Crystallography Open Database
Search results
Result: there are 779 entries in the selection
Switch to the old layout of the pageDownload all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)
Searching journal of publication like 'Catalysis science & technology'
COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
---|---|---|---|---|---|---|
1548131 | CIF | C44 H66 Ir2 N2 O4 P4 | P 1 21/n 1 | 14.6367; 11.0939; 14.9574 90; 93.785; 90 | 2423.5 | Cano, 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 | CIF | C44 H42 Mn | P 43 | 10.52378; 10.52378; 30.7376 90; 90; 90 | 3404.19 | Sharpe, 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 | CIF | C24 H27 Cl2 Co N7 O8 | C 1 2/c 1 | 27.9963; 10.5409; 19.1609 90; 100.453; 90 | 5560.7 | Leung, 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 | CIF | C30 H44 N6 O12 S2 Zn2 | P -4 21 c | 20.4693; 20.4693; 19.1467 90; 90; 90 | 8022.32 | Tan, 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 | CIF | C15 H23 Br2 Co N3 O2 | P 1 21/n 1 | 10.2514; 14.6308; 12.6552 90; 92.105; 90 | 1896.82 | Landge, 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 | CIF | C25 H17 Au Cl F4 N2 O P | P 1 21/n 1 | 19.942; 10.9697; 24.135 90; 112.7; 90 | 4870.7 | Arif, 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 | CIF | C25 H17 Au Cl F4 N2 O P | P 1 21/n 1 | 16.0034; 8.3754; 19.2521 90; 111.188; 90 | 2406.01 | Arif, 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 | CIF | C37.85 H26.29 Au2 Cl7.11 F4 N2 P2 | P -1 | 11.051; 15.816; 16.857 109.459; 103.933; 104.747 | 2509.4 | Arif, 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 | CIF | C36.8 H24.8 Au2 Cl4.4 F4 N2 P2 | P 1 21/c 1 | 18.453; 18.5065; 11.1568 90; 97.085; 90 | 3781 | Arif, 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 | CIF | C39.1 H24.5 Fe3 N2.1 O15.7 | P 1 21/c 1 | 12.6797; 13.5123; 23.948 90; 90; 90 | 4103.1 | Pham, 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 | CIF | C27 H33 Cl3 Cr N7 O2 | P b c a | 18.2412; 14.5616; 23.1101 90; 90; 90 | 6138.53 | Nobbs, 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 | CIF | C25 H33 Cl3 Cr N7 O2 | P 1 21/c 1 | 18.3091; 11.3311; 13.9361 90; 100.163; 90 | 2845.85 | Nobbs, 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 | CIF | C43 H29 N6 O4 Ru | P 1 21/c 1 | 12.139; 15.53; 24.301 90; 98.77; 90 | 4528 | Xiang, 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 | CIF | C18 H32 F3 Mn O6 P2 S | P 21 21 21 | 8.6949; 13.9549; 19.9508 90; 90; 90 | 2420.8 | Garduño, 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 | CIF | C15 H20 Cl2 O6 Pd | C 1 2/m 1 | 11.6869; 8.8935; 8.551 90; 90.223; 90 | 888.76 | Eremin, 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 | CIF | C10 H8 F6 O4 Pd | P -1 | 4.7881; 7.9629; 8.7923 80.994; 77.33; 72.621 | 310.64 | Eremin, 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 | CIF | C26 H44 Cl Ir N O7 P | P 1 21/c 1 | 15.0632; 12.3425; 16.2371 90; 107.643; 90 | 2876.77 | Gregor, 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 | CIF | C26 H43 Ir N O7 P | P -1 | 7.7588; 15.5942; 24.116 89.185; 82.743; 89.582 | 2894.1 | Gregor, 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 | CIF | C17 H16 O2 Se | P 1 | 6.7562; 7.5182; 8.7692 107.83; 98.976; 113.06 | 370.28 | García-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 | CIF | C15 H23 Br2 Co N3 O2 | P 1 21/n 1 | 10.2514; 14.6308; 12.6552 90; 92.105; 90 | 1896.82 | Midya, 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 | CIF | C15 H29 B2 Cl2 Co F8 N5 O | P -1 | 6.838; 13.077; 13.377 89.44; 78.44; 82.78 | 1162.5 | Midya, 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 | CIF | C28 H18 Cu3 N10 O15 | C 1 2/c 1 | 31.977; 18.3536; 14.7633 90; 91.413; 90 | 8661.8 | Ahmad, 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 | CIF | C86 H157 K2 Mn8 N O42 | P 1 21/n 1 | 18.998; 15.678; 20.236 90; 100.84; 90 | 5920 | Mousazade, 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 | CIF | C8 H4.19 Al I0.82 O5 | I m m a | 16.501; 6.6194; 13.21 90; 90; 90 | 1442.9 | Tahmouresilerd, 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 | CIF | C8 H4.3 Al I0.7 O5.25 | I m m a | 17.107; 6.622; 12.229 90; 90; 90 | 1385.3 | Tahmouresilerd, 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 | CIF | C31 H53 Rh2 S2 | P 1 21/n 1 | 10.855; 28.6007; 10.8441 90; 119.239; 90 | 2937.7 | Serrano-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 | CIF | C40 H74 Rh2 S2 | P 1 21/m 1 | 8.734; 26.987; 8.39 90; 90; 90 | 1977.6 | Serrano-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 | CIF | C21 H33 Cl2 N Si Ti | P -1 | 8.268; 11.8794; 12.9943 71.395; 78.04; 70.734 | 1134.41 | Williams, 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 | CIF | C32 H49 Cl2 N Si Ti | P -1 | 9.966; 12.4507; 15.2615 112.445; 108.902; 90.786 | 1635.29 | Williams, 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 | CIF | C20 H31 Cl2 N Si Ti | P 1 21/c 1 | 11.5225; 12.9843; 15.2891 90; 104.979; 90 | 2209.7 | Williams, 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 | CIF | C23 H26 Ir N O3 | P b c a | 16.13031; 14.54437; 17.33703 