Crystallography Open Database

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7116521 CIFC78.5 H93 Cl N O17 P4P 1 21 113.9589; 37.935; 15.3453
90; 91.459; 90
8123.2Biavardi, Elisa; Ugozzoli, Franco; Massera, Chiara
Chemoselective recognition with phosphonate cavitands: the ephedrine over pseudoephedrine case
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3426-3429
7116522 CIFC79 H90 Cl N O15 P4P 1 21 113.917; 37.798; 15.357
90; 91.273; 90
8076Biavardi, Elisa; Ugozzoli, Franco; Massera, Chiara
Chemoselective recognition with phosphonate cavitands: the ephedrine over pseudoephedrine case
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3426-3429
7116523 CIFC78.5 H90 Cl N O15.5 P4P 1 21 113.898; 37.849; 15.383
90; 91.633; 90
8088.6Biavardi, Elisa; Ugozzoli, Franco; Massera, Chiara
Chemoselective recognition with phosphonate cavitands: the ephedrine over pseudoephedrine case
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3426-3429
7116556 CIFC324 H558 Co2 Cr21 F24 Fe4 N9 Ni3 O122C 1 2/c 163.4959; 38.2021; 71.4099
90; 114.799; 90
157244Whitehead, George F. S.; Teat, Simon J.; Gagnon, Kevin J.; Timco, Grigore A.; Winpenny, Richard E. P.
An extended framework of cages formed of pre-synthesised and functionalised heterometallic cages
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3533-3536
7116562 CIFC15 H26 O5 SiP c a 2115.0354; 6.2653; 36.895
90; 90; 90
3475.6Abe, Hideki; Itaya, Satoko; Sasaki, Kei; Kobayashi, Toyoharu; Ito, Hisanaka
Total synthesis of the proposed structure of a polyketide from Phialomyces macrosporus
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3586-3589
7116563 CIFC13 H16 O5P -17.353; 12.521; 13.79
109.346; 90.415; 98.193
1183.7Abe, Hideki; Itaya, Satoko; Sasaki, Kei; Kobayashi, Toyoharu; Ito, Hisanaka
Total synthesis of the proposed structure of a polyketide from Phialomyces macrosporus
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3586-3589
7116564 CIFC22 H36 O5 SiP 1 21/n 114.836; 9.2966; 18.3676
90; 113.488; 90
2323.4Abe, Hideki; Itaya, Satoko; Sasaki, Kei; Kobayashi, Toyoharu; Ito, Hisanaka
Total synthesis of the proposed structure of a polyketide from Phialomyces macrosporus
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3586-3589
7116565 CIFC89 H106 F12 N4 O22 P2C 1 2/c 118.69; 26.43; 43.505
90; 97.138; 90
21324Wang, Qi; Cheng, Ming; Zhao, Yue; Wu, Lin; Jiang, Juli; Wang, Leyong; Pan, Yi
A pillar[5]arene-fused cryptand: from orthogonal self-assembly to supramolecular polymer
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3623-3626
7116566 CIFC64 H76 N4 Sm2P b c a16.6036; 17.8851; 18.2024
90; 90; 90
5405.33Nocton, Grégory; Ricard, Louis
Reversible C‒C coupling in phenanthroline complexes of divalent samarium and thulium
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3578-3581
7116567 CIFC120 H164 N4 Sm2P -110.225; 12.304; 20.627
87.677; 87.886; 83.688
2575.8Nocton, Grégory; Ricard, Louis
Reversible C‒C coupling in phenanthroline complexes of divalent samarium and thulium
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3578-3581
7116568 CIFC94 H136 N4 O4.5 Sm2P 1 21/c 110.9726; 18.7116; 19.7467
90; 91.3117; 90
4053.23Nocton, Grégory; Ricard, Louis
Reversible C‒C coupling in phenanthroline complexes of divalent samarium and thulium
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3578-3581
7116569 CIFC113 H156 N4 Tm2P -110.148; 12.286; 20.481
87.531; 88.273; 84.59
2538.9Nocton, Grégory; Ricard, Louis
Reversible C‒C coupling in phenanthroline complexes of divalent samarium and thulium
