Crystallography Open Database

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1552352 CIFC7 H7 Au Cl4 N2 O3P -17.831; 7.931; 11.079
97.173; 95.533; 96.097		674.6Ahmad, 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 CIFC50 H39 F18 N12 P3 Ru2P -110.6161; 15.1085; 16.911
90.103; 94.853; 105.573		2602.6Hennessey, 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 CIFC51 H42 Cl F12 N11 O P2 Ru2P -112.918; 13.831; 17.552
92.997; 100.953; 105.668		2946.61Hennessey, 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 CIFC46 H41 Au Cl N2 P3P 1 21/n 117.5516; 12.9246; 17.7238
90; 93.431; 90		4013.4Schwarz, 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 CIFC44 H39 Au Cl N2 P3P 1 21/n 110.8276; 33.9018; 11.4594
90; 113.03; 90		3871.21Schwarz, 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 CIFC47 H37 Cl2 N2 P3P 1 21 110.3342; 22.3144; 17.0157
90; 92.007; 90		3921.4Schwarz, 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 CIFC47 H37 Au Cl3 N2 P3P -112.5994; 13.2954; 13.5256
70.09; 84.549; 78.391		2085.9Schwarz, 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 CIFC28 H33 Au Cl N P2P 1 21/c 111.78322; 9.40736; 24.667
90; 102.482; 90		2669.68Schwarz, 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 CIFC62 H72 N2 P4P -110.1896; 17.4204; 17.4304
67.712; 73.191; 73.1212		2682.92Schwarz, 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 CIFC60 H45 N3 P4P -335.1836; 35.1836; 9.7068
90; 90; 120		10406.1Schwarz, 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 CIFC55 H51 Cl9 N2 O3 P3 RhP 1 21/c 111.00739; 22.02102; 24.05162
90; 102.989; 90		5680.79Schwarz, 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 CIFC45 H41 Cl2 N2 P3P 1 21/n 19.8538; 22.9455; 17.3019
90; 93.031; 90		3906.5Schwarz, 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 CIFC97 H92 Cl10 N4 P6P -110.2673; 12.11; 19.82
103.947; 99.881; 100.687		2289Schwarz, 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 CIFC18 H22 Br F5 N2P 1 21/c 17.8536; 8.5571; 29.1438
90; 90.415; 90		1958.53Anthofer, 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 CIFC20 H29 Cl Mo N2 O3P 1 21/c 110.9605; 15.9334; 13.4384
90; 112.447; 90		2169Gomes, 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 CIFC41 H53 Cl17 Mo2 N4 O4F d -3 c :258.3972; 58.3972; 58.3972
90; 90; 90		199148Gomes, 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 CIFC40 H60 Cl2 Mo2 N4 O6P -112.2348; 14.0396; 14.2351
92.035; 107.553; 104.751		2237.7Gomes, 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 CIFC29 H31 Cl2 O3 P RuP 1 21/n 110.0354; 12.4751; 22.059
90; 93.55; 90		2756.3Amenuvor, 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 CIFC123.3 Cl8 O8 P4 Ru4 Zn2P 1 21/n 116.387; 27.97; 26.66
90; 101.396; 90		11979Amenuvor, 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 CIFC25 H29 Cl2 O2 P RuP 1 21/n 110.595; 12.873; 18.387
90; 106.74; 90		2401.5Amenuvor, 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 CIFC24 H38 F6 Fe P Ru S3C m c e15.867; 20.073; 18.513
90; 90; 90		5896.4Zhang, 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 CIFC14 H23 Co S3P 1 21/c 113.1028; 8.6112; 14.2219
90; 101.551; 90		1572.17Zhang, 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 CIFC30 H43 F6 Fe P Ru S4P 1 21/n 114.3616; 13.9373; 16.9737
90; 99.0564; 90		3355.1Zhang, 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 CIFC26 H41 F12 Fe N P2 Ru S3P n m a11.8; 15.608; 18.603
90; 90; 90		3426Zhang, 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 CIFC48 H58 B Co Fe S3P n a 2120.2817; 17.2944; 12.4241
90; 90; 90		4357.9Zhang, 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 CIFC47 H56 B Co Fe S3P n a 2120.576; 16.9755; 12.0227
90; 90; 90		4199.4Zhang, 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 CIFC48 H59 B Fe Ru S3P 1 21/c 115.5349; 15.8332; 18.3897
90; 90.694; 90		4522.9Zhang, 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 CIFC28 H27 N O6P 21 21 2110.42; 12.888; 19.103
90; 90; 90		2565.4Wang, 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 CIFC24 H28 Br2 N2 NiC 1 2/c 129.331; 10.775; 15.226
90; 105.3; 90		4641.5Song, 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 CIFC23 H26 Br2 N2 NiP 1 21/n 115.834; 8.6441; 17.665
90; 114.28; 90		2204Song, 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 CIFC60 H53 Cl4 O5 P5 Rh2P 1 21/c 117.0585; 17.1534; 19.5448
90; 90.797; 90		5718.5Castro, 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 CIFC44 H48 F6 O12 S8 ZnR -3 :H12.5877; 12.5877; 29.1803
90; 90; 120		4004.2Enthaler, Stephan
A straightforward zinc-catalysed reduction of sulfoxides to sulfides
Catalysis Science & Technology, 2011, 1, 104
1556271 CIFC33.33 H0 F4 O6.67 S4 Zn0.67P -110.5817; 13.8939; 19.8576
83.554; 88.085; 73.117		2775.99Enthaler, Stephan
A straightforward zinc-catalysed reduction of sulfoxides to sulfides
Catalysis Science & Technology, 2011, 1, 104
1556272 CIFC18 H22 N O5 PC 1 2/c 122.1091; 10.4184; 18.2639
90; 118.495; 90		3697.3Kidwai, 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 CIFC22 H24 Cl2 Co N2P 1 21/n 111.337; 15.712; 11.611
90; 95.49; 90		2058.7Xiao, 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 CIFC24 H28 Cl2 Co N2P 1 21/n 110.125; 16.885; 13.533
90; 90.01; 90		2313.6Xiao, 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 CIFC24 H34 N O4 VP 1 21/c 18.4832; 11.5025; 24.14
90; 94.873; 90		2347Lorber, 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 CIFC26 H26 Cl2 N2 O TiC 1 2/c 123.852; 13.832; 16.89
90; 118.68; 90		4889Huang, 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 CIFC27 H28 Cl2 N2 O TiP 1 21/c 117.098; 8.1446; 17.624
90; 98.7; 90		2426Huang, 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 CIFC16 H24 Cl2 N2 O4 Pd S2P -18.4783; 11.6061; 13.1535
67.125; 89.797; 68.971		1099.1Tomás-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 CIFC14 H14 Cl2 N2 O5 Pd SP -17.6738; 10.4974; 12.5545
112.689; 90.017; 108.646		875.2Tomás-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 CIFC54.2 H48.4 Cl0.4 N2 O P2P -111.5434; 14.8956; 15.1659
62.313; 86.134; 78.115		2258.4Wheaton, 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 CIFC50 H40 N2 O P2P 1 21/c 118.0198; 14.0045; 16.7584
90; 109.646; 90		3982.9Wheaton, 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 CIFC51 H39 N2 O P2P -19.373; 13.769; 17.95
104.285; 90.99; 92.535		2242Wheaton, 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 CIFC85 H77 B N2 O P2 ZnP -114.3702; 15.2542; 17.2588
81.451; 66.469; 76.867		3370.8Wheaton, 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 CIFC76.18 H63.47 B N2 O P2 ZnP -19.9214; 17.1175; 18.4747
86.754; 78.725; 80.859		3036.9Wheaton, 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 CIFC80.65 H63.86 B N2 O P2 ZnP -19.9023; 16.867; 20.7112
101.974; 91.114; 95.296		3366.9Wheaton, 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 CIFC86.83 H60.66 B Cl1.66 F24 N2 O4 P2 ZnP -111.4655; 19.564; 19.662
99.64; 103.416; 92.916		4210.9Wheaton, 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 CIFC90 H60 B Br0.38 F24 N2 O4 P2 ZnP 1 21/c 118.781; 27.1179; 18.6506
90; 116.785; 90		8479.6Wheaton, 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 CIFC57 H50 Br2 N2 NiP 1 21/c 110.378; 16.008; 31.765
90; 95.61; 90		5251.9Liu, 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 CIFC56 H48 Br2 N2 NiP 1 21/c 115.352; 22.551; 15.38
90; 106.96; 90		5093Liu, 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 CIFC54 H44 Cl2 N2 Ni O0P 1 21/c 115.33; 22.285; 14.954
90; 106.33; 90		4902.6Liu, 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 CIFC28 H33 Cl4 Co N3 O2P b c a15.492; 17.191; 25.784
90; 90; 90		6867Smit, 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 CIFC28 H33 Cl4 Fe N3 S2C 1 2/c 123.2849; 16.2809; 17.6654
90; 106.957; 90		6405.8Smit, 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 CIFC41 H43 Cl2 Fe N3 O3P 1 21/n 116.114; 8.9394; 27.383
90; 99.828; 90		3886.6Smit, 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 CIFC38 H37 Cl4 Fe N3 S2P b c a17.148; 20.564; 22.319
90; 90; 90		7870Smit, 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 CIFC38.5 H38 Cl6 N3 S2 VP 1 21/n 112.3896; 19.617; 16.797
90; 95.449; 90		4064Smit, 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 CIFC38.5 H38 Cl6 Cr N3 S2P 1 21/n 112.3561; 19.623; 16.75
90; 95.756; 90		4040.8Smit, 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 CIFC38 H37 Cl4 Mn N3 S2P b c a17.056; 20.693; 22.231