90; 90; 90 | 4067.36 | Pèrez-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 | CIF | C28 H34 Cl Ir N2 | P -1 | 9.7423; 11.066; 12.1673 100.717; 104.685; 96.543 | 1228.72 | Wong, 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 | CIF | C17 H21 N O2 S | P -1 | 7.4134; 8.4142; 12.1239 84.72; 88.99; 84.549 | 749.62 | Llorente, 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 | CIF | C16 H22 O4 | P -1 | 6.2605; 9.8392; 12.7844 67.7938; 88.4599; 84.1325 | 725.21 | Llorente, 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 | CIF | C49 H50 N6 O Y | P 1 2/n 1 | 22.637; 9.781; 23.089 90; 118.062; 90 | 4511 | Zhang, 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 | CIF | C37 H46 B Cl2 Cu F4 N8 | P 1 21/c 1 | 20.808; 31.071; 12.2164 90; 90.694; 90 | 7897.6 | Zelenay, 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 | CIF | C33.5 H41 Cl Cu F3 N4 O3 S | P 1 21/n 1 | 12.3905; 19.0233; 14.481 90; 102.996; 90 | 3325.86 | Zelenay, 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 | CIF | C37 H44 Cu F3 N4 O3 S | P -1 | 9.1002; 10.9858; 19.3481 89.693; 79.192; 82.793 | 1884.64 | Zelenay, 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 | CIF | C22 H26 I Ir N4 | P -1 | 8.5611; 10.9802; 13.2254 109.051; 102.4; 90.413 | 1143.69 | Semwal, 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 | CIF | C22 H23 N | P -1 | 9.7438; 9.9224; 10.984 64.086; 78.354; 63.503 | 854.8 | Abdellah, 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 | CIF | C24 H27 N | P -1 | 8.3046; 10.7954; 12.0469 109.64; 100.96; 104.352 | 940.16 | Abdellah, 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 | CIF | C38 H60 Mo13 N10 O34 | C m c m | 24.715; 23.137; 13.595 90; 90; 90 | 7774 | Luo, Benlong; Sang, Rui-LI; Lin, Lifang; Xu, Li Mo3IV-Polyoxomolybdates with Frustrated Lewis Pairs For High-Performance Hydrogenation Catalysis Catalysis Science & Technology, 2019 |
1550279 | CIF | C20 H32 Cl4 Co2 N4 S2 | P -1 | 7.6862; 11.1085; 17.7851 72.8236; 88.0499; 70.2746 | 1362.03 | Puylaert, 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 | CIF | C11 H18 Cl2 Co N2 S | P -1 | 7.0681; 9.014; 12.2372 108.21; 98.899; 99.291 | 713.18 | Puylaert, 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 | CIF | C53.5 H66 Cl3 N4 O1.5 Ru | P -1 | 11.961; 16.591; 26.614 93.877; 90.681; 98.321 | 5212.6 | DUMAS, 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 | CIF | C63 H82 Cl2 N4 Ru | P 1 21/n 1 | 11.206; 15.0047; 33.7602 90; 96.909; 90 | 5635.3 | DUMAS, 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 | CIF | C53 H62 Cl2 N4 Ru | P -1 | 12.017; 12.562; 16.608 80.103; 89.839; 70.644 | 2326.2 | DUMAS, 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 | CIF | C56 H68 Cl4 N4 Ru | P 1 21/c 1 | 21.792; 10.9906; 22.5146 90; 107.445; 90 | 5144.4 | DUMAS, 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 | CIF | C55 H66 Cl2 N4 Ru | P -1 | 10.9047; 11.6314; 19.7689 95.343; 101.998; 100.664 | 2387.6 | Dumas, 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 | CIF | C26 H34 B N O4 S | P 1 21/c 1 | 6.4192; 32.5924; 11.989 90; 99.366; 90 | 2474.9 | Cabrera-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 | CIF | C45 H61 Cl N4 Ni O2 | P 1 21/n 1 | 13.217; 20.737; 16.3 90; 112.083; 90 | 4140 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550590 | CIF | C45 H52 Br N4 Ni O2 | P 1 21/n 1 | 13.1252; 20.65; 16.188 90; 112.956; 90 | 4040 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550591 | CIF | C45 H50 N5 Ni | P 1 21/c 1 | 14.185; 10.668; 25.257 90; 94.686; 90 | 3809 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550592 | CIF | C94 H104 Br2 N8 Ni2 O | P -1 | 12.62; 16.578; 20.317 77.4; 84.597; 86.947 | 4127.5 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550593 | CIF | C49 H54 N5 Ni | P 1 21/c 1 | 11.812; 21.544; 16.48 90; 91.636; 90 | 4192.1 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550594 | CIF | C46 H46 N3 Ni | C 1 2/c 1 | 29.913; 13.087; 20.428 90; 99.079; 90 | 7896.8 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550595 | CIF | C57 H69 N5 Ni O | P -1 | 12.662; 12.701; 16.94 72.52; 78.286; 84.831 | 2543.1 | Inatomi, Takahiro; Fukahori, Yukino; Yamada, Yuji; Ishikawa, Ryuta; Kanegawa, Shinji; Koga, Yuji; Matsubara, Kouki Ni(I)-Ni(III) Cycle in Buchwald-Hartwig Amination of Aryl Bromide Mediated by NHC-ligated Ni(I) Complexes Catalysis Science & Technology, 2019 |
1550632 | CIF | C15 H18 N2 O S | P 1 21/n 1 | 5.9659; 16.3145; 14.5127 90; 99.253; 90 | 1394.15 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
1550633 | CIF | C12 H12 O2 S | P b c a | 16.151; 7.314; 19.036 90; 90; 90 | 2249 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
1550634 | CIF | C9 H14 N2 O S | P 1 21/n 1 | 7.5382; 12.2061; 10.8739 90; 95.949; 90 | 995.14 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
1550635 | CIF | C15 H16 O2 S | P 1 21/c 1 | 11.978; 7.388; 16.198 90; 109.288; 90 | 1353 | Zhou, Hui; Zhang, Rui; zhang, hui; Mu, Sen; Lu, Xiaobing Organocatalytic Cycloaddition of Carbonyl Sulfide with Propargylic Alcohols to 1,3-Oxathiolan-2-ones Catalysis Science & Technology, 2019 |
