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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7121452 CIFC21 H25 N O2 SP 1 21/c 118.5181; 8.291; 12.5064
90; 99.496; 90
1893.84Lu, Xiao-Yu; Hong, Mei-Lan; Zhou, Hai-Pin; Wang, Yue; Wang, Jin-Yu; Ge, Xiu-Tao
Trisubstituted olefin synthesis via Ni-catalyzed hydroalkylation of internal alkynes with non-activated alkyl halides.
Chemical communications (Cambridge, England), 2018, 54, 4417-4420
7121453 CIFC103.5 H144 N8 P4 Sm2P -114.1425; 14.9026; 26.1273
98.343; 96.438; 111.506
4986.58Schoo, Christoph; Bestgen, Sebastian; Köppe, Ralf; Konchenko, Serygey N.; Roesky, Peter W.
Reactivity of bulky Ln(ii) amidinates towards P<sub>4</sub>, As<sub>4</sub>, and As<sub>4</sub>S<sub>4</sub>.
Chemical communications (Cambridge, England), 2018, 54, 4770-4773
7121454 CIFC54 H78 As N4 O S2 SmP 1 21/c 114.6528; 17.1717; 21.7016
90; 96.826; 90
5421.7Schoo, Christoph; Bestgen, Sebastian; Köppe, Ralf; Konchenko, Serygey N.; Roesky, Peter W.
Reactivity of bulky Ln(ii) amidinates towards P<sub>4</sub>, As<sub>4</sub>, and As<sub>4</sub>S<sub>4</sub>.
Chemical communications (Cambridge, England), 2018, 54, 4770-4773
7121455 CIFC100 H140 As4 N8 Sm2P -113.6808; 16.1681; 22.4917
99.664; 94.939; 95.996
4850.2Schoo, Christoph; Bestgen, Sebastian; Köppe, Ralf; Konchenko, Serygey N.; Roesky, Peter W.
Reactivity of bulky Ln(ii) amidinates towards P<sub>4</sub>, As<sub>4</sub>, and As<sub>4</sub>S<sub>4</sub>.
Chemical communications (Cambridge, England), 2018, 54, 4770-4773
7121456 CIFC54 H78 As N4 O S2 YbP 1 21/c 114.5485; 17.054; 21.7258
90; 96.905; 90
5351.3Schoo, Christoph; Bestgen, Sebastian; Köppe, Ralf; Konchenko, Serygey N.; Roesky, Peter W.
Reactivity of bulky Ln(ii) amidinates towards P<sub>4</sub>, As<sub>4</sub>, and As<sub>4</sub>S<sub>4</sub>.
Chemical communications (Cambridge, England), 2018, 54, 4770-4773
7121457 CIFC6 H42 Mn3 N3 O18 P9P 1 21/c 114.6139; 13.305; 19.3418
90; 109.188; 90
3551.85Wu, Yue; Binford, Trevor; Hill, Joshua A.; Shaker, Sammy; Wang, John; Cheetham, Anthony K.
Hypophosphite hybrid perovskites: a platform for unconventional tilts and shifts.
Chemical communications (Cambridge, England), 2018, 54, 3751-3754
7121458 CIFC94 H98 B2 N10 O7 U2P -114.7593; 15.6981; 20.1394
74.615; 87.841; 69.604
4209.1Cowie, Bradley E.; Nichol, Gary S.; Love, Jason B.; Arnold, Polly L.
Double uranium oxo cations derived from uranyl by borane or silane reduction.
Chemical communications (Cambridge, England), 2018, 54, 3839-3842
7121459 CIFC89 H79 B2 N11 O8 U2P -114.8167; 15.0681; 18.9308
68.593; 79.072; 86.228
3863.52Cowie, Bradley E.; Nichol, Gary S.; Love, Jason B.; Arnold, Polly L.
Double uranium oxo cations derived from uranyl by borane or silane reduction.
Chemical communications (Cambridge, England), 2018, 54, 3839-3842
7121460 CIFC98 H102 N8 O7 Si2 U2C 1 2/c 122.5124; 19.8405; 20.141
90; 110.283; 90
8438.29Cowie, Bradley E.; Nichol, Gary S.; Love, Jason B.; Arnold, Polly L.
Double uranium oxo cations derived from uranyl by borane or silane reduction.
Chemical communications (Cambridge, England), 2018, 54, 3839-3842
7121461 CIFC97 H85 N11 O3 Si2 U2C 1 2/c 123.8381; 17.7807; 21.4711
90; 114.099; 90
8307.5Cowie, Bradley E.; Nichol, Gary S.; Love, Jason B.; Arnold, Polly L.
Double uranium oxo cations derived from uranyl by borane or silane reduction.
Chemical communications (Cambridge, England), 2018, 54, 3839-3842
7121462 CIFC96 H108 N10 O7 U2P 1 21/m 114.0792; 21.2447; 14.5359
90; 105.081; 90
4198.07Cowie, Bradley E.; Nichol, Gary S.; Love, Jason B.; Arnold, Polly L.
