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 | CIF | C21 H25 N O2 S | P 1 21/c 1 | 18.5181; 8.291; 12.5064 90; 99.496; 90 | 1893.84 | Lu, 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 | CIF | C103.5 H144 N8 P4 Sm2 | P -1 | 14.1425; 14.9026; 26.1273 98.343; 96.438; 111.506 | 4986.58 | Schoo, 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 | CIF | C54 H78 As N4 O S2 Sm | P 1 21/c 1 | 14.6528; 17.1717; 21.7016 90; 96.826; 90 | 5421.7 | Schoo, 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 | CIF | C100 H140 As4 N8 Sm2 | P -1 | 13.6808; 16.1681; 22.4917 99.664; 94.939; 95.996 | 4850.2 | Schoo, 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 | CIF | C54 H78 As N4 O S2 Yb | P 1 21/c 1 | 14.5485; 17.054; 21.7258 90; 96.905; 90 | 5351.3 | Schoo, 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 | CIF | C6 H42 Mn3 N3 O18 P9 | P 1 21/c 1 | 14.6139; 13.305; 19.3418 90; 109.188; 90 | 3551.85 | Wu, 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 | CIF | C94 H98 B2 N10 O7 U2 | P -1 | 14.7593; 15.6981; 20.1394 74.615; 87.841; 69.604 | 4209.1 | Cowie, 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 | CIF | C89 H79 B2 N11 O8 U2 | P -1 | 14.8167; 15.0681; 18.9308 68.593; 79.072; 86.228 | 3863.52 | Cowie, 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 | CIF | C98 H102 N8 O7 Si2 U2 | C 1 2/c 1 | 22.5124; 19.8405; 20.141 90; 110.283; 90 | 8438.29 | Cowie, 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 | CIF | C97 H85 N11 O3 Si2 U2 | C 1 2/c 1 | 23.8381; 17.7807; 21.4711 90; 114.099; 90 | 8307.5 | Cowie, 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 | CIF | C96 H108 N10 O7 U2 | P 1 21/m 1 | 14.0792; 21.2447; 14.5359 90; 105.081; 90 | 4198.07 | Cowie, 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 | CIF | C33 H28 N4 O4 | P 1 21/n 1 | 5.1541; 15.3053; 31.936 90; 91.791; 90 | 2518 | Shanmugaraju, 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 | CIF | C105 H92 F6 N6 O22 Ru2 S2 | P -1 | 14.8532; 18.9099; 19.3296 80.7; 78.221; 84.014 | 5230.7 | Shanmugaraju, 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 | CIF | C44 H66 Al Cl Si2 Zr | P 1 21/n 1 | 11.2015; 18.847; 20.042 90; 90.198; 90 | 4231.1 | Nakamura, 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 | CIF | C668 H828 Ag90 Cl18 N8 O121 S46 W10 | P 1 21/n 1 | 24.0308; 35.6613; 45.039 90; 92.815; 90 | 38550 | Liu, 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 | CIF | C78 H128 B4 Cl6 Cu12 F12 N28 P2 S12 W4 | C 1 2/m 1 | 16.85; 35.352; 17.915 90; 116.535; 90 | 9547 | Qiu, 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 | CIF | C72 H87 B2 Cl5 Cu6 F6 N18 O6 S8 W2 | C 1 2/c 1 | 26.5566; 22.6712; 36.931 90; 91.034; 90 | 22231 | Qiu, 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 | CIF | C54 H56 N2 | P -1 | 7.2956; 10.3483; 14.0315 96.97; 98.026; 100.566 | 1019.36 | Nakazato, 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 | CIF | C34 H24 N2 S4 | P 1 2/c 1 | 15.9885; 6.2625; 14.7453 90; 111.597; 90 | 1372.77 | Nakazato, 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 | CIF | C34 H48 N2 | P n a 21 | 21.6241; 4.7229; 27.9845 90; 90; 90 | 2858 | Nakazato, 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 | CIF | C384 H396 N108 O12 Pt24 | P 2 2 2 | 33.966; 19.359; 26.794 90; 90; 90 | 17618 | Bhat, 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 | CIF | C20 H16 O8 S | P -1 | 6.1387; 12.306; 12.412 97.997; 100.495; 96.136 | 904.5 | Vibhute, 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 | CIF | C14 H12 O8 S | P -1 | 6.2082; 7.2693; 16.148 93.364; 96.808; 109.758 | 677.2 | Vibhute, 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 | CIF | C23 H22 O8 | P 21 21 21 | 6.5124; 