1550749 | CIF | C9 H9 N7 O | P n a 21 | 12.569; 22.176; 3.6728 90; 90; 90 | 1023.7 | Wang, 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 | CIF | C36 H40 N14 Ni3 O22 | C 1 2/c 1 | 20.1497; 7.1876; 34.937 90; 94.669; 90 | 5043.1 | Wang, 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 | CIF | C45 H63 Cl2 Fe N3 O | P 1 21/c 1 | 13.3638; 34.6037; 18.3685 90; 102.6; 90 | 8289.7 | Wang, 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 | CIF | C41 H55 Cl4 Fe2 N3 O | P 1 21/c 1 | 12.228; 21.82; 16.338 90; 104.2; 90 | 4226 | Wang, 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 | CIF | C42 H81 As2 Co K5 Mo12 N6 O74 | P -1 | 11.6422; 12.1336; 17.7687 76.661; 89.632; 84.551 | 2430.98 | Hou, 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 | CIF | C42 H83 As2 K5 Mo12 N6 Ni O75 | P -1 | 11.6585; 12.1103; 17.742 76.859; 89.702; 84.663 | 2428.46 | Hou, 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 | CIF | C42 H86 Co Cs4 Mo12 N6 Na2 O78 Te2 | P -1 | 11.7267; 12.4654; 18.6945 74.384; 85.99; 84.238 | 2615.9 | Hou, 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 | CIF | C42 H75 Cs4 K Mo12 N6 O72 Te2 Zn | P -1 | 11.6855; 12.386; 18.6191 74.699; 85.651; 83.954 | 2581.64 | Hou, 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 | CIF | C16 H78 As2 Co2 Mo12 N4 O75 Rb2 | P 1 21/c 1 | 13.8787; 23.7424; 15.8044 90; 120.032; 90 | 4508.6 | Hou, 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 | CIF | C16 H82 As2 Mo12 N4 O77 Rb2 Zn2 | P 1 21/c 1 | 13.8717; 23.7484; 15.8204 90; 119.884; 90 | 4518.8 | Hou, 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 | CIF | C42 H83 Cs4 K Mn Mo12 N6 O76 Te2 | P -1 | 11.651; 12.303; 18.63 74.094; 85.386; 84.132 | 2550.9 | Hou, 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 | CIF | C42 H85 As2 K5 Mn Mo12 N6 O76 | P -1 | 11.6211; 12.093; 17.7264 76.501; 89.846; 84.725 | 2411.63 | Hou, 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 | CIF | C16 H71 As2 K2 Mn2 Mo12 N4 Na O72 | P 1 21/c 1 | 13.702; 23.542; 15.546 90; 119.466; 90 | 4366 | Hou, 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 | CIF | C42 H81 As2 K5 Mo12 N6 O74 Zn | P -1 | 11.6516; 12.123; 17.7391 76.692; 89.874; 84.635 | 2427.2 | Hou, 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 | CIF | C42 H70 Cs4 K2 Mo12 N6 Ni O70 Te2 | P -1 | 11.686; 12.336; 18.569 75.76; 86.017; 84.106 | 2578 | Hou, 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 | CIF | C16 H99 As2 Mo12 N4 Na Ni2 O86 Rb2 | P 1 21/n 1 | 13.842; 23.8125; 14.9785 90; 113.996; 90 | 4510.4 | Hou, 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 | CIF | C20 H11 Br O4 S | P 1 21 1 | 5.7841; 12.278; 11.6933 90; 102.57; 90 | 810.52 | Almeida, 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 | CIF | C20 H11 Br O2 S | P -1 | 8.0446; 9.3059; 11.5017 106.28; 102.659; 90.396 | 804.28 | Almeida, 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 | CIF | C32 H29 B F2 N2 O S2 | I 1 a 1 | 18.217; 7.6976; 20.1851 90; 98.631; 90 | 2798.4 | Almeida, 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 | CIF | C32 H48 Cl2 Ir2 N4 O4 Si4 | I 1 2/a 1 | 17.8492; 10.6328; 43.5137 90; 96.227; 90 | 8209.6 | Guzman, 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 | CIF | C38 H53 F6 Ir2 N4 O8.5 Si4 | P -1 | 11.4358; 13.0237; 17.6415 90.226; 106.899; 101.886 | 2454.4 | Guzman, 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 | CIF | C18 H16 Mn2 N6 O8 | C 1 2/c 1 | 14.6208; 10.5924; 15.2131 90; 108.231; 90 | 2237.78 | Pinto, 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 | CIF | C30 H34 Cl Fe N3 | P 1 21 1 | 8.9968; 18.444; 9.3737 90; 117.856; 90 | 1375.21 | Gomes, 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 | CIF | C39 H51 Fe N2 | P -1 | 9.606; 10.504; 17.317 103.9; 93.89; 91.43 | 1690.7 | Gomes, 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 | CIF | C46 H42 Cl Fe N3 | P 1 21/c 1 | 20.583; 11.705; 19.314 90; 116.648; 90 | 4158.9 | Gomes, 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 | CIF | C69 H93 Fe2 N5 | P -1 | 14.0411; 16.3354; 17.4433 107.001; 92.917; 100.939 | 3732.4 | Gomes, 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 | CIF | C40 H39 Cu3 N8 O16.5 | P 1 2/c 1 | 16.471; 13.801; 18.659 90; 91.86; 90 | 4239.3 | Muthukumar, 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 | CIF | C24 H20 Cu2 N4 O11 | C 1 2/c 1 | 14.695; 5.165; 31.873 90; 94.29; 90 | 2412.4 | Muthukumar, 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 | CIF | C12 H8 Cu N2 O4 | C 1 2/c 1 | 7.8977; 13.599; 10.051 90; 91.65; 90 | 1079 | Muthukumar, 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 | CIF | C7 H5 Cu N O5 | C 1 2/c 1 | 12.072; 10.473; 7.6968 90; 127.27; 90 | 774.4 | Muthukumar, 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 | CIF | C68 H44 Cu6 N12 O16 | C 1 2/c 1 | 41.526; 10.852; 13.786 90; 95.84; 90 | 6180 | Muthukumar, 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 | CIF | C10 H13 Cu N2 O6 | P 1 21/n 1 | 6.421; 15.619; 11.765 90; 98.52; 90 | 1166.9 | Muthukumar, 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 | CIF | C45 