Crystallography Open Database

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1548131 CIFC44 H66 Ir2 N2 O4 P4P 1 21/n 114.6367; 11.0939; 14.9574
90; 93.785; 90
2423.5Cano, Israel; Martínez-Prieto, Luis M.; Vendier, Laure; van Leeuwen, Piet W. N. M.
An iridium‒SPO complex as bifunctional catalyst for the highly selective hydrogenation of aldehydes
Catalysis Science & Technology, 2018, 8, 221
1548132 CIFC44 H42 MnP 4310.52378; 10.52378; 30.7376
90; 90; 90
3404.19Sharpe, Helen R.; Geer, Ana M.; Blundell, Toby J.; Hastings, Fiona R.; Fay, Michael W.; Rance, Graham A.; Lewis, William; Blake, Alexander J.; Kays, Deborah L.
Dehydrocoupling of dimethylamine‒borane promoted by manganese(ii) m-terphenyl complexes
Catalysis Science & Technology, 2018, 8, 229
1548133 CIFC24 H27 Cl2 Co N7 O8C 1 2/c 127.9963; 10.5409; 19.1609
90; 100.453; 90
5560.7Leung, C.-F.; Cheng, S.-C.; Yang, Y.; Xiang, J.; Yiu, S.-M.; Ko, C.-C.; Lau, T.-C.
Efficient photocatalytic water reduction by a cobalt(ii) tripodal iminopyridine complex
Catalysis Science & Technology, 2018, 8, 307
1548157 CIFC30 H44 N6 O12 S2 Zn2P -4 21 c20.4693; 20.4693; 19.1467
90; 90; 90
8022.32Tan, Ai-Dong; Wan, Kai; Wang, Yi-Fang; Fu, Zhi-Yong; Liang, Zhen-Xing
N, S-containing MOF-derived dual-doped mesoporous carbon as a highly effective oxygen reduction reaction electrocatalyst
Catalysis Science & Technology, 2018, 8, 335
1548362 CIFC15 H23 Br2 Co N3 O2P 1 21/n 110.2514; 14.6308; 12.6552
90; 92.105; 90
1896.82Landge, Vinod G.; Pitchaimani, Jayaraman; Midya, Siba P.; Subaramanian, Murugan; Madhu, Vedichi; Balaraman, Ekambaram
Phosphine-free cobalt pincer complex catalyzed Z-selective semi-hydrogenation of unbiased alkynes
Catalysis Science & Technology, 2018, 8, 428
1548586 CIFC25 H17 Au Cl F4 N2 O PP 1 21/n 119.942; 10.9697; 24.135
90; 112.7; 90
4870.7Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548587 CIFC25 H17 Au Cl F4 N2 O PP 1 21/n 116.0034; 8.3754; 19.2521
90; 111.188; 90
2406.01Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548588 CIFC37.85 H26.29 Au2 Cl7.11 F4 N2 P2P -111.051; 15.816; 16.857
109.459; 103.933; 104.747
2509.4Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548589 CIFC36.8 H24.8 Au2 Cl4.4 F4 N2 P2P 1 21/c 118.453; 18.5065; 11.1568
90; 97.085; 90
3781Arif, T.; Cazorla, C.; Bogliotti, N.; Saleh, N.; Blanchard, F.; Gandon, V.; Métivier, R.; Xie, J.; Voituriez, A.; Marinetti, A.
Bimetallic gold(i) complexes of photoswitchable phosphines: synthesis and uses in cooperative catalysis
Catalysis Science & Technology, 2018, 8, 710
1548784 CIFC39.1 H24.5 Fe3 N2.1 O15.7P 1 21/c 112.6797; 13.5123; 23.948
90; 90; 90
4103.1Pham, Phuc H.; Doan, Son H.; Tran, Hang T. T.; Nguyen, Ngoc N.; Phan, Anh N. Q.; Le, Ha V.; Tu, Thach N.; Phan, Nam T. S.
A new transformation of coumarins via direct C‒H bond activation utilizing an iron‒organic framework as a recyclable catalyst
Catalysis Science & Technology, 2018, 8, 1267
1548827 CIFC27 H33 Cl3 Cr N7 O2P b c a18.2412; 14.5616; 23.1101
90; 90; 90
6138.53Nobbs, James D.; Tomov, Atanas K.; Young, Craig T.; White, Andrew J. P.; Britovsek, George J. P.
From alternating to selective distributions in chromium-catalysed ethylene oligomerisation with asymmetric BIMA ligands
Catalysis Science & Technology, 2018, 8, 1314
1548828 CIFC25 H33 Cl3 Cr N7 O2P 1 21/c 118.3091; 11.3311; 13.9361
90; 100.163; 90
2845.85Nobbs, James D.; Tomov, Atanas K.; Young, Craig T.; White, Andrew J. P.; Britovsek, George J. P.
