Crystallography Open Database

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Searching year of publication is 2019

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1550367 CIFC280 H132 Eu2 N12 Ni3C 1 2/m 124.307; 18.191; 22.087
90; 100.995; 90
9587Bao, Lipiao; Yu, Pengyuan; Pan, Changwang; Shen, Wangqiang; Lu, Xing
Crystallographic identification of Eu@C2n (2n = 88, 86 and 84): completing a transformation map for existing metallofullerenes
Chemical Science, 2019
1550368 CIFC130.05 H53.66 Eu N4 Ni S0.78C 1 2/m 125.3346; 15.1339; 19.9751
90; 95.659; 90
7621.4Bao, Lipiao; Yu, Pengyuan; Pan, Changwang; Shen, Wangqiang; Lu, Xing
Crystallographic identification of Eu@C2n (2n = 88, 86 and 84): completing a transformation map for existing metallofullerenes
Chemical Science, 2019
1550369 CIFC132 H56 Eu N4 NiC 1 2/m 125.386; 15.123; 19.953
90; 95.2; 90
7629Bao, Lipiao; Yu, Pengyuan; Pan, Changwang; Shen, Wangqiang; Lu, Xing
Crystallographic identification of Eu@C2n (2n = 88, 86 and 84): completing a transformation map for existing metallofullerenes
Chemical Science, 2019
1550370 CIF
Paper
C4 H9 Co N O6P n m a8.2674; 11.66; 8.1483
90; 90; 90
785.48Canadillas-Delgado, Laura; Mazzuca, Lidia; Fabelo, Oscar; Rodriguez-Velamazan, J. Alberto; Rodriguez-Carvajal, Juan
Incommensurate structures of the [CH~3~NH~3~][Co(COOH)~3~] compound
IUCrJ, 2019, 6, 105-115
1550371 CIF
Paper
C4 H9 Co N O6P n m a8.2556; 11.6519; 8.1508
90; 90; 90
784.05Canadillas-Delgado, Laura; Mazzuca, Lidia; Fabelo, Oscar; Rodriguez-Velamazan, J. Alberto; Rodriguez-Carvajal, Juan
Incommensurate structures of the [CH~3~NH~3~][Co(COOH)~3~] compound
IUCrJ, 2019, 6, 105-115
1550372 CIF
Paper
C4 H9 Co N O6P n m a8.2702; 11.6766; 8.1631
90; 90; 90
788.29Canadillas-Delgado, Laura; Mazzuca, Lidia; Fabelo, Oscar; Rodriguez-Velamazan, J. Alberto; Rodriguez-Carvajal, Juan
Incommensurate structures of the [CH~3~NH~3~][Co(COOH)~3~] compound
IUCrJ, 2019, 6, 105-115
1550373 CIF
Paper
C4 H9 Co N O6P n m a8.2548; 11.6547; 8.1521
90; 90; 90
784.29Canadillas-Delgado, Laura; Mazzuca, Lidia; Fabelo, Oscar; Rodriguez-Velamazan, J. Alberto; Rodriguez-Carvajal, Juan
Incommensurate structures of the [CH~3~NH~3~][Co(COOH)~3~] compound
IUCrJ, 2019, 6, 105-115
1550375 CIFC77 H51.5 Cl6 S5C 1 2/c 121.7713; 21.459; 27.4874
90; 92.893; 90
12825.5Lin, Hsing-An; Kato, Kenta; Segawa, Yasutomo; Scott, Lawrence T.; Itami, Kenichiro
Synthesis and Structural Features of Thiophene-fused Analogues of Warped Nanographene and Quintuple Helicene
Chemical Science, 2019
1550376 CIFC24 H22 OP -18.4646; 10.2366; 11.8274
77.022; 69.293; 74.924
915.6Zhang, Yuchen; Wu, Wangteng; Fu, Chunling; Huang, Xin; Ma, Shengming
Benzene Construction via Pd-catalyzed Cyclization of 2,7-Alkadiynylic Carbonates in the Presence of Alkynes
Chemical Science, 2019
1550377 CIFC24 H22 O2P 1 21/n 16.8864; 33.272; 8.5011
90; 104.932; 90
1882Zhang, Yuchen; Wu, Wangteng; Fu, Chunling; Huang, Xin; Ma, Shengming