90; 90; 90		7846Smit, 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 CIFC41 H43 Br2 N3 Ni O S2P b c a17.54; 20.405; 22.23
90; 90; 90		7956Smit, 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 CIFC44.5 H50 Cl5 Fe N3 O2P 1 21/n 19.2178; 29.17; 16.7749
90; 92.674; 90		4505.6Smit, 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 CIFC44.25 H49.5 Cl4.5 Co N3 O2P 1 21/c 112.8687; 19.6515; 18.0924
90; 90.931; 90		4574.8Smit, 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 CIFC44.5 H50 Cl5 Fe N3 S2C 1 2/c 134.005; 10.0092; 27.105
90; 94.482; 90		9197.3Smit, 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 CIFC44.5 H50 Cl5 Co N3 S2C 1 2/c 134.234; 10.0665; 27.315
90; 93.888; 90		9392Smit, 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 CIFC19 H26 Cl O3 P PdP -17.8175; 16.296; 16.654
100.4; 100.58; 102.97		1977.2Fuentes, 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 CIFC22 H32 Cl O4 P PdP 1 21/n 19.552; 15.094; 16.038
90; 100.126; 90		2276.3Fuentes, 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 CIFC18 H18 F12 N2 O2P -18.301; 10.979; 11.71
80.225; 85.04; 89.69		1047.7Legros, 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 CIFC18 H18 F12 N2 O2C 1 c 125.06; 6.782; 13.057
90; 110.81; 90		2074Legros, 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 CIFC25 H24 Br N3 O5 Pd SP -17.724; 13.385; 14
68.935; 83.939; 89.447		1342.5Srinivas, 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 CIFC90 H84 Br0 N2 Ni O2P -110.515; 13.887; 15.272
80.61; 71.05; 70.1		1979.8Zhou, 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 CIFC78 H56 F4 N2 Ni O2C 1 2/c 147.225; 16.333; 17.278
90; 110.26; 90		12502Zhou, 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 CIFC17 H17 N O5P c a b8.8191; 17.5507; 20.7531
90; 90; 90		3212.2Ananthakrishnan, 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 CIFC40 H54 N2 O3 ZnP -110.9698; 12.9718; 13.3427
91.834; 104.278; 92.66		1836.16Taherimehr, 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 CIFC68.5 H85 N4 O9 Zn2C 1 2/c 142.19; 9.719; 31.932
90; 110.08; 90		12297.6Taherimehr, 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 CIFC48 H38 Cl2 N2 O TiP b c a17.529; 18.752; 25.656
90; 90; 90		8433Huang, 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 CIFC37 H32 Cl2 N2 O TiC 1 2/c 153.675; 10.021; 24.886
90; 100.29; 90		13170Huang, 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 CIFC12 H12 Au Cl3 N2P 1 21/n 118.108; 9.5124; 18.3546
90; 113.59; 90		2897.4O'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 CIFC12 H13 Au Cl4 N2C 1 2/c 122.1175; 14.791; 9.5257
90; 99.676; 90		3071.9O'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 CIFC12 H12 Au Cl N2 O5P -17.6032; 9.2289; 9.96
82.321; 85.907; 88.085		690.65O'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 CIFC40 H54 Cl4 N2 O3 RuP 1 21/c 120.5265; 13.4139; 29.7267
90; 91.812; 90		8180.9Leitgeb, 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 CIFC15 H29 Cl2 N3 PdP -18.1051; 11.1155; 22.6264
77.784; 89.987; 71.894		1888.9Peral, 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 CIFC15 H28 Cl2 N2 Pd SP -18.1752; 15.2655; 15.457
94.321; 90.451; 93.185		1920.4Peral, 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 CIFC30 H56 Cl2 N4 O2 PdP 18.1693; 9.1162; 22.9935
93.592; 91.806; 89.939		1708.2Peral, 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 CIFC23 H45 Cl2 N3 PdP 1 21/c 115.7877; 21.0937; 8.109
90; 102.061; 90		2640.9Peral, 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 CIFC66 H64 Cl2 N4 O7.5 V2P 1 21/a 117.8598; 10.775; 31.054
90; 101.73; 90		5851.2Clowes, 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 CIFC44 H56 N2 O2P 1 21/a 19.6297; 12.1792; 16.2276
90; 100.851; 90		1869.18Clowes, 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 CIFC60 H86 Cl4 N2 O6 V2P b c a15.4851; 12.3449; 33.0323
90; 90; 90		6314.5Clowes, 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 CIFC42 H52 Cl2 N4 O3 VP 21 n b11.0873; 17.9157; 20.6832
90; 90; 90		4108.4Clowes, 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 CIFC54 H84 B Cl2 F4 P6 Rh3P 41 21 214.483; 14.483; 58.042
90; 90; 90		12175Preetz, 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 CIFC85 H86 B Cl4 F4 O6 P6 Rh3P 113.136; 13.405; 14.779
85.58; 68.44; 68.06		2239.6Preetz, 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 CIFC44 H72 Cl2 P4 Rh2P 21 21 2114.1975; 16.3823; 20.5561
90; 90; 90		4781.1Preetz, 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 CIFC135 H100 Cl6 F3 O3 P6 Rh3 SP 1 21 116.493; 23.276; 16.775
90; 118.1; 90		5681Preetz, 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 CIFC54 H84 B Br0.8 Cl1.2 F4 P6 Rh3P 21 21 2116.431; 20.348; 21.116
90; 90; 90		7060Preetz, 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 CIFC36 H56 Br2 P4 Rh2P 1 21 111.2912; 16.6047; 11.4464
90; 105.766; 90		2065.32Preetz, 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 CIFC36 H86 B F4 O2 P6 Rh3P 112.416; 12.444; 18.186
95.81; 94.37; 111.98		2572.3Preetz, 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 CIFC37 H86 B Cl4 F4 P6 Rh3P 19.6676; 12.005; 12.658
109.83; 94.19; 90.56		1377.3Preetz, 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 CIFC30.5 H30 Cl2 F6 N6 O3 P2 RuC 1 2/c 129.0844; 15.042; 16.3344
90; 108.315; 90		6784.1Vaquer, 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 CIFC30.5 H30.5 Cl2 F6 N6 O3.25 P2 RuP -110.9643; 11.9921; 15.491
110.491; 99.026; 107.666		1737.2Vaquer, 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 CIFC80 H102 Al Cl N4 O6 S2P 41 21 213.6143; 13.6143; 38.6616
90; 90; 90		7165.9Ternel, 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 CIFC17 H15 Cl N4 O3P 21 21 217.129; 11.454; 19.387
90; 90; 90		1583.1Siddiqui, 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
1556372 CIFC48 H44 Cu2 O12P -110.53; 10.579; 10.773
109.248; 93.156; 106.287		1073Sunil, Abraham C.; Langner, Ernst H. G.; Marais, Charlene; Bezuidenhoudt, Barend C. B.
Thermo-analytical determination of intermediates in the copper catalysed rearrangement of o-toluic acid to meta-cresol
Catalysis Science & Technology, 2013, 3, 2227
1556373 CIFC19 H24 Br2 Cl2 N4 NiC 2 2 2114.2034; 11.5066; 14.6836
90; 90; 90		2399.8Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556374 CIFC18 H22 Cl2 N4 NiP -19.2765; 10.7428; 12.1287
110.976; 96.346; 113.712		986.47Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556375 CIFC18 H22 Br2 N4 NiP -19.3446; 14.994; 15.681
75.599; 78.411; 81.522		2073.7Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556376 CIFC45 H41 Br2 Cl N2 NiP 1 21/c 19.6013; 16.927; 24.799
90; 100.77; 90		3959.4Jia, Dedong; Zhang, Wenjuan; Liu, Weiliang; Wang, Lin; Redshaw, Carl; Sun, Wen-Hua
Unsymmetrical α-diiminonickel bromide complexes: synthesis, characterization and their catalytic behavior toward ethylene
Catalysis Science & Technology, 2013, 3, 2737
1556377 CIFC47 H45 Br2 Cl N2 NiP 1 21/c 19.922; 16.84; 24.975
90; 98.41; 90		4128.1Jia, Dedong; Zhang, Wenjuan; Liu, Weiliang; Wang, Lin; Redshaw, Carl; Sun, Wen-Hua
Unsymmetrical α-diiminonickel bromide complexes: synthesis, characterization and their catalytic behavior toward ethylene
Catalysis Science & Technology, 2013, 3, 2737
1556378 CIFC25 H35 N3 ZnP -19.6343; 9.6463; 14.2834
76.36; 88.829; 63.062		1144.29Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556379 CIFC31 H39 N3 O ZnP 1 21/n 112.765; 16.025; 13.594
90; 98.6; 90		2750Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556380 CIFC35 H47 N3 O ZnP -110.889; 14.2911; 20.7227
92.804; 92.129; 92.212		3216.1Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556381 CIFC3 H5 Au Cl4 N2P 1 2/m 13.8864; 7.7824; 7.5103
90; 98.573; 90		224.61de Almeida, M. Peixoto; Martins, L. M. D. R. S.; Carabineiro, S. A. C.; Lauterbach, T.; Rominger, F.; Hashmi, A. S. K.; Pombeiro, A. J. L.; Figueiredo, J. L.
Homogeneous and heterogenised new gold C-scorpionate complexes as catalysts for cyclohexane oxidation
Catalysis Science & Technology, 2013, 3, 3056
1556382 CIFC14 H16 N2 O2P 1 21/n 15.8113; 23.7797; 9.2207
90; 95.959; 90		1267.33Ray, Suman; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda
Porous silica nanoparticles with mesoscopic void spaces for the domino intermolecular aerobic oxidative synthesis of novel β,β′-diketoenamines
Catalysis Science & Technology, 2013, 3, 1267
1556383 CIFC99 H102 N9 O6 P Zn3P -3 c 120.8644; 20.8644; 52.9489
90; 90; 120		19961.8Jacobs, Ivo; van Duin, Adri C. T.; Kleij, Arjan W.; Kuil, Mark; Tooke, Duncan M.; Spek, Anthony L.; Reek, Joost N. H.
