Crystallography Open Database
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Searching journal of publication like 'Catalysis science & technology'
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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1552352 | CIF | C7 H7 Au Cl4 N2 O3 | P -1 | 7.831; 7.931; 11.079 97.173; 95.533; 96.097 | 674.6 | Ahmad, Ahmad A. L.; Panicker, Seema; Chehimi, Mohamed M.; Monge, Miguel; López-de-Luzuriaga, José M.; Mohamed, Ahmed A.; Bruce, Alice E.; Bruce, Mitchell R. M. Synthesis of Water-Soluble Gold-Aryl Nanoparticles with Distinct Catalytic Performance in the Reduction of the Environmental Pollutant 4-Nitrophenol Catalysis Science & Technology, 2019 |
1552752 | CIF | C50 H39 F18 N12 P3 Ru2 | P -1 | 10.6161; 15.1085; 16.911 90.103; 94.853; 105.573 | 2602.6 | Hennessey, Seán; Farras Costa, Pau; Benet-Buchholz, Jordi; Llobet, Antoni A Bpp-based Dinuclear Ruthenium Photocatalyst for Visible Light-Driven Oxidation Reactions Catalysis Science & Technology, 2019 |
1552753 | CIF | C51 H42 Cl F12 N11 O P2 Ru2 | P -1 | 12.918; 13.831; 17.552 92.997; 100.953; 105.668 | 2946.61 | Hennessey, Seán; Farras Costa, Pau; Benet-Buchholz, Jordi; Llobet, Antoni A Bpp-based Dinuclear Ruthenium Photocatalyst for Visible Light-Driven Oxidation Reactions Catalysis Science & Technology, 2019 |
1552866 | CIF | C46 H41 Au Cl N2 P3 | P 1 21/n 1 | 17.5516; 12.9246; 17.7238 90; 93.431; 90 | 4013.4 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552867 | CIF | C44 H39 Au Cl N2 P3 | P 1 21/n 1 | 10.8276; 33.9018; 11.4594 90; 113.03; 90 | 3871.21 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552868 | CIF | C47 H37 Cl2 N2 P3 | P 1 21 1 | 10.3342; 22.3144; 17.0157 90; 92.007; 90 | 3921.4 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552869 | CIF | C47 H37 Au Cl3 N2 P3 | P -1 | 12.5994; 13.2954; 13.5256 70.09; 84.549; 78.391 | 2085.9 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552870 | CIF | C28 H33 Au Cl N P2 | P 1 21/c 1 | 11.78322; 9.40736; 24.667 90; 102.482; 90 | 2669.68 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552871 | CIF | C62 H72 N2 P4 | P -1 | 10.1896; 17.4204; 17.4304 67.712; 73.191; 73.1212 | 2682.92 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552872 | CIF | C60 H45 N3 P4 | P -3 | 35.1836; 35.1836; 9.7068 90; 90; 120 | 10406.1 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552873 | CIF | C55 H51 Cl9 N2 O3 P3 Rh | P 1 21/c 1 | 11.00739; 22.02102; 24.05162 90; 102.989; 90 | 5680.79 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552874 | CIF | C45 H41 Cl2 N2 P3 | P 1 21/n 1 | 9.8538; 22.9455; 17.3019 90; 93.031; 90 | 3906.5 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552875 | CIF | C97 H92 Cl10 N4 P6 | P -1 | 10.2673; 12.11; 19.82 103.947; 99.881; 100.687 | 2289 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552963 | CIF | C18 H22 Br F5 N2 | P 1 21/c 1 | 7.8536; 8.5571; 29.1438 90; 90.415; 90 | 1958.53 | Anthofer, Michael H.; Wilhelm, Michael E.; Cokoja, Mirza; Markovits, Iulius I. E.; Pöthig, Alexander; Mink, János; Herrmann, Wolfgang A.; Kühn, Fritz E. Cycloaddition of CO2 and epoxides catalyzed by imidazolium bromides under mild conditions: influence of the cation on catalyst activity Catalysis Science & Technology, 2014, 4, 1749 |
