Crystallography Open Database
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COD ID  |
Links | Formula  |
Space group |
Cell parameters | Cell volume |
Bibliography |
|---|---|---|---|---|---|---|
| 1518527 | CIF | C38 H48 N2 O4 | P 1 21/c 1 | 14.93217; 14.22602; 15.93712 90; 100.89; 90 | 3324.49 | Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S. Increased carrier mobility in end-functionalized oligosilanes Chem. Sci., 2015, 6, 1905 |
| 1518528 | CIF | C30 H40 N2 O4 Si4 | P -1 | 8.5558; 11.887; 17.0071 99.115; 92.129; 94.397 | 1700.67 | Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S. Increased carrier mobility in end-functionalized oligosilanes Chem. Sci., 2015, 6, 1905 |
| 1518529 | CIF | C34 H52 N2 O4 Si6 | P -1 | 8.6514; 11.8373; 20.4256 82.751; 87.339; 86.175 | 2068.9 | Surampudi, S.; Yeh, M.-L.; Siegler, M. A.; Hardigree, J. F. Martinez; Kasl, T. A.; Katz, H. E.; Klausen, R. S. Increased carrier mobility in end-functionalized oligosilanes Chem. Sci., 2015, 6, 1905 |
| 1518530 | CIF | C152.05 H75.74 Cl2.21 F40 N12 S8 | P -1 | 18.9073; 20.7452; 21.091 67.38; 77.21; 65.257 | 6917.2 | Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro 5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents Chem. Sci., 2015, 6, 1696 |
| 1518531 | CIF | C87.05 H40.13 Cl3.96 F20 N6 S6 | C 1 2/c 1 | 49.998; 12.402; 35.242 90; 131.613; 90 | 16338 | Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro 5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents Chem. Sci., 2015, 6, 1696 |
| 1518532 | CIF | C95.3 H48 Cl2.3 F20 N6 O0.5 S8 | P -1 | 17.2734; 18.9028; 30.1289 105; 92.92; 107.23 | 8989 | Mori, Hirotaka; Suzuki, Masaaki; Kim, Woojae; Lim, Jong Min; Kim, Dongho; Osuka, Atsuhiro 5,20-Bis(α-oligothienyl)-substituted [26]hexaphyrins possessing electronic circuits strongly perturbed by meso-oligothienyl substituents Chem. Sci., 2015, 6, 1696 |
| 1518536 | CIF | C18 H11 F6 N O3 | C 1 2/c 1 | 32.403; 6.8959; 15.25 90; 97.03; 90 | 3382 | Lu, Yi; Wang, Huai-Wei; Spangler, Jillian E.; Chen, Kai; Cui, Pei-Pei; Zhao, Yue; Sun, Wei-Yin; Yu, Jin-Quan Rh(iii)-catalyzed C‒H olefination of N-pentafluoroaryl benzamides using air as the sole oxidant Chem. Sci., 2015, 6, 1923 |
| 1518540 | CIF | C18 H33 N2 O8 S2 | P -1 | 7.8956; 9.6557; 14.916 77.311; 81.835; 86.214 | 1097.43 | Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water Chem. Sci., 2015, 6, 2079 |
| 1518541 | CIF | C36 H66 N4 O16 S4 | I 1 2/c 1 | 19.4827; 7.7013; 30.1416 90; 101.758; 90 | 4427.61 | Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water Chem. Sci., 2015, 6, 2079 |
| 1518542 | CIF | C28.7552 H49.5104 N8 O14 S4 | P -1 | 9.7673; 9.8143; 10.2046 94.88; 96.822; 95.184 | 962.76 | Dumitrescu, Dan; Legrand, Yves-Marie; Petit, Eddy; van der Lee, Arie; Barboiu, Mihail Adaptive binding and selection of compressed 1,ω-diammonium-alkanes via molecular encapsulation in water Chem. Sci., 2015, 6, 2079 |
| 1518545 | CIF | C14 H34 Cl Mo P3 | P 21 21 21 | 11.8282; 12.449; 13.6005 90; 90; 90 | 2002.7 | Neary, Michelle C.; Parkin, Gerard Dehydrogenation, disproportionation and transfer hydrogenation reactions of formic acid catalyzed by molybdenum hydride compounds Chem. Sci., 2015, 6, 1859 |
| 1518548 | CIF | C44.71 H22.16 Cl4 F14 N6 Na2 O7.22 | P -1 | 14.6741; 15.8676; 24.1918 91.946; 106.327; 115.228 | 4812.8 | Seifert, Sabine; Schmidt, David; Würthner, Frank An ambient stable core-substituted perylene bisimide dianion: isolation and single crystal structure analysis Chem. Sci., 2015, 6, 1663 |
| 1518587 | CIF | C56 H92 Cl2 Co2 I2 N4 P4 Ti2 | P b c a | 18.6991; 16.4217; 21.8753 90; 90; 90 | 6717.3 | Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M. A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes Chem. Sci., 2015, 6, 2044 |
| 1518588 | CIF | C31 H55 Cl Co N2 P3 Ti | P 1 21/n 1 | 9.0138; 18.8395; 21.5085 90; 90.54; 90 | 3652.3 | Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M. A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes Chem. Sci., 2015, 6, 2044 |
| 1518589 | CIF | C68 H104 Co2 I2 N4 O2 P4 Ti2 | P -1 | 12.5912; 13.4571; 13.5956 110.682; 94.623; 117.15 | 1835.07 | Wu, Bing; Bezpalko, Mark W.; Foxman, Bruce M.; Thomas, Christine M. A heterobimetallic complex featuring a Ti‒Co multiple bond and its application to the reductive coupling of ketones to alkenes Chem. Sci., 2015, 6, 2044 |
| 1518590 | CIF | C24 H16 Au2 F8 N4 O2 | P -1 | 3.5452; 14.0087; 14.249 109.292; 91.673; 91.322 | 667.23 | Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence Chem. Sci., 2015, 6, 2187 |
| 1518591 | CIF | C18 H4 Au2 F8 N4 | P -1 | 3.5707; 10.3087; 14.2742 107.689; 92.505; 100.205 | 489.99 | Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence Chem. Sci., 2015, 6, 2187 |
| 1518592 | CIF | C18 H4 Au2 F8 N4 | P 1 21/c 1 | 7.79058; 18.7202; 6.74157 90; 103.167; 90 | 957.35 | Seki, Tomohiro; Ozaki, Taichi; Okura, Takuma; Asakura, Kiyotaka; Sakon, Aya; Uekusa, Hidehiro; Ito, Hajime Interconvertible multiple photoluminescence color of a gold(i) isocyanide complex in the solid state: solvent-induced blue-shifted and mechano-responsive red-shifted photoluminescence Chem. Sci., 2015, 6, 2187 |
| 1518593 | CIF | C30 H51 Ir P2 | P -1 | 10.264; 16.311; 19.425 103.753; 105.008; 93.129 | 3027.6 | Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F. Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex Chem. Sci., 2015, 6, 2060 |
| 1518594 | CIF | C31 H55 Ir O P2 | P 1 21/c 1 | 17.003; 20.0591; 9.4403 90; 102.986; 90 | 3137.41 | Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F. Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex Chem. Sci., 2015, 6, 2060 |
| 1518595 | CIF | C24 H46 Cl Ir P2 | P 1 21/c 1 | 11.4108; 13.6574; 17.7933 90; 104.097; 90 | 2689.4 | Polukeev, Alexey V.; Marcos, Rocío; Ahlquist, Mårten S. G.; Wendt, Ola F. Formation of a C‒C double bond from two aliphatic carbons. Multiple C‒H activations in an iridium pincer complex Chem. Sci., 2015, 6, 2060 |
| 1518596 | CIF | C34 H26 F4 P2 | P 1 21/n 1 | 9.2062; 16.7452; 17.6319 90; 101.286; 90 | 2665.6 | Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Chem. Sci., 2015, 6, 2016 |
