Crystallography Open Database

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Searching journal of publication like 'Journal of the American Chemical Society' volume of publication is 138

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4125052 CIFC39 H96 Ce N9 Si6P 1 21/n 114.4193; 22.9467; 17.0665
90; 97.255; 90
5601.7Yin, Haolin; Carroll, Patrick J.; Manor, Brian C.; Anna, Jessica M.; Schelter, Eric J.
Cerium Photosensitizers: Structure-Function Relationships and Applications in Photocatalytic Aryl Coupling Reactions.
Journal of the American Chemical Society, 2016, 138, 5984-5993
4125053 CIFC73 H112 B Ce Cl4 F24 N9 Si6P 1 21/n 123.2747; 18.2692; 24.82
90; 115.313; 90
9540.4Yin, Haolin; Carroll, Patrick J.; Manor, Brian C.; Anna, Jessica M.; Schelter, Eric J.
Cerium Photosensitizers: Structure-Function Relationships and Applications in Photocatalytic Aryl Coupling Reactions.
Journal of the American Chemical Society, 2016, 138, 5984-5993
4125054 CIFC27 H76 Ce Cl3 N4 Si6P 1 21/n 115.9152; 15.6395; 18.7462
90; 91.845; 90
4663.6Yin, Haolin; Carroll, Patrick J.; Manor, Brian C.; Anna, Jessica M.; Schelter, Eric J.
Cerium Photosensitizers: Structure-Function Relationships and Applications in Photocatalytic Aryl Coupling Reactions.
Journal of the American Chemical Society, 2016, 138, 5984-5993
4125055 CIFNd9.553 O25.776 Si6P 63/m9.5507; 9.5507; 7.0155
90; 90; 120
554.191An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125056 CIFNd9.606 O25.924 Si6P 63/m9.5507; 9.5507; 7.0155
90; 90; 120
554.191An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125057 CIFAl1.5 Nd9.959 O26 Si4.5P 63/m9.5611; 9.5611; 7.0607
90; 90; 120
558.977An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125058 CIFNd9.605 O25.789 Si6P 63/m9.5507; 9.5507; 7.0155
90; 90; 120
554.191An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125059 CIFNd9.58 O25.84 Si6P 63/m9.5507; 9.5507; 7.0155
90; 90; 120
554.191An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125060 CIFAl Nd9.906 O26 Si5P 63/m9.553; 9.553; 7.0496
90; 90; 120
557.153An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125061 CIFAl0.5 Nd9.652 O26 Si5.5P 63/m9.5515; 9.5515; 7.042
90; 90; 120
556.378An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125062 CIFNd9.569 O25.905 Si6P 63/m9.5507; 9.5507; 7.0155
90; 90; 120
554.191An, Tao; Baikie, Tom; Orera, Alodia; Piltz, Ross O.; Meven, Martin; Slater, Peter R.; Wei, Jun; Sanjuán, María L; White, T. J.
Interstitial Oxide Ion Distribution and Transport Mechanism in Aluminum-Doped Neodymium Silicate Apatite Electrolytes.
Journal of the American Chemical Society, 2016, 138, 4468-4483
4125063 CIFC24 H24 B F10 NP -16.0559; 12.211; 16.663
104.66; 95.819; 103.157
1144.1Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125064 CIFC24 H26 B F10 N OP -110.9865; 11.3039; 12.1268
111.608; 90.925; 116.464
1223.73Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125065 CIFC29 H30 B F10 NP 1 21/n 19.3348; 18.8671; 15.8074
90; 91.077; 90
2783.52Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125066 CIFC36 H25 B2 F20 NP 1 21/n 112.3941; 19.3768; 17.7912
90; 99.37; 90
4215.7Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125067 CIFC24 H26 B F10 NC 1 2/c 136.0335; 8.0228; 19.5293
90; 121.688; 90
4804.1Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125068 CIFC48 H48 B2 F20 N2 O2P 1 21/n 112.633; 22.0052; 17.6449
90; 104.135; 90
4756.6Wang, Tongdao; Kehr, Gerald; Liu, Lei; Grimme, Stefan; Daniliuc, Constantin G.; Erker, Gerhard
Selective Oxidation of an Active Intramolecular Amine/Borane Frustrated Lewis Pair with Dioxygen.
Journal of the American Chemical Society, 2016, 138, 4302-4305
4125069 CIFC22 H23 F3 N O5 PP 19.548; 10.705; 12.059
87.745; 67.638; 83.773
1133.1Morisaki, Kazuhiro; Sawa, Masanao; Yonesaki, Ryohei; Morimoto, Hiroyuki; Mashima, Kazushi; Ohshima, Takashi
Mechanistic Studies and Expansion of the Substrate Scope of Direct Enantioselective Alkynylation of α-Ketiminoesters Catalyzed by Adaptable (Phebox)Rhodium(III) Complexes.
Journal of the American Chemical Society, 2016, 138, 6194-6203
4125070 CIFC34 H27 N2 O4 RhP 21 21 2110.73; 14.3916; 18.13
90; 90; 90
2799.7Morisaki, Kazuhiro; Sawa, Masanao; Yonesaki, Ryohei; Morimoto, Hiroyuki; Mashima, Kazushi; Ohshima, Takashi
Mechanistic Studies and Expansion of the Substrate Scope of Direct Enantioselective Alkynylation of α-Ketiminoesters Catalyzed by Adaptable (Phebox)Rhodium(III) Complexes.
Journal of the American Chemical Society, 2016, 138, 6194-6203
4125071 CIFC24 H20 N2 O4 SP 1 21 15.73; 20.761; 8.5902
90; 100.442; 90
1005Morisaki, Kazuhiro; Sawa, Masanao; Yonesaki, Ryohei; Morimoto, Hiroyuki; Mashima, Kazushi; Ohshima, Takashi
Mechanistic Studies and Expansion of the Substrate Scope of Direct Enantioselective Alkynylation of α-Ketiminoesters Catalyzed by Adaptable (Phebox)Rhodium(III) Complexes.
Journal of the American Chemical Society, 2016, 138, 6194-6203
4125072 CIFBa Hg Se2P m c 214.358; 14.881; 7.59
90; 90; 90
492.22Li, Chao; Yin, Wenlong; Gong, Pifu; Li, Xiaoshuang; Zhou, Molin; Mar, Arthur; Lin, Zheshuai; Yao, Jiyong; Wu, Yicheng; Chen, Chuangtian
Trigonal Planar [HgSe3](4-) Unit: A New Kind of Basic Functional Group in IR Nonlinear Optical Materials with Large Susceptibility and Physicochemical Stability.
Journal of the American Chemical Society, 2016, 138, 6135-6138
4125073 CIFC32 H40 B2 O2C 1 2/c 121.179; 18.427; 14.466
90; 99.82; 90
5563Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125074 CIFC32 H40 B2 O2P 21 21 219.147; 9.787; 31.937
90; 90; 90
2859.1Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125075 CIFC32 H40 B2 O2P 1 21/n 18.818; 36.059; 8.85
90; 90.252; 90
2814Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125076 CIFC32 H39 B2 Br O2P 1 21/c 115.857; 10.022; 19.656
90; 111.004; 90
2916.2Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125077 CIFC32 H39 B2 Br O2P 1 21/c 111.783; 15.689; 15.773
90; 99.815; 90
2873.2Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125078 CIFC32 H39 B2 Br O2C 1 2/c 123.103; 16.332; 15.614
90; 99.64; 90
5808.3Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125079 CIFC32 H39 B2 Br O2P 1 21/c 111.801; 15.554; 16.698
90; 104.974; 90
2960.9Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125080 CIFC34 H45 B2 N O2P 1 n 19.667; 11.589; 14.115
90; 96.22; 90
1572Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125081 CIFC32 H39 B2 F O2C 1 2/c 121.448; 18.667; 14.378
90; 100.147; 90
5666Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125082 CIFC32 H39 B2 F O2P 1 21/n 18.705; 35.874; 9.064
90; 90.276; 90
2830.5Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125083 CIFC33 H39 B2 F3 O2P -114.316; 14.506; 15.944
90.042; 112.231; 94.799
3052.3Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125084 CIFC33 H39 B2 F3 O2P -18.4771; 12.1269; 16.329
70.166; 81.088; 69.721
1479.9Kojima, Chiemi; Lee, Ka-Ho; Lin, Zhenyang; Yamashita, Makoto
Direct and Base-Catalyzed Diboration of Alkynes Using the Unsymmetrical Diborane(4), pinB-BMes2.