From alternating to selective distributions in chromium-catalysed ethylene oligomerisation with asymmetric BIMA ligands
Catalysis Science & Technology, 2018, 8, 1314
1549079 CIFC43 H29 N6 O4 RuP 1 21/c 112.139; 15.53; 24.301
90; 98.77; 90
4528Xiang, Wenjing; Li, Lin; Dai, Zengjin; Meng, Xianggao; Li, Renjie; Zhang, Jing; Peng, Tianyou
TiO2 modified with a Ru(ii)‒N′NN′ 8-hydroxyquinolyl complex for efficient gaseous photoreduction of CO2
Catalysis Science & Technology, 2018, 8, 2098
1549242 CIFC18 H32 F3 Mn O6 P2 SP 21 21 218.6949; 13.9549; 19.9508
90; 90; 90
2420.8Garduño, Jorge A.; Arévalo, Alma; Flores-Alamo, Marcos; García, Juventino J.
Mn(i) organometallics containing the iPr2P(CH2)2PiPr2 ligand for the catalytic hydration of aromatic nitriles
Catalysis Science & Technology, 2018, 8, 2606
1549488 CIFC15 H20 Cl2 O6 PdC 1 2/m 111.6869; 8.8935; 8.551
90; 90.223; 90
888.76Eremin, Dmitry B.; Boiko, Daniil A.; Borkovskaya, Eugenia V.; Khrustalev, Victor N.; Chernyshev, Victor M.; Ananikov, Valentine P.
Ten-fold boost of catalytic performance in thiol‒yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand
Catalysis Science & Technology, 2018, 8, 3073
1549489 CIFC10 H8 F6 O4 PdP -14.7881; 7.9629; 8.7923
80.994; 77.33; 72.621
310.64Eremin, Dmitry B.; Boiko, Daniil A.; Borkovskaya, Eugenia V.; Khrustalev, Victor N.; Chernyshev, Victor M.; Ananikov, Valentine P.
Ten-fold boost of catalytic performance in thiol‒yne click reaction enabled by a palladium diketonate complex with a hexafluoroacetylacetonate ligand
Catalysis Science & Technology, 2018, 8, 3073
1549495 CIFC26 H44 Cl Ir N O7 PP 1 21/c 115.0632; 12.3425; 16.2371
90; 107.643; 90
2876.77Gregor, Lauren C.; Grajeda, Javier; White, Peter S.; Vetter, Andrew J.; Miller, Alexander J. M.
Salt-promoted catalytic methanol carbonylation using iridium pincer-crown ether complexes
Catalysis Science & Technology, 2018, 8, 3133
1549496 CIFC26 H43 Ir N O7 PP -17.7588; 15.5942; 24.116
89.185; 82.743; 89.582
2894.1Gregor, Lauren C.; Grajeda, Javier; White, Peter S.; Vetter, Andrew J.; Miller, Alexander J. M.
Salt-promoted catalytic methanol carbonylation using iridium pincer-crown ether complexes
Catalysis Science & Technology, 2018, 8, 3133
1549588 CIFC17 H16 O2 SeP 16.7562; 7.5182; 8.7692
107.83; 98.976; 113.06
370.28García-López, Diego; Civit, Marc G.; Vogels, Christopher M.; Ricart, Josep M.; Westcott, Stephen A.; Fernández, Elena; Carbó, Jorge J.
