Crystallography Open Database
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COD ID | Links | Formula | Space group | Cell parameters | Cell volume | Bibliography |
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4511774 | CIF | C22 H42 Cl N Ni P2 | P 21 21 21 | 11.354; 14.53; 14.976 90; 90; 90 | 2470.6 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511775 | CIF | C36 H56 N2 Ni P2 | P 42 b c | 18.924; 18.924; 19.322 90; 90; 90 | 6919.6 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511776 | CIF | C36 H55 N Ni O P2 | P 42 b c | 18.927; 18.927; 19.275 90; 90; 90 | 6904.9 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511777 | CIF | C36 H31 N Ni O P2 | P 1 n 1 | 14.1636; 11.3071; 18.0536 90; 90.216; 90 | 2891.2 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511778 | CIF | C42 H61 N Ni P2 S | P 1 21/n 1 | 11.218; 17.049; 20.543 90; 103.831; 90 | 3815 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511779 | CIF | C36 H31 N Ni P2 S | P c a 21 | 10.107; 17.521; 17.023 90; 90; 90 | 3015 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511780 | CIF | C30 H46.8 Cl0.2 N Ni O0.8 P2 | P 1 21/c 1 | 10.3866; 18.0201; 15.5109 90; 92.576; 90 | 2900.2 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511781 | CIF | C30 H51 N Ni P2 S | P 1 21/c 1 | 10.2239; 18.5337; 15.7104 90; 91.024; 90 | 2976.4 | Venkanna, Gopaladasu T.; Arman, Hadi D.; Tonzetich, Zachary J. Catalytic C‒S Cross-Coupling Reactions Employing Ni Complexes of Pyrrole-Based Pincer Ligands ACS Catalysis, 2014, 4, 2941 |
4511782 | CIF | C32 H57 B2 F8 N3 Ni P2 | P 1 21/c 1 | 12.2559; 15.9677; 19.9262 90; 102.37; 90 | 3809 | Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M. Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines ACS Catalysis, 2014, 4, 2951 |
4511783 | CIF | C26 H53 B2 F8 N5 Ni P2 | P 1 21 1 | 10.6454; 10.5867; 17.3734 90; 90.393; 90 | 1957.9 | Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M. Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines ACS Catalysis, 2014, 4, 2951 |
4511784 | CIF | C148 H222 B3 F12 N14 Ni3 P12 | P 1 2/n 1 | 14.8297; 11.6379; 43.244 90; 92.88; 90 | 7453.9 | Weiss, Charles J.; Das, Parthapratim; Miller, Deanna L.; Helm, Monte L.; Appel, Aaron M. Catalytic Oxidation of Alcohol via Nickel Phosphine Complexes with Pendant Amines ACS Catalysis, 2014, 4, 2951 |
4511901 | CIF | C32 H40 Cl Ir P2 | P n a 21 | 15.2261; 11.1905; 17.3055 90; 90; 90 | 2948.64 | Bézier, David; Brookhart, Maurice Applications of PC(sp3)P Iridium Complexes in Transfer Dehydrogenation of Alkanes ACS Catalysis, 2014, 4, 3411 |
4511978 | CIF | C46 H74 O P4 Pd2 S4 | P 1 21/c 1 | 18.0562; 14.0451; 22.0832 90; 113.61; 90 | 5131.5 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2014, 4, 3605 |
4511979 | CIF | C75 H138 Cl4 N2 P4 Pd2 S4 | P -1 | 10.2156; 16.2747; 26.6821 91.603; 90.239; 103.725 | 4307.4 | Espinosa-Jalapa, Noel Ángel; Ke, Diandian; Nebra, Noel; Le Goanvic, Lucas; Mallet-Ladeira, Sonia; Monot, Julien; Martin-Vaca, Blanca; Bourissou, Didier Enhanced Catalytic Performance of Indenediide Palladium Pincer Complexes for Cycloisomerization: Efficient Synthesis of Alkylidene Lactams ACS Catalysis, 2014, 4, 3605 |
4511980 | CIF | C18 H16 O6 | P -1 | 10.209; 11.5382; 15.259 72.37; 89.09; 66.272 | 1556.57 | Mbofana, Curren T.; Miller, Scott J. Phosphine-Catalyzed Annulation Reactions of 2-Butynoate and α-Keto Esters: Synthesis of Cyclopentene Derivatives ACS Catalysis, 2014, 4, 3671 |
4511995 | CIF | C16 H39 N4 O5 P | P -1 | 8.8946; 9.599; 14.595 105.46; 94.446; 114.78 | 1064.6 | Jeletic, Matthew S.; Helm, Monte L.; Hulley, Elliott B.; Mock, Michael T.; Appel, Aaron M.; Linehan, John C. A Cobalt Hydride Catalyst for the Hydrogenation of CO2: Pathways for Catalysis and Deactivation ACS Catalysis, 2014, 4, 3755 |
4511996 | CIF | C16 H35 N4 O2 P | P -1 | 9.492; 10.0652; 11.6878 72.135; 84.493; 64.509 | 958.49 | Jeletic, Matthew S.; Helm, Monte L.; Hulley, Elliott B.; Mock, Michael T.; Appel, Aaron M.; Linehan, John C. A Cobalt Hydride Catalyst for the Hydrogenation of CO2: Pathways for Catalysis and Deactivation ACS Catalysis, 2014, 4, 3755 |