15.0561; 20.2887 90; 90; 90 | 1989.33 | Vibhute, 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 | CIF | C20 H16 O9 S | P -1 | 12.1168; 12.9658; 25.4643 100.531; 97.317; 90.034 | 3900 | Vibhute, 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 | CIF | C21 H16 O9 S | P -1 | 5.9531; 12.597; 14.559 72.156; 88.823; 84.441 | 1034.3 | Vibhute, 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 | CIF | C13 H12 O8 S | P -1 | 7.8234; 9.9598; 9.9951 107.61; 102.745; 109.14 | 655.56 | Vibhute, 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 | CIF | C21 H16 O8 | P -1 | 9.1816; 13.2228; 14.5348 88.475; 87.657; 88.007 | 1761.52 | Vibhute, 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 | CIF | C14 H7 N3 S4 | P 1 21/n 1 | 7.2126; 17.1917; 10.7279 90; 94.846; 90 | 1325.47 | Park, 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 | CIF | C26 H19 N3 S6 | C 1 2/c 1 | 29.9118; 20.1932; 9.8958 90; 102.473; 90 | 5836.1 | Park, 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 | CIF | C36 H34 Cl3 N3 O8 S9 | P -1 | 10.8535; 12.4996; 18.2429 109.371; 93.9288; 103.089 | 2246.2 | Park, 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 | CIF | C22 H16 N2 O | P 1 21/c 1 | 23.5316; 6.7006; 24.2907 90; 115.166; 90 | 3466.51 | Xie, 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 | CIF | C19 H17 Br N4 O4 | P n a 21 | 18.4667; 8.4993; 12.0129 90; 90; 90 | 1885.47 | Zhao, 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 | CIF | C9 H12 Au F5 N4 O3 S | P 1 21/n 1 | 8.1155; 6.7521; 27.4966 90; 97.325; 90 | 1494.43 | Albayer, Mohammad; Corbo, Robert; Dutton, Jason L. Well defined difluorogold(iii) complexes supported by N-ligands. Chemical communications (Cambridge, England), 2018, 54, 6832-6834 |
| 7121488 | CIF | C50 H58 Al N3 O3 | P 1 21/c 1 | 9.9221; 22.0031; 20.2879 90; 101.001; 90 | 4347.8 | Kwak, 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 | CIF | C7 H4 N O3 Zn | P 41 2 2 | 12.8863; 12.8863; 13.2102 90; 90; 90 | 2193.64 | Zhang, 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 | CIF | C40 H61 Cl N4 Zn | P 21 21 21 | 11.8352; 17.5939; 18.329 90; 90; 90 | 3816.6 | Ballestero-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 | CIF | C39 H61 As N4 Si Zn | P 1 21/c 1 | 13.8602; 21.5672; 12.9197 90; 95.682; 90 | 3843.06 | Ballestero-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 | CIF | C41 H61 As N4 O Zn | P 1 21/n 1 | 17.2926; 11.8957; 19.9787 90; 104.184; 90 | 3984.48 | Ballestero-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 | CIF | C55 H77 As N4 Si Zn | P 1 21/c 1 | 14.0308; 13.9065; 26.737 90; 90.031; 90 | 5216.9 | Ballestero-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 | CIF | C50 H81 As N6 Si Zn | P -1 | 13.577; 14.7552; 14.8121 92.378; 107.476; 112.237 | 2579.1 | Ballestero-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 | CIF | C86 H30 N2 O52 S13.97 Zn12 | P 1 2 1 | 23.5616; 10.817; 28.5728 90; 90.096; 90 | 7282.2 | Kusaka, 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 | CIF | C92 H66 O52 S20 Zn12 | P 1 2 1 | 23.7128; 10.805; 28.5974 90; 90.017; 90 | 7327.1 | Kusaka, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.4028; 13.7025; 23.9113 90; 90; 90 | 5701.9 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.5861; 13.7084; 23.9914 90; 90; 90 | 5783.8 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.7039; 13.7664; 24.2192 90; 90; 90 | 5902.7 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.4184; 13.6963; 23.9378 90; 90; 90 | 5710.8 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.5771; 13.7282; 24.1464 90; 90; 90 | 5826.6 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.5344; 13.7273; 24.1221 90; 90; 90 | 5806.2 