Benzene Construction via Pd-catalyzed Cyclization of 2,7-Alkadiynylic Carbonates in the Presence of Alkynes
Chemical Science, 2019
1550378 CIFC27 H23 N O2P b c a37.682; 6.9971; 15.2009
90; 90; 90
4007.9Zhang, Yuchen; Wu, Wangteng; Fu, Chunling; Huang, Xin; Ma, Shengming
Benzene Construction via Pd-catalyzed Cyclization of 2,7-Alkadiynylic Carbonates in the Presence of Alkynes
Chemical Science, 2019
1550379 CIFC21 H24 O4P 21 21 216.2996; 14.6723; 19.1704
90; 90; 90
1771.9Gupta, Saswata; Lin, Yongjia; Xia, Yuanzhi; Wink, Donald; Lee, Daesung
Alder-Ene Reactions Driven by High Steric Strain and Bond Angle Distortion to Form Benzocyclobutenes
Chemical Science, 2019
1550380 CIFC42 H30 O14 Ti3R -3 m25.8366; 25.8366; 13.6675
90; 90; 120
7901.2Feng, Xuanyu; Song, Yang; Chen, Justin S.; Li, Zhe; Chen, Emily Y.; Kaufmann, Michael; Wang, Cheng; Lin, Wenbin
Cobalt-Bridged Secondary Building Units in a Titanium Metal-Organic Framework Catalyze Cascade Reduction of N-Heteroarenes
Chemical Science, 2019
1550381 CIFC78.74 H94.11 Cl4 N9.37 O6 P2P 1 21/n 113.8833; 29.9782; 18.874
90; 93.677; 90
7839.1Peñuelas-Haro, Guillem; Ballester, Pablo
Efficient Hydrogen Bonding Recognition in Water using Aryl-extended Calix[4]pyrrole Receptors
Chemical Science, 2019
1550382 CIFC74 H87 Cl4 N7 O6 P2I 41 m d19.6411; 19.6411; 18.4185
90; 90; 90
7105.4Peñuelas-Haro, Guillem; Ballester, Pablo
Efficient Hydrogen Bonding Recognition in Water using Aryl-extended Calix[4]pyrrole Receptors
Chemical Science, 2019
1550383 CIFAl2 Eu4 F2 O8P 1 21/c 17.5885; 10.8399; 11.0776
90; 108.788; 90
862.67Morán-Ruiz, Aroa; Wain-Martin, Aritza; Orera, Alodia; Sanjuán, María Luisa; Larrañaga, Aitor; Slater, Peter R.; Arriortua, Maribel
Synthesis of new Ln~4~(Al~2~O~6~F~2~)O~2~ (Ln = Sm, Eu, Gd) phases with a cuspidine-related structure
IUCrJ, 2019, 6, 128-135
1550384 CIFAl2 F2 O8 Sm4P 1 21/c 17.6188; 10.8705; 11.1077
90; 108.805; 90
870.84Morán-Ruiz, Aroa; Wain-Martin, Aritza; Orera, Alodia; Sanjuán, María Luisa; Larrañaga, Aitor; Slater, Peter R.; Arriortua, Maribel
Synthesis of new Ln~4~(Al~2~O~6~F~2~)O~2~ (Ln = Sm, Eu, Gd) phases with a cuspidine-related structure
IUCrJ, 2019, 6, 128-135
1550400 CIFC55 H66 Cl2 N4 RuP -110.9047; 11.6314; 19.7689
95.343; 101.998; 100.664
2387.6Dumas, Adrien; Colombel-Rouen, Sophie; Curbet, Idriss; Forcher, Gwénael; Tripoteau, Fabien; Caijo, Frédéric; Queval, Pierre; Rouen, Mathieu; Baslé, Olivier; Mauduit, Marc
Highly selective macrocyclic ring-closing metathesis of terminal olefins in non-chlorinated solvents at low dilution
Catalysis Science & Technology, 2019
1550401 CIFC77 H66 Cl2 N10 O12P -113.861; 15.962; 17.258
69.871; 75.157; 81.221
3457Chen, Huaiyu; Huang, Chao; Ding, Yazhou; Zhang, Qi-Long; Zhu, Bi-Xue; Ni, Xin-Long
Organic core‒shell-shaped micro/nanoparticles from twisted macrocycles in Schiff base reaction
Chemical Science, 2019, 10, 490
1550402 CIFC15 H12 O4P 1 21/n 17.804; 11.72; 13.252
90; 94.565; 90
1208.2Chen, Huaiyu; Huang, Chao; Ding, Yazhou; Zhang, Qi-Long; Zhu, Bi-Xue; Ni, Xin-Long