Double uranium oxo cations derived from uranyl by borane or silane reduction.
Chemical communications (Cambridge, England), 2018, 54, 3839-3842
7121465 CIFC33 H28 N4 O4P 1 21/n 15.1541; 15.3053; 31.936
90; 91.791; 90
2518Shanmugaraju, Sankarasekaran; la Cour Poulsen, Bjørn; Arisa, Tobi; Umadevi, Deivasigamani; Dalton, Hannah L.; Hawes, Chris S.; Estalayo-Adrián, Sandra; Savyasachi, Aramballi J.; Watson, Graeme W.; Williams, D. Clive; Gunnlaugsson, Thorfinnur
Synthesis, structural characterisation and antiproliferative activity of a new fluorescent 4-amino-1,8-naphthalimide Tröger's base-Ru(ii)-curcumin organometallic conjugate.
Chemical communications (Cambridge, England), 2018, 54, 4120-4123
7121466 CIFC105 H92 F6 N6 O22 Ru2 S2P -114.8532; 18.9099; 19.3296
80.7; 78.221; 84.014
5230.7Shanmugaraju, Sankarasekaran; la Cour Poulsen, Bjørn; Arisa, Tobi; Umadevi, Deivasigamani; Dalton, Hannah L.; Hawes, Chris S.; Estalayo-Adrián, Sandra; Savyasachi, Aramballi J.; Watson, Graeme W.; Williams, D. Clive; Gunnlaugsson, Thorfinnur
Synthesis, structural characterisation and antiproliferative activity of a new fluorescent 4-amino-1,8-naphthalimide Tröger's base-Ru(ii)-curcumin organometallic conjugate.
Chemical communications (Cambridge, England), 2018, 54, 4120-4123
7121467 CIFC44 H66 Al Cl Si2 ZrP 1 21/n 111.2015; 18.847; 20.042
90; 90.198; 90
4231.1Nakamura, Taichi; Suzuki, Katsunori; Yamashita, Makoto
A zwitterionic aluminabenzene-alkylzirconium complex having half-zirconocene structure: synthesis and application for additive-free ethylene polymerization.
Chemical communications (Cambridge, England), 2018, 54, 4180-4183
7121468 CIFC668 H828 Ag90 Cl18 N8 O121 S46 W10P 1 21/n 124.0308; 35.6613; 45.039
90; 92.815; 90
38550Liu, Jia-Wei; Su, Hai-Feng; Wang, Zhi; Li, Yan-An; Zhao, Quan-Qin; Wang, Xing-Po; Tung, Chen-Ho; Sun, Di; Zheng, Lan-Sun
A giant 90-nucleus silver cluster templated by hetero-anions.
Chemical communications (Cambridge, England), 2018, 54, 4461-4464
7121469 CIFC78 H128 B4 Cl6 Cu12 F12 N28 P2 S12 W4C 1 2/m 116.85; 35.352; 17.915
90; 116.535; 90
9547Qiu, Xiao-Ting; Yao, Rui; Zhou, Wen-Fa; Liu, Meng-Di; Liu, Quan; Song, Ying-Lin; Young, David J.; Zhang, Wen-Hua; Lang, Jian-Ping
Rectangle and [2]catenane from cluster modular construction.
Chemical communications (Cambridge, England), 2018, 54, 4168-4171
7121470 CIFC72 H87 B2 Cl5 Cu6 F6 N18 O6 S8 W2C 1 2/c 126.5566; 22.6712; 36.931
90; 91.034; 90
22231Qiu, Xiao-Ting; Yao, Rui; Zhou, Wen-Fa; Liu, Meng-Di; Liu, Quan; Song, Ying-Lin; Young, David J.; Zhang, Wen-Hua; Lang, Jian-Ping
Rectangle and [2]catenane from cluster modular construction.
Chemical communications (Cambridge, England), 2018, 54, 4168-4171
7121471 CIFC54 H56 N2P -17.2956; 10.3483; 14.0315
96.97; 98.026; 100.566
1019.36Nakazato, Takumi; Kamatsuka, Takuto; Inoue, Junichi; Sakurai, Tsuneaki; Seki, Shu; Shinokubo, Hiroshi; Miyake, Yoshihiro
The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes.
Chemical communications (Cambridge, England), 2018, 54, 5177-5180
7121472 CIFC34 H24 N2 S4P 1 2/c 115.9885; 6.2625; 14.7453
90; 111.597; 90
1372.77Nakazato, Takumi; Kamatsuka, Takuto; Inoue, Junichi; Sakurai, Tsuneaki; Seki, Shu; Shinokubo, Hiroshi; Miyake, Yoshihiro
The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes.
