Crystallography Open Database
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Searching year of publication is 2019
COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1550585 | CIF | C43 H24 F6 Ir N5 S2 | P 1 21/n 1 | 8.4135; 22.5714; 19.5667 90; 95.368; 90 | 3699.5 | Lu, Guang-Zhao; Su, ning; Yang, Huiqing; Zhu, Qi; Zhang, Wen-Wei; Zheng, Youxuan; Zhou, Liang; Zuo, Jing-Lin; Chen, Zhao-Xu; Zhang, Hongjie Rapid room temperature synthesis of red iridium(III) complexes containing four-membered Ir-S-C-S chelating ring for highly efficient OLEDs with EQE over 30% Chemical Science, 2019 |
| 1550586 | CIF | C37 H30 F6 Ir N5 S2 | P 1 21/n 1 | 13.9038; 34.924; 15.0724 90; 92.347; 90 | 7312.7 | Lu, Guang-Zhao; Su, ning; Yang, Huiqing; Zhu, Qi; Zhang, Wen-Wei; Zheng, Youxuan; Zhou, Liang; Zuo, Jing-Lin; Chen, Zhao-Xu; Zhang, Hongjie Rapid room temperature synthesis of red iridium(III) complexes containing four-membered Ir-S-C-S chelating ring for highly efficient OLEDs with EQE over 30% Chemical Science, 2019 |
| 1550587 | CIF HKL Paper | C27 H17 Cl F N3 O2 S | P b c a | 7.9243; 23.7112; 24.927 90; 90; 90 | 4683.7 | El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alqahtani, Alaa; Hegazy, Amany S.; Kariuki, Benson M. 3-{2-[3-(4-Chlorophenyl)-5-(4-fluorophenyl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl]thiazol-4-yl}-3,8a-dihydro-2<i>H</i>-chromen-2-one IUCrData, 2019, 4, x190170 |
| 1550588 | CIF HKL Paper | C23 H17 Cl F N5 O S | P 1 21/c 1 | 5.2879; 26.3742; 15.7872 90; 98.293; 90 | 2178.73 | El-Hiti, Gamal A; Abdel-Wahab, Bakr F.; Yousif, Emad; Alotaibi, Mohammad Hayal; Hegazy, Amany S.; Kariuki, Benson M. 5-[(4-Chlorophenyl)diazenyl]-2-[5-(4-fluorophenyl)-3-(furan-2-yl)-4,5-dihydro-1<i>H</i>-pyrazol-1-yl]-4-methylthiazole IUCrData, 2019, 4, x190211 |
| 1550589 | CIF | C45 H61 Cl N4 Ni O2 | P 1 21/n 1 | 13.217; 20.737; 16.3 90; 112.083; 90 | 4140 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550590 | CIF | C45 H52 Br N4 Ni O2 | P 1 21/n 1 | 13.1252; 20.65; 16.188 90; 112.956; 90 | 4040 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550591 | CIF | C45 H50 N5 Ni | P 1 21/c 1 | 14.185; 10.668; 25.257 90; 94.686; 90 | 3809 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550592 | CIF | C94 H104 Br2 N8 Ni2 O | P -1 | 12.62; 16.578; 20.317 77.4; 84.597; 86.947 | 4127.5 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550593 | CIF | C49 H54 N5 Ni | P 1 21/c 1 | 11.812; 21.544; 16.48 90; 91.636; 90 | 4192.1 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550594 | CIF | C46 H46 N3 Ni | C 1 2/c 1 | 29.913; 13.087; 20.428 90; 99.079; 90 | 7896.8 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550595 | CIF | C57 H69 N5 Ni O | P -1 | 12.662; 12.701; 16.94 72.52; 78.286; 84.831 | 2543.1 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
| 1550596 | CIF | C22 H18 Br N O2 | P 21 21 21 | 9.3465; 10.4901; 18.9441 90; 90; 90 | 1857.4 | Rezayee, Nomaan Mohammed; Lauridsen, Vibeke Henriette; Næsborg, Line; Nguyen, Thanh V. Q.; Tobiesen, Henriette Natorp; Jorgensen, Karl Anker Oxidative Organocatalysed Enantioselective Coupling of Indoles with Aldehydes that Forms Quaternary Carbon Stereocentres Chemical Science, 2019 |
