Crystallography Open Database

Result: there are 709 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 'Chemical Communications' volume of publication is 53

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 8 | Next 100 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
7119273 CIFC18 H13 F3 I NP 1 21/c 111.015; 14.627; 11.621
90; 112.793; 90
1726.1Zhou, Xiaofan; Huang, Chaoqian; Zeng, Yu; Xiong, Jiarui; Xiao, Yuanjing; Zhang, Junliang
Silver-catalysed tandem hydroamination and cyclization of 2-trifluoromethyl-1,3-enynes with primary amines: modular entry to 4-trifluoromethyl-3-pyrrolines.
Chemical communications (Cambridge, England), 2017, 53, 1084-1087
7119274 CIFC18 H36 Cu4 N10 O12P 63 2 219.613; 19.613; 13.849
90; 90; 120
4613.6Song, Bai-Qiao; Chen, Da-Qin; Ji, Zhenguo; Tang, Junhong; Wang, Xin-Long; Zang, Hong-Ying; Su, Zhong-Min
Control of bulk homochirality and proton conductivity in isostructural chiral metal-organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 1892-1895
7119275 CIFC24 H48 Cu4 N10 O6P 63 2 219.603; 19.603; 13.939
90; 90; 120
4639Song, Bai-Qiao; Chen, Da-Qin; Ji, Zhenguo; Tang, Junhong; Wang, Xin-Long; Zang, Hong-Ying; Su, Zhong-Min
Control of bulk homochirality and proton conductivity in isostructural chiral metal-organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 1892-1895
7119276 CIFC24 H48 Cu4 N10 O6P 63 2 219.593; 19.593; 13.927
90; 90; 120
4630.1Song, Bai-Qiao; Chen, Da-Qin; Ji, Zhenguo; Tang, Junhong; Wang, Xin-Long; Zang, Hong-Ying; Su, Zhong-Min
Control of bulk homochirality and proton conductivity in isostructural chiral metal-organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 1892-1895
7119277 CIFC18 H30 Cu4 N10 O12P 63 2 219.6977; 19.6977; 13.8757
90; 90; 120
4662.5Song, Bai-Qiao; Chen, Da-Qin; Ji, Zhenguo; Tang, Junhong; Wang, Xin-Long; Zang, Hong-Ying; Su, Zhong-Min
Control of bulk homochirality and proton conductivity in isostructural chiral metal-organic frameworks.
Chemical communications (Cambridge, England), 2017, 53, 1892-1895
7119278 CIFC247 H240 Cl4 La4 N16 O8P -121.2533; 21.617; 25.3669
75.244; 83.199; 82.524
11129.9Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119279 CIFC255 H280 La4 N20 O4 Si8P 1 2/n 120.8963; 22.8615; 25.1772
90; 94.338; 90
11993.2Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119280 CIFC38 H62 N5 O Si2 SmP 1 21/n 113.2427; 19.5465; 16.2
90; 106.627; 90
4018.01Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119281 CIFC46 H48 N4 O3 S2P -19.7749; 10.2099; 21.6219
78.582; 80.858; 89.827
2087.41Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119282 CIFC28 H38 N4P 1 21/n 117.381; 8.9219; 18.17
90; 114.373; 90
2566.5Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119283 CIFC116 H144 N10 O7 Si4 Sm2P -116.7981; 18.7804; 19.323
82.107; 81.378; 68.045
5567.9Kazeminejad, Neda; Munzel, Denise; Gamer, Michael T.; Roesky, Peter W.
Bis(amidinate) ligands in early lanthanide chemistry - synthesis, structures, and hydroamination catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1060-1063
7119284 CIFC46 H29 B2 Cl2 F20 O3 P SP -110.6838; 11.7958; 20.5532
81.999; 81.481; 65.83
2328.18Ye, Ke-Yin; Bursch, Markus; Qu, Zheng-Wang; Daniliuc, Constantin G.; Grimme, Stefan; Kehr, Gerald; Erker, Gerhard
Reversible formylborane/SO2 coupling at a frustrated Lewis pair framework.
Chemical communications (Cambridge, England), 2017, 53, 633-635
7119285 CIFC43 H23 B2 F20 O3 P SC 1 2/c 119.6527; 18.1222; 23.6282
90; 99.171; 90
8307.6Ye, Ke-Yin; Bursch, Markus; Qu, Zheng-Wang; Daniliuc, Constantin G.; Grimme, Stefan; Kehr, Gerald; Erker, Gerhard
Reversible formylborane/SO2 coupling at a frustrated Lewis pair framework.
Chemical communications (Cambridge, England), 2017, 53, 633-635
7119286 CIFC22 H15 F N2 OC 1 2/c 138.444; 6.2239; 14.5234
90; 96.834; 90
3450.3Lingayya, Rajaka; Vellakkaran, Mari; Nagaiah, Kommu; Tadikamalla, Prabhakar Rao; Nanubolu, Jagadeesh Babu
Palladium(ii)-catalyzed direct O-alkenylation of 2-arylquinazolinones with N-tosylhydrazones: an efficient route to O-alkenylquinazolines.
