Crystallography Open Database

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4511551 CIFC56 H38 N8 Ni2 O13P 1 21/n 116.2122; 16.0154; 20.1031
90; 110.772; 90
4880.4Han, Zheng-Bo; Cheng, Xiao-Ning; Chen, Xiao-Ming
Effect of the Size of Aromatic Chelate Ligands on the Frameworks of Metal Dicarboxylate Polymers: From Helical Chains to 2-D Networks
Crystal Growth & Design, 2005, 5, 695
4511552 CIFC24 H21 Cl N4 O2P 21 21 216.852; 17.012; 17.31
90; 90; 90
2017.8Arora, Kapildev K.; Pedireddi, V. R.
Poly(pseudo)rotaxane-like Network Mediated by Hydrogen Bonds in the Solid-State Structure of 1,7-Phenanthroline
Crystal Growth & Design, 2005, 5, 1309
4511553 CIFC24 H16 N4P -18.926; 9.101; 12.193
72.56; 72.35; 88.1
898.7Arora, Kapildev K.; Pedireddi, V. R.
Poly(pseudo)rotaxane-like Network Mediated by Hydrogen Bonds in the Solid-State Structure of 1,7-Phenanthroline
Crystal Growth & Design, 2005, 5, 1309
4511554 CIFC22 H25 Ag2 F12 N7 P2 SP 1 2/c 116.309; 14.636; 13.941
90; 93.67; 90
3320.9Amoore, Jarrod J. M.; Black, Cory A.; Hanton, Lyall R.; Spicer, Mark D.
Increasing Structural Dimensionality in Ag(I) Coordination Polymers Formed from the Same Flexible Multimodal Thioether Pyrazine Ligand
Crystal Growth & Design, 2005, 5, 1255
4511555 CIFC10 H10 Ag F6 N4 P SP 1 21/c 19.9188; 12.8858; 11.7449
90; 100.646; 90
1475.3Amoore, Jarrod J. M.; Black, Cory A.; Hanton, Lyall R.; Spicer, Mark D.
Increasing Structural Dimensionality in Ag(I) Coordination Polymers Formed from the Same Flexible Multimodal Thioether Pyrazine Ligand
Crystal Growth & Design, 2005, 5, 1255
4511556 CIFC21 H23 Ag2 B2 F8 N9 O2 S2P 1 21/a 110.7108; 13.2616; 20.7926
90; 92.5034; 90
2950.61Amoore, Jarrod J. M.; Black, Cory A.; Hanton, Lyall R.; Spicer, Mark D.
Increasing Structural Dimensionality in Ag(I) Coordination Polymers Formed from the Same Flexible Multimodal Thioether Pyrazine Ligand
Crystal Growth & Design, 2005, 5, 1255
4511557 CIFC12 H20 Cd N14 O8P 1 21/c 18.767; 12.523; 10.476
90; 100.963; 90
1129.2Yi, Long; Yang, Xing; Lu, Tongbu; Cheng, Peng
Self-Assembly of Right-Handed Helical Infinite Chain, One- and Two-Dimensional Coordination Polymers Tuned via Anions
Crystal Growth & Design, 2005, 5, 1215
4511558 CIFC12 H20 N14 O8 ZnP 1 21/c 18.661; 12.412; 10.288
90; 100.717; 90
1086.7Yi, Long; Yang, Xing; Lu, Tongbu; Cheng, Peng
Self-Assembly of Right-Handed Helical Infinite Chain, One- and Two-Dimensional Coordination Polymers Tuned via Anions
Crystal Growth & Design, 2005, 5, 1215
4511559 CIFC6 H8 Cl2 N6 ZnP 41 21 29.631; 9.631; 12.325
90; 90; 90
1143.2Yi, Long; Yang, Xing; Lu, Tongbu; Cheng, Peng
Self-Assembly of Right-Handed Helical Infinite Chain, One- and Two-Dimensional Coordination Polymers Tuned via Anions
Crystal Growth & Design, 2005, 5, 1215
4511560 CIFC12 H24 Cd Cl2 N12 O12P -18.404; 8.618; 10.385
66.379; 76.161; 77.081
662.2Yi, Long; Yang, Xing; Lu, Tongbu; Cheng, Peng
Self-Assembly of Right-Handed Helical Infinite Chain, One- and Two-Dimensional Coordination Polymers Tuned via Anions
Crystal Growth & Design, 2005, 5, 1215
4511561 CIFC23 H25 N11 O16P -17.604; 13.403; 16.366
109.47; 98.36; 99.17
1516.8MacDonald, John C.; Yigit, Mehmet V.; Mychajlonka, Kyle
Two Concomitant Polymorphs of a Supramolecular Model of the Asp···His···Ser Catalytic Triad
Crystal Growth & Design, 2005, 5, 2248
4511562 CIFC23 H25 N11 O16C 1 2/c 133.908; 7.765; 25.389
90; 114.74; 90
6071MacDonald, John C.; Yigit, Mehmet V.; Mychajlonka, Kyle
Two Concomitant Polymorphs of a Supramolecular Model of the Asp···His···Ser Catalytic Triad
Crystal Growth & Design, 2005, 5, 2248
4511563 CIFC50 H43 Mn2 N5 O16P -112.6912; 13.367; 16.295
97; 102.73; 117.685
2305.8Dobrzyńska, Danuta; Jerzykiewicz, Lucjan B.; Jezierska, Julia; Duczmal, Marek
Crystal Structure and Characterization of Manganese(II) Carboxylates: 3D Metal−Organic Frameworks
Crystal Growth & Design, 2005, 5, 1945
4511564 CIFC12 H11 N3 O4P 1 21/c 111.3931; 15.4265; 7.6611
90; 106.208; 90
1292.97Naumov, Panče; Sakurai, Kenji
Reversible Thermal Gating of the Photochromic Properties of 3-Methyl-2-(2‘,4‘-dinitrobenzyl)pyridine in a Single Crystal
Crystal Growth & Design, 2005, 5, 1699
4511565 CIFC12 H11 N3 O4P 1 21/c 111.5668; 15.3271; 7.6407
90; 105.885; 90
1302.86Naumov, Panče; Sakurai, Kenji
Reversible Thermal Gating of the Photochromic Properties of 3-Methyl-2-(2‘,4‘-dinitrobenzyl)pyridine in a Single Crystal
Crystal Growth & Design, 2005, 5, 1699
4511566 CIFC12 H11 N3 O4P 1 21/c 111.386; 15.422; 7.658
90; 106.188; 90
1291.39Naumov, Panče; Sakurai, Kenji
Reversible Thermal Gating of the Photochromic Properties of 3-Methyl-2-(2‘,4‘-dinitrobenzyl)pyridine in a Single Crystal
Crystal Growth & Design, 2005, 5, 1699
4511567 CIFC12 H11 N3 O4P 1 21/c 111.62; 15.38; 7.668
90; 105.948; 90
1317.65Naumov, Panče; Sakurai, Kenji
Reversible Thermal Gating of the Photochromic Properties of 3-Methyl-2-(2‘,4‘-dinitrobenzyl)pyridine in a Single Crystal
Crystal Growth & Design, 2005, 5, 1699
4511568 CIFC12 H11 N3 O4P 1 21/c 111.385; 15.422; 7.659
90; 106.176; 90
1291.52Naumov, Panče; Sakurai, Kenji
Reversible Thermal Gating of the Photochromic Properties of 3-Methyl-2-(2‘,4‘-dinitrobenzyl)pyridine in a Single Crystal
Crystal Growth & Design, 2005, 5, 1699
4511569 CIFC42 H58 N12 O16 S2 Zn2P 1 21/n 115.796; 13.704; 24.555
90; 92.42; 90
5310.6Carlucci, Lucia; Ciani, Gianfranco; Proserpio, Davide M.
Parallel and Inclined (1D →2D) Interlacing Modes in New Polyrotaxane Frameworks [M2(bix)3(SO4)2] [M = Zn(II), Cd(II); Bix = 1,4-Bis(imidazol-1-ylmethyl)benzene]
Crystal Growth & Design, 2005, 5, 37
4511570 CIFC21 H21 Cd N6 O4 SP 1 21/n 113.8132; 11.1759; 14.4009
90; 96.37; 90
2209.4Carlucci, Lucia; Ciani, Gianfranco; Proserpio, Davide M.
Parallel and Inclined (1D →2D) Interlacing Modes in New Polyrotaxane Frameworks [M2(bix)3(SO4)2] [M = Zn(II), Cd(II); Bix = 1,4-Bis(imidazol-1-ylmethyl)benzene]
Crystal Growth & Design, 2005, 5, 37
4511571 CIFC21 H25 Cd N6 O6 SP 1 21/c 110.1323; 18.6237; 12.6038
90; 100.3; 90
2340Carlucci, Lucia; Ciani, Gianfranco; Proserpio, Davide M.
Parallel and Inclined (1D →2D) Interlacing Modes in New Polyrotaxane Frameworks [M2(bix)3(SO4)2] [M = Zn(II), Cd(II); Bix = 1,4-Bis(imidazol-1-ylmethyl)benzene]
Crystal Growth & Design, 2005, 5, 37
4511572 CIFC32 H40 Cl2 Cu2 N6 O12P -18.6613; 10.5768; 11.0798
81.366; 80.022; 69.272
930.59Marin, Geanina; Tudor, Violeta; Kravtsov, Victor Ch.; Schmidtmann, Marc; Simonov, Yurii A.; Müller, Achim; Andruh, Marius
Extended Structures Constructed from Alkoxo-Bridged Binuclear Complexes as Nodes and Bis(4-pyridyl)ethylene as a Spacer
Crystal Growth & Design, 2005, 5, 279
4511573 CIFC14 H16 Cl Cu N3 O5P 1 21/c 110.238; 11.749; 14.548
90; 95.35; 90
1742.3Marin, Geanina; Tudor, Violeta; Kravtsov, Victor Ch.; Schmidtmann, Marc; Simonov, Yurii A.; Müller, Achim; Andruh, Marius
Extended Structures Constructed from Alkoxo-Bridged Binuclear Complexes as Nodes and Bis(4-pyridyl)ethylene as a Spacer
Crystal Growth & Design, 2005, 5, 279
4511574 CIFC19 H42 N2 O2 SP 1 21/n 15.6334; 39.286; 9.6819
90; 91.276; 90
2142.2Morris, David G.; Ryder, Karl S.; Muir, Kenneth W.