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3578-3581
7116591 CIFC45 H62 N4 O9 RuP -116.0973; 18.0969; 20.125
90.43; 113.25; 99.817
5289.5Ivry, Elisa; Ben-Asuly, Amos; Goldberg, Israel; Lemcoff, N. Gabriel
Amino acids as chiral anionic ligands for ruthenium based asymmetric olefin metathesis
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3870-3873
7116592 CIFGe3.88 In22.12 O Se50I 41/a :222.4956; 22.4956; 37.984
90; 90; 90
19221.9Han, Xiaohui; Xu, Jin; Wang, Zhenqing; Liu, Dan; Wang, Cheng
A hybrid linkage mode between T2,2 and T3 selenide clusters
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3919-3922
7116593 CIFC432 H360 B28 F112 N72 O0 Pd6 Zn8P -3 1 c31.0248; 31.0248; 42.9572
90; 90; 120
35808Yang, Yang; Jia, Jian-Hua; Pei, Xiao-Li; Zheng, Hao; Nan, Zi-Ang; Wang, Quan-Ming
Diastereoselective synthesis of O symmetric heterometallic cubic cages
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3804-3807
7116594 CIFC456 H408 B28 F112 N72 O0 Pd6 Zn8P 4 3 225.9101; 25.9101; 25.9101
90; 90; 90
17394.3Yang, Yang; Jia, Jian-Hua; Pei, Xiao-Li; Zheng, Hao; Nan, Zi-Ang; Wang, Quan-Ming
Diastereoselective synthesis of O symmetric heterometallic cubic cages
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3804-3807
7116595 CIFC456 H408 B28 F112 N72 O0 Pd6 Zn8P 4 3 225.9709; 25.9709; 25.9709
90; 90; 90
17517.1Yang, Yang; Jia, Jian-Hua; Pei, Xiao-Li; Zheng, Hao; Nan, Zi-Ang; Wang, Quan-Ming
Diastereoselective synthesis of O symmetric heterometallic cubic cages
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3804-3807
7116596 CIFC67 H40 Cl2 N4 O7 Re2P 1 21/c 115.67; 16.5072; 21.2401
90; 96.244; 90
5461.54Saleh, Nidal; Srebro, Monika; Reynaldo, Thibault; Vanthuyne, Nicolas; Toupet, Loïc; Chang, Victoria Y.; Muller, Gilles; Williams, J. A. Gareth; Roussel, Christian; Autschbach, Jochen; Crassous, Jeanne
enantio-Enriched CPL-active helicene‒bipyridine‒rhenium complexes
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3754-3757
7116597 CIFC32 H23 B Cl4 F4 N3 O3 ReP 1 21/n 110.854; 24.7778; 13.4316
90; 110.589; 90
3381.54Saleh, Nidal; Srebro, Monika; Reynaldo, Thibault; Vanthuyne, Nicolas; Toupet, Loïc; Chang, Victoria Y.; Muller, Gilles; Williams, J. A. Gareth; Roussel, Christian; Autschbach, Jochen; Crassous, Jeanne
enantio-Enriched CPL-active helicene‒bipyridine‒rhenium complexes
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3754-3757
7116598 CIFC36.5 H25 Cl3 F6 N3 O3 P ReF d d 222.7551; 54.882; 11.6412
90; 90; 90
14538.1Saleh, Nidal; Srebro, Monika; Reynaldo, Thibault; Vanthuyne, Nicolas; Toupet, Loïc; Chang, Victoria Y.; Muller, Gilles; Williams, J. A. Gareth; Roussel, Christian; Autschbach, Jochen; Crassous, Jeanne
enantio-Enriched CPL-active helicene‒bipyridine‒rhenium complexes
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 3754-3757
7116611 CIFC24 H24 ZrP b c n8.3971; 12.4057; 17.927
90; 90; 90
1867.49Thapa, Surendra; Basnet, Prakash; Gurung, Santosh K.; Giri, Ramesh
Copper-catalysed cross-coupling of arylzirconium reagents with aryl and heteroaryl iodides
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 4009-4012
7116612 CIFCs2 H30.8 K10 Nb12 O65.4 Pt2P -110.5213; 12.6202; 15.122
96.136; 98.791; 96.912
1953.8Abramov, P. A.; Vicent, C.; Kompankov, N. B.; Gushchin, A. L.; Sokolov, M. N.
Platinum polyoxoniobates
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 4021-4023
7116613 CIFH36 K10 Na2 Nb12 O56 PtP a -318.1811; 18.1811; 18.1811
90; 90; 90
6009.8Abramov, P. A.; Vicent, C.; Kompankov, N. B.; Gushchin, A. L.; Sokolov, M. N.