Understanding the mechanism of transition metal-free anti addition to alkynes: the selenoboration case
Catalysis Science & Technology, 2018, 8, 3617
1549589 CIFC15 H23 Br2 Co N3 O2P 1 21/n 110.2514; 14.6308; 12.6552
90; 92.105; 90
1896.82Midya, Siba P.; Pitchaimani, Jayaraman; Landge, Vinod G.; Madhu, Vedichi; Balaraman, Ekambaram
Direct access toN-alkylated amines and iminesviaacceptorless dehydrogenative coupling catalyzed by a cobalt(ii)-NNN pincer complex
Catalysis Science & Technology, 2018, 8, 3469
1549590 CIFC15 H29 B2 Cl2 Co F8 N5 OP -16.838; 13.077; 13.377
89.44; 78.44; 82.78
1162.5Midya, Siba P.; Pitchaimani, Jayaraman; Landge, Vinod G.; Madhu, Vedichi; Balaraman, Ekambaram
Direct access toN-alkylated amines and iminesviaacceptorless dehydrogenative coupling catalyzed by a cobalt(ii)-NNN pincer complex
Catalysis Science & Technology, 2018, 8, 3469
1549609 CIFC28 H18 Cu3 N10 O15C 1 2/c 131.977; 18.3536; 14.7633
90; 91.413; 90
8661.8Ahmad, Nazir; Younus, Hussein A.; Chughtai, Adeel H.; Van Hecke, Kristof; Khattak, Zafar A. K.; Gaoke, Zhang; Danish, Muhammad; Verpoort, Francis
Synthesis of 2D MOF having potential for efficient dye adsorption and catalytic applications
Catalysis Science & Technology, 2018, 8, 4010
1549715 CIFC86 H157 K2 Mn8 N O42P 1 21/n 118.998; 15.678; 20.236
90; 100.84; 90
5920Mousazade, Younes; Mohammadi, Mohammad Reza; Chernev, Petko; Bikas, Rahman; Bagheri, Robabeh; Song, Zhenlun; Lis, Tadeusz; Dau, Holger; Najafpour, Mohammad Mahdi
Water oxidation by a manganese‒potassium cluster: Mn oxide as a kinetically dominant “true” catalyst for water oxidation
Catalysis Science & Technology, 2018, 8, 4390
1549739 CIFC8 H4.19 Al I0.82 O5I m m a16.501; 6.6194; 13.21
90; 90; 90
1442.9Tahmouresilerd, Babak; Larson, Patrick J.; Unruh, Daniel K.; Cozzolino, Anthony F.
Make room for iodine: systematic pore tuning of multivariate metal‒organic frameworks for the catalytic oxidation of hydroquinones using hypervalent iodine
Catalysis Science & Technology, 2018, 8, 4349
1549740 CIFC8 H4.3 Al I0.7 O5.25I m m a17.107; 6.622; 12.229
90; 90; 90
1385.3Tahmouresilerd, Babak; Larson, Patrick J.; Unruh, Daniel K.; Cozzolino, Anthony F.
Make room for iodine: systematic pore tuning of multivariate metal‒organic frameworks for the catalytic oxidation of hydroquinones using hypervalent iodine
Catalysis Science & Technology, 2018, 8, 4349
1549749 CIFC31 H53 Rh2 S2P 1 21/n 110.855; 28.6007; 10.8441
90; 119.239; 90
2937.7Serrano-Maldonado, A.; Rozenel, S. S.; Jimenez-Santiago, J. L.; Guerrero-Ríos, I.; Martin, E.
Rh nanoparticles from thiolate dimers: selective and reusable hydrogenation catalysts in ionic liquids
Catalysis Science & Technology, 2018, 8, 4373
1549750 CIFC40 H74 Rh2 S2P 1 21/m 18.734; 26.987; 8.39
90; 90; 90
1977.6Serrano-Maldonado, A.; Rozenel, S. S.; Jimenez-Santiago, J. L.; Guerrero-Ríos, I.; Martin, E.
Rh nanoparticles from thiolate dimers: selective and reusable hydrogenation catalysts in ionic liquids
Catalysis Science & Technology, 2018, 8, 4373
1549855 CIFC21 H33 Cl2 N Si TiP -18.268; 11.8794; 12.9943
71.395; 78.04; 70.734
1134.41Williams, Thomas J.; Buffet, Jean-Charles; Turner, Zoë R.; O'Hare, Dermot
Group 4 permethylindenyl constrained geometry complexes for ethylene polymerisation catalysis
Catalysis Science & Technology, 2018, 8, 5454
1549856 CIFC32 H49 Cl2 N Si TiP -19.966; 12.4507; 15.2615
112.445; 108.902; 90.786
1635.29Williams, Thomas J.; Buffet, Jean-Charles; Turner, Zoë R.; O'Hare, Dermot
Group 4 permethylindenyl constrained geometry complexes for ethylene polymerisation catalysis
Catalysis Science & Technology, 2018, 8, 5454
1549857 CIFC20 H31 Cl2 N Si TiP 1 21/c 111.5225; 12.9843; 15.2891
90; 104.979; 90
2209.7Williams, Thomas J.; Buffet, Jean-Charles; Turner, Zoë R.; O'Hare, Dermot
Group 4 permethylindenyl constrained geometry complexes for ethylene polymerisation catalysis
Catalysis Science & Technology, 2018, 8, 5454
1549858 CIFC23 H26 Ir N O3P b c a16.13031; 14.54437; 17.33703
90; 90; 90
4067.36Pèrez-Miqueo, Jorge; San Nacianceno, Virginia; Urquiola, F. Borja; Freixa, Zoraida
Revisiting the iridacycle-catalyzed hydrosilylation of enolizable imines
Catalysis Science & Technology, 2018, 8, 6316
1549873 CIFC28 H34 Cl Ir N2P -19.7423; 11.066; 12.1673
100.717; 104.685; 96.543
1228.72Wong, Chin Min; Fekete, Marianna; Nelson-Forde, Rhianna; Gatus, Mark R. D.; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.; Messerle, Barbara A.