| 1550597 | CIF | C6 H20 Cl2 Cu N4 O | P 21 21 21 | 7.0684; 10.5124; 16.554 90; 90; 90 | 1230.06 | Fu, Chunyan; Lizhao, Junhong; Luo, Zhenghui; Wang, Tao; Grapperhaus, Craig A.; Ding, Xueqin; Kang, Y. James Active uptake of hydrophilic copper complex Cu(ii)-TETA in primary cultures of neonatal rat cardiomyocytes. Metallomics : integrated biometal science, 2019, 11, 565-575 |
| 1550598 | CIF | Al2 H4 O9 Si2 | P 1 | 5.17375; 8.98502; 7.35224 91.6843; 105.128; 89.7549 | 329.789 | Richard, D.; Rendtorff, N. M. First principles study of structural properties and electric field gradients in kaolinite Applied Clay Science, 2019, 169, 67-73 |
| 1550599 | CIF | C64 H36 Cl4 N22 Ru2 | P -1 | 12.9007; 14.8064; 18.5391 89.44; 81.175; 87.749 | 3496.6 | Archer, Stuart; Raza, Ahtasham; Dröge, Fabian; Robertson, Craig C.; Auty, Alexander J.; Chekulaev, Dimitri M.; Weinstein, Julia; Keane, Theo; Meijer, Anthony J. H. M.; Haycock, John; MacNeil, Sheila; Thomas, Jim A. A dinuclear ruthenium(II) phototherapeutic that targets duplex and quadruplex DNA Chemical Science, 2019 |
| 1550600 | CIF | C30 H46 Cl2 Ge2 N4 O2 | P -1 | 8.2234; 10.4654; 11.0901 105.331; 105.474; 104.265 | 833.9 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550601 | CIF | C42 H58 Ge2 N6 O2 | P 1 21/n 1 | 9.571; 13.665; 15.943 90; 91.027; 90 | 2084.8 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550602 | CIF | C39 H28 B F15 Ge N2 O S | P 1 21/c 1 | 15.032; 11.229; 23.3 90; 104.94; 90 | 3800 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550603 | CIF | C52 H70 Ge2 N6 O2 | P 1 21/n 1 | 10.595; 15.635; 14.875 90; 92.261; 90 | 2462.2 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550604 | CIF | C40 H30 B Cl2 F15 Ge N2 O | P -1 | 12.501; 12.739; 15.229 97.161; 106.18; 115.904 | 2008.1 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550605 | CIF | C42 H30 B Cl F15 Ge N2 O | P -1 | 11.7566; 13.7449; 13.7689 65.642; 74.276; 74.609 | 1920.9 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550606 | CIF | C39 H41 B F15 Ge N3 O Si2 | P -1 | 11.6826; 12.4053; 17.1901 83.572; 87.402; 73.342 | 2371.5 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550607 | CIF | C34 H25 B Cl3 F15 Ge N2 O | P -1 | 11.7309; 13.344; 13.627 62.827; 73.967; 81.201 | 1823 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550608 | CIF | C35 H28 B Cl2 F15 Ge N2 O | P 21 21 21 | 12.1298; 15.8356; 19.4206 90; 90; 90 | 3730.4 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550609 | CIF | C44 H62 Ge2 N6 O2 | P -1 | 12.9207; 12.9316; 14.5928 69.991; 89.472; 71.225 | 2155.2 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550610 | CIF | C38 H29 B Cl2 F15 Ge N3 O | P -1 | 12.436; 12.462; 15.186 106.723; 96.368; 115.028 | 1967.5 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550611 | CIF | C51 H38 B F15 Ge N2 O2 Si | P -1 | 11.625; 15.0956; 15.2052 82.564; 69.443; 69.839 | 2345.2 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550612 | CIF | C37 H32 B F15 Ge N2 O2 | P 1 21/n 1 | 11.415; 38.762; 17.556 90; 96.277; 90 | 7721 | Sharma, Mahendra Kumar; Sinhababu, Soumen; Mahawar, Pritam; Mukherjee, Goutam; Pandey, Bhawana; Rajaraman, Gopalan; Selvarajan, Nagendran Donor-Acceptor-Stabilized Germanium Analogues of Acid Chloride, Ester, and Acyl Pyrrole Compounds: Synthesis and Reactivity Chemical Science, 2019 |
