Daniliuc; Gerhard Erker
Unusual product formation in a 1,1-carboboration reaction
Chem.Commun., 2015, 51, 8436
7117142 CIFC23 H20 Fe O4P 1 21/n 18.6879; 6.4163; 34.7054
90; 94.776; 90
1927.91Tatsuo Okauchi; Naoki Sata; Akihiro Urakawa; Mitsuru Kitamura
Unprecedented formation of eta^46-(vinylketene)iron complexes from eta^4^-(diene)iron complexes and aromatic compounds in the presence of a Lewis acid
Chem.Commun., 2015, 51, 8454
7117143 CIFC21 H33 Cu N3 O11.5R -3 m :H18.483; 18.483; 46.758
90; 90; 120
13833Chengling Song; Yajing Ling; Yunlong Feng; Wei Zhou; Taner Yildirim; Yabing He
A NbO-type metal-organic framework exhibiting high deliverable capacity for methane storage
Chem.Commun., 2015, 51, 8508
7117144 CIFC147 H182 N14 O56 Zn6P m n a19.7928; 17.7591; 28.543
90; 90; 90
10032.9Fei-Yan Yi; Hai-Long Jiang; Zhong-Ming Sun
Linearly bridging CO2 in a metal-organic framework
Chem.Commun., 2015, 51, 8446
7117145 CIFC24 H17 NP 1 21/c 113.0849; 9.1297; 13.5767
90; 93.893; 90
1618.15Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117146 CIFC22 H17 NP 1 21/n 14.2713; 14.11; 25.725
90; 91.832; 90
1549.6Sisir Lohar; Damir A. Safin; Archya Sengupta; Ansuman Chattopadhyay; Jesus Sanmartin Matalobos; Maria G. Babashkina; Koen Robeyns; Mariusz P. Mitoraj; Piotr Kubisiak; Yann Garcia; Debasis Das
Ratiometric sensing of lysine through the formation of the pyrene excimer: experimental and computational studies
Chem.Commun., 2015, 51, 8536
7117147 CIFC31 H30 Al Cr F24 O7P 1 21/n 125.012; 13.9336; 25.099
90; 111.913; 90
8115.2Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117148 CIFC48 H33 Al Cr F36 O6 PP 1 21/n 119.1442; 34.536; 19.5979
90; 119.074; 90
11324.7Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117149 CIFC32 H33 Cr O2 PP -18.649; 9.593; 17.771
90.671; 99.551; 116.355
1296.8Wenqing Wang; Xingyong Wang; Zaichao Zhang; Ningning Yuan; Xinping Wang
The long-sought seventeen-electron radical [(C6Me6)Cr(CO)3]+: isolation, crystal structure and substitution reaction
Chem.Commun., 2015, 51, 8410
7117150 CIFC18 H20 O2 SP 1 21 17.323; 12.346; 9.152
90; 108.447; 90
784.9Ryosuke Takechi; Takahiro Nishimura
Enantioselective 1,4-addition of cyclopropylboronic acid catalyzed by rhodium/chiral diene complexes
Chem.Commun., 2015, 51, 8528
7117151 CIFC51 H50 N2 O2 S6C 1 2/c 137.215; 14.101; 9.619
90; 96.595; 90
5014.3Minh T. Nguyen; Bradley J. Holliday
Direct insights into metal-induced conductivity enhancement in conducting metallopolymers
Chem.Commun., 2015, 51, 8610
7117152 CIFC18.86 H19 Ag I0.14 N3.86P 1 21/n 19.6546; 10.6457; 17.115
90; 90.385; 90
1759.04Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117153 CIFC19 H19 Ag N4P 1 21/n 19.59019; 10.57651; 17.1999
90; 90.1567; 90
1744.59Rachael Heath; Helge Muller-Bunz; Martin Albrecht
Silver(I) NHC mediated C-C bond activation of alkyl nitriles and catalytic efficiency in oxazoline synthesis
Chem.Commun., 2015, 51, 8699
7117154 CIFC20 H16 Cl F3 N2 O2P 1 21 110.4449; 7.9864; 11.2224
90; 93.069; 90
934.8Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117155 CIFC11 H8 Br F3 N2 OP 1 21/n 16.8291; 12.139; 14.882
90; 101.467; 90
1209.1Mingxia Ma; Yuanyuan Zhu; Quantao Sun; Xiaoyuan Li; Jinhuan Su; Long Zhao; Yanyan Zhao; Shuai Qiu; Wenjin Yan; Kairong Wang; Rui Wang
The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2'-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Chem.Commun., 2015, 51, 8789