Harnessing asymmetric N-heterocyclic carbene ligands to optimise SABRE hyperpolarisation.
Catalysis science & technology, 2018, 8, 4925-4933
1549904 CIFC17 H21 N O2 SP -17.4134; 8.4142; 12.1239
84.72; 88.99; 84.549
749.62Llorente, Nuria; Fernández-Pérez, Héctor; Bauzá, Antonio; Frontera, Antonio; Vidal-Ferran, Anton
Ni-Catalysed Intramolecular [4+4]-cycloadditions of bis-dienes towards eight-membered fused bicyclic systems: a combined experimental and computational study
Catalysis Science & Technology, 2018, 8, 5251
1549905 CIFC16 H22 O4P -16.2605; 9.8392; 12.7844
67.7938; 88.4599; 84.1325
725.21Llorente, Nuria; Fernández-Pérez, Héctor; Bauzá, Antonio; Frontera, Antonio; Vidal-Ferran, Anton
Ni-Catalysed Intramolecular [4+4]-cycloadditions of bis-dienes towards eight-membered fused bicyclic systems: a combined experimental and computational study
Catalysis Science & Technology, 2018, 8, 5251
1549933 CIFC49 H50 N6 O YP 1 2/n 122.637; 9.781; 23.089
90; 118.062; 90
4511Zhang, Dexing; Liu, Ruiting; Zhou, Xigeng
Intramolecular alkene hydroamination and degradation of amidines: divergent behavior of rare earth metal amidinate intermediates
Catalysis Science & Technology, 2018, 8, 5573
1550033 CIFC37 H46 B Cl2 Cu F4 N8P 1 21/c 120.808; 31.071; 12.2164
90; 90.694; 90
7897.6Zelenay, Benjamin; Besora, Maria; Monasterio, Zaira; Ventura-Espinosa, David; White, Andrew J. P.; Maseras, Feliu; Díez-González, Silvia
Copper-mediated reduction of azides under seemingly oxidising conditions: catalytic and computational studies
Catalysis Science & Technology, 2018, 8, 5763
1550034 CIFC33.5 H41 Cl Cu F3 N4 O3 SP 1 21/n 112.3905; 19.0233; 14.481
90; 102.996; 90
3325.86Zelenay, Benjamin; Besora, Maria; Monasterio, Zaira; Ventura-Espinosa, David; White, Andrew J. P.; Maseras, Feliu; Díez-González, Silvia
Copper-mediated reduction of azides under seemingly oxidising conditions: catalytic and computational studies
Catalysis Science & Technology, 2018, 8, 5763
1550035 CIFC37 H44 Cu F3 N4 O3 SP -19.1002; 10.9858; 19.3481
89.693; 79.192; 82.793
1884.64Zelenay, Benjamin; Besora, Maria; Monasterio, Zaira; Ventura-Espinosa, David; White, Andrew J. P.; Maseras, Feliu; Díez-González, Silvia
Copper-mediated reduction of azides under seemingly oxidising conditions: catalytic and computational studies
Catalysis Science & Technology, 2018, 8, 5763
1550044 CIFC22 H26 I Ir N4P -18.5611; 10.9802; 13.2254
109.051; 102.4; 90.413
1143.69Semwal, Shrivats; Kumar, Abhishek; Choudhury, Joyanta
Iridium‒NHC-based catalyst for ambient pressure storage and low temperature release of H2via the CO2/HCO2H couple
Catalysis Science & Technology, 2018, 8, 6137
1550236 CIFC22 H23 NP -19.7438; 9.9224; 10.984
64.086; 78.354; 63.503
854.8Abdellah, Ibrahim; Poater, Albert; Lohier, Jean-François; Gaumont, Annie-Claude
Au(i)-Catalyzed hydroarylation of alkenes with N,N-dialkylanilines: a dual gold catalysis concept
Catalysis Science & Technology, 2018, 8, 6486
1550237 CIFC24 H27 NP -18.3046; 10.7954; 12.0469
109.64; 100.96; 104.352
940.16Abdellah, Ibrahim; Poater, Albert; Lohier, Jean-François; Gaumont, Annie-Claude
Au(i)-Catalyzed hydroarylation of alkenes with N,N-dialkylanilines: a dual gold catalysis concept
Catalysis Science & Technology, 2018, 8, 6486
1550265 CIFC38 H60 Mo13 N10 O34C m c m24.715; 23.137; 13.595
90; 90; 90
7774Luo, Benlong; Sang, Rui-LI; Lin, Lifang; Xu, Li
Mo3IV-Polyoxomolybdates with Frustrated Lewis Pairs For High-Performance Hydrogenation Catalysis
Catalysis Science & Technology, 2019
1550279 CIFC20 H32 Cl4 Co2 N4 S2P -17.6862; 11.1085; 17.7851
72.8236; 88.0499; 70.2746
1362.03Puylaert, Pim; Dell'Acqua, Andrea; El Ouahabi, Fatima; Spannenberg, Anke; Roisnel, Thierry; Lefort, Laurent; Hinze, Sandra; Tin, Sergey; de Vries, Johannes G.