| 1518597 | CIF | C25 H22 F4 P2 | C 1 2 1 | 21.0973; 8.3882; 6.3567 90; 102.383; 90 | 1098.76 | Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Chem. Sci., 2015, 6, 2016 |
| 1518598 | CIF | C58 H26 B F21 P2 | P 1 21 1 | 8.4256; 21.123; 13.804 90; 95.055; 90 | 2447.2 | Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Chem. Sci., 2015, 6, 2016 |
| 1518599 | CIF | C59.25 H28.5 B Cl2.5 F23 P2 | P 1 21/c 1 | 18.8002; 17.1372; 17.8001 90; 102.564; 90 | 5597.6 | Holthausen, Michael H.; Hiranandani, Rashi R.; Stephan, Douglas W. Electrophilic bis-fluorophosphonium dications: Lewis acid catalysts from diphosphines Chem. Sci., 2015, 6, 2016 |
| 1518609 | CIF | C35 H28 F6 N3 P S2 Se4 | P 1 21/n 1 | 19.6176; 7.5992; 25.2231 90; 93.7263; 90 | 3752.3 | Bedics, Matthew A.; Kearns, Hayleigh; Cox, Jordan M.; Mabbott, Sam; Ali, Fatima; Shand, Neil C.; Faulds, Karen; Benedict, Jason B.; Graham, Duncan; Detty, Michael R. Extreme red shifted SERS nanotags Chem. Sci., 2015, 6, 2302 |
| 1518610 | CIF | C20 H14 | P -1 | 9.6321; 11.0943; 14.7022 67.862; 79.883; 69.219 | 1359 | Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C Chem. Sci., 2015, 6, 1816 |
| 1518611 | CIF | C24 H16 | P 1 21/c 1 | 19.1157; 5.7556; 29.6669 90; 108.002; 90 | 3104.2 | Collins, Karl D.; Honeker, Roman; Vásquez-Céspedes, Suhelen; Tang, Dan-Tam D.; Glorius, Frank C‒H arylation of triphenylene, naphthalene and related arenes using Pd/C Chem. Sci., 2015, 6, 1816 |
| 1518661 | CIF | C64 H48 S4 | P 1 21/n 1 | 20.159; 5.0166; 25.728 90; 109.164; 90 | 2457.7 | Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 2015, 6, 2354 |
| 1518662 | CIF | C65 H50 S4 | P 1 21/n 1 | 20.1; 5.1652; 25.159 90; 109.501; 90 | 2462.2 | Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 2015, 6, 2354 |
| 1518663 | CIF | C68 H56 Cl2 S4 | P 1 21/c 1 | 7.6706; 17.4871; 20.506 90; 100.272; 90 | 2706.5 | Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 2015, 6, 2354 |
| 1518664 | CIF | C66 H52 S4 | P 1 21/n 1 | 21.43; 5.2798; 24.95 90; 111.599; 90 | 2624.8 | Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 2015, 6, 2354 |
| 1518665 | CIF | C66 H52 S4 | P 1 21/n 1 | 20.0834; 5.2324; 24.6005 90; 109.019; 90 | 2444.01 | Chou, Chih-Ming; Nobusue, Shunpei; Saito, Shohei; Inoue, Daishi; Hashizume, Daisuke; Yamaguchi, Shigehiro Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 2015, 6, 2354 |
| 1518666 | CIF | C8 H16 F7 O6 P2 S2 Sb | P 1 21/n 1 | 14.5029; 8.9034; 14.9927 90; 97.26; 90 | 1920.41 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518667 | CIF | C43 H71 F9 N3 O9 P3 S3 Sb4 | P -1 | 11.4789; 11.9874; 26.0864 91.82; 97.564; 112.074 | 3284.57 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518668 | CIF | C29 H61.5 F12 N0.5 O12 P4 S4 Sb4 | P 1 21/c 1 | 23.986; 21.83; 22.193 90; 106.57; 90 | 11138 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518669 | CIF | C31 H41 F6 N2 O6 S2 Sb | P 1 21/c 1 | 12.3127; 17.4575; 17.0214 90; 91.03; 90 | 3658.1 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518670 | CIF | C4 H9 F4 O3 P S | P 1 21/m 1 | 10.2147; 8.6511; 11.0323 90; 94.5503; 90 | 971.83 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518671 | CIF | C14 H30 F6 O6 P2 S2 | P 1 21/n 1 | 13.4271; 11.8532; 15.7504 90; 110.993; 90 | 2340.4 | Chitnis, Saurabh S.; Robertson, Alasdair P. M.; Burford, Neil; Weigand, Jan J.; Fischer, Roland Synthesis and reactivity of cyclo-tetra(stibinophosphonium) tetracations: redox and coordination chemistry of phosphine‒antimony complexes Chem. Sci., 2015, 6, 2559 |
| 1518672 | CIF | C27 H24 Cl5 F6 N5 O P2 Ru | P -1 | 11.1445; 12.0548; 14.8726 67.197; 84.942; 67.025 | 1691.09 | Walden, Andrew G.; Miller, Alexander J. M. Rapid water oxidation electrocatalysis by a ruthenium complex of the tripodal ligand tris(2-pyridyl)phosphine oxide Chem. Sci., 2015, 6, 2405 |
| 1518676 | CIF | C17 H25 N O2 Si | P 1 21/n 1 | 7.8451; 10.8055; 41.681 90; 92.188; 90 | 3530.7 | Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams Chem. Sci., 2015, 6, 2275 |
| 1518677 | CIF | C19 H19 Cl2 N O S | P 1 21/c 1 | 9.4678; 22.465; 8.4857 90; 94.892; 90 | 1798.3 | Wu, Shangze; Zeng, Rong; Fu, Chunling; Yu, Yihua; Zhang, Xue; Ma, Shengming Rhodium-catalyzed C‒H functionalization-based approach to eight-membered lactams Chem. Sci., 2015, 6, 2275 |
| 1518714 | CIF | C14 H26 Cl3 N4 O P Ru | P 1 21/n 1 | 6.9163; 23.66; 11.8396 90; 97.078; 90 | 1922.7 | Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G. Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action Chem. Sci., 2015, 6, 2449 |
| 1518715 | CIF | C15 H23 Cl2 N4 O P Ru | P -1 | 10.5379; 12.8283; 13.7451 100.766; 97.279; 91.491 | 1808.34 | Babak, Maria V.; Meier, Samuel M.; Huber, Kilian V. M.; Reynisson, Jóhannes; Legin, Anton A.; Jakupec, Michael A.; Roller, Alexander; Stukalov, Alexey; Gridling, Manuela; Bennett, Keiryn L.; Colinge, Jacques; Berger, Walter; Dyson, Paul J.; Superti-Furga, Giulio; Keppler, Bernhard K.; Hartinger, Christian G. Target profiling of an antimetastatic RAPTA agent by chemical proteomics: relevance to the mode of action Chem. Sci., 2015, 6, 2449 |
| 1518716 | CIF | C42 H55 Cl2 N5 O10 | C 1 2 1 | 25.187; 8.1556; 21.154 90; 99.308; 90 | 4288.1 | Rose, Tristan E.; Lawson, Kenneth V.; Harran, Patrick. G. Large ring-forming alkylations provide facile access to composite macrocycles Chem. Sci., 2015, 6, 2219 |
| 1518727 | CIF | C53 H53 F3 N4 O3 P2 S | C 1 c 1 | 24.05898; 12.60445; 17.26646 90; 109.899; 90 | 4923.42 | Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H. Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system Chem. Sci., 2015, 6, 2506 |
| 1518728 | CIF | C67 H72 Cl Ir N4 P2 | P -1 | 11.53121; 15.09347; 16.48026 91.4726; 100.955; 90.9436 | 2814.45 | Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H. Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system Chem. Sci., 2015, 6, 2506 |
| 1518729 | CIF | C54 H52 Cl Ir N4 O2 P2 | R -3 | 30.1754; 30.1754; 27.5094 90; 90; 120 | 21692.9 | Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H. Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system Chem. Sci., 2015, 6, 2506 |