Chemical communications (Cambridge, England), 2018, 54, 5177-5180
7121473 CIFC34 H48 N2P n a 2121.6241; 4.7229; 27.9845
90; 90; 90
2858Nakazato, Takumi; Kamatsuka, Takuto; Inoue, Junichi; Sakurai, Tsuneaki; Seki, Shu; Shinokubo, Hiroshi; Miyake, Yoshihiro
The reductive aromatization of naphthalene diimide: a versatile platform for 2,7-diazapyrenes.
Chemical communications (Cambridge, England), 2018, 54, 5177-5180
7121474 CIFC384 H396 N108 O12 Pt24P 2 2 233.966; 19.359; 26.794
90; 90; 90
17618Bhat, Imtiyaz Ahmad; Devaraj, Anthonisamy; Howlader, Prodip; Chi, Ki-Whan; Mukherjee, Partha Sarathi
Preparation of a chiral Pt<sub>12</sub> tetrahedral cage and its use in catalytic Michael addition reaction.
Chemical communications (Cambridge, England), 2018, 54, 4814-4817
7121475 CIFC20 H16 O8 SP -16.1387; 12.306; 12.412
97.997; 100.495; 96.136
904.5Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121476 CIFC14 H12 O8 SP -16.2082; 7.2693; 16.148
93.364; 96.808; 109.758
677.2Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121477 CIFC23 H22 O8P 21 21 216.5124; 15.0561; 20.2887
90; 90; 90
1989.33Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121478 CIFC20 H16 O9 SP -112.1168; 12.9658; 25.4643
100.531; 97.317; 90.034
3900Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121479 CIFC21 H16 O9 SP -15.9531; 12.597; 14.559
72.156; 88.823; 84.441
1034.3Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121480 CIFC13 H12 O8 SP -17.8234; 9.9598; 9.9951
107.61; 102.745; 109.14
655.56Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121481 CIFC21 H16 O8P -19.1816; 13.2228; 14.5348
88.475; 87.657; 88.007
1761.52Vibhute, Amol M.; Deva Priyakumar, U.; Ravi, Arthi; Sureshan, Kana M.
Model molecules to classify CHO hydrogen-bonds.
Chemical communications (Cambridge, England), 2018, 54, 4629-4632
7121482 CIFC14 H7 N3 S4P 1 21/n 17.2126; 17.1917; 10.7279
90; 94.846; 90
1325.47Park, Jung Su; Tran, Trang Thu; Kim, Jongmin; Sessler, Jonathan L.
Electrochemical amphotericity and NIR absorption induced via the step-wise protonation of fused quinoxaline-tetrathiafulvalene-pyrroles.
Chemical communications (Cambridge, England), 2018, 54, 4553-4556
7121483 CIFC26 H19 N3 S6C 1 2/c 129.9118; 20.1932; 9.8958
90; 102.473; 90
5836.1Park, Jung Su; Tran, Trang Thu; Kim, Jongmin; Sessler, Jonathan L.
Electrochemical amphotericity and NIR absorption induced via the step-wise protonation of fused quinoxaline-tetrathiafulvalene-pyrroles.
Chemical communications (Cambridge, England), 2018, 54, 4553-4556
7121484 CIFC36 H34 Cl3 N3 O8 S9P -110.8535; 12.4996; 18.2429
109.371; 93.9288; 103.089
2246.2Park, Jung Su; Tran, Trang Thu; Kim, Jongmin; Sessler, Jonathan L.
Electrochemical amphotericity and NIR absorption induced via the step-wise protonation of fused quinoxaline-tetrathiafulvalene-pyrroles.
Chemical communications (Cambridge, England), 2018, 54, 4553-4556
7121485 CIFC22 H16 N2 OP 1 21/c 123.5316; 6.7006; 24.2907
90; 115.166; 90
3466.51Xie, Yangxi; Wang, Jian
N-Heterocyclic carbene-catalyzed annulation of ynals with amidines: access to 1,2,6-trisubstituted pyrimidin-4-ones.
Chemical communications (Cambridge, England), 2018, 54, 4597-4600
7121486 CIFC19 H17 Br N4 O4P n a 2118.4667; 8.4993; 12.0129
90; 90; 90
1885.47Zhao, Hua; Shao, Xiaoru; Wang, Taimin; Zhai, Shengxian; Qiu, Shuxian; Tao, Cheng; Wang, Huifei; Zhai, Hongbin
A 2-(1-methylhydrazinyl)pyridine-directed C-H functionalization/spirocyclization cascade: facile access to spirosuccinimide derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4927-4930
7121487 CIFC9 H12 Au F5 N4 O3 SP 1 21/n 18.1155; 6.7521; 27.4966
90; 97.325; 90
1494.43Albayer, Mohammad; Corbo, Robert; Dutton, Jason L.
Well defined difluorogold(iii) complexes supported by N-ligands.
