Crystallography Open Database

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Searching journal of publication like 'Chemical communications (Cambridge, England)' volume of publication is 54

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7120959 CIFC48 H50 Al2P -111.0642; 11.5289; 16.885
99.424; 98.234; 111.443
1928.7Urwin, Stephanie J.; Nichol, Gary S.; Cowley, Michael J.
Aluminium-mediated carbon-carbon coupling of an isonitrile.
Chemical communications (Cambridge, England), 2018, 54, 378-380
7120960 CIFC37 H26 Br N O3P 21 21 218.0961; 18.4979; 9.1885
90; 90; 90
3075.8Yan, Jun; Shi, Kuangxi; Zhao, Chengtao; Ding, Liyuan; Jiang, Shengsheng; Yang, Limin; Zhong, Guofu
NHC-catalyzed [4+2] cycloaddition reactions for the synthesis of 3'-spirocyclic oxindoles via a C-F bond cleavage protocol.
Chemical communications (Cambridge, England), 2018, 54, 1567-1570
7120961 CIFC18 H19 N O4P -19.8925; 12.4541; 14.3675
96.459; 109.369; 103.883
1585.09Zheng, Long-Sheng; Férard, Charlène; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Rhodium-mediated asymmetric transfer hydrogenation: a diastereo- and enantioselective synthesis of syn-α-amido β-hydroxy esters.
Chemical communications (Cambridge, England), 2018, 54, 283-286
7120962 CIFC15 H15 N O4 SP 21 21 217.9135; 9.874; 19.0229
90; 90; 90
1486.41Zheng, Long-Sheng; Férard, Charlène; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Rhodium-mediated asymmetric transfer hydrogenation: a diastereo- and enantioselective synthesis of syn-α-amido β-hydroxy esters.
Chemical communications (Cambridge, England), 2018, 54, 283-286
7120963 CIFC16 H18 N2 O5P 21 21 219.0313; 11.8519; 14.6499
90; 90; 90
1568.1Zheng, Long-Sheng; Férard, Charlène; Phansavath, Phannarath; Ratovelomanana-Vidal, Virginie
Rhodium-mediated asymmetric transfer hydrogenation: a diastereo- and enantioselective synthesis of syn-α-amido β-hydroxy esters.
Chemical communications (Cambridge, England), 2018, 54, 283-286
7120964 CIFC16 H13 N SP 1 21/n 19.8465; 10.1124; 26.1644
90; 90.975; 90
2604.9Wang, Tong-Lin; Liu, Xiao-Jun; Huo, Cong-De; Wang, Xi-Cun; Quan, Zheng-Jun
Base-catalyzed thio-lactamization of 2-(1-arylvinyl)anilines with CS<sub>2</sub> for the synthesis of quinoline-2-thiones.
Chemical communications (Cambridge, England), 2018, 54, 499-502
7120965 CIFC45.5 H24 N4 Ni2 O14 P4P -19.561; 15.086; 16.722
94.723; 97.602; 97.88
2356Rhauderwiek, Timo; Wolkersdörfer, Konrad; Øien-Ødegaard, Sigurd; Lillerud, Karl-Petter; Wark, Michael; Stock, Norbert
Crystalline and permanently porous porphyrin-based metal tetraphosphonates.
Chemical communications (Cambridge, England), 2018, 54, 389-392
7120966 CIFC107 H95 Cl25 N4 O2 Pd2P c c n20.571; 23.494; 24.097
90; 90; 90
11646Vasiuta, Roman; Stockert, Alexander; Plenio, Herbert
Alternating ring-opening metathesis polymerization by Grubbs-type catalysts with N-pentiptycenyl, N-alkyl-NHC ligands.
Chemical communications (Cambridge, England), 2018, 54, 1706-1709
7120967 CIFC100 H52 Cu5 N4 O20I m m m26.294; 34.046; 34.098
90; 90; 90
30525Wang, Xun; Gao, Wen-Yang; Niu, Zheng; Wojtas, Lukasz; Perman, Jason A.; Chen, Yu-Sheng; Li, Zhong; Aguila, Briana; Ma, Shengqian
A metal-metalloporphyrin framework based on an octatopic porphyrin ligand for chemical fixation of CO<sub>2</sub> with aziridines.
Chemical communications (Cambridge, England), 2018, 54, 1170-1173
7120968 CIFC74 H142 Ge2 Si14P 1 21/n 113.4049; 33.992; 20.3454
90; 91.9033; 90
9265.5Sugahara, Tomohiro; Guo, Jing-Dong; Sasamori, Takahiro; Nagase, Shigeru; Tokitoh, Norihiro
Reversible addition of terminal alkenes to digermynes.