| 1518730 | CIF | C71.5 H80 Cl2 Ir2 N4 P2 | P -1 | 13.28816; 15.4534; 18.6095 66.4438; 87.7181; 64.8361 | 3131.28 | Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H. Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system Chem. Sci., 2015, 6, 2506 |
| 1518731 | CIF | C55.5 H62 Au2 Cl3 Ir N4 P2 | P 1 21/c 1 | 12.88426; 13.46559; 30.9781 90; 99.5872; 90 | 5299.46 | Roth, Torsten; Vasilenko, Vladislav; Benson, Callum G. M.; Wadepohl, Hubert; Wright, Dominic S.; Gade, Lutz H. Extending N-heterocyclic carbene ligands into the third dimension: a new type of hybrid phosphazane/NHC system Chem. Sci., 2015, 6, 2506 |
| 1518738 | CIF | C19.5 H18.5 As3 Cl6.5 S6 | P n m a | 20.703; 9.885; 14.702 90; 90; 90 | 3008.8 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518739 | CIF | C24 H24 Cl3 S6 Sb3 | R -3 c :H | 14.2066; 14.2066; 33.41 90; 90; 120 | 5839.7 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518740 | CIF | C36 H42 As3 Cl3 S6 | P -1 | 10.0055; 12.424; 16.522 81.285; 88.456; 84.579 | 2020.9 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518741 | CIF | C30 H42 As3 Cl3 S6 | R -3 :H | 16.413; 16.413; 23.8 90; 90; 120 | 5552.4 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518742 | CIF | C24 H30 Cl3 S6 Sb3 | P 1 21/n 1 | 16.0971; 11.4604; 16.3368 90; 91.867; 90 | 3012.2 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518743 | CIF | C30 H42 Cl3 S6 Sb3 | R -3 :H | 16.458; 16.458; 23.9449 90; 90; 120 | 5616.9 | Collins, Mary S.; Choi, Robert Y.; Zakharov, Lev N.; Watson, Lori A.; Hay, Benjamin P.; Johnson, Darren W. Self-assembled trinuclear arsenic and antimony macrobicycles Chem. Sci., 2015, 6, 2444 |
| 1518744 | CIF | C32 H30 N8 O5 Zn4 | P 42/m c m | 11.5382; 11.5382; 25.813 90; 90; 90 | 3436.5 | Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications Chem. Sci., 2015, 6, 2516 |
| 1518745 | CIF | C34 H32 N8 O5 Zn4 | P 42/m c m | 11.517; 11.517; 34.474 90; 90; 90 | 4573 | Lin, Rui-Biao; Li, Tai-Yang; Zhou, Hao-Long; He, Chun-Ting; Zhang, Jie-Peng; Chen, Xiao-Ming Tuning fluorocarbon adsorption in new isoreticular porous coordination frameworks for heat transformation applications Chem. Sci., 2015, 6, 2516 |
| 1518753 | CIF | C37 H31 Cu F12 N4 | P -1 | 12.1667; 12.1867; 13.5954 81.549; 77.873; 65.444 | 1788.5 | Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions Chem. Sci., 2015, 6, 2474 |
| 1518754 | CIF | C16 H6 F12 N2 | I 41/a :2 | 36.71; 36.71; 4.9148 90; 90; 90 | 6623.3 | Tomson, Neil C.; Williams, Kamille D.; Dai, Xuliang; Sproules, Stephen; DeBeer, Serena; Warren, Timothy H.; Wieghardt, Karl Re-evaluating the Cu K pre-edge XAS transition in complexes with covalent metal‒ligand interactions Chem. Sci., 2015, 6, 2474 |
| 1518755 | CIF | C18 H27 Au B Cl N2 O2 | P 1 21/n 1 | 11.295; 10.512; 16.9583 90; 102.328; 90 | 1967.1 | Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors Chem. Sci., 2015, 6, 2893 |
| 1518756 | CIF | C53 H79 Au B Cl N4 O4 | P 1 21/c 1 | 15.396; 14.4925; 24.966 90; 100.935; 90 | 5469.4 | Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors Chem. Sci., 2015, 6, 2893 |
| 1518757 | CIF | C19 H27 B F3 Li N2 O5 S | P -1 | 5.9513; 10.9562; 17.3953 96.176; 93.242; 97.646 | 1114.73 | Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors Chem. Sci., 2015, 6, 2893 |
| 1518758 | CIF | C26 H39 B Cl N2 O2 Rh | P 1 21/c 1 | 16.46; 13.8072; 11.9483 90; 104.628; 90 | 2627.4 | Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors Chem. Sci., 2015, 6, 2893 |
| 1518759 | CIF | C33 H47 B Cl Ir N2 O2 | C 1 2/c 1 | 35.4699; 10.667; 18.1337 90; 115.404; 90 | 6197.6 | Kong, Lingbing; Ganguly, Rakesh; Li, Yongxin; Kinjo, Rei Diverse reactivity of a tricoordinate organoboron L2PhB: (L = oxazol-2-ylidene) towards alkali metal, group 9 metal, and coinage metal precursors Chem. Sci., 2015, 6, 2893 |
| 1518761 | CIF | C25 H23 F12 Fe2 O10 | P -1 | 9.507; 11.729; 16.605 102.703; 96.771; 112.595 | 1625 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518762 | CIF | C35 H25 F24 Fe3 O14 | P 1 21 1 | 9.7834; 20.8414; 12.0955 90; 102.57; 90 | 2407.2 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518763 | CIF | C35 H25 F24 Fe3 O14 | P 1 21 1 | 9.7979; 20.819; 12.0998 90; 102.659; 90 | 2408.2 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518764 | CIF | C35 H19 F30 Fe3 O14 | C 1 2/c 1 | 20.934; 13.481; 17.739 90; 92.848; 90 | 5000 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518765 | CIF | C25 H23 F12 Fe Mn O10 | P -1 | 9.464; 11.8255; 16.508 102.022; 97.859; 112.682 | 1618.3 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518766 | CIF | C35 H25 F24 Fe Ni2 O14 | P 1 21 1 | 9.7682; 20.7583; 12.0575 90; 103.126; 90 | 2381 | Lieberman, Craig M.; Filatov, Alexander S.; Wei, Zheng; Rogachev, Andrey Yu.; Abakumov, Artem M.; Dikarev, Evgeny V. Mixed-valent, heteroleptic homometallic diketonates as templates for the design of volatile heterometallic precursors Chem. Sci., 2015, 6, 2835 |
| 1518779 | CIF | C38 H34 Cl2 Ir N P2 | I b a m | 30.868; 17.517; 24.155 90; 90; 90 | 13061 | Liu, Chong; Xie, Jian-Hua; Tian, Gui-Long; Li, Wei; Zhou, Qi-Lin Highly efficient hydrogenation of carbon dioxide to formate catalyzed by iridium(iii) complexes of imine‒diphosphine ligands Chem. Sci., 2015, 6, 2928 |
| 1518780 | CIF | Ga1.67 O10 P2.5 Zn0.83 | C 1 2/m 1 | 16.767; 19.047; 10.248 90; 127.038; 90 | 2612.5 | Wu, Junbiao; Tao, Chunyao; Li, Yi; Li, Jiyang; Yu, Jihong Methyl viologen-templated zinc gallophosphate zeolitic material with dual photo-/thermochromism and tuneable photovoltaic activity Chem. Sci., 2015, 6, 2922 |
| 1518781 | CIF | C63 H59 B F29 Fe N3 P2 | P -1 | 12.7767; 13.894; 38.0545 90.4567; 92.9881; 96.475 | 6702.5 | Darmon, Jonathan M.; Kumar, Neeraj; Hulley, Elliott B.; Weiss, Charles J.; Raugei, Simone; Bullock, R. Morris; Helm, Monte L. Increasing the rate of hydrogen oxidation without increasing the overpotential: a bio-inspired iron molecular electrocatalyst with an outer coordination sphere proton relay Chem. Sci., 2015, 6, 2737 |