H31 Cl N4 Zn | I 1 2/a 1 | 18.7682; 13.7292; 31.4518 90; 106.951; 90 | 7752.2 | Ge, 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 | CIF | C18 H15 N O2 | P -1 | 6.1964; 8.1764; 14.4347 94.139; 93.272; 107.361 | 693.81 | Yuan, 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 | CIF | C25 H21 N O3 | P 1 21/n 1 | 8.2186; 14.7157; 16.7006 90; 93.695; 90 | 2015.61 | Yuan, 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 | CIF | C22 H17 N O | P 1 21/n 1 | 6.0929; 16.8891; 15.9338 90; 91.658; 90 | 1639 | Yuan, 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 | CIF | C19 H17 N O3 | P -1 | 6.9823; 10.9866; 11.6209 110.95; 97.555; 105.365 | 777.03 | Yuan, 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 | CIF | C19 H17 N O4 | P -1 | 7.0659; 10.6181; 11.7282 111.09; 100.172; 102.895 | 767.69 | Yuan, 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 | CIF | C69 H70 B2 N6 Ni | P b c a | 35.8282; 18.7973; 17.4964 90; 90; 90 | 11783.4 | Sethuraman, Muthuramalingam; Anandababu, Karunanithi; Velusamy, Marappan; Ramasamy, Mayilmurugan One Step Phenol Synthesis from Benzene Catalysed by Nickel(II) Complexes Catalysis Science & Technology, 2019 |
1552352 | CIF | C7 H7 Au Cl4 N2 O3 | P -1 | 7.831; 7.931; 11.079 97.173; 95.533; 96.097 | 674.6 | Ahmad, Ahmad A. L.; Panicker, Seema; Chehimi, Mohamed M.; Monge, Miguel; López-de-Luzuriaga, José M.; Mohamed, Ahmed A.; Bruce, Alice E.; Bruce, Mitchell R. M. Synthesis of Water-Soluble Gold-Aryl Nanoparticles with Distinct Catalytic Performance in the Reduction of the Environmental Pollutant 4-Nitrophenol Catalysis Science & Technology, 2019 |
1552752 | CIF | C50 H39 F18 N12 P3 Ru2 | P -1 | 10.6161; 15.1085; 16.911 90.103; 94.853; 105.573 | 2602.6 | Hennessey, Seán; Farras Costa, Pau; Benet-Buchholz, Jordi; Llobet, Antoni A Bpp-based Dinuclear Ruthenium Photocatalyst for Visible Light-Driven Oxidation Reactions Catalysis Science & Technology, 2019 |
1552753 | CIF | C51 H42 Cl F12 N11 O P2 Ru2 | P -1 | 12.918; 13.831; 17.552 92.997; 100.953; 105.668 | 2946.61 | Hennessey, Seán; Farras Costa, Pau; Benet-Buchholz, Jordi; Llobet, Antoni A Bpp-based Dinuclear Ruthenium Photocatalyst for Visible Light-Driven Oxidation Reactions Catalysis Science & Technology, 2019 |
1552866 | CIF | C46 H41 Au Cl N2 P3 | P 1 21/n 1 | 17.5516; 12.9246; 17.7238 90; 93.431; 90 | 4013.4 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552867 | CIF | C44 H39 Au Cl N2 P3 | P 1 21/n 1 | 10.8276; 33.9018; 11.4594 90; 113.03; 90 | 3871.21 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552868 | CIF | C47 H37 Cl2 N2 P3 | P 1 21 1 | 10.3342; 22.3144; 17.0157 90; 92.007; 90 | 3921.4 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552869 | CIF | C47 H37 Au Cl3 N2 P3 | P -1 | 12.5994; 13.2954; 13.5256 70.09; 84.549; 78.391 | 2085.9 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552870 | CIF | C28 H33 Au Cl N P2 | P 1 21/c 1 | 11.78322; 9.40736; 24.667 90; 102.482; 90 | 2669.68 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552871 | CIF | C62 H72 N2 P4 | P -1 | 10.1896; 17.4204; 17.4304 67.712; 73.191; 73.1212 | 2682.92 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552872 | CIF | C60 H45 N3 P4 | P -3 | 35.1836; 35.1836; 9.7068 90; 90; 120 | 10406.1 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552873 | CIF | C55 H51 Cl9 N2 O3 P3 Rh | P 1 21/c 1 | 11.00739; 22.02102; 24.05162 90; 102.989; 90 | 5680.79 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552874 | CIF | C45 H41 Cl2 N2 P3 | P 1 21/n 1 | 9.8538; 22.9455; 17.3019 90; 93.031; 90 | 3906.5 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552875 | CIF | C97 H92 Cl10 N4 P6 | P -1 | 10.2673; 12.11; 19.82 103.947; 99.881; 100.687 | 2289 | Schwarz, Christopher; Handelmann, Jens; Baier, Daniel M.; Ouissa, Alina; Gessner, Viktoria H. Mono- and Diylide-substituted Phosphines (YPhos): Impact of the Ligand Properties on the Catalytic Activity in Gold(I)-Catalysed Hydroaminations Catalysis Science & Technology, 2019 |
1552963 | CIF | C18 H22 Br F5 N2 | P 1 21/c 1 | 7.8536; 8.5571; 29.1438 90; 90.415; 90 | 1958.53 | Anthofer, Michael H.; Wilhelm, Michael E.; Cokoja, Mirza; Markovits, Iulius I. E.; Pöthig, Alexander; Mink, János; Herrmann, Wolfgang A.; Kühn, Fritz E. Cycloaddition of CO2 and epoxides catalyzed by imidazolium bromides under mild conditions: influence of the cation on catalyst activity Catalysis Science & Technology, 2014, 4, 1749 |
1553092 | CIF | C20 H29 Cl Mo N2 O3 | P 1 21/c 1 | 10.9605; 15.9334; 13.4384 90; 112.447; 90 | 2169 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1553093 | CIF | C41 H53 Cl17 Mo2 N4 O4 | F d -3 c :2 | 58.3972; 58.3972; 58.3972 90; 90; 90 | 199148 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1553094 | CIF | C40 H60 Cl2 Mo2 N4 O6 | P -1 | 12.2348; 14.0396; 14.2351 92.035; 107.553; 104.751 | 2237.7 | Gomes, Ana C.; Neves, Patrícia; Cunha-Silva, Luís; Valente, Anabela A.; Gonçalves, Isabel S.; Pillinger, Martyn Oxidomolybdenum complexes for acid catalysis using alcohols as solvents and reactants Catalysis Science & Technology, 2016, 6, 5207 |