1553092 | CIF | C20 H29 Cl Mo N2 O3 | P 1 21/c 1 | 10.9605; 15.9334; 13.4384 90; 112.447; 90 | 2169 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1553093 | CIF | C41 H53 Cl17 Mo2 N4 O4 | F d -3 c :2 | 58.3972; 58.3972; 58.3972 90; 90; 90 | 199148 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1553094 | CIF | C40 H60 Cl2 Mo2 N4 O6 | P -1 | 12.2348; 14.0396; 14.2351 92.035; 107.553; 104.751 | 2237.7 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1554189 | CIF | C29 H31 Cl2 O3 P Ru | P 1 21/n 1 | 10.0354; 12.4751; 22.059 90; 93.55; 90 | 2756.3 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554190 | CIF | C123.3 Cl8 O8 P4 Ru4 Zn2 | P 1 21/n 1 | 16.387; 27.97; 26.66 90; 101.396; 90 | 11979 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554191 | CIF | C25 H29 Cl2 O2 P Ru | P 1 21/n 1 | 10.595; 12.873; 18.387 90; 106.74; 90 | 2401.5 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554620 | CIF | C24 H38 F6 Fe P Ru S3 | C m c e | 15.867; 20.073; 18.513 90; 90; 90 | 5896.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554621 | CIF | C14 H23 Co S3 | P 1 21/c 1 | 13.1028; 8.6112; 14.2219 90; 101.551; 90 | 1572.17 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554622 | CIF | C30 H43 F6 Fe P Ru S4 | P 1 21/n 1 | 14.3616; 13.9373; 16.9737 90; 99.0564; 90 | 3355.1 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554623 | CIF | C26 H41 F12 Fe N P2 Ru S3 | P n m a | 11.8; 15.608; 18.603 90; 90; 90 | 3426 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554624 | CIF | C48 H58 B Co Fe S3 | P n a 21 | 20.2817; 17.2944; 12.4241 90; 90; 90 | 4357.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554625 | CIF | C47 H56 B Co Fe S3 | P n a 21 | 20.576; 16.9755; 12.0227 90; 90; 90 | 4199.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554626 | CIF | C48 H59 B Fe Ru S3 | P 1 21/c 1 | 15.5349; 15.8332; 18.3897 90; 90.694; 90 | 4522.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1556266 | CIF | C28 H27 N O6 | P 21 21 21 | 10.42; 12.888; 19.103 90; 90; 90 | 2565.4 | Wang, Ming; Shi, Yu-Hua; Luo, Jun-Fei; Du, Wenting; Shi, Xiao-Xin; Fossey, John S.; Deng, Wei-Ping Novel N,O-Cu(OAc)2 complex catalysed diastereo- and enantioselective 1,4-addition of glycine derivatives to alkylidene malonates Catalysis Science & Technology, 2011, 1, 100 |
1556267 | CIF | C24 H28 Br2 N2 Ni | C 1 2/c 1 | 29.331; 10.775; 15.226 90; 105.3; 90 | 4641.5 | Song, Shengju; Xiao, Tianpengfei; Liang, Tongling; Wang, Fosong; Redshaw, Carl; Sun, Wen-Hua Synthesis, characterization and ethylene oligomerization behaviour of 8-(1-aryliminoethylidene)quinaldinylnickel dihalides Catalysis Science & Technology, 2011, 1, 69 |
1556268 | CIF | C23 H26 Br2 N2 Ni | P 1 21/n 1 | 15.834; 8.6441; 17.665 90; 114.28; 90 | 2204 | Song, Shengju; Xiao, Tianpengfei; Liang, Tongling; Wang, Fosong; Redshaw, Carl; Sun, Wen-Hua Synthesis, characterization and ethylene oligomerization behaviour of 8-(1-aryliminoethylidene)quinaldinylnickel dihalides Catalysis Science & Technology, 2011, 1, 69 |
1556269 | CIF | C60 H53 Cl4 O5 P5 Rh2 | P 1 21/c 1 | 17.0585; 17.1534; 19.5448 90; 90.797; 90 | 5718.5 | Castro, Pascal M.; Gulyás, Henrik; Benet-Buchholz, Jordi; Bo, Carles; Freixa, Zoraida; van Leeuwen, Piet W. N. M. SPOs as new ligands in Rh(iii) catalyzed enantioselective transfer hydrogenation Catalysis Science & Technology, 2011, 1, 401 |
1556270 | CIF | C44 H48 F6 O12 S8 Zn | R -3 :H | 12.5877; 12.5877; 29.1803 90; 90; 120 | 4004.2 | Enthaler, Stephan A straightforward zinc-catalysed reduction of sulfoxides to sulfides Catalysis Science & Technology, 2011, 1, 104 |
1556271 | CIF | C33.33 H0 F4 O6.67 S4 Zn0.67 | P -1 | 10.5817; 13.8939; 19.8576 83.554; 88.085; 73.117 | 2775.99 | Enthaler, Stephan A straightforward zinc-catalysed reduction of sulfoxides to sulfides Catalysis Science & Technology, 2011, 1, 104 |