A Model for a Lipid Membrane Stabilized by C−H···X Bonds: The Crystal Structure of the Paraffinic Ylide Trimethylammonion-Hexadecylsulfonamidate CH3(CH2)15SO2N(−)N(+)Me3
Crystal Growth & Design, 2005, 5, 361
4511662 CIFC42 H45 N O13P 1 21 115.5024; 6.2258; 20.953
90; 101.598; 90
1981Calosso, Mickael; Tambutet, Guillaume; Charpentier, Daniel; St-Pierre, Gabrielle; Vaillancourt, Marc; Bencheqroun, Mohammed; Gratton, Jean-Philippe; Prévost, Michel; Guindon, Yvan
Acyclic tethers mimicking subunits of polysaccharide ligands: selectin antagonists.
ACS medicinal chemistry letters, 2014, 5, 1054-1059
4511858 CIFC30 H22 Cl N O5P 1 21/c 120.3663; 6.5008; 18.3376
90; 104.897; 90
2346.25Li, Bingbing X.; Xie, Fuchun; Fan, Qiuhua; Barnhart, Kerry M.; Moore, Curtis E.; Rheingold, Arnold L.; Xiao, Xiangshu
Novel Type of Prodrug Activation through a Long-Range O,N-Acyl Transfer: A Case of Water-Soluble CREB Inhibitor.
ACS medicinal chemistry letters, 2014, 5, 1104-1109
4512454 CIFC17 H26 O4P 1 21/c 15.4051; 35.529; 16.8799
90; 99.541; 90
3196.7Weiss, Marcel; Peters, René
Catalytic Direct Dehydrogenative Cross-Couplings of C–H (Pro)Nucleophiles and Allylic Alcohols without an Additional Oxidant
ACS Catalysis, 2015, 5, 310
4512455 CIFC23 H27 N OP 1 21 15.1067; 11.928; 15.558
90; 96.711; 90
941.19Weiss, Marcel; Peters, René
Catalytic Direct Dehydrogenative Cross-Couplings of C–H (Pro)Nucleophiles and Allylic Alcohols without an Additional Oxidant
ACS Catalysis, 2015, 5, 310
4512456 CIFC22 H19 F4 N O4P 21 21 2112.878; 15.68; 19.97
90; 90; 90
4032Avidan-Shlomovich, Shlomit; Ghosh, Harisadhan; Szpilman, Alex M.
Synthetic and Mechanistic Study of the Catalytic Enantioselective Preparation of Primary β-Amino Ketones from Enones and a Fluorinated Gabriel Reagent
ACS Catalysis, 2015, 5, 336
4512457 CIFC22 H27.5 Cl2 N3.5 Ni O8 PC 1 2/c 128.443; 8.4569; 22.9631
90; 107.39; 90
5271.1Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512458 CIFC15 H25 Cl2 N3 Ni O8 SP -18.7289; 8.7999; 13.9708
93.47; 106.608; 93.681
1022.76Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512459 CIFC30 H42 Cl4 N6 Ni2 O8 S2P -18.0156; 12.2115; 19.7215
91.373; 99.117; 93.388
1901.6Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512460 CIFC24 H36 Cl2 N3 Ni O9 PP -19.3883; 13.0308; 13.093
79.943; 89.364; 73.953
1514.52Chen, Lingjing; Chen, Gui; Leung, Chi-Fai; Yiu, Shek-Man; Ko, Chi-Chiu; Anxolabéhère-Mallart, Elodie; Robert, Marc; Lau, Tai-Chu
Dual Homogeneous and Heterogeneous Pathways in Photo- and Electrocatalytic Hydrogen Evolution with Nickel(II) Catalysts Bearing Tetradentate Macrocyclic Ligands
ACS Catalysis, 2015, 5, 356
4512489 CIFC20 H16 Br Fe N5C 1 2/c 116.847; 13.0275; 16.3223
90; 96.25; 90
3561Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512490 CIFC25 H24 F3 Fe N5 O4 SP 18.4756; 8.8071; 18.6806
99.732; 90.796; 112.598
1264.06Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512491 CIFC23 H19 F6 Fe N5 O6 S2P -110.7036; 12.1278; 12.2733
66.351; 73.133; 69.747
1347.8Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Regulation of Iron-Catalyzed Olefin Hydroboration by Ligand Modifications at a Remote Site
ACS Catalysis, 2015, 5, 411
4512510 CIFC40 H36 Cl2 F3 N3 O7 P Re SP 1 21/n 112.089; 9.0476; 36.982
90; 91.534; 90
4043.5Liu, Jinyong; Choe, Jong Kwon; Wang, Yin; Shapley, John R.; Werth, Charles J.; Strathmann, Timothy J.
Bioinspired Complex-Nanoparticle Hybrid Catalyst System for Aqueous Perchlorate Reduction: Rhenium Speciation and Its Influence on Catalyst Activity
ACS Catalysis, 2015, 5, 511
4512511 CIFC55 H46 F3 N2 O7 P2 Re SP 21 21 2111.209; 11.6194; 37.5809
90; 90; 90
4894.6Liu, Jinyong; Choe, Jong Kwon; Wang, Yin; Shapley, John R.; Werth, Charles J.; Strathmann, Timothy J.
Bioinspired Complex-Nanoparticle Hybrid Catalyst System for Aqueous Perchlorate Reduction: Rhenium Speciation and Its Influence on Catalyst Activity
ACS Catalysis, 2015, 5, 511
4512512 CIFC37 H56 Co N3 SiP 1 21/n 117.8016; 12.0498; 18.7953
90; 117.63; 90
3571.93Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512513 CIFC31 H45 Co N2C 1 2/c 116.1764; 9.2233; 18.8751
90; 92.623; 90
2813.2Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512514 CIFC38 H57 Co N2C 1 2/c 138.978; 10.046; 18.259
90; 104.3; 90
6928Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512515 CIFC19 H22 Co N3 SiP 1 21/n 111.086; 19.096; 16.774
90; 94.52; 90
3540Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512516 CIFC14 H21 Cl Co N2 SiR -3 :H31.103; 31.103; 9.4729
90; 90; 120
7936.3Palmer, W. Neil; Diao, Tianning; Pappas, Iraklis; Chirik, Paul J.
High-Activity Cobalt Catalysts for Alkene Hydroboration with Electronically Responsive Terpyridine and α-Diimine Ligands
ACS Catalysis, 2015, 5, 622
4512529 CIFC45 H40 F4 N3 O P RuP 21 21 2113.869; 16.834; 16.985
90; 90; 90
3965.5McKay, David; Riddlestone, Ian M.; Macgregor, Stuart A.; Mahon, Mary F.; Whittlesey, Michael K.
Mechanistic Study of Ru-NHC-Catalyzed Hydrodefluorination of Fluoropyridines: The Influence of the NHC on the Regioselectivity of C‒F Activation and Chemoselectivity of C‒F versus C‒H Bond Cleavage
ACS Catalysis, 2015, 5, 776
4512584 CIFC12 H20 Cl N3 NiP c a 2116.1973; 9.2551; 18.251
90; 90; 90
2736Pérez García, Pablo M.; Ren, Peng; Scopelliti, Rosario; Hu, Xile
Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
ACS Catalysis, 2015, 5, 1164
4512585 CIFC20 H25 N3 NiP 1 21/n 19.7694; 14.6639; 12.8939
90; 100.806; 90
1814.4Pérez García, Pablo M.; Ren, Peng; Scopelliti, Rosario; Hu, Xile
Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
ACS Catalysis, 2015, 5, 1164
4512586 CIFC144 H154 B2 Fe3 O13 P8P -114.7034; 15.3502; 30.5317
81.607; 77.192; 79.041
6558.1Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512587 CIFC42 H44 Fe P4P -111.3961; 11.8042; 14.9611
88.014; 81.462; 63.904
1786.33Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512588 CIFC49 H58 B F4 Fe N P4P -111.6311; 12.2422; 18.0737
104.224; 98.681; 106.392
2325.12Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512589 CIFC66 H63 B Fe P4P -112.4918; 13.5351; 19.2058
92.091; 105.612; 94.273
3113.4Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512590 CIFC103 H117 B4 F16 Fe2 N7 P8C 1 2/c 133.6116; 14.8734; 20.7957
90; 105.833; 90
10001.7Bertini, Federica; Mellone, Irene; Ienco, Andrea; Peruzzini, Maurizio; Gonsalvi, Luca
Iron(II) Complexes of the Linearrac-Tetraphos-1 Ligand as Efficient Homogeneous Catalysts for Sodium Bicarbonate Hydrogenation and Formic Acid Dehydrogenation
ACS Catalysis, 2015, 5, 1254
4512815 CIFC58 H58 B2 F8 N2 Ni P4P 1 21/n 19.2602; 20.7179; 14.2353
90; 97.2; 90
2709.5Brown, Houston J. S.; Wiese, Stefan; Roberts, John A. S.; Bullock, R. Morris; Helm, Monte L.