Organic core–shell-shaped micro/nanoparticles from twisted macrocycles in Schiff base reaction
Chemical Science, 2019, 10, 490
1550403 CIFC32 H47 Al N2P 1 21/c 110.5476; 13.0639; 22.5422
90; 99.217; 90
3066Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550404 CIFC38.5 H57 Al N2C 1 2/c 119.4468; 18.4781; 20.5105
90; 102.346; 90
7199.8Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550405 CIFC39 H53 Al N2 OP 1 21/n 112.3296; 16.8397; 17.7035
90; 106.384; 90
3526.5Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550406 CIFC31 H45 Al N2P 1 21/n 112.3658; 17.1209; 14.023
90; 104.507; 90
2874.2Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550407 CIFC38 H50 Al N2P 21 21 2111.227; 14.6841; 21.0838
90; 90; 90
3475.8Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550408 CIFC62 H90 Al2 N4C 1 2/c 124.6053; 15.38681; 14.82658
90; 96.6729; 90
5575.27Bakewell, Clare; White, Andrew J. P.; Crimmin, Mark Richard
Reversible Alkene Binding and Allylic C‒H Activation with an Aluminium(I) Complex
Chemical Science, 2019
1550409 CIFC48 H36 Cu F12 N8 O14.13 S4P -116.1504; 16.2726; 17.8745
99.297; 112.765; 102.854
4059.7Liu, Yanju; Han, Yongzhen; Zhang, Zongyao; Zhang, Wei; Lai, Wenzhen; Wang, Yong; Cao, Rui
Low overpotential water oxidation at neutral pH catalyzed by a copper(II) porphyrin
Chemical Science, 2019
1550410 CIFC35 H21 Al2 F55 O6 SiP -110.4039; 12.682; 21.4037
88.235; 80.175; 82.373
2757.92Martens, Arthur; Kreuzer, Marvin; Ripp, Alexander Johannes Christoph; Schneider, Marius; Himmel, Daniel; Scherer, Harald; Krossing, Ingo
Investigations on Non-Classical Silylium Ions Leading to a Cyclobutenyl Cation
Chemical Science, 2019
1550411 CIFC30 H31 Al F28 N2 O3 SiP -19.4236; 10.9684; 20.6676
78.207; 88.952; 83.352
2077.06Martens, Arthur; Kreuzer, Marvin; Ripp, Alexander Johannes Christoph; Schneider, Marius; Himmel, Daniel; Scherer, Harald; Krossing, Ingo
Investigations on Non-Classical Silylium Ions Leading to a Cyclobutenyl Cation
Chemical Science, 2019
1550412 CIFC19 H10 Al F27 N2 O3P 1 21/c 112.2182; 11.395; 21.1752
90; 105.383; 90
2842.5Martens, Arthur; Kreuzer, Marvin; Ripp, Alexander Johannes Christoph; Schneider, Marius; Himmel, Daniel; Scherer, Harald; Krossing, Ingo
Investigations on Non-Classical Silylium Ions Leading to a Cyclobutenyl Cation
Chemical Science, 2019
1550413 CIFC24 H22 F N O4P 1 21 115.3747; 7.2401; 18.684
90; 102.066; 90
2033.85Royal, Titouan; Baudoin, Olivier
Pd-catalyzed γ-arylation of γ,δ-unsaturated O-carbamates via an unusual haptotropic rearrangement
Chemical Science, 2019
1550414 CIFC24 H22 F N O4P 1 21 115.3844; 7.2248; 18.6689
90; 102.133; 90
2028.68Royal, Titouan; Baudoin, Olivier
Pd-catalyzed γ-arylation of γ,δ-unsaturated O-carbamates via an unusual haptotropic rearrangement
Chemical Science, 2019
1550415 CIFC39 H32 Br2 N4 OP c c n18.5184; 19.9443; 9.0043
90; 90; 90
3325.6Sindt, Ammon J.; DeHaven, Baillie A.; McEachern, David F.; Dissanayake, Madushanka M.; Smith, Mark D.; Vannucci, Aaron K.; Shimizu, Linda S.