1554189 | CIF | C29 H31 Cl2 O3 P Ru | P 1 21/n 1 | 10.0354; 12.4751; 22.059 90; 93.55; 90 | 2756.3 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554190 | CIF | C123.3 Cl8 O8 P4 Ru4 Zn2 | P 1 21/n 1 | 16.387; 27.97; 26.66 90; 101.396; 90 | 11979 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554191 | CIF | C25 H29 Cl2 O2 P Ru | P 1 21/n 1 | 10.595; 12.873; 18.387 90; 106.74; 90 | 2401.5 | Amenuvor, Gershon; Darkwa, James; Makhubela, Banothile C. E. Homogeneous polymetallic ruthenium(ii)^zinc(ii) complexes: robust catalysts for the efficient hydrogenation of levulinic acid to γ-valerolactone Catalysis Science & Technology, 2018, 8, 2370 |
1554620 | CIF | C24 H38 F6 Fe P Ru S3 | C m c e | 15.867; 20.073; 18.513 90; 90; 90 | 5896.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554621 | CIF | C14 H23 Co S3 | P 1 21/c 1 | 13.1028; 8.6112; 14.2219 90; 101.551; 90 | 1572.17 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554622 | CIF | C30 H43 F6 Fe P Ru S4 | P 1 21/n 1 | 14.3616; 13.9373; 16.9737 90; 99.0564; 90 | 3355.1 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554623 | CIF | C26 H41 F12 Fe N P2 Ru S3 | P n m a | 11.8; 15.608; 18.603 90; 90; 90 | 3426 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554624 | CIF | C48 H58 B Co Fe S3 | P n a 21 | 20.2817; 17.2944; 12.4241 90; 90; 90 | 4357.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554625 | CIF | C47 H56 B Co Fe S3 | P n a 21 | 20.576; 16.9755; 12.0227 90; 90; 90 | 4199.4 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1554626 | CIF | C48 H59 B Fe Ru S3 | P 1 21/c 1 | 15.5349; 15.8332; 18.3897 90; 90.694; 90 | 4522.9 | Zhang, Yahui; Yang, Dawei; Li, Ying; Zhao, Xiangyu; Wang, Baomin; Qu, Jingping Biomimetic catalytic oxidative coupling of thiols using thiolate-bridged dinuclear metal complexes containing iron in water under mild conditions Catalysis Science & Technology, 2019, 9, 6492 |
1556266 | CIF | C28 H27 N O6 | P 21 21 21 | 10.42; 12.888; 19.103 90; 90; 90 | 2565.4 | Wang, Ming; Shi, Yu-Hua; Luo, Jun-Fei; Du, Wenting; Shi, Xiao-Xin; Fossey, John S.; Deng, Wei-Ping Novel N,O-Cu(OAc)2 complex catalysed diastereo- and enantioselective 1,4-addition of glycine derivatives to alkylidene malonates Catalysis Science & Technology, 2011, 1, 100 |
1556267 | CIF | C24 H28 Br2 N2 Ni | C 1 2/c 1 | 29.331; 10.775; 15.226 90; 105.3; 90 | 4641.5 | Song, Shengju; Xiao, Tianpengfei; Liang, Tongling; Wang, Fosong; Redshaw, Carl; Sun, Wen-Hua Synthesis, characterization and ethylene oligomerization behaviour of 8-(1-aryliminoethylidene)quinaldinylnickel dihalides Catalysis Science & Technology, 2011, 1, 69 |
1556268 | CIF | C23 H26 Br2 N2 Ni | P 1 21/n 1 | 15.834; 8.6441; 17.665 90; 114.28; 90 | 2204 | Song, Shengju; Xiao, Tianpengfei; Liang, Tongling; Wang, Fosong; Redshaw, Carl; Sun, Wen-Hua Synthesis, characterization and ethylene oligomerization behaviour of 8-(1-aryliminoethylidene)quinaldinylnickel dihalides Catalysis Science & Technology, 2011, 1, 69 |
1556269 | CIF | C60 H53 Cl4 O5 P5 Rh2 | P 1 21/c 1 | 17.0585; 17.1534; 19.5448 90; 90.797; 90 | 5718.5 | Castro, Pascal M.; Gulyás, Henrik; Benet-Buchholz, Jordi; Bo, Carles; Freixa, Zoraida; van Leeuwen, Piet W. N. M. SPOs as new ligands in Rh(iii) catalyzed enantioselective transfer hydrogenation Catalysis Science & Technology, 2011, 1, 401 |
1556270 | CIF | C44 H48 F6 O12 S8 Zn | R -3 :H | 12.5877; 12.5877; 29.1803 90; 90; 120 | 4004.2 | Enthaler, Stephan A straightforward zinc-catalysed reduction of sulfoxides to sulfides Catalysis Science & Technology, 2011, 1, 104 |
1556271 | CIF | C33.33 H0 F4 O6.67 S4 Zn0.67 | P -1 | 10.5817; 13.8939; 19.8576 83.554; 88.085; 73.117 | 2775.99 | Enthaler, Stephan A straightforward zinc-catalysed reduction of sulfoxides to sulfides Catalysis Science & Technology, 2011, 1, 104 |
1556272 | CIF | C18 H22 N O5 P | C 1 2/c 1 | 22.1091; 10.4184; 18.2639 90; 118.495; 90 | 3697.3 | Kidwai, Mazaahir; Bhardwaj, Saurav; Mishra, Neeraj Kumar; Jain, Arti; Kumar, Ajeet; Mozzumdar, Subho Application of mobilized Cu-nanoparticles as heterogeneous catalyst for the synthesis of α-amino phosphonates via A2-P coupling Catalysis Science & Technology, 2011, 1, 426 |
1556279 | CIF | C22 H24 Cl2 Co N2 | P 1 21/n 1 | 11.337; 15.712; 11.611 90; 95.49; 90 | 2058.7 | Xiao, Tianpengfei; Lai, Jingjuan; Zhang, Shu; Hao, Xiang; Sun, Wen-Hua 2-(1-Aryliminopropylidene)quinolylcobalt(ii) dichlorides: synthesis, characterization and catalytic behaviour towards ethylene Catalysis Science & Technology, 2011, 1, 462 |
1556280 | CIF | C24 H28 Cl2 Co N2 | P 1 21/n 1 | 10.125; 16.885; 13.533 90; 90.01; 90 | 2313.6 | Xiao, Tianpengfei; Lai, Jingjuan; Zhang, Shu; Hao, Xiang; Sun, Wen-Hua 2-(1-Aryliminopropylidene)quinolylcobalt(ii) dichlorides: synthesis, characterization and catalytic behaviour towards ethylene Catalysis Science & Technology, 2011, 1, 462 |
1556281 | CIF | C24 H34 N O4 V | P 1 21/c 1 | 8.4832; 11.5025; 24.14 90; 94.873; 90 | 2347 | Lorber, Christian; Despagnet-Ayoub, Emmanuelle; Vendier, Laure; Arbaoui, Abdessamad; Redshaw, Carl Amine influence in vanadium-based ethylene polymerisation pro-catalysts bearing bis(phenolate) ligands with ‘pendant’ arms Catalysis Science & Technology, 2011, 1, 489 |