Electrocatalytic Hydrogen Production by [Ni(7PPh2NH)2]2+: Removing the Distinction Between Endo- and Exo-Protonation Sites
ACS Catalysis, 2015, 5, 2116
4512816 CIFC38 H44 B2 Cl4 F14 N2 Ni O4 P4P -110.3197; 13.2465; 19.7249
94.91; 101.046; 109.554
2460.92Brown, Houston J. S.; Wiese, Stefan; Roberts, John A. S.; Bullock, R. Morris; Helm, Monte L.
Electrocatalytic Hydrogen Production by [Ni(7PPh2NH)2]2+: Removing the Distinction Between Endo- and Exo-Protonation Sites
ACS Catalysis, 2015, 5, 2116
4512852 CIFC58 H81 F12 Fe2 N9 O18 S4P 21 21 2116.9742; 17.1155; 50.282
90; 90; 90
14608Lyakin, Oleg Y.; Zima, Alexandra M.; Samsonenko, Denis G.; Bryliakov, Konstantin P.; Talsi, Evgenii P.
EPR Spectroscopic Detection of the Elusive FeV═O Intermediates in Selective Catalytic Oxofunctionalizations of Hydrocarbons Mediated by Biomimetic Ferric Complexes
ACS Catalysis, 2015, 5, 2702
4512854 CIFC31 H27 F3 N2 O4 SP -19.4555; 12.671; 13.141
89.372; 83.024; 70.301
1470.6Ghorai, Debasish; Choudhury, Joyanta
Rhodium(III)‒N-Heterocyclic Carbene-Driven Cascade C‒H Activation Catalysis
ACS Catalysis, 2015, 5, 2692
4512855 CIFC45 H31 F3 N2 O3 SP -110.6172; 12.7911; 14.6372
102.793; 106.868; 96.17
1823.39Ghorai, Debasish; Choudhury, Joyanta
Rhodium(III)‒N-Heterocyclic Carbene-Driven Cascade C‒H Activation Catalysis
ACS Catalysis, 2015, 5, 2692
4512856 CIFC12 H10 N2 Ni S2P 1 21/c 112.301; 5.883; 8.098
90; 95.547; 90
583.3Das, Amit; Han, Zhiji; Brennessel, William W.; Holland, Patrick L.; Eisenberg, Richard
Nickel Complexes for Robust Light-Driven and Electrocatalytic Hydrogen Production from Water
ACS Catalysis, 2015, 5, 1397
4512857 CIFC20 H36 N2 Ni O4 S6P -18.3237; 11.0567; 15.928
92.197; 99.883; 94.145
1438.4Das, Amit; Han, Zhiji; Brennessel, William W.; Holland, Patrick L.; Eisenberg, Richard
Nickel Complexes for Robust Light-Driven and Electrocatalytic Hydrogen Production from Water
ACS Catalysis, 2015, 5, 1397
4512930 CIFC10 H17 N O3P 21 21 219.8502; 13.6853; 16.4912
90; 90; 90
2223.1Bae, Han Yong; Song, Choong Eui
Unprecedented Hydrophobic Amplification in Noncovalent Organocatalysis “on Water”: Hydrophobic Chiral Squaramide Catalyzed Michael Addition of Malonates to Nitroalkenes
ACS Catalysis, 2015, 5, 3613
4512945 CIFC36 H52 Br Co N2 O2P 110.795; 12.6416; 14.6957
65.979; 89.9734; 71.994
1723.83North, Michael; Quek, Sophie C. Z.; Pridmore, Natalie E.; Whitwood, Adrian C.; Wu, Xiao
Aluminum(salen) Complexes as Catalysts for the Kinetic Resolution of Terminal Epoxides via CO2Coupling
ACS Catalysis, 2015, 5, 3398
4512946 CIFC16 H12 F3 N O2P -18.167; 8.306; 10.825
91.64; 99.308; 92.741
723.3Albaladejo, María José; Alonso, Francisco; González-Soria, María José
Synthetic and Mechanistic Studies on the Solvent-Dependent Copper-Catalyzed Formation of Indolizines and Chalcones
ACS Catalysis, 2015, 5, 3446
4512947 CIFBi4 Na20.72 O213.36 W36 Zn8P 1 21/n 113.234; 17.661; 20.966
90; 93.12; 90
4893Amanchi, Srinivasa Rao; Khenkin, Alexander M.; Diskin-Posner, Yael; Neumann, Ronny
Bismuth-Substituted “Sandwich” Type Polyoxometalate Catalyst for Activation of Peroxide: Umpolung of the Peroxo Intermediate and Change of Chemoselectivity
ACS Catalysis, 2015, 5, 3336
4512948 CIFBi2 Na4 O98.55 W18 Zn6P n n m16.187; 19.43; 14.641
90; 90; 90
4604.8Amanchi, Srinivasa Rao; Khenkin, Alexander M.; Diskin-Posner, Yael; Neumann, Ronny
Bismuth-Substituted “Sandwich” Type Polyoxometalate Catalyst for Activation of Peroxide: Umpolung of the Peroxo Intermediate and Change of Chemoselectivity
ACS Catalysis, 2015, 5, 3336
4513027 CIFC23 H24 Br N OP 21 21 217.2425; 15.4541; 17.01
90; 90; 90
1903.9Hu, Haoxiang; Meng, Chunna; Dong, Yun; Li, Xin; Ye, Jinxing
Catalytic Asymmetric Formal Aza-Diels–Alder Reactions of α,β-Unsaturated Ketones and 3H-Indoles
ACS Catalysis, 2015, 5, 3700
4513028 CIFC15 H B Br3 F18 N6 TlP -19.4814; 10.765; 13.9827
111.406; 92.343; 99.301
1303.49Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C–H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513029 CIFC17 H4 B Br3 Cu F18 N7C 1 2/c 121.9569; 16.6067; 17.0174
90; 105.863; 90
5968.8Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C–H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513030 CIFC19 H9 Ag B Br3 F18 N6 OP -19.5396; 12.6988; 12.9452
100.867; 94.371; 98.592
1514Gava, Riccardo; Olmos, Andrea; Noverges, Bárbara; Varea, Teresa; Álvarez, Eleuterio; Belderrain, Tomás R.; Caballero, Ana; Asensio, Gregorio; Pérez, Pedro J.
Discovering Copper for Methane C–H Bond Functionalization
ACS Catalysis, 2015, 5, 3726
4513043 CIFC24 H20 N4 O5 Ru SP -18.7507; 10.3497; 14.1618
79.212; 73.228; 77.234
1187.17Wang, Ying; Duan, Lele; Wang, Lei; Chen, Hong; Sun, Junliang; Sun, Licheng; Ahlquist, Mårten S. G.
Alkene Epoxidation Catalysts [Ru(pdc)(tpy)] and [Ru(pdc)(pybox)] Revisited: Revealing a Unique RuIV═O Structure from a Dimethyl Sulfoxide Coordinating Complex
ACS Catalysis, 2015, 5, 3966
4513044 CIFC45 H57 Cl F N2 O3 P RuP -19.25; 10.543; 21.668
84.919; 89.766; 81.66
2082.5Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513045 CIFC45 H57 F2 N2 O3 P RuP -19.123; 10.569; 21.751
94.901; 90.209; 99.166
2062.6Guidone, Stefano; Songis, Olivier; Falivene, Laura; Nahra, Fady; Slawin, Alexandra M. Z.; Jacobsen, Heiko; Cavallo, Luigi; Cazin, Catherine S. J.
Ruthenium Olefin Metathesis Catalysts Containing Fluoride
ACS Catalysis, 2015, 5, 3932
4513186 CIFC49 H47 Cl F6 N2 P2 RuP -111.185; 12.2337; 15.712
87.763; 85.343; 75.988
2078.7Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513187 CIFC45 H47 Cl F6 N2 P2 RuC 1 c 118.524; 15.304; 14.862
90; 98.269; 90
4169.4Xie, Xiaoke; Huynh, Han Vinh
Tunable Dehydrogenative Amidation versus Amination Using a Single Ruthenium-NHC Catalyst
ACS Catalysis, 2015, 5, 4143
4513215 CIFC32 H28 B Fe PP 21 21 217.8373; 11.1807; 28.7574
90; 90; 90
2519.91Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513216 CIFC20 H25 NP 1 21 18.4925; 18.0565; 21.7726
90; 92.034; 90
3336.61Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513217 CIFC18 H21 NP -17.6079; 9.9255; 10.7036
113.746; 100.964; 95.416
713.05Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C–H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513218 CIFC25 H29 Fe N OP 21 21 2110.843; 12.6988; 15.1797
90; 90; 90
2090.14Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C‒H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513219 CIFC43 H38 N O3.5 P Pd SP 41 21 214.5165; 14.5165; 37.1387
90; 90; 90
7826.2Holstein, Philipp M.; Vogler, Maria; Larini, Paolo; Pilet, Guillaume; Clot, Eric; Baudoin, Olivier
Efficient Pd0-Catalyzed Asymmetric Activation of Primary and Secondary C–H Bonds Enabled by Modular Binepine Ligands and Carbonate Bases
ACS Catalysis, 2015, 5, 4300
4513383 CIFC72 H78 N4 O11 Ti2P 43 21 212.3687; 12.3687; 44.436
90; 90; 90
6798Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513384 CIFC76 H78 N4 O11 Ti2P 31 2 119.0457; 19.0457; 41.0671
90; 90; 120
12900.9Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513385 CIFC65 H61 Cl3 N4 O6 Ti2P 1 21 111.5315; 19.176; 13.4627
90; 98.481; 90
2944.4Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513386 CIFC68 H66 Br4 N4 O7 Ti2P 43 21 212.2324; 12.2324; 45.9762
90; 90; 90
6879.5Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513387 CIFC64 H56 Br4 N4 O6 Ti2P 113.8302; 15.4438; 16.7517
108.353; 90.647; 116.089
3002.56Talsi, Evgenii P.; Rybalova, Tatyana V.; Bryliakov, Konstantin P.
Isoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
ACS Catalysis, 2015, 5, 4673
4513439 CIFC54 H47 N4 O7P 21 21 2112.3766; 16.424; 28.578
90; 90; 90
5809.1Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513440 CIFC22 H22 N2 O3P 1 21 110.202; 7.487; 11.933
90; 100.922; 90
895Alcaide, Benito; Almendros, Pedro; Fernández, Israel; Martín-Montero, Raúl; Martínez-Peña, Francisco; Ruiz, M. Pilar; Torres, M. Rosario
Gold-Catalyzed Reactivity Reversal of Indolizidinone-Tethered β-Amino Allenes Controlled by the Stereochemistry
ACS Catalysis, 2015, 5, 4842
4513441 CIFC22 H16 F3 N O3 SC 1 2/c 140.887; 9.2404; 27.6197
90; 131.709; 90
7790.1Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)–H and C(sp2)–H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513442 CIFC21 H16 B F4 NP 21 21 216.1068; 15.2343; 18.4646
90; 90; 90
1717.81Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)–H and C(sp2)–H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513443 CIFC21 H16 F6 N SbC 1 2/c 113.0833; 9.1095; 33.015
90; 91.371; 90
3933.7Luo, Ching-Zong; Gandeepan, Parthasarathy; Wu, Yun-Ching; Tsai, Chia-Hung; Cheng, Chien-Hong
Cooperative C(sp3)‒H and C(sp2)‒H Activation of 2-Ethylpyridines by Copper and Rhodium: A Route toward Quinolizinium Salts
ACS Catalysis, 2015, 5, 4837
4513454 CIFC15 H13 Br N2P 4115.9607; 15.9607; 5.4313
90; 90; 90
1383.59Zhang, De-Yang; Shao, Long; Xu, Jie; Hu, Xiang-Ping
Copper-Catalyzed Asymmetric Formal [3 + 2] Cycloaddition of Propargylic Acetates with Hydrazines: Enantioselective Synthesis of Optically Active 2-Pyrazolines
ACS Catalysis, 2015, 5, 5026
4513487 CIFC38 H46 Au N3 O2P 1 21/n 19.1636; 36.3601; 21.4472
90; 97.684; 90
7081.8Hase, Shun; Kayaki, Yoshihito; Ikariya, Takao
Mechanistic Aspects of the Carboxylative Cyclization of Propargylamines and Carbon Dioxide Catalyzed by Gold(I) Complexes Bearing anN-Heterocyclic Carbene Ligand
ACS Catalysis, 2015, 5, 5135
4513497 CIFC39 H14 Cl6 Cu F10 N5 O2P -110.2256; 13.2327; 15.2136
75.791; 82.911; 77.348
1941.9Lei, Haitao; Fang, Huayi; Han, Yongzhen; Lai, Wenzhen; Fu, Xuefeng; Cao, Rui
Reactivity and Mechanism Studies of Hydrogen Evolution Catalyzed by Copper Corroles
ACS Catalysis, 2015, 5, 5145
4513498 CIFC39 H12 Cl4 Cu F15 N4P 1 21/c 113.6323; 13.187; 21.0645
90; 105.96; 90
3640.78Lei, Haitao; Fang, Huayi; Han, Yongzhen; Lai, Wenzhen; Fu, Xuefeng; Cao, Rui
Reactivity and Mechanism Studies of Hydrogen Evolution Catalyzed by Copper Corroles
ACS Catalysis, 2015, 5, 5145
4513610 CIFC20 H20 Cl N O4P 21 21 218.1602; 11.357; 20.59
90; 90; 90
1908.2Bai, Xing-Feng; Xu, Zheng; Xia, Chun-Gu; Zheng, Zhan-Jiang; Xu, Li-Wen
Aromatic-Amide-Derived Nonbiaryl Atropisomer as Highly Efficient Ligand for Asymmetric Silver-Catalyzed [3 + 2] Cycloaddition
ACS Catalysis, 2015, 5, 6016
4513611 CIFC25 H23 N O3P 1 21 16.0364; 17.033; 10.4225
90; 102.271; 90
1047.1Bai, Xing-Feng; Xu, Zheng; Xia, Chun-Gu; Zheng, Zhan-Jiang; Xu, Li-Wen
Aromatic-Amide-Derived Nonbiaryl Atropisomer as Highly Efficient Ligand for Asymmetric Silver-Catalyzed [3 + 2] Cycloaddition
ACS Catalysis, 2015, 5, 6016
4513656 CIFC29 H27 N O6 SC 1 2 127.301; 8.7461; 10.8469
90; 96.239; 90
2574.7Hao, Xiaoyu; Lin, Lili; Tan, Fei; Yin, Chengkai; Liu, Xiaohua; Feng, Xiaoming
Ligand Control of Diastereodivergency in Asymmetric Inverse Electron Demand Diels–Alder Reaction
ACS Catalysis, 2015, 5, 6052
4513657 CIFC29 H27 N O6 SP 21 21 2112.1813; 12.9222; 16.9425
90; 90; 90
2666.9Hao, Xiaoyu; Lin, Lili; Tan, Fei; Yin, Chengkai; Liu, Xiaohua; Feng, Xiaoming
Ligand Control of Diastereodivergency in Asymmetric Inverse Electron Demand Diels–Alder Reaction
ACS Catalysis, 2015, 5, 6052
4513663 CIFC32 H42 Ag N2C 1 2/c 116.043; 6.7774; 27.121
90; 94.443; 90
2940Liu, Qilun; Yuan, Zheliang; Wang, Hao-yang; Li, Yang; Wu, Yichen; Xu, Tao; Leng, Xuebing; Chen, Pinhong; Guo, Yin-long; Lin, Zhenyang; Liu, Guosheng
Abnormal Mesoionic Carbene Silver Complex: Synthesis, Reactivity, and Mechanistic Insight on Oxidative Fluorination
ACS Catalysis, 2015, 5, 6732
4513664 CIFC32 H40 Ag F2 N3 O3C 1 2/c 130.342; 14.1754; 27.882
90; 98.13; 90
11872Liu, Qilun; Yuan, Zheliang; Wang, Hao-yang; Li, Yang; Wu, Yichen; Xu, Tao; Leng, Xuebing; Chen, Pinhong; Guo, Yin-long; Lin, Zhenyang; Liu, Guosheng
Abnormal Mesoionic Carbene Silver Complex: Synthesis, Reactivity, and Mechanistic Insight on Oxidative Fluorination
ACS Catalysis, 2015, 5, 6732
4513677 CIFC25 H28 Cr N O4 PP 21 21 2110.0194; 14.8755; 33.308
90; 90; 90
4964.3Radcliffe, James E.; Batsanov, Andrei S.; Smith, David M.; Scott, John A.; Dyer, Philip W.; Hanton, Martin J.
Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium
ACS Catalysis, 2015, 5, 7095
4513678 CIFC29 H36 Cr N O4 PP 1 21/n 111.79138; 14.69577; 16.3394
90; 94.4771; 90
2822.71Radcliffe, James E.; Batsanov, Andrei S.; Smith, David M.; Scott, John A.; Dyer, Philip W.; Hanton, Martin J.
Phosphanyl Methanimine (PCN) Ligands for the Selective Trimerization/Tetramerization of Ethylene with Chromium
ACS Catalysis, 2015, 5, 7095
4513679 CIFC32 H38 Cl3 N P2 Pd SP b c a11.77; 16.605; 35.069
90; 90; 90
6854Sui, Xuelin; Dai, Shengyu; Chen, Changle
Ethylene Polymerization and Copolymerization with Polar Monomers by Cationic Phosphine Phosphonic Amide Palladium Complexes
ACS Catalysis, 2015, 5, 5932
4513680 CIFC31 H36 Cl N O P2 PdC 1 c 112.1032; 15.8942; 16.1513
90; 106.192; 90
2983.8Sui, Xuelin; Dai, Shengyu; Chen, Changle
Ethylene Polymerization and Copolymerization with Polar Monomers by Cationic Phosphine Phosphonic Amide Palladium Complexes
ACS Catalysis, 2015, 5, 5932
4514605 CIFC27 H27 F3 N4 O3C 1 2/c 154.69; 5.385; 17.156
90; 102.882; 90
4925Parveen, Rumana; Jayamma, Bandi; Dastidar, Parthasarathi
Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
ACS Biomaterials Science & Engineering, 2019, 5, 2180
4514606 CIFC25 H21 F3 N2 O2P -16.96; 10.566; 14.887
82.157; 78.009; 88.874
1060.8Parveen, Rumana; Jayamma, Bandi; Dastidar, Parthasarathi
Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
ACS Biomaterials Science & Engineering, 2019, 5, 2180
4514607 CIFC96 H100 F12 N8 O17P 1 2/n 126.469; 6.0807; 28.774
90; 90.77; 90
4630.8Parveen, Rumana; Jayamma, Bandi; Dastidar, Parthasarathi
Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
ACS Biomaterials Science & Engineering, 2019, 5, 2180
4514608 CIFC22 H21 F3 N2 O2P c c n14.751; 33.72; 8.39
90; 90; 90
4173Parveen, Rumana; Jayamma, Bandi; Dastidar, Parthasarathi
Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
ACS Biomaterials Science & Engineering, 2019, 5, 2180
4514609 CIFC17 H19 F3 N2 O4P -16.55; 8.043; 16.75
86.878; 89.257; 87.524
880Parveen, Rumana; Jayamma, Bandi; Dastidar, Parthasarathi
Supramolecular Gels Derived from Simple Organic Salts of Flufenamic Acid: Design, Synthesis, Structures, and Plausible Biomedical Application
ACS Biomaterials Science & Engineering, 2019, 5, 2180
4514920 CIFCl5 H24 N9 O2 Ru2I 1 2/m 18.5277; 7.6795; 13.5715
90; 91.593; 90
888.433Woods, Joshua J.; Nemani, Neeharika; Shanmughapriya, Santhanam; Kumar, Akshay; Zhang, MengQi; Nathan, Sarah R.; Thomas, Manfred; Carvalho, Edmund; Ramachandran, Karthik; Srikantan, Subramanya; Stathopulos, Peter B.; Wilson, Justin J.; Madesh, Muniswamy
A Selective and Cell-Permeable Mitochondrial Calcium Uniporter (MCU) Inhibitor Preserves Mitochondrial Bioenergetics after Hypoxia/Reoxygenation Injury.