Platinum polyoxoniobates
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 4021-4023
7116723 CIFC121 H149 N6 O2 P4 Y2P 1 21/c 118.5724; 19.0815; 33.6472
90; 101.101; 90
11701.1Rong, Weifeng; He, Dongliang; Wang, Meiyan; Mou, Zehuai; Cheng, Jianhua; Yao, Changguang; Li, Shihui; Trifonov, Alexander A.; Lyubov, Dmitrii M.; Cui, Dongmei
Neutral binuclear rare-earth metal complexes with four μ2-bridging hydrides
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 5063-5065
7116724 CIFC48 H56 Lu N3 P2I 2 2 213.164; 18.573; 19.615
90; 90; 90
4795.8Rong, Weifeng; He, Dongliang; Wang, Meiyan; Mou, Zehuai; Cheng, Jianhua; Yao, Changguang; Li, Shihui; Trifonov, Alexander A.; Lyubov, Dmitrii M.; Cui, Dongmei
Neutral binuclear rare-earth metal complexes with four μ2-bridging hydrides
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 5063-5065
7116725 CIFC108 H112 N6 P4 Y2I 2 2 213.1802; 18.73; 19.619
90; 90; 90
4843.2Rong, Weifeng; He, Dongliang; Wang, Meiyan; Mou, Zehuai; Cheng, Jianhua; Yao, Changguang; Li, Shihui; Trifonov, Alexander A.; Lyubov, Dmitrii M.; Cui, Dongmei
Neutral binuclear rare-earth metal complexes with four μ2-bridging hydrides
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 5063-5065
7116828 CIFC88 H60 F12 N12 O12 Zn2P 1 21/n 18.1943; 26.8625; 42.167
90; 90.213; 90
9281.7Prakasam, Thirumurugan; Lusi, Matteo; Nauha, Elisa; Olsen, John-Carl; Sy, Mohamadou; Platas-Iglesias, Carlos; Charbonnière, Loïc J.; Trabolsi, Ali
Dynamic stereoisomerization in inherently chiral bimetallic [2]catenanes
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 5840-5843
7116829 CIFC96 H68 F18 N12 O13 Zn2C 1 2 143.874; 8.3311; 29.743
90; 110.065; 90
10211.8Prakasam, Thirumurugan; Lusi, Matteo; Nauha, Elisa; Olsen, John-Carl; Sy, Mohamadou; Platas-Iglesias, Carlos; Charbonnière, Loïc J.; Trabolsi, Ali
Dynamic stereoisomerization in inherently chiral bimetallic [2]catenanes
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 5840-5843
7116868 CIFC28 H26 Er N5 O13A b a 217.572; 54.043; 9.58
90; 90; 90
9098Das, Chinmoy; Upadhyay, Apoorva; Vaidya, Shefali; Singh, Saurabh Kumar; Rajaraman, Gopalan; Shanmugam, Maheswaran
Origin of SMM behaviour in an asymmetric Er(III) Schiff base complex: a combined experimental and theoretical study
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 6137-6140
7116869 CIFC28 H26 Lu N5 O13A b a 217.439; 54.451; 9.5702
90; 90; 90
9088Das, Chinmoy; Upadhyay, Apoorva; Vaidya, Shefali; Singh, Saurabh Kumar; Rajaraman, Gopalan; Shanmugam, Maheswaran
Origin of SMM behaviour in an asymmetric Er(III) Schiff base complex: a combined experimental and theoretical study
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 6137-6140
7116960 CIFC26 H28 N8 O2P -19.5863; 13.8917; 20.1426
83.305; 76.31; 81.1
2565.9Haridas, V.; Sapala, Appa Rao; Jasinski, Jerry P.
Self-assembling triazolophanes: from croissants through donuts to spherical vesicles
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 6905-6908
7116979 CIFC10 H9 N O2 SP 1 21/n 111.222; 12.458; 13.769
90; 91.055; 90
1924.6Perez, Christian; Monserrat, Jean-Philippe; Chen, Yao; Cohen, Seth M.
Exploring hydrogen peroxide responsive thiazolidinone-based prodrugs
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7116-7119
7116980 CIFC10 H9 N O2 SP c a 2113.7485; 5.436; 25.063
90; 90; 90
1873.13Perez, Christian; Monserrat, Jean-Philippe; Chen, Yao; Cohen, Seth M.
Exploring hydrogen peroxide responsive thiazolidinone-based prodrugs
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7116-7119
7117009 CIFC38 H21 F5 S2C 1 2/c 145.2352; 6.6395; 22.441
90; 119.467; 90
5868Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117010 CIFC42 H29 F5 S2P -111.1959; 12.3836; 12.6296
101.538; 91.211; 91.197
1714.71Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117011 CIFC25 H21 B F10 SP 1 21/c 113.6064; 16.1319; 11.023
90; 91.753; 90
2418.38Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117012 CIFC24 H18 B Cl F10 SP 1 21/c 113.609; 16.1094; 10.9768
90; 91.466; 90
2405.69Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117013 CIFC31 H20 B Cl2 F15 SP -110.3691; 10.8688; 15.4492
85.529; 80.114; 69.229
1603.51Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117014 CIFC30 H18 B F15 SP -18.964; 10.7186; 15.817
78.9; 87.821; 81.241
1473.84Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117015 CIFC33 H27 B F15 P SP 1 21/n 110.6872; 20.2903; 16.7936
90; 96.71; 90
3616.7Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117016 CIFC24 H23 F5 SP 1 21/c 124.4977; 10.2132; 19.1177
90; 112.3; 90
4425.51Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117017 CIFC22 H21 F5 S2P 1 21/c 123.7477; 10.2283; 19.1342
90; 111.487; 90
4324.66Eller, Christina; Kehr, Gerald; Daniliuc, Constantin G.; Stephan, Douglas W.; Erker, Gerhard