Journal of the American Chemical Society, 2016, 138, 6662-6669
4125085 CIFC41 H37 Au N O PP 1 21/c 115.935; 13.013; 17.978
90; 112.28; 90
3449.6Hong, Eugene Yau-Hin; Poon, Chun-Ting; Yam, Vivian Wing-Wah
A Phosphole Oxide-Containing Organogold(III) Complex for Solution-Processable Resistive Memory Devices with Ternary Memory Performances.
Journal of the American Chemical Society, 2016, 138, 6368-6371
4125086 CIFC10 H11 N O3 SP 1 21 19.1983; 16.7173; 13.7123
90; 90.549; 90
2108.5Huang, Yuan; Huang, Rui-Zhi; Zhao, Yu
Cobalt-Catalyzed Enantioselective Vinylation of Activated Ketones and Imines.
Journal of the American Chemical Society, 2016, 138, 6571-6576
4125087 CIFC19 H17 Cl O3P 1 21 15.9854; 7.5004; 18.085
90; 97.565; 90
804.82Huang, Yuan; Huang, Rui-Zhi; Zhao, Yu
Cobalt-Catalyzed Enantioselective Vinylation of Activated Ketones and Imines.
Journal of the American Chemical Society, 2016, 138, 6571-6576
4125088 CIFC11 H12 O3P 21 21 215.8398; 21.5974; 23.1903
90; 90; 90
2924.86Huang, Yuan; Huang, Rui-Zhi; Zhao, Yu
Cobalt-Catalyzed Enantioselective Vinylation of Activated Ketones and Imines.
Journal of the American Chemical Society, 2016, 138, 6571-6576
4125091 CIFC45 H38 P2P 1 21/c 114.8855; 11.3406; 20.3764
90; 94.041; 90
3431.2Transue, Wesley J.; Velian, Alexandra; Nava, Matthew; Martin-Drumel, Marie-Aline; Womack, Caroline C.; Jiang, Jun; Hou, Gao-Lei; Wang, Xue-Bin; McCarthy, Michael C.; Field, Robert W.; Cummins, Christopher C.
A Molecular Precursor to Phosphaethyne and Its Application in Synthesis of the Aromatic 1,2,3,4-Phosphatriazolate Anion.
Journal of the American Chemical Society, 2016, 138, 6731-6734
4125092 CIFC33 H59 K N5 O7 PP -111.0044; 12.0737; 13.946
83.904; 82.249; 85.085
1820.8Transue, Wesley J.; Velian, Alexandra; Nava, Matthew; Martin-Drumel, Marie-Aline; Womack, Caroline C.; Jiang, Jun; Hou, Gao-Lei; Wang, Xue-Bin; McCarthy, Michael C.; Field, Robert W.; Cummins, Christopher C.
A Molecular Precursor to Phosphaethyne and Its Application in Synthesis of the Aromatic 1,2,3,4-Phosphatriazolate Anion.
Journal of the American Chemical Society, 2016, 138, 6731-6734
4125093 CIFC7 H19 N6 P SP -16.0072; 10.1348; 10.3082
90.002; 89.996; 83.296
623.29Transue, Wesley J.; Velian, Alexandra; Nava, Matthew; Martin-Drumel, Marie-Aline; Womack, Caroline C.; Jiang, Jun; Hou, Gao-Lei; Wang, Xue-Bin; McCarthy, Michael C.; Field, Robert W.; Cummins, Christopher C.
A Molecular Precursor to Phosphaethyne and Its Application in Synthesis of the Aromatic 1,2,3,4-Phosphatriazolate Anion.
Journal of the American Chemical Society, 2016, 138, 6731-6734
4125094 CIFC29 H36 Cl2 O8P -110.1108; 12.5567; 12.7249
91.518; 110.105; 113.487
1366.1Kaplan, Will; Khatri, Hem Raj; Nagorny, Pavel
Concise Enantioselective Total Synthesis of Cardiotonic Steroids 19-Hydroxysarmentogenin and Trewianin Aglycone.
Journal of the American Chemical Society, 2016, 138, 7194-7198
4125095 CIFC28 H19 Br4 N O6C 1 2/c 126.4265; 11.8821; 19.8835
90; 115.18; 90
5650.2Quint, Valentin; Morlet-Savary, Fabrice; Lohier, Jean-François; Lalevée, Jacques; Gaumont, Annie-Claude; Lakhdar, Sami
Metal-Free, Visible Light-Photocatalyzed Synthesis of Benzo[b]phosphole Oxides: Synthetic and Mechanistic Investigations.
Journal of the American Chemical Society, 2016, 138, 7436-7441
4125096 CIFC10 H14 O5P 1 21/c 13.9342; 27.324; 9.9305
90; 96.314; 90
1061Li, Gang; Kuo, Jonathan L.; Han, Arthur; Abuyuan, Janine M.; Young, Lily C.; Norton, Jack R.; Palmer, Joshua H.
Radical Isomerization and Cycloisomerization Initiated by H• Transfer.
Journal of the American Chemical Society, 2016, 138, 7698-7704
4125097 CIFC22 H18 Br2 N S7 Si2C 1 2/c 121.1775; 18.3158; 7.0825
90; 93.269; 90
2742.7Wang, Ying; Zhang, Hui; Pink, Maren; Olankitwanit, Arnon; Rajca, Suchada; Rajca, Andrzej
Radical Cation and Neutral Radical of Aza-thia[7]helicene with SOMO-HOMO Energy Level Inversion.
Journal of the American Chemical Society, 2016, 138, 7298-7304
4125098 CIFC14 H32 N6 O5P b c n8.8452; 16.0629; 13.7551
90; 90; 90
1954.32Kim, Byoungmoo; Chinn, Alex J.; Fandrick, Daniel R.; Senanayake, Chris H.; Singer, Robert A.; Miller, Scott J.
Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.
Journal of the American Chemical Society, 2016, 138, 7939-7945
4125099 CIFC18 H40 Li N5 O11P 1 21 111.543; 7.5993; 14.3503
90; 99.189; 90
1242.64Kim, Byoungmoo; Chinn, Alex J.; Fandrick, Daniel R.; Senanayake, Chris H.; Singer, Robert A.; Miller, Scott J.
Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.
Journal of the American Chemical Society, 2016, 138, 7939-7945
4125100 CIFC21 H18 Br2 F6 N2 O2P 1 21/c 112.3264; 13.9962; 13.345
90; 100.34; 90
2264.9Kim, Byoungmoo; Chinn, Alex J.; Fandrick, Daniel R.; Senanayake, Chris H.; Singer, Robert A.; Miller, Scott J.
Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.
Journal of the American Chemical Society, 2016, 138, 7939-7945
4125101 CIFC10 H23 N3 O3P 21 21 218.1091; 9.773; 16.327
90; 90; 90
1293.9Kim, Byoungmoo; Chinn, Alex J.; Fandrick, Daniel R.; Senanayake, Chris H.; Singer, Robert A.; Miller, Scott J.
Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.
Journal of the American Chemical Society, 2016, 138, 7939-7945
4125102 CIFC8 H18 F6 N3 O2 PP 1 21/n 110.8788; 8.3292; 15.9771
90; 97.955; 90
1433.78Kim, Byoungmoo; Chinn, Alex J.; Fandrick, Daniel R.; Senanayake, Chris H.; Singer, Robert A.; Miller, Scott J.
Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.
Journal of the American Chemical Society, 2016, 138, 7939-7945
4125103 CIFC12 H15 B F4 N2 OP 1 21/n 111.6467; 10.9394; 11.9902
90; 117.808; 90
1351.23Lau, Genevieve P. S.; Schreier, Marcel; Vasilyev, Dmitry; Scopelliti, Rosario; Grätzel, Michael; Dyson, Paul J.