Phosphine-Free Pincer Cobalt Catalyst Precursors for the Selective Hydrogenation of Olefins
Catalysis Science & Technology, 2019
1550280 CIFC11 H18 Cl2 Co N2 SP -17.0681; 9.014; 12.2372
108.21; 98.899; 99.291
713.18Puylaert, Pim; Dell'Acqua, Andrea; El Ouahabi, Fatima; Spannenberg, Anke; Roisnel, Thierry; Lefort, Laurent; Hinze, Sandra; Tin, Sergey; de Vries, Johannes G.
Phosphine-Free Pincer Cobalt Catalyst Precursors for the Selective Hydrogenation of Olefins
Catalysis Science & Technology, 2019
1550289 CIFC53.5 H66 Cl3 N4 O1.5 RuP -111.961; 16.591; 26.614
93.877; 90.681; 98.321
5212.6DUMAS, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénaël; Tripoteau, Fabien; Caijo, Frédéric; Rouen, Mathieu; Queval, Pierre; Basle, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550290 CIFC63 H82 Cl2 N4 RuP 1 21/n 111.206; 15.0047; 33.7602
90; 96.909; 90
5635.3DUMAS, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénaël; Tripoteau, Fabien; Caijo, Frédéric; Rouen, Mathieu; Queval, Pierre; Basle, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550291 CIFC53 H62 Cl2 N4 RuP -112.017; 12.562; 16.608
80.103; 89.839; 70.644
2326.2DUMAS, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénaël; Tripoteau, Fabien; Caijo, Frédéric; Rouen, Mathieu; Queval, Pierre; Basle, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550292 CIFC56 H68 Cl4 N4 RuP 1 21/c 121.792; 10.9906; 22.5146
90; 107.445; 90
5144.4DUMAS, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénaël; Tripoteau, Fabien; Caijo, Frédéric; Rouen, Mathieu; Queval, Pierre; Basle, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550400 CIFC55 H66 Cl2 N4 RuP -110.9047; 11.6314; 19.7689
95.343; 101.998; 100.664
2387.6Dumas, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénael; Tripoteau, Fabien; Caijo, Frédéric; Queval, Pierre; Rouen, Mathieu; Baslé, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550519 CIFC26 H34 B N O4 SP 1 21/c 16.4192; 32.5924; 11.989
90; 99.366; 90
2474.9Cabrera-Lobera, Natalia; Quirós, M. Teresa; Buñuel, Elena; Cardenas, Diego J.
Atom-Economical Regioselective Ni-Catalyzed Hydroborylative Cyclization of Enynes: Development and Mechanism
Catalysis Science & Technology, 2019
1550589 CIFC45 H61 Cl N4 Ni O2P 1 21/n 113.217; 20.737; 16.3
90; 112.083; 90
4140Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550590 CIFC45 H52 Br N4 Ni O2P 1 21/n 113.1252; 20.65; 16.188
90; 112.956; 90
4040Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550591 CIFC45 H50 N5 NiP 1 21/c 114.185; 10.668; 25.257
90; 94.686; 90
3809Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550592 CIFC94 H104 Br2 N8 Ni2 OP -112.62; 16.578; 20.317
77.4; 84.597; 86.947
4127.5Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550593 CIFC49 H54 N5 NiP 1 21/c 111.812; 21.544; 16.48
90; 91.636; 90
4192.1Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550594 CIFC46 H46 N3 NiC 1 2/c 129.913; 13.087; 20.428
90; 99.079; 90
7896.8Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550595 CIFC57 H69 N5 Ni OP -112.662; 12.701; 16.94
72.52; 78.286; 84.831
2543.1Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki
Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes
Catalysis Science & Technology, 2019
1550632 CIFC15 H18 N2 O SP 1 21/n 15.9659; 16.3145; 14.5127
90; 99.253; 90
1394.15Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing
Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones
Catalysis Science & Technology, 2019
1550633 CIFC12 H12 O2 SP b c a16.151; 7.314; 19.036
90; 90; 90
2249Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing
Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones
Catalysis Science & Technology, 2019
1550634 CIFC9 H14 N2 O SP 1 21/n 17.5382; 12.2061; 10.8739
90; 95.949; 90
995.14Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing
Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones
Catalysis Science & Technology, 2019
1550635 CIFC15 H16 O2 SP 1 21/c 111.978; 7.388; 16.198