1556282 | CIF | C26 H26 Cl2 N2 O Ti | C 1 2/c 1 | 23.852; 13.832; 16.89 90; 118.68; 90 | 4889 | Huang, Wei; Li, Baixiang; Wang, Youhong; Zhang, Wenjuan; Wang, Lin; Li, Yuesheng; Sun, Wen-Hua; Redshaw, Carl Synthesis, characterization and ethylene (co-)polymerization behavior of half-titanocene 2-(1-(arylimino)ethyl)quinolin-8-olate chlorides Catalysis Science & Technology, 2011, 1, 1208 |
1556283 | CIF | C27 H28 Cl2 N2 O Ti | P 1 21/c 1 | 17.098; 8.1446; 17.624 90; 98.7; 90 | 2426 | Huang, Wei; Li, Baixiang; Wang, Youhong; Zhang, Wenjuan; Wang, Lin; Li, Yuesheng; Sun, Wen-Hua; Redshaw, Carl Synthesis, characterization and ethylene (co-)polymerization behavior of half-titanocene 2-(1-(arylimino)ethyl)quinolin-8-olate chlorides Catalysis Science & Technology, 2011, 1, 1208 |
1556284 | CIF | C16 H24 Cl2 N2 O4 Pd S2 | P -1 | 8.4783; 11.6061; 13.1535 67.125; 89.797; 68.971 | 1099.1 | Tomás-Mendivil, Eder; Díez, Josefina; Cadierno, Victorio Conjugate addition of arylboronic acids to α,β-unsaturated carbonyl compounds in aqueous medium using Pd(ii) complexes with dihydroxy-2,2′-bipyridine ligands: homogeneous or heterogeneous nano-catalysis? Catalysis Science & Technology, 2011, 1, 1605 |
1556285 | CIF | C14 H14 Cl2 N2 O5 Pd S | P -1 | 7.6738; 10.4974; 12.5545 112.689; 90.017; 108.646 | 875.2 | Tomás-Mendivil, Eder; Díez, Josefina; Cadierno, Victorio Conjugate addition of arylboronic acids to α,β-unsaturated carbonyl compounds in aqueous medium using Pd(ii) complexes with dihydroxy-2,2′-bipyridine ligands: homogeneous or heterogeneous nano-catalysis? Catalysis Science & Technology, 2011, 1, 1605 |
1556286 | CIF | C54.2 H48.4 Cl0.4 N2 O P2 | P -1 | 11.5434; 14.8956; 15.1659 62.313; 86.134; 78.115 | 2258.4 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556287 | CIF | C50 H40 N2 O P2 | P 1 21/c 1 | 18.0198; 14.0045; 16.7584 90; 109.646; 90 | 3982.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556288 | CIF | C51 H39 N2 O P2 | P -1 | 9.373; 13.769; 17.95 104.285; 90.99; 92.535 | 2242 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556289 | CIF | C85 H77 B N2 O P2 Zn | P -1 | 14.3702; 15.2542; 17.2588 81.451; 66.469; 76.867 | 3370.8 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556290 | CIF | C76.18 H63.47 B N2 O P2 Zn | P -1 | 9.9214; 17.1175; 18.4747 86.754; 78.725; 80.859 | 3036.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556291 | CIF | C80.65 H63.86 B N2 O P2 Zn | P -1 | 9.9023; 16.867; 20.7112 101.974; 91.114; 95.296 | 3366.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556292 | CIF | C86.83 H60.66 B Cl1.66 F24 N2 O4 P2 Zn | P -1 | 11.4655; 19.564; 19.662 99.64; 103.416; 92.916 | 4210.9 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556293 | CIF | C90 H60 B Br0.38 F24 N2 O4 P2 Zn | P 1 21/c 1 | 18.781; 27.1179; 18.6506 90; 116.785; 90 | 8479.6 | Wheaton, Craig A.; Hayes, Paul G. Exploring the versatility of a bis(phosphinimine) pincer ligand: effect of sterics on structure and lactide polymerization activity of cationic zinc complexes Catal. Sci. Technol., 2012, 2, 125 |
1556294 | CIF | C57 H50 Br2 N2 Ni | P 1 21/c 1 | 10.378; 16.008; 31.765 90; 95.61; 90 | 5251.9 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556295 | CIF | C56 H48 Br2 N2 Ni | P 1 21/c 1 | 15.352; 22.551; 15.38 90; 106.96; 90 | 5093 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556296 | CIF | C54 H44 Cl2 N2 Ni O0 | P 1 21/c 1 | 15.33; 22.285; 14.954 90; 106.33; 90 | 4902.6 | Liu, Hao; Zhao, Weizhen; Yu, Jiangang; Yang, Wenhong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Synthesis, characterization and ethylenepolymerization behavior of nickel dihalide complexes bearing bulky unsymmetrical α-diimine ligands Catal. Sci. Technol., 2012, 2, 415 |
1556297 | CIF | C28 H33 Cl4 Co N3 O2 | P b c a | 15.492; 17.191; 25.784 90; 90; 90 | 6867 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556298 | CIF | C28 H33 Cl4 Fe N3 S2 | C 1 2/c 1 | 23.2849; 16.2809; 17.6654 90; 106.957; 90 | 6405.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556299 | CIF | C41 H43 Cl2 Fe N3 O3 | P 1 21/n 1 | 16.114; 8.9394; 27.383 90; 99.828; 90 | 3886.6 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556300 | CIF | C38 H37 Cl4 Fe N3 S2 | P b c a | 17.148; 20.564; 22.319 90; 90; 90 | 7870 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556301 | CIF | C38.5 H38 Cl6 N3 S2 V | P 1 21/n 1 | 12.3896; 19.617; 16.797 90; 95.449; 90 | 4064 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556302 | CIF | C38.5 H38 Cl6 Cr N3 S2 | P 1 21/n 1 | 12.3561; 19.623; 16.75 90; 95.756; 90 | 4040.