Chemical communications (Cambridge, England), 2018, 54, 6832-6834
7121488 CIFC50 H58 Al N3 O3P 1 21/c 19.9221; 22.0031; 20.2879
90; 101.001; 90
4347.8Kwak, Sang Woo; Jin, Hyomin; Shin, Heuiseok; Lee, Ji Hye; Hwang, Hyonseok; Lee, Junseong; Kim, Min; Chung, Yongseog; Kim, Youngjo; Lee, Kang Mun; Park, Myung Hwan
A salen-Al/carbazole dyad-based guest-host assembly: enhancement of luminescence efficiency via intramolecular energy transfer.
Chemical communications (Cambridge, England), 2018, 54, 4712-4715
7121491 CIFC7 H4 N O3 ZnP 41 2 212.8863; 12.8863; 13.2102
90; 90; 90
2193.64Zhang, Ling; Jiang, Ke; Li, Libo; Xia, Yu-Pei; Hu, Tong-Liang; Yang, Yu; Cui, Yuanjing; Li, Bin; Chen, Banglin; Qian, Guodong
Efficient separation of C<sub>2</sub>H<sub>2</sub> from C<sub>2</sub>H<sub>2</sub>/CO<sub>2</sub> mixtures in an acid-base resistant metal-organic framework.
Chemical communications (Cambridge, England), 2018, 54, 4846-4849
7121492 CIFC40 H61 Cl N4 ZnP 21 21 2111.8352; 17.5939; 18.329
90; 90; 90
3816.6Ballestero-Martínez, Ernesto; Hadlington, Terrance J.; Szilvási, Tibor; Yao, Shenglai; Driess, Matthias
From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes.
Chemical communications (Cambridge, England), 2018, 54, 6124-6127
7121493 CIFC39 H61 As N4 Si ZnP 1 21/c 113.8602; 21.5672; 12.9197
90; 95.682; 90
3843.06Ballestero-Martínez, Ernesto; Hadlington, Terrance J.; Szilvási, Tibor; Yao, Shenglai; Driess, Matthias
From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes.
Chemical communications (Cambridge, England), 2018, 54, 6124-6127
7121494 CIFC41 H61 As N4 O ZnP 1 21/n 117.2926; 11.8957; 19.9787
90; 104.184; 90
3984.48Ballestero-Martínez, Ernesto; Hadlington, Terrance J.; Szilvási, Tibor; Yao, Shenglai; Driess, Matthias
From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes.
Chemical communications (Cambridge, England), 2018, 54, 6124-6127
7121495 CIFC55 H77 As N4 Si ZnP 1 21/c 114.0308; 13.9065; 26.737
90; 90.031; 90
5216.9Ballestero-Martínez, Ernesto; Hadlington, Terrance J.; Szilvási, Tibor; Yao, Shenglai; Driess, Matthias
From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes.
Chemical communications (Cambridge, England), 2018, 54, 6124-6127
7121496 CIFC50 H81 As N6 Si ZnP -113.577; 14.7552; 14.8121
92.378; 107.476; 112.237
2579.1Ballestero-Martínez, Ernesto; Hadlington, Terrance J.; Szilvási, Tibor; Yao, Shenglai; Driess, Matthias
From zinco(ii) arsaketenes to silylene-stabilised zinco arsinidene complexes.
Chemical communications (Cambridge, England), 2018, 54, 6124-6127
7121497 CIFC86 H30 N2 O52 S13.97 Zn12P 1 2 123.5616; 10.817; 28.5728
90; 90.096; 90
7282.2Kusaka, Shinpei; Matsuda, Ryotaro; Kitagawa, Susumu
Generation of thiyl radicals in a zinc(ii) porous coordination polymer by light-induced post-synthetic deprotection.
Chemical communications (Cambridge, England), 2018, 54, 4782-4785
7121498 CIFC92 H66 O52 S20 Zn12P 1 2 123.7128; 10.805; 28.5974
90; 90.017; 90
7327.1Kusaka, Shinpei; Matsuda, Ryotaro; Kitagawa, Susumu
Generation of thiyl radicals in a zinc(ii) porous coordination polymer by light-induced post-synthetic deprotection.