90; 109.288; 90
1353Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing
Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones
Catalysis Science & Technology, 2019
1550749 CIFC9 H9 N7 OP n a 2112.569; 22.176; 3.6728
90; 90; 90
1023.7Wang, Chunling; Song, Chuanqqi; Shen, Wen-Hui; Qi, Yuan-Yuan; Xue, Ying; Shi, Yao-Cheng; Yu, Huaguang; Feng, Ligang
A two-dimensional Ni(II) coordination polymer based on 3,5-bis(1’,2’,4’-triazol-1’-yl) pyridine ligand for water electro-oxidation
Catalysis Science & Technology, 2019
1550750 CIFC36 H40 N14 Ni3 O22C 1 2/c 120.1497; 7.1876; 34.937
90; 94.669; 90
5043.1Wang, Chunling; Song, Chuanqqi; Shen, Wen-Hui; Qi, Yuan-Yuan; Xue, Ying; Shi, Yao-Cheng; Yu, Huaguang; Feng, Ligang
A two-dimensional Ni(II) coordination polymer based on 3,5-bis(1’,2’,4’-triazol-1’-yl) pyridine ligand for water electro-oxidation
Catalysis Science & Technology, 2019
1550762 CIFC45 H63 Cl2 Fe N3 OP 1 21/c 113.3638; 34.6037; 18.3685
90; 102.6; 90
8289.7Wang, Zheng; Zhang, Randi; Zhang, Wenjuan; Solan, Gregory; Liu, Qingbin; tongling, liang; Sun, Wen Hua
Enhancing thermostability of iron ethylene polymerization catalysts through N,N,N-chelation of doubly fused α,α′-bis(arylimino)-2,3:5,6-bis(hexamethylene)pyridines
Catalysis Science & Technology, 2019
1550763 CIFC41 H55 Cl4 Fe2 N3 OP 1 21/c 112.228; 21.82; 16.338
90; 104.2; 90
4226Wang, Zheng; Zhang, Randi; Zhang, Wenjuan; Solan, Gregory; Liu, Qingbin; tongling, liang; Sun, Wen Hua
Enhancing thermostability of iron ethylene polymerization catalysts through N,N,N-chelation of doubly fused α,α′-bis(arylimino)-2,3:5,6-bis(hexamethylene)pyridines
Catalysis Science & Technology, 2019
1550781 CIFC42 H81 As2 Co K5 Mo12 N6 O74P -111.6422; 12.1336; 17.7687
76.661; 89.632; 84.551
2430.98Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550782 CIFC42 H83 As2 K5 Mo12 N6 Ni O75P -111.6585; 12.1103; 17.742
76.859; 89.702; 84.663
2428.46Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550783 CIFC42 H86 Co Cs4 Mo12 N6 Na2 O78 Te2P -111.7267; 12.4654; 18.6945
74.384; 85.99; 84.238
2615.9Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550784 CIFC42 H75 Cs4 K Mo12 N6 O72 Te2 ZnP -111.6855; 12.386; 18.6191
74.699; 85.651; 83.954
2581.64Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550785 CIFC16 H78 As2 Co2 Mo12 N4 O75 Rb2P 1 21/c 113.8787; 23.7424; 15.8044
90; 120.032; 90
4508.6Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550786 CIFC16 H82 As2 Mo12 N4 O77 Rb2 Zn2P 1 21/c 113.8717; 23.7484; 15.8204
90; 119.884; 90
4518.8Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550787 CIFC42 H83 Cs4 K Mn Mo12 N6 O76 Te2P -111.651; 12.303; 18.63
74.094; 85.386; 84.132
2550.9Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550788 CIFC42 H85 As2 K5 Mn Mo12 N6 O76P -111.6211; 12.093; 17.7264
76.501; 89.846; 84.725
2411.63Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550789 CIFC16 H71 As2 K2 Mn2 Mo12 N4 Na O72P 1 21/c 113.702; 23.542; 15.546
90; 119.466; 90
4366Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550790 CIFC42 H81 As2 K5 Mo12 N6 O74 ZnP -111.6516; 12.123; 17.7391
76.692; 89.874; 84.635
2427.2Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550791 CIFC42 H70 Cs4 K2 Mo12 N6 Ni O70 Te2P -111.686; 12.336; 18.569
75.76; 86.017; 84.106
2578Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550792 CIFC16 H99 As2 Mo12 N4 Na Ni2 O86 Rb2P 1 21/n 113.842; 23.8125; 14.9785
90; 113.996; 90
4510.4Hou, Yujiao; An, Haiyan; Chang, Shenzhen; Zhang, Jie
Versatile catalysts constructed from hybrid polyoxomolybdates for simultaneously detoxifying sulfur mustard and organophosphate simulants
Catalysis Science & Technology, 2019
1550881 CIFC20 H11 Br O4 SP 1 21 15.7841; 12.278; 11.6933
90; 102.57; 90
810.52Almeida, Renata G.; Carvalho, Renato; Nunes, Mateus P.; Gomes, Roberto; Pedrosa, Leandro; Simone, Carlos; Elumalai, Gopi; Geertsen, Valerie; Gravel, Edmond; Doris, Eric; da Silva Júnior, Eufrânio N.