UV-irradiation of self-assembled triphenylamines affords persistent and regenerable radicals
Chemical Science, 2019
1550416 CIFC79 H106 N18 O14 PP n a 2120.4627; 15.7895; 25.0638
90; 90; 90
8098Zuo, Wei; Jia, Chuandong; Zhang, Huizheng; Zhao, Yanxia; Yang, Xiao-Juan; Wu, Biao
Selective recognition of choline phosphate by tripodal hexa-urea receptors with dual binding sites: crystal and solution evidence
Chemical Science, 2019
1550417 CIFC142 H157 N32 O20 P2P -115.948; 16.487; 16.568
98.9391; 95.3315; 117.154
3762Zuo, Wei; Jia, Chuandong; Zhang, Huizheng; Zhao, Yanxia; Yang, Xiao-Juan; Wu, Biao
Selective recognition of choline phosphate by tripodal hexa-urea receptors with dual binding sites: crystal and solution evidence
Chemical Science, 2019
1550418 CIFC142 H201 N36 O33 P2P 1 21/n 122.7938; 18.9289; 23.1163
90; 119.257; 90
8701.5Zuo, Wei; Jia, Chuandong; Zhang, Huizheng; Zhao, Yanxia; Yang, Xiao-Juan; Wu, Biao
Selective recognition of choline phosphate by tripodal hexa-urea receptors with dual binding sites: crystal and solution evidence
Chemical Science, 2019
1550419 CIFC27 H20 Cl2 O3P 21 21 217.6102; 10.7051; 27.326
90; 90; 90
2226.2Yao, Lu; Ishihara, Kazuaki
Enantioselecive [1,3] O-to-C rearrangement: Dearomatization of alkyl 2-allyloxy/benzyloxy-1/3-naphthoates catalyzed by a chiral π–Cu(II) complex
Chemical Science, 2019
1550420 CIFC50 H64 Cu F6 N4 O8 S2P 21 21 2114.293; 16.823; 21.7
90; 90; 90
5217.8Yao, Lu; Ishihara, Kazuaki
Enantioselecive [1,3] O-to-C rearrangement: Dearomatization of alkyl 2-allyloxy/benzyloxy-1/3-naphthoates catalyzed by a chiral π–Cu(II) complex
Chemical Science, 2019
1550421 CIFC50 H46 N6 O6P 1 21/c 116.393; 12.1248; 20.3969
90; 96.964; 90
4024.22Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550422 CIFC66 H52 Cl12 N8 O6P -110.6274; 12.6722; 13.0666
76.113; 81.646; 68.89
1590.27Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550423 CIFC60 H46 N8 O7P 19.1177; 10.6349; 13.6347
84.797; 86.884; 73.337
1260.8Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550424 CIFC62 H50 Cl8 N8 O6P -19.5459; 10.8943; 14.704
77.534; 84.269; 68.203
1386.03Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550425 CIFC62 H46 Cl8 N8 O5P n a 2134.5017; 10.56728; 14.7887
90; 90; 90
5391.8Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550426 CIFC66 H50 Cl16 N8 O6P -110.5616; 23.6815; 27.6022
94.092; 92.874; 92.603
6869.1Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550427 CIFC134 H110 Cl24 N16 O17P -110.653; 12.928; 51.06
92.18; 90.93; 111.37
6540Gozálvez, Cristian; Zafra, José L.; Saeki, Akinori; Melle-Franco, Manuel; Casado Cordón, Juan; Mateo-Alonso, Aurelio
Charge Transport Modulation in Pseudorotaxane 1D Stacks of Acene and Azaacene Derivatives
Chemical Science, 2019
1550428 CIFC29 H21 B Cl F10 NP -110.2284; 11.0264; 12.5397
88.589; 80.364; 79.511
1371Erker, Gerhard; Tao, Xin; Wölke, Christian; Daniliuc, Constantin Gabriel; Kehr, Gerald
Halogenoborane mediated allene cyclooligomerization
Chemical Science, 2019
1550429 CIFC29 H21 B Br F10 NP -110.2011; 11.0143; 12.5252
88.743; 80.865; 79.649
1366.81Erker, Gerhard; Tao, Xin; Wölke, Christian; Daniliuc, Constantin Gabriel; Kehr, Gerald