New Insights Into the Role of Imidazolium-Based Promoters for the Electroreduction of CO2 on a Silver Electrode.
Journal of the American Chemical Society, 2016, 138, 7820-7823
4125104 CIFC12 H12 B F4 N3P -16.6104; 9.5196; 10.5103
93.681; 98.829; 91.89
651.6Lau, Genevieve P. S.; Schreier, Marcel; Vasilyev, Dmitry; Scopelliti, Rosario; Grätzel, Michael; Dyson, Paul J.
New Insights Into the Role of Imidazolium-Based Promoters for the Electroreduction of CO2 on a Silver Electrode.
Journal of the American Chemical Society, 2016, 138, 7820-7823
4125105 CIFC11 H12 B F5 N2P -110.4842; 10.524; 12.4159
114.73; 90.775; 90.061
1244.1Lau, Genevieve P. S.; Schreier, Marcel; Vasilyev, Dmitry; Scopelliti, Rosario; Grätzel, Michael; Dyson, Paul J.
New Insights Into the Role of Imidazolium-Based Promoters for the Electroreduction of CO2 on a Silver Electrode.
Journal of the American Chemical Society, 2016, 138, 7820-7823
4125106 CIFC11 H13 B F4 N2P -110.153; 10.7563; 12.182
88.021; 65.88; 85.439
1210.4Lau, Genevieve P. S.; Schreier, Marcel; Vasilyev, Dmitry; Scopelliti, Rosario; Grätzel, Michael; Dyson, Paul J.
New Insights Into the Role of Imidazolium-Based Promoters for the Electroreduction of CO2 on a Silver Electrode.
Journal of the American Chemical Society, 2016, 138, 7820-7823
4125107 CIFC20 H30 Cl Cu I NP 1 21/c 110.0336; 9.9876; 21.8458
90; 95.333; 90
2179.7Chu, Jiaxiang; Munz, Dominik; Jazzar, Rodolphe; Melaimi, Mohand; Bertrand, Guy
Synthesis of Hemilabile Cyclic (Alkyl)(amino)carbenes (CAACs) and Applications in Organometallic Chemistry.
Journal of the American Chemical Society, 2016, 138, 7884-7887
4125108 CIFC78 H68 Au B F20 N2P -113.7142; 15.7707; 15.8385
88.698; 87.417; 82.569
3392.9Chu, Jiaxiang; Munz, Dominik; Jazzar, Rodolphe; Melaimi, Mohand; Bertrand, Guy
Synthesis of Hemilabile Cyclic (Alkyl)(amino)carbenes (CAACs) and Applications in Organometallic Chemistry.
Journal of the American Chemical Society, 2016, 138, 7884-7887
4125109 CIFC36 H54 Au Cl N2P -110.0911; 18.5601; 19.6959
106.828; 94.902; 98.618
3458.6Chu, Jiaxiang; Munz, Dominik; Jazzar, Rodolphe; Melaimi, Mohand; Bertrand, Guy
Synthesis of Hemilabile Cyclic (Alkyl)(amino)carbenes (CAACs) and Applications in Organometallic Chemistry.
Journal of the American Chemical Society, 2016, 138, 7884-7887
4125110 CIFC22 H36 Cl Cu N2P 1 21 18.4234; 16.0108; 8.5636
90; 101.32; 90
1132.47Chu, Jiaxiang; Munz, Dominik; Jazzar, Rodolphe; Melaimi, Mohand; Bertrand, Guy
Synthesis of Hemilabile Cyclic (Alkyl)(amino)carbenes (CAACs) and Applications in Organometallic Chemistry.
Journal of the American Chemical Society, 2016, 138, 7884-7887
4125111 CIFC13 H19 N3 SP 1 21 16.3999; 18.9408; 11.3358
90; 92.523; 90
1372.78Howe, Ethan N. W.; Busschaert, Nathalie; Wu, Xin; Berry, Stuart N.; Ho, Junming; Light, Mark E.; Czech, Dawid D.; Klein, Harry A.; Kitchen, Jonathan A.; Gale, Philip A.
pH-Regulated Nonelectrogenic Anion Transport by Phenylthiosemicarbazones.
Journal of the American Chemical Society, 2016, 138, 8301-8308
4125112 CIFC14 H21 N3 O SP b c a10.5978; 10.4507; 27.0588
90; 90; 90
2996.9Howe, Ethan N. W.; Busschaert, Nathalie; Wu, Xin; Berry, Stuart N.; Ho, Junming; Light, Mark E.; Czech, Dawid D.; Klein, Harry A.; Kitchen, Jonathan A.; Gale, Philip A.
pH-Regulated Nonelectrogenic Anion Transport by Phenylthiosemicarbazones.
Journal of the American Chemical Society, 2016, 138, 8301-8308
4125113 CIFC14 H18 F3 N3 SP 1 21/c 113.7959; 13.3873; 8.3649
90; 92.859; 90
1542.99Howe, Ethan N. W.; Busschaert, Nathalie; Wu, Xin; Berry, Stuart N.; Ho, Junming; Light, Mark E.; Czech, Dawid D.; Klein, Harry A.; Kitchen, Jonathan A.; Gale, Philip A.
pH-Regulated Nonelectrogenic Anion Transport by Phenylthiosemicarbazones.
Journal of the American Chemical Society, 2016, 138, 8301-8308
4125114 CIFC13 H17 N3 SP 1 21/c 115.8157; 7.5474; 11.0448
90; 91.419; 90
1317.98Howe, Ethan N. W.; Busschaert, Nathalie; Wu, Xin; Berry, Stuart N.; Ho, Junming; Light, Mark E.; Czech, Dawid D.; Klein, Harry A.; Kitchen, Jonathan A.; Gale, Philip A.
pH-Regulated Nonelectrogenic Anion Transport by Phenylthiosemicarbazones.
Journal of the American Chemical Society, 2016, 138, 8301-8308
4125115 CIFC23 H24 N2 O3P 21 21 217.9683; 10.4097; 22.0972
90; 90; 90
1832.91Allemann, Oliver; Brutsch, Manuela; Lukesh, 3rd, John C; Brody, Daniel M.; Boger, Dale L.
Synthesis of a Potent Vinblastine: Rationally Designed Added Benign Complexity.
Journal of the American Chemical Society, 2016, 138, 8376-8379
4125116 CIFC25 H38 Cl7 NP 1 21/n 19.8718; 16.9815; 36.212
90; 97.081; 90
6024.2Zhukhovitskiy, Aleksandr V.; Mavros, Michael G.; Queeney, K. T.; Wu, Tony; Voorhis, Troy Van; Johnson, Jeremiah A.
Reactions of Persistent Carbenes with Hydrogen-Terminated Silicon Surfaces.
Journal of the American Chemical Society, 2016, 138, 8639-8652
4125117 CIFC19 H29 F3 N2 O5 SP -112.6127; 15.2311; 17.9955
69.5328; 88.0275; 88.8565
3236.8Zhukhovitskiy, Aleksandr V.; Mavros, Michael G.; Queeney, K. T.; Wu, Tony; Voorhis, Troy Van; Johnson, Jeremiah A.
Reactions of Persistent Carbenes with Hydrogen-Terminated Silicon Surfaces.
Journal of the American Chemical Society, 2016, 138, 8639-8652
4125118 CIFC32 H63 N Si4P 1 21/n 112.4987; 16.0655; 17.6184
90; 94.9451; 90
3524.6Zhukhovitskiy, Aleksandr V.; Mavros, Michael G.; Queeney, K. T.; Wu, Tony; Voorhis, Troy Van; Johnson, Jeremiah A.
Reactions of Persistent Carbenes with Hydrogen-Terminated Silicon Surfaces.
Journal of the American Chemical Society, 2016, 138, 8639-8652
4125119 CIFC25 H29 F3 N2 O5 SP 1 21/n 18.7865; 21.4221; 13.4402
90; 94.5721; 90
2521.7Zhukhovitskiy, Aleksandr V.; Mavros, Michael G.; Queeney, K. T.; Wu, Tony; Voorhis, Troy Van; Johnson, Jeremiah A.