| 1518782 | CIF | C38 H55 Co N2 O4 | P 1 21/n 1 | 17.569; 10.302; 19.781 90; 100.629; 90 | 3518.8 | Zhao, Yaguang; Yu, Mengmeng; Zhang, Shuailin; Wu, Zhenqiang; Liu, Yuchu; Peng, Chi-How; Fu, Xuefeng A well-defined, versatile photoinitiator (salen)Co‒CO2CH3for visible light-initiated living/controlled radical polymerization Chem. Sci., 2015, 6, 2979 |
| 1518784 | CIF | C16 H29 B I N3 | C 1 2/c 1 | 17.3182; 19.7092; 12.0924 90; 120.773; 90 | 3546.3 | Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts Chem. Sci., 2015, 6, 2938 |
| 1518785 | CIF | C17 H30 B N3 O4 | P 21 21 21 | 7.1546; 12.8526; 20.4294 90; 90; 90 | 1878.59 | Chauvier, Clément; Tlili, Anis; Das Neves Gomes, Christophe; Thuéry, Pierre; Cantat, Thibault Metal-free dehydrogenation of formic acid to H2and CO2using boron-based catalysts Chem. Sci., 2015, 6, 2938 |
| 1518786 | CIF | C23 H17 N | P n a 21 | 7.4701; 19.7919; 11.1894 90; 90; 90 | 1654.32 | Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J. Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters Chem. Sci., 2015, 6, 2843 |
| 1518787 | CIF | C58 H46 F6 Ir N4 O P | P n a 21 | 13.128; 37.8916; 10.29 90; 90; 90 | 5118.7 | Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J. Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters Chem. Sci., 2015, 6, 2843 |
| 1518788 | CIF | C44 H32 F6 Ir N4 P | P 1 21/n 1 | 15.0877; 13.1747; 18.093 90; 96.094; 90 | 3576.1 | Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J. Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters Chem. Sci., 2015, 6, 2843 |
| 1518789 | CIF | C76 H60 F6 Ir N4 P | P -1 | 10.8073; 13.5065; 20.8777 80.953; 86.577; 78.797 | 2950.9 | Bünzli, Andreas M.; Constable, Edwin C.; Housecroft, Catherine E.; Prescimone, Alessandro; Zampese, Jennifer A.; Longo, Giulia; Gil-Escrig, Lidón; Pertegás, Antonio; Ortí, Enrique; Bolink, Henk J. Exceptionally long-lived light-emitting electrochemical cells: multiple intra-cation π-stacking interactions in [Ir(C^N)2(N^N)][PF6] emitters Chem. Sci., 2015, 6, 2843 |
| 1518821 | CIF | C65 H80 Au N O | P -1 | 11.6132; 14.7425; 16.9669 87.393; 71.112; 80.062 | 2707 | Ming Tong, Glenna So; Chan, Kaai Tung; Chang, Xiaoyong; Che, Chi-Ming Theoretical studies on the photophysical properties of luminescent pincer gold(iii) arylacetylide complexes: the role of π-conjugation at the C-deprotonated [C^N^C] ligand Chem. Sci., 2015, 6, 3026 |
| 1518822 | CIF | C35 H34 Au B Mn O2 P | P -1 | 10.071; 11.844; 13.4 86.394; 79.387; 74.371 | 1512.8 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518823 | CIF | C43 H40 Au B Mn O2 P | C 1 2/c 1 | 41.848; 10.898; 15.941 90; 91.024; 90 | 7269 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518824 | CIF | C30 H29 Au B Mn N O2 P S | P 1 21/n 1 | 13.491; 13.559; 16.412 90; 101.959; 90 | 2937 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518825 | CIF | C46 H40 Au B3 Cl8 Mn2 O4 | P 1 21/c 1 | 18.435; 33.798; 17.288 90; 113.832; 90 | 9853 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518826 | CIF | C98 H85 Ag2 B6 Cl16 F Mn4 O8 | P -1 | 12.2946; 13.8214; 16.0619 88.083; 67.993; 83.916 | 2516.2 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518827 | CIF | C53 H48 Ag B3 Cl8 Mn2 O4 | P 1 21/n 1 | 11.184; 36.556; 13.609 90; 93.434; 90 | 5554 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518828 | CIF | C46 H40 Ag B3 Cl8 Mn2 O4 | P 1 21/c 1 | 18.444; 33.901; 17.285 90; 113.909; 90 | 9880 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518829 | CIF | C53 H48 B3 Cl8 Cu Mn2 O4 | P 1 21/n 1 | 11.0743; 36.198; 13.711 90; 93.21; 90 | 5488 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518830 | CIF | C55 H50 B3 Cl12 Cu2 Mn3 O6 | P -1 | 11.952; 14.576; 20.573 70.672; 73.21; 68.233 | 3084 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518831 | CIF | C67 H62 B3 Cl8 Cu2 Mn3 O6 | P -1 | 11.301; 14.461; 21.311 97.172; 96.19; 102.139 | 3345.8 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518832 | CIF | C75 H50 Au B F24 P2 | P -1 | 12.38; 15.772; 18.327 83.065; 74.699; 81.63 | 3402.1 | Braunschweig, Holger; Radacki, Krzysztof; Shang, Rong Side-on coordination of boryl and borylene complexes to cationic coinage metal fragments Chem. Sci., 2015, 6, 2989 |
| 1518843 | CIF | C22 H23 N O3 | P 1 21/n 1 | 6.0325; 20.594; 14.3515 90; 97.425; 90 | 1768 | Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans Chem. Sci., 2015, 6, 2903 |
| 1518844 | CIF | C25 H27 N O3 | P 1 21/n 1 | 10.6026; 12.0053; 16.5199 90; 105.806; 90 | 2023.27 | Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans Chem. Sci., 2015, 6, 2903 |
| 1518845 | CIF | C24 H25 N O3 | P 1 21/c 1 | 19.6584; 6.7792; 14.62 90; 104.609; 90 | 1885.39 | Faustino, Hélio; Varela, Iván; Mascareñas, José L.; López, Fernando Gold(i)-catalyzed [2 + 2 + 2] cycloaddition of allenamides, alkenes and aldehydes: a straightforward approach to tetrahydropyrans Chem. Sci., 2015, 6, 2903 |
| 1518846 | CIF | C10 H9 Br Cl N O2 | P 1 21 1 | 5.928; 7.6682; 11.3533 90; 95.944; 90 | 513.31 | Zhu, Cheng-Liang; Tian, Jun-Shan; Gu, Zhen-Yuan; Xing, Guo-Wen; Xu, Hao Iron(ii)-catalyzed asymmetric intramolecular olefin aminochlorination using chloride ion Chem. Sci., 2015, 6, 3044 |
| 1518866 | CIF | C11 H9 Dy N3 O6 | P 1 21/c 1 | 13.672; 7.313; 12.481 90; 94.296; 90 | 1244.4 | Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer Chem. Sci., 2015, 6, 3095 |
| 1518867 | CIF | C11 H9 N3 O6 Y | P 1 21/c 1 | 13.655; 7.278; 12.428 90; 94.424; 90 | 1231.4 | Yin, Dan-Dan; Chen, Qi; Meng, Yin-Shan; Sun, Hao-Ling; Zhang, Yi-Quan; Gao, Song Slow magnetic relaxation in a novel carboxylate/oxalate/hydroxyl bridged dysprosium layer Chem. Sci., 2015, 6, 3095 |
| 1518869 | CIF | C42 H34 N6 O10 | P -1 | 8.8838; 20.6864; 22.5136 68.276; 78.717; 89.509 | 3760 | Martinez-Cuezva, Alberto; Pastor, Aurelia; Cioncoloni, Giacomo; Orenes, Raul-Angel; Alajarin, Mateo; Symes, Mark D.; Berna, Jose Versatile control of the submolecular motion of di(acylamino)pyridine-based [2]rotaxanes Chem. Sci., 2015, 6, 3087 |
| 1518870 | CIF | C67 H57.75 N7 O7 | P -1 | 10.4583; 13.5669; 19.947 76.564; 75.557; 80.757 | 2649.9 | Martinez-Cuezva, Alberto; Pastor, Aurelia; Cioncoloni, Giacomo; Orenes, Raul-Angel; Alajarin, Mateo; Symes, Mark D.; Berna, Jose Versatile control of the submolecular motion of di(acylamino)pyridine-based [2]rotaxanes Chem. Sci., 2015, 6, 3087 |