Conformational studies of ligand-template assemblies and the consequences for encapsulation of rhodium complexes and hydroformylation catalysis
Catalysis Science & Technology, 2013, 3, 1955
1556384 CIFC25.63 H25.25 Cl3.25 Fe N6 O8P 1 21/c 112.2117; 20.6062; 23.4209
90; 90.957; 90		5892.7Wong, Emma; Jeck, Jonathan; Grau, Michaela; White, Andrew J. P.; Britovsek, George J. P.
A strong-field pentadentate ligand in iron-based alkane oxidation catalysis and implications for iron(iv) oxo intermediates
Catalysis Science & Technology, 2013, 3, 1116
1556385 CIFC48 H47 Cl4 Fe2 N11 O18P 1 21/c 112.4043; 38.877; 12.3737
90; 117.208; 90		5306.9Wong, Emma; Jeck, Jonathan; Grau, Michaela; White, Andrew J. P.; Britovsek, George J. P.
A strong-field pentadentate ligand in iron-based alkane oxidation catalysis and implications for iron(iv) oxo intermediates
Catalysis Science & Technology, 2013, 3, 1116
1556599 CIFC87.5 H82 Ag2 Fe O7.5 P4P 1 21 113.2313; 30.795; 18.556
90; 94.183; 90		7540.6Liu, Kuan-Guan; Rouhani, Farzaneh; Gao, Xue-Mei; Abbasi-Azad, Mahsa; Li, Jing-Zhe; Hu, Xiu-De; Wang, Wei; Hu, Mao-Lin; Morsali, Ali
Bilateral photocatalytic mechanism of dye degradation by a designed ferrocene-functionalized cluster under natural sunlight
Catalysis Science & Technology, 2020, 10, 757-767
1556600 CIFC122.5 H108.5 Cu2 Fe O7 P6P b c a24.582; 20.281; 40.461
90; 90; 90		20172Liu, Kuan-Guan; Rouhani, Farzaneh; Gao, Xue-Mei; Abbasi-Azad, Mahsa; Li, Jing-Zhe; Hu, Xiu-De; Wang, Wei; Hu, Mao-Lin; Morsali, Ali
Bilateral photocatalytic mechanism of dye degradation by a designed ferrocene-functionalized cluster under natural sunlight
Catalysis Science & Technology, 2020, 10, 757-767
1556927 CIFC9 H19 I2 N3 PdC 1 2/c 114.7908; 7.8079; 27.592
90; 99.197; 90		3145.5Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556928 CIFC13 H21 I2 N3 PdP 1 21/c 117.5721; 12.5994; 8.4655
90; 99.55; 90		1848.27Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556929 CIFC15 H17 I2 N3 PdC 1 2/c 121.6545; 8.657; 20.1671
90; 95.408; 90		3763.8Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556930 CIFC16 H19 I2 N3 PdP -19.5333; 10.964; 11.3716
62.48; 79.571; 67.896		976.59Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1557055 CIFC20 H21 B Cl2 O2C 1 2/c 127.001; 6.0841; 25.1455
90; 108.298; 90		3922Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557056 CIFC22 H27 B O2C 1 2/c 135.07; 6.2286; 20.596
90; 119.212; 90		3926.8Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557057 CIFC22 H27 B O2P c a 2125.447; 6.3811; 24.281
90; 90; 90		3942.7Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557058 CIFC36.5 H57 B Cl F4 N4 P4 RhP 31 2 113.824; 13.824; 40.089
90; 90; 120		6635Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557059 CIFC27 H42 B Cl2 F4 N2 P2 RhP 1 21 19.7105; 14.3281; 11.2851
90; 96.031; 90		1561.44Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557155 CIFC116 H154 Cl N9 O9 Ti2P 1 21/n 126.5998; 13.18144; 32.7719
90; 104.629; 90		11118.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557156 CIFC30 H44 Cl2 O2 TiP 1 21 111.0509; 9.6943; 14.8668
90; 108.131; 90		1513.61Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557157 CIFC220 H283 Cl6 N15 O20 Ti6P -117.651; 18.2749; 19.8507
67.4531; 68.6833; 73.3966		5428.93Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557158 CIFC125 H172.5 Cl N8.5 O9 Ti2P -117.4371; 17.7765; 21.1345
100.63; 93.526; 104.426		6195.8Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557159 CIFC120 H164 Cl2 N6 O8 Ti2P -112.5697; 18.1183; 27.5282
104.559; 98.781; 102.093		5792.04Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557160 CIFC108 H140 Cl N7 O9 Ti2P -113.9465; 17.4744; 23.5392
85.6028; 74.2347; 74.5316		5320.83Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557161 CIFC130.71 H174.42 Cl N2.85 O11.43 Ti2P -116.3253; 17.3213; 23.5069
102.481; 91.495; 101.593		6340.9Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557162 CIFC113 H149.5 Cl N7.5 O9 Ti2P 1 21/n 126.6007; 13.18235; 32.7812
90; 104.622; 90		11122.7Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557163 CIFC49 H61 Cl N2 O4 TiP -112.14575; 18.0271; 21.0909
95.2564; 105.355; 90.2869		4432.27Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557164 CIFC54 H72 Cl2 N2 O4 TiC 1 2/c 143.9803; 12.41683; 19.4608
90; 94.9954; 90		10587.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557173 CIFC54.28 H49.13 Ir O0.28 P3P 1 21/c 117.31801; 12.99024; 19.71788
90; 94.4442; 90		4422.5Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557174 CIFC57 H68 Cl2 Ir2 N4 O S2P 1 21/c 112.9317; 16.6; 25.5365
90; 90.2757; 90		5481.76Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557528 CIFC39 H72 Cd Mo12 N6 O68 P8 Zn2P -113.126; 25.198; 30.034
113.698; 101.194; 90.634		8879Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557529 CIFC26 H24 Cd1.2 Co0.8 Mo12 N4 Na4 O69 P8C 1 2/c 121.0842; 18.3743; 21.9022
90; 100.716; 90		8337.1Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557530 CIFC65 H116 Al2 Cd2 Mo24 N10 O137 P16P 1 n 115.882; 21.676; 25.338
90; 94.559; 90		8695.2Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557594 CIFC16 H22 Cl2 Co N4 O4P 1 21/n 19.5079; 32.3832; 13.8528
90; 110.045; 90		4006.9Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557595 CIFC17 H22 Cl2 Co N4 O4P 1 21/c 112.2832; 7.3066; 22.5865
90; 95.779; 90		2016.8Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557596 CIFC41 H44 B Cl Co N4P 21 21 219.8205; 14.0434; 26.706
90; 90; 90		3683.1Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557597 CIFC43 H46 B Cl Co N4P 1 21/c 116.0327; 10.7162; 22.6792
90; 107.025; 90		3725.7Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557658 CIFC36 H46 Cl10 Fe4 N6 O9P 1 21/n 113.612; 13.537; 14.409
90; 109.931; 90		2496.1Karim, Suhana; Chakraborty, Aratrika; Samanta, Debabrata; Zangrando, Ennio; Ghosh, Totan; Das, Debasis
A dinuclear iron complex as an efficient electrocatalyst for homogeneous water oxidation reaction
Catalysis Science & Technology, 2020, 10, 2830-2837
1557659 CIFC32 H40 Cl4 Fe2 N6 O10P 1 21/c 111.8719; 16.9617; 9.4064
90; 102.136; 90		1851.81Karim, Suhana; Chakraborty, Aratrika; Samanta, Debabrata; Zangrando, Ennio; Ghosh, Totan; Das, Debasis
A dinuclear iron complex as an efficient electrocatalyst for homogeneous water oxidation reaction
Catalysis Science & Technology, 2020, 10, 2830-2837
1557722 CIFC36 H46 N4 O6 P2P -19.437; 10.4908; 18.5143
96.9776; 99.2858; 104.161		1728.97Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557723 CIFC27 H30 Br2 Co N4 O7 S2P -18.1545; 11.7917; 16.3115
107.981; 96.136; 103.72		1421.47Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557724 CIFC26 H28 Br2 Co N4 O4P 1 21/n 18.0833; 11.8214; 13.6272
90; 95.751; 90		1295.61Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557862 CIFC20 H35 Al N6P n a 2118.8949; 10.1078; 23.9918
90; 90; 90		4582.1Navarro, Marta; Sánchez-Barba, Luis F.; Garcés, Andrés; Fernández-Baeza, Juan; Fernández, Israel; Lara-Sánchez, Agustín; Rodríguez, Ana M.
Bimetallic scorpionate-based helical organoaluminum complexes for efficient carbon dioxide fixation into a variety of cyclic carbonates
Catalysis Science & Technology, 2020, 10, 3265-3278
1557863 CIFC33.5 H44 Al2 N6P 1 21/c 118.637; 9.384; 26.354
90; 125.325; 90		3760.4Navarro, Marta; Sánchez-Barba, Luis F.; Garcés, Andrés; Fernández-Baeza, Juan; Fernández, Israel; Lara-Sánchez, Agustín; Rodríguez, Ana M.
Bimetallic scorpionate-based helical organoaluminum complexes for efficient carbon dioxide fixation into a variety of cyclic carbonates
Catalysis Science & Technology, 2020, 10, 3265-3278
1557983 CIFC23 H33 Br Ir N3 OP 1 21/c 18.5663; 11.0966; 24.1272
90; 98.595; 90		2267.7González-Lainez, Miguel; Jiménez, M. Victoria; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.
Effective N-methylation of nitroarenes with methanol catalyzed by a functionalized NHC-based iridium catalyst: a green approach to N-methyl amines
Catalysis Science & Technology, 2020, 10, 3458-3467
1557984 CIFC17 H21 Br Ir N3 O3P -19.2294; 11.1211; 11.892
99.157; 110.946; 114.394		968.3González-Lainez, Miguel; Jiménez, M. Victoria; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.