ACS central science, 2019, 5, 153-166
4514921 CIFC8 H32 Cl5 N9 O Ru2P 65 2 210.0036; 10.0036; 37.9277
90; 90; 120
3287Woods, Joshua J.; Nemani, Neeharika; Shanmughapriya, Santhanam; Kumar, Akshay; Zhang, MengQi; Nathan, Sarah R.; Thomas, Manfred; Carvalho, Edmund; Ramachandran, Karthik; Srikantan, Subramanya; Stathopulos, Peter B.; Wilson, Justin J.; Madesh, Muniswamy
A Selective and Cell-Permeable Mitochondrial Calcium Uniporter (MCU) Inhibitor Preserves Mitochondrial Bioenergetics after Hypoxia/Reoxygenation Injury.
ACS central science, 2019, 5, 153-166
4514922 CIFC H6 I3 N3 PbP 1 21/n 14.5694; 11.748; 19.504
90; 94.147; 90
1044.3Fu, Yongping; Hautzinger, Matthew P.; Luo, Ziyu; Wang, Feifan; Pan, Dongxu; Aristov, Michael M.; Guzei, Ilia A.; Pan, Anlian; Zhu, Xiaoyang; Jin, Song
Incorporating Large A Cations into Lead Iodide Perovskite Cages: Relaxed Goldschmidt Tolerance Factor and Impact on Exciton-Phonon Interaction.
ACS central science, 2019, 5, 1377-1386
4514923 CIFC13 H38 I7 N3 Pb2C 1 2/c 145.146; 8.814; 8.695
90; 100.03; 90
3407Fu, Yongping; Hautzinger, Matthew P.; Luo, Ziyu; Wang, Feifan; Pan, Dongxu; Aristov, Michael M.; Guzei, Ilia A.; Pan, Anlian; Zhu, Xiaoyang; Jin, Song
Incorporating Large A Cations into Lead Iodide Perovskite Cages: Relaxed Goldschmidt Tolerance Factor and Impact on Exciton-Phonon Interaction.
ACS central science, 2019, 5, 1377-1386
4514924 CIFC38.51 H46.04 B18 Cl18 O2.49 P2 Pd2P 1 21/c 115.4952; 15.2588; 27.3371
90; 91.4479; 90
6461.5Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514925 CIFC44 H56 B18 Cl18 O2 P2 Pd2P -113.05; 12.04; 13.06
107.57; 91.15; 123.19
1592.4Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514926 CIFC220 H184 O4 P12 Rh4P 1 21/n 110.01; 31.78; 13.34
90; 90.15; 90
4243.7Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514927 CIFC136 H112 Cl8 Fe4 Ni4 P8P n a 2119.76; 10.1; 14.58
90; 90; 90
2909.8Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514928 CIFC120 H168 Fe8 O48P b c a15.52; 13.41; 16.49
90; 90; 90
3432Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514929 CIFC10 H11 Cl ZrP n n m7.21; 9.2; 13.84
90; 90; 90
918Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514930 CIFC172 H288 Cl8 P8 Ru4P 1 21/n 19.68; 25.65; 16.08
90; 92.63; 90
3988.3Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4514931 CIFC168 H160 N4 O8 P4 Pd4P 21 21 2110.2; 17.04; 19.9
90; 90; 90
3458.8Jones, Christopher G.; Asay, Matthew; Kim, Lee Joon; Kleinsasser, Jack F.; Saha, Ambarneil; Fulton, Tyler J.; Berkley, Kevin R.; Cascio, Duilio; Malyutin, Andrey G.; Conley, Matthew P.; Stoltz, Brian M.; Lavallo, Vincent; Rodríguez, José A; Nelson, Hosea M.
Characterization of Reactive Organometallic Species via MicroED.
ACS central science, 2019, 5, 1507-1513
4515176 CIFC46 H70 N4 O15P 21 21 2110.1242; 13.9473; 35.3927
90; 90; 90
4997.6Pyta, Krystian; Janas, Anna; Skrzypczak, Natalia; Schilf, Wojciech; Wicher, Barbara; Gdaniec, Maria; Bartl, Franz; Przybylski, Piotr
Specific Interactions between Rifamycin Antibiotics and Water Influencing Ability To Overcome Natural Cell Barriers and the Range of Antibacterial Potency.
ACS infectious diseases, 2019, 5, 1754-1763
4515177 CIFC53 H62 N2 O9 SiP 1 21 114.868; 10.1272; 31.874
90; 90.165; 90
4799.3Sati, Girish C.; Sarpe, Vikram A.; Furukawa, Takayuki; Mondal, Sujit; Mantovani, Matilde; Hobbie, Sven N.; Vasella, Andrea; Böttger, Erik C; Crich, David
Modification at the 2'-Position of the 4,5-Series of 2-Deoxystreptamine Aminoglycoside Antibiotics To Resist Aminoglycoside Modifying Enzymes and Increase Ribosomal Target Selectivity.
ACS infectious diseases, 2019, 5, 1718-1730
4516658 CIFC17 H16 OP -110.073; 10.958; 25.373
100.784; 100.991; 90.485
2697.9Qin, Guiping; Chen, Xiangning; Yang, Lei; Huang, Hanmin
Copper-Catalyzed α-Benzylation of Enones via Radical-Triggered Oxidative Coupling of Two C–H Bonds
ACS Catalysis, 2015, 5, 2882
4516659 CIFC15 H19 F3 N4 O7P 1 21/c 110.6111; 9.3941; 19.1315
90; 91.384; 90
1906.5Huang, Lin; Lin, Jin-Shun; Tan, Bin; Liu, Xin-Yuan
Alkene Trifluoromethylation-Initiated Remote α-Azidation of Carbonyl Compounds toward Trifluoromethyl γ-Lactam and Spirobenzofuranone-Lactam
ACS Catalysis, 2015, 5, 2826
4516660 CIFC17 H15 Cl F3 N O5P n a 2115.896; 8.7193; 25.283
90; 90; 90
3504.3Huang, Lin; Lin, Jin-Shun; Tan, Bin; Liu, Xin-Yuan
Alkene Trifluoromethylation-Initiated Remote α-Azidation of Carbonyl Compounds toward Trifluoromethyl γ-Lactam and Spirobenzofuranone-Lactam
ACS Catalysis, 2015, 5, 2826
4516661 CIFC55 H40 Cl3 O3 P3 Si3P -3 c 115.5297; 15.5297; 24.1564
90; 90; 120
5045.3Iwai, Tomohiro; Konishi, Shota; Miyazaki, Tatsuya; Kawamorita, Soichiro; Yokokawa, Natsumi; Ohmiya, Hirohisa; Sawamura, Masaya
Silica-Supported Triptycene-Type Phosphine. Synthesis, Characterization, and Application to Pd-Catalyzed Suzuki‒Miyaura Cross-Coupling of Chloroarenes
ACS Catalysis, 2015, 5, 7254
4516662 CIFC38 H31 Cl N5 P RuP 1 21/c 133.581; 10.1257; 19.1334
90; 101.527; 90
6374.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516663 CIFC44.5 H38 Cl F6 N5 O6 P Ru S2C 1 2/c 131.847; 12.7757; 25.6211
90; 117.055; 90
9283.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516664 CIFC40 H33 F3 N5 O P RuP -19.4999; 10.3978; 18.4333
79.884; 84.512; 68.604
1667.97Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal–Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516665 CIFC54 H42 Cl N5 P2 RuP 1 21/c 111.5459; 20.4778; 18.8418
90; 104.485; 90
4313.2Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516666 CIFC56 H46 Cl N5 P2 RuP -111.8598; 13.6537; 16.6403
89.614; 87.952; 69.915
2529Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516667 CIFC60 H54 Cl N5 O3.5 P2 RuP 1 21/c 123.8181; 11.25; 20.994
90; 115.986; 90
5056.7Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516668 CIFC57 H49 Cl4 N5 P2 RuP n a 2121.7779; 23.4319; 9.6235
90; 90; 90
4910.8Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516669 CIFC97 H81 N10 P2 Ru2P -113.7897; 15.8415; 19.6154
71.991; 73.73; 81.086
3900.9Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516670 CIFC38 H32 Cl F6 N5 P2 RuP -19.0716; 12.721; 15.6504
93.195; 103.235; 93.102
1751.2Tseng, Kuei-Nin T.; Kampf, Jeff W.; Szymczak, Nathaniel K.