1556272 | CIF | C18 H22 N O5 P | C 1 2/c 1 | 22.1091; 10.4184; 18.2639 90; 118.495; 90 | 3697.3 | Kidwai, Mazaahir; Bhardwaj, Saurav; Mishra, Neeraj Kumar; Jain, Arti; Kumar, Ajeet; Mozzumdar, Subho Application of mobilized Cu-nanoparticles as heterogeneous catalyst for the synthesis of α-amino phosphonates via A2-P coupling Catalysis Science & Technology, 2011, 1, 426 |
1556279 | CIF | C22 H24 Cl2 Co N2 | P 1 21/n 1 | 11.337; 15.712; 11.611 90; 95.49; 90 | 2058.7 | Xiao, Tianpengfei; Lai, Jingjuan; Zhang, Shu; Hao, Xiang; Sun, Wen-Hua 2-(1-Aryliminopropylidene)quinolylcobalt(ii) dichlorides: synthesis, characterization and catalytic behaviour towards ethylene Catalysis Science & Technology, 2011, 1, 462 |
1556280 | CIF | C24 H28 Cl2 Co N2 | P 1 21/n 1 | 10.125; 16.885; 13.533 90; 90.01; 90 | 2313.6 | Xiao, Tianpengfei; Lai, Jingjuan; Zhang, Shu; Hao, Xiang; Sun, Wen-Hua 2-(1-Aryliminopropylidene)quinolylcobalt(ii) dichlorides: synthesis, characterization and catalytic behaviour towards ethylene Catalysis Science & Technology, 2011, 1, 462 |
1556281 | CIF | C24 H34 N O4 V | P 1 21/c 1 | 8.4832; 11.5025; 24.14 90; 94.873; 90 | 2347 | Lorber, Christian; Despagnet-Ayoub, Emmanuelle; Vendier, Laure; Arbaoui, Abdessamad; Redshaw, Carl Amine influence in vanadium-based ethylene polymerisation pro-catalysts bearing bis(phenolate) ligands with ‘pendant’ arms Catalysis Science & Technology, 2011, 1, 489 |
1556282 | CIF | C26 H26 Cl2 N2 O Ti | C 1 2/c 1 | 23.852; 13.832; 16.89 90; 118.68; 90 | 4889 | Huang, Wei; Li, Baixiang; Wang, Youhong; Zhang, Wenjuan; Wang, Lin; Li, Yuesheng; Sun, Wen-Hua; Redshaw, Carl Synthesis, characterization and ethylene (co-)polymerization behavior of half-titanocene 2-(1-(arylimino)ethyl)quinolin-8-olate chlorides Catalysis Science & Technology, 2011, 1, 1208 |
1556283 | CIF | C27 H28 Cl2 N2 O Ti | P 1 21/c 1 | 17.098; 8.1446; 17.624 90; 98.7; 90 | 2426 | Huang, Wei; Li, Baixiang; Wang, Youhong; Zhang, Wenjuan; Wang, Lin; Li, Yuesheng; Sun, Wen-Hua; Redshaw, Carl Synthesis, characterization and ethylene (co-)polymerization behavior of half-titanocene 2-(1-(arylimino)ethyl)quinolin-8-olate chlorides Catalysis Science & Technology, 2011, 1, 1208 |
1556284 | CIF | C16 H24 Cl2 N2 O4 Pd S2 | P -1 | 8.4783; 11.6061; 13.1535 67.125; 89.797; 68.971 | 1099.1 | Tomás-Mendivil, Eder; Díez, Josefina; Cadierno, Victorio Conjugate addition of arylboronic acids to α,β-unsaturated carbonyl compounds in aqueous medium using Pd(ii) complexes with dihydroxy-2,2′-bipyridine ligands: homogeneous or heterogeneous nano-catalysis? Catalysis Science & Technology, 2011, 1, 1605 |
1556285 | CIF | C14 H14 Cl2 N2 O5 Pd S | P -1 | 7.6738; 10.4974; 12.5545 112.689; 90.017; 108.646 | 875.2 | Tomás-Mendivil, Eder; Díez, Josefina; Cadierno, Victorio Conjugate addition of arylboronic acids to α,β-unsaturated carbonyl compounds in aqueous medium using Pd(ii) complexes with dihydroxy-2,2′-bipyridine ligands: homogeneous or heterogeneous nano-catalysis? Catalysis Science & Technology, 2011, 1, 1605 |