Chemical communications (Cambridge, England), 2018, 54, 519-522
7120969 CIFC56 H106 Ge2 Si8P -112.8999; 16.643; 17.7075
88.806; 75.528; 67.21
3381.4Sugahara, Tomohiro; Guo, Jing-Dong; Sasamori, Takahiro; Nagase, Shigeru; Tokitoh, Norihiro
Reversible addition of terminal alkenes to digermynes.
Chemical communications (Cambridge, England), 2018, 54, 519-522
7120970 CIFC66 H146 Ge2 Si14P -114.6873; 17.2952; 18.3289
92.502; 104.946; 91.16
4491.71Sugahara, Tomohiro; Guo, Jing-Dong; Sasamori, Takahiro; Nagase, Shigeru; Tokitoh, Norihiro
Reversible addition of terminal alkenes to digermynes.
Chemical communications (Cambridge, England), 2018, 54, 519-522
7120971 CIFC76 H65 Cr N8 O3 P2P -112.6533; 13.479; 19.7139
78.895; 81.527; 80.413
3230.1Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120972 CIFC38 H21 Cr N8P 1 21/n 110.0731; 12.0863; 22.7664
90; 96.395; 90
2754.48Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120973 CIFC60 H71 Cr Li N8 O10P 1 21/c 112.259; 27.9724; 17.8044
90; 108.65; 90
5784.8Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120974 CIFC36 H25.51 Cr K N8 OP 1 21/c 112.4386; 14.7836; 16.988
90; 108.199; 90
2967.61Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120975 CIFC79 H44 Cr2 N16 O4P m -3 n17.1137; 17.1137; 17.1137
90; 90; 90
5012.2Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120976 CIFC182 H84 Cr4 I2 Li2.04 N32 O10I b c a24.4994; 24.2314; 35.7646
90; 90; 90
21232Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120977 CIFC36 H27 Cr N8 SiP 1 21/n 111.3864; 25.8865; 41.3004
90; 91.612; 90
12168.6Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120978 CIFC34 H21 Cr N8P 1 21/n 115.768; 8.5743; 19.542
90; 93.19; 90
2638Zhou, Wen; Leznoff, Daniel B.
Phthalocyanine as a redox-active platform for organometallic chemistry.
Chemical communications (Cambridge, England), 2018, 54, 1829-1832
7120983 CIFC33 H62 N8 O16P -16.196; 13.132; 13.815
73.83; 83.92; 78.69
1057.1Prohens, Rafel; Portell, Anna; Font-Bardia, Mercè; Bauzá, Antonio; Frontera, Antonio
H-Bonded anion-anion complex trapped in a squaramido-based receptor.
Chemical communications (Cambridge, England), 2018, 54, 1841-1844
7120984 CIFC38 H30 B F13 O4 S TeP -112.199; 13.1459; 13.2577
70.801; 79.133; 76.956
1940.9Tsao, Fu An; Stephan, Douglas W.
Synthesis and reactions of 4H-1,4-telluraborine.
Chemical communications (Cambridge, England), 2017, 54, 208-211
7120985 CIFC35 H24.5 B F10 O TeP -19.092; 13.245; 14.772
72.11; 79.179; 87.274
1662.7Tsao, Fu An; Stephan, Douglas W.
Synthesis and reactions of 4H-1,4-telluraborine.
Chemical communications (Cambridge, England), 2017, 54, 208-211
7120990 CIFC21 H22 N2 O2P n a 2110.467; 6.9909; 23.485
90; 90; 90
1718.5Kumari, Pratibha; Verma, Sanjay K.; Mobin, Shaikh M.
Water soluble two-photon fluorescent organic probes for long-term imaging of lysosomes in live cells and tumor spheroids.
Chemical communications (Cambridge, England), 2018, 54, 539-542
7120991 CIFC36 H20 Au3 B2 Br3 F12 N12 PbP -3 c 113.2426; 13.2426; 35.7164
90; 90; 120
5424.31Echeverría, Raquel; López-de-Luzuriaga, José M; Monge, Miguel; Moreno, Sonia; Olmos, M. Elena; Rodríguez-Castillo, María
Lead encapsulation by a golden clamp through multiple electrostatic, metallophilic, hydrogen bonding and weak interactions.
Chemical communications (Cambridge, England), 2018, 54, 295-298
7120992 CIFC43 H46 Au3 B Br3 F12 N7P 1 21/c 117.6281; 15.3378; 18.8338
90; 91.372; 90
5090.8Echeverría, Raquel; López-de-Luzuriaga, José M; Monge, Miguel; Moreno, Sonia; Olmos, M. Elena; Rodríguez-Castillo, María
Lead encapsulation by a golden clamp through multiple electrostatic, metallophilic, hydrogen bonding and weak interactions.