7117156 CIFC15 H11 N O SP 1 21/c 116.112; 7.8274; 9.593
90; 101.081; 90
1187.27Bhaskar Garg; Yong-Chien Ling
A highly selective phenothiazine-based fluorescence 'turn-on' indicator based on cyanide-promoted novel protection/deprotection mechanism
Chem.Commun., 2015, 51, 8809
7117157 CIFC29 H23 Br O2P -19.845; 10.37; 12.763
89.509; 70.585; 71.497
1158.5Ya-Jing Chen; Tian-Jiao Hu; Chen-Guo Feng; Guo-Qiang Lin
Synthesis of chiral cyclobutanes via rhodium/diene-catalyzed asymmetric 1,4-addition: a dramatic ligand effect on the diastereoselectivity
Chem.Commun., 2015, 51, 8773
7117158 CIFC15 H4 F4 I NP -17.4665; 9.3784; 10.5061
85.468; 75.25; 67.203
655.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117159 CIFC15 H8 I NF d d 218.421; 7.6185; 17.387
90; 90; 90
2440.1Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117160 CIFC15 H4 Br F4 NP 1 21/c 113.2997; 9.7019; 19.917
90; 102.415; 90
2509.8Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117161 CIFC15 H6 Br F2 NP -15.7972; 8.6736; 12.715
73.612; 85.418; 86.061
610.7Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117162 CIFC15 H8 Br NF d d 217.893; 7.5409; 17.168
90; 90; 90
2316.5Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117163 CIFC15 H9 NP -19.404; 9.48; 13.047
94.412; 102.356; 103.038
1097.3Fanny Frausto; Zachary C. Smith; Terry E. Haas; Samuel W. Thomas III
Two-dimensional bricklayer arrangements of tolans using halogen bonding interactions
Chem.Commun., 2015, 51, 8825
7117164 CIFC16 H12 F2 N O4P 1 21/c 122.639; 5.0207; 11.438
90; 93.54; 90
1297.6Rui Guo; Haodong Yang; Pingping Tang
Silver-catalyzed Meerwein arylation: intermolecular and intramolecular fluoroarylation of styrenes
Chem.Commun., 2015, 51, 8829
7117166 CIFC10 H16 N4 O4 SC 1 2/c 19.642; 15.986; 9.334
90; 92.708; 90
1437Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117167 CIFC14 H14 N4 O4 SF d d 214.6766; 18.8388; 11.8862
90; 90; 90
3286.4Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117168 CIFC16 H18 N4 O4 SC 1 2/c 117.398; 7.4436; 14.051
90; 105.38; 90
1754.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117169 CIFC28 H28 N4 O5 SP b c n16.62; 8.218; 19.159
90; 90; 90
2616.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117170 CIFC28 H30 N4 O6 SP b c n16.933; 8.0337; 19.688
90; 90; 90
2678.3Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117171 CIFC14 H14 N4 O4 SeP 43 21 218.5107; 18.5107; 18.953
90; 90; 90
6494.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117172 CIFC17 H23 N4 O5.5 SeC 1 2/c 125.917; 8.7717; 17.5915
90; 100.377; 90
3933.8Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117173 CIFC26 H22 N4 O4 SeP -19.611; 10.852; 11.918
83.339; 72.175; 88.808
1175.2Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117174 CIFC28 H30 N4 O6 SeP b c n17.3442; 8.0712; 19.5768
90; 90; 90
2740.5Cristina Mottillo; Tomislav Friscic
Supramolecular imidazolium frameworks: direct analogues of metal azolate frameworks with charge-inverted node-and-linker structure
Chem.Commun., 2015, 51, 8924
7117175 CIFC30 H24 O2C 1 2/c 131.067; 13.835; 15.67
90; 93.254; 90
6724Suman Kalyan Samanta; Eduard Preis; Christian W. Lehmann; Richard Goddard; Saientan Bag; Prabal K. Maiti; Gunther Brunklaus; Ullrich Scherf
