Crystallography Open Database

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1567442 CIFC41 H63 Fe N3P -19.6054; 19.7203; 20.7848
104.662; 92.247; 90.183
3805.6Yang, Po-Chun; Yu, Kuan-Po; Hsieh, Chi-Tien; Zou, Junjie; Fang, Chia-Te; Liu, Hsin-Kuan; Pao, Chih-Wen; Deng, Liang; Cheng, Mu-Jeng; Lin, Chun-Yi
Stabilization of a high-spin three-coordinate Fe(iii) imidyl complex by radical delocalization
Chemical Science, 2022, 13, 9637-9643
1567443 CIFC32 H52 Li2 N2P -18.9896; 9.3153; 10.4649
74.635; 87.557; 62.337
745.1Yang, Po-Chun; Yu, Kuan-Po; Hsieh, Chi-Tien; Zou, Junjie; Fang, Chia-Te; Liu, Hsin-Kuan; Pao, Chih-Wen; Deng, Liang; Cheng, Mu-Jeng; Lin, Chun-Yi
Stabilization of a high-spin three-coordinate Fe(iii) imidyl complex by radical delocalization
Chemical Science, 2022, 13, 9637-9643
1567444 CIFC32 H52 Fe N2C 1 2/c 19.3375; 15.828; 21.069
90; 96.519; 90
3093.7Yang, Po-Chun; Yu, Kuan-Po; Hsieh, Chi-Tien; Zou, Junjie; Fang, Chia-Te; Liu, Hsin-Kuan; Pao, Chih-Wen; Deng, Liang; Cheng, Mu-Jeng; Lin, Chun-Yi
Stabilization of a high-spin three-coordinate Fe(iii) imidyl complex by radical delocalization
Chemical Science, 2022, 13, 9637-9643
1567445 CIFC42 H67 Fe N3P 1 21/n 19.9409; 36.563; 10.6275
90; 95.047; 90
3847.8Yang, Po-Chun; Yu, Kuan-Po; Hsieh, Chi-Tien; Zou, Junjie; Fang, Chia-Te; Liu, Hsin-Kuan; Pao, Chih-Wen; Deng, Liang; Cheng, Mu-Jeng; Lin, Chun-Yi
Stabilization of a high-spin three-coordinate Fe(iii) imidyl complex by radical delocalization
Chemical Science, 2022, 13, 9637-9643
1567447 CIFC40 H26 B N3 O2P 21 21 219.9788; 15.3329; 19.7187
90; 90; 90
3017.04van Vliet, Sven; Alachouzos, Georgios; de Vries, Folkert; Pfeifer, Lukas; Feringa, Ben L.
Visible light activated BINOL-derived chiroptical switches based on boron integrated hydrazone complexes
Chemical Science, 2022, 13, 9713-9718
1567448 CIFC40 H28 B Cl2 N3 O2P 1 21 113.375; 6.5182; 18.2995
90; 98.281; 90
1578.73van Vliet, Sven; Alachouzos, Georgios; de Vries, Folkert; Pfeifer, Lukas; Feringa, Ben L.
Visible light activated BINOL-derived chiroptical switches based on boron integrated hydrazone complexes
Chemical Science, 2022, 13, 9713-9718
1567449 CIFC58 H4 Al2 F80 O22 Ru3P -111.298; 14.164; 15.698
71.621; 71.685; 73.388
2214Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567450 CIFC2.76 H0.19 Al0.1 F3.81 O1.05 Os0.14P -111.283; 14.143; 15.714
71.674; 71.73; 73.486
2211.9Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567451 CIFC29 Al F36 N O17 Ru4P 1 21/c 115.639; 15.156; 41.36
90; 95.87; 90
9752Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567452 CIFC38 Al2 Cl2 F63 O6P 1 21/n 114.514; 10.566; 18.161
90; 98.81; 90
2752Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567453 CIFC68 H2 Al4 F114 O26 Os3P -111.81; 12.939; 19.507
102.689; 103.941; 92.667
2806.8Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567454 CIFC22 Al F36 I3 O10 Ru2P n m a18.581; 13.756; 16.816
90; 90; 90
4298.2Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567455 CIFC57 H3 Ag Al2 F61 O30 Os6P 1 21/c 120.504; 17.81; 25.217
90; 107.09; 90
8802Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567456 CIFC21 Al F36 I O9 RuP 4/n :213.768; 13.768; 9.5388
90; 90; 90
1808.2Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567457 CIFC68 H2 Al4 F114 O26 Ru3P -111.819; 12.94; 19.477
102.636; 103.912; 92.736
2805.5Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567458 CIFC46 H2 Ag Al F40 O28 Ru6P -112.349; 12.385; 23.041
90.85; 94.031; 93.152
3509Sellin, Malte; Friedmann, Christian; Mayländer, Maximilian; Richert, Sabine; Krossing, Ingo
Towards clustered carbonyl cations [M3(CO)14]2+ (M = Ru, Os): the need for innocent deelectronation
Chemical Science, 2022, 13, 9147-9158
1567461 CIFC19 H21 N O2P 1 21/c 19.0815; 11.6927; 14.7988
90; 102.05; 90
1536.82Plöger, Stefanie; Mück-Lichtenfeld, Christian; Daniliuc, Constantin G.; Studer, Armido
Azodioxy compounds as precursors for C-radicals and their application in thermal styrene difunctionalization
Chemical Science, 2022, 13, 9749-9754
1567476 CIFC62 H49 F12.1 N6 Ni2 O6P 21 21 2115.4863; 16.5824; 22.2267
90; 90; 90
5707.82Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567477 CIFC8 H8 F6 O2I 1 a 16.2917; 16.636; 9.166
90; 102.361; 90
937.15Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567478 CIFC31 H25 F7 N3 Ni O3P 21 21 2111.0205; 13.9185; 19.0776
90; 90; 90
2926.29Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567479 CIFC7 H4 F6 N2P 1 21/c 113.7855; 5.6753; 11.6678
90; 103.923; 90
886.03Delamare, Aline; Naulet, Guillaume; Kauffmann, Brice; Guichard, Gilles; Compain, Guillaume
Hexafluoroisobutylation of enolates through a tandem elimination/allylic shift/hydrofluorination reaction
Chemical Science, 2022, 13, 9507-9514
1567487 CIFC16 H17 N O2 S2P 21 21 216.2635; 11.4411; 20.8675
90; 90; 90
1495.4Lai, Junshan; Reid, Jolene P.
Interrogating the thionium hydrogen bond as a noncovalent stereocontrolling interaction in chiral phosphate catalysis
Chemical Science, 2022, 13, 11065-11073
1567538 CIFC33 H39 N O4P 1 21 19.28; 17.0143; 10.0461
90; 115.351; 90
1433.5Balanna, Kuruva; Barik, Soumen; Shee, Sayan; Gonnade, Rajesh G.; Biju, Akkattu T.
Dynamic kinetic resolution of γ,γ-disubstituted indole 2-carboxaldehydes <i>via</i> NHC-Lewis acid cooperative catalysis for the synthesis of tetracyclic ε-lactones.