Chemical communications (Cambridge, England), 2018, 54, 4782-4785
7121499 CIFC12 H32 N2 Se7 Sn3P b c a17.4028; 13.7025; 23.9113
90; 90; 90
5701.9Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121500 CIFC12 H32 N2 Se7 Sn3P b c a17.5861; 13.7084; 23.9914
90; 90; 90
5783.8Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121501 CIFC12 H32 N2 Se7 Sn3P b c a17.7039; 13.7664; 24.2192
90; 90; 90
5902.7Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121502 CIFC12 H32 N2 Se7 Sn3P b c a17.4184; 13.6963; 23.9378
90; 90; 90
5710.8Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121503 CIFC12 H32 N2 Se7 Sn3P b c a17.5771; 13.7282; 24.1464
90; 90; 90
5826.6Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121504 CIFC12 H32 N2 Se7 Sn3P b c a17.5344; 13.7273; 24.1221
90; 90; 90
5806.2Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121505 CIFC12 H32 N2 Se7 Sn3P b c a17.4508; 13.6959; 23.9469
90; 90; 90
5723.4Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121506 CIFC12 H32 N2 Se7 Sn3P b c a17.645; 13.7539; 24.1705
90; 90; 90
5865.9Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121507 CIFC12 H32 N2 Se7 Sn3P b c a17.7542; 13.831; 24.2599
90; 90; 90
5957.2Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121508 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.9739; 13.7151; 21.1612
90; 91.969; 90
2893Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121509 CIFC12 H32 N2 Se7 Sn3P b c a17.4944; 13.7191; 24.0762
90; 90; 90
5778.5Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121510 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.8761; 13.597; 20.7839
90; 92.484; 90
2788.35Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121511 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.8469; 13.5734; 20.7529
90; 92.642; 90
2770.8Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121512 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.8956; 13.611; 20.8327
90; 92.368; 90
2803.54Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121513 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.8365; 13.5796; 20.7384
90; 92.727; 90
2767.01Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121514 CIFC10 H30 N2 O3 Se7 Sn3P 1 21/n 19.9152; 13.6371; 20.9056
90; 92.274; 90
2824.52Wang, Kai-Yao; Ding, Dong; Zhang, Shu; Wang, Yanlong; Liu, Wei; Wang, Shuao; Wang, Shuai-Hua; Liu, Dan; Wang, Cheng
Preparation of thermochromic selenidostannates in deep eutectic solvents.
Chemical communications (Cambridge, England), 2018, 54, 4806-4809
7121515 CIFC17 H21 F2 N O4P n a 219.3962; 10.839; 33.4374
90; 90; 90
3405.45Hofman, Gert-Jan; Ottoy, Emile; Light, Mark E.; Kieffer, Bruno; Kuprov, Ilya; Martins, Jose C.; Sinnaeve, Davy; Linclau, Bruno
Minimising conformational bias in fluoroprolines through vicinal difluorination.
Chemical communications (Cambridge, England), 2018, 54, 5118-5121
7121516 CIFC18 H48 Eu I2 N8P c a 2115.77; 12.1249; 13.749
90; 90; 90
2628.9Jenks, Tyler C.; Bailey, Matthew D.; Corbin, Brooke A.; Kuda-Wedagedara, Akhila N W; Martin, Philip D.; Schlegel, H. Bernhard; Rabuffetti, Federico A.; Allen, Matthew J.
Photophysical characterization of a highly luminescent divalent-europium-containing azacryptate.
Chemical communications (Cambridge, England), 2018, 54, 4545-4548
7121517 CIFC25 H57 Eu I2 N8 OP 21 314.9671; 14.9671; 14.9671
90; 90; 90
3352.8Jenks, Tyler C.; Bailey, Matthew D.; Corbin, Brooke A.; Kuda-Wedagedara, Akhila N W; Martin, Philip D.; Schlegel, H. Bernhard; Rabuffetti, Federico A.; Allen, Matthew J.
Photophysical characterization of a highly luminescent divalent-europium-containing azacryptate.
Chemical communications (Cambridge, England), 2018, 54, 4545-4548
7121518 CIFC24 H34 B2 Fe2 N18 Ni O7C 1 2/c 128.851; 9.668; 13.718
90; 101.205; 90
3753.4Jiménez, Juan-Ramón; Sugahara, Akira; Okubo, Masashi; Yamada, Atsuo; Chamoreau, Lise-Marie; Lisnard, Laurent; Lescouëzec, Rodrigue
A [Fe<sup>III</sup>(Tp)(CN)<sub>3</sub>]<sup>-</sup> scorpionate-based complex as a building block for designing ion storage hosts (Tp: hydrotrispyrazolylborate).
Chemical communications (Cambridge, England), 2018, 54, 5189-5192
7121519 CIFC28 H48 B2 N2P 1 21/a 113.356; 10.8079; 18.731
90; 102.739; 90
2637.3Kitamura, Ryo; Suzuki, Katsunori; Yamashita, Makoto
Dimerization of boryl- and amino-substituted acetylenes by B<sub>2</sub>C<sub>2</sub> four-membered ring formation.
Chemical communications (Cambridge, England), 2018, 54, 5819-5822
7121520 CIFC36 H40 B2 N2P -19.3775; 9.7968; 10.2151
62.343; 79.192; 65.439
756Kitamura, Ryo; Suzuki, Katsunori; Yamashita, Makoto
Dimerization of boryl- and amino-substituted acetylenes by B<sub>2</sub>C<sub>2</sub> four-membered ring formation.