Chemical communications (Cambridge, England), 2018, 54, 295-298
7120993 CIFC42 H32 Ag F3 N2 O3 SP 1 21/m 19.4002; 20.3414; 9.8392
90; 104.762; 90
1819.28Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120994 CIFC95.5 H74 Ag B F24 N2P -113.0012; 16.8587; 20.2367
93.9117; 100.458; 99.6917
4277.23Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120995 CIFC76.8 H49.8 Ag B Cl3.4 F24 N2P 1 21/n 115.318; 25.8009; 18.7754
90; 101.5; 90
7271.4Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120996 CIFC79 H49 Ag B F25 N2P 1 21/n 115.165; 26.0219; 18.5838
90; 101.23; 90
7193.2Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120997 CIFC50 H48 Ag N2 O3 PP -111.15213; 11.75148; 16.7352
83.7416; 85.9962; 71.1237
2061.5Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120998 CIFC158 H116 Ag2 B2 F48 N4P -115.6902; 16.2845; 16.4921
117.748; 92.4871; 105.908
3513.3Roy, Matthew M. D.; Ferguson, Michael J.; McDonald, Robert; Rivard, Eric
Approaching monocoordination at a silver(i) cation.
Chemical communications (Cambridge, England), 2018, 54, 483-486
7120999 CIFC41 H55 N O3P 1 21 114.4864; 11.3225; 22.708
90; 106.085; 90
3578.8Mou, Xue-Qing; Chen, Xiang-Yu; Chen, Gong; He, Gang
Radical-mediated intramolecular β-C(sp<sup>3</sup>)-H amidation of alkylimidates: facile synthesis of 1,2-amino alcohols.
Chemical communications (Cambridge, England), 2018, 54, 515-518
7121000 CIFC12 H14 Cl3 I2 N OP 1 21/c 112.7496; 10.1118; 12.9485
90; 96.469; 90
1658.71Mou, Xue-Qing; Chen, Xiang-Yu; Chen, Gong; He, Gang
Radical-mediated intramolecular β-C(sp<sup>3</sup>)-H amidation of alkylimidates: facile synthesis of 1,2-amino alcohols.
Chemical communications (Cambridge, England), 2018, 54, 515-518
7121001 CIFC58.56 H54.68 Cl0.88 O3.78 P4 RuP 1 21/c 112.4387; 16.867; 24.294
90; 90.103; 90
5097Tan, Xuefeng; Zeng, Weijun; Zhang, Xiaoyong; Chung, Lung Wa; Zhang, Xumu
Development of a novel secondary phosphine oxide-ruthenium(ii) catalyst and its application for carbonyl reduction.
Chemical communications (Cambridge, England), 2018, 54, 535-538
7121002 CIFC57 H36 Br I4 PI 1 2/a 117.4076; 17.4445; 34.0495
90; 90.184; 90
10339.7Gunawardana, C. A.; Đaković, M; Aakeröy, C B
Diamondoid architectures from halogen-bonded halides.
Chemical communications (Cambridge, England), 2018, 54, 607-610
7121003 CIFC57 H36 I5 PI 1 2/a 117.419; 17.3989; 34.9081
90; 90.638; 90
10579Gunawardana, C. A.; Đaković, M; Aakeröy, C B
Diamondoid architectures from halogen-bonded halides.
Chemical communications (Cambridge, England), 2018, 54, 607-610
7121004 CIFC57 H36 Cl I4 PI 1 2/a 117.373; 17.4497; 33.5122
90; 90.168; 90
10159.3Gunawardana, C. A.; Đaković, M; Aakeröy, C B
Diamondoid architectures from halogen-bonded halides.
Chemical communications (Cambridge, England), 2018, 54, 607-610
7121009 CIFC76.96 H55.54 Cu8 O49P 21 334.773; 34.773; 34.773
90; 90; 90
42046Lal, Garima; Lee, Shiron J.; Spasyuk, Denis M.; Shimizu, George K. H.
Amphiphile-like self assembly of metal organic polyhedra having both polar and non-polar groups.