Effective N-methylation of nitroarenes with methanol catalyzed by a functionalized NHC-based iridium catalyst: a green approach to N-methyl amines
Catalysis Science & Technology, 2020, 10, 3458-3467
1558022 CIFC15 H19 N O6 SP b c a13.3705; 7.2739; 31.8622
90; 90; 90		3098.78Wu, Xiao-Yun; Gui, Hou-Ze; Jangra, Harish; Wei, Yin; Zipse, Hendrik; Shi, Min
Phosphine-catalyzed [3 + 2] annulation of 2-aminoacrylates with allenoates and mechanistic studies
Catalysis Science & Technology, 2020, 10, 3959-3964
1558045 CIFC23 H22 F9 Fe N10 O9 S3P -19.1084; 11.7267; 16.3308
85.341; 89.88; 70.285		1636.05Dyckhoff, Florian; Schlagintweit, Jonas F.; Reich, Robert M.; Kühn, Fritz E.
Pushing the limits of activity and stability: the effects of Lewis acids on non-heme iron‒NHC epoxidation catalysts
Catalysis Science & Technology, 2020, 10, 3532-3536
1558072 CIFC15 H19 N2 O4 ReP 1 21/c 114.6069; 8.871; 12.0927
90; 90.801; 90		1566.79Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558073 CIFC23 H35 N2 O4 ReC 1 2/c 123.927; 9.4928; 22.1646
90; 106.575; 90		4825.1Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558074 CIFC15 H18 N3 O6 ReP b c a8.90063; 11.9803; 31.8099
90; 90; 90		3391.96Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558149 CIFC28 H24 Co N2 O10 S2C 1 2/c 120.1441; 12.2778; 11.4937
90; 92.993; 90		2838.8Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558150 CIFC28 H24 Co0.79 Fe0.21 N2 O10 S2C 1 2/c 120.1868; 12.2668; 11.4817
90; 92.862; 90		2839.64Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558151 CIFC28 H24 Co0.29 N2 Ni0.71 O10 S2C 1 2/c 120.1616; 12.1398; 11.4274
90; 92.792; 90		2793.63Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558164 CIFC16 H29 Cl F6 N2 O P Ru SbP 1 21/n 111.7394; 14.7656; 14.6955
90; 108.172; 90		2420.26González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558165 CIFC17 H31 Cl F6 N2 O P Ru SbP 1 21/n 18.3717; 21.574; 14.8558
90; 105.025; 90		2591.39González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558270 CIFC70.98 H100.97 Fe2 N4 O7.98 Ti2P 1 21/c 122.6283; 8.7736; 18.5643
90; 105.17; 90		3557.2Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558271 CIFC39 H57.63 Fe N2 O4 ZrP 1 21/c 122.8642; 9.1582; 19.4463
90; 106.447; 90		3905.3Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558272 CIFC31.51 H58.93 N2 O4 ZrP -19.0808; 9.9464; 21.5037
93.147; 91.175; 115.995		1741Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558273 CIFC30.5 H58 N2 O4 TiP 1 21/c 126.1034; 13.6068; 18.7389
90; 90.427; 90		6655.6Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558490 CIFC95 H104 B2 Cl2 Co2 F10 O12 P6P b c a26.2086; 27.5599; 28.9629
90; 90; 90		20920.1Papa, Veronica; Cabrero-Antonino, Jose R.; Spannenberg, Anke; Junge, Kathrin; Beller, Matthias
Homogeneous cobalt-catalyzed deoxygenative hydrogenation of amides to amines
Catalysis Science & Technology, 2020, 10, 6116-6128
1558540 CIFC19 H21 Cl2 N RuP c a 217.1672; 13.7037; 17.9697
90; 90; 90		1764.93Chatterjee, Basujit; Kalsi, Deepti; Kaithal, Akash; Bordet, Alexis; Leitner, Walter; Gunanathan, Chidambaram
One-pot dual catalysis for the hydrogenation of heteroarenes and arenes
Catalysis Science & Technology, 2020, 10, 5163-5170
1558696 CIFC30 H47 Cl Ir NP 1 21/c 110.1037; 11.6662; 23.623
90; 97.789; 90		2758.8Zhang, Dejin; Yang, Guoqiang; Zhao, Yue; Shao, Shouyan; Zhu, Guisheng; Liu, Peijun; Liu, Jia; Hu, Xingbang; Zhang, Zhibing
Efficient methanol carbonylation to methyl acetate catalyzed by a cyclic(alkyl)(amino)carbene iridium complex
Catalysis Science & Technology, 2020, 10, 6045-6049
1558697 CIFC24 H35 Cl I0 Ir N O2P 1 21/n 19.4294; 15.2306; 16.4958
90; 94.904; 90		2360.38Zhang, Dejin; Yang, Guoqiang; Zhao, Yue; Shao, Shouyan; Zhu, Guisheng; Liu, Peijun; Liu, Jia; Hu, Xingbang; Zhang, Zhibing
Efficient methanol carbonylation to methyl acetate catalyzed by a cyclic(alkyl)(amino)carbene iridium complex
Catalysis Science & Technology, 2020, 10, 6045-6049
1559097 CIFC25 H19 NP 1 21/n 18.7417; 11.0177; 19.073
90; 101.123; 90		1802.48Nori, Valeria; Dasgupta, Ayan; Babaahmadi, Rasool; Carlone, Armando; Ariafard, Alireza; Melen, Rebecca L.
Triarylborane catalysed N-alkylation of amines with aryl esters
Catalysis Science & Technology, 2020, 10, 7523-7530
1559098 CIFC23 H19 F2 NP 1 21/c 18.9007; 11.1893; 18.1967
90; 93.764; 90		1808.35Nori, Valeria; Dasgupta, Ayan; Babaahmadi, Rasool; Carlone, Armando; Ariafard, Alireza; Melen, Rebecca L.
Triarylborane catalysed N-alkylation of amines with aryl esters
Catalysis Science & Technology, 2020, 10, 7523-7530
1559113 CIFC65 H89 In N2 O3 P2P 1 21/c 115.1464; 16.9612; 26.1549
90; 103.943; 90		6521.25Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559114 CIFC50 H74 N2 O2 P2P -111.4385; 15.3688; 15.4343
83.413; 78.85; 78.526		2600.66Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559115 CIFC57 H85 In N2 O5 P2P 21 21 2111.128; 18.2363; 30.9376
90; 90; 90		6278.28Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559116 CIFC65 H87 In N2 O4 P2P n a 2120.6809; 18.5748; 15.7154
90; 90; 90		6036.97Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559117 CIFC63 H102 In N2 O3 P2P 1 21/n 110.9894; 28.7519; 19.81
90; 91.214; 90		6257.9Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559118 CIFC52 H77 In N2 O3 P2P -114.2993; 14.3196; 17.8201
105.16; 107.065; 96.826		3290.3Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559240 CIFC18 H32 Co O4 PP -19.1926; 18.6959; 18.8899
93.315; 103.878; 98.222		3105Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559241 CIFC15 H8 Co F18 O4 PP -18.808; 11.2727; 11.4608
87.2767; 86.0751; 81.5105		1122.03Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559242 CIFC27 H40 Co O6 PP 1 21/c 19.342; 12.6826; 22.4709
90; 93.041; 90		2658.6Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559243 CIFC24 H40 Co O6 PP 1 21/n 110.925; 12.6105; 20.1341
90; 104.561; 90		2684.77Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559244 CIFC21 H34 Co N2 O6 PP 1 21/c 117.748; 8.4442; 16.239
90; 91.117; 90		2433.2Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559245 CIFC33 H29 Co N O5 PP 21 21 2110.7864; 11.5313; 22.3359
90; 90; 90		2778.2Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559279 CIFC58 H53 Cl3 Cu F6 N2 O5 P3C 1 2/c 135.7359; 12.1275; 27.9938
90; 112.354; 90		11220.4Li, Chenfei; Dickson, Robert; Rockstroh, Nils; Rabeah, Jabor; Cordes, David B.; Slawin, Alexandra M. Z.; Hünemörder, Paul; Spannenberg, Anke; Bühl, Michael; Mejía, Esteban; Zysman-Colman, Eli; Kamer, Paul C. J.
Ligand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry reaction
Catalysis Science & Technology, 2020, 10, 7745-7756
1559280 CIFC57 H40 Cu F18 N2 O P3P 1 21/n 111.4434; 20.2661; 27.9804
90; 99.805; 90		6394.24Li, Chenfei; Dickson, Robert; Rockstroh, Nils; Rabeah, Jabor; Cordes, David B.; Slawin, Alexandra M. Z.; Hünemörder, Paul; Spannenberg, Anke; Bühl, Michael; Mejía, Esteban; Zysman-Colman, Eli; Kamer, Paul C. J.