4512057 | CIF | C16 H22 O6 | P 1 21 1 | 9.64383; 5.51183; 14.44803 90; 95.6537; 90 | 764.251 | Kim, Junghwa; Lee, Dong-Hwan; Kalutharage, Nishantha; Yi, Chae S. Selective Catalytic Synthesis of Unsymmetrical Ethers from the Dehydrative Etherification of Two Different Alcohols ACS Catalysis, 2014, 4, 3881 |
4512058 | CIF | C35 H54 O2 | P 1 21 1 | 12.0622; 9.18339; 13.6306 90; 94.3; 90 | 1505.64 | Kim, Junghwa; Lee, Dong-Hwan; Kalutharage, Nishantha; Yi, Chae S. Selective Catalytic Synthesis of Unsymmetrical Ethers from the Dehydrative Etherification of Two Different Alcohols ACS Catalysis, 2014, 4, 3881 |
4512105 | CIF | C44 H31 Cl Ir N2 O2 P | P -1 | 11.7801; 14.2655; 17.1787 88.278; 80.64; 69.608 | 2668.8 | Wang, Dawei; Zhao, Keyan; Xu, Chongying; Miao, Hongyan; Ding, Yuqiang Synthesis, Structures of Benzoxazolyl Iridium(III) Complexes, and Applications on C‒C and C‒N Bond Formation Reactions under Solvent-Free Conditions: Catalytic Activity Enhanced by Noncoordinating Anion without Silver Effect ACS Catalysis, 2014, 4, 3910 |
4512106 | CIF | C38 H43 Cl Ir N2 O2 P | P 1 21/c 1 | 9.2237; 23.848; 16.3363 90; 103.348; 90 | 3496.4 | Wang, Dawei; Zhao, Keyan; Xu, Chongying; Miao, Hongyan; Ding, Yuqiang Synthesis, Structures of Benzoxazolyl Iridium(III) Complexes, and Applications on C‒C and C‒N Bond Formation Reactions under Solvent-Free Conditions: Catalytic Activity Enhanced by Noncoordinating Anion without Silver Effect ACS Catalysis, 2014, 4, 3910 |
4512210 | CIF | C46 H51 B Cl6 Cu N7 O | P -1 | 11.8005; 12.088; 18.1433 101.21; 93.076; 105.213 | 2434.7 | Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J. Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles ACS Catalysis, 2014, 4, 4215 |
4512211 | CIF | C16.5 H7 B Br9 Cl Cu N7 S | P -1 | 11.1605; 13.8447; 19.6313 83.707; 80.497; 79.114 | 2928.2 | Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J. Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles ACS Catalysis, 2014, 4, 4215 |
4512212 | CIF | C17 H17 N O4 | P -1 | 7.9337; 8.6976; 11.8982 110.549; 102.752; 93.549 | 741.04 | Corro, Macarena; Besora, Maria; Maya, Celia; Álvarez, Eleuterio; Urbano, Juan; Fructos, Manuel R.; Maseras, Feliu; Pérez, Pedro J. Catalytic Copper-Mediated Ring Opening and Functionalization of Benzoxazoles ACS Catalysis, 2014, 4, 4215 |
4512224 | CIF | C34 H46 Cl N4 Rh | P 1 21/c 1 | 24.481; 13.201; 20.184 90; 93.847; 90 | 6508.2 | Azpíroz, Ramón; Rubio-Pérez, Laura; Di Giuseppe, Andrea; Passarelli, Vincenzo; Lahoz, Fernando J.; Castarlenas, Ricardo; Pérez-Torrente, Jesús J.; Oro, Luis A. Rhodium(I)-N-Heterocyclic Carbene Catalyst for Selective Coupling ofN-Vinylpyrazoles with Alkynes via C‒H Activation ACS Catalysis, 2014, 4, 4244 |
4512225 | CIF | C39 H51 Cl N5 Rh | P 1 21/n 1 | 15.579; 13.803; 18.6728 90; 112.173; 90 | 3718.4 | Azpíroz, Ramón; Rubio-Pérez, Laura; Di Giuseppe, Andrea; Passarelli, Vincenzo; Lahoz, Fernando J.; Castarlenas, Ricardo; Pérez-Torrente, Jesús J.; Oro, Luis A. Rhodium(I)-N-Heterocyclic Carbene Catalyst for Selective Coupling ofN-Vinylpyrazoles with Alkynes via C‒H Activation ACS Catalysis, 2014, 4, 4244 |
4512242 | CIF | C26 H26 N3 O7 S2 | P 1 21 1 | 10.08; 20.648; 13.183 90; 107.503; 90 | 2616.8 | Ohmatsu, Kohsuke; Kawai, Shinya; Imagawa, Naomichi; Ooi, Takashi Palladium-Catalyzed Asymmetric [3 + 2] Cycloaddition of 5-Vinyloxazolidinones with Imines Using Chiral Ammonium-Phosphine Hybrid Ligand ACS Catalysis, 2014, 4, 4304 |
4512275 | CIF | C15 H11 Cl O | P 1 21/c 1 | 5.8543; 22.954; 8.9509 90; 96.206; 90 | 1195.8 | Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides ACS Catalysis, 2014, 4, 4485 |
4512276 | CIF | C22 H18 O | P 1 21/n 1 | 5.8215; 8.3087; 33.2148 90; 94.567; 90 | 1601.47 | Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides ACS Catalysis, 2014, 4, 4485 |
4512277 | CIF | C17 H16 O | P 1 21/c 1 | 12.7973; 6.1187; 16.9311 90; 101.782; 90 | 1297.82 | Gandeepan, Parthasarathy; Rajamalli, P.; Cheng, Chien-Hong Palladium-Catalyzed Dehydrogenative β-Arylation of Simple Saturated Carbonyls by Aryl Halides ACS Catalysis, 2014, 4, 4485 |
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