Chemical communications (Cambridge, England), 2018, 54, 5819-5822
7121521 CIFC7 H9 OP 1 21/c 18.8275; 6.0025; 12.1333
90; 103.211; 90
625.89Saito, Yuki; Higuchi, Masayuki; Yoshioka, Shota; Senboku, Hisanori; Inokuma, Yasuhide
Bioinspired synthesis of pentalene-based chromophores from an oligoketone chain.
Chemical communications (Cambridge, England), 2018, 54, 6788-6791
7121522 CIFC10 H9 N2P 1 21/n 19.8253; 6.718; 13.1473
90; 110.128; 90
814.81Saito, Yuki; Higuchi, Masayuki; Yoshioka, Shota; Senboku, Hisanori; Inokuma, Yasuhide
Bioinspired synthesis of pentalene-based chromophores from an oligoketone chain.
Chemical communications (Cambridge, England), 2018, 54, 6788-6791
7121523 CIFC17 H18 N2 OP n a 2112.1379; 7.1688; 16.6494
90; 90; 90
1448.73Saito, Yuki; Higuchi, Masayuki; Yoshioka, Shota; Senboku, Hisanori; Inokuma, Yasuhide
Bioinspired synthesis of pentalene-based chromophores from an oligoketone chain.
Chemical communications (Cambridge, England), 2018, 54, 6788-6791
7121524 CIFC20 H14 N2 O5P 21 21 216.6428; 14.2542; 17.8105
90; 90; 90
1686.44Khan, Ijaz; Zhao, Can; Zhang, Yong Jian
Pd-Catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with 3-cyanochromones.
Chemical communications (Cambridge, England), 2018, 54, 4708-4711
7121525 CIFC20 H14 N2 O5P 1 21/c 111.4782; 14.6774; 10.854
90; 115.824; 90
1645.97Khan, Ijaz; Zhao, Can; Zhang, Yong Jian
Pd-Catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with 3-cyanochromones.
Chemical communications (Cambridge, England), 2018, 54, 4708-4711
7121526 CIFC21 H19 N O3P 21 21 217.0542; 14.1154; 17.6777
90; 90; 90
1760.22Khan, Ijaz; Zhao, Can; Zhang, Yong Jian
Pd-Catalyzed asymmetric decarboxylative cycloaddition of vinylethylene carbonates with 3-cyanochromones.
Chemical communications (Cambridge, England), 2018, 54, 4708-4711
7121527 CIFC12 H28 Cl5 N2 SbP 21 21 217.5861; 13.2521; 20.2623
90; 90; 90
2037Zhang, Jing; Han, Shiguo; Liu, Xitao; Wu, Zhenyue; Ji, Chengmin; Sun, Zhihua; Luo, Junhua
A lead-free perovskite-like hybrid with above-room-temperature switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2018, 54, 5614-5617
7121528 CIFC12 H28 Cl5 N2 SbP n m a13.0708; 7.9573; 20.1605
90; 90; 90
2096.9Zhang, Jing; Han, Shiguo; Liu, Xitao; Wu, Zhenyue; Ji, Chengmin; Sun, Zhihua; Luo, Junhua
A lead-free perovskite-like hybrid with above-room-temperature switching of quadratic nonlinear optical properties.
Chemical communications (Cambridge, England), 2018, 54, 5614-5617
7121529 CIFC48 H68 N4 O8 S4P -19.7664; 10.1835; 14.4361
106.574; 96.681; 101.627
1324.56Ravi, Anil; Oshchepkov, Aleksandr S.; German, Konstantin E.; Kirakosyan, Gayana A.; Safonov, Aleksey V.; Khrustalev, Victor N.; Kataev, Evgeny A.
Finding a receptor design for selective recognition of perrhenate and pertechnetate: hydrogen vs. halogen bonding.
Chemical communications (Cambridge, England), 2018, 54, 4826-4829
7121533 CIFC28 H24 O2C 1 2/c 114.55; 12.0209; 25.0181
90; 99.828; 90
4311.55Lou, Dandan; Lu, Xiangcheng; Zhang, Mengxing; Bai, Ming; Jiang, Jianzhuang
Regulating the emission of tetraphenylethenes by changing the alkoxyl linkage length between two neighboring phenyl moieties.
Chemical communications (Cambridge, England), 2018, 54, 6987-6990
7121534 CIFC29 H24 O2P 1 21/c 114.1335; 9.122; 17.8477
90; 109.798; 90
2165.02Lou, Dandan; Lu, Xiangcheng; Zhang, Mengxing; Bai, Ming; Jiang, Jianzhuang
Regulating the emission of tetraphenylethenes by changing the alkoxyl linkage length between two neighboring phenyl moieties.
Chemical communications (Cambridge, England), 2018, 54, 6987-6990
7121535 CIFC27 H20 O2P 1 21/n 19.2661; 8.4682; 25.032
90; 97.682; 90
1946.56Lou, Dandan; Lu, Xiangcheng; Zhang, Mengxing; Bai, Ming; Jiang, Jianzhuang
Regulating the emission of tetraphenylethenes by changing the alkoxyl linkage length between two neighboring phenyl moieties.