Chemical communications (Cambridge, England), 2017, 53, 1672-1675
7119287 CIFC12 H15 N5 OP c a 2112.406; 5.786; 34.77
90; 90; 90
2496Wu, Zhongkai; Xu, Pan; Zhou, Nengneng; Duan, Yingqian; Zhang, Muliang; Zhu, Chengjian
[3+2] Cycloaddition of azide with aldehyde hydrazone through an aminyl radical-polar crossover strategy.
Chemical communications (Cambridge, England), 2017, 53, 1045-1047
7119288 CIFC35 H41 Cu F6 N2P 1 21/n 19.7652; 25.1903; 13.2123
90; 95.217; 90
3236.61Sakhaei, Zeinab; Kundu, Subrata; Donnelly, Jane M.; Bertke, Jeffery A.; Kim, William Y.; Warren, Timothy H.
Nitric oxide release via oxygen atom transfer from nitrite at copper(ii).
Chemical communications (Cambridge, England), 2017, 53, 549-552
7119289 CIFC45 H71 Cu F6 N4 O2P 1 21/c 124.3428; 16.7818; 23.2483
90; 93.793; 90
9476.5Sakhaei, Zeinab; Kundu, Subrata; Donnelly, Jane M.; Bertke, Jeffery A.; Kim, William Y.; Warren, Timothy H.
Nitric oxide release via oxygen atom transfer from nitrite at copper(ii).
Chemical communications (Cambridge, England), 2017, 53, 549-552
7119290 CIFC58 H70 Cu2 F12 N5 O2C 1 2/c 121.7216; 22.2834; 16.5124
90; 103.473; 90
7772.6Sakhaei, Zeinab; Kundu, Subrata; Donnelly, Jane M.; Bertke, Jeffery A.; Kim, William Y.; Warren, Timothy H.
Nitric oxide release via oxygen atom transfer from nitrite at copper(ii).
Chemical communications (Cambridge, England), 2017, 53, 549-552
7119291 CIFC47 H50 Cu F6 N2 PP -112.7356; 16.3289; 23.5452
81.7; 82.851; 73.675
4631.6Sakhaei, Zeinab; Kundu, Subrata; Donnelly, Jane M.; Bertke, Jeffery A.; Kim, William Y.; Warren, Timothy H.
Nitric oxide release via oxygen atom transfer from nitrite at copper(ii).
Chemical communications (Cambridge, England), 2017, 53, 549-552
7119292 CIFC83 H96 Cu2 F12 N6C 1 2/c 128.6867; 15.4462; 37.041
90; 107.702; 90
15635.7Sakhaei, Zeinab; Kundu, Subrata; Donnelly, Jane M.; Bertke, Jeffery A.; Kim, William Y.; Warren, Timothy H.
Nitric oxide release via oxygen atom transfer from nitrite at copper(ii).
Chemical communications (Cambridge, England), 2017, 53, 549-552
7119293 CIFC14 H9 F3 N2P 41 21 211.5964; 11.5964; 17.7913
90; 90; 90
2392.51Gao, Guo-Lin; Yang, Chao; Xia, Wujiong
Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1041-1044
7119294 CIFC9 H7 F3 N2P n m a12.8186; 6.8399; 9.8413
90; 90; 90
862.86Gao, Guo-Lin; Yang, Chao; Xia, Wujiong
Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1041-1044
7119295 CIFC15 H11 F3 N2P 1 21/c 19.7224; 11.5982; 11.6209
90; 92.78; 90
1308.86Gao, Guo-Lin; Yang, Chao; Xia, Wujiong
Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1041-1044
7119296 CIFC12 H11 F3 N2 O2P -17.2208; 9.3833; 9.5826
102.706; 105.918; 97.358
596.67Gao, Guo-Lin; Yang, Chao; Xia, Wujiong
Selective C-H trifluoromethylation of benzimidazoles through photoredox catalysis.
Chemical communications (Cambridge, England), 2017, 53, 1041-1044
7119297 CIFC19 H20 Cl2 F6 Ge N4 O6 S2P -18.4372; 13.0507; 13.307
69.771; 85.531; 81.999
1360.79Raut, Ravindra K.; Majumdar, Moumita
Direct coordination of a germanium(ii) dicationic center to transition metals.
Chemical communications (Cambridge, England), 2017, 53, 1467-1469
7119298 CIFC17 H18 Cl F3 Ge N4 O3 SP 1 21/c 120.5748; 13.4785; 14.7382
90; 99.802; 90
4027.5Raut, Ravindra K.; Majumdar, Moumita
Direct coordination of a germanium(ii) dicationic center to transition metals.
Chemical communications (Cambridge, England), 2017, 53, 1467-1469
7119299 CIFC37 H36 Au F15 Ge2 N8 O15 S5P -112.421; 12.98; 17.648
85.383; 72.526; 75.017
2621.7Raut, Ravindra K.; Majumdar, Moumita
Direct coordination of a germanium(ii) dicationic center to transition metals.