Ligand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry reaction
Catalysis Science & Technology, 2020, 10, 7745-7756
1559301 CIFC21.5 H32 Cl2 N3 O2.5 RuP 1 21/n 112.5519; 23.6646; 16.9746
90; 94.02; 90		5029.7Das, Kanu; Yasmin, Eileen; Das, Babulal; Srivastava, Hemant Kumar; Kumar, Akshai
Phosphine-free pincer-ruthenium catalyzed biofuel production: high rates, yields and turnovers of solventless alcohol alkylation
Catalysis Science & Technology, 2020, 10, 8347-8358
1559302 CIFC14 H21 Cl2 N3 O2 RuP 1 21/c 19.2304; 10.8098; 18.2395
90; 96.278; 90		1809Das, Kanu; Yasmin, Eileen; Das, Babulal; Srivastava, Hemant Kumar; Kumar, Akshai
Phosphine-free pincer-ruthenium catalyzed biofuel production: high rates, yields and turnovers of solventless alcohol alkylation
Catalysis Science & Technology, 2020, 10, 8347-8358
1559556 CIFC68 H156 O28 Si14 Zr2P -113.346; 17.309; 23.753
86.026; 89.28; 76.624		5325.4Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559557 CIFC96 H184 O28 Si14 Zr2P b c a20.0054; 24.0516; 27.5739
90; 90; 90		13267.5Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559558 CIFC68 H156 Hf2 O28 Si14P b c a18.563; 22.017; 26.445
90; 90; 90		10808Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559559 CIFC96 H184 Hf2 O28 Si14P b c a20.061; 24.064; 27.568
90; 90; 90		13308Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559560 CIFC86 H109 N9 Na2 O11 V2P -113.4214; 14.2596; 25.2549
85.709; 78.946; 69.251		4435.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559561 CIFC104 H120 N8 O8 V2P -112.0966; 12.3373; 17.8971
90.8728; 107.997; 99.2458		2501.28Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559562 CIFC80 H90 Cl2 N2 O8 V2P 1 21/n 119.7039; 20.0862; 20.6921
90; 113.114; 90		7532Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559563 CIFC178 H213 N11 O20 V4P -114.0354; 17.3396; 20.1906
71.168; 84.459; 66.456		4260.59Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559564 CIFC86 H114 N6 O16 V4P -112.4983; 13.6976; 14.1554
68.166; 79.128; 75.546		2165.92Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559565 CIFC82 H90 F6 N2 O8 V2P 1 21/c 120.0005; 19.9315; 22.023
90; 116.08; 90		7885.4Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559566 CIFC355 H421 Cl2 N21 O32 V8P -119.7899; 20.6775; 22.7696
69.271; 76.567; 78.627		8407.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559567 CIFC49 H38 Cl2 Co F5 N3P -111.8773; 12.8721; 14.5308
97.115; 92.063; 98.641		2176.04Zhang, Qiuyue; Li, Zilong; Han, Mingyang; Xiang, Junfeng; Solan, Gregory A.; Ma, Yanping; Liang, Tongling; Sun, Wen-Hua
Fluorinated cobalt catalysts and their use in forming narrowly dispersed polyethylene waxes of high linearity and incorporating vinyl functionality
Catalysis Science & Technology, 2021, 11, 656-670
1559568 CIFC260 H220 Cl10 Co5 F25 N15P -120.2887; 22.5854; 30.0093
94.052; 105.348; 102.898		12802.4Zhang, Qiuyue; Li, Zilong; Han, Mingyang; Xiang, Junfeng; Solan, Gregory A.; Ma, Yanping; Liang, Tongling; Sun, Wen-Hua
Fluorinated cobalt catalysts and their use in forming narrowly dispersed polyethylene waxes of high linearity and incorporating vinyl functionality
Catalysis Science & Technology, 2021, 11, 656-670
1559569 CIFC75 H60 B Cl2 F24 N3 PdP -112.4888; 16.9952; 19.3546
69.171; 75.05; 81.715		3703.33Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559570 CIFC41 H45 Br2 Cl N2 PdP 1 21/n 112.8172; 18.0795; 16.7528
90; 96.977; 90		3853.36Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559571 CIFC44 H53 Cl3 N2 O2 PdP 1 21/n 111.7251; 18.4561; 19.821
90; 101.805; 90		4198.5Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559572 CIFC41 H45 Cl3 N2 PdP -111.0716; 16.373; 21.6279
89.42; 76.403; 88.652		3809.6Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559573 CIFC78 H67 B F24 I2 N3 PdP -113.006; 16.863; 19.2164
98.154; 96.07; 99.498		4078.6Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559574 CIFC77.25 H66.5 B Cl0.5 F24 N3 O2 PdP -114.4315; 16.2211; 18.6665
109.704; 107.844; 95.369		3820.3Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559575 CIFC41 H45 Cl I2 N2 PdP 1 21/c 110.0308; 19.7307; 20.2309
90; 101.055; 90		3929.69Zheng, Handou; Zhong, Liu; Du, Cheng; Du, Wenbo; Cheung, Chi Shing; Ruan, Jingjing; Gao, Haiyang
Combining hydrogen bonding interactions with steric and electronic modifications for thermally robust α-diimine palladium catalysts toward ethylene (co)polymerization
Catalysis Science & Technology, 2021, 11, 124-135
1559893 CIFC12 H14 Br2 OP 1 21/c 115.797; 10.6695; 7.533
90; 91.679; 90		1269.11Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559894 CIFC18 H22 N6 OP 1 21/c 114.654; 7.0476; 17.0806
90; 91.653; 90		1763.3Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559895 CIFC23 H32 N6 OP 1 21/n 15.4266; 52.494; 8.032
90; 107.835; 90		2178.1Roemer, Max; Gonçales, Vinicius R.; Keaveney, Sinead T.; Pernik, Indrek; Lian, Jiaxin; Downes, James; Gooding, J. Justin; Messerle, Barbara A.
Carbon supported hybrid catalysts for controlled product selectivity in the hydrosilylation of alkynes
Catalysis Science & Technology, 2021, 11, 1888-1898
1559971 CIFC20 H30 Fe N2 O4 Si2P 1 21/n 18.4055; 18.3319; 15.0466
90; 92.57; 90		2316.2Cingolani, Andrea; Gualandi, Isacco; Scavetta, Erika; Cesari, Cristiana; Zacchini, Stefano; Tonelli, Domenica; Zanotti, Valerio; Franchi, Paola; Lucarini, Marco; Sicilia, Emilia; Mazzone, Gloria; Nanni, Daniele; Mazzoni, Rita
Cyclopentadienone‒NHC iron(0) complexes as low valent electrocatalysts for water oxidation
Catalysis Science & Technology, 2021, 11, 1407-1418
1560073 CIFC18 H18 O3P 1 21 15.656; 8.202; 16.2422
90; 92.949; 90		752.49Mu, Yu; Zhang, Tao; Cheng, Yaping; Fu, Wenzhen; Wei, Zuting; Chen, Wanjun; Liu, Guodu
Efficient synthesis of tetrahydrofurans with chiral tertiary allylic alcohols catalyzed by Ni/P-chiral ligand DI-BIDIME
Catalysis Science & Technology, 2021, 11, 2306-2315
1560074 CIFC18 H18 O2P 21 21 216.5109; 8.5749; 26.234
90; 90; 90		1464.7Mu, Yu; Zhang, Tao; Cheng, Yaping; Fu, Wenzhen; Wei, Zuting; Chen, Wanjun; Liu, Guodu
Efficient synthesis of tetrahydrofurans with chiral tertiary allylic alcohols catalyzed by Ni/P-chiral ligand DI-BIDIME
Catalysis Science & Technology, 2021, 11, 2306-2315
1560075 CIFC23 H27 Al N2 O6P 1 21/c 18.9958; 12.8818; 19.2304
90; 96.615; 90		2213.62Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560076 CIFC23 H27 Co N2 O6P 1 21/c 18.9996; 12.8364; 19.0472
90; 96.745; 90		2185.15Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560077 CIFC23 H29 Al N2 O4P 21 21 217.869; 15.7511; 17.6113
90; 90; 90		2182.84Diment, Wilfred T.; Stößer, Tim; Kerr, Ryan W. F.; Phanopoulos, Andreas; Durr, Christopher B.; Williams, Charlotte K.
Ortho-vanillin derived Al(iii) and Co(iii) catalyst systems for switchable catalysis using ε-decalactone, phthalic anhydride and cyclohexene oxide
Catalysis Science & Technology, 2021, 11, 1737-1745
1560115 CIFC6 H8 Mo N4 O4C m c 2118.363; 3.83; 14.745
90; 90; 90		1037Amarante, Tatiana R.; Neves, Patrícia; Almeida Paz, Filipe A.; Gomes, Ana C.; Pillinger, Martyn; Valente, Anabela A.; Gonçalves, Isabel S.
Heterogeneous catalysis with an organic‒inorganic hybrid based on MoO3 chains decorated with 2,2′-biimidazole ligands
Catalysis Science & Technology, 2021, 11, 2214-2228
1560129 CIFC22 H19 N O3 S SeP 1 21 17.2473; 12.2693; 10.9251
90; 90.353; 90		971.43Hua, Jiawei; Bian, Mixue; Ma, Tao; Yang, Man; He, Wei; Yang, Zhao; Liu, ChengKou; Fang, Zheng; Guo, Kai
The sunlight-promoted aerobic selective cyclization of olefinic amides and diselenides
Catalysis Science & Technology, 2021, 11, 2299-2305
1560130 CIFC22 H19 N O3 S SeP 1 21/n 15.8297; 16.2078; 20.9813
90; 93.402; 90		1979Hua, Jiawei; Bian, Mixue; Ma, Tao; Yang, Man; He, Wei; Yang, Zhao; Liu, ChengKou; Fang, Zheng; Guo, Kai
The sunlight-promoted aerobic selective cyclization of olefinic amides and diselenides
Catalysis Science & Technology, 2021, 11, 2299-2305
1560262 CIFC57 H73 Cl2 N2 O3.5 P2 RuP 116.268; 17.763; 23.082
87.715; 81.35; 66.621		6051.3León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560263 CIFC55 H68 Cl2 N2 O3 P2 RuP 41 21 214.0362; 14.0362; 55.098
90; 90; 90		10855León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560264 CIFC55 H68 Cl2 N2 O3 P2 RuP 1 21 114.485; 13.276; 16.008
90; 104.344; 90		2982.4León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560265 CIFC50 H58 Cl4 N2 O5 P2 RuC 1 2 129.604; 12.869; 29.396
90; 114.68; 90		10176León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560266 CIFC123 H142 Cl10 F4 N4 O6 P4 Ru2P 113.3642; 15.0349; 18.4697
89.212; 76.738; 66.771		3307.09León, Félix; Comas-Vives, Aleix; Álvarez, Eleuterio; Pizzano, Antonio
A combined experimental and computational study to decipher complexity in the asymmetric hydrogenation of imines with Ru catalysts bearing atropisomerizable ligands
Catalysis Science & Technology, 2021, 11, 2497-2511
1560480 CIFC25 H24 O6 SnP b c a11.9618; 16.8603; 23.0411
90; 90; 90		4646.9Wolzak, Lukas A.; Hermans, Joen J.; de Vries, Folkert; van den Berg, Keimpe J.; Reek, Joost N. H.; Tromp, Moniek; Korstanje, Ties J.