| 1518871 | CIF | C31 H22 O S | P 1 21 1 | 5.594; 47.1662; 9.2545 90; 103.425; 90 | 2375.06 | Xu, Bingjia; He, Jiajun; Mu, Yingxiao; Zhu, Qiangzhong; Wu, Sikai; Wang, Yifan; Zhang, Yi; Jin, Chongjun; Lo, Changcheng; Chi, Zhenguo; Lien, Alan; Liu, Siwei; Xu, Jiarui Very bright mechanoluminescence and remarkable mechanochromism using a tetraphenylethene derivative with aggregation-induced emission Chem. Sci., 2015, 6, 3236 |
| 1518875 | CIF | C42 H84 N0 O26 Zn8 | C 1 2/c 1 | 22.502; 12.882; 21.773 90; 98.995; 90 | 6233.7 | Kubisiak, Marcin; Zelga, Karolina; Bury, Wojciech; Justyniak, Iwona; Budny-Godlewski, Krzysztof; Ochal, Zbigniew; Lewiński, Janusz Development of zinc alkyl/air systems as radical initiators for organic reactions Chem. Sci., 2015, 6, 3102 |
| 1518876 | CIF | C38 H64 O26 Zn8 | P -1 | 9.5731; 10.8542; 13.0771 77.371; 83.044; 80.914 | 1304.01 | Kubisiak, Marcin; Zelga, Karolina; Bury, Wojciech; Justyniak, Iwona; Budny-Godlewski, Krzysztof; Ochal, Zbigniew; Lewiński, Janusz Development of zinc alkyl/air systems as radical initiators for organic reactions Chem. Sci., 2015, 6, 3102 |
| 1518882 | CIF | C82.5 H86 B Cr F24 N2 | P -1 | 13.468; 14.272; 20.836 85.98; 89.96; 87.39 | 3991 | Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S. Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes Chem. Sci., 2015, 6, 3148 |
| 1518883 | CIF | C40 H62 Cl2 Cr N2 | C 1 2/c 1 | 16.958; 10.973; 22.073 90; 108.91; 90 | 3885.7 | Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S. Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes Chem. Sci., 2015, 6, 3148 |
| 1518884 | CIF | C47 H70 Cl Cr N2 | P -1 | 9.636; 12.053; 19.94 102.29; 95.37; 106.71 | 2137.4 | Samuel, Prinson P.; Neufeld, Roman; Chandra Mondal, Kartik; Roesky, Herbert W.; Herbst-Irmer, Regine; Stalke, Dietmar; Demeshko, Serhiy; Meyer, Franc; Rojisha, Vallyanga Chalil; De, Susmita; Parameswaran, Pattiyil; Stückl, A. Claudia; Kaim, Wolfgang; Christian, Jonathan H.; Bindra, Jasleen K.; Dalal, Naresh S. Cr(i)Cl as well as Cr+are stabilised between two cyclic alkyl amino carbenes Chem. Sci., 2015, 6, 3148 |
| 1518906 | CIF | C34 H18 O2 | C 1 2 1 | 13.707; 6.3468; 13.269 90; 103.472; 90 | 1122.6 | Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties Chem. Sci., 2015, 6, 3402 |
| 1518907 | CIF | C34 H16 O2 | P b c n | 18.9562; 15.493; 14.8168 90; 90; 90 | 4351.5 | Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties Chem. Sci., 2015, 6, 3402 |
| 1518908 | CIF | C59 H61 Si2 | P b c a | 34.006; 7.6167; 36.832 90; 90; 90 | 9540 | Sbargoud, Kamal; Mamada, Masashi; Marrot, Jérôme; Tokito, Shizuo; Yassar, Abderrahim; Frigoli, Michel Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties Chem. Sci., 2015, 6, 3402 |
| 1518942 | CIF | C26 H40 O5 Si | P 1 21 1 | 6.7367; 22.9731; 16.5877 90; 90.862; 90 | 2566.9 | Mukai, Ken; Kasuya, Satoshi; Nakagawa, Yuki; Urabe, Daisuke; Inoue, Masayuki A convergent total synthesis of ouabagenin Chem. Sci., 2015, 6, 3383 |
| 1518943 | CIF | C18 H30 O5 Si | P 1 21 1 | 11.0079; 6.36439; 13.7975 90; 110.712; 90 | 904.16 | Mukai, Ken; Kasuya, Satoshi; Nakagawa, Yuki; Urabe, Daisuke; Inoue, Masayuki A convergent total synthesis of ouabagenin Chem. Sci., 2015, 6, 3383 |
| 1518946 | CIF | C11 H9 F3 N2 O | P -1 | 11.5587; 11.8263; 17.672 92.233; 102.972; 108.187 | 2220.9 | Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers Chem. Sci., 2015, 6, 3415 |
| 1518947 | CIF | C10 H9 F3 N2 O | P 1 21 1 | 9.0634; 5.8062; 9.8369 90; 90.567; 90 | 517.63 | Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers Chem. Sci., 2015, 6, 3415 |
| 1518948 | CIF | C17 H15 F3 N2 O | P 21 21 21 | 5.7467; 9.4574; 27.5934 90; 90; 90 | 1499.67 | Chen, Zhang-Pei; Chen, Mu-Wang; Shi, Lei; Yu, Chang-Bin; Zhou, Yong-Gui Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers Chem. Sci., 2015, 6, 3415 |
| 1518949 | CIF | C46 H46 N2 S2 | P 1 21/c 1 | 23.6399; 5.207; 15.042 90; 107.545; 90 | 1765.4 | He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors Chem. Sci., 2015, 6, 3180 |
| 1518950 | CIF | C42 H42 N2 S4 | R -3 :H | 43.2109; 43.2109; 5.0578 90; 90; 120 | 8178.6 | He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors Chem. Sci., 2015, 6, 3180 |
| 1518951 | CIF | C46 H46 N2 O2 | P 1 21/c 1 | 15.3148; 5.2027; 21.5181 90; 93.605; 90 | 1711.13 | He, Bo; Dai, Jing; Zherebetskyy, Danylo; Chen, Teresa L.; Zhang, Benjamin A.; Teat, Simon J.; Zhang, Qichun; Wang, Linwang; Liu, Yi A divergent route to core- and peripherally functionalized diazacoronenes that act as colorimetric and fluorescence proton sensors Chem. Sci., 2015, 6, 3180 |
| 1518952 | CIF | C34 H36 Cl2 Mo2 N6 O4 | P 1 21/c 1 | 12.536; 12.3769; 13.069 90; 115.499; 90 | 1830.2 | Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes Chem. Sci., 2015, 6, 3434 |
| 1518953 | CIF | C62 H102 Cl4 Mo2 N6 O4 | P 1 21/n 1 | 12.6064; 14.1061; 19.183 90; 101.372; 90 | 3344.3 | Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes Chem. Sci., 2015, 6, 3434 |
| 1518954 | CIF | C48 H69 Cl4 Mo2 N6 O4 | P -1 | 12.142; 13.615; 17.274 78.896; 84.467; 69.112 | 2616.8 | Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes Chem. Sci., 2015, 6, 3434 |
| 1518955 | CIF | C34 H36 Cl4 Mo2 N6 O4 | P 1 21/c 1 | 11.752; 15.014; 11.14 90; 109.276; 90 | 1855.4 | Tsurugi, Hayato; Hayakawa, Akio; Kando, Shun; Sugino, Yoshitaka; Mashima, Kazushi Mixed-ligand complexes of paddlewheel dinuclear molybdenum as hydrodehalogenation catalysts for polyhaloalkanes Chem. Sci., 2015, 6, 3434 |
| 1518956 | CIF | C216 H130 N12 O32 Zr6 | P m -3 m | 25.4376; 25.4376; 25.4376 90; 90; 90 | 16459.9 | Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses Chem. Sci., 2015, 6, 3466 |
| 1518957 | CIF | C216 H124 Cu3 N12 O32 Zr6 | P m -3 m | 25.4213; 25.4213; 25.4213 90; 90; 90 | 16428.3 | Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses Chem. Sci., 2015, 6, 3466 |
| 1518958 | CIF | C216 H130 Hf6 N12 O32 | P m -3 m | 25.3976; 25.3976; 25.3976 90; 90; 90 | 16382.4 | Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses Chem. Sci., 2015, 6, 3466 |