1556286 | CIF | C54.2 H48.4 Cl0.4 N2 O P2 | P -1 | 11.5434; 14.8956; 15.1659 62.313; 86.134; 78.115 | 2258.4 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556287 | CIF | C50 H40 N2 O P2 | P 1 21/c 1 | 18.0198; 14.0045; 16.7584 90; 109.646; 90 | 3982.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556288 | CIF | C51 H39 N2 O P2 | P -1 | 9.373; 13.769; 17.95 104.285; 90.99; 92.535 | 2242 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556289 | CIF | C85 H77 B N2 O P2 Zn | P -1 | 14.3702; 15.2542; 17.2588 81.451; 66.469; 76.867 | 3370.8 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556290 | CIF | C76.18 H63.47 B N2 O P2 Zn | P -1 | 9.9214; 17.1175; 18.4747 86.754; 78.725; 80.859 | 3036.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556291 | CIF | C80.65 H63.86 B N2 O P2 Zn | P -1 | 9.9023; 16.867; 20.7112 101.974; 91.114; 95.296 | 3366.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556292 | CIF | C86.83 H60.66 B Cl1.66 F24 N2 O4 P2 Zn | P -1 | 11.4655; 19.564; 19.662 99.64; 103.416; 92.916 | 4210.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556293 | CIF | C90 H60 B Br0.38 F24 N2 O4 P2 Zn | P 1 21/c 1 | 18.781; 27.1179; 18.6506 90; 116.785; 90 | 8479.6 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556294 | CIF | C57 H50 Br2 N2 Ni | P 1 21/c 1 | 10.378; 16.008; 31.765 90; 95.61; 90 | 5251.9 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556295 | CIF | C56 H48 Br2 N2 Ni | P 1 21/c 1 | 15.352; 22.551; 15.38 90; 106.96; 90 | 5093 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556296 | CIF | C54 H44 Cl2 N2 Ni O0 | P 1 21/c 1 | 15.33; 22.285; 14.954 90; 106.33; 90 | 4902.6 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556297 | CIF | C28 H33 Cl4 Co N3 O2 | P b c a | 15.492; 17.191; 25.784 90; 90; 90 | 6867 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556298 | CIF | C28 H33 Cl4 Fe N3 S2 | C 1 2/c 1 | 23.2849; 16.2809; 17.6654 90; 106.957; 90 | 6405.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556299 | CIF | C41 H43 Cl2 Fe N3 O3 | P 1 21/n 1 | 16.114; 8.9394; 27.383 90; 99.828; 90 | 3886.6 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556300 | CIF | C38 H37 Cl4 Fe N3 S2 | P b c a | 17.148; 20.564; 22.319 90; 90; 90 | 7870 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556301 | CIF | C38.5 H38 Cl6 N3 S2 V | P 1 21/n 1 | 12.3896; 19.617; 16.797 90; 95.449; 90 | 4064 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556302 | CIF | C38.5 H38 Cl6 Cr N3 S2 | P 1 21/n 1 | 12.3561; 19.623; 16.75 90; 95.756; 90 | 4040.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556303 | CIF | C38 H37 Cl4 Mn N3 S2 | P b c a | 17.056; 20.693; 22.231 90; 90; 90 | 7846 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556304 | CIF | C41 H43 Br2 N3 Ni O S2 | P b c a | 17.54; 20.405; 22.23 90; 90; 90 | 7956 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556305 | CIF | C44.5 H50 Cl5 Fe N3 O2 | P 1 21/n 1 | 9.2178; 29.17; 16.7749 90; 92.674; 90 | 4505.6 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556306 | CIF | C44.25 H49.5 Cl4.5 Co N3 O2 | P 1 21/c 1 | 12.8687; 19.6515; 18.0924 90; 90.931; 90 | 4574.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556307 | CIF | C44.5 H50 Cl5 Fe N3 S2 | C 1 2/c 1 | 34.005; 10.0092; 27.105 90; 94.482; 90 | 9197.3 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556308 | CIF | C44.5 H50 Cl5 Co N3 S2 | C 1 2/c 1 | 34.234; 10.0665; 27.315 90; 93.888; 90 | 9392 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556309 | CIF | C19 H26 Cl O3 P Pd | P -1 | 7.8175; 16.296; 16.654 100.4; 100.58; 102.97 | 1977.2 | Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L. Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene Catalysis Science & Technology, 2012, 2, 715 |
1556310 | CIF | C22 H32 Cl O4 P Pd | P 1 21/n 1 | 9.552; 15.094; 16.038 90; 100.126; 90 | 2276.3 | Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L. Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene Catalysis Science & Technology, 2012, 2, 715 |