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556303 | CIF | C38 H37 Cl4 Mn N3 S2 | P b c a | 17.056; 20.693; 22.231 90; 90; 90 | 7846 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556304 | CIF | C41 H43 Br2 N3 Ni O S2 | P b c a | 17.54; 20.405; 22.23 90; 90; 90 | 7956 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556305 | CIF | C44.5 H50 Cl5 Fe N3 O2 | P 1 21/n 1 | 9.2178; 29.17; 16.7749 90; 92.674; 90 | 4505.6 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556306 | CIF | C44.25 H49.5 Cl4.5 Co N3 O2 | P 1 21/c 1 | 12.8687; 19.6515; 18.0924 90; 90.931; 90 | 4574.8 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556307 | CIF | C44.5 H50 Cl5 Fe N3 S2 | C 1 2/c 1 | 34.005; 10.0092; 27.105 90; 94.482; 90 | 9197.3 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556308 | CIF | C44.5 H50 Cl5 Co N3 S2 | C 1 2/c 1 | 34.234; 10.0665; 27.315 90; 93.888; 90 | 9392 | Smit, Theo M.; Tomov, Atanas K.; Britovsek, George J. P.; Gibson, Vernon C.; White, Andrew J. P.; Williams, David J. The effect of imine-carbon substituents in bis(imino)pyridine-based ethylene polymerisation catalysts across the transition series Catalysis Science & Technology, 2012, 2, 643 |
1556309 | CIF | C19 H26 Cl O3 P Pd | P -1 | 7.8175; 16.296; 16.654 100.4; 100.58; 102.97 | 1977.2 | Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L. Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene Catalysis Science & Technology, 2012, 2, 715 |
1556310 | CIF | C22 H32 Cl O4 P Pd | P 1 21/n 1 | 9.552; 15.094; 16.038 90; 100.126; 90 | 2276.3 | Fuentes, José A.; Slawin, Alexandra M. Z.; Clarke, Matthew L. Application of palladium (trioxo-adamantyl cage phosphine)chloride complexes as catalysts for the alkoxycarbonylation of styrene; Pd catalysed tert-butoxycarbonylation of styrene Catalysis Science & Technology, 2012, 2, 715 |
1556311 | CIF | C18 H18 F12 N2 O2 | P -1 | 8.301; 10.979; 11.71 80.225; 85.04; 89.69 | 1047.7 | Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z. Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling Catalysis Science & Technology, 2012, 2, 934 |
1556312 | CIF | C18 H18 F12 N2 O2 | C 1 c 1 | 25.06; 6.782; 13.057 90; 110.81; 90 | 2074 | Legros, Julien; Bonnet-Delpon, Danièle; Crousse, Benoit; Slawin, Alexandra M. Z. Self-assembly between 1,4-diazabicyclo[2.2.2]octane and bis(hexafluoroalcohols): solid/liquid phase switching for catalyst recycling Catalysis Science & Technology, 2012, 2, 934 |
1556313 | CIF | C25 H24 Br N3 O5 Pd S | P -1 | 7.724; 13.385; 14 68.935; 83.939; 89.447 | 1342.5 | Srinivas, Keesara; Srinivas, Pottabathula; Prathima, Parvathaneni Sai; Balaswamy, Kodicherla; Sridhar, Balsubramanian; Rao, Mandapati Mohan Thiopseudourea ligated palladium complexes: synthesis, characterization and application as catalysts for Suzuki‒Miyaura, Sonogashira, Heck and Hiyama reactions Catalysis Science & Technology, 2012, 2, 1180 |
1556314 | CIF | C90 H84 Br0 N2 Ni O2 | P -1 | 10.515; 13.887; 15.272 80.61; 71.05; 70.1 | 1979.8 | Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene Catalysis Science & Technology, 2012, 2, 1340 |
1556315 | CIF | C78 H56 F4 N2 Ni O2 | C 1 2/c 1 | 47.225; 16.333; 17.278 90; 110.26; 90 | 12502 | Zhou, Zihong; Hao, Xiang; Redshaw, Carl; Chen, Langqiu; Sun, Wen-Hua Nickel bis{4,6-dibenzhydryl-2-[(arylimino)methyl]phenoxylate} complexes: Synthesis, structures, and catalytic behaviour towards ethylene and norbornene Catalysis Science & Technology, 2012, 2, 1340 |
1556316 | CIF | C17 H17 N O5 | P c a b | 8.8191; 17.5507; 20.7531 90; 90; 90 | 3212.2 | Ananthakrishnan, Rajakumar; Gazi, Sarifuddin [Ru(bpy)3]2+ aided photocatalytic synthesis of 2-arylpyridines via Hantzsch reaction under visible irradiation and oxygen atmosphere Catalysis Science & Technology, 2012, 2, 1463 |
1556317 | CIF | C40 H54 N2 O3 Zn | P -1 | 10.9698; 12.9718; 13.3427 91.834; 104.278; 92.66 | 1836.16 | Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P. A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium Catalysis Science & Technology, 2012, 2, 2231 |
1556318 | CIF | C68.5 H85 N4 O9 Zn2 | C 1 2/c 1 | 42.19; 9.719; 31.932 90; 110.08; 90 | 12297.6 | Taherimehr, Masoumeh; Decortes, Antonello; Al-Amsyar, Syed M.; Lueangchaichaweng, Warunee; Whiteoak, Christopher J.; Escudero-Adán, Eduardo C.; Kleij, Arjan W.; Pescarmona, Paolo P. A highly active Zn(salphen) catalyst for production of organic carbonates in a green CO2 medium Catalysis Science & Technology, 2012, 2, 2231 |
1556319 | CIF | C48 H38 Cl2 N2 O Ti | P b c a | 17.529; 18.752; 25.656 90; 90; 90 | 8433 | Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates Catalysis Science & Technology, 2012, 2, 2090 |
1556320 | CIF | C37 H32 Cl2 N2 O Ti | C 1 2/c 1 | 53.675; 10.021; 24.886 90; 100.29; 90 | 13170 | Huang, Wei; Zhang, Wenjuan; Sun, Wen-Hua; Wang, Lin; Redshaw, Carl Synthesis, characterization, and the ethylene (co-)polymerization behaviour of half-titanocene dichloride 2-aryliminoquinolin-8-olates Catalysis Science & Technology, 2012, 2, 2090 |
1556321 | CIF | C12 H12 Au Cl3 N2 | P 1 21/n 1 | 18.108; 9.5124; 18.3546 90; 113.59; 90 | 2897.4 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)–oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556322 | CIF | C12 H13 Au Cl4 N2 | C 1 2/c 1 | 22.1175; 14.791; 9.5257 90; 99.676; 90 | 3071.9 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556323 | CIF | C12 H12 Au Cl N2 O5 | P -1 | 7.6032; 9.2289; 9.96 82.321; 85.907; 88.085 | 690.65 | O'Neill, James A. T.; Rosair, Georgina M.; Lee, Ai-Lan Gold(iii)‒oxo complexes as catalysts in intramolecular hydroamination Catalysis Science & Technology, 2012, 2, 1818 |