Thiophene synthesis via 1,1-carboboration
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7226-7229
7117063 CIFC18 H24 N5 O13 P3 Zn3P -19.2153; 11.1328; 15.2684
70.278; 83.973; 71.336
1396.98Wang, Chih-Min; Chang, Tsung-Yuan; Lee, Li-Wei; Lin, Hsiu-Mei; Lu, Kuang-Lieh; Lii, Kwang-Hwa
The first zinc phosphite with remarkable structural and functional transformations
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7824-7826
7117064 CIFC18 H18 N5 O10 P3 Zn3P -19.149; 11.202; 14.628
73.526; 88.045; 71.284
1358.9Wang, Chih-Min; Chang, Tsung-Yuan; Lee, Li-Wei; Lin, Hsiu-Mei; Lu, Kuang-Lieh; Lii, Kwang-Hwa
The first zinc phosphite with remarkable structural and functional transformations
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7824-7826
7117065 CIFC18 H16 N5 O9 P3 Zn3P -19.578; 11.517; 13.244
76.705; 88.391; 69.043
1325.4Wang, Chih-Min; Chang, Tsung-Yuan; Lee, Li-Wei; Lin, Hsiu-Mei; Lu, Kuang-Lieh; Lii, Kwang-Hwa
The first zinc phosphite with remarkable structural and functional transformations
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 7824-7826
7117091 CIFC43 H39 Cu F12 N5 P2P 1 21/n 112.70025; 21.30927; 15.21998
90; 93.2975; 90
4112.21Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117092 CIFC90 H78 Cl2 Cu2 Fe N8 O8P 1 21/n 118.1611; 52.0625; 20.5495
90; 106.087; 90
18669Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117093 CIFC22 H15 Fe I N2P 1 21/c 15.8216; 15.604; 19.8079
90; 91.3; 90
1798.89Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117094 CIFC34 H22 Fe N4P 1 21/n 115.622; 9.169; 17.531
90; 102.084; 90
2455.5Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117095 CIFC22 H16 Fe N2P n a 2123.8585; 6.8313; 10.025
90; 90; 90
1633.92Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117096 CIFC18 H16 F6 Fe N PP 1 21 17.396; 10.9122; 11.2342
90; 104.382; 90
878.26Scottwell, Synøve Ø.; Elliott, Anastasia B. S.; Shaffer, Karl J.; Nafady, Ayman; McAdam, C. John; Gordon, Keith C.; Crowley, James D.
Chemically and electrochemically induced expansion and contraction of a ferrocene rotor
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8161-8164
7117132 CIFC18 H12 Cl N O3P 21 21 219.3195; 10.8944; 14.3609
90; 90; 90
1458.07Lin, Youqiang; Yang, Limin; Deng, Yue; Zhong, Guofu
Cooperative catalysis of N-heterocyclic carbene and Brønsted acid for a highly enantioselective route to unprotected spiro-indoline-pyrans
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 8330-8333
7117209 CIFC25 H21 Br N2 O2P 1 21 110.912; 8.3793; 11.228
90; 93.81; 90
1024.4Gao, Zhong-Hua; Chen, Xiang-Yu; Cheng, Jin-Tang; Liao, Wei-Lin; Ye, Song
N-Heterocyclic carbene-catalyzed [2+3] cyclocondensation of α-chloroaldehydes with azomethine imines
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 9328-9331
7117226 CIFC127 H224 In5 N29 O87P 1 21/c 115.3713; 37.512; 38.979
90; 105.255; 90
21684Song, Bai-Qiao; Wang, Xin-Long; Zhang, Yu-Teng; Wu, Xue-Song; Liu, Hong-Sheng; Shao, Kui-Zhan; Su, Zhong-Min
Periodic tiling of triangular and square nanotubes in a cationic metal-organic framework for selective anion exchange
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 9515-9518
7117402 CIFC20 H18 OP -19.39; 15.536; 17.758
64.69; 79.19; 85.9
2300Pérez, Manuel; Mahdi, Tayseer; Hounjet, Lindsay J.; Stephan, Douglas W.
Electrophilic phosphonium cations catalyze hydroarylation and hydrothiolation of olefins
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11301-11304
7117413 CIFC26 H21 N OC 1 2/c 128.0546; 9.681; 15.0716
90; 109.781; 90
3851.9Ghosh, Abhijit; Sengupta, Archya; Chattopadhyay, Ansuman; Das, Debasis
Lysine triggered ratiometric conversion of dynamic to static excimer of a pyrene derivative: aggregation-induced emission, nanomolar detection and human breast cancer cell (MCF7) imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11455-11458
7117463 CIFC11 H18 N2 OP 21 21 217.3992; 9.2492; 18.3176
90; 90; 90
1253.6Su, Wei; Gong, Tian-Jun; Xiao, Bin; Fu, Yao
Rhodium(III)-catalyzed cyanation of vinylic C‒H bonds: N-cyano-N-phenyl-p-toluenesulfonamide as a cyanation reagent
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11848-11851
7117464 CIFC26 H18P 1 21/c 117.973; 7.352; 6.245
90; 90.646; 90
825.1Liu, Jie; Dong, Huanli; Wang, Zongrui; Ji, Deyang; Cheng, Changli; Geng, Hua; Zhang, Hantang; Zhen, Yonggang; Jiang, Lang; Fu, Hongbing; Bo, Zhishan; Chen, Wei; Shuai, Zhigang; Hu, Wenping
Thin film field-effect transistors of 2,6-diphenyl anthracene (DPA)
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11777-11779
7117486 CIFC76 H92 Cu4 N8 SP -4 3 n21.82156; 21.82156; 21.82156
90; 90; 90
10391Johnson, Brittany J.; Antholine, William E.; Lindeman, Sergey V.; Mankad, Neal P.