| 1550613 | CIF | C60 H61.5 F0.5 N3 P2 | P -1 | 10.7104; 13.0233; 20.6386 87.872; 83.02; 65.815 | 2606.38 | Schulz, Axel; Bresien, Jonas; Kroeger-Badge, Thomas; Lochbrunner, Stefan; Michalik, Dirk; Müller, Henrik; Zander, Edgar A chemical reaction controlled by light-activated molecular switches based on hetero-cyclopentanediyls Chemical Science, 2019 |
| 1550614 | CIF | C60 H61.5 F0.5 N3 P2 | P -1 | 10.5944; 12.9038; 20.3409 85.38; 82.564; 66.245 | 2522.5 | Schulz, Axel; Bresien, Jonas; Kroeger-Badge, Thomas; Lochbrunner, Stefan; Michalik, Dirk; Müller, Henrik; Zander, Edgar A chemical reaction controlled by light-activated molecular switches based on hetero-cyclopentanediyls Chemical Science, 2019 |
| 1550615 | CIF | C72 H162 K N O24 Si6 U2 | P 1 21/c 1 | 14.21; 28.1537; 27.91 90; 104.632; 90 | 10804 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550616 | CIF | C73 H162 K2 N2 O26 Si6 U2 | P 1 21 1 | 13.9377; 17.9175; 22.0849 90; 92.306; 90 | 5510.8 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550617 | CIF | C73 H162 K2 N2 O24 S2 Si6 U2 | P 1 21 1 | 13.9065; 18.2338; 22.181 90; 92.45; 90 | 5619.3 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550618 | CIF | C81 H170 K2 N2 O26 Si6 U2 | P 1 21 1 | 13.9927; 18.2874; 22.208 90; 93.321; 90 | 5673.3 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550619 | CIF | C79 H172 K2 N2 O24 Si6 U2 | P 1 21/n 1 | 14.4207; 17.5321; 21.9098 90; 91.84; 90 | 5536.5 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550620 | CIF | C72 H162 K2 N4 O24 Si6 U2 | P 1 21/n 1 | 14.382; 17.661; 21.819 90; 92.012; 90 | 5538.6 | Barluzzi, Luciano; Chatelain, Lucile; Fadaei-Tirani, Farzaneh; Zivkovic, Ivica; Mazzanti, Marinella Facile N-functionalization and strong magnetic communication in a diuranium(v) bis-nitride complex Chemical Science, 2019 |
| 1550621 | CIF | C11 H20 B10 S2 | P 1 21/c 1 | 12.427; 12.068; 11.6342 90; 92.622; 90 | 1742.9 | Messina, Marco S.; Graefe, Christian T.; Chong, Paul; Ebrahim, Omar M.; Pathuri, Ramya S.; Bernier, Nicholas A.; Mills, Harrison A.; Rheingold, Arnold L.; Frontiera, Renee R.; Maynard, Heather D.; Spokoyny, Alexander M. Carborane RAFT agents as tunable and functional molecular probes for polymer materials Polymer Chemistry, 2019, 10, 1660 |
| 1550622 | CIF | C36 H21 F20 O3 P | P -1 | 9.973; 10.483; 19.394 88.696; 79.354; 62.57 | 1764.13 | Jiang, Xin-Dong; Toya, Yuya; Matsukawa, Shiro; Kojima, Satoshi; Jimenez-Halla, Jose Oscar Carlos; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P-O-C-C four-membered ring Chemical Science, 2019 |
| 1550623 | CIF | C37 H23 Cl2 F20 O3 P | C 1 2/c 1 | 39.273; 9.553; 26.355 90; 127.505; 90 | 7843.9 | Jiang, Xin-Dong; Toya, Yuya; Matsukawa, Shiro; Kojima, Satoshi; Jimenez-Halla, Jose Oscar Carlos; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P-O-C-C four-membered ring Chemical Science, 2019 |