One-step synthesis of a cyclic 2,17-dioxo[3,3](4,4') biphenylophane and first preparation of a microporous polymer network from a macrocyclic precursor by cyclotrimerization
Chem.Commun., 2015, 51, 9046
7117176 CIFC18 H11 F3 O SP 1 21 15.593; 8.107; 17.57
90; 95.029; 90
793.6Amparo Sanz-Marco; Gonzalo Blay; M. Carmen Munoz; Jose R. Pedro
Highly enantioselective copper(I)-catalyzed conjugate addition of 1,3-diynes to alpha,beta-unsaturated trifluoromethyl ketones
Chem.Commun., 2015, 51, 8958
7117177 CIFC29 H31 N3 O6P 1 21/c 119.2486; 10.9164; 12.4114
90; 93.117; 90
2604.09Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117178 CIFC116 H132 B4 F16 N12 O28 Pd2P -114.8562; 16.5839; 16.9982
117.401; 93.11; 114.691
3216.5Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117179 CIFC58 H62 Cl4 N6 O12 Pd2C 1 2/m 113.8958; 21.0537; 11.1192
90; 101.982; 90
3182.1Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117180 CIFC126 H150 N16 O38 Pd2 S4P 1 21/n 113.099; 17.179; 32.25
90; 91.566; 90
7254.4Dan Preston; Alyssa Fox-Charles; Warrick K. C. Lo; James D. Crowley
Chloride triggered reversible switching from a metallosupramolecular [Pd2L4]^4+^ cage to a [Pd2L2Cl4] metallo-macrocycle with release of endo- and exo-hedrally bound guests
Chem.Commun., 2015, 51, 9042
7117181 CIFC24 H44 Cu7 I8 N8R -3 :H25.9051; 25.9051; 20.4603
90; 90; 120
11890.9Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117182 CIFC15 H29 Cu4 I4 N4I 4 2 218.5097; 18.5097; 36.1113
90; 90; 90
12372.1Yao Kang; Wei-Hui Fang; Lei Zhang; Jian Zhang
A structure-directing method to prepare semiconductive zeolitic cluster-organic frameworks with Cu3I4 building units
Chem.Commun., 2015, 51, 8994
7117183 CIFC26 H16 N2 O8 S UP 21 21 218.435; 12.595; 22.468
90; 90; 90
2387Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117184 CIFC26 H18 N2 O9 S UP 1 21/c 114.395; 8.675; 20.368
90; 95.16; 90
2533.2Shu-wen An; Lei Mei; Cong-zhi Wang; Chuan-qin Xia; Zhi-fang Chai; Wei-qun Shi
The first case of actinide triple helices: pH-dependent structural evolution and kinetically-controlled transformation of two supramolecular conformational isomers
Chem.Commun., 2015, 51, 8978
7117185 CIFC11 H9 F3 N2 O3P -15.736; 7.686; 15.026
102.598; 92.769; 110.155
601.4Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117186 CIFC11 H9 Cl F3 N O2P 1 21/c 17.764; 22.824; 7.398
90; 112.915; 90
1207.5Ai-Jie Cai; Yan Zheng; Jun-An Ma
Copper-triggered three-component reaction of CF3CHN2, nitriles, and aldehydes: highly diastereoselective synthesis of CF3-substituted oxazolines and vicinal amino alcohols
Chem.Commun., 2015, 51, 8946
7117188 CIFC46 H43 Cl3 S6P b c a9.4165; 19.7949; 45.588
90; 90; 90
8497.5Shu-Wei Chang; Masaki Horie
A donor-acceptor conjugated block copolymer of poly(arylenevinylene)s by ring-opening metathesis polymerization
Chem.Commun., 2015, 51, 9113
7117189 CIFC16 H17.13 Cu2 O19.5 S2P -17.6226; 8.0332; 19.2709
89.772; 88.902; 76.322
1146.36Xiao-Qin Wu; Jian-Gong Ma; Han Li; Di-Ming Chen; Wen Gu; Guang-Ming Yang; Peng Cheng
Metal-organic framework biosensor with high stability and selectivity in a bio-mimic environment
Chem.Commun., 2015, 51, 9161
7117190 CIFC17 H21 F4 N O4 SP 21 21 217.7459; 9.8069; 25.602
90; 90; 90
1944.8Chen Xie; Yanling Dai; Haibo Mei; Jianlin Han; Vadim A. Soloshonok; Yi Pan
Asymmetric synthesis of quaternary alpha-fluoro-beta-keto-amines via detrifluoroacetylative Mannich reactions