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.4508; 13.6959; 23.9469 90; 90; 90 | 5723.4 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.645; 13.7539; 24.1705 90; 90; 90 | 5865.9 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.7542; 13.831; 24.2599 90; 90; 90 | 5957.2 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.9739; 13.7151; 21.1612 90; 91.969; 90 | 2893 | Wang, 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 | CIF | C12 H32 N2 Se7 Sn3 | P b c a | 17.4944; 13.7191; 24.0762 90; 90; 90 | 5778.5 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.8761; 13.597; 20.7839 90; 92.484; 90 | 2788.35 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.8469; 13.5734; 20.7529 90; 92.642; 90 | 2770.8 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.8956; 13.611; 20.8327 90; 92.368; 90 | 2803.54 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.8365; 13.5796; 20.7384 90; 92.727; 90 | 2767.01 | Wang, 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 | CIF | C10 H30 N2 O3 Se7 Sn3 | P 1 21/n 1 | 9.9152; 13.6371; 20.9056 90; 92.274; 90 | 2824.52 | Wang, 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 | CIF | C17 H21 F2 N O4 | P n a 21 | 9.3962; 10.839; 33.4374 90; 90; 90 | 3405.45 | Hofman, 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 | CIF | C18 H48 Eu I2 N8 | P c a 21 | 15.77; 12.1249; 13.749 90; 90; 90 | 2628.9 | Jenks, 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 | CIF | C25 H57 Eu I2 N8 O | P 21 3 | 14.9671; 14.9671; 14.9671 90; 90; 90 | 3352.8 | Jenks, 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 | CIF | C24 H34 B2 Fe2 N18 Ni O7 | C 1 2/c 1 | 28.851; 9.668; 13.718 90; 101.205; 90 | 3753.4 | Jiménez, 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 | CIF | C28 H48 B2 N2 | P 1 21/a 1 | 13.356; 10.8079; 18.731 90; 102.739; 90 | 2637.3 | Kitamura, 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 | CIF | C36 H40 B2 N2 | P -1 | 9.3775; 9.7968; 10.2151 62.343; 79.192; 65.439 | 756 | Kitamura, 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 | CIF | C7 H9 O | P 1 21/c 1 | 8.8275; 6.0025; 12.1333 90; 103.211; 90 | 625.89 | Saito, 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 | CIF | C10 H9 N2 | P 1 21/n 1 | 9.8253; 6.718; 13.1473 90; 110.128; 90 | 814.81 | Saito, 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 | CIF | C17 H18 N2 O | P n a 21 | 12.1379; 7.1688; 16.6494 90; 90; 90 | 1448.73 | Saito, 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 | CIF | C20 H14 N2 O5 | P 21 21 21 | 6.6428; 14.2542; 17.8105 90; 90; 90 | 1686.44 | Khan, 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 | CIF | C20 H14 N2 O5 | P 1 21/c 1 | 11.4782; 14.6774; 10.854 90; 115.824; 90 | 1645.97 | Khan, 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 | CIF | C21 H19 N O3 | P 21 21 21 | 7.0542; 14.1154; 17.6777 90; 90; 90 | 1760.22 | Khan, 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 | CIF | C12 H28 Cl5 N2 Sb | P 21 21 21 | 7.5861; 13.2521; 20.2623 90; 90; 90 | 2037 | Zhang, 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 | CIF | C12 H28 Cl5 N2 Sb | P n m a | 13.0708; 7.9573; 20.1605 90; 90; 90 | 2096.9 | Zhang, 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 | CIF | C48 H68 N4 O8 S4 | P -1 | 9.7664; 10.1835; 14.4361 106.574; 96.681; 101.627 | 1324.56 | Ravi, 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 | CIF | C28 H24 O2 | C 1 2/c 1 | 14.55; 12.0209; 25.0181 90; 99.828; 90 | 4311.55 | Lou, 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 | CIF | C29 H24 O2 | P 1 21/c 1 | 14.1335; 9.122; 17.8477 90; 109.798; 90 | 2165.02 | Lou, 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 | CIF | C27 H20 O2 | P 1 21/n 1 | 9.2661; 8.4682; 