Halogenoborane mediated allene cyclooligomerization
Chemical Science, 2019
1550430 CIFC36 H42 B F10 PP -19.9507; 11.7835; 16.007
71.517; 86.117; 70.299
1674.26Erker, Gerhard; Tao, Xin; Wölke, Christian; Daniliuc, Constantin Gabriel; Kehr, Gerald
Halogenoborane mediated allene cyclooligomerization
Chemical Science, 2019
1550431 CIFC27.5 H43 ClP -110.8108; 12.1099; 19.1989
76.703; 75.176; 87.966
2363.95Erker, Gerhard; Tao, Xin; Wölke, Christian; Daniliuc, Constantin Gabriel; Kehr, Gerald
Halogenoborane mediated allene cyclooligomerization
Chemical Science, 2019
1550432 CIFC65.56 H77.12 B2 Cl7.12 F8 N2 O8.38 P4 Pd0.98C 1 2/c 124.9341; 15.1575; 22.1525
90; 114.583; 90
7613.4Viertl, Wolfgang; Pann, Johann; Pehn, Richard; Roithmeyer, Helena; Bendig, Marvin; Rodríguez-Villalón, Alba; Bereiter, Raphael; Heiderscheid, Max; Müller, Thomas; Zhao, Xia; Hofer, Thomas S.; Thompson, Mark E.; Shi, Shuyang; Brueggeller, Peter
Performance of enhanced DuBois type water reduction catalysts (WRC) in artificial photosynthesis - effects of various proton relays during catalysis.
Faraday discussions, 2019, 215, 141-161
1550433 CIFC35 H30 Cl3 F6 N O4.4 P3 PdP 1 21/n 112.3522; 26.1118; 13.6448
90; 113.138; 90
4046.96Viertl, Wolfgang; Pann, Johann; Pehn, Richard; Roithmeyer, Helena; Bendig, Marvin; Rodríguez-Villalón, Alba; Bereiter, Raphael; Heiderscheid, Max; Müller, Thomas; Zhao, Xia; Hofer, Thomas S.; Thompson, Mark E.; Shi, Shuyang; Brueggeller, Peter
Performance of enhanced DuBois type water reduction catalysts (WRC) in artificial photosynthesis - effects of various proton relays during catalysis.
Faraday discussions, 2019, 215, 141-161
1550434 CIFC33 H38 Cl2 N2 O4 P2 PdP 1 21/n 112.9976; 18.6574; 14.6755
90; 105.169; 90
3434.83Viertl, Wolfgang; Pann, Johann; Pehn, Richard; Roithmeyer, Helena; Bendig, Marvin; Rodríguez-Villalón, Alba; Bereiter, Raphael; Heiderscheid, Max; Müller, Thomas; Zhao, Xia; Hofer, Thomas S.; Thompson, Mark E.; Shi, Shuyang; Brueggeller, Peter
Performance of enhanced DuBois type water reduction catalysts (WRC) in artificial photosynthesis - effects of various proton relays during catalysis.
Faraday discussions, 2019, 215, 141-161
1550435 CIFC35 H41 Cl8 N Ni O4 P2P 1 21/c 111.7989; 15.5485; 23.5593
90; 101.232; 90
4239.29Viertl, Wolfgang; Pann, Johann; Pehn, Richard; Roithmeyer, Helena; Bendig, Marvin; Rodríguez-Villalón, Alba; Bereiter, Raphael; Heiderscheid, Max; Müller, Thomas; Zhao, Xia; Hofer, Thomas S.; Thompson, Mark E.; Shi, Shuyang; Brueggeller, Peter
Performance of enhanced DuBois type water reduction catalysts (WRC) in artificial photosynthesis - effects of various proton relays during catalysis.
Faraday discussions, 2019, 215, 141-161
1550436 CIFC33 H38 Cl2 N2 Ni O4 P2P 1 21/n 112.8814; 18.6698; 14.5746
90; 105.006; 90
3385.56Viertl, Wolfgang; Pann, Johann; Pehn, Richard; Roithmeyer, Helena; Bendig, Marvin; Rodríguez-Villalón, Alba; Bereiter, Raphael; Heiderscheid, Max; Müller, Thomas; Zhao, Xia; Hofer, Thomas S.; Thompson, Mark E.; Shi, Shuyang; Brueggeller, Peter
Performance of enhanced DuBois type water reduction catalysts (WRC) in artificial photosynthesis - effects of various proton relays during catalysis.