| 1518959 | CIF | C216 H124 Cu3 Hf6 N12 O32 | P m -3 m | 25.357; 25.357; 25.357 90; 90; 90 | 16304 | Zheng, Jun; Wu, Mingyan; Jiang, Feilong; Su, Weiping; Hong, Maochun Stable porphyrin Zr and Hf metal‒organic frameworks featuring 2.5 nm cages: high surface areas, SCSC transformations and catalyses Chem. Sci., 2015, 6, 3466 |
| 1518983 | CIF | C40 H28 | P 1 21/c 1 | 9.0462; 22.0677; 14.1102 90; 91.134; 90 | 2816.25 | He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes Chem. Sci., 2015, 6, 3538 |
| 1518984 | CIF | C45 H31 Cl3 | P 1 21/n 1 | 9.6681; 17.2389; 20.8625 90; 90.222; 90 | 3477.07 | He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes Chem. Sci., 2015, 6, 3538 |
| 1518985 | CIF | C48 H32 | C 1 2/c 1 | 28.4; 12.0889; 20.7374 90; 110.271; 90 | 6678.7 | He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes Chem. Sci., 2015, 6, 3538 |
| 1518986 | CIF | C44 H30 | P 1 21 1 | 9.2686; 7.5344; 22.0069 90; 91.349; 90 | 1536.39 | He, Zikai; Shan, Liang; Mei, Ju; Wang, Hong; Lam, Jacky W. Y.; Sung, Herman H. Y.; Williams, Ian D.; Gu, Xiao; Miao, Qian; Tang, Ben Zhong Aggregation-induced emission and aggregation-promoted photochromism of bis(diphenylmethylene)dihydroacenes Chem. Sci., 2015, 6, 3538 |
| 1518987 | CIF | C93 H95 N2 P Pd | P 1 21/n 1 | 14.1659; 25.5435; 20.2558 90; 95.695; 90 | 7293.3 | Henwood, Adam F.; Lesieur, Mathieu; Bansal, Ashu K.; Lemaur, Vincent; Beljonne, David; Thompson, David G.; Graham, Duncan; Slawin, Alexandra M. Z.; Samuel, Ifor D. W.; Cazin, Catherine S. J.; Zysman-Colman, Eli Palladium(0) NHC complexes: a new avenue to highly efficient phosphorescence Chem. Sci., 2015, 6, 3248 |
| 1518988 | CIF | C54 H76 N4 Pd | P 1 21/n 1 | 12.889; 27.082; 14.073 90; 92.483; 90 | 4908 | Henwood, Adam F.; Lesieur, Mathieu; Bansal, Ashu K.; Lemaur, Vincent; Beljonne, David; Thompson, David G.; Graham, Duncan; Slawin, Alexandra M. Z.; Samuel, Ifor D. W.; Cazin, Catherine S. J.; Zysman-Colman, Eli Palladium(0) NHC complexes: a new avenue to highly efficient phosphorescence Chem. Sci., 2015, 6, 3248 |
| 1519000 | CIF | C136 H142 N4 Ni O2 | P -1 | 12.8361; 15.5717; 15.9281 100.921; 109.976; 108.18 | 2682 | Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan Phenalenyl-fused porphyrins with different ground states Chem. Sci., 2015, 6, 2427 |
| 1519001 | CIF | C136 H142 N4 Ni O2 | P -1 | 12.85; 15.5881; 15.9283 100.951; 110.033; 108.118 | 2687.2 | Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan Phenalenyl-fused porphyrins with different ground states Chem. Sci., 2015, 6, 2427 |
| 1519002 | CIF | C85.5 H87 N5 Ni | P -1 | 15.0498; 15.6708; 17.4668 111.901; 107.076; 102.416 | 3400.2 | Zeng, Wangdong; Lee, Sangsu; Son, Minjung; Ishida, Masatoshi; Furukawa, Ko; Hu, Pan; Sun, Zhe; Kim, Dongho; Wu, Jishan Phenalenyl-fused porphyrins with different ground states Chem. Sci., 2015, 6, 2427 |
| 1519367 | CIF | C10 H10 Cl I N2 O4 | P 1 21/n 1 | 12.2849; 16.0628; 14.7939 90; 113.273; 90 | 2681.74 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519368 | CIF | C10 H10 F6 I N2 P | C 1 2/m 1 | 13.6827; 6.7491; 8.4045 90; 106.045; 90 | 745.89 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519369 | CIF | C10 H10 F6 I N2 Sb | P -1 | 6.9674; 7.1797; 7.7358 91.775; 101.402; 96.682 | 376.18 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519370 | CIF | C11 H10 F3 I N2 O3 S | P -1 | 7.0091; 10.6722; 10.7542 93.455; 105.677; 104.138 | 744.16 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519371 | CIF | C17 H17 I N2 O3 S | P 1 21/n 1 | 9.0892; 21.1577; 10.0924 90; 115.781; 90 | 1747.65 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519372 | CIF | C10 H10 I N3 O3 | P -1 | 7.0864; 7.4613; 13.5366 99.491; 94.725; 117.637 | 614.97 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519373 | CIF | C12 H14 Ag B Cl2 F4 N2 | P 1 21/n 1 | 7.2894; 13.3581; 16.9874 90; 101.989; 90 | 1618.03 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519374 | CIF | C12 H14 Ag Cl3 N2 O4 | P 1 21/n 1 | 7.2442; 13.3604; 16.9657 90; 101.394; 90 | 1609.67 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519375 | CIF | C12 H14 Ag Cl2 F6 N2 P | P -1 | 9.968; 10.512; 10.679 111.37; 116.82; 97.43 | 869.9 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519376 | CIF | C12 H14 Ag Cl2 F6 N2 Sb | P 1 21/c 1 | 12.6882; 13.8467; 11.1581 90; 112.12; 90 | 1816.08 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519377 | CIF | C11 H10 Ag F3 N2 O3 S | P 1 21/c 1 | 7.952; 17.294; 10.7947 90; 95.624; 90 | 1477.36 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519378 | CIF | C17 H17 Ag N2 O3 S | P 1 21/c 1 | 9.8088; 15.4242; 11.5973 90; 100.033; 90 | 1727.76 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519379 | CIF | C15 H15 Ag2 N5 O6 | P -1 | 7.4958; 10.0405; 12.7988 82.991; 83.259; 76.743 | 926.59 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519380 | CIF | C10 H12 Ag N3 O4 | I 1 2/a 1 | 5.7265; 14.7681; 14.6482 90; 96.59; 90 | 1230.61 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519381 | CIF | C22.5 H17 Ag Cl5 N3 O3 | P -1 | 7.2198; 13.3083; 14.6862 116.693; 90.96; 90.319 | 1260.4 | Bedin, Michele; Karim, Alavi; Reitti, Marcus; Carlsson, Anna-Carin C.; Topić, Filip; Cetina, Mario; Pan, Fangfang; Havel, Vaclav; Al-Ameri, Fatima; Sindelar, Vladimir; Rissanen, Kari; Gräfenstein, Jürgen; Erdélyi, Máté Counterion influence on the N‒I‒N halogen bond Chem. Sci., 2015, 6, 3746 |
| 1519382 | CIF | C59 H79 B Cl N6 O13 S6 | P -1 | 17.809; 18.594; 22.412 73.894; 83.175; 71.769 | 6768.1 | Rudolf, Marc; Trukhina, Olga; Perles, Josefina; Feng, Lai; Akasaka, Takeshi; Torres, Tomas; Guldi, Dirk M. Taming C60fullerene: tuning intramolecular photoinduced electron transfer process with subphthalocyanines Chem. Sci., 2015, 6, 4141 |
| 1519383 | CIF | C72 H116 Fe2 Mo2 N12 P4 | P -1 | 14.749; 15.266; 18.081 72.467; 83.794; 81.014 | 3826.2 | Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site Chem. Sci., 2015, 6, 3940 |