Chem.Commun., 2015, 51, 9149
7117191 CIFC22 H19 Br Cl3 N2 O4P 21 21 2110.2175; 12.1386; 19.641
90; 90; 90
2436Wu-Lin Yang; Yang-Zi Liu; Shuai Luo; Xingxin Yu; John S. Fossey; Wei-Ping Deng
The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to alpha-alkylidene succinimides
Chem.Commun., 2015, 51, 9212
7117192 CIFC24 H18 F6 O6P -18.917; 11.888; 12.165
62.137; 81.719; 78.834
1116.3Jingbo Wu; Scott T. Iacono; Gregory T. McCandless; Dennis W. Smith; Bruce M. Novak
Utilization of a Meldrum's acid towards functionalized fluoropolymers possessing dual reactivity for thermal crosslinking and post-polymerization modification
Chem.Commun., 2015, 51, 9220
7117193 CIFC19 H14 B F2 N3 SP 1 21/c 113.4997; 13.9995; 10.1052
90; 111.458; 90
1777.4Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117194 CIFC23 H23 B F2 N3 SP 1 21/n 116.3271; 8.327; 16.9926
90; 109.759; 90
2174.2Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117195 CIFC20 H16 B F2 N3 O SP 1 21/c 110.5497; 19.995; 9.2865
90; 104.898; 90
1893.1Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117196 CIFC18 H11 B Cl F2 N3P 1 21/c 19.7361; 14.5464; 12.214
90; 111.146; 90
1613.33Roop Shikha Singh; Rakesh Kumar Gupta; Rajendra Prasad Paitandi; Mrigendra Dubey; Gunjan Sharma; Biplob Koch; Daya Shankar Pandey
Morphological tuning via structural modulations in AIE luminogens with the minimum number of possible variables and their use in live cell imaging
Chem.Commun., 2015, 51, 9125
7117197 CIFC90 H106 Cl4 N10 O92.75 V16P 1 21/a 121.2958; 21.33; 21.9581
90; 105.868; 90
9594.2Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117198 CIFC80 H80 Cl4 N4 O81.5 V16I 4/m m m14.9098; 14.9098; 38.069
90; 90; 90
8462.8Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117199 CIFC51.75 H64.75 Br4 Cl2 N7.25 O42.75 V8P -115.1975; 19.1532; 19.3115
103.817; 95.3294; 98.3478
5352.9Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117200 CIFC91 H119 Cl7 N9 O83.25 V16P -114.9214; 16.0334; 16.7794
79.476; 82.828; 81.284
3881.7Zhuxiu Zhang; Wen-Yang Gao; Lukasz Wojtas; Zhenjie Zhang; Michael J. Zaworotko
A new family of anionic organic-inorganic hybrid doughnut-like nanostructures
Chem.Commun., 2015, 51, 9223
7117201 CIFC45 H109 Cr Mo6 N6 O29P -113.554; 13.7899; 21.0955
86.768; 88.944; 63.016
3508Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117202 CIFC62 H143 Br Cr Mo6 N5 O27P 1 21/c 124.0245; 13.9963; 26.7955
90; 94.54; 90
8981.8Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117203 CIFC69 H158 Br Cr Mo6 N8 O29P 113.2494; 14.7378; 14.8892
119.221; 103.752; 96.589
2371.5Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117204 CIFC46 H108 Cr Mo6 N5 O28P -113.6865; 13.7366; 21.5248
86.727; 83.692; 62.304
3561.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117205 CIFC67 H155 Br Mn Mo6 N9 O29P 113.2671; 14.756; 14.887
119.33; 103.729; 96.883
2370.4Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117206 CIFC8 H43 Cr Mo6 N2 O30P 1 21/n 115.0834; 11.5341; 23.0245
90; 98.122; 90
3965.47Jiangwei Zhang; Zhenhua Liu; Yichao Huang; Jin zhang; Jian Hao; Yongge Wei
Unprecedented chi isomers of single-side triol-functionalized Anderson polyoxometalates and their proton-controlled isomer transformation
Chem.Commun., 2015, 51, 9097
7117207 CIFC62 H54 Cl6 P4 RuP -112.3129; 14.9215; 18.0053
67.588; 85.054; 78.028