Chemical communications (Cambridge, England), 2018, 54, 6987-6990
7121536 CIFC28 H22 O2P 1 21/n 19.1319; 19.4605; 12.3122
90; 97.242; 90
2170.56Lou, Dandan; Lu, Xiangcheng; Zhang, Mengxing; Bai, Ming; Jiang, Jianzhuang
Regulating the emission of tetraphenylethenes by changing the alkoxyl linkage length between two neighboring phenyl moieties.
Chemical communications (Cambridge, England), 2018, 54, 6987-6990
7121537 CIFC30 H26 O2P 1 21/c 19.3824; 9.3181; 25.644
90; 97.845; 90
2221Lou, Dandan; Lu, Xiangcheng; Zhang, Mengxing; Bai, Ming; Jiang, Jianzhuang
Regulating the emission of tetraphenylethenes by changing the alkoxyl linkage length between two neighboring phenyl moieties.
Chemical communications (Cambridge, England), 2018, 54, 6987-6990
7121538 CIFC20 H14 O3P b c a7.2027; 18.296; 22.189
90; 90; 90
2924.1Zhang, Huiwen; Ma, Chunmei; Zheng, Ziwei; Sun, Rengwei; Yu, Xinhong; Zhao, Jianhong
Synthesis of 2-arylbenzofuran-3-carbaldehydes via an organocatalytic [3+2] annulation/oxidative aromatization reaction.
Chemical communications (Cambridge, England), 2018, 54, 4935-4938
7121539 CIFC14 H42 O19 Ti2 V4P 1 21/n 110.2851; 24.103; 12.028
90; 92.176; 90
2979.6VanGelder, L. E.; Forrestel, P. L.; Brennessel, W. W.; Matson, E. M.
Site-selectivity in the halogenation of titanium-functionalized polyoxovanadate-alkoxide clusters.
Chemical communications (Cambridge, England), 2018, 54, 6839-6842
7121540 CIFC20 H54 Al Cl5 O19.5 Ti2 V4P 1 21/m 119.3992; 11.6179; 19.5185
90; 96.728; 90
4368.7VanGelder, L. E.; Forrestel, P. L.; Brennessel, W. W.; Matson, E. M.
Site-selectivity in the halogenation of titanium-functionalized polyoxovanadate-alkoxide clusters.
Chemical communications (Cambridge, England), 2018, 54, 6839-6842
7121542 CIFC68 H73 O8.5P -112.353; 14.6695; 16.1299
93.266; 105.038; 100.126
2762.64Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121543 CIFC70 H74 Cl6 O8P -113.6525; 15.3663; 17.4716
109.493; 102.788; 99.544
3253.02Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121544 CIFC139 H139 Cl9 O16P -114.3309; 18.0783; 24.9943
72.549; 80.55; 75.159
5944.5Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121545 CIFC96 H99 O8P -114.2685; 14.5929; 19.2492
101.482; 91.26; 95.436
3906.74Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121546 CIFC164 H212 O30 S14P -116.7858; 20.0431; 25.8482
87.859; 88.846; 68.982
8111.9Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121547 CIFC138 H132 Cl4 O16P -117.7109; 19.323; 21.2976
78.212; 65.437; 66.098
6054.9Smith, Jordan N.; Lucas, Nigel T.
Rigid tetraarylene-bridged cavitands from reduced-symmetry resorcin[4]arene derivatives.
Chemical communications (Cambridge, England), 2018, 54, 4716-4719
7121548 CIFC158 H155 F65 N25 O8 P11P -118.275; 22.178; 26.09
100.067; 91.197; 90.025
10409Wang, Cai-Yun; Wu, Guangcheng; Jiao, Tianyu; Shen, Libo; Ma, Ge; Pan, Yuanjiang; Li, Hao
Precursor control over the self-assembly of [2]catenanes via hydrazone condensation in water.
Chemical communications (Cambridge, England), 2018, 54, 5106-5109
7121549 CIFC192 H180 F48 N36 O10 P8C 1 2/c 134.3375; 27.6556; 43.5292
90; 105.457; 90
39841Wang, Cai-Yun; Wu, Guangcheng; Jiao, Tianyu; Shen, Libo; Ma, Ge; Pan, Yuanjiang; Li, Hao
Precursor control over the self-assembly of [2]catenanes via hydrazone condensation in water.
Chemical communications (Cambridge, England), 2018, 54, 5106-5109
7121554 CIFC97 H64 Eu2 F6 N4 O12P 1 21/c 111.765; 22.391; 16.151
90; 110.732; 90
3979Kalyakina, Alena S.; Utochnikova, Valentina V.; Zimmer, Manuel; Dietrich, Fabian; Kaczmarek, Anna M.; Van Deun, Rik; Vashchenko, Andrey A.; Goloveshkin, Alexander S.; Nieger, Martin; Gerhards, Markus; Schepers, Ute; Bräse, Stefan
Remarkable high efficiency of red emitters using Eu(iii) ternary complexes.