Chemical science, 2022, 13, 11513-11518
1567539 CIFC52 H84 Ag14 F24 N6 O22 S6C 1 2/c 121.4916; 18.1316; 23.7184
90; 91.945; 90
9237.2Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567540 CIFC68 H112 Ag24 F30 N8 O28 S9P -114.2139; 15.6549; 17.3498
94.12; 110.998; 104.208
3439.1Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567541 CIFC62 H77 Ag24 F50 N5 O25 S9P -114.9116; 16.3962; 18.2438
97.091; 112.841; 104.162
3864.89Luo, Xi-Ming; Huang, Shuo; Luo, Peng; Ma, Kai; Wang, Zhao-Yang; Dong, Xi-Yan; Zang, Shuang-Quan
Snapshots of key intermediates unveiling the growth from silver ions to Ag70 nanoclusters
Chemical Science, 2022, 13, 11110-11118
1567548 CIFC22 H17 N OP -17.4998; 11.4895; 18.504
98.672; 96.018; 90.007
1567.3Muraoka, Masanobu; Goto, Masahide; Minami, Masaki; Zhou, Dayang; Suzuki, Takeyuki; Yajima, Tatsuo; Hayashi, Jun'ichi; Sogawa, Hiromitsu; Sanda, Fumio
Ethynylene-linked multifunctional benzoxazines: the effect of the ethynylene group and packing on thermal behavior
Polymer Chemistry, 2022, 13, 5590-5596
1567549 CIFC8 H7 N O2F d d 211.8514; 30.185; 7.533
90; 90; 90
2694.8Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567550 CIFC16 H11 N OR -3 :H35.383; 35.383; 5.235
90; 90; 120
5675.9Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567551 CIFC34 H25 NP 1 21/n 19.928; 9.4716; 52.455
90; 90.791; 90
4932.1Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567552 CIFC21 H19 N O3C 1 c 114.0103; 35.603; 11.376
90; 117.174; 90
5048.1Wang, Bin; Ren, Hongyuan; Cao, Hou-Ji; Lu, Changsheng; Yan, Hong
A switchable redox annulation of 2-nitroarylethanols affording N-heterocycles: photoexcited nitro as a multifunctional handle
Chemical Science, 2022, 13, 11074-11082
1567572 CIFC44 H40 Br4 Co2 N4 O6P -19.4017; 10.5681; 12.696
66.4289; 77.1738; 84.9305
1127.35Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567573 CIFC31 H44 Co N3 O2P 1 21/c 111.59303; 11.77994; 21.25835
90; 91.1883; 90
2902.53Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567574 CIFC68 H68 Co2 N4 O6P b c a10.9817; 17.1391; 31.4588
90; 90; 90
5921.1Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567575 CIFC84 H100 Co2 N4 O6P -111.1838; 12.1674; 15.6011
72.164; 70.4512; 89.2308
1895.03Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567576 CIFC52 H60 Co2 N4 O6P -111.1341; 13.1609; 17.4589
81.674; 71.6133; 84.1723
2397.89Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567577 CIFC57 H72 Co2 N4 O10P 1 21/c 114.3182; 12.0109; 15.9104
90; 97.507; 90
2712.73Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567578 CIFC60 H80 Co2 N8 O6P -113.2692; 15.2605; 16.5352
77.6834; 76.0242; 66.204
2947.53Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567579 CIFC54 H58 Co2 N4 O6P 1 21/c 113.5589; 35.2233; 16.1183
90; 105.07; 90
7433.2Takebayashi, Satoshi; Fayzullin, Robert R.; Bansal, Richa
Direct observation of reversible bond homolysis by 2D EXSY NMR
Chemical Science, 2022, 13, 9202-9209
1567580 CIFC53 H76 N2 OP -114.2247; 18.7107; 19.0753
109.83; 93.98; 103.16
4590.5Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567581 CIFC53 H79 Cl N2 O2P 1 21/c 113.0058; 18.6532; 20.2559
90; 107.607; 90
4683.9Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567582 CIFC57 H84 F3 N2 O4.5 SI 1 2/a 117.3378; 16.0403; 38.924
90; 95.096; 90
10782.1Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567583 CIFC54 H78 Cl2 F12 N2 O P2P 1 21/n 112.152; 31.9515; 14.2567
90; 97.129; 90
5492.7Théry, Valentin; Molton, Florian; Sirach, Selim; Tillet, Neven; Pécaut, Jacques; Tomás-Mendivil, Eder; Martin, David
The curious case of a sterically crowded Stenhouse salt
Chemical Science, 2022, 13, 9755-9760
1567601 CIFC60 H68 Ga N4 PP 1 21/n 111.5827; 15.4151; 27.061
90; 90.708; 90
4831.3Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567602 CIFC52.5 H53 Cl Ga N4 PP 1 21/c 125.411; 16.6359; 23.7139
90; 107.797; 90
9545Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567603 CIFC56 H60 Ga N4 O PP 1 21/c 113.0677; 21.406; 17.1423
90; 108.63; 90
4543.9Sigmund, Lukas M.; Engels, Eliane; Richert, Nick; Greb, Lutz
Calix[4]pyrrolato gallate: square planar-coordinated gallium(iii) and its metal–ligand cooperative reactivity with CO2 and alcohols
Chemical Science, 2022, 13, 11215-11220
1567608 CIFC23 H29 NP 1 21 110.9102; 6.1038; 14.7452
90; 99.5; 90
968.47Sun, Yue; Ma, Chun; Li, Zhiming; Zhang, Junliang
Palladium/GF-Phos-catalyzed asymmetric carbenylative amination to access chiral pyrrolidines and piperidines
Chemical Science, 2022, 13, 11150-11155
1567609 CIFC23 H16 I3 NP b c n21.1343; 13.7339; 7.328
90; 90; 90
2127Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567610 CIFC22 H14 I3 NP -18.0838; 11.8898; 12.2871
64.355; 77.901; 77.39
1030.02Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567611 CIFC23 H14 F3 I2 N O3 SP -18.5783; 11.1636; 13.3063
74.307; 71.324; 79.269
1155.23Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567612 CIFC22 H15 I3 N2P b c n21.0883; 13.773; 7.3022
90; 90; 90
2120.9Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567613 CIFC22 H14 I3 NP b c n21.0383; 13.782; 7.3031
90; 90; 90
2117.5Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567614 CIFC24 H16 F3 I2 N O3 SP -17.2077; 12.3954; 14.0967
98.565; 101.823; 91.413
1216.98Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567615 CIFC23 H14 F3 I2 N O3 SP -17.1362; 12.3559; 14.2656
98.46; 103.067; 94.936
1202.63Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567616 CIFC23 H15 F3 I2 N2 O3 SP -4 21 c22.544; 22.544; 9.5927
90; 90; 90
4875.3Decato, Daniel A.; Sun, Jiyu; Boller, Madeleine R.; Berryman, Orion B.