Chemical communications (Cambridge, England), 2018, 54, 1722-1725
7121010 CIFC142 H220 F18 N18 O46 Rh4 S6P -115.772; 17.56; 19.223
67.479; 69.242; 86.897
4578.1Zhang, Hai-Ning; Gao, Wen-Xi; Deng, Yu-Xin; Lin, Yue-Jian; Jin, Guo-Xin
Stacking-interaction-induced host-guest chemistry and Borromean rings based on a polypyridyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 1559-1562
7121011 CIFC148 H208 F24 N24 O52 Rh4 S8P 1 21/n 121.482; 12.4683; 38.691
90; 101.321; 90
10162Zhang, Hai-Ning; Gao, Wen-Xi; Deng, Yu-Xin; Lin, Yue-Jian; Jin, Guo-Xin
Stacking-interaction-induced host-guest chemistry and Borromean rings based on a polypyridyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 1559-1562
7121012 CIFC169 H148 F24 N16 O31 Rh4 S8C 1 2/c 137.464; 13.3075; 36.173
90; 112.998; 90
16601Zhang, Hai-Ning; Gao, Wen-Xi; Deng, Yu-Xin; Lin, Yue-Jian; Jin, Guo-Xin
Stacking-interaction-induced host-guest chemistry and Borromean rings based on a polypyridyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 1559-1562
7121013 CIFC170 H152 F24 Ir4 N16 O32 S8P 1 21/c 119.945; 14.605; 31.218
90; 101.754; 90
8903Zhang, Hai-Ning; Gao, Wen-Xi; Deng, Yu-Xin; Lin, Yue-Jian; Jin, Guo-Xin
Stacking-interaction-induced host-guest chemistry and Borromean rings based on a polypyridyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 1559-1562
7121014 CIFC168 H192 F24 N28 O40 Rh4 S8P 1 21/n 126.607; 31.867; 33.813
90; 94.492; 90
28581Zhang, Hai-Ning; Gao, Wen-Xi; Deng, Yu-Xin; Lin, Yue-Jian; Jin, Guo-Xin
Stacking-interaction-induced host-guest chemistry and Borromean rings based on a polypyridyl ligand.
Chemical communications (Cambridge, England), 2018, 54, 1559-1562
7121016 CIFC68 H46 N4 S2P -113.296; 13.957; 17.986
87.92; 79.12; 75.01
3165.9Białek, Michał J; Latos-Grażyński, Lechosław
Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin.
Chemical communications (Cambridge, England), 2018, 54, 1837-1840
7121017 CIFC82 H44 D16 N4 O Pd S2P -111.111; 16.969; 18.186
106.13; 93.46; 90.79
3286.2Białek, Michał J; Latos-Grażyński, Lechosław
Aromaticity switching via azulene transformations in azulene-bridged A,D-dithiahexaphyrin.
Chemical communications (Cambridge, England), 2018, 54, 1837-1840
7121018 CIFC29 H35 N3 O13 UP 1 21 111.217; 10.2614; 14.346
90; 97.541; 90
1637Wang, Xia; Wang, Yanlong; Dai, Xing; Silver, Mark A.; Liu, Wei; Li, Yuxiang; Bai, Zhuanling; Gui, Daxiang; Chen, Lanhua; Diwu, Juan; Zhou, Ruhong; Chai, Zhifang; Wang, Shuao
Phase transition triggered aggregation-induced emission in a photoluminescent uranyl-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 627-630
7121019 CIFC23 H25.8 N O13.4 UP 1 21 111.4098; 9.3291; 14.383
90; 96.391; 90
1521.5Wang, Xia; Wang, Yanlong; Dai, Xing; Silver, Mark A.; Liu, Wei; Li, Yuxiang; Bai, Zhuanling; Gui, Daxiang; Chen, Lanhua; Diwu, Juan; Zhou, Ruhong; Chai, Zhifang; Wang, Shuao
Phase transition triggered aggregation-induced emission in a photoluminescent uranyl-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 627-630
7121020 CIFC27 H36 N2 O SiP 1 21/c 112.787; 16.559; 11.9492
90; 95.643; 90
2517.9Wu, Li-Jun; Yang, Yuan; Song, Ren-Jie; Yu, Jiang-Xi; Li, Jin-Heng; He, De-Liang
An access to 1,3-azasiline-fused quinolinones via oxidative heteroannulation involving silyl C(sp<sup>3</sup>)-H functionalization.
Chemical communications (Cambridge, England), 2018, 54, 1367-1370
7121021 CIFC65 H50 N2 O4P 1 21/n 114.9397; 9.2935; 34.6459
90; 98.609; 90
4756.1Schlüter, Friederike; Riehemann, Kristina; Kehr, Nermin Seda; Quici, Silvio; Daniliuc, Constantin G.; Rizzo, Fabio
A highly fluorescent water soluble spirobifluorene dye with a large Stokes shift: synthesis, characterization and bio-applications.
Chemical communications (Cambridge, England), 2018, 54, 642-645

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