A Cu4S model for the nitrous oxide reductase active sites supported only by nitrogen ligands
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 11860-11863
7117552 CIFC5 H8 B F3 N2P 1 21/m 17.169; 6.8769; 7.474
90; 105.675; 90
354.77Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]‒NHC‒BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117553 CIFC5 H7 B F3 N3 O2P 1 21/c 17.4533; 9.5695; 11.8645
90; 105.049; 90
817.21Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]‒NHC‒BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117554 CIFC9 H9 B F3 N3 O2P 21 21 217.5804; 7.9279; 18.431
90; 90; 90
1107.6Chansaenpak, Kantapat; Wang, Mengzhe; Wu, Zhanhong; Zaman, Rehmat; Li, Zibo; Gabbaï, François P
[^18^F]‒NHC‒BF~3~ adducts as water stable radio-prosthetic groups for PET imaging
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 12439-12442
7117651 CIFC32 H48 N5 PtP 1 21/c 122.614; 8.529; 17.808
90; 107.877; 90
3269Ogawa, Tomohiro; Yoshida, Masaki; Ohara, Hiroki; Kobayashi, Atsushi; Kato, Masako
A dual-emissive ionic liquid based on an anionic platinum(II) complex
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 13377-13380
7117652 CIFC31 H30 K2 N6 O3 Pt2P 1 21/c 119.743; 12.197; 14.509
90; 108.445; 90
3314.4Ogawa, Tomohiro; Yoshida, Masaki; Ohara, Hiroki; Kobayashi, Atsushi; Kato, Masako
A dual-emissive ionic liquid based on an anionic platinum(II) complex
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 13377-13380
7117995 CIFC26 H15 B F2 I2C 1 2/c 120.082; 9.3614; 14.777
90; 126.854; 90
2222.9Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117996 CIFC26 H15 B Br4P 1 21/c 112.6333; 14.6789; 12.1639
90; 94.908; 90
2247.4Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117997 CIFC26 H15 BP 21 21 213.9791; 19.948; 20.208
90; 90; 90
1604Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7117998 CIFC31 H20 B NF -4 3 c48.2907; 48.2907; 48.2907
90; 90; 90
112614Schickedanz, Kai; Trageser, Timo; Bolte, Michael; Lerner, Hans-Wolfram; Wagner, Matthias
A boron-doped helicene as a highly soluble, benchtop-stable green emitter
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 15808-15810
7118020 CIFC116 H128 Cl4 N12 O12P 1 21 19.2218; 27.5508; 24.8963
90; 92.701; 90
6318.3Zhao, Xiaohu; Liu, Xiaohua; Xiong, Qian; Mei, Hongjiang; Ma, Baiwei; Lin, Lili; Feng, Xiaoming
The asymmetric synthesis of polycyclic 3-spirooxindole alkaloids via the cascade reaction of 2-isocyanoethylindoles
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16076-16079
7118048 CIFC69 H66 Cd4 N12 O29R 3 2 :H26.9207; 26.9207; 20.9044
90; 90; 120
13120.2Wu, Xin; Zhang, Hua-Bin; Xu, Zhong-Xuan; Zhang, Jian
Asymmetric induction in homochiral MOFs: from interweaving double helices to single helices
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16331-16333
7118049 CIFC69 H66 Cd4 N12 O29R 3 2 :H26.8706; 26.8706; 20.9
90; 90; 120
13068.7Wu, Xin; Zhang, Hua-Bin; Xu, Zhong-Xuan; Zhang, Jian
Asymmetric induction in homochiral MOFs: from interweaving double helices to single helices
Chemical Communications (Cambridge, United Kingdom), 2015, 51, 16331-16333
7118180 CIFC34 H29 Cl2 N3 O6 SP -19.468; 12.672; 14.441
73.289; 72.517; 76.408
1561.7Blair, Lachlan M.; Sperry, Jonathan
Total syntheses of (±)-spiroindimicins B and C enabled by a late-stage Schöllkopf‒Magnus‒Barton‒Zard (SMBZ) reaction
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 800-802
7118181 CIFC13 H16 Fe N10 S2P 1 21/n 18.496; 9.275; 25.99
90; 97.228; 90
2032Hagiwara, Hiroaki; Okada, Shohei
A polymorphism-dependent T1/2 shift of 100 K in a hysteretic spin-crossover complex related to differences in intermolecular weak CH⋯X hydrogen bonds (X = S vs. S and N)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 815-818
7118182 CIFC13 H16 Fe N10 S2P 1 21/n 18.1325; 8.9739; 26.23
90; 93.858; 90
1909.9Hagiwara, Hiroaki; Okada, Shohei
A polymorphism-dependent T1/2 shift of 100 K in a hysteretic spin-crossover complex related to differences in intermolecular weak CH⋯X hydrogen bonds (X = S vs. S and N)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 815-818
7118183 CIFC13 H16 Fe N10 S2C 1 2/c 116.324; 8.928; 13.831
90; 105.685; 90
1940.7Hagiwara, Hiroaki; Okada, Shohei
A polymorphism-dependent T1/2 shift of 100 K in a hysteretic spin-crossover complex related to differences in intermolecular weak CH⋯X hydrogen bonds (X = S vs. S and N)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 815-818
7118184 CIFC13 H16 Fe N10 S2C 1 2/c 115.27; 9.786; 13.27
90; 110.53; 90
1857Hagiwara, Hiroaki; Okada, Shohei
A polymorphism-dependent T1/2 shift of 100 K in a hysteretic spin-crossover complex related to differences in intermolecular weak CH⋯X hydrogen bonds (X = S vs. S and N)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 815-818
7118191 CIFC39 H36 F9 N O9 P3 S3 SbP b c n12.2821; 16.7365; 44.4675
90; 90; 90
9140.7Chitnis, Saurabh S.; Vos, Kevin A.; Burford, Neil; McDonald, Robert; Ferguson, Michael J.