2991.6Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117208 CIFC63.5 H57 Cl5 P4 RuP -111.3506; 12.3819; 21.4222
80.7264; 74.684; 83.7147
2858.75Samantha G. Eaves; Sam J. Hart; Adrian C. Whitwood; Dmitry S. Yufit; Paul J. Low; Jason M. Lynam
Rapid Markovnikov addition of HCl to a pendant alkyne: evidence for a quinoidal cumulene
Chem.Commun., 2015, 51, 9362
7117210 CIFC67.99 H56.99 F11.99 N14 O P2 RuR -317.6408; 17.6408; 44.355
90; 90; 120
11953.9E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117211 CIFC60 H42 Cl2 N12 O5 RuP 41 3 221.1118; 21.1118; 21.1118
90; 90; 90
9409.7E. Rousset; D. Chartrand; I. Ciofini; V. Marvaud; G. S. Hanan
Red-light-driven photocatalytic hydrogen evolution using a ruthenium quaterpyridine complex
Chem.Commun., 2015, 51, 9261
7117212 CIFC17 H13 N3 OP 1 21/n 15.212; 17.471; 15.196
90; 92.267; 90
1382.6Liang Zhang; Mingzhu Zhao; Xiaoming Zhao
The synthesis of carbonyl 2-amino-pyrimidines via tandem regioselective heterocyclization of 1,3-diynes with guanidine and selective oxidation
Chem.Commun., 2015, 51, 9370
7117213 CIFAl4 H3 Na3 O19 P4P 1 21/m 17.537; 12.525; 9.7
90; 98.51; 90
905.6Yanjun Sun; Yan Yan; Yanyan Wang; Yi Li; Jiyang Li; Jihong Yu
High proton conduction in a new alkali metal-templated open-framework aluminophosphate
Chem.Commun., 2015, 51, 9317
7117214 CIFC96 H40 Cd5 O34R -3 c :H29.1653; 29.1653; 83.513
90; 90; 120
61520Hongming He; Yang Song; Chuanqi Zhang; Fuxing Sun; Rongrong Yuan; Zheng Bian; Lianxun Gao; Guangshan Zhu
A highly robust metal-organic framework based on an aromatic 12-carboxyl ligand with highly selective adsorption of CO2 over CH4
Chem.Commun., 2015, 51, 9463
7117215 CIFCl7 Cu10 O16 Pb2 Se4C 1 2/m 118.605; 6.204; 12.673
90; 109.869; 90
1376Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117216 CIFCl10 Cu12 O16 Pb2 Se4C 1 2/m 118.4956; 6.1454; 15.2985
90; 119.311; 90
1516.25Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117217 CIFCl11.6 Cu13.6 K1.6 O16 Pb0.4 Se4C 1 2/m 115.1158; 6.1853; 9.2672
90; 95.965; 90
861.75Vadim M. Kovrugin; Marie Colmont; Oleg I. Siidra; Olivier Mentre; Alexander Al-Shuray; Vladislav V. Gurzhiy; Sergey V. Krivovichev
Oxocentered Cu(II) lead selenite honeycomb lattices hosting Cu(I)Cl2 groups obtained by chemical vapor transport reactions
Chem.Commun., 2015, 51, 9563
7117218 CIFC15 H9 Ag Cl N9 O4I -4 3 d20.2313; 20.2313; 20.2313
90; 90; 90
8280.8Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117219 CIFC40 H27 Ag4 F12 N27 O12 S4P 1 21/n 110.6023; 18.0069; 33.316
90; 90.1374; 90
6360.5Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117220 CIFC24 H18 Ag2 F12 N18 P2P n m a10.6565; 16.8754; 19.1418
90; 90; 90
3442.3Damir A. Safin; Amelie Pialat; Alicea A. Leitch; Nikolay A. Tumanov; Ilia Korobkov; Yaroslav Filinchuk; Jaclyn L. Brusso; Muralee Murugesu
Anion-induced Ag^I^ self-assemblies with electron deficient aromatic ligands: anion-pi-system interactions as a driving force for templated coordination networks
Chem.Commun., 2015, 51, 9547
7117221 CIFC30 H24 Cl2 N Ni O3 PP -110.2518; 11.9007; 13.0245
111.438; 97.586; 98.593
1432.11Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117222 CIFC20 H40 N4 Ni O2C 1 2/c 114.857; 10.303; 15.562
90; 99.009; 90
2352.7Wenfeng Lo; Chunhua Hu; Tyler Berenson; Nathaniel Tracer; Daniel Shlian; Michael Khaloo; Avraham Benhaim; Jianfeng Jiang