Chemical communications (Cambridge, England), 2017, 53, 1467-1469
7119300 CIFC16 H18 Cl4 Ge2 N4P -18.872; 10.214; 12.585
90.296; 93.135; 107.603
1085.1Raut, Ravindra K.; Majumdar, Moumita
Direct coordination of a germanium(ii) dicationic center to transition metals.
Chemical communications (Cambridge, England), 2017, 53, 1467-1469
7119301 CIFC39 H39 Ag F15 Ge2 N9 O15 S5P -114.699; 15.176; 15.433
112.989; 103.063; 106.078
2819.6Raut, Ravindra K.; Majumdar, Moumita
Direct coordination of a germanium(ii) dicationic center to transition metals.
Chemical communications (Cambridge, England), 2017, 53, 1467-1469
7119302 CIFC32 H22 O2 SP 1 21/c 111.3812; 9.024; 23.553
90; 100.181; 90
2380.9Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119303 CIFC20 H12 F2 O2 SP 1 21/c 110.3524; 10.3346; 15.3392
90; 92.291; 90
1639.8Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119304 CIFC22 H18 O4 SP -19.6225; 10.5635; 10.9316
63.981; 64.608; 78.743
902.05Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119305 CIFC22 H18 O2 SP 1 21/n 19.9496; 12.5896; 14.3507
90; 99.202; 90
1774.5Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119306 CIFC20 H14 O2 SC 1 c 18.7763; 18.341; 19.844
90; 100.092; 90
3144.8Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119307 CIFC22 H18 O2 SP -110.134; 10.9037; 17.706
90.049; 92.799; 114.437
1778.61Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119308 CIFC22 H12 F6 O2 SP -17.5333; 10.9876; 11.6354
91.853; 90.826; 95.099
958.64Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119309 CIFC28 H30 O2 SP 1 21/c 116.9872; 11.0288; 12.9726
90; 101.237; 90
2383.8Guo, Jingjing; Hu, Shimin; Luo, Wenwen; Hu, Rongrong; Qin, Anjun; Zhao, Zujin; Tang, Ben Zhong
A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide.
Chemical communications (Cambridge, England), 2017, 53, 1463-1466
7119310 CIFC102 H98 Cd3 Cl6 K2 N36 O12P 1 2/c 116.136; 13.126; 34.238
90; 90.19; 90
7252Wang, Ying; Jia, Wei; Chen, Ran; Zhao, Xiao-Jun; Wang, Zhong-Liang
Guest-induced SC-SC transformation within the first K/Cd heterodimetallic triazole complex: a luminescent sensor for high-explosives and cyano molecules.
Chemical communications (Cambridge, England), 2017, 53, 636-639
7119311 CIFC43 H45 Cd N15 O8P -112.1538; 12.1574; 16.1536
77.045; 82.55; 83.527
2297.8Wang, Ying; Jia, Wei; Chen, Ran; Zhao, Xiao-Jun; Wang, Zhong-Liang
Guest-induced SC-SC transformation within the first K/Cd heterodimetallic triazole complex: a luminescent sensor for high-explosives and cyano molecules.
Chemical communications (Cambridge, England), 2017, 53, 636-639
7119312 CIFC244 H171 Cd8 N88 O28C 1 2 120.477; 23.839; 17.521
90; 111.11; 90
7979Wang, Ying; Jia, Wei; Chen, Ran; Zhao, Xiao-Jun; Wang, Zhong-Liang
Guest-induced SC-SC transformation within the first K/Cd heterodimetallic triazole complex: a luminescent sensor for high-explosives and cyano molecules.
Chemical communications (Cambridge, England), 2017, 53, 636-639
7119313 CIFC20 H15 F27 O4 SP 1 21/n 16.7936; 24.851; 17.591
90; 90.105; 90
2969.8Dichiarante, V.; Tirotta, I.; Catalano, L.; Terraneo, G.; Raffaini, G.; Chierotti, M. R.; Gobetto, R.; Baldelli Bombelli, F.; Metrangolo, P.
Superfluorinated and NIR-luminescent gold nanoclusters.
Chemical communications (Cambridge, England), 2017, 53, 621-624
7119314 CIFC16 H16 F3 N O2 SP 1 21/n 18.5653; 10.5123; 17.819
90; 94.319; 90
1599.9Dong, Jinhuan; Xin, Shuang; Wang, Yanqing; Pan, Ling; Liu, Qun
In situ generation and reactions of p-(trifluoromethyl)benzyl electrophiles: an efficient access to p-(trifluoromethyl)benzyl compounds.
Chemical communications (Cambridge, England), 2017, 53, 1668-1671
7119315 CIFC38 H44 N2 O6P 1 21/n 16.156; 23.845; 12.467
90; 100.295; 90
1800.6Hu, Wenbo; He, Tingchao; Jiang, Rongcui; Yin, Jun; Li, Lin; Lu, Xiaomei; Zhao, Hui; Zhang, Lei; Huang, Ling; Sun, Handong; Huang, Wei; Fan, Quli
Inner salt-shaped small molecular photosensitizer with extremely enhanced two-photon absorption for mitochondrial-targeted photodynamic therapy.