| 1550624 | CIF | C56 H60 F20 K O11 P | P -1 | 11.03; 12.802; 23.276 105.47; 92.07; 96.064 | 3142.8 | Jiang, Xin-Dong; Toya, Yuya; Matsukawa, Shiro; Kojima, Satoshi; Jimenez-Halla, Jose Oscar Carlos; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P-O-C-C four-membered ring Chemical Science, 2019 |
| 1550625 | CIF | C44 H36 F20 K O5 P | P 1 21/n 1 | 18.972; 13.493; 19.631 90; 111.443; 90 | 4677.5 | Jiang, Xin-Dong; Toya, Yuya; Matsukawa, Shiro; Kojima, Satoshi; Jimenez-Halla, Jose Oscar Carlos; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P-O-C-C four-membered ring Chemical Science, 2019 |
| 1550626 | CIF | C56 H68 F12 K O12 P | P 1 21/c 1 | 15.552; 13.58; 28.022 90; 95.733; 90 | 5889 | Jiang, Xin-Dong; Toya, Yuya; Matsukawa, Shiro; Kojima, Satoshi; Jimenez-Halla, Jose Oscar Carlos; Shang, Rong; Nakamoto, Masaaki; Yamamoto, Yohsuke Synthesis and characterization of a pair of O-fac/O-mer 12-P-6 alkyloxaphosphates with a P-O-C-C four-membered ring Chemical Science, 2019 |
| 1550627 | CIF | C44 H46 O4 | P -1 | 10.8484; 11.0591; 15.2489 76.98; 84.293; 86.909 | 1772.66 | Ye, Changqing; Li, Yajun; Zhu, Xiaotao; Hu, Shengmin; Yuan, Daqiang; Bao, Hongli Copper-Catalyzed 1,4-Alkylarylation of 1,3-Enynes with Masked Alkyl Electrophiles Chemical Science, 2019 |
| 1550628 | CIF HKL Paper | C20 H17 N5 O | P -1 | 9.7894; 10.983; 17.2596 93.49; 95.702; 107.729 | 1750.67 | El-Hiti, Gamal A.; Abdel-Wahab, Bakr F.; Alqahtani, Alaa; Hegazy, Amany S.; Kariuki, Benson M. 3-[5-Methyl-1-(4-methylphenyl)-1<i>H</i>-1,2,3-triazol-4-yl]-1-phenyl-1<i>H</i>-pyrazole-4-carbaldehyde IUCrData, 2019, 4, x190217 |
| 1550629 | CIF | C148.57 H175.16 B6 Cl5.16 Fe N10 | P 21 21 21 | 17.5522; 21.2914; 35.9929 90; 90; 90 | 13450.9 | McNicholas, Brendon James; Grubbs, Robert H.; Winkler, Jay; Gray, Harry B.; Despagnet-Ayoub, Emmanuelle Tuning the Formal Potential of Ferrocyanide over a 2.1 V Range Chemical Science, 2019 |
| 1550630 | CIF | C44 H99 Fe N13 O5 | C 1 c 1 | 16.3801; 15.2273; 22.2072 90; 92.0316; 90 | 5535.5 | McNicholas, Brendon James; Grubbs, Robert H.; Winkler, Jay; Gray, Harry B.; Despagnet-Ayoub, Emmanuelle Tuning the Formal Potential of Ferrocyanide over a 2.1 V Range Chemical Science, 2019 |
| 1550631 | CIF | C263.25 H130.49 B6 Cl10.49 F90 Fe N10 P8 | P -1 | 19.29; 19.912; 20.432 65.073; 68.449; 80.849 | 6619 | McNicholas, Brendon James; Grubbs, Robert H.; Winkler, Jay; Gray, Harry B.; Despagnet-Ayoub, Emmanuelle Tuning the Formal Potential of Ferrocyanide over a 2.1 V Range Chemical Science, 2019 |
| 1550632 | CIF | C15 H18 N2 O S | P 1 21/n 1 | 5.9659; 16.3145; 14.5127 90; 99.253; 90 | 1394.15 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
| 1550633 | CIF | C12 H12 O2 S | P b c a | 16.151; 7.314; 19.036 90; 90; 90 | 2249 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
| 1550634 | CIF | C9 H14 N2 O S | P 1 21/n 1 | 7.5382; 12.2061; 10.8739 90; 95.949; 90 | 995.14 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
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