Mechanism of N,N,N-Amide Ruthenium(II) Hydride Mediated Acceptorless Alcohol Dehydrogenation: Inner-Sphere β-H Elimination versus Outer-Sphere Bifunctional Metal‒Ligand Cooperativity
ACS Catalysis, 2015, 5, 5468
4516671 CIFC34 H25 B Cu F4 N4 O3 PP 1 21/n 112.5021; 13.6073; 19.1227
90; 108.373; 90
3087.32Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516672 CIFC42 H28 Cl10 N4 O6 P2 Pd2P -110.5194; 11.305; 12.8486
64.026; 86.154; 63.035
1207.7Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516673 CIFC47 H35 B Cl2 Cu F4 N4 O3 PP b c n30.0446; 11.56203; 24.6258
90; 90; 90
8554.4Knorn, Matthias; Rawner, Thomas; Czerwieniec, Rafał; Reiser, Oliver
[Copper(phenanthroline)(bisisonitrile)]±Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
ACS Catalysis, 2015, 5, 5186
4516674 CIFC44 H56 Fe Li N2 O Si2P 1 21/n 111.3913; 26.6073; 13.8664
90; 103.752; 90
4082.3Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516675 CIFC35 H33 Fe N2 O3 PP 1 21/c 114.14; 13.3999; 16.5218
90; 112.094; 90
2900.6Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516676 CIFC56 H53 Fe N2 PP 1 21/c 116.7305; 14.4122; 17.4229
90; 93.471; 90
4193.4Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516677 CIFC38 H33 Fe N5P n a 2116.9958; 10.2025; 17.6294
90; 90; 90
3056.9Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516678 CIFC368 H416 F24 Fe8 N16 Na4 O28.7 P4P 4/m n c17.2377; 17.2377; 27.3182
90; 90; 90
8117.3Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516679 CIFC32 H24 Cl2 Fe N2P 1 21/c 119.5314; 9.7274; 13.93
90; 99.058; 90
2613.55Lichtenberg, Crispin; Adelhardt, Mario; Gianetti, Thomas L.; Meyer, Karsten; de Bruin, Bas; Grützmacher, Hansjörg
Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application
ACS Catalysis, 2015, 5, 6230
4516680 CIFC46 H64 Fe N2 O4 TiP 21 21 2110.8375; 14.8073; 27.377
90; 90; 90
4393.3Brown, Lauren A.; Rhinehart, Jennifer L.; Long, Brian K.
Effects of Ferrocenyl Proximity and Monomer Presence during Oxidation for the Redox-Switchable Polymerization of l-Lactide
ACS Catalysis, 2015, 5, 6057
4516681 CIFC20 H18 F4P 1 21/a 16.1162; 15.02; 17.666
90; 96.537; 90
1612.3Ichitsuka, Tomohiro; Fujita, Takeshi; Ichikawa, Junji
Nickel-Catalyzed Allylic C(sp3)–F Bond Activation of Trifluoromethyl Groups via β-Fluorine Elimination: Synthesis of Difluoro-1,4-dienes
ACS Catalysis, 2015, 5, 5947
4516682 CIFC35 H30 Cl2 N2 O4 SP 1 21 110.9711; 7.3155; 19.9974
90; 93.418; 90
1602.1Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita–Baylis–Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516683 CIFC20 H22 N2 O3 SP 1 21/c 17.7705; 22.437; 11.0377
90; 105.525; 90
1854.2Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita–Baylis–Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516684 CIFC35 H28 Cl2 N2 O4 SP -111.9029; 15.3015; 19.0001
85.692; 79.538; 67.684
3148.1Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita–Baylis–Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516685 CIFC24 H26 N2 O4 SP -19.3454; 9.7516; 14.35
92.675; 101.306; 115.481
1144.9Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita–Baylis–Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516686 CIFC34 H28 Cl2 N2 O4 SP 21 21 2110.3652; 10.371; 28.86
90; 90; 90
3102.4Gao, Yuning; Xu, Qin; Shi, Min
Enantioselective Synthesis of Polycyclic Indole Derivatives Based on aza-Morita–Baylis–Hillman Reaction
ACS Catalysis, 2015, 5, 6608
4516687 CIFC25 H23 N O5 SP 21 21 218.8035; 14.912; 17.9438
90; 90; 90
2355.62Liu, Ren-Rong; Wang, Dan-Jie; Wu, Liang; Xiang, Bin; Zhang, Guo-Qi; Gao, Jian-Rong; Jia, Yi-Xia
Nickel-Catalyzed Enantioselective Addition of Styrenes to Cyclic N-Sulfonyl α-Ketiminoesters
ACS Catalysis, 2015, 5, 6524
4516688 CIFC66 H68 N4 Pd2 S4P 1 21/n 115.6832; 11.3541; 16.787
90; 92.189; 90
2987.1Degtyareva, Evgeniya S.; Burykina, Julia V.; Fakhrutdinov, Artem N.; Gordeev, Evgeniy G.; Khrustalev, Victor N.; Ananikov, Valentine P.
Pd-NHC Catalytic System for the Efficient Atom-Economic Synthesis of Vinyl Sulfides from Tertiary, Secondary, or Primary Thiols
ACS Catalysis, 2015, 5, 7208
4516689 CIFC22 H15 P SP n a 218.233; 13.912; 15.188
90; 90; 90
1739.6Unoh, Yuto; Satoh, Tetsuya; Hirano, Koji; Miura, Masahiro
Rhodium(III)-Catalyzed Direct Coupling of Arylphosphine Derivatives with Heterobicyclic Alkenes: A Concise Route to Biarylphosphines and Dibenzophosphole Derivatives
ACS Catalysis, 2015, 5, 6634
4516690 CIFC24 H32 F3 I O3 SP 1 21/c 19.6451; 25.6279; 10.7472
90; 102.565; 90
2592.91Berzina, Beatrise; Sokolovs, Igors; Suna, Edgars
Copper-Catalyzed para-Selective C–H Amination of Electron-Rich Arenes
ACS Catalysis, 2015, 5, 7008
4516691 CIFC50 H32 B F24 N3 Ni O2P -111.4773; 13.0681; 18.2775
70.951; 80.767; 78.887
2528.57Escobar, Manuel A.; Trofymchuk, Oleksandra S.; Rodriguez, Barbara E.; Lopez-Lira, Claudia; Tapia, Ricardo; Daniliuc, Constantin; Berke, Heinz; Nachtigall, Fabiane M.; Santos, Leonardo S.; Rojas, Rene S.
Lewis Acid Enhanced Ethene Dimerization and Alkene Isomerization—ESI-MS Identification of the Catalytically Active Pyridyldimethoxybenzimidazole Nickel(II) Hydride Species
ACS Catalysis, 2015, 5, 7338
4516692 CIFC124 H186 F24 Ir4 N12 O25 S8P 1 21/c 111.1326; 28.0168; 13.6059
90; 96.8149; 90
4213.7Kim, Hyunwoo; Chang, Sukbok
Iridium-Catalyzed Direct C‒H Amination with Alkylamines: Facile Oxidative Insertion of Amino Group into Iridacycle
ACS Catalysis, 2015, 5, 6665
4516693 CIFC26 H24 N2 O3P 1 21 19.4911; 9.8015; 12.0673
90; 103.604; 90
1091.09Li, Dan; Wang, Linqing; Yang, Dongxu; Zhang, Bangzhi; Wang, Rui
Catalytic Desymmetrization of meso-Aziridines with Benzofuran-2(3H)-Ones Employing a Simple In Situ-Generated Magnesium Catalyst
ACS Catalysis, 2015, 5, 7432
4516804 CIFC24 H23 N2 O5 PP 1 21/c 111.359; 21.291; 9.219
90; 97.196; 90
2212Mitchell, Lauren A.; Holliday, Bradley J.
Polymeric Materials for the Separation of f-Elements Utilizing Carbamoylmethylphosphine Oxide Chelating Ligands
ACS Macro Letters, 2016, 5, 1100
4517008 CIFC22 H28 Na O9 SI 1 a 119.0828; 11.0641; 21.971
90; 99.81; 90
4571Miles-Barrett, Daniel M.; Montgomery, James R. D.; Lancefield, Christopher S.; Cordes, David B.; Slawin, Alexandra M. Z.; Lebl, Tomas; Carr, Reuben; Westwood, Nicholas J.