Oxidation of carbon monoxide in basic solution catalyzed by nickel cyano carbonyls under ambient conditions and the prototype of a CO-powered alkaline fuel cell
Chem.Commun., 2015, 51, 9432
7117223 CIFC62 H42 N6 Ni2 O18P 1 21/n 113.142; 12.337; 17.656
90; 108.519; 90
2714Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117224 CIFC36 H21 N4 Ni2 O8C m c a31.395; 13.702; 15.808
90; 90; 90
6800Jun Zhao; Yenan Wang; Wenwen Dong; Yapan Wu; Dongsheng Li; Bin Liu; Qichun Zhang
A new surfactant-introduction strategy for separating the pure single-phase of metal-organic frameworks
Chem.Commun., 2015, 51, 9479
7117225 CIFC18 H12 N2 O2P 1 21/n 17.72; 21.073; 8.161
90; 92.202; 90
1326.7David E. Stephens; Johant Lakey-Beitia; Gabriel Chavez; Carla Ilie; Hadi D. Arman; Oleg V. Larionov
Experimental and mechanistic analysis of the palladium-catalyzed oxidative C8-selective C-H homocoupling of quinoline N-oxides
Chem.Commun., 2015, 51, 9507
7117227 CIFC28 H31 N3C 1 2/c 131.282; 8.8017; 19.4725
90; 121.27; 90
4582.6Qian Gao; Peng Zhou; Feng Liu; Wen-Juan Hao; Changsheng Yao; Bo Jiang; Shu-Jiang Tu
Cobalt(II)/silver relay catalytic isocyanide insertion/cycloaddition cascades: a new access to pyrrolo[2,3-b]indoles
Chem.Commun., 2015, 51, 9519
7117228 CIFC23 H18 N2 O4P 1 21/c 110.8247; 12.1491; 14.009
90; 96.356; 90
1831Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117229 CIFC24 H20 Cl3 N O3P 1 21/c 115.3285; 11.4221; 12.7961
90; 95.471; 90
2230.2Subrata Mukherjee; Santigopal Mondal; Atanu Patra; Rajesh G. Gonnade; Akkattu T. Biju
N-Heterocyclic carbene-catalyzed diastereoselective synthesis of beta-lactone-fused cyclopentanes using homoenolate annulation reaction
Chem.Commun., 2015, 51, 9559
7117230 CIFC50 H60 B F24 Na P6P 1 21/c 118.4514; 13.2631; 26.133
90; 90.826; 90
6394.7Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117231 CIFC62 H60 B F24 Na P6P -112.5084; 16.4798; 17.5637
79.047; 78.403; 81.625
3460.2Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117232 CIFC46 H48 Al F36 Li O4 P6P n a 2115.092; 27.737; 15.405
90; 90; 90
6448.6Marina Carravetta; Maria Concistre; William Levason; Gillian Reid; Wenjian Zhang
Unique Group 1 cations stabilised by homoleptic neutral phosphine coordination
Chem.Commun., 2015, 51, 9555
7117233 CIFC48 H68 Cl Fe In N2 O4P 21 21 2110.3658; 18.6942; 23.794
90; 90; 90
4610.8Stephanie M. Quan; Paula L. Diaconescu
High activity of an indium alkoxide complex toward ring opening polymerization of cyclic esters
Chem.Commun., 2015, 51, 9643
7117234 CIFC27 H18 Br N3 OP 1 21 18.1413; 13.747; 10.606
90; 108.05; 90
1128.6Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117235 CIFC32 H24 N2 O SP -19.4724; 12.292; 12.563
104; 109.97; 102.72
1258.3Tianyou Qin; Lu Cheng; Sean Xiao-An Zhang; Weiwei Liao
Stereoselective synthesis of organosulfur compounds incorporating N-aromatic heterocyclic motifs and quaternary carbon centers via a sulfa-Michael triggered tandem reaction
Chem.Commun., 2015, 51, 9714
7117236 CIFC33 H15 Cu6 N6 O19F m -3 m44.588; 44.588; 44.588
90; 90; 90
88645Wen-Yang Gao; Tony Pham; Katherine A. Forrest; Brian Space; Lukasz Wojtas; Yu-Sheng Chen; Shengqian Ma
The local electric field favours more than exposed nitrogen atoms on CO2 capture: a case study on the rht-type MOF platform
Chem.Commun., 2015, 51, 9636
7117237 CIFC69 H65 Au2 F6 N P SbP 1 21/c 116.83401; 18.4515; 19.639