Mechanistic elucidation of monoalkyltin(iv)-catalyzed esterification
Catalysis Science & Technology, 2021, 11, 3326-3332
1560497 CIFC18 H23 Cl Ir N O2P 21 21 218.2268; 14.3426; 14.7546
90; 90; 90		1740.95Gatto, Giordano; De Palo, Alice; Carrasco, Ana C.; Pizarro, Ana M.; Zacchini, Stefano; Pampaloni, Guido; Marchetti, Fabio; Macchioni, Alceo
Modulating the water oxidation catalytic activity of iridium complexes by functionalizing the Cp*-ancillary ligand: hints on the nature of the active species
Catalysis Science & Technology, 2021, 11, 2885-2895
1560498 CIFC30 H32 Cl4 F2 Ir2P -18.7487; 17.713; 20.308
73.261; 89.913; 83.794		2994.6Gatto, Giordano; De Palo, Alice; Carrasco, Ana C.; Pizarro, Ana M.; Zacchini, Stefano; Pampaloni, Guido; Marchetti, Fabio; Macchioni, Alceo
Modulating the water oxidation catalytic activity of iridium complexes by functionalizing the Cp*-ancillary ligand: hints on the nature of the active species
Catalysis Science & Technology, 2021, 11, 2885-2895
1561024 CIFC33 H48 I2 N2 O7 Zn2P 1 21 110.3649; 17.385; 10.4787
90; 93.802; 90		1884.04Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561025 CIFC33 H48 Ca I2 N2 O7 ZnP b c a13.906; 14.3422; 37.8508
90; 90; 90		7549.06Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561026 CIFC25 H32 Br Li Mg N2 O5P 1 21/c 112.3544; 10.9625; 19.5187
90; 90.048; 90		2643.52Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561027 CIFC63 H72 Mg3 N6 O12P n a 2126.6385; 12.1506; 18.5863
90; 90; 90		6015.9Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561028 CIFC42 H48 Li4 N4 O8P 41 21 211.2287; 11.2287; 32.691
90; 90; 90		4121.8Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561029 CIFC25 H32 I Li N2 O5 ZnP 1 21/c 112.2484; 11.1331; 19.8508
90; 91.174; 90		2706.34Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561030 CIFC42 H48 N4 O8 Zn2P 1 21/c 110.7086; 20.5174; 8.9876
90; 98.462; 90		1953.19Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561031 CIFC25 H30 Cd I2 Mg N4 O4P 1 21/c 110.7707; 17.2439; 19.6341
90; 90.981; 90		3646.1Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561032 CIFC33 H46 I2 N2 O7 Zn2P 1 21 110.3649; 17.385; 10.4787
90; 93.802; 90		1884.04Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561033 CIFC29 H40 Cd I2 N2 O6 ZnP -110.1985; 10.9552; 15.6105
86.416; 87.592; 73.094		1664.95Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561034 CIFC33 H48 I N2 Na O7 ZnP 1 21/c 121.0024; 10.5844; 15.9024
90; 91.002; 90		3534.53Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561035 CIFC37 H56 Br2 Mg2 N2 O8P 1 21/n 110.7118; 20.0019; 18.6537
90; 91.671; 90		3994.97Deacy, Arron C.; Durr, Christopher B.; Kerr, Ryan W. F.; Williams, Charlotte K.
Heterodinuclear catalysts Zn(ii)/M and Mg(ii)/M, where M = Na(i), Ca(ii) or Cd(ii), for phthalic anhydride/cyclohexene oxide ring opening copolymerisation
Catalysis Science & Technology, 2021, 11, 3109-3118
1561513 CIFC23 H37 Cl N P2 Rh S2P 1 21/c 118.425; 8.8088; 17.927
90; 113.42; 90		2669.89Hasche, Patrick; Haak, Julia; Anke, Felix; Kubis, Christoph; Baumann, Wolfgang; Drexler, Hans-Joachim; Jiao, Haijun; Beweries, Torsten
Dehydropolymerisation of methylamine borane using highly active rhodium(iii) bis(thiophosphinite) pincer complexes: catalytic and mechanistic insights
Catalysis Science & Technology, 2021, 11, 3514-3526
1561514 CIFC18 H32 Cl P2 Rh S2P 1 21/c 111.1268; 11.9807; 17.1003
90; 92.141; 90		2278Hasche, Patrick; Haak, Julia; Anke, Felix; Kubis, Christoph; Baumann, Wolfgang; Drexler, Hans-Joachim; Jiao, Haijun; Beweries, Torsten
Dehydropolymerisation of methylamine borane using highly active rhodium(iii) bis(thiophosphinite) pincer complexes: catalytic and mechanistic insights
Catalysis Science & Technology, 2021, 11, 3514-3526
1561515 CIFC35 H29 Cl N P2 Rh S2P 1 21/n 19.2984; 15.248; 22.7278
90; 100.479; 90		3168.65Hasche, Patrick; Haak, Julia; Anke, Felix; Kubis, Christoph; Baumann, Wolfgang; Drexler, Hans-Joachim; Jiao, Haijun; Beweries, Torsten
Dehydropolymerisation of methylamine borane using highly active rhodium(iii) bis(thiophosphinite) pincer complexes: catalytic and mechanistic insights
Catalysis Science & Technology, 2021, 11, 3514-3526
1562424 CIFC37 H27 Cr N O4 P2P 1 21/c 110.2734; 14.333; 21.7148
90; 99.339; 90		3155.09Wang, Zhichao; Liu, Lin; Ma, Xufeng; Liu, Yao; Mi, Puke; Liu, Zhen; Zhang, Jun
Effect of an additional donor on decene formation in ethylene oligomerization catalyzed by a Cr/PCCP system: a combined experimental and DFT study
Catalysis Science & Technology, 2021, 11, 4596-4604
1562548 CIFC33 H50 N2 Si2 Zr2P 1 21/c 116.1662; 12.7556; 16.3557
90; 96.7815; 90		3349.1Lindenau, Kevin; Jannsen, Nora; Rippke, Mirko; Al Hamwi, Hanan; Selle, Carmen; Drexler, Hans-Joachim; Spannenberg, Anke; Sawall, Mathias; Neymeyr, Klaus; Heller, Detlef; Reiß, Fabian; Beweries, Torsten
Mechanistic insights into dehydrocoupling of amine boranes using dinuclear zirconocene complexes
Catalysis Science & Technology, 2021, 11, 4034-4050
1562549 CIFC29 H40 Si2 Zr2P -18.4309; 8.6096; 10.3197
89.1575; 78.2307; 74.7766		706.99Lindenau, Kevin; Jannsen, Nora; Rippke, Mirko; Al Hamwi, Hanan; Selle, Carmen; Drexler, Hans-Joachim; Spannenberg, Anke; Sawall, Mathias; Neymeyr, Klaus; Heller, Detlef; Reiß, Fabian; Beweries, Torsten
Mechanistic insights into dehydrocoupling of amine boranes using dinuclear zirconocene complexes
Catalysis Science & Technology, 2021, 11, 4034-4050
1562550 CIFC33 H40 Si Zr2P 1 21/n 18.3405; 25.5764; 14.2103
90; 100.188; 90		2983.54Lindenau, Kevin; Jannsen, Nora; Rippke, Mirko; Al Hamwi, Hanan; Selle, Carmen; Drexler, Hans-Joachim; Spannenberg, Anke; Sawall, Mathias; Neymeyr, Klaus; Heller, Detlef; Reiß, Fabian; Beweries, Torsten
Mechanistic insights into dehydrocoupling of amine boranes using dinuclear zirconocene complexes
Catalysis Science & Technology, 2021, 11, 4034-4050
1562551 CIFC30.11 H41.33 Cl0.89 Si2 Zr2P -112.9147; 16.0454; 16.0971
73.455; 74.142; 82.668		3071.4Lindenau, Kevin; Jannsen, Nora; Rippke, Mirko; Al Hamwi, Hanan; Selle, Carmen; Drexler, Hans-Joachim; Spannenberg, Anke; Sawall, Mathias; Neymeyr, Klaus; Heller, Detlef; Reiß, Fabian; Beweries, Torsten
Mechanistic insights into dehydrocoupling of amine boranes using dinuclear zirconocene complexes
Catalysis Science & Technology, 2021, 11, 4034-4050
1562893 CIFC25 H28 Cl N O2 OsP 1 21/c 19.4652; 9.6082; 24.647
90; 90.999; 90		2241.1Biriukov, Klim O.; Vinogradov, Mikhail M.; Afanasyev, Oleg I.; Vasilyev, Dmitry V.; Tsygankov, Alexey A.; Godovikova, Maria; Nelyubina, Yulia V.; Loginov, Dmitry A.; Chusov, Denis
Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power
Catalysis Science & Technology, 2021, 11, 4922-4930
1562894 CIFC26 H16 Cl2 N2 O2 OsP 1 21/n 16.961; 19.454; 16.217
90; 95.607; 90		2185.6Biriukov, Klim O.; Vinogradov, Mikhail M.; Afanasyev, Oleg I.; Vasilyev, Dmitry V.; Tsygankov, Alexey A.; Godovikova, Maria; Nelyubina, Yulia V.; Loginov, Dmitry A.; Chusov, Denis
Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power
Catalysis Science & Technology, 2021, 11, 4922-4930
1563131 CIFC85 H71 Cl2 F8 Fe N3P 1 21/c 136.1891; 13.7667; 33.3782
90; 107.739; 90		15838.5Zhang, Qiuyue; Yang, Wenhong; Wang, Zheng; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Doubly fused N,N,N-iron ethylene polymerization catalysts appended with fluoride substituents; probing catalytic performance via a combined experimental and MLR study
Catalysis Science & Technology, 2021, 11, 4605-4618
1563132 CIFC57 H51 Cl2 F4 Fe N3P 3114.6606; 14.6606; 22.0189
90; 90; 120		4098.55Zhang, Qiuyue; Yang, Wenhong; Wang, Zheng; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Doubly fused N,N,N-iron ethylene polymerization catalysts appended with fluoride substituents; probing catalytic performance via a combined experimental and MLR study
Catalysis Science & Technology, 2021, 11, 4605-4618
1563133 CIFC58 H53 Cl4 F4 Fe N3P 1 21/c 120.1017; 15.0497; 18.8974
90; 117.144; 90		5087.3Zhang, Qiuyue; Yang, Wenhong; Wang, Zheng; Solan, Gregory A.; Liang, Tongling; Sun, Wen-Hua
Doubly fused N,N,N-iron ethylene polymerization catalysts appended with fluoride substituents; probing catalytic performance via a combined experimental and MLR study
Catalysis Science & Technology, 2021, 11, 4605-4618
1563267 CIFC17 H22 N2 O2 SP 1 21/n 110.3118; 9.8749; 16.4567
90; 105.396; 90		1615.62Schulz, Emmanuelle; Abi Fayssal, Sandra; Naret, Timothée; Huc, Vincent; Buendia, Julien; Martini, Cyril
Benzyloxycalix[8]arene supported Pd-NHC cinnamyl complexes for Buchwald-Hartwig C-N cross-couplings
Catalysis Science & Technology, 2021
1564316 CIFC33 H35 Cl3 Cr N O P2P 1 21/c 116.1058; 12.1316; 17.2976
90; 100.554; 90		3322.6Wang, Zhichao; Liu, Lin; Ma, Xufeng; Liu, Yao; Mi, Puke; Liu, Zhen; Zhang, Jun
Effect of an additional donor on decene formation in ethylene oligomerization catalyzed by a Cr/PCCP system: a combined experimental and DFT study
Catalysis Science & Technology, 2021, 11, 4596-4604
1564378 CIFC56 H41 Cl Cu3 N15 O8P -112.4454; 13.2667; 16.8433
76.118; 87.983; 82.56		2677.01Benkó, Tímea; Lukács, Dávid; Frey, Krisztina; Németh, Miklós; Móricz, Márta M.; Liu, Dongyu; Kováts, Éva; May, Nóra V.; Vayssieres, Lionel; Li, Mingtao; Pap, József S.