Faraday discussions, 2019, 215, 141-161
1550437 CIFC26 H18 La N9 O9P 1 21/n 19.1366; 14.1095; 20.9641
90; 90.052; 90
2702.54Gajarushi, Ashwini S.; Wasim, Mohd; Nabi, Rizwan; Kancharlapalli, Srinivasu; Rao, V. Ramgopal; Rajaraman, Gopalan; Subramaniam, Chandramouli; Shanmugam, Maheswaran
Lanthanide complexes as molecular dopants for realizing air-stable n-type graphene logic inverters with symmetric transconductance
Materials Horizons, 2019, 6, 743
1550438 CIFC26 H18 Ce N9 O9C 1 2/c 115.0921; 10.8118; 19.5232
90; 118.32; 90
2804.4Gajarushi, Ashwini S.; Wasim, Mohd; Nabi, Rizwan; Kancharlapalli, Srinivasu; Rao, V. Ramgopal; Rajaraman, Gopalan; Subramaniam, Chandramouli; Shanmugam, Maheswaran
Lanthanide complexes as molecular dopants for realizing air-stable n-type graphene logic inverters with symmetric transconductance
Materials Horizons, 2019, 6, 743
1550439 CIFC16 H26P 1 21/n 114.3334; 5.56223; 8.53021
90; 92.0219; 90
679.65van de Streek, Jacco; Alig, Edith; Parsons, Simon; Vella-Zarb, Liana
A jumping crystal predicted with molecular dynamics and analysed with TLS refinement against powder diffraction data
IUCrJ, 2019, 6, 136-144
1550440 CIFC7 H15 Cl N2 OP 1 21 17.2588; 8.9399; 22.7927
90; 95.818; 90
1471.47Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550441 CIFC7 H15 I N2 OP b c a13.4725; 9.8551; 32.7259
90; 90; 90
4345.11Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550442 CIFC7 H15 Cl N2 OP 1 21 17.2902; 8.9099; 7.8789
90; 107.024; 90
489.35Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550443 CIFC7 H15 Br N2 OP 1 21 17.5269; 9.1017; 7.93
90; 107.161; 90
519.08Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550444 CIFC7 H15 I N2 OP 21 21 217.585; 10.8242; 13.0468
90; 90; 90
1071.16Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550445 CIFC14 H30 B Cl F4 N4 O2P 21 21 219.4006; 13.2619; 16.6581
90; 90; 90
2076.76Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550446 CIFC22 H27 Br N2 O4 SP 21 21 216.106; 9.0317; 42.33
90; 90; 90
2334.4Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550447 CIFC22 H27 I N2 O4 SP 21 21 216.2219; 9.0228; 43.0569
90; 90; 90
2417.17Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550448 CIFC22 H27 N3 O7 SP 21 21 216.3765; 8.8174; 42.942
90; 90; 90
2414.38Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550449 CIFC22 H32 N2 O9.5 P SP 18.7929; 12.6645; 23.7867
82.3345; 81.4117; 89.9824
2595.2Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550450 CIFC15 H24 N2 O5P 1 21 111.47377; 6.14747; 11.71348
90; 111.978; 90
766.164Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550451 CIFC19 H23 Cl N6 O4P 1 21/c 112.6065; 13.0726; 12.6694
90; 106.397; 90
2003Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550452 CIFC20 H23 Cl N6 O SP -112.1482; 13.1848; 13.8251