Distinction between coordination and phosphine ligand oxidation: interactions of di- and triphosphines with Pn^3+^ (Pn = P, As, Sb, Bi)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 685-688
7118192 CIFC30 H25 F9 N O9 P2 S3 SbP 1 21/n 19.1263; 19.3196; 21.6426
90; 99.3749; 90
3765Chitnis, Saurabh S.; Vos, Kevin A.; Burford, Neil; McDonald, Robert; Ferguson, Michael J.
Distinction between coordination and phosphine ligand oxidation: interactions of di- and triphosphines with Pn^3+^ (Pn = P, As, Sb, Bi)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 685-688
7118193 CIFC29 H24 F9 O9 P2 S3 SbP 1 21/n 113.3718; 17.5496; 15.4871
90; 102.96; 90
3541.8Chitnis, Saurabh S.; Vos, Kevin A.; Burford, Neil; McDonald, Robert; Ferguson, Michael J.
Distinction between coordination and phosphine ligand oxidation: interactions of di- and triphosphines with Pn^3+^ (Pn = P, As, Sb, Bi)
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 685-688
7118194 CIFC14 H13 Dy N8 O8 SP -19.3478; 10.5315; 11.3151
69.422; 77.825; 77.336
1006.5Yutronkie, Nathan J.; Kühne, Irina A; Korobkov, Ilia; Brusso, Jaclyn L.; Murugesu, Muralee
Connecting mononuclear dysprosium single-molecule magnets to form dinuclear complexes via in situ ligand oxidation
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 677-680
7118195 CIFC14 H13 N8 O8 S YP -19.347; 10.531; 11.323
69.422; 77.684; 77.232
1006.4Yutronkie, Nathan J.; Kühne, Irina A; Korobkov, Ilia; Brusso, Jaclyn L.; Murugesu, Muralee
Connecting mononuclear dysprosium single-molecule magnets to form dinuclear complexes via in situ ligand oxidation
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 677-680
7118228 CIFC25 H21 Co N7 O5 S2P 21 21 2110.692; 11.464; 24.031
90; 90; 90
2945.6Dey, Mamon; Dutta, Snigdha; Sarma, Bipul; Deka, Ramesh Ch.; Gogoi, Nayanmoni
Modulation of the coordination environment: a convenient approach to tailor magnetic anisotropy in seven coordinate Co(II) complexes
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 753-756
7118229 CIFC23 H21 Co N5 O4C m c 2126.039; 11.4044; 7.3288
90; 90; 90
2176.35Dey, Mamon; Dutta, Snigdha; Sarma, Bipul; Deka, Ramesh Ch.; Gogoi, Nayanmoni
Modulation of the coordination environment: a convenient approach to tailor magnetic anisotropy in seven coordinate Co(II) complexes
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 753-756
7118453 CIFC78 H58 Cu7 I6 N22 O2C 1 2/c 132.206; 8.802; 30.44
90; 108.12; 90
8201.1Jiang, Wei; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang
Porphyrin-based mixed-valent Ag(I)/Ag(II) and Cu(I)/Cu(II) networks as efficient heterogeneous catalysts for the azide-alkyne "click" reaction and promising oxidation of ethylbenzene
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 1373-1376
7118454 CIFC158 H108 Ag4 N42 O6C 1 2/c 122.375; 17.788; 35.564
90; 95.971; 90
14077.9Jiang, Wei; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang
Porphyrin-based mixed-valent Ag(I)/Ag(II) and Cu(I)/Cu(II) networks as efficient heterogeneous catalysts for the azide-alkyne "click" reaction and promising oxidation of ethylbenzene
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 1373-1376
7118455 CIFC15 H13 N3P 1 21 17.982; 5.766; 13.788
90; 100.341; 90
624.3Jiang, Wei; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang
Porphyrin-based mixed-valent Ag(I)/Ag(II) and Cu(I)/Cu(II) networks as efficient heterogeneous catalysts for the azide-alkyne "click" reaction and promising oxidation of ethylbenzene
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 1373-1376
7118456 CIFC15 H12 F N3P 1 c 15.673; 15.311; 15.16
90; 103.5; 90
1280.4Jiang, Wei; Yang, Jin; Liu, Ying-Ying; Ma, Jian-Fang
Porphyrin-based mixed-valent Ag(I)/Ag(II) and Cu(I)/Cu(II) networks as efficient heterogeneous catalysts for the azide-alkyne "click" reaction and promising oxidation of ethylbenzene