Redox-inactive metal single-site molecular complexes: a new generation of electrocatalysts for oxygen evolution?
Catalysis Science & Technology, 2021, 11, 6411-6424
1564379 CIFC19 H18 Cl Cu N5 O6P -17.881; 10.7847; 12.077
91.738; 105.882; 95.876		980.28Benkó, Tímea; Lukács, Dávid; Frey, Krisztina; Németh, Miklós; Móricz, Márta M.; Liu, Dongyu; Kováts, Éva; May, Nóra V.; Vayssieres, Lionel; Li, Mingtao; Pap, József S.
Redox-inactive metal single-site molecular complexes: a new generation of electrocatalysts for oxygen evolution?
Catalysis Science & Technology, 2021, 11, 6411-6424
1564529 CIFC6 H15 N3 O3P 1 21/n 17.4094; 9.2008; 14.0802
90; 94.27; 90		957.22Mannisto, Jere K.; Pavlovic, Ljiljana; Tiainen, Tony; Nieger, Martin; Sahari, Aleksi; Hopmann, Kathrin H.; Repo, Timo
Mechanistic insights into carbamate formation from CO2 and amines: the role of guanidine–CO2 adducts
Catalysis Science & Technology, 2021, 11, 6877-6886
1564635 CIFC21 H26 Cl N2 RhP 1 21/n 112.4856; 10.6263; 15.2385
90; 98.181; 90		2001.2Sambou, Sasaline Salomon; Hromov, Roman; Ruzhylo, Illia; Wang, Hui; Allandrieu, Audrey; Sabatier, Cassandra; Coppel, Yannick; Daran, Jean-Claude; Gayet, Florence; Labande, Agnès; Manoury, Eric; Poli, Rinaldo
Amphiphilic polymeric nanoreactors containing Rh(i)–NHC complexes for the aqueous biphasic hydrogenation of alkenes
Catalysis Science & Technology, 2021, 11, 6811-6824
1564636 CIFC29 H34 Cl N2 RhP 1 21/c 117.8663; 15.711; 9.4111
90; 96.939; 90		2622.32Sambou, Sasaline Salomon; Hromov, Roman; Ruzhylo, Illia; Wang, Hui; Allandrieu, Audrey; Sabatier, Cassandra; Coppel, Yannick; Daran, Jean-Claude; Gayet, Florence; Labande, Agnès; Manoury, Eric; Poli, Rinaldo
Amphiphilic polymeric nanoreactors containing Rh(i)–NHC complexes for the aqueous biphasic hydrogenation of alkenes
Catalysis Science & Technology, 2021, 11, 6811-6824
1564764 CIFC60 H48 B F24 N3 NiP 1 21/n 112.6058; 36.234; 13.4322
90; 91.713; 90		6132.5Trofymchuk, Oleksandra S.; Ortega, Daniela E.; Cortés-Arriagada, Diego; Pereira, Alfredo; Daniliuc, Constantin G.; Klitzke, Clecio F.; Santos, Leonardo S.; Rojas, Rene S.
Neutral and cationic methallyl nickel complexes in alkene activation: a combined DFT, ESI-MS and chemometric approach
Catalysis Science & Technology, 2021, 11, 7475-7485
1564765 CIFC56 H76 Cl8 N4 Pd2P b c a14.2641; 19.0639; 22.615
90; 90; 90		6149.7Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1564766 CIFC54 H74 Br2 N4 O2 Pd2P 1 21 112.4263; 14.7841; 16.2288
90; 103.567; 90		2898.23Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1564767 CIFC56 H76 Br4 Cl4 N4 Pd2P b c a14.6417; 19.3275; 22.4789
90; 90; 90		6361.2Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1564768 CIFC55 H74 Cl2 I4 N4 Pd2P 1 21 112.5373; 15.0465; 16.1547
90; 100.064; 90		3000.57Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1564769 CIFC54.5 H75 Cl3 N4 O2 Pd2C 1 2/c 129.8011; 13.1568; 30.6277
90; 95.8028; 90		11947.2Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1564770 CIFC54 H74 I2 N4 O2 Pd2C 1 2/c 125.3642; 12.2415; 18.7483
90; 105.03; 90		5622.1Prima, Darya O.; Madiyeva, Malena; Burykina, Julia V.; Minyaev, Mikhail E.; Boiko, Daniil A.; Ananikov, Valentine P.
Evidence for “cocktail”-type catalysis in Buchwald–Hartwig reaction. A mechanistic study
Catalysis Science & Technology, 2021, 11, 7171-7188
1565037 CIFC23 H24 Cl Ir N2 O3P 1 21/c 112.4748; 16.3845; 21.7988
90; 94.3271; 90		4442.8Zhao, Li-Jun; Yin, Zequn; Shi, Yusheng; Sun, Wen; Sun, Libo; Su, Huijuan; Sun, Xun; Zhang, Weiling; Xia, Linyan; Qi, Caixia
A highly active Cp*Ir complex with an anionic N,N-donor chelate ligand catalyzes the robust regeneration of NADH under physiological conditions
Catalysis Science & Technology, 2021, 11, 7982-7991
1565038 CIFC36 H44 F8 Mn N6 O6 S2P 21 21 2110.2605; 15.2842; 26.1552
90; 90; 90		4101.75Masferrer-Rius, Eduard; Li, Fanshi; Lutz, Martin; Klein Gebbink, Robertus J. M.
Exploration of highly electron-rich manganese complexes in enantioselective oxidation catalysis; a focus on enantioselective benzylic oxidation
Catalysis Science & Technology, 2021, 11, 7751-7763
1565039 CIFC34 H48 F6 Fe N6 O7 S2P 21 21 2110.2594; 15.1887; 25.5178
90; 90; 90		3976.36Masferrer-Rius, Eduard; Li, Fanshi; Lutz, Martin; Klein Gebbink, Robertus J. M.
Exploration of highly electron-rich manganese complexes in enantioselective oxidation catalysis; a focus on enantioselective benzylic oxidation
Catalysis Science & Technology, 2021, 11, 7751-7763
1565040 CIFC10 H12 F N O3P 1 21 15.9384; 5.3053; 15.9518
90; 93.289; 90		501.734Zhang, Rui; Tan, Jiamu; Luo, Zhenzhen; Dong, Haihong; Ma, Ningshan; Liao, Cangsong
Stereo-selective synthesis of non-canonical γ-hydroxy-α-amino acids by enzymatic carbon–carbon bond formation
Catalysis Science & Technology, 2021, 11, 7380-7385
1565138 CIFC16 H23 Br Mn N3 O4P -17.94037; 10.1189; 12.8889
87.2665; 76.201; 70.5516		947.75Wang, Zheng; Lin, Qing; Ma, Ning; Liu, Song; Han, Mingyang; Yan, Xiuli; Liu, Qingbin; Solan, Gregory A.; Sun, Wen-Hua
Direct synthesis of ring-fused quinolines and pyridines catalyzed by NNHY-ligated manganese complexes (Y = NR2 or SR)
Catalysis Science & Technology, 2021, 11, 8026-8036
1565139 CIFC16 H20 Br Mn N2 O3 SP -17.71788; 10.1753; 13.2154
103.067; 101.353; 108.667		916.12Wang, Zheng; Lin, Qing; Ma, Ning; Liu, Song; Han, Mingyang; Yan, Xiuli; Liu, Qingbin; Solan, Gregory A.; Sun, Wen-Hua
Direct synthesis of ring-fused quinolines and pyridines catalyzed by NNHY-ligated manganese complexes (Y = NR2 or SR)
Catalysis Science & Technology, 2021, 11, 8026-8036
1565140 CIFC26 H24 Br Mn N2 O3 PP 1 21/n 19.1878; 28.171; 10.117
90; 105.67; 90		2521.3Wang, Zheng; Lin, Qing; Ma, Ning; Liu, Song; Han, Mingyang; Yan, Xiuli; Liu, Qingbin; Solan, Gregory A.; Sun, Wen-Hua
Direct synthesis of ring-fused quinolines and pyridines catalyzed by NNHY-ligated manganese complexes (Y = NR2 or SR)
Catalysis Science & Technology, 2021, 11, 8026-8036
1565172 CIFC20 H23 Br N4 O2 RuP 1 21/n 17.918; 17.8; 14.7128
90; 95.2089; 90		2065.06Illam, Praseetha Mathoor; Rit, Arnab
Electronically tuneable orthometalated RuII–NHC complexes as efficient catalysts for C–C and C–N bond formations via borrowing hydrogen strategy
Catalysis Science & Technology, 2022, 12, 67-74
1565173 CIFH4 N2 O3P m m n :25.446; 5.7605; 4.9406
90; 90; 90		154.99Nesterova, Oksana V.; Kuznetsov, Maxim L.; Pombeiro, Armando J. L.; Shul'pin, Georgiy B.; Nesterov, Dmytro S.