Chemical communications (Cambridge, England), 2017, 53, 1680-1683
7119316 CIFC36 H40 N2 O6P 4/n :231.2361; 31.2361; 8.08
90; 90; 90
7883.6Hu, Wenbo; He, Tingchao; Jiang, Rongcui; Yin, Jun; Li, Lin; Lu, Xiaomei; Zhao, Hui; Zhang, Lei; Huang, Ling; Sun, Handong; Huang, Wei; Fan, Quli
Inner salt-shaped small molecular photosensitizer with extremely enhanced two-photon absorption for mitochondrial-targeted photodynamic therapy.
Chemical communications (Cambridge, England), 2017, 53, 1680-1683
7119317 CIFC25 H19 F N2 OP -17.2657; 15.2058; 19.3128
110.971; 99.332; 95.705
1937.08Yang, Xinglin; Shan, Gang; Yang, Zimo; Huang, Guiyi; Dong, Guoqiang; Sheng, Chunquan; Rao, Yu
One-pot synthesis of quaternary carbon centered cyclobutanes via Pd(ii)-catalyzed cascade C(sp(3))-H activations.
Chemical communications (Cambridge, England), 2017, 53, 1534-1537
7119318 CIFC21 H19 F N2 OP 1 21/c 19.4896; 14.7995; 12.088
90; 91; 90
1697.4Yang, Xinglin; Shan, Gang; Yang, Zimo; Huang, Guiyi; Dong, Guoqiang; Sheng, Chunquan; Rao, Yu
One-pot synthesis of quaternary carbon centered cyclobutanes via Pd(ii)-catalyzed cascade C(sp(3))-H activations.
Chemical communications (Cambridge, England), 2017, 53, 1534-1537
7119319 CIFC84 H114 O18 S3P 110.542; 12.791; 15.052
97.91; 98.81; 96.16
1969.5Hou, Xueqing; Zhu, Yongtao; Qin, Yunke; Chen, Lichuan; Li, Xuexiang; Zhang, Hao-Li; Xu, Wei; Zhu, Daoben; Shao, Xiangfeng
Tris(S,S-dioxide)-trithiasumanene: strong fluorescence and cocrystal with 1,2,6,7,10,11-hexabutoxytriphenylene.
Chemical communications (Cambridge, England), 2017, 53, 1546-1549
7119320 CIFC62 H54 S2C 1 2/c 141.379; 6.0824; 20.059
90; 106.27; 90
4846.3Wu, Hongzhuo; Fang, Renren; Tao, Jingwei; Wang, Deliang; Qiao, Xiaolan; Yang, Xiaodi; Hartl, František; Li, Hongxiang
Diacenaphthylene-fused benzo[1,2-b:4,5-b']dithiophenes: polycyclic heteroacenes containing full-carbon five-membered aromatic rings.
Chemical communications (Cambridge, England), 2017, 53, 751-754
7119321 CIFC46 H46 O2 S2P -113.094; 14.5388; 20.6868
76.383; 82.589; 80.352
3756.8Wu, Hongzhuo; Fang, Renren; Tao, Jingwei; Wang, Deliang; Qiao, Xiaolan; Yang, Xiaodi; Hartl, František; Li, Hongxiang
Diacenaphthylene-fused benzo[1,2-b:4,5-b']dithiophenes: polycyclic heteroacenes containing full-carbon five-membered aromatic rings.
Chemical communications (Cambridge, England), 2017, 53, 751-754
7119322 CIFC15 H14 Cl N O2 SP c a 2115.601; 13.4615; 7.0024
90; 90; 90
1470.6Song, Bo; Yu, Chang-Bin; Ji, Yue; Chen, Mu-Wang; Zhou, Yong-Gui
Synthesis of chiral sultams via palladium-catalyzed intramolecular asymmetric reductive amination.
Chemical communications (Cambridge, England), 2017, 53, 1704-1707
7119323 CIFC14 H19 N O2 SP 21 21 2110.1064; 12.4748; 21.895
90; 90; 90
2760.4Song, Bo; Yu, Chang-Bin; Ji, Yue; Chen, Mu-Wang; Zhou, Yong-Gui
Synthesis of chiral sultams via palladium-catalyzed intramolecular asymmetric reductive amination.
Chemical communications (Cambridge, England), 2017, 53, 1704-1707
7119324 CIFC21 H12 O2P 329.98192; 9.98192; 11.95006
90; 90; 120
1031.17Ngamsomprasert, Niti; Dang, Jing-Shuang; Higashibayashi, Shuhei; Yakiyama, Yumi; Sakurai, Hidehiro
Sumanene derivatives functionalized at the internal carbon.
Chemical communications (Cambridge, England), 2017, 53, 697-700
7119325 CIFC21 H12 O2P 319.98291; 9.98291; 11.95223
90; 90; 120
1031.56Ngamsomprasert, Niti; Dang, Jing-Shuang; Higashibayashi, Shuhei; Yakiyama, Yumi; Sakurai, Hidehiro
Sumanene derivatives functionalized at the internal carbon.