Pushing the limits of the hydrogen bond enhanced halogen bond—the case of the C–H hydrogen bond
Chemical Science, 2022, 13, 11156-11162
1567617 CIFC59 H51 F6 N5 O6 S2C 1 2/c 122.116; 17.029; 16.379
90; 124.27; 90
5098Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567618 CIFC51 H45 N5P 1 21/n 18.4766; 15.6816; 28.099
90; 95.655; 90
3716.9Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567619 CIFC57 H49 Cl4 N5P 1 21/n 117.0926; 16.467; 17.5046
90; 113.674; 90
4512.3Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567620 CIFC59 H55 Cl6 I2 N5 Rh2C 1 2/c 115.6999; 18.4945; 20.4988
90; 91.779; 90
5949.2Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567621 CIFC57 H55 Cl2 F6 N5 O6 S2P 1 21/c 116.175; 18.4493; 18.016
90; 102.497; 90
5248.9Karak, Pirudhan; Choudhury, Joyanta
Conformationally flexible heterohelicenes as stimuli-controlled soft molecular springs
Chemical Science, 2022, 13, 11163-11173
1567622 CIFC18 H21 N O6P -18.1602; 10.1021; 11.5212
88.2151; 69.4794; 72.0806
843.2Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567623 CIFC16 H17 N O6P 1 21/c 112.998; 7.7936; 15.3862
90; 106.506; 90
1494.41Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567624 CIFC18 H21 N O6C 1 c 15.03; 20.5537; 16.8829
90; 97.379; 90
1730.99Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567625 CIFC18 H21 N O6P 1 21/c 117.15; 9.733; 10.702
90; 106.541; 90
1712.5Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567626 CIFC16 H17 N O6P 1 21/c 18.1387; 24.2934; 8.5069
90; 117.414; 90
1493.08Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567627 CIFC16 H17 N O6P 1 21/n 17.8712; 16.4752; 11.757
90; 91.5968; 90
1524.05Koo, Bonwoo; Kim, Dopil; Song, Da Yong; Han, Woo Joo; Kim, Dongwook; Park, Jae Woo; Kim, Min; Kim, Cheoljae
The formation of photodegradable nitrophenylene polymers via ring-opening metathesis polymerization
Polymer Chemistry, 2022, 13, 6268-6273
1567630 CIFC22 H13 F2 N OC 1 2/c 124.1916; 9.9649; 14.5436
90; 112.784; 90
3232.4Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567631 CIFC17 H11 F2 N OP 1 21/n 113.16; 7.282; 14.2
90; 99.631; 90
1341.6Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567632 CIFC25 H30 N2 O2P -4 21 c20.192; 20.192; 11.043
90; 90; 90
4502.4Wang, Gang; Li, Wenqi; Liu, Tianxiang; Zhang, Yonghong; Wang, Bin; Xue, Fei; Jin, Weiwei; Ma, Caiyan; Xia, Yu; Liu, Chenjiang
Palladium-catalyzed intramolecular Heck dearomative <i>gem</i>-difluorovinylation of indoles.
Chemical science, 2022, 13, 11594-11599
1567633 CIFC96 H85 N3 O4 S2P 1 21/c 120.891; 8.271; 44.433
90; 102.813; 90
7486Zhu, Jiangyu; Li, Wenhao; Zhang, Ning; An, Dongyue; Zhao, Yan; Lu, Xuefeng; Liu, Yunqi
Size-dependent properties and unusual reactivity of novel nonplanar heterocycloarenes
Chemical Science, 2022, 13, 11174-11182
1567634 CIFC80 H48 Cl6 N2 O8 S2P -112.745; 14.782; 19.522
82.434; 83.954; 80.211
3579.8Zhu, Jiangyu; Li, Wenhao; Zhang, Ning; An, Dongyue; Zhao, Yan; Lu, Xuefeng; Liu, Yunqi
Size-dependent properties and unusual reactivity of novel nonplanar heterocycloarenes
Chemical Science, 2022, 13, 11174-11182
1567637 CIFC20 H27 N O2P 1 21/c 16.3182; 39.6141; 7.7124
90; 111.769; 90
1792.68Cooper, Phillippa; Dalling, Andrew G.; Farrar, Elliot H. E.; Aldhous, Timothy P.; Grélaud, Simon; Lester, Eleanor; Feron, Lyman J.; Kemmitt, Paul D.; Grayson, Matthew N.; Bower, John F.
Atom and step economical synthesis of acyclic quaternary centers via iridium-catalyzed hydroarylative cross-coupling of 1,1-disubstituted alkenes
Chemical Science, 2022, 13, 11183-11189
1567641 CIFC21 H29 Br O4P -16.36017; 7.8529; 20.1551
91.523; 91.016; 93.88
1003.81Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567642 CIFC21 H29 Br O4P b c a10.6941; 8.218; 46.3766
90; 90; 90
4075.8Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567643 CIFC21 H29 Br O4P -16.41587; 12.0405; 13.3039
94.139; 91.6023; 101.288
1004.29Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567644 CIFC14 H26 O3P 1 21/n 15.8614; 15.5412; 14.8746
90; 90.764; 90
1354.85Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567645 CIFC21 H29 Br O4P 1 21/c 114.0432; 7.0309; 21.1186
90; 100.447; 90
2050.61Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567646 CIFC35 H38 O4P -16.28197; 12.2599; 19.1503
89.562; 87.114; 78.209
1441.93Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567647 CIFC21 H29 Br O4P -17.44418; 11.53654; 12.84945
69.1422; 81.678; 84.3027
1018.98Chen, Hao; Li, Tian-Ren; Sakai, Naomi; Besnard, Celine; Guénée, Laure; Pupier, Marion; Viger-Gravel, Jasmine; Tiefenbacher, Konrad; Matile, Stefan
Decoded fingerprints of hyperresponsive, expanding product space: polyether cascade cyclizations as tools to elucidate supramolecular catalysis
Chemical Science, 2022, 13, 10273-10280
1567648 CIFC25 H25 N O3P 1 21 110.5777; 41.8595; 10.6059
90; 115.198; 90
4249.18Guo, Wengang; Jiang, Feng; Li, Shijia; Sun, Jianwei
Organocatalytic asymmetric azidation of sulfoxonium ylides: mild synthesis of enantioenriched α-azido ketones bearing a labile tertiary stereocenter.