Carbon nanotube-ruthenium hybrid towards mild oxidation of sulfides to sulfones: Efficient synthesis of diverse sulfonyl compounds
Catalysis Science & Technology, 2019
1550882 CIFC20 H11 Br O2 SP -18.0446; 9.3059; 11.5017
106.28; 102.659; 90.396
804.28Almeida, Renata G.; Carvalho, Renato; Nunes, Mateus P.; Gomes, Roberto; Pedrosa, Leandro; Simone, Carlos; Elumalai, Gopi; Geertsen, Valerie; Gravel, Edmond; Doris, Eric; da Silva Júnior, Eufrânio N.
Carbon nanotube-ruthenium hybrid towards mild oxidation of sulfides to sulfones: Efficient synthesis of diverse sulfonyl compounds
Catalysis Science & Technology, 2019
1550883 CIFC32 H29 B F2 N2 O S2I 1 a 118.217; 7.6976; 20.1851
90; 98.631; 90
2798.4Almeida, Renata G.; Carvalho, Renato; Nunes, Mateus P.; Gomes, Roberto; Pedrosa, Leandro; Simone, Carlos; Elumalai, Gopi; Geertsen, Valerie; Gravel, Edmond; Doris, Eric; da Silva Júnior, Eufrânio N.
Carbon nanotube-ruthenium hybrid towards mild oxidation of sulfides to sulfones: Efficient synthesis of diverse sulfonyl compounds
Catalysis Science & Technology, 2019
1550934 CIFC32 H48 Cl2 Ir2 N4 O4 Si4I 1 2/a 117.8492; 10.6328; 43.5137
90; 96.227; 90
8209.6Guzman, Jefferson; García-Orduña, Pilar; Polo, Victor; Lahoz, Fernando J.; Oro, Luis A.; Fernandez-Alvarez, Francisco J
Ir-Catalyzed Selective Reduction of CO2 to Methoxy or Formate Level with HSiMe(OSiMe3)2
Catalysis Science & Technology, 2019
1550935 CIFC38 H53 F6 Ir2 N4 O8.5 Si4P -111.4358; 13.0237; 17.6415
90.226; 106.899; 101.886
2454.4Guzman, Jefferson; García-Orduña, Pilar; Polo, Victor; Lahoz, Fernando J.; Oro, Luis A.; Fernandez-Alvarez, Francisco J
Ir-Catalyzed Selective Reduction of CO2 to Methoxy or Formate Level with HSiMe(OSiMe3)2
Catalysis Science & Technology, 2019
1550941 CIFC18 H16 Mn2 N6 O8C 1 2/c 114.6208; 10.5924; 15.2131
90; 108.231; 90
2237.78Pinto, Mara F.; Olivares, Marta; Vivancos, Angela; Guisado Barrios, Gregorio; Albrecht, Martin; Royo, Beatriz
(Di)Triazolylidene Manganese Complexes in Catalytic Oxidation of Alcohols to Ketones and Aldehydes
Catalysis Science & Technology, 2019
1551065 CIFC30 H34 Cl Fe N3P 1 21 18.9968; 18.444; 9.3737
90; 117.856; 90
1375.21Gomes, Pedro T.; Cruz, Tiago Carpinteiro; Pereira, Laura C. J.; Waerenborgh, João Carlos; Veiros, Luis F.
Hydroboration of terminal olefins with pinacolborane catalyzed by new 2-iminopyrrolyl iron(II) complexes
Catalysis Science & Technology, 2019
1551066 CIFC39 H51 Fe N2P -19.606; 10.504; 17.317
103.9; 93.89; 91.43
1690.7Gomes, Pedro T.; Cruz, Tiago Carpinteiro; Pereira, Laura C. J.; Waerenborgh, João Carlos; Veiros, Luis F.
Hydroboration of terminal olefins with pinacolborane catalyzed by new 2-iminopyrrolyl iron(II) complexes
Catalysis Science & Technology, 2019
1551067 CIFC46 H42 Cl Fe N3P 1 21/c 120.583; 11.705; 19.314
90; 116.648; 90
4158.9Gomes, Pedro T.; Cruz, Tiago Carpinteiro; Pereira, Laura C. J.; Waerenborgh, João Carlos; Veiros, Luis F.