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 1373-1376
7118643 CIFC6 F5 NC 1 2 113.77; 5.569; 9.822
90; 127.333; 90
598.9Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118644 CIFC12 H2 Br2 F6 N2P 1 21/c 111.412; 10.891; 11.216
90; 104.541; 90
1349.4Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118645 CIFC12 H2 Br2 F6 N2P 1 21/c 111.822; 5.6611; 20.062
90; 92.243; 90
1341.6Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118646 CIFC26 H14 F8 I2 N4C 1 2/c 128.3; 5.4157; 17.841
90; 96.287; 90
2717.9Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118647 CIFC18 H12 F8 I2 N4P 1 2/c 120.39; 6.3311; 17.654
90; 108.999; 90
2154.8Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118648 CIFC16 H8 F8 I2 N2 S2C 1 2/c 132.485; 5.4079; 11.3764
90; 91.042; 90
1998.2Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118649 CIFC12 F10 N2C 1 2/c 117.098; 7.5871; 8.8151
90; 95.309; 90
1138.6Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118650 CIFC12 H2 Br2 F6 N2P 1 21/c 110.63; 4.7239; 12.695
90; 101.917; 90
623.74Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118651 CIFC6 H Br F3 NP 1 21/c 14.446; 15.197; 9.65
90; 91.628; 90
651.7Bushuyev, Oleksandr S.; Tomberg, Anna; Vinden, Joanna R.; Moitessier, Nicolas; Barrett, Christopher J.; Friščić, Tomislav
Azo⋯phenyl stacking: a persistent self-assembly motif guides the assembly of fluorinated cis-azobenzenes into photo-mechanical needle crystals
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 2103-2106
7118895 CIFBa25 Cl18 N19 Nb5P -112.5942; 13.5297; 20.635
89.813; 89.59; 87.684
3513.1Francesconi, M. Grazia; Barker, Marten G.; Wilson, Claire
Novel ternary N-containing mixed-anion compounds with ionic and covalent features
Chemical Communications (Cambridge, United Kingdom), 2002, 1358-1359
7118896 CIFC44 H43 Ag3 N9 O10.5 S4P 1 21/n 118.749; 12.78; 21.716
90; 99.729; 90
5129Caradoc-Davies, Paula L.; Hanton, Lyall R.; Lee, Kitty
Extension of a π-stacked N~2~S ligand to form bi- and tri-nuclear silver(I) complexes
Chemical Communications (Cambridge, United Kingdom), 2000, 783-784
7118978 CIFC21 H15 N O6P 1 21/n 17.235; 27.116; 50.042
90; 92.752; 90
9806Nandi, Shyamapada; Chakraborty, Debanjan; Vaidhyanathan, Ramanathan
A permanently porous single molecule H-bonded organic framework for selective CO2 capture
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 7249-7252
7118979 CIFC21 H15 N O6P 1 21/n 17.235; 27.116; 50.042
90; 92.752; 90
9806Nandi, Shyamapada; Chakraborty, Debanjan; Vaidhyanathan, Ramanathan
A permanently porous single molecule H-bonded organic framework for selective CO2 capture
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 7249-7252
7119100 CIFC21 H17 Br N4 O5 SC 1 2 138.802; 5.04894; 10.781
90; 94.337; 90
2106.05Knipe, Peter C.; Thompson, Sam; Hamilton, Andrew D.
Acid-mediated topological control in a functionalized foldamer
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 6521-6524
7119154 CIFC4 H Ne0.46 Ni O3R -3 :H25.7542; 25.7542; 6.755
90; 90; 120
3880.18Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119155 CIFC4 H Ne1.045 Ni O3R -3 :H25.7611; 25.7611; 6.7565
90; 90; 120
3883.12Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119156 CIFC8.5 H7 Cu N5 Ne0.446 O2C 1 2/c 128.6315; 9.2743; 9.2833
90; 116.615; 90
2203.9Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119157 CIFC8.5 H7 Cu N5 Ne0.316 O2C 1 2/c 128.6841; 9.2655; 9.3005
90; 116.369; 90
2214.63Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119158 CIFC4 H Ne0.223 Ni O3R -3 :H25.7522; 25.7522; 6.7576
90; 90; 120
3881.07Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119159 CIFC8.5 H7 Cu N5 Ne0.179 O2C 1 2/c 128.7444; 9.2672; 9.3295
90; 116.097; 90
2231.83Wood, Peter A.; Sarjeant, Amy A.; Yakovenko, Andrey A.; Ward, Suzanna C.; Groom, Colin R.