Chemical science, 2022, 13, 11648-11655
1567649 CIFC24 H48 Cl2 Cr2 Si4P 1 21/c 113.2426; 7.9314; 15.6465
90; 101.402; 90
1610.96Trummer, David; Nobile, Anna Giorgia; Payard, Pierre-Adrien; Ashuiev, Anton; Kakiuchi, Yuya; Klose, Daniel; Jeschke, Gunnar; Copéret, Christophe
Union carbide polymerization catalysts: from uncovering active site structures to designing molecularly-defined analogs
Chemical Science, 2022, 13, 11091-11098
1567650 CIFC26 H36 CrP 1 21/n 19.3657; 16.7589; 14.5402
90; 105.649; 90
2197.6Trummer, David; Nobile, Anna Giorgia; Payard, Pierre-Adrien; Ashuiev, Anton; Kakiuchi, Yuya; Klose, Daniel; Jeschke, Gunnar; Copéret, Christophe
Union carbide polymerization catalysts: from uncovering active site structures to designing molecularly-defined analogs
Chemical Science, 2022, 13, 11091-11098
1567652 CIFC29.5 H31 Cl N2I 1 2/a 122.0567; 7.5133; 32.5379
90; 109.612; 90
5079.32Cui, Xian-Chao; Zhang, Hu; Wang, Yi-Ping; Qu, Jian-Ping; Kang, Yan-Biao
Synthesis of carbinoxamine via α-C(sp3)–H 2-pyridylation of O, S or N-containing compounds enabled by non-D–A-type super organoreductants and sulfoxide- or sulfide HAT reagents
Chemical Science, 2022, 13, 11246-11251
1567653 CIFC27 H26 N2 OP -17.8864; 9.9577; 15.3148
75.304; 85.678; 67.535
1074.74Cui, Xian-Chao; Zhang, Hu; Wang, Yi-Ping; Qu, Jian-Ping; Kang, Yan-Biao
Synthesis of carbinoxamine via α-C(sp3)–H 2-pyridylation of O, S or N-containing compounds enabled by non-D–A-type super organoreductants and sulfoxide- or sulfide HAT reagents
Chemical Science, 2022, 13, 11246-11251
1567654 CIFC21 H16 Cl NP 1 21/n 110.7317; 5.511; 27.4878
90; 99.361; 90
1604.05Li, Quanzhe; Gu, Xintao; Wei, Yin; Shi, Min
Visible-light-induced indole synthesis <i>via</i> intramolecular C-N bond formation: desulfonylative C(sp<sup>2</sup>)-H functionalization.
Chemical science, 2022, 13, 11623-11632
1567655 CIFC24 H28 Br4 N4 O4I 1 2/a 120.6359; 5.1809; 27.7349
90; 104.528; 90
2870.4Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567656 CIFC18 H14 I4 N2 O4P 1 21/c 114.0017; 8.2362; 19.1456
90; 104.636; 90
2136.24Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567657 CIFC14 H8 I4 N8P -111.9316; 12.2715; 15.2444
73.159; 73.857; 79.026
2037.41Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567658 CIFC26 H34 N2 O4 S4P -17.2152; 8.0923; 12.5451
87.957; 82.964; 66.841
668.32Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567659 CIFC24 H30 F2 N4 O4P -110.1072; 11.4012; 11.5402
94.868; 95.841; 112.726
1208.99Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567660 CIFC16 H18 N2 Se4P 1 2/n 115.5783; 7.9499; 29.5587
90; 90.3204; 90
3660.67Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567661 CIFC22 H26 N2 O4 Se4P b c n16.0349; 15.8463; 19.0464
90; 90; 90
4839.57Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567662 CIFC16 H18 N2 S4P 1 2/n 115.105; 7.8801; 28.9196
90; 90.6804; 90
3442.03Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567663 CIFC14 H12 F2 N2 Te2P 1 21/n 16.4567; 8.6728; 13.3795
90; 92.32; 90
748.61Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567664 CIFC16 H18 N2 Te4P 1 21 110.7335; 10.5743; 18.0208
90; 95.2723; 90
2036.69Kerckhoffs, Aidan; Christensen, Kirsten E.; Langton, Matthew J.
Fast relaxing red and near-IR switchable azobenzenes with chalcogen and halogen substituents: periodic trends, tuneable thermal half-lives and chalcogen bonding.
Chemical science, 2022, 13, 11551-11559
1567665 CIFC34 H44 Br0 N4 O4P -14.7183; 12.508; 13.014
78.569; 86.876; 82.105
745.4Bansal, Deepak; Kundu, Arup; Singh, Vijay Pal; Pal, Arun K.; Datta, Ayan; Dasgupta, Jyotishman; Mukhopadhyay, Pritam
A highly contorted push-pull naphthalenediimide dimer and evidence of intramolecular singlet exciton fission.
Chemical science, 2022, 13, 11506-11512
1567666 CIFC56 H64 N8 O8P 43 21 214.7104; 14.7104; 23.995
90; 90; 90
5192.4Bansal, Deepak; Kundu, Arup; Singh, Vijay Pal; Pal, Arun K.; Datta, Ayan; Dasgupta, Jyotishman; Mukhopadhyay, Pritam
A highly contorted push-pull naphthalenediimide dimer and evidence of intramolecular singlet exciton fission.
Chemical science, 2022, 13, 11506-11512
1567667 CIFCd S4 Si SrA m a 210.2821; 10.1551; 6.3699
90; 90; 90
665.12Yang, He-Di; Ran, Mao-Yin; Zhou, Sheng-Hua; Wu, Xin-Tao; Lin, Hua; Zhu, Qi-Long
Rational design via dual-site aliovalent substitution leads to an outstanding IR nonlinear optical material with well-balanced comprehensive properties
Chemical Science, 2022, 13, 10725-10733
1567668 CIFGa2 S4 SrF d d d :212.2216; 20.5008; 20.8426
90; 90; 90
5222.2Yang, He-Di; Ran, Mao-Yin; Zhou, Sheng-Hua; Wu, Xin-Tao; Lin, Hua; Zhu, Qi-Long
Rational design via dual-site aliovalent substitution leads to an outstanding IR nonlinear optical material with well-balanced comprehensive properties
Chemical Science, 2022, 13, 10725-10733
1567671 CIFC19 H17 N O3P 1 21/n 18.9115; 18.9555; 9.6086
90; 104.43; 90
1571.9Tavernier, Romain; Granado, Lérys; Tillard, Monique; Van Renterghem, Louis; Métro, Thomas-Xavier; Lamaty, Frédéric; Bonnaud, Leïla; Raquez, Jean-Marie; David, Ghislain; Caillol, Sylvain
Solvent-free synthesis of a formaldehyde-free benzoxazine monomer: study of its curing acceleration effect for commercial benzoxazine
Polymer Chemistry, 2022, 13, 5745-5756
1567676 CIFC39 H36 Ge N2P 1 21/c 115.0811; 11.4764; 18.5521
90; 90.197; 90
3210.9Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567677 CIFC39 H36 Ge N2 SP 1 21/n 17.9949; 21.1802; 19.6152
90; 99.409; 90
3276.8Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567678 CIFC39 H49 Ge N3 Si2P 1 21/n 113.302; 9.7758; 28.456
90; 93.909; 90
3691.7Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567679 CIFC78 H98 Cu2 Ge2 I2 N6 Se2 Si4P 1 21/c 113.7954; 12.2314; 23.9124
90; 90.032; 90
4034.9Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567680 CIFC39 H36 Ge N2 SeP 1 21/n 18.0415; 21.217; 19.7259
90; 99.617; 90
3318.3Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567681 CIFC39 H49 Ge N3 Se Si2P -18.9661; 11.2946; 19.9064
86.969; 77.252; 73.433
1884.5Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567682 CIFC42 H55 Ge N3 S Si2P -18.7695; 11.3819; 21.887
76.889; 86.438; 72.957
2034.2Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567683 CIFC39 H49 Cl Cu Ge N3 S Si2P -110.915; 12.0113; 17.7694
83.36; 76.387; 69.278
2116.37Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567684 CIFC35 H36 Ge N2 O SP 1 21/n 114.9611; 14.0451; 15.5244
