Crystallography Open Database

Result: there are 1796 entries in the selection

Switch to the old layout of the page

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

Searching journal of publication like 'Chem.Commun.' volume of publication is 51

Left arrow Left arrow First | Left arrow Previous 500 | of 4 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
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

Left arrow Left arrow First | Left arrow Previous 500 | of 4 | Next 500 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!