90; 100.054; 90
6006.44Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117238 CIFC58.01 H55.02 Au2 F6 N P SbP b c n24.291; 17.933; 24.334
90; 90; 90
10600Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117239 CIFC66 H64 Au3 F6 N2 SbP 1 21/c 116.33309; 18.64797; 18.79354
90; 91.0581; 90
5723.14Luisa Ciano; Natalie Fey; Connor J. V. Halliday; Jason M. Lynam; Lucy M. Milner; Nimesh Mistry; Natalie E. Pridmore; Nell S. Townsend; Adrian C. Whitwood
Dispersion, solvent and metal effects in the binding of gold cations to alkynyl ligands: implications for Au(I) catalysis
Chem.Commun., 2015, 51, 9702
7117240 CIFC32 H42 Cl3 N3 PdP 1 21/c 19.2943; 21.212; 18.121
90; 114.171; 90
3259.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117241 CIFC26 H30 Cl3 N3 PtP 21 21 235.0384; 9.1217; 16.6331
90; 90; 90
5316.1Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117242 CIFC32 H42 Cl3 N3 PtP 1 21/c 19.3227; 21.1418; 18.1068
90; 115.162; 90
3230.18Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117243 CIFC32 H41 Cl2 N3 PdP 1 21/c 19.7411; 22.3057; 14.8046
90; 98.163; 90
3184.2Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117244 CIFC33 H43 Cl4 N3 PdI 41/a :233.4882; 33.4882; 12.9635
90; 90; 90
14538Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117245 CIFC39 H49 Cl2 N3 PdP 1 21/c 114.8545; 17.1043; 14.8749
90; 102.243; 90
3693.4Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117246 CIFC22 H21 Cl2 N3 PdP 1 21/c 19.0414; 25.274; 10.5618
90; 120.856; 90
2071.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117247 CIFC44 H42 Br1.81 Cl2.18 N6 Pd2C 1 c 114.907; 15.9956; 18.4249
90; 99.438; 90
4333.9Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117248 CIFC26 H29 Cl2 N3 PdP 1 21/c 111.5869; 14.0962; 15.7142
90; 100.524; 90
2523.45Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117249 CIFC27 H31 Cl4 N3 PtP 1 21/c 116.5349; 11.8855; 14.5488
90; 91.162; 90
2858.62Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117250 CIFC22 H21 Cl2 N3 PtP 1 21/c 19.0255; 25.338; 10.5412
90; 120.716; 90
2072.5Christopher J. Adams; Matteo Lusi; Emily M. Mutambi; A. Guy Orpen
Two-step solid-state synthesis of PEPPSI-type compounds
Chem.Commun., 2015, 51, 9632
7117251 CIFC79 H21 Cl2 NP 1 21/c 110.4764; 25.5317; 16.5265
90; 102.296; 90
4319.1Bolong Zhang; Jegadesan Subbiah; Yu-Ying Lai; Jonathan M. White; David J. Jones; Wallace W. H. Wong
One-pot selective synthesis of a fullerene bisadduct for organic solar cell applications
Chem.Commun., 2015, 51, 9837
7117252 CIFC21 H19 Cl N2 O3P 21 21 216.1999; 13.2765; 23.277
90; 90; 90
1916Santosh Agrawal; Nagaraju Molleti; Vinod K. Singh
Organocatalytic enantio- and diastereoselective synthesis of highly substituted ?-lactones via a Michael-cyclization cascade
Chem.Commun., 2015, 51, 9793
7117253 CIFC116 H150 Ag24 F12 N2 O16P 1 21/n 123.5527; 20.9694; 29.346
90; 95.231; 90
14433.2Kuan-Guan Liu; Su-Kun Chen; Yu-Mei Lin; Quan-Ming Wang
An organic anion template: a 24-nucleus silver cluster encapsulating a squarate dimer
Chem.Commun., 2015, 51, 9896
7117254 CIFC12 H18P -15.246; 6.1956; 7.9824
103.859; 98.602; 100.131
242.93Viswanadha G. Saraswatula; Binoy K. Saha
A thermal expansion investigation of the melting point anomaly in trihalomesitylenes
Chem.Commun., 2015, 51, 9829

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