Chemical communications (Cambridge, England), 2017, 53, 697-700
7119326 CIFC53 H32 F6 N6 O8 S2 Zn2C 1 2/c 122.4106; 23.6354; 15.2117
90; 126.403; 90
6485.1Fan, Cong Bin; Liu, Zhi Qiang; Gong, Le Le; Zheng, An Min; Zhang, Le; Yan, Chang Sheng; Wu, Hui Qiong; Feng, Xue Feng; Luo, Feng
Photoswitching adsorption selectivity in a diarylethene-azobenzene MOF.
Chemical communications (Cambridge, England), 2017, 53, 763-766
7119327 CIFC18 H16 F N OP 1 21/c 19.793; 9.5921; 15.8816
90; 98.943; 90
1473.71Lonca, Geoffroy Hervé; Tejo, Ciputra; Chan, Hui Ling; Chiba, Shunsuke; Gagosz, Fabien
Gold(i)-catalyzed 6-endo-dig azide-yne cyclization: efficient access to 2H-1,3-oxazines.
Chemical communications (Cambridge, England), 2017, 53, 736-739
7119328 CIFC17 H13 Br F N OP c a 219.5444; 10.0871; 15.2076
90; 90; 90
1464.12Lonca, Geoffroy Hervé; Tejo, Ciputra; Chan, Hui Ling; Chiba, Shunsuke; Gagosz, Fabien
Gold(i)-catalyzed 6-endo-dig azide-yne cyclization: efficient access to 2H-1,3-oxazines.
Chemical communications (Cambridge, England), 2017, 53, 736-739
7119329 CIFC17 H13 Br F N OP 1 21/c 111.855; 16.44; 15.069
90; 91.469; 90
2935.9Lonca, Geoffroy Hervé; Tejo, Ciputra; Chan, Hui Ling; Chiba, Shunsuke; Gagosz, Fabien
Gold(i)-catalyzed 6-endo-dig azide-yne cyclization: efficient access to 2H-1,3-oxazines.
Chemical communications (Cambridge, England), 2017, 53, 736-739
7119330 CIFC16 H12 F N O2P 1 21/c 112.1739; 11.0034; 9.8232
90; 90.269; 90
1315.85Lonca, Geoffroy Hervé; Tejo, Ciputra; Chan, Hui Ling; Chiba, Shunsuke; Gagosz, Fabien
Gold(i)-catalyzed 6-endo-dig azide-yne cyclization: efficient access to 2H-1,3-oxazines.
Chemical communications (Cambridge, England), 2017, 53, 736-739
7119331 CIFC18 H13 B F7 N3 OP 1 21/c 115.2794; 9.0171; 13.5025
90; 111.891; 90
1726.18Sekhar, Adiki Raja; Sariki, Santhosh Kumar; Reddy, R. V. Ramana; Bisai, Alakesh; Sahu, Pushpendra Kumar; Tomar, Raghuvir S.; Sankar, Jeyaraman
Zwitterionic BODIPYs with large stokes shift: small molecular biomarkers for live cells.
Chemical communications (Cambridge, England), 2017, 53, 1096-1099
7119332 CIFC19 H16 B F7 N4P 1 21/c 115.712; 9.184; 13.544
90; 111.297; 90
1820.9Sekhar, Adiki Raja; Sariki, Santhosh Kumar; Reddy, R. V. Ramana; Bisai, Alakesh; Sahu, Pushpendra Kumar; Tomar, Raghuvir S.; Sankar, Jeyaraman
Zwitterionic BODIPYs with large stokes shift: small molecular biomarkers for live cells.
Chemical communications (Cambridge, England), 2017, 53, 1096-1099
7119333 CIFC35 H53 Br O2 P2 WP 1 21/n 111.41025; 13.66762; 23.3661
90; 100.054; 90
3588.01Hill, Anthony F.; Kong, Richard Y.
High oxidation state bromocarbyne complexes.
Chemical communications (Cambridge, England), 2017, 53, 759-762
7119334 CIFC66 H106 Br6 P4 W2P -111.714; 15.844; 20.4006
81.812; 88.384; 84.131
3727.68Hill, Anthony F.; Kong, Richard Y.
High oxidation state bromocarbyne complexes.
Chemical communications (Cambridge, England), 2017, 53, 759-762
7119335 CIFC56 H98 Br8 Cl4 P4 W2P 1 21/c 118.5723; 15.8298; 25.1171
90; 100.001; 90
7272.1Hill, Anthony F.; Kong, Richard Y.
High oxidation state bromocarbyne complexes.
Chemical communications (Cambridge, England), 2017, 53, 759-762
7119336 CIFC16.5 H11 N3 Ni0.5C 1 2/c 110.7913; 23.085; 9.7956
90; 98.37; 90
2414.3Yoshida, Takuya; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Enhancing the low-energy absorption band and charge mobility of antiaromatic Ni(II) norcorroles by their substituent effects.