1556311 | CIF | C18 H18 F12 N2 O2 | P -1 | 8.301; 10.979; 11.71 80.225; 85.04; 89.69 | 1047.7 | Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z. Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling Catalysis Science & Technology, 2012, 2, 934 |
1556312 | CIF | C18 H18 F12 N2 O2 | C 1 c 1 | 25.06; 6.782; 13.057 90; 110.81; 90 | 2074 | Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z. Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling Catalysis Science & Technology, 2012, 2, 934 |
1556313 | CIF | C25 H24 Br N3 O5 Pd S | P -1 | 7.724; 13.385; 14 68.935; 83.939; 89.447 | 1342.5 | Srinivas, Keesara; Srinivas, Pottabathula; Prathima, Parvathaneni Sai; Balaswamy, Kodicherla; Sridhar, Balsubramanian; Rao, Mandapati Mohan Thiopseudourea ligated palladium complexes: synthesis, characterization and application as catalysts for Suzuki‒Miyaura, Sonogashira, Heck and Hiyama reactions Catalysis Science & Technology, 2012, 2, 1180 |
1556314 | CIF | C90 H84 Br0 N2 Ni O2 | P -1 | 10.515; 13.887; 15.272 80.61; 71.05; 70.1 | 1979.8 | Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene Catalysis Science & Technology, 2012, 2, 1340 |
1556315 | CIF | C78 H56 F4 N2 Ni O2 | C 1 2/c 1 | 47.225; 16.333; 17.278 90; 110.26; 90 | 12502 | Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene Catalysis Science & Technology, 2012, 2, 1340 |
1556316 | CIF | C17 H17 N O5 | P c a b | 8.8191; 17.5507; 20.7531 90; 90; 90 | 3212.2 | Ananthakrishnan, Rajakumar; Gazi, Sarifuddin [Ru(bpy)3]2+ aided photocatalytic synthesis of 2-arylpyridines via Hantzsch reaction under visible irradiation and oxygen atmosphere Catalysis Science & Technology, 2012, 2, 1463 |
1556317 | CIF | C40 H54 N2 O3 Zn | P -1 | 10.9698; 12.9718; 13.3427 91.834; 104.278; 92.66 | 1836.16 | Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P. A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium Catalysis Science & Technology, 2012, 2, 2231 |
1556318 | CIF | C68.5 H85 N4 O9 Zn2 | C 1 2/c 1 | 42.19; 9.719; 31.932 90; 110.08; 90 | 12297.6 | Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P. A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium Catalysis Science & Technology, 2012, 2, 2231 |
1556319 | CIF | C48 H38 Cl2 N2 O Ti | P b c a | 17.529; 18.752; 25.656 90; 90; 90 | 8433 | Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates Catalysis Science & Technology, 2012, 2, 2090 |
1556320 | CIF | C37 H32 Cl2 N2 O Ti | C 1 2/c 1 | 53.675; 10.021; 24.886 90; 100.29; 90 | 13170 | Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates Catalysis Science & Technology, 2012, 2, 2090 |
1556321 | CIF | C12 H12 Au Cl3 N2 | P 1 21/n 1 | 18.108; 9.5124; 18.3546 90; 113.59; 90 | 2897.4 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)–oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556322 | CIF | C12 H13 Au Cl4 N2 | C 1 2/c 1 | 22.1175; 14.791; 9.5257 90; 99.676; 90 | 3071.9 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556323 | CIF | C12 H12 Au Cl N2 O5 | P -1 | 7.6032; 9.2289; 9.96 82.321; 85.907; 88.085 | 690.65 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556324 | CIF | C40 H54 Cl4 N2 O3 Ru | P 1 21/c 1 | 20.5265; 13.4139; 29.7267 90; 91.812; 90 | 8180.9 | Leitgeb, Anita; Abbas, Mudassar; Fischer, Roland C.; Poater, Albert; Cavallo, Luigi; Slugovc, Christian A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand Catalysis Science & Technology, 2012, 2, 1640 |