90.263; 90.218; 108.005
2105.9Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550453 CIFC19 H23 B Cl F4 N5 OP 1 21/c 112.46473; 12.98315; 13.42014
90; 106.765; 90
2079.49Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550454 CIFC16 H21 N O4 SP 1 21 15.72587; 20.83882; 6.92054
90; 98.3547; 90
816.998Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550455 CIFC24 H38 N2 O8P 15.8213; 7.27088; 15.90214
94.7215; 96.6693; 109.525
624.781Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550456 CIFC24 H38 N2 O9P 1 21 16.07189; 32.9414; 7.1383
90; 114.168; 90
1302.63Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550457 CIFC10 H16 N2 O4P 1 21 16.0401; 29.3553; 7.3828
90; 112.806; 90
1206.7Babor, Martin; Nievergelt, Philipp P.; Čejka, Jan; Zvoníček, Vít; Spingler, Bernhard
Microbatch under-oil salt screening of organic cations: single-crystal growth of active pharmaceutical ingredients
IUCrJ, 2019, 6, 145-151
1550458 CIF
HKL
Paper
C25 H24 Cl4 N2 P2 PdP 1 21/n 111.7085; 16.9319; 15.2399
90; 105.324; 90
2913.85Höhne, Martha; Aluri, Bhaskar R.; Spannenberg, Anke; Müller, Bernd H.; Peulecke, Normen; Rosenthal, Uwe
Dichlorido[1,1-(diphenylphosphino)hydrazide]palladium(II) dichloromethane monosolvate
IUCrData, 2019, 4, x181803
1550459 CIF
HKL
Paper
C12 H14 Cl N O3P 1 21/c 15.7323; 9.2537; 21.6899
90; 91.168; 90
1150.3Rodriguez-Vega, Gibran; Aguirre, Gerardo; Chávez, Daniel
Ethyl 4-chloro-2-oxo-1,2,5,6,7,8-hexahydroquinoline-3-carboxylate
IUCrData, 2019, 4, x190016
1550460 CIF
HKL
Paper
C20 H21 N5 OP 1 2/n 112.241; 5.9386; 25.2112
90; 90.317; 90
1832.69Slassi, Siham; Stetsiuk, Oleh; Amine, Amina; Aarjane, Mohammed; El-Ghayoury, Abdelkrim; Zouihri, Hafid; Yamni, Khalid
2-[(<i>E</i>)-{[3-(1<i>H</i>-Imidazol-1-yl)propyl]imino}methyl]-4-[(<i>E</i>)-(4-methylphenyl)diazenyl]phenol
IUCrData, 2019, 4, x190036
1550461 CIF
HKL
Paper
C17 H14 O2P 1 21/n 19.0801; 15.4598; 10.092
90; 109.453; 90
1335.81Pineda, Leslie W.; Amey, Adam; Cabezas, Jorge A.
5,5-Diphenyl-<i>cis</i>-penta-2,4-dienoic acid
IUCrData, 2019, 4, x181799
1550462 CIF
HKL
C52 H50 Cl2 N4 O7P 1 21/n 113.702; 11.349; 28.538
90; 92.999; 90
4431.7Lee, Jae Myoung; Kim, Sung Baek; Sim, Wonbo; Lee, Jai Young
25,27-(3,6,9-Trioxaundecane-1,11-dioxy)-26,28-[3-(4-tricyanoethylene)phenyl]-3-aza-pentane-1,5-dioxy)calix[4]arene dichloromethane monosolvate
IUCrData, 2019, 4, x190026
1550463 CIFCu Mg O5 VC m c m5.7716; 8.7145; 6.3052
90; 90; 90
317.13Gake, T.; Matsushita, S.; Arai, M.; Obata, K.
Electronic structures and optical properties of CuMgVO4 and AgMgVO4: a first-principles study
Journal of the Ceramic Society of Japan, 2019, 127, 50-55
1550464 CIFAg Mg O5 VP n m a9.5314; 6.7696; 5.3618
90; 90; 90
345.964Gake, T.; Matsushita, S.; Arai, M.; Obata, K.