Reactions of Persistent Carbenes with Hydrogen-Terminated Silicon Surfaces.
Journal of the American Chemical Society, 2016, 138, 8639-8652
4125120 CIFC14 H15 Cl4 N4 O Ru SP 1 21/n 17.1525; 23.0424; 11.829
90; 90.688; 90
1949.4Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125121 CIFC14 H15 Cl4 F6 N2 O Ru SP 1 21/n 17.8013; 10.8212; 25.017
90; 95.03; 90
2103.79Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125122 CIFC26.5 H30 Cl5 N2 O Ru SP -115.1499; 17.3913; 23.9791
76.679; 89.978; 77.344
5990.2Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125123 CIFC14 H21 Cl4 N2 O Rh SP -19.2004; 15.21; 15.6366
71.257; 73.832; 72.534
1936.04Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125124 CIFC14 H15 Cl4 N4 O Rh SP 1 21/n 17.1887; 22.9114; 11.8104
90; 90.63; 90
1945.09Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125125 CIFC14 H15 Cl4 F6 N2 O Rh SP 1 21/n 17.7976; 10.7641; 25.0618
90; 95.151; 90
2095Novotný, Jan; Sojka, Martin; Komorovsky, Stanislav; Nečas, Marek; Marek, Radek
Interpreting the Paramagnetic NMR Spectra of Potential Ru(III) Metallodrugs: Synergy between Experiment and Relativistic DFT Calculations.
Journal of the American Chemical Society, 2016, 138, 8432-8445
4125126 CIFC22 H27 I N O PP -112.0966; 12.7937; 16.0697
81.918; 70.076; 64.935
2117.9Yang, Youqing; Li, Ruirui; Zhao, Yue; Zhao, Dongbing; Shi, Zhuangzhi
Cu-Catalyzed Direct C6-Arylation of Indoles.
Journal of the American Chemical Society, 2016, 138, 8734-8737
4125127 CIFC22 H28 N O PP b c a13.0319; 12.8304; 23.089
90; 90; 90
3860.6Yang, Youqing; Li, Ruirui; Zhao, Yue; Zhao, Dongbing; Shi, Zhuangzhi
Cu-Catalyzed Direct C6-Arylation of Indoles.
Journal of the American Chemical Society, 2016, 138, 8734-8737
4125128 CIFC23 H24 O8P 1 21/n 14.581; 20.94; 21.9
90; 92.86; 90
2098Lahive, Ciaran W.; Deuss, Peter J.; Lancefield, Christopher S.; Sun, Zhuohua; Cordes, David B.; Young, Claire M.; Tran, Fanny; Slawin, Alexandra M. Z.; de Vries, Johannes G.; Kamer, Paul C. J.; Westwood, Nicholas J.; Barta, Katalin
Advanced Model Compounds for Understanding Acid-Catalyzed Lignin Depolymerization: Identification of Renewable Aromatics and a Lignin-Derived Solvent.
Journal of the American Chemical Society, 2016, 138, 8900-8911
4125129 CIFC20 H20 O7P 1 21/c 18.6085; 26.787; 7.8482
90; 97.903; 90
1792.6Lahive, Ciaran W.; Deuss, Peter J.; Lancefield, Christopher S.; Sun, Zhuohua; Cordes, David B.; Young, Claire M.; Tran, Fanny; Slawin, Alexandra M. Z.; de Vries, Johannes G.; Kamer, Paul C. J.; Westwood, Nicholas J.; Barta, Katalin
Advanced Model Compounds for Understanding Acid-Catalyzed Lignin Depolymerization: Identification of Renewable Aromatics and a Lignin-Derived Solvent.
Journal of the American Chemical Society, 2016, 138, 8900-8911
4125130 CIFC64 H48 O40 Zr6P 42/m m c24.263; 24.263; 14.615
90; 90; 90
8604Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125131 CIFC56 H24 N8 O48 Zr6P 42/m m c24.25; 24.25; 15.232
90; 90; 90
8957Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125132 CIFC64 H56 O32 Zr6P 42/m m c24.348; 24.348; 14.918
90; 90; 90
8844Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125133 CIFC56 H24 I8 O32 Zr6P 42/m m c24.35; 24.354; 14.797
90; 90; 90
8775Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125134 CIFC64 H24 F24 O32 Zr6P 42/n c m :234.882; 34.882; 12.086
90; 90; 90
14706Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125135 CIFC56 H16 N16 O64 Zr6P 42/m m c23.024; 23.024; 18.6484
90; 90; 90
9885.6Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125136 CIFC72 H64 O32 Zr6P 42/m m c24.218; 24.218; 15.359
90; 90; 90
9008Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125137 CIFC98 H70 Cu0.53 I0.27 N2.27 O32 Zr6P 42/m m c23.0867; 23.087; 18.8049
90; 90; 90
10023.1Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125138 CIFC68 H50 O32 Zr6P 42/n c m :235.053; 35.053; 12.665
90; 90; 90
15562Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125139 CIFC72 H58 O32 Zr6P 42/m m c24.4; 24.401; 14.88
90; 90; 90
8859Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125140 CIFC76 H54 O32 Zr6P 42/m m c23.679; 23.679; 16.816
90; 90; 90
9429Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125141 CIFC70 H40 O32 Zr6P 42/m m c23.07; 23.075; 19.16
90; 90; 90
10200Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125142 CIFC86 H70 O32 Zr6P 42/m m c23.91; 23.91; 16.057
90; 90; 90
9180Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125143 CIFC74 H54 O32 Zr6P 42/m m c24.378; 24.378; 15.017
90; 90; 90
8924Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125144 CIFC83 H65 O32 Zr6P 42/m n m34.29; 34.293; 14.665
90; 90; 90
17245Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125145 CIFC82 H58 O32 Zr6P 42/m m c24.288; 24.288; 14.859
90; 90; 90
8765Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125146 CIFC87 H62 O32 Zr6P 42/m n m33.505; 33.505; 16.824
90; 90; 90
18886Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125147 CIFC96 H66 O32 Zr6P 42/m m c23.9; 23.9; 16.817
90; 90; 90
9606Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125148 CIFC80.8 H49.6 O28.8 Zr6P 42/m m c23.33; 23.332; 19.07
90; 90; 90
10380Yuan, Shuai; Chen, Ying-Pin; Qin, Jun-Sheng; Lu, Weigang; Zou, Lanfang; Zhang, Qiang; Wang, Xuan; Sun, Xing; Zhou, Hong-Cai
Linker Installation: Engineering Pore Environment with Precisely Placed Functionalities in Zirconium MOFs.
Journal of the American Chemical Society, 2016, 138, 8912-8919
4125149 CIFC30 H16 B2 O4P -17.0696; 10.6921; 16.9433
105.252; 91.082; 103.892
1194.9Wang, Xiao-Ye; Narita, Akimitsu; Zhang, Wen; Feng, Xinliang; Müllen, Klaus
Synthesis of Stable Nanographenes with OBO-Doped Zigzag Edges Based on Tandem Demethylation-Electrophilic Borylation.
Journal of the American Chemical Society, 2016, 138, 9021-9024
4125150 CIFC6 H16 B10 N2P n a 2112.788; 10.8486; 9.2601
90; 90; 90
1284.7Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125151 CIFC10 H20 B10 OP 1 21/n 18.6489; 13.1773; 13.8649
90; 94.794; 90
1574.64Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125152 CIFC3 H11 B10 NP b c a12.862; 12.2276; 13.0826
90; 90; 90
2057.5Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125153 CIFC18 H28 B10 O2P -17.7608; 11.8506; 13.1031
103.335; 100.977; 103.535
1101.34Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125154 CIFC2 H11 B10 Br OP b c a12.5493; 13.4359; 24.2837
90; 90; 90
4094.5Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125155 CIFC10 H20 B10 OP 21 21 217.6501; 13.2544; 15.2454
90; 90; 90
1545.85Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125156 CIFC10 H21 B10 N O2P -112.7259; 12.9299; 20.6344
100.156; 98.573; 96.338
3272Dziedzic, Rafal M.; Saleh, Liban M. A.; Axtell, Jonathan C.; Martin, Joshua L.; Stevens, Simone L.; Royappa, A. Timothy; Rheingold, Arnold L.; Spokoyny, Alexander M.