1556325 | CIF | C15 H29 Cl2 N3 Pd | P -1 | 8.1051; 11.1155; 22.6264 77.784; 89.987; 71.894 | 1888.9 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556326 | CIF | C15 H28 Cl2 N2 Pd S | P -1 | 8.1752; 15.2655; 15.457 94.321; 90.451; 93.185 | 1920.4 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556327 | CIF | C30 H56 Cl2 N4 O2 Pd | P 1 | 8.1693; 9.1162; 22.9935 93.592; 91.806; 89.939 | 1708.2 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556328 | CIF | C23 H45 Cl2 N3 Pd | P 1 21/c 1 | 15.7877; 21.0937; 8.109 90; 102.061; 90 | 2640.9 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556329 | CIF | C66 H64 Cl2 N4 O7.5 V2 | P 1 21/a 1 | 17.8598; 10.775; 31.054 90; 101.73; 90 | 5851.2 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556330 | CIF | C44 H56 N2 O2 | P 1 21/a 1 | 9.6297; 12.1792; 16.2276 90; 100.851; 90 | 1869.18 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556331 | CIF | C60 H86 Cl4 N2 O6 V2 | P b c a | 15.4851; 12.3449; 33.0323 90; 90; 90 | 6314.5 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556332 | CIF | C42 H52 Cl2 N4 O3 V | P 21 n b | 11.0873; 17.9157; 20.6832 90; 90; 90 | 4108.4 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556333 | CIF | C54 H84 B Cl2 F4 P6 Rh3 | P 41 21 2 | 14.483; 14.483; 58.042 90; 90; 90 | 12175 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556334 | CIF | C85 H86 B Cl4 F4 O6 P6 Rh3 | P 1 | 13.136; 13.405; 14.779 85.58; 68.44; 68.06 | 2239.6 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556335 | CIF | C44 H72 Cl2 P4 Rh2 | P 21 21 21 | 14.1975; 16.3823; 20.5561 90; 90; 90 | 4781.1 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556336 | CIF | C135 H100 Cl6 F3 O3 P6 Rh3 S | P 1 21 1 | 16.493; 23.276; 16.775 90; 118.1; 90 | 5681 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556337 | CIF | C54 H84 B Br0.8 Cl1.2 F4 P6 Rh3 | P 21 21 21 | 16.431; 20.348; 21.116 90; 90; 90 | 7060 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556338 | CIF | C36 H56 Br2 P4 Rh2 | P 1 21 1 | 11.2912; 16.6047; 11.4464 90; 105.766; 90 | 2065.32 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556339 | CIF | C36 H86 B F4 O2 P6 Rh3 | P 1 | 12.416; 12.444; 18.186 95.81; 94.37; 111.98 | 2572.3 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556340 | CIF | C37 H86 B Cl4 F4 P6 Rh3 | P 1 | 9.6676; 12.005; 12.658 109.83; 94.19; 90.56 | 1377.3 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556341 | CIF | C30.5 H30 Cl2 F6 N6 O3 P2 Ru | C 1 2/c 1 | 29.0844; 15.042; 16.3344 90; 108.315; 90 | 6784.1 | Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A. Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts Catal. Sci. Technol., 2013, 3, 706 |
1556342 | CIF | C30.5 H30.5 Cl2 F6 N6 O3.25 P2 Ru | P -1 | 10.9643; 11.9921; 15.491 110.491; 99.026; 107.666 | 1737.2 | Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A. Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts Catal. Sci. Technol., 2013, 3, 706 |
1556343 | CIF | C80 H102 Al Cl N4 O6 S2 | P 41 21 2 | 13.6143; 13.6143; 38.6616 90; 90; 90 | 7165.9 | Ternel, Jérémy; Roussel, Pascal; Agbossou-Niedercorn, Francine; Gauvin, Régis M. Dismantling the salen framework: design of new asymmetric silylcyanation catalysts Catal. Sci. Technol., 2013, 3, 580 |
1556371 | CIF | C17 H15 Cl N4 O3 | P 21 21 21 | 7.129; 11.454; 19.387 90; 90; 90 | 1583.1 | Siddiqui, Zeba N.; Khan, Tabassum P2O5/SiO2 as an efficient heterogeneous catalyst for the synthesis of heterocyclic alkene derivatives under thermal solvent-free conditions Catalysis Science & Technology, 2013, 3, 2032 |
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