Use of Bisulfite Processing To Generate High-β-O-4 Content Water-Soluble Lignosulfonates
ACS Sustainable Chemistry & Engineering, 2017, 5, 1831
4517009 CIFC20 H15 Cl2 F N4 O8P 1 21/n 17.8249; 22.011; 12.217
90; 99.059; 90
2077.9Chen, Liang; Huang, Rong; Du, Xuan-Xuan; Yan, Sheng-Jiao; Lin, Jun
One-Pot Synthesis of Highly Functionalized Bicyclic Imidazopyridinium Derivatives in Ethanol
ACS Sustainable Chemistry & Engineering, 2017, 5, 1899
4517010 CIFC28 H16 N O4 ZnP 1 21/c 17.8228; 19.98; 17.1179
90; 91.087; 90
2675Zhao, Hongmei; Xia, Qiansu; Xing, Hongzhu; Chen, Dashu; Wang, Hong
Construction of Pillared-Layer MOF as Efficient Visible-Light Photocatalysts for Aqueous Cr(VI) Reduction and Dye Degradation
ACS Sustainable Chemistry & Engineering, 2017, 5, 4449
4517011 CIFC21 H18 N2 O2 SP 1 21/c 116.376; 5.782; 19.03
90; 100.86; 90
1769.6Pigulski, Bartłomiej; Cichos, Jakub; Szafert, Sławomir
Polyynes as Precursors of Photoluminescent Solvent Polarity Probes
ACS Sustainable Chemistry & Engineering, 2017, 5, 7077
4517012 CIFC16 H20 N2 O5 SP n n a6.7039; 10.6697; 22.602
90; 90; 90
1616.7Mehrotra, Sonam; Raje, Sakthi; Jain, Anant Kumar; Angamuthu, Raja
Benzimidazolines Convert Sulfur Dioxide to Bisulfate at Room Temperature and Atmospheric Pressure Utilizing Aerial Oxygen
ACS Sustainable Chemistry & Engineering, 2017, 5, 6322
4517013 CIFC20 H20 N5 O5 SP -110.8743; 12.9713; 13.3718
64.0149; 71.014; 70.772
1564Mehrotra, Sonam; Raje, Sakthi; Jain, Anant Kumar; Angamuthu, Raja
Benzimidazolines Convert Sulfur Dioxide to Bisulfate at Room Temperature and Atmospheric Pressure Utilizing Aerial Oxygen
ACS Sustainable Chemistry & Engineering, 2017, 5, 6322
4517014 CIFC14 H14 Br N3 O4 SP -17.907; 8.536; 11.911
83.119; 78.561; 83.567
779.1Mehrotra, Sonam; Raje, Sakthi; Jain, Anant Kumar; Angamuthu, Raja
Benzimidazolines Convert Sulfur Dioxide to Bisulfate at Room Temperature and Atmospheric Pressure Utilizing Aerial Oxygen
ACS Sustainable Chemistry & Engineering, 2017, 5, 6322
4517015 CIFC36 H34 Fe I2 N10P b c a17.516; 19.233; 23.482
90; 90; 90
7911Chen, Fei; Liu, Ning; Dai, Bin
Iron(II) Bis-CNN Pincer Complex-Catalyzed Cyclic Carbonate Synthesis at Room Temperature
ACS Sustainable Chemistry & Engineering, 2017, 5, 9065
4517016 CIFC13 H9 N2 O4 ZnP 1 21/c 112.549; 7.632; 16.158
90; 109.74; 90
1456.6Senthilkumar, S.; Goswami, Ranadip; Obasi, Nnamdi Lawrence; Neogi, Subhadip
Construction of Pillar-Layer Metal‒Organic Frameworks for CO2 Adsorption under Humid Climate: High Selectivity and Sensitive Detection of Picric Acid in Water
ACS Sustainable Chemistry & Engineering, 2017, 5, 11307
4517017 CIFC13 H9 N3 O4 ZnP 1 21/c 114.702; 7.736; 15.973
90; 107.124; 90
1736.1Senthilkumar, S.; Goswami, Ranadip; Obasi, Nnamdi Lawrence; Neogi, Subhadip
Construction of Pillar-Layer Metal‒Organic Frameworks for CO2 Adsorption under Humid Climate: High Selectivity and Sensitive Detection of Picric Acid in Water
ACS Sustainable Chemistry & Engineering, 2017, 5, 11307
4517018 CIFC14 H10 N2 O4 ZnC 1 2/c 135.331; 7.6491; 16.0546
90; 108.658; 90
4110.7Senthilkumar, S.; Goswami, Ranadip; Obasi, Nnamdi Lawrence; Neogi, Subhadip
Construction of Pillar-Layer Metal‒Organic Frameworks for CO2 Adsorption under Humid Climate: High Selectivity and Sensitive Detection of Picric Acid in Water
ACS Sustainable Chemistry & Engineering, 2017, 5, 11307
4517019 CIFC11 H7 N5 O7P 1 21/n 15.535; 19.583; 11.673
90; 97.599; 90
1254.1Senthilkumar, S.; Goswami, Ranadip; Obasi, Nnamdi Lawrence; Neogi, Subhadip
Construction of Pillar-Layer Metal‒Organic Frameworks for CO2 Adsorption under Humid Climate: High Selectivity and Sensitive Detection of Picric Acid in Water
ACS Sustainable Chemistry & Engineering, 2017, 5, 11307
4517020 CIFC38 H36 N2 O7P -111.2185; 13.1576; 13.44
111.204; 93.969; 112.787
1653.87García-Montero, Angel; Rodriguez, Antonio M.; Juan, Alberto; Velders, Aldrik H.; Denisi, Antonio; Jiménez-Osés, Gonzalo; Gómez-Bengoa, Enrique; Cativiela, Carlos; Gómez, Maria Victoria; Urriolabeitia, Esteban P.
Metal-Free [2 + 2]-Photocycloaddition of (Z)-4-Aryliden-5(4H)-Oxazolones as Straightforward Synthesis of 1,3-Diaminotruxillic Acid Precursors: Synthetic Scope and Mechanistic Studies
ACS Sustainable Chemistry & Engineering, 2017, 5, 8370
4517021 CIFC34 H26 N2 O4P -17.5802; 9.6279; 10.5678
69.46; 73.023; 68.198
658.87García-Montero, Angel; Rodriguez, Antonio M.; Juan, Alberto; Velders, Aldrik H.; Denisi, Antonio; Jiménez-Osés, Gonzalo; Gómez-Bengoa, Enrique; Cativiela, Carlos; Gómez, Maria Victoria; Urriolabeitia, Esteban P.
Metal-Free [2 + 2]-Photocycloaddition of (Z)-4-Aryliden-5(4H)-Oxazolones as Straightforward Synthesis of 1,3-Diaminotruxillic Acid Precursors: Synthetic Scope and Mechanistic Studies
ACS Sustainable Chemistry & Engineering, 2017, 5, 8370
4517022 CIFC38 H34 Cl4 N2 O8P 1 21/c 113.9228; 17.8301; 16.472
90; 111.643; 90
3800.8García-Montero, Angel; Rodriguez, Antonio M.; Juan, Alberto; Velders, Aldrik H.; Denisi, Antonio; Jiménez-Osés, Gonzalo; Gómez-Bengoa, Enrique; Cativiela, Carlos; Gómez, Maria Victoria; Urriolabeitia, Esteban P.
Metal-Free [2 + 2]-Photocycloaddition of (Z)-4-Aryliden-5(4H)-Oxazolones as Straightforward Synthesis of 1,3-Diaminotruxillic Acid Precursors: Synthetic Scope and Mechanistic Studies
ACS Sustainable Chemistry & Engineering, 2017, 5, 8370
4517023 CIFC18 H15 N O4P 1 21/c 112.4183; 13.3678; 8.9785
90; 93.613; 90
1487.52García-Montero, Angel; Rodriguez, Antonio M.; Juan, Alberto; Velders, Aldrik H.; Denisi, Antonio; Jiménez-Osés, Gonzalo; Gómez-Bengoa, Enrique; Cativiela, Carlos; Gómez, Maria Victoria; Urriolabeitia, Esteban P.
Metal-Free [2 + 2]-Photocycloaddition of (Z)-4-Aryliden-5(4H)-Oxazolones as Straightforward Synthesis of 1,3-Diaminotruxillic Acid Precursors: Synthetic Scope and Mechanistic Studies
ACS Sustainable Chemistry & Engineering, 2017, 5, 8370
4517024 CIFC32 H34 F3 N3 O3P 1 21/c 113.96; 19.71; 15.38
90; 116.32; 90
3793.1Wang, Bao-Qu; Luo, Qin; Xiao, Qiang; Lin, Jun; Yan, Sheng-Jiao
Synthesis of Quinone Methide Substituted Neonicotinoid Derivatives via 1,6-Conjugate Addition of N-Benzyl Nitro Ketene Aminals with para-Quinone Methides Accompanying Oxidation
ACS Sustainable Chemistry & Engineering, 2017, 5, 8382
4517297 CIFC84 H54 Cl2 P2 PdP 1 n 116.66; 15.5656; 28.2198
90; 97.375; 90
7257.5Beránek, Tomáš; Žádný, Jaroslav; Strašák, Tomáš; Karban, Jindřich; Císařová, Ivana; Sýkora, Jan; Storch, Jan
Synthesis of a Helical Phosphine and a Catalytic Study of Its Palladium Complex.
ACS omega, 2020, 5, 882-892
4517306 CIFC22 H33 N3 O4 S SiP 63/m23.6621; 23.6621; 7.5296
90; 90; 120
3650.98Prybil, Joshua W.; Wallace, Rodney; Warren, Alexandra; Klingman, Jordan; Vaillant, Romane; Hall, Michael B.; Yang, Xin; Brennessel, William W.; Chin, Robert M.
Silylation of Pyridine, Picolines, and Quinoline with a Zinc Catalyst
ACS Omega, 2020, 5, 1528-1539
4517307 CIFC41 H50 B2 N4 P2 TiP 1 21/c 111.0617; 24.4886; 17.3459
90; 122.08; 90
3981.29Bhattacharjee, Jayeeta; Harinath, Adimulam; Bano, Kulsum; Panda, Tarun K.
Highly Chemoselective Hydroboration of Alkynes and Nitriles Catalyzed by Group 4 Metal Amidophosphine–Borane Complexes
ACS Omega, 2020, 5, 1595-1606
4517308 CIFC40 H40 B2 Cl0 N2 P2 ZrP -110.8835; 13.0462; 26.353
95.711; 101.515; 101.049
3561.4Bhattacharjee, Jayeeta; Harinath, Adimulam; Bano, Kulsum; Panda, Tarun K.
Highly Chemoselective Hydroboration of Alkynes and Nitriles Catalyzed by Group 4 Metal Amidophosphine‒Borane Complexes
ACS Omega, 2020, 5, 1595-1606
4517309 CIFC60 H60 B4 N4 P4 ZrP 1 21/n 112.6729; 21.3485; 23.3993
90; 96.078; 90
6295.03Bhattacharjee, Jayeeta; Harinath, Adimulam; Bano, Kulsum; Panda, Tarun K.
Highly Chemoselective Hydroboration of Alkynes and Nitriles Catalyzed by Group 4 Metal Amidophosphine–Borane Complexes
ACS Omega, 2020, 5, 1595-1606
4517386 CIFC14 H18 N6 O3 SP b c a15.3961; 13.602; 16.0574
90; 90; 90
3362.7Oliveira, Ana P. A.; Freitas, Jennifer T. J.; Diniz, Renata; Pessoa, Claudia; Maranhão, Sarah S; Ribeiro, Juliana M.; Souza-Fagundes, Elaine M; Beraldo, Heloisa
Triethylphosphinegold(I) Complexes with Secnidazole-Derived Thiosemicarbazones: Cytotoxic Activity against HCT-116 Colorectal Cancer Cells under Hypoxia Conditions.