Chemical communications (Cambridge, England), 2018, 54, 5221-5224
7121555 CIFC66 H34 Eu2 F12 N4 O12P 1 21/n 114.583; 13.1391; 15.364
90; 103.713; 90
2859.9Kalyakina, Alena S.; Utochnikova, Valentina V.; Zimmer, Manuel; Dietrich, Fabian; Kaczmarek, Anna M.; Van Deun, Rik; Vashchenko, Andrey A.; Goloveshkin, Alexander S.; Nieger, Martin; Gerhards, Markus; Schepers, Ute; Bräse, Stefan
Remarkable high efficiency of red emitters using Eu(iii) ternary complexes.
Chemical communications (Cambridge, England), 2018, 54, 5221-5224
7121556 CIFC14 H15 N O2 SP 1 21 18.4454; 7.2057; 10.9962
90; 96.797; 90
664.47Yang, Fan; Chen, Jingchao; Shen, Guoli; Zhang, Xuexin; Fan, Baomin
Asymmetric transfer hydrogenation reactions of N-sulfonylimines by using alcohols as hydrogen sources.
Chemical communications (Cambridge, England), 2018, 54, 4963-4966
7121557 CIFC39 H123 N18 O28 Rh5 S15 Zn4R 3 :H20.209; 20.209; 21.1201
90; 90; 120
7469.9Yasukawa, Yuhei; Yoshinari, Nobuto; Konno, Takumi
Two-step chiral transfer from d-penicillamine to metallosupramolecular ionic crystals.
Chemical communications (Cambridge, England), 2018, 54, 5003-5006
7121558 CIFC39 H139 N18 O36 Rh5 S15 Zn4P 113.279; 13.782; 14.45
95.771; 94.901; 96.534
2601Yasukawa, Yuhei; Yoshinari, Nobuto; Konno, Takumi
Two-step chiral transfer from d-penicillamine to metallosupramolecular ionic crystals.
Chemical communications (Cambridge, England), 2018, 54, 5003-5006
7121559 CIFC46 H32 Cl3 N5 Ni SP -110.2159; 14.359; 15.0898
113.223; 103.443; 98.599
1905.05Berthelot, Mathieu; Hoffmann, Guillaume; Bousfiha, Asmae; Echaubard, Julie; Roger, Julien; Cattey, Hélène; Romieu, Anthony; Lucas, Dominique; Fleurat-Lessard, Paul; Devillers, Charles H.
Oxidative C-N fusion of pyridinyl-substituted porphyrins.
Chemical communications (Cambridge, England), 2018, 54, 5414-5417
7121560 CIFC45 H30 F6 N5 Ni P SP 1 21/c 119.386; 20.956; 9.2559
90; 96.226; 90
3738.1Berthelot, Mathieu; Hoffmann, Guillaume; Bousfiha, Asmae; Echaubard, Julie; Roger, Julien; Cattey, Hélène; Romieu, Anthony; Lucas, Dominique; Fleurat-Lessard, Paul; Devillers, Charles H.
Oxidative C-N fusion of pyridinyl-substituted porphyrins.
Chemical communications (Cambridge, England), 2018, 54, 5414-5417
7121561 CIFC39 H27 N5 Ni SP 1 21/c 110.9758; 12.6253; 23.005
90; 93.015; 90
3183.5Berthelot, Mathieu; Hoffmann, Guillaume; Bousfiha, Asmae; Echaubard, Julie; Roger, Julien; Cattey, Hélène; Romieu, Anthony; Lucas, Dominique; Fleurat-Lessard, Paul; Devillers, Charles H.
Oxidative C-N fusion of pyridinyl-substituted porphyrins.
Chemical communications (Cambridge, England), 2018, 54, 5414-5417
7121562 CIFC14 H10 N2 O2P 1 21/c 114.66; 5.7506; 14.623
90; 109.41; 90
1162.7Zhou, Lijing; Li, Hongji; Zhang, Wenge; Wang, Lei
Tuning chemoselectivity in O-/N-arylation of 3-aryl-1,2,4-oxadiazolones with ortho-(trimethylsilyl)phenyl triflates via aryne insertion.
Chemical communications (Cambridge, England), 2018, 54, 4822-4825
7121563 CIFC360 H198 Cu12 N18 O60R -3 c :H32.322; 32.322; 78.505
90; 90; 120
71027Omoto, Kenichiro; Hosono, Nobuhiko; Gochomori, Mika; Albrecht, Ken; Yamamoto, Kimihisa; Kitagawa, Susumu
Anisotropic convergence of dendritic macromolecules facilitated by a heteroleptic metal-organic polyhedron scaffold.
Chemical communications (Cambridge, England), 2018, 54, 5209-5212

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