B-N, B-O, and B-CN Bond Formation via Palladium-Catalyzed Cross-Coupling of B-Bromo-Carboranes.
Journal of the American Chemical Society, 2016, 138, 9081-9084
4125157 CIFC49 H32 Cl2 F12 I2 O6P -110.0301; 11.1977; 12.2876
89.531; 71.447; 64.321
1165.47Wu, Junliang; Deng, Xiaozhou; Hirao, Hajime; Yoshikai, Naohiko
Pd-Catalyzed Conversion of Alkynyl-λ(3)-iodanes to Alkenyl-λ(3)-iodanes via Stereoselective 1,2-Iodine(III) Shift/1,1-Hydrocarboxylation.
Journal of the American Chemical Society, 2016, 138, 9105-9108
4125158 CIFC24 H15 F6 I O3P -18.8713; 10.9507; 11.5619
86.324; 83.416; 88.711
1113.37Wu, Junliang; Deng, Xiaozhou; Hirao, Hajime; Yoshikai, Naohiko
Pd-Catalyzed Conversion of Alkynyl-λ(3)-iodanes to Alkenyl-λ(3)-iodanes via Stereoselective 1,2-Iodine(III) Shift/1,1-Hydrocarboxylation.
Journal of the American Chemical Society, 2016, 138, 9105-9108
4125159 CIFC56 H80 Cl N2 Os PP 1 21/c 112.5093; 13.2893; 31.967
90; 93.927; 90
5301.7Buil, María L; Cardo, Juan J. F.; Esteruelas, Miguel A.; Oñate, Enrique
Square-Planar Alkylidyne-Osmium and Five-Coordinate Alkylidene-Osmium Complexes: Controlling the Transformation from Hydride-Alkylidyne to Alkylidene.
Journal of the American Chemical Society, 2016, 138, 9720-9728
4125160 CIFC45.5 H68 Cl N2 Os PP 42/n :224.642; 24.642; 16.016
90; 90; 90
9725Buil, María L; Cardo, Juan J. F.; Esteruelas, Miguel A.; Oñate, Enrique
Square-Planar Alkylidyne-Osmium and Five-Coordinate Alkylidene-Osmium Complexes: Controlling the Transformation from Hydride-Alkylidyne to Alkylidene.
Journal of the American Chemical Society, 2016, 138, 9720-9728
4125161 CIFC196 Cu24 O120P -124.307; 24.5206; 25.3072
118.393; 111.787; 93.769
11767.2Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125162 CIFC192 Cu24 N24 O168R -336.076; 36.076; 29.2307
90; 90; 120
32946Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125163 CIFC192 Cu24 O144I 4/m27.401; 27.401; 35.409
90; 90; 90
26586Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125164 CIFC36 Cu4 O20R -335.66; 35.66; 30.219
90; 90; 120
33279Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125165 CIFC192 H96 Cu24 O120I m -3 m27.57; 27.57; 27.57
90; 90; 90
20956Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125166 CIFC192 Cu28 N24 O132I 4/m m m26.217; 26.217; 44.813
90; 90; 90
30801Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125167 CIFC198 Cu24 N24 O168R -3 :H36.173; 36.173; 29.289
90; 90; 120
33190Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125168 CIFC200 Cu24 O145I 4/m27.571; 27.571; 35.456
90; 90; 90
26952Chen, Teng-Hao; Wang, Le; Trueblood, Jonathan V.; Grassian, Vicki H.; Cohen, Seth M.
Poly(isophthalic acid)(ethylene oxide) as a Macromolecular Modulator for Metal-Organic Polyhedra.
Journal of the American Chemical Society, 2016, 138, 9646-9654
4125169 CIFC30 H21 N2 P SP -19.5544; 11.6505; 12.0027
72.481; 69.051; 73.391
1165.8Tao, Ye; Xu, Lijia; Zhang, Zhen; Chen, Runfeng; Li, Huanhuan; Xu, Hui; Zheng, Chao; Huang, Wei
Achieving Optimal Self-Adaptivity for Dynamic Tuning of Organic Semiconductors through Resonance Engineering.
Journal of the American Chemical Society, 2016, 138, 9655-9662
4125170 CIFC24 H18 N P SP -19.731; 9.785; 11.1276
95.858; 101.602; 109.696
960.46Tao, Ye; Xu, Lijia; Zhang, Zhen; Chen, Runfeng; Li, Huanhuan; Xu, Hui; Zheng, Chao; Huang, Wei
Achieving Optimal Self-Adaptivity for Dynamic Tuning of Organic Semiconductors through Resonance Engineering.
Journal of the American Chemical Society, 2016, 138, 9655-9662
4125171 CIFC16 H19 N O2C 1 2/c 121.61; 7.777; 16.839
90; 93.812; 90
2824Paolino, Marco; Gueye, Moussa; Pieri, Elisa; Manathunga, Madushanka; Fusi, Stefania; Cappelli, Andrea; Latterini, Loredana; Pannacci, Danilo; Filatov, Michael; Léonard, Jérémie; Olivucci, Massimo
Design, Synthesis, and Dynamics of a Green Fluorescent Protein Fluorophore Mimic with an Ultrafast Switching Function.
Journal of the American Chemical Society, 2016, 138, 9807-9825
4125172 CIFC15 H19 N O3P -17.491; 8.603; 11.623
71.9; 71.38; 87.8
673.17Paolino, Marco; Gueye, Moussa; Pieri, Elisa; Manathunga, Madushanka; Fusi, Stefania; Cappelli, Andrea; Latterini, Loredana; Pannacci, Danilo; Filatov, Michael; Léonard, Jérémie; Olivucci, Massimo
Design, Synthesis, and Dynamics of a Green Fluorescent Protein Fluorophore Mimic with an Ultrafast Switching Function.
Journal of the American Chemical Society, 2016, 138, 9807-9825
4125173 CIFC22 H24 N2 O2P 21 21 216.3942; 11.6678; 24.848
90; 90; 90
1853.8Chapman, Lauren M.; Beck, Jordan C.; Wu, Linglin; Reisman, Sarah E.
Enantioselective Total Synthesis of (+)-Psiguadial B.
Journal of the American Chemical Society, 2016, 138, 9803-9806
4125174 CIFC57 H46 N2 O6P -112.002; 12.2342; 15.114
102.499; 99.728; 92.966
2126.5Ip, Ho-Wang; Ng, Chun-Fai; Chow, Hak-Fun; Kuck, Dietmar
Three-Fold Scholl-Type Cycloheptatriene Ring Formation around a Tribenzotriquinacene Core: Toward Warped Graphenes.
Journal of the American Chemical Society, 2016, 138, 13778
4125175 CIFC20 H35 F3 N2 O2P -15.2753; 7.7876; 25.903
90.414; 95.771; 98.112
1047.91Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125176 CIFC20 H35 F3 N4 O2 SP -15.424; 9.1759; 23.7616
88.7; 83.798; 83.935
1169.04Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125177 CIFC20 H35 F6 N3 O4 S2P -18.0522; 13.2016; 25.7191
75.731; 85.109; 88.052
2639.8Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125178 CIFC18 H35 Cl N2 O4P 1 21/n 18.4858; 56.257; 8.7349
90; 97.052; 90
4138.4Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125179 CIFC20 H35 N5P -15.3155; 7.3072; 27.5134
87.006; 85.0705; 73.2054
1018.87Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125180 CIFC19 H35 F3 N2 O3 SP 1 21/n 19.6318; 8.3408; 56.7289
90; 92.107; 90
4554.3Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125181 CIFC18 H37 Br N2 OP -15.315; 7.8401; 24.302
91.377; 94.775; 98.629
997Nelyubina, Yulia V.; Shaplov, Alexander S.; Lozinskaya, Elena I.; Buzin, Mikhail I.; Vygodskii, Yakov S.