| 1519384 | CIF | C72 H116 Mo2 N12 P4 Ru2 | P -1 | 14.7212; 15.3604; 18.0121 72.7582; 84.4816; 81.1096 | 3837.72 | Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site Chem. Sci., 2015, 6, 3940 |
| 1519385 | CIF | C39 H65 Cl3 Fe Mo N P2 | C 1 c 1 | 21.9221; 15.852; 14.007 90; 121.631; 90 | 4144.4 | Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site Chem. Sci., 2015, 6, 3940 |
| 1519386 | CIF | C39 H64 Cl5 Fe Mo N P2 | P -1 | 13.2456; 15.6143; 24.2272 90.538; 102.695; 112.964 | 4475.5 | Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site Chem. Sci., 2015, 6, 3940 |
| 1519387 | CIF | C40 H57 Cl5 Fe Mo N P2 | C 1 c 1 | 18.9384; 19.521; 13.7984 90; 120.86; 90 | 4379 | Kuriyama, Shogo; Arashiba, Kazuya; Nakajima, Kazunari; Tanaka, Hiromasa; Yoshizawa, Kazunari; Nishibayashi, Yoshiaki Nitrogen fixation catalyzed by ferrocene-substituted dinitrogen-bridged dimolybdenum‒dinitrogen complexes: unique behavior of ferrocene moiety as redox active site Chem. Sci., 2015, 6, 3940 |
| 1519388 | CIF | C27 H25 N5 O2 | P 21 21 21 | 11.295; 12.39; 16.088 90; 90; 90 | 2251.4 | Li, Qi; Xia, Tingting; Yao, Licheng; Deng, Haiteng; Liao, Xuebin Enantioselective and diastereoselective azo-coupling/iminium-cyclizations: a unified strategy for the total syntheses of (−)-psychotriasine and (+)-pestalazine B Chem. Sci., 2015, 6, 3599 |
| 1519389 | CIF | C60 H70 N2 O4 | P -1 | 10.8676; 12.3446; 19.476 75.286; 86.422; 86.274 | 2518.9 | Yatham, Veera Reddy; Neudörfl, Jörg-M.; Schlörer, Nils E.; Berkessel, Albrecht Carbene catalyzed umpolung of α,β-enals: a reactivity study of diamino dienols vs. azolium enolates, and the characterization of advanced reaction intermediates Chem. Sci., 2015, 6, 3706 |
| 1519390 | CIF | C55 H72 N2 O6 | P 1 21/c 1 | 12.309; 37.444; 10.6821 90; 91.78; 90 | 4921 | Yatham, Veera Reddy; Neudörfl, Jörg-M.; Schlörer, Nils E.; Berkessel, Albrecht Carbene catalyzed umpolung of α,β-enals: a reactivity study of diamino dienols vs. azolium enolates, and the characterization of advanced reaction intermediates Chem. Sci., 2015, 6, 3706 |
| 1519391 | CIF | C18 H54 Cl N3 Si6 Th | R 3 c :H | 18.4298; 18.4298; 16.84 90; 90; 120 | 4953.5 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519392 | CIF | C36 H82 Cl2 N3 Na O4.5 Si6 Th | R -3 :H | 18.404; 18.404; 29.626 90; 90; 120 | 8690 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519393 | CIF | C18 H54 I N3 Si6 Th | R 3 c :H | 18.328; 18.328; 17.356 90; 90; 120 | 5049 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519394 | CIF | C53 H73 N2 O2 Si4 Th | P -1 | 12.955; 13.0253; 16.867 85.654; 77.178; 79.336 | 2725.5 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519395 | CIF | C37 H69 N3 S Si6 Th | P -1 | 10.5938; 11.5867; 19.595 96.883; 91.006; 96.27 | 2372.5 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519396 | CIF | C32 H83 K N3 O7.5 Si6 Th | P b c a | 20.457; 20.307; 25.358 90; 90; 90 | 10534 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519397 | CIF | C30 H78 K N3 O6 S Si6 Th | P -1 | 12.7484; 18.891; 21.817 91.554; 105.863; 92.564 | 5044.8 | Smiles, Danil E.; Wu, Guang; Kaltsoyannis, Nikolas; Hayton, Trevor W. Thorium‒ligand multiple bonds via reductive deprotection of a trityl group Chem. Sci., 2015, 6, 3891 |
| 1519398 | CIF | C8 H6 F4 O6 | P 1 21/c 1 | 8.5417; 8.0442; 7.4465 90; 99.017; 90 | 505.33 | Gong, Yongyang; Zhao, Lifang; Peng, Qian; Fan, Di; Yuan, Wang Zhang; Zhang, Yongming; Tang, Ben Zhong Crystallization-induced dual emission from metal- and heavy atom-free aromatic acids and esters Chem. Sci., 2015, 6, 4438 |
| 1519399 | CIF | C10 H6 F4 O4 | P 1 21/n 1 | 6.332; 4.701; 17.423 90; 95.605; 90 | 516.1 | Gong, Yongyang; Zhao, Lifang; Peng, Qian; Fan, Di; Yuan, Wang Zhang; Zhang, Yongming; Tang, Ben Zhong Crystallization-induced dual emission from metal- and heavy atom-free aromatic acids and esters Chem. Sci., 2015, 6, 4438 |
| 1519400 | CIF | C94 H93.62 Ga4 Gd2 N15 O31.31 | C 1 2/c 1 | 25.233; 22.054; 17.997 90; 99.09; 90 | 9889 | Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative Chem. Sci., 2015, 6, 4148 |
| 1519401 | CIF | C94 H93 Ga4 N15 O31 Tb2 | C 1 2/c 1 | 25.1697; 22.1217; 17.9895 90; 99.302; 90 | 9884.8 | Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative Chem. Sci., 2015, 6, 4148 |
| 1519402 | CIF | C94 H93 Dy2 Ga4 N15 O31 | C 1 2/c 1 | 25.1638; 22.1781; 18.0649 90; 99.353; 90 | 9947.7 | Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative Chem. Sci., 2015, 6, 4148 |
| 1519403 | CIF | C93 H91 Er2 Ga4 N15 O31 | C 1 2/c 1 | 25.1476; 22.138; 18.0285 90; 99.177; 90 | 9908.3 | Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative Chem. Sci., 2015, 6, 4148 |
| 1519404 | CIF | C94 H93 Ga4 N15 O31 Y2 | C 1 2/c 1 | 25.1053; 22.1794; 18.0733 90; 99.377; 90 | 9929.1 | Chow, Chun Y.; Bolvin, Hélène; Campbell, Victoria E.; Guillot, Régis; Kampf, Jeff W.; Wernsdorfer, Wolfgang; Gendron, Frédéric; Autschbach, Jochen; Pecoraro, Vincent L.; Mallah, Talal Assessing the exchange coupling in binuclear lanthanide(iii) complexes and the slow relaxation of the magnetization in the antiferromagnetically coupled Dy2derivative Chem. Sci., 2015, 6, 4148 |
| 1519405 | CIF | C26 H20 O3 | P 21 21 21 | 5.8732; 11.684; 28.383 90; 90; 90 | 1947.7 | Li, Guo-Tai; Gu, Qing; You, Shu-Li Enantioselective annulation of enals with 2-naphthols by triazolium salts derived froml-phenylalanine Chem. Sci., 2015, 6, 4273 |
| 1519406 | CIF | C35 H38 B F4 N3 O Si | P 31 2 1 | 11.541; 11.541; 52.812 90; 90; 120 | 6091.9 | Li, Guo-Tai; Gu, Qing; You, Shu-Li Enantioselective annulation of enals with 2-naphthols by triazolium salts derived froml-phenylalanine Chem. Sci., 2015, 6, 4273 |
| 1519407 | CIF | C154 H96 N14 O32 Ti7 | P 1 2/m 1 | 17.6073; 17.0188; 25.0871 90; 101.722; 90 | 7360.7 | Yuan, Shuai; Liu, Tian-Fu; Feng, Dawei; Tian, Jian; Wang, Kecheng; Qin, Junsheng; Zhang, Qiang; Chen, Ying-Pin; Bosch, Mathieu; Zou, Lanfang; Teat, Simon J.; Dalgarno, Scott J.; Zhou, Hong-Cai A single crystalline porphyrinic titanium metal‒organic framework Chem. Sci., 2015, 6, 3926 |