Electronic structures and optical properties of CuMgVO4 and AgMgVO4: a first-principles study
Journal of the Ceramic Society of Japan, 2019, 127, 50-55
1550465 CIFC52 H15 Cl2 F20 Ga N4 O2P 1 21/c 113.125; 17.799; 21.46
90; 106.821; 90
4798.8Wang, Ni; Lei, Haitao; Zhang, Zongyao; Li, Jianfeng; Zhang, Wei; Cao, Rui
Electrocatalytic hydrogen evolution with gallium hydride and ligand-centered reduction
Chemical Science, 2019
1550466 CIFC52 H32 Cl0 F20 Ga N4 O5P 1 21/c 114.3965; 25.5948; 13.8025
90; 93.422; 90
5076.8Wang, Ni; Lei, Haitao; Zhang, Zongyao; Li, Jianfeng; Zhang, Wei; Cao, Rui
Electrocatalytic hydrogen evolution with gallium hydride and ligand-centered reduction
Chemical Science, 2019
1550467 CIFC8 H20 Cl3 Ga N4P n a 2114.5269; 7.3499; 12.7491
90; 90; 90
1361.2Wang, Ni; Lei, Haitao; Zhang, Zongyao; Li, Jianfeng; Zhang, Wei; Cao, Rui
Electrocatalytic hydrogen evolution with gallium hydride and ligand-centered reduction
Chemical Science, 2019
1550468 CIFC44 H8 F20 Ga N4 O2P 1 21/n 114.0662; 5.607; 26.055
90; 95.056; 90
2046.9Wang, Ni; Lei, Haitao; Zhang, Zongyao; Li, Jianfeng; Zhang, Wei; Cao, Rui
Electrocatalytic hydrogen evolution with gallium hydride and ligand-centered reduction
Chemical Science, 2019
1550469 CIFC2 H6 F3 N O6 S2P n a 218.9227; 18.531; 5.5268
90; 90; 90
913.8D'Amato, Erica M.; Börgel, Jonas; Ritter, Tobias
Aromatic C–H amination in hexafluoroisopropanol
Chemical Science, 2019
1550470 CIFC34 H58 Al2 Br2P -110.367; 12.452; 15.704
69.094; 88.918; 67.783
1737.3Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550471 CIFC34 H58 Al2 Br2C 1 c 119.582; 8.479; 21.301
90; 93.33; 90
3530.8Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550472 CIFC27 H44 Al2 Br2P 1 21/c 18.824; 29.234; 12.125
90; 108.8; 90
2960.9Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550473 CIFC46 H68 Al2 N2P b c a17.2467; 13.0572; 18.6141
90; 90; 90
4191.8Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550474 CIFC17 H29 Al Br2P 1 21/c 19.4; 14.876; 13.886
90; 105.24; 90
1873Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550475 CIFC17 H29 Al2 Br3P -110.6448; 10.6844; 11.1041
63.541; 81.455; 73.465
1083.5Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550476 CIFC51 H87 Al3 O3P 1 21/c 114.173; 19.091; 19.858
90; 109.37; 90
5069Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550477 CIFC21 H38 Al2 Cl2P 1 21 19.8915; 21.5331; 11.5146
90; 90.457; 90
2452.47Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550478 CIFC34 H58 Al3 Br3P 1 21/c 110.1424; 38.371; 10.1825
90; 105.719; 90
3814.6Braunschweig, Holger; Kupfer, Thomas; Hofmann, Alexander; Tröster, Tobias
Monomeric Cp3tAl(I): Synthesis, reactivity, and the concept of valence isomerism
Chemical Science, 2019
1550479 CIFC19 H22 O5C 1 2 122.5468; 10.4722; 7.3277
90; 107.751; 90
1647.8Craig, Robert A.; Roizen, Jennifer L.; Smith, Russell C.; Jones, Amanda C.; Virgil, Scott C.; Stoltz, Brian M.
Correction: Enantioselective, convergent synthesis of the ineleganolide core by a tandem annulation cascade
Chemical Science, 2019
1550480 CIFC17 H17 Cl N2 O3P 1 21 17.599; 10.249; 10.488
90; 109.1; 90
771.861Wu, Zijun; Wang, Jian
A tandem dearomatization/rearomatization strategy: enantioselective N-heterocyclic carbene-catalyzed α-arylation
Chemical Science, 2019
1550481 CIF
HKL
Paper
C23 H26 Br Cl N6P 1 21/n 116.252; 5.3787; 27.109
90; 90.551; 90
2369.6Bourichi, Selma; Kandri Rodi, Youssef; Hökelek, Tuncer; Chakroune, Said; Ouzidan, Younes; Capet, Frédéric
6-Bromo-2-(4-chlorophenyl)-3-[(1-octyl-1<i>H</i>-1,2,3-triazol-4-yl)methyl]-3<i>H</i>-imidazo[4,5-<i>b</i>]pyridine
IUCrData, 2019, 4, x190053
1550482 CIF
HKL
Paper
C95 H90 Cl2 F3 Fe N12 O7 SP -112.2257; 19.3422; 19.5199
88.061; 72.058; 77.104
4277.6Li, Jianfeng; Oliver, Allen G.; Scheidt, W. Robert
Bis(1-phenylimidazole)[5,10,15,20-tetrakis(2-pivalamidophenyl)porphinato]iron(III) trifluoromethanesulfonate chlorobenzene disolvate
IUCrData, 2019, 4, x190015

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