Capturing neon – the first experimental structure of neon trapped within a metal-organic environment
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 10048-10051
7119444 CIFC26 H18 F2 N2 O4P -16.0426; 12.222; 15.374
78.111; 79.431; 87.801
1092.2Xu, Hui; Zhou, Bei; Zhou, Pan; Zhou, Jie; Shen, Yuehai; Yu, Fu-Chao; Lu, Ling-Ling
Insights into the unexpected chemoselectivity in Brønsted acid catalyzed cyclization of isatins with enaminones: convenient synthesis of pyrrolo[3,4-c]quinolin-1-ones and spirooxindoles
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 8002-8005
7119445 CIFC31 H21 F N4 O4C 1 c 16.522; 19.035; 20.25
90; 92.66; 90
2511.3Xu, Hui; Zhou, Bei; Zhou, Pan; Zhou, Jie; Shen, Yuehai; Yu, Fu-Chao; Lu, Ling-Ling
Insights into the unexpected chemoselectivity in Brønsted acid catalyzed cyclization of isatins with enaminones: convenient synthesis of pyrrolo[3,4-c]quinolin-1-ones and spirooxindoles
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 8002-8005
7119452 CIFC111 H98 Ag2 Au6 B4 F16 N6 O17 P6P -115.9788; 16.3669; 29.5491
78.976; 80.628; 61.755
6658.6Liu, Xiao-Yun; Yang, Yang; Lei, Zhen; Guan, Zong-Jie; Wang, Quan-Ming
Luminescence responsive intracluster rearrangements of gold(I)-silver(I) clusters triggered by acetonitrile
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 8022-8025
7119453 CIFC121 H102 Ag2 Au6 B4 F16 N12 O12 P6R -3 c23.7002; 23.7002; 49.407
90; 90; 120
24033.8Liu, Xiao-Yun; Yang, Yang; Lei, Zhen; Guan, Zong-Jie; Wang, Quan-Ming
Luminescence responsive intracluster rearrangements of gold(I)-silver(I) clusters triggered by acetonitrile
Chemical Communications (Cambridge, United Kingdom), 2016, 52, 8022-8025
7119524 CIFC148 H166 F24 N14 O33 P4P 1 21/c 126.2806; 10.5229; 28.8376
90; 104.925; 90
7705.9Wei, Peifa; Wang, Haoze; Jie, Kecheng; Huang, Feihe
Taco complex-templated highly regio- and stereo-selective photodimerization of a coumarin-containing crown ether
Chemical Communications (Cambridge, United Kingdom), 2017, 53, 1688-1691
7119525 CIFC74 H87 F18 N3 O18 P3P -112.9533; 13.437; 26.4914
82.573; 79.383; 65.221
4107.7Wei, Peifa; Wang, Haoze; Jie, Kecheng; Huang, Feihe
Taco complex-templated highly regio- and stereo-selective photodimerization of a coumarin-containing crown ether
Chemical Communications (Cambridge, United Kingdom), 2017, 53, 1688-1691
7120979 CIFC26 H42 B N7 O2 Te WP -110.0038; 10.0481; 16.8445
96.049; 93.448; 111.328
1559.57Frogley, Benjamin J.; Hill, Anthony F.; Manzano, Richard A.; Sharma, Manab
Bis(alkylidynyl)tellurides and ditellurides
Chemical Communications (Cambridge, United Kingdom), 2018, 54, 1702-1705
7120980 CIFC24 H27 B N6 O2 Te WP -111.1515; 14.7348; 17.8819
70.872; 89.962; 75.377
2675.28Frogley, Benjamin J.; Hill, Anthony F.; Manzano, Richard A.; Sharma, Manab
Bis(alkylidynyl)tellurides and ditellurides
Chemical Communications (Cambridge, United Kingdom), 2018, 54, 1702-1705
7120981 CIFC36 H44 B2 N12 O4 Te2 W2I 1 2/a 120.1187; 13.9835; 36.0701
90; 104.18; 90
9838.4Frogley, Benjamin J.; Hill, Anthony F.; Manzano, Richard A.; Sharma, Manab
Bis(alkylidynyl)tellurides and ditellurides
Chemical Communications (Cambridge, United Kingdom), 2018, 54, 1702-1705
7120982 CIFC51 H74 B2 N12 O4 Te W2P 1 21/c 110.4143; 25.0854; 22.5482
90; 102.335; 90
5754.7Frogley, Benjamin J.; Hill, Anthony F.; Manzano, Richard A.; Sharma, Manab
Bis(alkylidynyl)tellurides and ditellurides
Chemical Communications (Cambridge, United Kingdom), 2018, 54, 1702-1705
7121272 CIFC19 H25 B N6 O2 Te WP -110.285; 11.7366; 20.8637
90.5; 100.717; 103.866
2398.69Frogley, Benjamin J.; Hill, Anthony F.; Manzano, Richard A.; Sharma, Manab
Bis(alkylidynyl)tellurides and ditellurides
Chemical Communications (Cambridge, United Kingdom), 2018, 54, 1702-1705

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