| 1519408 | CIF | C25 H21 Cl N5 O4 Pt | P -1 | 7.2307; 12.06; 14.471 74.425; 82.9797; 79.6363 | 1192.09 | Tsai, Johnson Lui-Lui; Zou, Taotao; Liu, Jia; Chen, Tianfeng; Chan, Anna On-Yee; Yang, Chen; Lok, Chun-Nam; Che, Chi-Ming Luminescent platinum(ii) complexes with self-assembly and anti-cancer properties: hydrogel, pH dependent emission color and sustained-release properties under physiological conditions Chem. Sci., 2015, 6, 3823 |
| 1519409 | CIF | C17 H17 Cl O3 | P 21 21 21 | 6.2836; 12.6214; 37.0026 90; 90; 90 | 2934.6 | Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations Chem. Sci., 2015, 6, 3550 |
| 1519410 | CIF | C17 H18 O3 | P 1 21 1 | 12.1037; 6.87725; 16.6432 90; 92.6683; 90 | 1383.88 | Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations Chem. Sci., 2015, 6, 3550 |
| 1519411 | CIF | C18 H19 Cl O3 | P 1 21 1 | 7.0438; 11.6921; 9.8846 90; 108.47; 90 | 772.13 | Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations Chem. Sci., 2015, 6, 3550 |
| 1519412 | CIF | C18 H19 N O5 | P 21 21 21 | 6.71816; 13.19234; 17.888 90; 90; 90 | 1585.38 | Burns, Alan R.; Madec, Amaël G. E.; Low, Darryl W.; Roy, Iain D.; Lam, Hon Wai Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations Chem. Sci., 2015, 6, 3550 |
| 1519413 | CIF | C12 H9 Cl O3 | P 21 21 21 | 9.632; 9.726; 11.729 90; 90; 90 | 1098.8 | Yin, Qin; Wang, Shou-Guo; Liang, Xiao-Wei; Gao, De-Wei; Zheng, Jun; You, Shu-Li Organocatalytic asymmetric chlorinative dearomatization of naphthols Chem. Sci., 2015, 6, 4179 |
| 1519414 | CIF | C12 H8 Br Cl O3 | P 21 21 21 | 7.45; 7.796; 21.193 90; 90; 90 | 1230.9 | Yin, Qin; Wang, Shou-Guo; Liang, Xiao-Wei; Gao, De-Wei; Zheng, Jun; You, Shu-Li Organocatalytic asymmetric chlorinative dearomatization of naphthols Chem. Sci., 2015, 6, 4179 |
| 1519415 | CIF | C114 H86 O52 Y6 | P m -3 m | 19.3042; 19.3042; 19.3042 90; 90; 90 | 7193.8 | Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs Chem. Sci., 2015, 6, 4095 |
| 1519416 | CIF | C138 H78 O35 Y6 | I m -3 | 40.048; 40.048; 40.048 90; 90; 90 | 64231 | Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs Chem. Sci., 2015, 6, 4095 |
| 1519417 | CIF | C162 H78 O32 Y6 | I m -3 | 48.111; 48.111; 48.111 90; 90; 90 | 111361 | Luebke, Ryan; Belmabkhout, Youssef; Weseliński, Łukasz J.; Cairns, Amy J.; Alkordi, Mohamed; Norton, George; Wojtas, Łukasz; Adil, Karim; Eddaoudi, Mohamed Versatile rare earth hexanuclear clusters for the design and synthesis of highly-connectedftw-MOFs Chem. Sci., 2015, 6, 4095 |
| 1519418 | CIF | C17 H17 F S | P 21 21 21 | 7.9685; 11.0136; 16.1416 90; 90; 90 | 1416.6 | Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R. Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect? Chem. Sci., 2015, 6, 3565 |
| 1519419 | CIF | C17 H17 F O S | P 21 21 21 | 9.4841; 9.9993; 14.7157 90; 90; 90 | 1395.55 | Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R. Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect? Chem. Sci., 2015, 6, 3565 |
| 1519420 | CIF | C17 H17 F O2 S | P 1 21/c 1 | 14.663; 9.5972; 10.7876 90; 109.646; 90 | 1429.7 | Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R. Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect? Chem. Sci., 2015, 6, 3565 |
| 1519421 | CIF | C8 H8 F N O3 S | P n a 21 | 20.3421; 4.6595; 9.8133 90; 90; 90 | 930.14 | Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R. Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect? Chem. Sci., 2015, 6, 3565 |
| 1519422 | CIF | C8 H8 F N O4 S | P -1 | 7.2161; 7.3574; 9.1736 86.045; 76.993; 78.266 | 464.49 | Thiehoff, C.; Holland, M. C.; Daniliuc, C.; Houk, K. N.; Gilmour, R. Can acyclic conformational control be achieved via a sulfur‒fluorine gauche effect? Chem. Sci., 2015, 6, 3565 |
| 1519423 | CIF | C15 H20 N2 O2 | P 1 21 1 | 9.4882; 10.3774; 15.575 90; 107.509; 90 | 1462.5 | Kim, Jinhee; Sim, Mikyung; Kim, Namhoon; Hong, Sungwoo Asymmetric C‒H functionalization of cyclopropanes using an isoleucine-NH2bidentate directing group Chem. Sci., 2015, 6, 3611 |
| 1519424 | CIF | C19 H21 Cu N4 O4.5 | P 1 21/c 1 | 12.1843; 13.6819; 22.5624 90; 99.683; 90 | 3707.7 | Moore, Cameron M.; Szymczak, Nathaniel K. Nitrite reduction by copper through ligand-mediated proton and electron transfer Chem. Sci., 2015, 6, 3373 |
| 1519425 | CIF | C36 H34 Cu2 N8 O6 | P b c n | 14.1161; 15.8051; 14.538 90; 90; 90 | 3243.5 | Moore, Cameron M.; Szymczak, Nathaniel K. Nitrite reduction by copper through ligand-mediated proton and electron transfer Chem. Sci., 2015, 6, 3373 |
| 1519426 | CIF | C26 H44 B Cl2 N2 | P 1 21/n 1 | 8.7727; 16.781; 18.22 90; 91.317; 90 | 2681.5 | Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C. Generation of 1,2-azaboretidines via reduction of ADC borane adducts Chem. Sci., 2015, 6, 3461 |
| 1519427 | CIF | C22 H39 B Cl2 N2 | P 1 21/n 1 | 8.4091; 23.915; 13.429 90; 91.008; 90 | 2700.2 | Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C. Generation of 1,2-azaboretidines via reduction of ADC borane adducts Chem. Sci., 2015, 6, 3461 |
| 1519428 | CIF | C13 H28 B Br2 N2 | P 1 21/n 1 | 7.1189; 15.9168; 15.0043 90; 91.677; 90 | 1699.4 | Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C. Generation of 1,2-azaboretidines via reduction of ADC borane adducts Chem. Sci., 2015, 6, 3461 |
| 1519429 | CIF | C23 H41 B N2 | P -1 | 8.8938; 9.258; 15.064 73.468; 79.717; 77.485 | 1151.7 | Braunschweig, H.; Gackstatter, A.; Kupfer, T.; Scheller, T.; Hupp, F.; Damme, A.; Arnold, N.; Ewing, W. C. Generation of 1,2-azaboretidines via reduction of ADC borane adducts Chem. Sci., 2015, 6, 3461 |
| 1519430 | CIF | C20 H16 N2 O2 | C 1 2/c 1 | 17.37; 29.0684; 8.8805 90; 94.498; 90 | 4470.1 | He, Xiaoyan; Benniston, Andrew C.; Saarenpää, Hanna; Lemmetyinen, Helge; Tkachenko, Nikolia V.; Baisch, Ulrich Polymorph crystal packing effects on charge transfer emission in the solid state Chem. Sci., 2015, 6, 3525 |
| 1519431 | CIF | C20 H16 N2 O2 | P -1 | 9.4336; 9.5749; 9.9183 115.803; 97.324; 104.839 | 749.69 | He, Xiaoyan; Benniston, Andrew C.; Saarenpää, Hanna; Lemmetyinen, Helge; Tkachenko, Nikolia V.; Baisch, Ulrich Polymorph crystal packing effects on charge transfer emission in the solid state Chem. Sci., 2015, 6, 3525 |
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