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

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