ACS omega, 2020, 5, 2939-2946
4517387 CIFC9 H14 N6 O2 SP -18.1536; 8.732; 9.8349
89.139; 81.378; 68.29
642.57Oliveira, Ana P. A.; Freitas, Jennifer T. J.; Diniz, Renata; Pessoa, Claudia; Maranhão, Sarah S; Ribeiro, Juliana M.; Souza-Fagundes, Elaine M; Beraldo, Heloisa
Triethylphosphinegold(I) Complexes with Secnidazole-Derived Thiosemicarbazones: Cytotoxic Activity against HCT-116 Colorectal Cancer Cells under Hypoxia Conditions.
ACS omega, 2020, 5, 2939-2946
4517388 CIFC27 H29 B Br2P -19.1165; 10.8798; 13.0957
73.946; 88.38; 77.43
1217.6Ru, Chenglong; Wei, Qiuyu; Chen, Wenhao; Guan, Qiye; Zhang, Qianqian; Ling, Yuan; Tao, Chunlan; Qin, Dongdong; Wu, Jincai; Pan, Xiaobo
Tunable Conjugated Organoborane Oligomers for Visible-Light-Driven Hydrogen Evolution
ACS Energy Letters, 2020, 5, 669-675
4517403 CIFC6 H6 Cl2 O7 U0.5C 1 2/c 113.7293; 11.363; 12.5175
90; 95.847; 90
1942.65Refn, Vanja E.; Kubus, Mariusz; Mossin, Susanne; Larsen, René Wugt; Pedersen, Kasper S.
A Redox-Innocent Uranium(IV)-Quinoid Metal-Organic Framework.
ACS omega, 2020, 5, 3462-3466
4517404 CIFC12 H12 Cl4 O14 UC 1 2/c 113.8598; 11.496; 12.61
90; 96.415; 90
1996.6Refn, Vanja E.; Kubus, Mariusz; Mossin, Susanne; Larsen, René Wugt; Pedersen, Kasper S.
A Redox-Innocent Uranium(IV)-Quinoid Metal-Organic Framework.
ACS omega, 2020, 5, 3462-3466
4517405 CIFC25 H17 N O2P -19.529; 10.567; 20.407
87.353; 86.97; 63.261
1832Panday, Anoop Kumar; Ali, Danish; Choudhury, Lokman H.
Cs<sub>2</sub>CO<sub>3</sub>-Mediated Rapid Room-Temperature Synthesis of 3-Amino-2-aroyl Benzofurans and Their Copper-Catalyzed <i>N</i>-Arylation Reactions.
ACS omega, 2020, 5, 3646-3660
4517407 CIFC17 H23 N3 O3 SP 17.9413; 7.9555; 8.0755
81.685; 63.54; 72.764
436.18Chiou, Wen-Hua; Hsu, Kuo-Hsun; Huang, Wen-Wei
Rh-Catalyzed Hydroformylation-Initiated Bicyclization: Construction of Azabicyclic Systems.
ACS omega, 2020, 5, 3717-3724
4517414 CIFC26 H28 N6 O14 ZnP 1 21/n 17.8574; 19.2849; 9.9755
90; 102.355; 90
1476.57Brahma, Rinki; Baruah, Jubaraj B.
Self-Assemblies of Zinc Complexes for Aggregation-Induced Emission Luminogen Precursors.
ACS omega, 2020, 5, 3774-3785
4517415 CIFC20 H20 N4 O12 ZnP -15.9866; 8.7293; 22.354
96.624; 90.797; 90.264
1160.3Brahma, Rinki; Baruah, Jubaraj B.
Self-Assemblies of Zinc Complexes for Aggregation-Induced Emission Luminogen Precursors.
ACS omega, 2020, 5, 3774-3785
4517416 CIFC28 H28 N6 O12 ZnC 1 2/c 120.1428; 6.2816; 25.1031
90; 104.399; 90
3076.5Brahma, Rinki; Baruah, Jubaraj B.
Self-Assemblies of Zinc Complexes for Aggregation-Induced Emission Luminogen Precursors.
ACS omega, 2020, 5, 3774-3785
4517417 CIFC42 H36 N8 O20 Zn2C 1 2/c 122.0343; 13.6328; 15.1548
90; 100.715; 90
4473Brahma, Rinki; Baruah, Jubaraj B.
Self-Assemblies of Zinc Complexes for Aggregation-Induced Emission Luminogen Precursors.
ACS omega, 2020, 5, 3774-3785
4517418 CIFC26 H22 N6 O11 ZnP -18.0671; 12.718; 14.3069
81.172; 76.06; 74.624
1367.3Brahma, Rinki; Baruah, Jubaraj B.
Self-Assemblies of Zinc Complexes for Aggregation-Induced Emission Luminogen Precursors.
ACS omega, 2020, 5, 3774-3785
4517430 CIFC49 H30 N2 OP 1 21/n 19.6783; 23.209; 14.9411
90; 95.11; 90
3342.8Wang, Sha-Sha; Rong, Rong; Liu, Yi-Ran; Hu, Xiao; Zhang, He; Yu, Yang; Wei, Ying; Xie, Ling-Hai; Huang, Wei
The Dimensionality Transition between Three-Dimensional and Two-Dimensional Organic Microcrystals: Specific Symmetry and Selective Adhesion.
ACS omega, 2020, 5, 3749-3754
4517432 CIFC18 H14 F4 O4P 1 21/c 113.7445; 17.581; 7.2542
90; 101.283; 90
1719Liu, Guangyuan; Zhang, Xingxing; Kuang, Guanghua; Lu, Naihao; Fu, Yang; Peng, Yiyuan; Xiao, Qiang; Zhou, Yirong
Phosphine-Free Ru-Catalyzed Regio- and Stereoselective Addition of Benzoic Acids to Trifluoromethylated Alkynes toward Facile Access to Trifluoromethyl Group-Substituted (E)-Enol Esters
ACS Omega, 2020, 5, 4158-4166
4517503 CIFC5 H3 Au Cl2 N2 O2P b c a7.2868; 14.4003; 16.4259
90; 90; 90
1723.6Stenger-Smith, Jenny; Kamariza, Mireille; Chakraborty, Indranil; Ouattara, Ramatoulaye; Bertozzi, Carolyn R.; Mascharak, Pradip K.
Enhanced Bactericidal Effects of Pyrazinamide Toward Mycobacterium smegmatis and Mycobacterium tuberculosis upon Conjugation to a {Au(I)-triphenylphosphine}+ Moiety
ACS Omega, 2020, 5, 6826-6833
4517504 CIFC24 H22 Au F3 N3 O5 P SP -17.0334; 12.6524; 15.688
79.435; 81.214; 89.464
1356Stenger-Smith, Jenny; Kamariza, Mireille; Chakraborty, Indranil; Ouattara, Ramatoulaye; Bertozzi, Carolyn R.; Mascharak, Pradip K.
Enhanced Bactericidal Effects of Pyrazinamide Toward Mycobacterium smegmatis and Mycobacterium tuberculosis upon Conjugation to a {Au(I)-triphenylphosphine}+ Moiety
ACS Omega, 2020, 5, 6826-6833
4517505 CIFC5 H4 Au Cl2 N3 OP -16.6857; 7.2848; 8.9057
94.664; 106.878; 91.649
413.06Stenger-Smith, Jenny; Kamariza, Mireille; Chakraborty, Indranil; Ouattara, Ramatoulaye; Bertozzi, Carolyn R.; Mascharak, Pradip K.
Enhanced Bactericidal Effects of Pyrazinamide Toward Mycobacterium smegmatis and Mycobacterium tuberculosis upon Conjugation to a {Au(I)-triphenylphosphine}+ Moiety
ACS Omega, 2020, 5, 6826-6833
4517506 CIFC15 H8 Cl4 F6 N4 OP 21 21 212.627; 16.99; 4.5162
90; 90; 90
968.9Mondal, Amita; Hazra, Abhijit; Chakrabarty, Jitamanyu; Bose K, Jagadeesh C.; Banerjee, Priyabrata
Tandem Detection of Sub-Nano Molar Level CN– and Hg2+ in Aqueous Medium by a Suitable Molecular Sensor: A Viable Solution for Detection of CN– and Development of the RGB-Based Sensory Device
ACS Omega, 2020, 5, 6576-6587
4517507 CIFC4 H10 Cd Cl4 F6 N2C 1 2/c 125.831; 7.3258; 7.3487
90; 90; 90
1390.6Song, Ning; Chen, Shao-Peng; Fan, Xiao-Wei; Tan, Yu-Hui; Wei, Wen-Juan; Tang, Yun-Zhi
Regulating Reversible Phase Transition Behaviors by Poly-H/F Substitution in Hybrid Perovskite-Like 2[CH2FCH2NH3]·[CdCl4]
ACS Omega, 2020, 5, 6773-6780
4517508 CIFC4 H12 Cd Cl4 F4 N2P b c a7.5273; 7.4027; 23.054
90; 90; 90
1284.6Song, Ning; Chen, Shao-Peng; Fan, Xiao-Wei; Tan, Yu-Hui; Wei, Wen-Juan; Tang, Yun-Zhi
Regulating Reversible Phase Transition Behaviors by Poly-H/F Substitution in Hybrid Perovskite-Like 2[CH2FCH2NH3]·[CdCl4]
ACS Omega, 2020, 5, 6773-6780
4517509 CIFC4 H14 Cd Cl4 F2 N2P 1 21/c 111.2047; 7.6515; 7.305
90; 104.162; 90
607.24Song, Ning; Chen, Shao-Peng; Fan, Xiao-Wei; Tan, Yu-Hui; Wei, Wen-Juan; Tang, Yun-Zhi
Regulating Reversible Phase Transition Behaviors by Poly-H/F Substitution in Hybrid Perovskite-Like 2[CH2FCH2NH3]·[CdCl4]
ACS Omega, 2020, 5, 6773-6780

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