A New Volume-Based Approach for Predicting Thermophysical Behavior of Ionic Liquids and Ionic Liquid Crystals.
Journal of the American Chemical Society, 2016, 138, 10076-10079
4125182 CIFC72 H112 I5 K2 O91P 42 21 219.826; 19.826; 30.613
90; 90; 90
12033Zhou, Hongyao; Yamada, Teppei; Kimizuka, Nobuo
Supramolecular Thermo-Electrochemical Cells: Enhanced Thermoelectric Performance by Host-Guest Complexation and Salt-Induced Crystallization.
Journal of the American Chemical Society, 2016, 138, 10502-10507
4125183 CIFC32 H48 N2 Si3P 21 21 219.8511; 16.512; 20.18
90; 90; 90
3282.5Wang, Zhendong; Zhang, Jianying; Li, Jianfeng; Cui, Chunming
NHC-Stabilized Silicon-Carbon Mixed Cumulene.
Journal of the American Chemical Society, 2016, 138, 10421-10424
4125184 CIFC21 H47 Cl N2 Si4P 1 21/n 19.1735; 17.478; 18.2
90; 101.25; 90
2862Wang, Zhendong; Zhang, Jianying; Li, Jianfeng; Cui, Chunming
NHC-Stabilized Silicon-Carbon Mixed Cumulene.
Journal of the American Chemical Society, 2016, 138, 10421-10424
4125185 CIFC22 H17 N OP 21 21 217.5669; 14.1761; 15.2272
90; 90; 90
1633.41Wang, Jie; Chen, Mu-Wang; Ji, Yue; Hu, Shu-Bo; Zhou, Yong-Gui
Kinetic Resolution of Axially Chiral 5- or 8-Substituted Quinolines via Asymmetric Transfer Hydrogenation.
Journal of the American Chemical Society, 2016, 138, 10413-10416
4125186 CIFC20 H15 NP 21 21 217.3982; 7.3861; 27.199
90; 90; 90
1486.3Wang, Jie; Chen, Mu-Wang; Ji, Yue; Hu, Shu-Bo; Zhou, Yong-Gui
Kinetic Resolution of Axially Chiral 5- or 8-Substituted Quinolines via Asymmetric Transfer Hydrogenation.
Journal of the American Chemical Society, 2016, 138, 10413-10416
4125189 CIFC16 H36 B10 O4 P2 RuP n m a14.5078; 17.5364; 10.1577
90; 90; 90
2584.27Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125190 CIFC16 H37 B10 Cl O4 P2 RuP 21 21 2111.9543; 14.3559; 16.4299
90; 90; 90
2819.6Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125191 CIFC21 H42 B10 O6 P2 RuP 1 21/c 118.6818; 8.9257; 19.5607
90; 91.606; 90
3260.4Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125192 CIFC18 H36 B10 D3 I2 O3 P2 RuC 1 2/m 115.7357; 12.9295; 15.8165
90; 103.388; 90
3130.5Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125193 CIFC22 H46 B10 O4 P2 RuP 1 21/c 110.908; 13.3367; 21.9824
90; 99.305; 90
3155.8Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125194 CIFC16 H39 B11 O4 P2 RuP 1 21/n 19.2907; 14.0608; 20.6883
90; 94.379; 90
2694.7Eleazer, Bennett J.; Smith, Mark D.; Popov, Alexey A.; Peryshkov, Dmitry V.
(BB)-Carboryne Complex of Ruthenium: Synthesis by Double B-H Activation at a Single Metal Center.
Journal of the American Chemical Society, 2016, 138, 10531-10538
4125195 CIFC34 H54 B Li N4 OP 111.97; 12.297; 17.763
80.063; 76.452; 82.123
2491Mukherjee, Debabrata; Osseili, Hassan; Spaniol, Thomas P.; Okuda, Jun
Alkali Metal Hydridotriphenylborates [(L)M][HBPh3] (M = Li, Na, K): Chemoselective Catalysts for Carbonyl and CO2 Hydroboration.
Journal of the American Chemical Society, 2016, 138, 10790-10793
4125196 CIFC30 H46 B K N4P 1 21/c 116.436; 10.063; 18
90; 91.481; 90
2976Mukherjee, Debabrata; Osseili, Hassan; Spaniol, Thomas P.; Okuda, Jun
Alkali Metal Hydridotriphenylborates [(L)M][HBPh3] (M = Li, Na, K): Chemoselective Catalysts for Carbonyl and CO2 Hydroboration.
Journal of the American Chemical Society, 2016, 138, 10790-10793
4125197 CIFC31 H46 B Li N4 O2P -311.66; 11.66; 13.306
90; 90; 120
1566.7Mukherjee, Debabrata; Osseili, Hassan; Spaniol, Thomas P.; Okuda, Jun
Alkali Metal Hydridotriphenylborates [(L)M][HBPh3] (M = Li, Na, K): Chemoselective Catalysts for Carbonyl and CO2 Hydroboration.
Journal of the American Chemical Society, 2016, 138, 10790-10793
4125198 CIFC31 H46 B N4 Na O2P -113.3224; 17.05; 17.6861
99.8463; 111.99; 112.862
3188.3Mukherjee, Debabrata; Osseili, Hassan; Spaniol, Thomas P.; Okuda, Jun
Alkali Metal Hydridotriphenylborates [(L)M][HBPh3] (M = Li, Na, K): Chemoselective Catalysts for Carbonyl and CO2 Hydroboration.
Journal of the American Chemical Society, 2016, 138, 10790-10793
4125199 CIFC31 H46 B K N4 O2P 1 21/c 19.57; 19.486; 17.762
90; 102.244; 90
3236.9Mukherjee, Debabrata; Osseili, Hassan; Spaniol, Thomas P.; Okuda, Jun
Alkali Metal Hydridotriphenylborates [(L)M][HBPh3] (M = Li, Na, K): Chemoselective Catalysts for Carbonyl and CO2 Hydroboration.
Journal of the American Chemical Society, 2016, 138, 10790-10793
4125200 CIFC43 H42 Co2 O4 P2 S SiP 21 21 2112.8244; 12.9947; 24.5725
90; 90; 90
4095Terada, Masahiro; Ota, Yusuke; Li, Feng; Toda, Yasunori; Kondoh, Azusa
Enantioconvergent Nucleophilic Substitution Reaction of Racemic Alkyne-Dicobalt Complex (Nicholas Reaction) Catalyzed by Chiral Brønsted Acid.
Journal of the American Chemical Society, 2016, 138, 11038-11043
4125201 CIFC21 H15 F3P n a 2116.638; 5.481; 33.4803
90; 90; 90
3053.2Toriyama, Fumihiko; Cornella, Josep; Wimmer, Laurin; Chen, Tie-Gen; Dixon, Darryl D.; Creech, Gardner; Baran, Phil S.
Redox-Active Esters in Fe-Catalyzed C-C Coupling.
Journal of the American Chemical Society, 2016, 138, 11132-11135
4125202 CIFC21 H18 OC 1 2/c 117.8244; 7.5148; 22.276
90; 99.79; 90
2940.35Toriyama, Fumihiko; Cornella, Josep; Wimmer, Laurin; Chen, Tie-Gen; Dixon, Darryl D.; Creech, Gardner; Baran, Phil S.
Redox-Active Esters in Fe-Catalyzed C-C Coupling.
Journal of the American Chemical Society, 2016, 138, 11132-11135
4125203 CIFC19 H20 OP 1 2/c 118.758; 5.7669; 13.563
90; 110.826; 90
1371.3Toriyama, Fumihiko; Cornella, Josep; Wimmer, Laurin; Chen, Tie-Gen; Dixon, Darryl D.; Creech, Gardner; Baran, Phil S.
Redox-Active Esters in Fe-Catalyzed C-C Coupling.
Journal of the American Chemical Society, 2016, 138, 11132-11135
4125204 CIFC105 H141 Fe3 K N10 O6P -113.9066; 18.4465; 20.5506
89.068; 71.963; 81.667
4957.5MacLeod, K. Cory; Menges, Fabian S.; McWilliams, Sean F.; Craig, Stephanie M.; Mercado, Brandon Q.; Johnson, Mark A.; Holland, Patrick L.
Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.
Journal of the American Chemical Society, 2016, 138, 11185-11191
4125205 CIFC71 H94 Fe3 N8 OP 1 21/c 113.6536; 18.9103; 25.4722
90; 101.305; 90
6449.2MacLeod, K. Cory; Menges, Fabian S.; McWilliams, Sean F.; Craig, Stephanie M.; Mercado, Brandon Q.; Johnson, Mark A.; Holland, Patrick L.
Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.
Journal of the American Chemical Society, 2016, 138, 11185-11191
4125206 CIFC66 H81 Fe3 N8P -111.7403; 13.7572; 21.6519
97.973; 92.876; 107.661
3284.2MacLeod, K. Cory; Menges, Fabian S.; McWilliams, Sean F.; Craig, Stephanie M.; Mercado, Brandon Q.; Johnson, Mark A.; Holland, Patrick L.
Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.
Journal of the American Chemical Society, 2016, 138, 11185-11191
4125207 CIFC86 H122 Fe3 K N8 O8P -113.5997; 18.2403; 20.2851
88.986; 84.849; 85.023
4992.5MacLeod, K. Cory; Menges, Fabian S.; McWilliams, Sean F.; Craig, Stephanie M.; Mercado, Brandon Q.; Johnson, Mark A.; Holland, Patrick L.
Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.
Journal of the American Chemical Society, 2016, 138, 11185-11191
4125208 CIFC78 H107 Fe3 K N8 O6C 1 c 127.2669; 18.0306; 20.0074
90; 95.201; 90
9795.9MacLeod, K. Cory; Menges, Fabian S.; McWilliams, Sean F.; Craig, Stephanie M.; Mercado, Brandon Q.; Johnson, Mark A.; Holland, Patrick L.
Alkali-Controlled C-H Cleavage or N-C Bond Formation by N2-Derived Iron Nitrides and Imides.
Journal of the American Chemical Society, 2016, 138, 11185-11191
4125209 CIFC56 H88 Fe2 N2 S8P -112.6555; 15.1068; 16.1136
85.1546; 88.2286; 75.2419
2968.2Lv, Hongjin; Ruberu, T Purnima A; Fleischauer, Valerie E.; Brennessel, William W.; Neidig, Michael L.; Eisenberg, Richard
Catalytic Light-Driven Generation of Hydrogen from Water by Iron Dithiolene Complexes.
Journal of the American Chemical Society, 2016, 138, 11654-11663
4125210 CIFC60 H96 Fe2 N2 S8R -3 :H34.115; 34.115; 15.1763
90; 90; 120
15296.3Lv, Hongjin; Ruberu, T Purnima A; Fleischauer, Valerie E.; Brennessel, William W.; Neidig, Michael L.; Eisenberg, Richard
Catalytic Light-Driven Generation of Hydrogen from Water by Iron Dithiolene Complexes.
Journal of the American Chemical Society, 2016, 138, 11654-11663
4125211 CIFC56 H80 Cl8 Fe2 N2 S8P 1 21/n 114.0308; 16.9507; 14.2666
90; 103.778; 90
3295.4Lv, Hongjin; Ruberu, T Purnima A; Fleischauer, Valerie E.; Brennessel, William W.; Neidig, Michael L.; Eisenberg, Richard
Catalytic Light-Driven Generation of Hydrogen from Water by Iron Dithiolene Complexes.
Journal of the American Chemical Society, 2016, 138, 11654-11663
4125212 CIFC56 H72 Cl16 Fe2 N2 S8P 1 21/c 113.9394; 18.7636; 15.3821
90; 115.958; 90
3617.3Lv, Hongjin; Ruberu, T Purnima A; Fleischauer, Valerie E.; Brennessel, William W.; Neidig, Michael L.; Eisenberg, Richard
Catalytic Light-Driven Generation of Hydrogen from Water by Iron Dithiolene Complexes.
Journal of the American Chemical Society, 2016, 138, 11654-11663
4125213 CIFC84 H152 Au Cl4 O76 RbP 1 21 115.7207; 24.401; 19.1401
90; 108.67; 90
6955.8Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125214 CIFC72 H130 Au0.75 Cl4 Na O65P 113.6582; 13.9202; 15.6235
93.585; 89.976; 118.879
2594.4Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125215 CIFC288 H504 Au Cl4 O256 Rb2P 4 21 223.7355; 23.7355; 22.8031
90; 90; 90
12846.7Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125216 CIFC72 H130 Au Cl4 O65 RbP 1 21 113.951; 23.8573; 16.0436
90; 96.2619; 90
5308Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125217 CIFC84 H152 Au0.8 Cl3.2 Na0.8 O76P 1 21 115.7324; 24.3405; 19.2739
90; 108.952; 90
6980.5Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125218 CIFC72 H122 Au Br4 Na O61P 21 21 223.7683; 14.1475; 16.2856
90; 90; 90
5476.2Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125219 CIFC144 H264 Au Br4 Na O135P 4 21 223.6486; 23.6486; 22.7925
90; 90; 90
12746.8Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125220 CIFC288 H488 Au Br4 O248 Rb2P 4 21 223.7386; 23.7386; 22.7883
90; 90; 90
12841.7Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125221 CIFC84 H164 Au0.78 Br3.1 O82 Rb0.78P 1 21 115.8404; 24.5602; 19.0823
90; 108.399; 90
7044.3Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125222 CIFC288 H480 Au Cl4 Na O241P 4 21 223.761; 23.761; 22.836
90; 90; 90
12893Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125223 CIFC72 H139 Au0.89 Br3.76 Cs1.1 O69.5P 1 21 116.3326; 14.2587; 23.6886
90; 90.021; 90
5516.6Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125224 CIFC74 H142 Au Br4 O69 RbP 1 21 116.3791; 14.2585; 23.6538
90; 90.259; 90
5524.1Liu, Zhichang; Samanta, Avik; Lei, Juying; Sun, Junling; Wang, Yuping; Stoddart, J. Fraser
Cation-Dependent Gold Recovery with α-Cyclodextrin Facilitated by Second-Sphere Coordination.
Journal of the American Chemical Society, 2016, 138, 11643-11653
4125225 CIFC42 H45 B N2P -19.3703; 9.8045; 17.2896
92.27; 92.092; 93.949
1582.17Wang, Xinyang; Zhang, Fan; Schellhammer, Karl Sebastian; Machata, Peter; Ortmann, Frank; Cuniberti, Gianaurelio; Fu, Yubin; Hunger, Jens; Tang, Ruizhi; Popov, Alexey A.; Berger, Reinhard; Müllen, Klaus; Feng, Xinliang
Synthesis of NBN-Type Zigzag-Edged Polycyclic Aromatic Hydrocarbons: 1,9-Diaza-9a-boraphenalene as a Structural Motif.
Journal of the American Chemical Society, 2016, 138, 11606-11615
4125226 CIFC30 H37 B N2C 1 c 123.6678; 21.434; 9.937
90; 96.896; 90
5004.5Wang, Xinyang; Zhang, Fan; Schellhammer, Karl Sebastian; Machata, Peter; Ortmann, Frank; Cuniberti, Gianaurelio; Fu, Yubin; Hunger, Jens; Tang, Ruizhi; Popov, Alexey A.; Berger, Reinhard; Müllen, Klaus; Feng, Xinliang
Synthesis of NBN-Type Zigzag-Edged Polycyclic Aromatic Hydrocarbons: 1,9-Diaza-9a-boraphenalene as a Structural Motif.
Journal of the American Chemical Society, 2016, 138, 11606-11615
4125227 CIFC247 H395 N101 O45 Zn16I 4 m m27.373; 27.373; 18.5827
90; 90; 90
13923.7Ramirez, Joseph R.; Yang, Haiyang; Kane, Christopher M.; Ley, Amanda N.; Holman, K. Travis
Reproducible Synthesis and High Porosity of mer-Zn(Im)2 (ZIF-10): Exploitation of an Apparent Double-Eight Ring Template.