Chemical communications (Cambridge, England), 2017, 53, 1112-1115
7119337 CIFC32 H23 N5 NiP 1 21/n 114.9222; 10.1071; 16.9856
90; 111.902; 90
2376.9Yoshida, Takuya; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Enhancing the low-energy absorption band and charge mobility of antiaromatic Ni(II) norcorroles by their substituent effects.
Chemical communications (Cambridge, England), 2017, 53, 1112-1115
7119338 CIFC32 H18 Cl2 F5 N5 NiP 1 21/c 116.003; 10.6329; 17.07
90; 100.125; 90
2859.4Yoshida, Takuya; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Enhancing the low-energy absorption band and charge mobility of antiaromatic Ni(II) norcorroles by their substituent effects.
Chemical communications (Cambridge, England), 2017, 53, 1112-1115
7119339 CIFC35 H29 N5 NiP 1 21/c 111.547; 7.327; 32.081
90; 96.234; 90
2698.2Yoshida, Takuya; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Enhancing the low-energy absorption band and charge mobility of antiaromatic Ni(II) norcorroles by their substituent effects.
Chemical communications (Cambridge, England), 2017, 53, 1112-1115
7119340 CIFC51 H31.5 F9 N7.5 Ni1.5P 1 21/c 117.128; 11.539; 21.492
90; 94.759; 90
4233Yoshida, Takuya; Sakamaki, Daisuke; Seki, Shu; Shinokubo, Hiroshi
Enhancing the low-energy absorption band and charge mobility of antiaromatic Ni(II) norcorroles by their substituent effects.
Chemical communications (Cambridge, England), 2017, 53, 1112-1115
7119341 CIFC34 H31 Cl N2 OP 1 21 19.9447; 9.7882; 14.404
90; 99.979; 90
1380.9Liu, Suna; Yang, Pu; Peng, Shiyong; Zhu, Chenghao; Cao, Shengyu; Li, Jian; Sun, Jiangtao
Gold-catalyzed sequential annulations towards 3,4-fused bi/tri-cyclic furans involving a [3+2+2]-cycloaddition.
Chemical communications (Cambridge, England), 2017, 53, 1152-1155
7119342 CIFC52 H84 P2 S4 Zr2C 1 2/c 124.7202; 13.679; 16.2972
90; 95.893; 90
5481.74Seitz, A. E.; Heinl, V.; Timoshkin, A. Y.; Scheer, M.
Transformation of nortricyclane type cage compounds P4S3, P4Se3 and As4S3 by [Cp''2Zr(CO)2].
Chemical communications (Cambridge, England), 2017, 53, 1172-1175
7119343 CIFC52 H84 P2 Se4 Zr2P 1 21/n 115.2831; 9.91947; 18.625
90; 102.835; 90
2753Seitz, A. E.; Heinl, V.; Timoshkin, A. Y.; Scheer, M.
Transformation of nortricyclane type cage compounds P4S3, P4Se3 and As4S3 by [Cp''2Zr(CO)2].
Chemical communications (Cambridge, England), 2017, 53, 1172-1175
7119344 CIFC80 H116 As2 S4 Zr2P 1 21/n 112.6043; 12.6538; 24.3651
90; 95.3864; 90
3868.89Seitz, A. E.; Heinl, V.; Timoshkin, A. Y.; Scheer, M.
Transformation of nortricyclane type cage compounds P4S3, P4Se3 and As4S3 by [Cp''2Zr(CO)2].
Chemical communications (Cambridge, England), 2017, 53, 1172-1175
7119345 CIFC17 H35 K N2 Si2P 1 21/c 18.7354; 23.0026; 11.6433
90; 100.207; 90
2302.5Boteju, Kasuni C.; Ellern, Arkady; Sadow, Aaron D.
Homoleptic organolanthanide compounds supported by the bis(dimethylsilyl)benzyl ligand.
Chemical communications (Cambridge, England), 2017, 53, 716-719
7119346 CIFC35.5 H63 La Si6P -312.438; 12.438; 16.1574
90; 90; 120
2164.7Boteju, Kasuni C.; Ellern, Arkady; Sadow, Aaron D.
Homoleptic organolanthanide compounds supported by the bis(dimethylsilyl)benzyl ligand.
Chemical communications (Cambridge, England), 2017, 53, 716-719
7119347 CIFC33 H57 Ce Si6P 1 21/c 122.3238; 19.8412; 19.9211
90; 116.076; 90
7925.5Boteju, Kasuni C.; Ellern, Arkady; Sadow, Aaron D.
Homoleptic organolanthanide compounds supported by the bis(dimethylsilyl)benzyl ligand.
Chemical communications (Cambridge, England), 2017, 53, 716-719
7119348 CIFC33 H57 Nd Si6P 1 21/c 122.3348; 19.8432; 19.8549
90; 116.017; 90
7907.9Boteju, Kasuni C.; Ellern, Arkady; Sadow, Aaron D.
Homoleptic organolanthanide compounds supported by the bis(dimethylsilyl)benzyl ligand.