1556324 | CIF | C40 H54 Cl4 N2 O3 Ru | P 1 21/c 1 | 20.5265; 13.4139; 29.7267 90; 91.812; 90 | 8180.9 | Leitgeb, Anita; Abbas, Mudassar; Fischer, Roland C.; Poater, Albert; Cavallo, Luigi; Slugovc, Christian A latent ruthenium based olefin metathesis catalyst with a sterically demanding NHC ligand Catalysis Science & Technology, 2012, 2, 1640 |
1556325 | CIF | C15 H29 Cl2 N3 Pd | P -1 | 8.1051; 11.1155; 22.6264 77.784; 89.987; 71.894 | 1888.9 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556326 | CIF | C15 H28 Cl2 N2 Pd S | P -1 | 8.1752; 15.2655; 15.457 94.321; 90.451; 93.185 | 1920.4 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556327 | CIF | C30 H56 Cl2 N4 O2 Pd | P 1 | 8.1693; 9.1162; 22.9935 93.592; 91.806; 89.939 | 1708.2 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556328 | CIF | C23 H45 Cl2 N3 Pd | P 1 21/c 1 | 15.7877; 21.0937; 8.109 90; 102.061; 90 | 2640.9 | Peral, Daniel; Gómez-Villarraga, Fernando; Sala, Xavier; Pons, Josefina; Carles Bayón, J.; Ros, Josep; Guerrero, Miguel; Vendier, Laure; Lecante, Pierre; García-Antón, Jordi; Philippot, Karine Palladium catalytic systems with hybrid pyrazole ligands in C‒C coupling reactions. Nanoparticles versus molecular complexes Catal. Sci. Technol., 2013, 3, 475 |
1556329 | CIF | C66 H64 Cl2 N4 O7.5 V2 | P 1 21/a 1 | 17.8598; 10.775; 31.054 90; 101.73; 90 | 5851.2 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556330 | CIF | C44 H56 N2 O2 | P 1 21/a 1 | 9.6297; 12.1792; 16.2276 90; 100.851; 90 | 1869.18 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556331 | CIF | C60 H86 Cl4 N2 O6 V2 | P b c a | 15.4851; 12.3449; 33.0323 90; 90; 90 | 6314.5 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556332 | CIF | C42 H52 Cl2 N4 O3 V | P 21 n b | 11.0873; 17.9157; 20.6832 90; 90; 90 | 4108.4 | Clowes, Lucy; Walton, Mark; Redshaw, Carl; Chao, Yimin; Walton, Alex; Elo, Pertti; Sumerin, Victor; Hughes, David L. Vanadium(iii) phenoxyimine complexes for ethylene or ε-caprolactone polymerization: mononuclear versus binuclear pre-catalysts Catal. Sci. Technol., 2013, 3, 152 |
1556333 | CIF | C54 H84 B Cl2 F4 P6 Rh3 | P 41 21 2 | 14.483; 14.483; 58.042 90; 90; 90 | 12175 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556334 | CIF | C85 H86 B Cl4 F4 O6 P6 Rh3 | P 1 | 13.136; 13.405; 14.779 85.58; 68.44; 68.06 | 2239.6 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556335 | CIF | C44 H72 Cl2 P4 Rh2 | P 21 21 21 | 14.1975; 16.3823; 20.5561 90; 90; 90 | 4781.1 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556336 | CIF | C135 H100 Cl6 F3 O3 P6 Rh3 S | P 1 21 1 | 16.493; 23.276; 16.775 90; 118.1; 90 | 5681 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556337 | CIF | C54 H84 B Br0.8 Cl1.2 F4 P6 Rh3 | P 21 21 21 | 16.431; 20.348; 21.116 90; 90; 90 | 7060 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556338 | CIF | C36 H56 Br2 P4 Rh2 | P 1 21 1 | 11.2912; 16.6047; 11.4464 90; 105.766; 90 | 2065.32 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556339 | CIF | C36 H86 B F4 O2 P6 Rh3 | P 1 | 12.416; 12.444; 18.186 95.81; 94.37; 111.98 | 2572.3 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556340 | CIF | C37 H86 B Cl4 F4 P6 Rh3 | P 1 | 9.6676; 12.005; 12.658 109.83; 94.19; 90.56 | 1377.3 | Preetz, Angelika; Kohrt, Christina; Meißner, Antje; Wei, Siping; Drexler, Hans-Joachim; Buschmann, Helmut; Heller, Detlef Halide bridged trinuclear rhodium complexes and their inhibiting influence on catalysis Catal. Sci. Technol., 2013, 3, 462 |
1556341 | CIF | C30.5 H30 Cl2 F6 N6 O3 P2 Ru | C 1 2/c 1 | 29.0844; 15.042; 16.3344 90; 108.315; 90 | 6784.1 | Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A. Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts Catal. Sci. Technol., 2013, 3, 706 |
1556342 | CIF | C30.5 H30.5 Cl2 F6 N6 O3.25 P2 Ru | P -1 | 10.9643; 11.9921; 15.491 110.491; 99.026; 107.666 | 1737.2 | Vaquer, Lydia; Riente, Paola; Sala, Xavier; Jansat, Susanna; Benet-Buchholz, Jordi; Llobet, Antoni; Pericàs, Miquel A. Molecular ruthenium complexes anchored on magnetic nanoparticles that act as powerful and magnetically recyclable stereospecific epoxidation catalysts Catal. Sci. Technol., 2013, 3, 706 |
1556343 | CIF | C80 H102 Al Cl N4 O6 S2 | P 41 21 2 | 13.6143; 13.6143; 38.6616 90; 90; 90 | 7165.9 | Ternel, Jérémy; Roussel, Pascal; Agbossou-Niedercorn, Francine; Gauvin, Régis M. Dismantling the salen framework: design of new asymmetric silylcyanation catalysts Catal. Sci. Technol., 2013, 3, 580 |
1556371 | CIF | C17 H15 Cl N4 O3 | P 21 21 21 | 7.129; 11.454; 19.387 90; 90; 90 | 1583.1 | Siddiqui, Zeba N.; Khan, Tabassum P2O5/SiO2 as an efficient heterogeneous catalyst for the synthesis of heterocyclic alkene derivatives under thermal solvent-free conditions Catalysis Science & Technology, 2013, 3, 2032 |
Back to the search form
Your own data is not in the COD? Deposit it, thanks!