25.032 90; 97.682; 90 | 1946.56 | Lou, 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 | CIF | C28 H22 O2 | P 1 21/n 1 | 9.1319; 19.4605; 12.3122 90; 97.242; 90 | 2170.56 | Lou, 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 | CIF | C30 H26 O2 | P 1 21/c 1 | 9.3824; 9.3181; 25.644 90; 97.845; 90 | 2221 | Lou, 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 | CIF | C20 H14 O3 | P b c a | 7.2027; 18.296; 22.189 90; 90; 90 | 2924.1 | Zhang, 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 | CIF | C14 H42 O19 Ti2 V4 | P 1 21/n 1 | 10.2851; 24.103; 12.028 90; 92.176; 90 | 2979.6 | VanGelder, 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 | CIF | C20 H54 Al Cl5 O19.5 Ti2 V4 | P 1 21/m 1 | 19.3992; 11.6179; 19.5185 90; 96.728; 90 | 4368.7 | VanGelder, 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 | CIF | C68 H73 O8.5 | P -1 | 12.353; 14.6695; 16.1299 93.266; 105.038; 100.126 | 2762.64 | Smith, 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 | CIF | C70 H74 Cl6 O8 | P -1 | 13.6525; 15.3663; 17.4716 109.493; 102.788; 99.544 | 3253.02 | Smith, 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 | CIF | C139 H139 Cl9 O16 | P -1 | 14.3309; 18.0783; 24.9943 72.549; 80.55; 75.159 | 5944.5 | Smith, 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 | CIF | C96 H99 O8 | P -1 | 14.2685; 14.5929; 19.2492 101.482; 91.26; 95.436 | 3906.74 | Smith, 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 | CIF | C164 H212 O30 S14 | P -1 | 16.7858; 20.0431; 25.8482 87.859; 88.846; 68.982 | 8111.9 | Smith, 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 | CIF | C138 H132 Cl4 O16 | P -1 | 17.7109; 19.323; 21.2976 78.212; 65.437; 66.098 | 6054.9 | Smith, 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 | CIF | C158 H155 F65 N25 O8 P11 | P -1 | 18.275; 22.178; 26.09 100.067; 91.197; 90.025 | 10409 | Wang, 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 | CIF | C192 H180 F48 N36 O10 P8 | C 1 2/c 1 | 34.3375; 27.6556; 43.5292 90; 105.457; 90 | 39841 | Wang, 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 | CIF | C97 H64 Eu2 F6 N4 O12 | P 1 21/c 1 | 11.765; 22.391; 16.151 90; 110.732; 90 | 3979 | Kalyakina, 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 | CIF | C66 H34 Eu2 F12 N4 O12 | P 1 21/n 1 | 14.583; 13.1391; 15.364 90; 103.713; 90 | 2859.9 | Kalyakina, 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 | CIF | C14 H15 N O2 S | P 1 21 1 | 8.4454; 7.2057; 10.9962 90; 96.797; 90 | 664.47 | Yang, 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 | CIF | C39 H123 N18 O28 Rh5 S15 Zn4 | R 3 :H | 20.209; 20.209; 21.1201 90; 90; 120 | 7469.9 | Yasukawa, 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 | CIF | C39 H139 N18 O36 Rh5 S15 Zn4 | P 1 | 13.279; 13.782; 14.45 95.771; 94.901; 96.534 | 2601 | Yasukawa, 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 | CIF | C46 H32 Cl3 N5 Ni S | P -1 | 10.2159; 14.359; 15.0898 113.223; 103.443; 98.599 | 1905.05 | Berthelot, 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 | CIF | C45 H30 F6 N5 Ni P S | P 1 21/c 1 | 19.386; 20.956; 9.2559 90; 96.226; 90 | 3738.1 | Berthelot, 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 | CIF | C39 H27 N5 Ni S | P 1 21/c 1 | 10.9758; 12.6253; 23.005 90; 93.015; 90 | 3183.5 | Berthelot, 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 | CIF | C14 H10 N2 O2 | P 1 21/c 1 | 14.66; 5.7506; 14.623 90; 109.41; 90 | 1162.7 | Zhou, 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 | CIF | C360 H198 Cu12 N18 O60 | R -3 c :H | 32.322; 32.322; 78.505 90; 90; 120 | 71027 | Omoto, 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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