Chemical communications (Cambridge, England), 2017, 53, 716-719
7119349 CIFC33 H57 Pr Si6P 1 21/c 122.331; 19.8399; 19.8802
90; 116.047; 90
7913.2Boteju, Kasuni C.; Ellern, Arkady; Sadow, Aaron D.
Homoleptic organolanthanide compounds supported by the bis(dimethylsilyl)benzyl ligand.
Chemical communications (Cambridge, England), 2017, 53, 716-719
7119364 CIFC32 H20 Cl2 Fe N4 O2P 1 21/n 110.2044; 12.8835; 19.3776
90; 93.6752; 90
2542.3Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119365 CIFC32 H20 Cl2 Fe N4 O2P 1 21/n 110.2113; 12.9889; 19.6876
90; 93.2672; 90
2606.99Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119366 CIFC32 H20 Cl2 Fe N4 O2P -110.2926; 13.0726; 19.6371
90.988; 93.801; 90.596
2635.8Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119367 CIFC32 H20 Cl2 Fe N4 O2P -110.3266; 13.1023; 19.6014
90.696; 93.869; 90.429
2645.8Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119368 CIFC32 H20 Cl2 Fe N4 O2P 1 21/n 110.3632; 13.1281; 19.5466
90; 94.034; 90
2652.71Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119369 CIFC32 H20 Cl2 Fe N4 O2P 1 21/n 110.397; 13.1513; 19.5205
90; 94.14; 90
2662.15Phonsri, Wasinee; Davies, Casey G.; Jameson, Guy N. L.; Moubaraki, Boujemaa; Ward, Jas S.; Kruger, Paul E.; Chastanet, Guillaume; Murray, Keith S.
Symmetry breaking above room temperature in an Fe(ii) spin crossover complex with an N4O2 donor set.
Chemical communications (Cambridge, England), 2017, 53, 1374-1377
7119370 CIFC35 H43 Fe N4 O11 SP 21 21 219.0301; 16.641; 25.46
90; 90; 90
3825.9Pulukkody, Randara; Chupik, Rachel B.; Montalvo, Steven K.; Khan, Sarosh; Bhuvanesh, Nattamai; Lim, Soon-Mi; Darensbourg, Marcetta Y.
Toward biocompatible dinitrosyl iron complexes: sugar-appended thiolates.
Chemical communications (Cambridge, England), 2017, 53, 1180-1183
7119371 CIFC30 H30 B N SC 1 2/c 113.7895; 19.91; 18.5249
90; 95.484; 90
5062.7Neena, Kalluvettukuzhy K.; Sudhakar, Pagidi; Dipak, Kumbhar; Thilagar, Pakkirisamy
Diarylboryl-phenothiazine based multifunctional molecular siblings.
Chemical communications (Cambridge, England), 2017, 53, 3641-3644
7119372 CIFC28 H26 B N SR 3 c :H18.7282; 18.7282; 34.3232
90; 90; 120
10425.8Neena, Kalluvettukuzhy K.; Sudhakar, Pagidi; Dipak, Kumbhar; Thilagar, Pakkirisamy
Diarylboryl-phenothiazine based multifunctional molecular siblings.
Chemical communications (Cambridge, England), 2017, 53, 3641-3644
7119390 CIFC55 H43 Cl N O6 S2C 1 2/c 131.6875; 12.3025; 24.4541
90; 111.423; 90
8874.4Du, Yanlong; Yu, Aimin; Jia, Jiru; Zhang, Youquan; Meng, Xiangtai
Direct N-H/α,α,β,β-C(sp(3))-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles.
Chemical communications (Cambridge, England), 2017, 53, 1684-1687
7119391 CIFC39 H36 Cl3 N3 O6 S2P -112.092; 12.945; 13.599
98.723; 112.832; 96.192
1906.4Du, Yanlong; Yu, Aimin; Jia, Jiru; Zhang, Youquan; Meng, Xiangtai
Direct N-H/α,α,β,β-C(sp(3))-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles.
Chemical communications (Cambridge, England), 2017, 53, 1684-1687
7119392 CIFC30 H28 N4 O4 SP 1 21/c 114.539; 10.3664; 17.82
90; 108.211; 90
2551.3Du, Yanlong; Yu, Aimin; Jia, Jiru; Zhang, Youquan; Meng, Xiangtai
Direct N-H/α,α,β,β-C(sp(3))-H functionalization of piperidine via an azomethine ylide route: synthesis of spirooxindoles bearing 3-substituted oxindoles.
Chemical communications (Cambridge, England), 2017, 53, 1684-1687
7119393 CIFC93 H110 Mg2 N10P 1 21/n 115.3537; 14.2772; 19.1707
90; 104.615; 90
4066.4Davin, Laia; McLellan, Ross; Hernán-Gómez, Alberto; Clegg, William; Kennedy, Alan R.; Mertens, Maria; Stepek, Iain A.; Hevia, Eva
Regioselective magnesiation of N-heterocyclic molecules: securing insecure cyclic anions by a β-diketiminate-magnesium clamp.