90; 107.287; 90
3114.79Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567685 CIFC84 H112 Br2 Cu2 Ge2 N6 S2 Si4P -112.3707; 12.4183; 16.7015
89.009; 74.715; 61.241
2151.41Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567686 CIFC78 H98 Cu2 Ge2 I2 N6 S2 Si4P 1 21/c 113.947; 12.306; 23.936
90; 90.327; 90
4108.1Mahawar, Pritam; Shukla, Pratima; Chandra Joshi, Prakash; Singh, Dharmendra; Kumar, Hemant; Mukherjee, Goutam; Nagendran, Selvarajan
Air and water stable germacarbonyl compounds
Chemical Science, 2022, 13, 12382-12388
1567695 CIFC32 H30 O2P 1 21 19.5099; 9.8152; 13.7004
90; 105.846; 90
1230.22Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567696 CIFC34 H26 O2P 1 21 19.2899; 10.6993; 13.1402
90; 107.074; 90
1248.51Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567697 CIFC36 H36 F2 O2P 1 21/c 110.356; 31.286; 9.517
90; 108.01; 90
2932.4Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567698 CIFC33 H29 Cl3 F2 O2P 1 21/n 113.893; 9.559; 23.43
90; 98.908; 90
3074Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567699 CIFC48 H57 P3 Si3C 1 2/c 126.6644; 42.3661; 9.7021
90; 104.927; 90
10590.3Arkhypchuk, Anna I.; D'Imperio, Nicolas; Wells, Jordann A. L.; Ott, Sascha
[2 + 2] Cycloaddition of phosphaalkenes as a key step for the reductive coupling of diaryl ketones to tetraaryl olefins
Chemical Science, 2022, 13, 12239-12244
1567702 CIFC24 H23 N O3P 21 21 217.9494; 10.2838; 24.4594
90; 90; 90
1999.56Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567703 CIFC28 H25 N O2 SP 3110.2503; 10.2503; 18.6428
90; 90; 120
1696.35Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567704 CIFC27 H23 N O2 SP 1 21 19.4589; 9.3504; 12.948
90; 110.298; 90
1074.06Li, Wendeng; Zhang, He; Chen, Kai; Jiang, Huanfeng; Sun, Jianwei; Zhu, Shifa
Palladium-catalyzed intramolecular enantioselective C(sp3)–H insertion of donor/donor carbenes
Chemical Science, 2022, 13, 12396-12402
1567721 CIFC148 H108 Au8 O10 P6 S2P 21 21 2118.8119; 27.697; 31.3398
90; 90; 90
16329.1Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567722 CIFC146 H104 Au8 O4 P6 S2P 21 21 2120.5564; 25.7288; 26.0976
90; 90; 90
13802.8Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567723 CIFC148 H108 Au8 O10 P6 S2P 21 21 2118.4744; 27.7085; 31.2344
90; 90; 90
15988.8Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567724 CIFC146 H104 Au8 O4 P6 S2P 21 21 2120.333; 25.812; 26.048
90; 90; 90
13671Si, Wei-Dan; Sheng, Kai; Zhang, Chengkai; Wang, Zhi; Zhang, Shan-Shan; Dou, Jian-Min; Feng, Lei; Gao, Zhi-Yong; Tung, Chen-Ho; Sun, Di
Bicarbonate insertion triggered self-assembly of chiral octa-gold nanoclusters into helical superstructures in the crystalline state
Chemical Science, 2022, 13, 10523-10531
1567725 CIFC26 H26 F N2 OP 1 21/c 111.1117; 20.386; 9.6205
90; 107.152; 90
2082.34Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567726 CIFC20 H17 F OF d d 238.8063; 15.6732; 9.8717
90; 90; 90
6004.15Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567727 CIFC23 H19 F N2 OP 1 21/c 112.6548; 7.2987; 20.6049
90; 98.643; 90
1881.53Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567728 CIFC20 H17 Cl OP 1 21/c 19.4028; 19.5701; 9.3681
90; 115.798; 90
1552.05Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567729 CIFC22 H19 F O3P 1 21/c 113.8641; 10.5226; 12.1171
90; 103.029; 90
1722.21Rai, Pramod; Maji, Kakoli; Jana, Sayan K.; Maji, Biplab
Intermolecular dearomative [4 + 2] cycloaddition of naphthalenes via visible-light energy-transfer-catalysis
Chemical Science, 2022, 13, 12503-12510
1567732 CIFC27 H28 N2 O4 S2P 1 21/n 19.4288; 10.4362; 26.2815
90; 96.065; 90
2571.65Chen, Zhi; Li, Yu-Fan; Tan, Shun-Zhong; Ouyang, Qin; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Formal nucleophilic pyrrolylmethylation via palladium-based auto-tandem catalysis: switchable regiodivergent synthesis and remote chirality transfer
Chemical Science, 2022, 13, 12433-12439
1567733 CIFC31 H30 N2 O4 S3C 1 2/c 129.5374; 9.77; 24.882
90; 122.932; 90
6026.7Chen, Zhi; Li, Yu-Fan; Tan, Shun-Zhong; Ouyang, Qin; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Formal nucleophilic pyrrolylmethylation via palladium-based auto-tandem catalysis: switchable regiodivergent synthesis and remote chirality transfer
Chemical Science, 2022, 13, 12433-12439
1567740 CIFC92 H90 Al8 F72 Ga2 O8P 1 21/c 144.352; 18.147; 30.839
90; 102.49; 90
24234Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567741 CIFC55 H66 Al4 F36 Ga N3 O4P -117.181; 21.399; 21.691
117.464; 90.245; 90.863
7075Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567742 CIFC56.88 H67.67 Al4 F36.06 Ga N3 O3.97P -110.927; 17.637; 19.087
94.601; 97.945; 98.66
3582Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567743 CIFC55 H66 Al5 F36 N3 O4P 1 21/c 121.369; 17.024; 21.581
90; 116.118; 90
7049Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567744 CIFC52.45 H49.31 Al4 F38.14 Ga O4P -116.445; 16.685; 28.346
80.473; 83.826; 60.715
6687Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567745 CIFC48.13 H46.42 Al4 F36.71 O4 TlP -122.345; 26.95; 29.77
88.88; 70.81; 70.94
15925Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567746 CIFC48.1 H46.39 Al4 F36.73 In O4P -122.327; 26.903; 29.692
88.983; 70.929; 70.884
15847Dabringhaus, Philipp; Krossing, Ingo
From mixed group 13 cations [M(AlCp*)3]+ (M = Ga/In/Tl) to an Al4+ cluster
Chemical Science, 2022, 13, 12078-12086
1567748 CIFC3 H6 N2 OF d d d :29.97; 11.8236; 13.3559
90; 90; 90
1574.41Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567749 CIFC3 H10 F6 N3 O PP -15.25069; 7.8976; 11.4023
82.781; 79.266; 84.108
459.35Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567750 CIFC2 H12 N8 O6P 1 21/n 114.6572; 3.71857; 20.3958
90; 108.778; 90
1052.48Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567751 CIFC3 H10 N6 O5C 1 2/c 124.756; 4.29; 17.8827
90; 107.988; 90
1806.37Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567752 CIFC2 H12 N8 O6P 1 21/n 114.7309; 3.59237; 20.2453
90; 108.791; 90
1014.25Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567753 CIFC2 H6 F6 N2 O PP 1 21/c 111.4292; 5.5925; 11.1451
90; 92.547; 90
711.67Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567754 CIFC H8 F6 N3 O PP b c a7.67243; 8.07957; 24.2351
90; 90; 90
1502.33Bellas, Michael K.; Matzger, Adam J.