Hydroboration of terminal olefins with pinacolborane catalyzed by new 2-iminopyrrolyl iron(II) complexes
Catalysis Science & Technology, 2019
1551068 CIFC69 H93 Fe2 N5P -114.0411; 16.3354; 17.4433
107.001; 92.917; 100.939
3732.4Gomes, Pedro T.; Cruz, Tiago Carpinteiro; Pereira, Laura C. J.; Waerenborgh, João Carlos; Veiros, Luis F.
Hydroboration of terminal olefins with pinacolborane catalyzed by new 2-iminopyrrolyl iron(II) complexes
Catalysis Science & Technology, 2019
1551866 CIFC40 H39 Cu3 N8 O16.5P 1 2/c 116.471; 13.801; 18.659
90; 91.86; 90
4239.3Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1551867 CIFC24 H20 Cu2 N4 O11C 1 2/c 114.695; 5.165; 31.873
90; 94.29; 90
2412.4Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1551868 CIFC12 H8 Cu N2 O4C 1 2/c 17.8977; 13.599; 10.051
90; 91.65; 90
1079Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1551869 CIFC7 H5 Cu N O5C 1 2/c 112.072; 10.473; 7.6968
90; 127.27; 90
774.4Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1551870 CIFC68 H44 Cu6 N12 O16C 1 2/c 141.526; 10.852; 13.786
90; 95.84; 90
6180Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1551871 CIFC10 H13 Cu N2 O6P 1 21/n 16.421; 15.619; 11.765
90; 98.52; 90
1166.9Muthukumar, P.; Moon, Dohyun; Anthony, Philip Philip
Copper Coordination Polymer Electrocatalyst for Strong Hydrogen Evolution Reaction Activity in Neutral Medium: Influence of Coordination Environment and Network Structure
Catalysis Science & Technology, 2019
1552107 CIFC45 H31 Cl N4 ZnI 1 2/a 118.7682; 13.7292; 31.4518
90; 106.951; 90
7752.2Ge, Yuansheng; Cheng, Guoe; Xu, Nanfeng; Wang, Weizhou; Ke, Hanzhong
Zinc 2-N-Methyl N-confused porphyrin: An Efficient Catalyst for the Conversion of CO2 into Cyclic Carbonates
Catalysis Science & Technology, 2019
1552138 CIFC18 H15 N O2P -16.1964; 8.1764; 14.4347
94.139; 93.272; 107.361
693.81Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Site-selective Ru-catalyzed C-H bond alkenylation with biologically relevant isoindolinones: a case of catalyst performance controlled by subtle stereo-electronic effects of the weak directing group
Catalysis Science & Technology, 2019
1552139 CIFC25 H21 N O3P 1 21/n 18.2186; 14.7157; 16.7006
90; 93.695; 90
2015.61Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Site-selective Ru-catalyzed C-H bond alkenylation with biologically relevant isoindolinones: a case of catalyst performance controlled by subtle stereo-electronic effects of the weak directing group
Catalysis Science & Technology, 2019
1552140 CIFC22 H17 N OP 1 21/n 16.0929; 16.8891; 15.9338
90; 91.658; 90
1639Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Site-selective Ru-catalyzed C-H bond alkenylation with biologically relevant isoindolinones: a case of catalyst performance controlled by subtle stereo-electronic effects of the weak directing group
Catalysis Science & Technology, 2019
1552141 CIFC19 H17 N O3P -16.9823; 10.9866; 11.6209
110.95; 97.555; 105.365
777.03Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Site-selective Ru-catalyzed C-H bond alkenylation with biologically relevant isoindolinones: a case of catalyst performance controlled by subtle stereo-electronic effects of the weak directing group
Catalysis Science & Technology, 2019
1552142 CIFC19 H17 N O4P -17.0659; 10.6181; 11.7282
111.09; 100.172; 102.895
767.69Yuan, Yu-Chao; Bruneau, Christian; Roisnel, Thierry; Gramage-Doria, Rafael
Site-selective Ru-catalyzed C-H bond alkenylation with biologically relevant isoindolinones: a case of catalyst performance controlled by subtle stereo-electronic effects of the weak directing group
Catalysis Science & Technology, 2019
1552351 CIFC69 H70 B2 N6 NiP b c a35.8282; 18.7973; 17.4964
90; 90; 90
11783.4Sethuraman, Muthuramalingam; Anandababu, Karunanithi; Velusamy, Marappan; Ramasamy, Mayilmurugan
One Step Phenol Synthesis from Benzene Catalysed by Nickel(II) Complexes
Catalysis Science & Technology, 2019
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

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