Chemical communications (Cambridge, England), 2017, 53, 3653-3656
7119394 CIFC32 H45 Mg N5P 1 21/n 111.5906; 15.2013; 17.8446
90; 98.976; 90
3105.6Davin, Laia; McLellan, Ross; Hernán-Gómez, Alberto; Clegg, William; Kennedy, Alan R.; Mertens, Maria; Stepek, Iain A.; Hevia, Eva
Regioselective magnesiation of N-heterocyclic molecules: securing insecure cyclic anions by a β-diketiminate-magnesium clamp.
Chemical communications (Cambridge, England), 2017, 53, 3653-3656
7119395 CIFC44 H55 F2 Mg N3 OP -19.2553; 12.7671; 16.8484
84.318; 82.946; 86.524
1963.7Davin, Laia; McLellan, Ross; Hernán-Gómez, Alberto; Clegg, William; Kennedy, Alan R.; Mertens, Maria; Stepek, Iain A.; Hevia, Eva
Regioselective magnesiation of N-heterocyclic molecules: securing insecure cyclic anions by a β-diketiminate-magnesium clamp.
Chemical communications (Cambridge, England), 2017, 53, 3653-3656
7119396 CIFC74 H102 Mg2 N6 OP -112.3525; 12.408; 22.7369
101.488; 92.55; 93.804
3401.6Davin, Laia; McLellan, Ross; Hernán-Gómez, Alberto; Clegg, William; Kennedy, Alan R.; Mertens, Maria; Stepek, Iain A.; Hevia, Eva
Regioselective magnesiation of N-heterocyclic molecules: securing insecure cyclic anions by a β-diketiminate-magnesium clamp.
Chemical communications (Cambridge, England), 2017, 53, 3653-3656
7119397 CIFC73 H96 Mg2 N8P -110.7648; 12.8654; 13.4034
96.729; 109.851; 103.994
1653.3Davin, Laia; McLellan, Ross; Hernán-Gómez, Alberto; Clegg, William; Kennedy, Alan R.; Mertens, Maria; Stepek, Iain A.; Hevia, Eva
Regioselective magnesiation of N-heterocyclic molecules: securing insecure cyclic anions by a β-diketiminate-magnesium clamp.
Chemical communications (Cambridge, England), 2017, 53, 3653-3656
7119398 CIFC24 H20 N0 O12 P4 Si ZrP 1 21/c 19.9688; 19.2157; 14.5392
90; 99.702; 90
2745.26Gao, Chao-Ying; Ai, Jing; Tian, Hong-Rui; Wu, Dai; Sun, Zhong-Ming
An ultrastable zirconium-phosphonate framework as bifunctional catalyst for highly active CO2 chemical transformation.
Chemical communications (Cambridge, England), 2017, 53, 1293-1296
7119399 CIFC39 H36 O4 SeP -19.1407; 10.98; 18.0686
105.432; 91.962; 108.604
1642.6Hu, Yimin; Ma, Jie; Li, Lidong; Hu, Qiong; Lv, Shuang; Liu, Baohua; Wang, Shaowu
Fused multifunctionalized dibenzoselenophenes from tetraynes.
Chemical communications (Cambridge, England), 2017, 53, 1542-1545
7119400 CIFC39 H36 O4 SeP 1 21/n 114.263; 8.8263; 27.54
90; 97.494; 90
3437.4Hu, Yimin; Ma, Jie; Li, Lidong; Hu, Qiong; Lv, Shuang; Liu, Baohua; Wang, Shaowu
Fused multifunctionalized dibenzoselenophenes from tetraynes.
Chemical communications (Cambridge, England), 2017, 53, 1542-1545
7119401 CIFC33 H22 Cl2 O4 SeP -111.1578; 11.3581; 12.6856
86.395; 80.464; 64.078
1425.9Hu, Yimin; Ma, Jie; Li, Lidong; Hu, Qiong; Lv, Shuang; Liu, Baohua; Wang, Shaowu
Fused multifunctionalized dibenzoselenophenes from tetraynes.
Chemical communications (Cambridge, England), 2017, 53, 1542-1545
7119402 CIFC38 H34 O4 SeP 1 21/c 111.8983; 24.716; 12.991
90; 120.114; 90
3304.7Hu, Yimin; Ma, Jie; Li, Lidong; Hu, Qiong; Lv, Shuang; Liu, Baohua; Wang, Shaowu
Fused multifunctionalized dibenzoselenophenes from tetraynes.
Chemical communications (Cambridge, England), 2017, 53, 1542-1545
7119403 CIFC54 H84 B Fe K N6 O10P 1 21/n 112.8202; 14.9253; 30.2522
90; 95.4151; 90
5762.8Hickey, Anne K.; Lutz, Sean A.; Chen, Chun-Hsing; Smith, Jeremy M.
Two-state reactivity in C-H activation by a four-coordinate iron(0) complex.
Chemical communications (Cambridge, England), 2017, 53, 1245-1248

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 8 | Next 100 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!