Discovery strategy leads to the first melt-castable cocrystal based on an energetic oxidizing salt
Chemical Science, 2022, 13, 12100-12106
1567756 CIFC66.95 H108.34 N0.52 O21.95 V6P b c m14.4807; 27.8595; 18.7836
90; 90; 90
7577.77Cooney, Shannon E.; Fertig, Alex A.; Buisch, Madeleine R.; Brennessel, William W.; Matson, Ellen M.
Coordination-induced bond weakening of water at the surface of an oxygen-deficient polyoxovanadate cluster.
Chemical science, 2022, 13, 12726-12737
1567757 CIFC21 H23 F O4P 1 21 18.092; 5.9484; 19.5057
90; 98.051; 90
929.64Liao, Ling; Zhang, Ying; Wu, Zhong-Wei; Ye, Zhong-Tian; Zhang, Xue-Xin; Chen, Guangying; Yu, Jin-Sheng
Nickel-catalyzed regio- and enantio-selective Markovnikov hydromonofluoroalkylation of 1,3-dienes
Chemical Science, 2022, 13, 12519-12526
1567758 CIFC23 H21 F O4 S2P 21 21 217.5543; 10.058; 28.1125
90; 90; 90
2136.02Liao, Ling; Zhang, Ying; Wu, Zhong-Wei; Ye, Zhong-Tian; Zhang, Xue-Xin; Chen, Guangying; Yu, Jin-Sheng
Nickel-catalyzed regio- and enantio-selective Markovnikov hydromonofluoroalkylation of 1,3-dienes
Chemical Science, 2022, 13, 12519-12526
1567759 CIFC13 H20.2 N2 O2.1P -15.7302; 9.9783; 11.5048
83.662; 89.167; 86.054
652.23Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567760 CIFC13 H19 N O5P 1 21/c 111.2115; 11.5329; 11.145
90; 104.981; 90
1392.08Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567761 CIFC13 H20 B F3 N2 O3C 1 2/c 131.0762; 9.4685; 12.1756
90; 91.156; 90
3581.9Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567762 CIFC22 H34 N2 O5 SP b c a16.617; 11.8972; 22.9385
90; 90; 90
4534.8Tien, Chieh-Hung; Lough, Alan J.; Yudin, Andrei K.
Iminologous epoxide ring-closure
Chemical Science, 2022, 13, 12175-12179
1567763 CIFC12 H10 Br F N2 SP 14.5926; 5.6626; 12.165
86.311; 88.909; 81.003
311.81Zhao, Ruyan; Zhu, Tong; Wang, Sasa; Jarrett-Wilkins, Charlie; Najjarian, Amin Morteza; Lough, Alan J.; Hoogland, Sjoerd; Sargent, Edward H.; Seferos, Dwight S.
Engineering hydrogen bonding to align molecular dipoles in organic solids for efficient second harmonic generation
Chemical Science, 2022, 13, 12144-12148
1567764 CIFC12 H11 Br2 F N2 SP -14.5711; 12.769; 13.073
69.971; 89.227; 85.826
714.9Zhao, Ruyan; Zhu, Tong; Wang, Sasa; Jarrett-Wilkins, Charlie; Najjarian, Amin Morteza; Lough, Alan J.; Hoogland, Sjoerd; Sargent, Edward H.; Seferos, Dwight S.
Engineering hydrogen bonding to align molecular dipoles in organic solids for efficient second harmonic generation
Chemical Science, 2022, 13, 12144-12148
1567775 CIFC15 H14 O3P 21 21 217.7082; 12.0888; 12.3892
90; 90; 90
1154.46Guan, Fujun; Zhou, Rong; Ren, Xiaoyu; Guo, Zhen; Wang, Chengming; Zhou, Cong-Ying
Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds.
Chemical science, 2022, 13, 13015-13019
1567776 CIFC15 H13 Br O2P 21 21 217.0572; 10.6743; 15.6753
90; 90; 90
1180.83Guan, Fujun; Zhou, Rong; Ren, Xiaoyu; Guo, Zhen; Wang, Chengming; Zhou, Cong-Ying
Asymmetric dearomative cyclopropanation of naphthalenes to construct polycyclic compounds.
Chemical science, 2022, 13, 13015-13019
1567779 CIFC11 H14 Cl Fe O2 PP b c a12.2903; 13.3012; 15.6001
90; 90; 90
2550.24Xin, Tiansi; Geeson, Michael B.; Zhu, Hui; Qu, Zheng-Wang; Grimme, Stefan; Cummins, Christopher C.
Synthesis of phosphiranes <i>via</i> organoiron-catalyzed phosphinidene transfer to electron-deficient olefins.
Chemical science, 2022, 13, 12696-12702
1567780 CIFC15 H20 Cl Fe O4 PP 1 21/c 18.0716; 22.6406; 9.6109
90; 107.934; 90
1671.01Xin, Tiansi; Geeson, Michael B.; Zhu, Hui; Qu, Zheng-Wang; Grimme, Stefan; Cummins, Christopher C.
Synthesis of phosphiranes <i>via</i> organoiron-catalyzed phosphinidene transfer to electron-deficient olefins.
Chemical science, 2022, 13, 12696-12702
1567781 CIFC11 H14 F Fe O2 PP b c a21.4541; 9.6814; 23.524
90; 90; 90
4886.07Xin, Tiansi; Geeson, Michael B.; Zhu, Hui; Qu, Zheng-Wang; Grimme, Stefan; Cummins, Christopher C.
Synthesis of phosphiranes <i>via</i> organoiron-catalyzed phosphinidene transfer to electron-deficient olefins.
Chemical science, 2022, 13, 12696-12702
1567786 CIFC15 H20 O2P 21 21 215.60939; 10.26643; 22.2551
90; 90; 90
1281.64Tian, Peilin; Ye, Wenkang; Zhang, Xiayan; Tong, Yi; Qian, Pei-Yuan; Tong, Rongbiao
Ten-step asymmetric total syntheses of potent antibiotics anthracimycin and anthracimycin B.
Chemical science, 2022, 13, 12776-12781
1567787 CIFC25 H32 O4P 21 21 215.5419; 15.3789; 25.7913
90; 90; 90
2198.15Tian, Peilin; Ye, Wenkang; Zhang, Xiayan; Tong, Yi; Qian, Pei-Yuan; Tong, Rongbiao
Ten-step asymmetric total syntheses of potent antibiotics anthracimycin and anthracimycin B.