Homogeneous oxidation of C–H bonds with m-CPBA catalysed by a Co/Fe system: mechanistic insights from the point of view of the oxidant
Catalysis Science & Technology, 2022, 12, 282-299
1565174 CIFC19 H25 Co N2 O6P -317.5321; 17.5321; 10.9885
90; 90; 120		2925.1Nesterova, Oksana V.; Kuznetsov, Maxim L.; Pombeiro, Armando J. L.; Shul'pin, Georgiy B.; Nesterov, Dmytro S.
Homogeneous oxidation of C–H bonds with m-CPBA catalysed by a Co/Fe system: mechanistic insights from the point of view of the oxidant
Catalysis Science & Technology, 2022, 12, 282-299
1565488 CIFC43 H44 N2 O P2P 21 21 2110.0784; 11.7543; 30.5885
90; 90; 90		3623.65Chakrabortty, Soumyadeep; Konieczny, Katharina; Müller, Bernd H.; Spannenberg, Anke; Kamer, Paul C. J.; de Vries, Johannes G.
Betti base derived P-stereogenic phosphine-diamidophosphite ligands with a single atom spacer and their application in asymmetric catalysis
Catalysis Science & Technology, 2022, 12, 1392-1399
1565975 CIFC113 H252 F4 N6 O71 V24P 1 21/n 115.755; 25.4335; 21.5604
90; 92.253; 90		8632.7Kikukawa, Yuji; Sakamoto, Yui; Hirasawa, Hikari; Kurimoto, Yushi; Iwai, Hiroya; Hayashi, Yoshihito
Synthesis and oxidation catalysis of a difluoride-incorporated polyoxovanadate and isolation of active vanadium alkylperoxo species
Catalysis Science & Technology, 2022, 12, 2438-2445
1565976 CIFC59 H126 F2 N4 O34 V12P 1 21/n 117.7995; 23.6442; 20.9424
90; 91.945; 90		8808.6Kikukawa, Yuji; Sakamoto, Yui; Hirasawa, Hikari; Kurimoto, Yushi; Iwai, Hiroya; Hayashi, Yoshihito
Synthesis and oxidation catalysis of a difluoride-incorporated polyoxovanadate and isolation of active vanadium alkylperoxo species
Catalysis Science & Technology, 2022, 12, 2438-2445
1565977 CIFC52 H117 F2 N3 O32 V12P c a 2117.199; 21.6914; 54.059
90; 90; 90		20167.8Kikukawa, Yuji; Sakamoto, Yui; Hirasawa, Hikari; Kurimoto, Yushi; Iwai, Hiroya; Hayashi, Yoshihito
Synthesis and oxidation catalysis of a difluoride-incorporated polyoxovanadate and isolation of active vanadium alkylperoxo species
Catalysis Science & Technology, 2022, 12, 2438-2445
1566090 CIFC21 H16 Cl N4 O5 P RuC 1 2/c 114.06525; 25.1567; 13.9309
90; 100.051; 90		4853.59Bühler, Jan; Zurflüh, Jonas; Siol, Sebastian; Blacque, Olivier; Sévery, Laurent; Tilley, S. David
Electrochemical ruthenium-catalysed C–H activation in water through heterogenization of a molecular catalyst
Catalysis Science & Technology, 2022, 12, 1512-1519
1566239 CIFC45.27 H22 Al Cl2 Cr0.18 O15.33 Zr3P 6/m m m39.433; 39.433; 16.2564
90; 90; 120		21891Goetjen, Timothy A.; Knapp, Julia G.; Syed, Zoha H.; Hackler, Ryan A.; Zhang, Xuan; Delferro, Massimiliano; Hupp, Joseph T.; Farha, Omar K.
Ethylene polymerization with a crystallographically well-defined metal–organic framework supported catalyst
Catalysis Science & Technology, 2022, 12, 1619-1627
1566376 CIFC15 H19 Cl2 Co N3 OP -17.3409; 8.2378; 14.1911
77.242; 85.133; 77.261		815.8Sharma, Dipesh M.; Gouda, Chandrakant; Gonnade, Rajesh G.; Punji, Benudhar
Room temperature Z-selective hydrogenation of alkynes by hemilabile and non-innocent (NNN)Co(ii) catalysts
Catalysis Science & Technology, 2022, 12, 1843-1849
1566377 CIFC15 H21 Cl2 Co N3P 1 21/c 116.65; 24.8705; 7.9667
90; 90.49; 90		3298.8Sharma, Dipesh M.; Gouda, Chandrakant; Gonnade, Rajesh G.; Punji, Benudhar
Room temperature Z-selective hydrogenation of alkynes by hemilabile and non-innocent (NNN)Co(ii) catalysts
Catalysis Science & Technology, 2022, 12, 1843-1849
1566663 CIFC36 H37 K N3 O3 P2 Ru SP c a 2112.6529; 18.7504; 15.5836
90; 90; 90		3697.2Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566664 CIFC100 H83 N6 O3 P6 Ru2P 1 21/c 114.8971; 22.753; 28.6172
90; 100.332; 90		9542.6Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566665 CIFC51 H48 Cl N4 O2 P3 RuP b c n25.849; 19.5041; 21.0152
90; 90; 90		10595Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566680 CIFC50.5 H47 Co O3 P2P 1 21/n 19.9652; 18.349; 23.3602
90; 96.462; 90		4244.3Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566681 CIFC45 H32 Co2 O7 P2P -110.8578; 11.6947; 17.4282
106.744; 95.84; 112.496		1900.9Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566688 CIFC29.4 H40.8 Cl8.8 N2 P2 PdP 1 21/n 115.262; 12.8154; 20.9917
90; 108.535; 90		3892.8Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566689 CIFC26 H40 B2 N2 P2P -19.1591; 11.3142; 15.1394
103.273; 102.525; 105.201		1408Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566690 CIFC28 H34 F6 N2 O6 P2 Pd S2P -111.2734; 12.1729; 13.5903
73.9005; 72.8892; 73.6404		1671.4Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566769 CIFC48 H28 Bi N4 O9P 21 21 2117.3; 17.4; 18.975
90; 90; 90		5711.9Xie, Dale; Wang, Sheng; Li, Shihao; Yang, Wenqing; Feng, Yi-Si
A two-dimensional Bi-based porphyrin metal–organic framework photocatalyst for white light-driven selective oxidation of sulfides
Catalysis Science & Technology, 2022, 12, 3254-3260
1566791 CIFC38 H63 In N2 O3P -111.4082; 13.035; 14.939
66.497; 68.941; 83.213		1900.3Bruckmoser, Jonas; Henschel, Daniel; Vagin, Sergei; Rieger, Bernhard
Combining high activity with broad monomer scope: indium salan catalysts in the ring-opening polymerization of various cyclic esters
Catalysis Science & Technology, 2022, 12, 3295-3302
1567084 CIFC24 H58 Cl10 Cr2 N10 P4P 1 21/c 111.9522; 13.5271; 14.8191
90; 104.592; 90		2318.65Lo, Quintin; Pye, Dominic; Gesslbauer, Sami; Sim, Ying; García, Felipe; White, Andrew J. P.; Britovsek, George J. P.
Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation
Catalysis Science & Technology, 2022, 12, 4544-4551
1567085 CIFC32 H72 Cr2 Li4 O4P c c n9.9307; 17.6625; 22.0161
90; 90; 90		3861.6Lo, Quintin; Pye, Dominic; Gesslbauer, Sami; Sim, Ying; García, Felipe; White, Andrew J. P.; Britovsek, George J. P.
Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation
Catalysis Science & Technology, 2022, 12, 4544-4551
1567086 CIFC24 H58 Cl10 Cr2 N10 P4P 1 21/c 19.3625; 12.7925; 19.2108
90; 96.406; 90		2286.51Lo, Quintin; Pye, Dominic; Gesslbauer, Sami; Sim, Ying; García, Felipe; White, Andrew J. P.; Britovsek, George J. P.
Single- and double-bridged PNP ligands in chromium-catalysed ethylene oligomerisation
Catalysis Science & Technology, 2022, 12, 4544-4551
1567159 CIFC56 H37 Co N5 PP -19.7214; 12.92; 17.269
77.514; 83.542; 79.876		2078.5Liu, Zheng-Yan; Lai, Jia-Wei; Yang, Gang; Ren, Bao-Ping; Lv, Zhou-Yan; Si, Li-Ping; Zhang, Hao; Liu, Hai-Yang
Electrocatalytic hydrogen production by CN– substituted cobalt triaryl corroles
Catalysis Science & Technology, 2022, 12, 5125-5135

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