Journal of the American Chemical Society, 2016, 138, 12017-12020
4125228 CIFC25 H29 N OP 21 21 218.1727; 12.9877; 19.1341
90; 90; 90
2030.98Zhou, Qi; Cobb, Kelsey M.; Tan, Tianyu; Watson, Mary P.
Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity.
Journal of the American Chemical Society, 2016, 138, 12057-12060
4125229 CIFC16 H18 O2C 1 2 121.7695; 5.8807; 10.4637
90; 97.282; 90
1328.76Zhou, Qi; Cobb, Kelsey M.; Tan, Tianyu; Watson, Mary P.
Stereospecific Cross Couplings To Set Benzylic, All-Carbon Quaternary Stereocenters in High Enantiopurity.
Journal of the American Chemical Society, 2016, 138, 12057-12060
4125230 CIFC20 H22 Cl2 N2 O4P c a 2119.756; 11.388; 8.946
90; 90; 90
2012.7Yao, Zi-Shuo; Yamamoto, Kaoru; Cai, Hong-Ling; Takahashi, Kazuyuki; Sato, Osamu
Above Room Temperature Organic Ferroelectrics: Diprotonated 1,4-Diazabicyclo[2.2.2]octane Shifts between Two 2-Chlorobenzoates.
Journal of the American Chemical Society, 2016, 138, 12005-12008
4125231 CIFC20 H20 Cl2 D2 N2 O4P b c a9.086; 11.473; 19.916
90; 90; 90
2076Yao, Zi-Shuo; Yamamoto, Kaoru; Cai, Hong-Ling; Takahashi, Kazuyuki; Sato, Osamu
Above Room Temperature Organic Ferroelectrics: Diprotonated 1,4-Diazabicyclo[2.2.2]octane Shifts between Two 2-Chlorobenzoates.
Journal of the American Chemical Society, 2016, 138, 12005-12008
4125232 CIFC20 H20 Cl2 D2 N2 O4P c a 2119.787; 11.403; 8.953
90; 90; 90
2020.1Yao, Zi-Shuo; Yamamoto, Kaoru; Cai, Hong-Ling; Takahashi, Kazuyuki; Sato, Osamu
Above Room Temperature Organic Ferroelectrics: Diprotonated 1,4-Diazabicyclo[2.2.2]octane Shifts between Two 2-Chlorobenzoates.
Journal of the American Chemical Society, 2016, 138, 12005-12008
4125233 CIFC20 H22 Cl2 N2 O4P c a 2119.745; 11.357; 8.896
90; 90; 90
1994.9Yao, Zi-Shuo; Yamamoto, Kaoru; Cai, Hong-Ling; Takahashi, Kazuyuki; Sato, Osamu
Above Room Temperature Organic Ferroelectrics: Diprotonated 1,4-Diazabicyclo[2.2.2]octane Shifts between Two 2-Chlorobenzoates.
Journal of the American Chemical Society, 2016, 138, 12005-12008
4125234 CIFC20 H22 Cl2 N2 O4P b c a9.083; 11.433; 19.797
90; 90; 90
2056Yao, Zi-Shuo; Yamamoto, Kaoru; Cai, Hong-Ling; Takahashi, Kazuyuki; Sato, Osamu
Above Room Temperature Organic Ferroelectrics: Diprotonated 1,4-Diazabicyclo[2.2.2]octane Shifts between Two 2-Chlorobenzoates.
Journal of the American Chemical Society, 2016, 138, 12005-12008
4125235 CIFC12 H10 N4P 1 21/n 117.5558; 7.0307; 17.5147
90; 106.484; 90
2073Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125236 CIFC39 H21 Cl3 F12 N8P 1 21/c 115.0395; 7.5585; 35.865
90; 101.24; 90
3998.8Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125237 CIFC23 H20.03 N6C 1 2/c 133.375; 8.0465; 32.417
90; 115.826; 90
7836.1Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125238 CIFC41 H25 Cl3 F12 N8P 1 21/n 120.468; 7.5319; 27.491
90; 101.425; 90
4154.1Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125239 CIFC20 H12 F6 N4I 1 2/c 113.35; 10.0002; 27.9606
90; 98.304; 90
3693.68Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125240 CIFC19 H16 Cl N5P -17.6508; 8.3307; 13.624
100.727; 99.114; 98.267
828.86Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125241 CIFC21 H15 F6 N5P -17.4714; 9.4834; 15.0286
77.253; 76.24; 83.065
1006.17Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125242 CIFC43 H32 Cl2 F12 N10P -17.8375; 14.804; 18.762
76.578; 86.891; 87.608
2113.36Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125243 CIFC20 H16 N6P 1 21/c 17.6566; 30.6548; 7.8558
90; 115.192; 90
1668.5Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125244 CIFC19 H10 F6 N4P -17.0493; 9.2417; 15.1514
94.912; 103.007; 111.772
877.41Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125245 CIFC14 H13 N4P 1 21/n 16.3116; 19.0781; 9.8328
90; 99.199; 90
1168.77Wu, Jie; Cheng, Yangyang; Lan, Jingbo; Wu, Di; Qian, Shengyou; Yan, Lipeng; He, Zhen; Li, Xiaoyu; Wang, Kai; Zou, Bo; You, Jingsong
Molecular Engineering of Mechanochromic Materials by Programmed C-H Arylation: Making a Counterpoint in the Chromism Trend.
Journal of the American Chemical Society, 2016, 138, 12803-12812
4125246 CIFC46 H58 Mg2 N4P 1 2/n 113.4857; 8.272; 19.9081
90; 101.058; 90
2179.59Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125247 CIFC39 H49 F5 Mg N2 OP -112.8601; 15.9403; 18.1538
84.244; 89.38; 88.675
3701.5Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125248 CIFC40 H49 F7 Mg N2 OI 1 2/a 114.9886; 14.8728; 36.1312
90; 98.802; 90
7959.6Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125249 CIFC38 H49 F4 Mg N3 OC 1 2/c 134.4121; 14.8141; 14.8714
90; 100.005; 90
7465.9Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125250 CIFC40 H45 F4 Mg N3C 1 2/c 131.6147; 16.0108; 15.04066
90; 101.334; 90
7464.76Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125251 CIFC52 H70 Mg2 N4C 1 2/c 118.253; 13.8247; 21.1714
90; 110.993; 90
4987.8Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125252 CIFC72 H112 F2 Mg2 N4 O2I 1 2/m 111.9516; 18.2934; 15.7645
90; 99.934; 90
3395Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark R.
Addition of Carbon-Fluorine Bonds to a Mg(I)-Mg(I) Bond: An Equivalent of Grignard Formation in Solution.
Journal of the American Chemical Society, 2016, 138, 12763-12766
4125253 CIFC23 H22 N2 OP -19.5297; 9.8101; 9.8488
79.725; 84.919; 89.558
902.38Liu, Zhen; Derosa, Joseph; Engle, Keary M.
Palladium(II)-Catalyzed Regioselective syn-Hydroarylation of Disubstituted Alkynes Using a Removable Directing Group.
Journal of the American Chemical Society, 2016, 138, 13076-13081
4125254 CIFC46 H68 F N5 O2P 1 2/n 111.004; 8.344; 24.0042
90; 97.4468; 90
2185.41Pfeifer, Lukas; Engle, Keary M.; Pidgeon, George W.; Sparkes, Hazel A.; Thompson, Amber L.; Brown, John M.; Gouverneur, Véronique
Hydrogen-Bonded Homoleptic Fluoride-Diarylurea Complexes: Structure, Reactivity, and Coordinating Power.
Journal of the American Chemical Society, 2016, 138, 13314
4125255 CIFC46 H56 F13 N5 O2P 1 21/n 110.9971; 17.064; 24.9997
90; 92.7108; 90
4686.06Pfeifer, Lukas; Engle, Keary M.; Pidgeon, George W.; Sparkes, Hazel A.; Thompson, Amber L.; Brown, John M.; Gouverneur, Véronique
Hydrogen-Bonded Homoleptic Fluoride-Diarylurea Complexes: Structure, Reactivity, and Coordinating Power.
Journal of the American Chemical Society, 2016, 138, 13314

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