Chemical science, 2022, 13, 12776-12781
1567790 CIFC10 H9 F7 N2 O3P -18.4543; 8.9233; 9.8274
111.704; 98.837; 101.362
654.12Deolka, Shubham; Govindarajan, Ramadoss; Vasylevskyi, Serhii; Roy, Michael C.; Khusnutdinova, Julia R.; Khaskin, Eugene
Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes.
Chemical science, 2022, 13, 12971-12979
1567791 CIFC9 H9 F5 N2 O3P -17.9519; 8.3267; 9.1611
82.449; 72.42; 77.031
562.18Deolka, Shubham; Govindarajan, Ramadoss; Vasylevskyi, Serhii; Roy, Michael C.; Khusnutdinova, Julia R.; Khaskin, Eugene
Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes.
Chemical science, 2022, 13, 12971-12979
1567792 CIFC11 H8 F5 NP 1 21/n 17.832; 6.1313; 22.493
90; 93.678; 90
1077.9Deolka, Shubham; Govindarajan, Ramadoss; Vasylevskyi, Serhii; Roy, Michael C.; Khusnutdinova, Julia R.; Khaskin, Eugene
Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes.
Chemical science, 2022, 13, 12971-12979
1567793 CIFC20 H18 F5 N O5I 1 2 120.3374; 7.1756; 14.0098
90; 92.999; 90
2041.69Deolka, Shubham; Govindarajan, Ramadoss; Vasylevskyi, Serhii; Roy, Michael C.; Khusnutdinova, Julia R.; Khaskin, Eugene
Ligand-free nickel catalyzed perfluoroalkylation of arenes and heteroarenes.
Chemical science, 2022, 13, 12971-12979
1567794 CIFC21.5 H25 Cu N6.75 O7P 1 21/c 114.2321; 13.2378; 14.6287
90; 93.153; 90
2751.9Zeng, Heng; Xie, Xiao-Jing; Wang, Ying; Luo, Dong; Wei, Rong-Jia; Lu, Weigang; Li, Dan
Spatial disposition of square-planar mononuclear nodes in metal-organic frameworks for C<sub>2</sub>H<sub>2</sub>/CO<sub>2</sub> separation.
Chemical science, 2022, 13, 12876-12882
1567803 CIFC34 H58 F6 N6 O6 S2P 1 21/c 19.4465; 20.428; 11.45
90; 112.936; 90
2034.9Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567804 CIFC32 H54 N6P -18.4164; 9.9098; 10.3761
101.12; 111.201; 93.802
782.89Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567805 CIFC35 H56 F9 N6 O9 S3I 1 2/a 111.2729; 20.2466; 19.5699
90; 92.742; 90
4461.5Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567806 CIFC36 H56 F12 N6 O12 S4P 1 21/n 112.7027; 13.3266; 14.3241
90; 93.044; 90
2421.42Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567807 CIFC32 H56 N6P 1 21/n 17.9568; 18.1921; 11.2323
90; 107.697; 90
1548.94Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567808 CIFC42 H72 F6 N6 O8 S2P 1 21/c 110.2368; 11.7148; 20.4531
90; 92.856; 90
2449.73Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567809 CIFC33 H56 N6P -18.4; 10.3658; 20.0368
78.183; 79.823; 82.783
1673.56Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567810 CIFC33 H58 N6P 1 21/c 111.5251; 28.9745; 11.6064
90; 119.306; 90
3379.7Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567811 CIFC38 H64 F6 N6 O6 S2P 1 21/c 19.1161; 46.1464; 11.2799
90; 105.642; 90
4569.4Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567812 CIFC35 H60 F6 N6 O6 S2P 1 21/c 116.4086; 22.9375; 11.3222
90; 97.679; 90
4223.1Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567813 CIFC40 H82 F12 N6 O22 S4P -111.1305; 11.429; 13.722
92.322; 99.653; 113.256
1570.03Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567814 CIFC41 H65 F9 N7 O9 S3P 1 21/n 113.7065; 11.8374; 32.3229
90; 91.669; 90
5242.1Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567815 CIFC42 H68 F6 N8 O6 S2P n a 2127.5528; 8.4292; 22.0477
90; 90; 90
5120.5Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567816 CIFC37 H59 F12 N6 O12.5 S4P 1 21/c 114.521; 11.291; 30.821
90; 93.8; 90
5042.2Nayak, Mithilesh Kumar; Sarkar, Pallavi; Elvers, Benedict J.; Mehta, Sakshi; Zhang, Fangyuan; Chrysochos, Nicolas; Krummenacher, Ivo; Vijayakanth, Thangavel; Narayanan, Ramakirushnan Suriya; Dolai, Ramapada; Roy, Biswarup; Malik, Vishal; Rawat, Hemant; Mondal, Abhishake; Boomishankar, Ramamoorthy; Pati, Swapan K.; Braunschweig, Holger; Schulzke, Carola; Ravat, Prince; Jana, Anukul
A bis-NHC–CAAC dimer derived dicationic diradical
Chemical Science, 2022, 13, 12533-12539
1567817 CIFC25 H19 N OP 1 21 18.5649; 10.4376; 9.9968
90; 98.418; 90
884.06Gu, Xiaodong; Liu, Kexin; Yang, Limin; Xie, Chengyi; Li, Mingliang; Wang, Jun (Joelle)
Nickel-catalyzed enantioselective α-heteroarylation of ketones via C–F bond activation to construct all-carbon quaternary stereocenters
Chemical Science, 2022, 13, 12498-12502
1567818 CIFC30 H32 Mn N2 S4P -111.3144; 11.4859; 12.22
88.259; 81.481; 65.401
1427.1Elsby, Matthew R.; Oh, Changjin; Son, Mina; Kim, Scott Y. H.; Baik, Mu-Hyun; Baker, R. Tom
Spin-state crossover in photo-catalyzed nitrile dihydroboration via Mn-thiolate cooperation
Chemical Science, 2022, 13, 12550-12559
1567819 CIFC44 H47 Mn N4 O S4P 1 21/n 113.8594; 19.0914; 16.2268
90; 103; 90
4183.5Elsby, Matthew R.; Oh, Changjin; Son, Mina; Kim, Scott Y. H.; Baik, Mu-Hyun; Baker, R. Tom
Spin-state crossover in photo-catalyzed nitrile dihydroboration via Mn-thiolate cooperation
Chemical Science, 2022, 13, 12550-12559
1567832 CIFC28 H33 N2 OP -16.2055; 11.319; 32.886
89.884; 85.258; 89.848
2302He, Xin; Ma, Pengchen; Tang, Yuhai; Li, Jing; Shen, Shenyu; Lear, Martin J.; Houk, K. N.; Xu, Silong
Phosphine-catalyzed activation of cyclopropenones: a versatile C<sub>3</sub> synthon for (3+2) annulations with unsaturated electrophiles.
Chemical science, 2022, 13, 12769-12775
1567833 CIFC25 H19 N O2R -3 :H32.848; 32.848; 10.842
90; 90; 120
10131He, Xin; Ma, Pengchen; Tang, Yuhai; Li, Jing; Shen, Shenyu; Lear, Martin J.; Houk, K. N.; Xu, Silong
Phosphine-catalyzed activation of cyclopropenones: a versatile C<sub>3</sub> synthon for (3+2) annulations with unsaturated electrophiles.
Chemical science, 2022, 13, 12769-12775
1567834 CIFC24 H19 N O2P 1 21/c 19.4143; 14.69; 13.927
90; 106.73; 90
1844.5He, Xin; Ma, Pengchen; Tang, Yuhai; Li, Jing; Shen, Shenyu; Lear, Martin J.; Houk, K. N.; Xu, Silong
Phosphine-catalyzed activation of cyclopropenones: a versatile C<sub>3</sub> synthon for (3+2) annulations with unsaturated electrophiles.
Chemical science, 2022, 13, 12769-12775
1567835 CIFC21 H27 N3 O6P -19.497; 14.1349; 16.2663
77.872; 89.269; 87.51
2132.8Cai, Bao-Gui; Bao, Ye-Peng; Pei, Chao; Li, Qian; Li, Lei; Koenigs, Rene M.; Xuan, Jun
Photochemical synthesis of 1,2,4-triazoles <i>via</i> addition reaction of triplet intermediates to diazoalkanes and azomethine ylide intermediates.
Chemical science, 2022, 13, 13141-13146
1567861 CIFC31 H37 N3 O6P 19.2497; 9.6644; 32.938
90.062; 92.44; 104.738
2844.7Misra, Rajkumar; Netti, Francesca; Koren, Gil; Dan, Yoav; Chakraborty, Priyadarshi; Cohen, Sidney R.; Shimon, Linda J. W.; Beck, Roy; Adler-Abramovich, Lihi
An atomistic view of rigid crystalline supramolecular polymers derived from short amphiphilic, α,β hybrid peptide
Polymer Chemistry, 2022, 13, 6223-6228
1567867 CIFC28 H37 Cl4 PP 1 21/n 18.2809; 22.5668; 16.3964
90; 103.932; 90
2973.9Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567868 CIFC31 H43 Cl2 N O RuP 1 21/n 18.8604; 17.881; 18.306
90; 95.479; 90
2887Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567869 CIFC34 H49 Cl4 N O RuP -110.4383; 12.2309; 13.85
99.897; 93.661; 99.297
1711.4Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567870 CIFC36 H45 Cl2 N O Ru S2P 1 21/c 115.6535; 12.8229; 17.9202
90; 100.381; 90
3538.1Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567871 CIFC35 H44 Cl2 N2 O3 RuP 21 21 218.7486; 19.3141; 43.739
90; 90; 90
7390.6Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567872 CIFC33 H40 Cl2 N2 O3 RuP 1 21 117.3665; 11.5707; 17.4342
90; 115.407; 90
3164.4Morvan, Jennifer; Vermersch, François; Lorkowski, Jan; Talcik, Jakub; Vives, Thomas; Roisnel, Thierry; Crévisy, Christophe; Vanthuyne, Nicolas; Bertrand, Guy; Jazzar, Rodolphe; Mauduit, Marc
Cyclic(alkyl)(amino)carbene ruthenium complexes for Z-stereoselective (asymmetric) olefin metathesis
Catalysis Science & Technology, 2023, 13, 381-388
1567877 CIFC52 H52 Ni P4P -110.507; 13.045; 16.585
81.696; 80.885; 84.254
2214Haibach, Michael C.; Ickes, Andrew R.; Tcyrulnikov, Sergei; Shekhar, Shashank; Monfette, Sebastien; Swiatowiec, Rafal; Kotecki, Brian J.; Wang, Jason; Wall, Amanda L.; Henry, Rodger F.; Hansen, Eric C.
Enabling Suzuki-Miyaura coupling of Lewis-basic arylboronic esters with a nonprecious metal catalyst.
Chemical science, 2022, 13, 12906-12912
1567878 CIFC26 H26 Cl2 Ni P2P 1 21/n 19.345; 15.097; 9.749
90; 113.171; 90
1264.5Haibach, Michael C.; Ickes, Andrew R.; Tcyrulnikov, Sergei; Shekhar, Shashank; Monfette, Sebastien; Swiatowiec, Rafal; Kotecki, Brian J.; Wang, Jason; Wall, Amanda L.; Henry, Rodger F.; Hansen, Eric C.
Enabling Suzuki-Miyaura coupling of Lewis-basic arylboronic esters with a nonprecious metal catalyst.
Chemical science, 2022, 13, 12906-12912
1567882 CIFC87 H48 O32 U4P -4 3 m20.902; 20.902; 20.902
90; 90; 90
9131.95Hanna, Sylvia L.; Debela, Tekalign T.; Mroz, Austin M.; Syed, Zoha H.; Kirlikovali, Kent O.; Hendon, Christopher H.; Farha, Omar K.
Identification of a metastable uranium metal-organic framework isomer through non-equilibrium synthesis.
Chemical science, 2022, 13, 13032-13039
1567883 CIFC81 H76 B2 Cl2 Dy N7 OP -112.7371; 14.2679; 22.1844
101.261; 93.525; 116.025
3503.18Zhang, Ben; Cheng, Zhijie; Wu, Yingying; Chen, Lei; Jing, Rong; Cai, Xingwei; Jiang, Chunhui; Zhang, Yi-Quan; Yuan, Aihua; Cui, Hui-Hui; Li, Zhao-Yang
Pseudo-mono-axial ligand fields that support high energy barriers in triangular dodecahedral Dy(iii) single-ion magnets.
Chemical science, 2022, 13, 13231-13240
1567884 CIFC86 H78 B2 Cl2 Dy N7 OP -114.0388; 14.481; 21.4518
91.27; 97.279; 111.868
4003.23Zhang, Ben; Cheng, Zhijie; Wu, Yingying; Chen, Lei; Jing, Rong; Cai, Xingwei; Jiang, Chunhui; Zhang, Yi-Quan; Yuan, Aihua; Cui, Hui-Hui; Li, Zhao-Yang
Pseudo-mono-axial ligand fields that support high energy barriers in triangular dodecahedral Dy(iii) single-ion magnets.
Chemical science, 2022, 13, 13231-13240
1567885 CIFC79 H71 B2 Cl Dy N7P 1 21/c 123.6641; 14.1103; 21.3612
90; 96.266; 90
7090.1Zhang, Ben; Cheng, Zhijie; Wu, Yingying; Chen, Lei; Jing, Rong; Cai, Xingwei; Jiang, Chunhui; Zhang, Yi-Quan; Yuan, Aihua; Cui, Hui-Hui; Li, Zhao-Yang
Pseudo-mono-axial ligand fields that support high energy barriers in triangular dodecahedral Dy(iii) single-ion magnets.
Chemical science, 2022, 13, 13231-13240
1567894 CIFC52 H40 B2 N2C 1 2/c 126.1224; 8.3077; 18.9832
90; 106.476; 90
3950.5Wu, Tien-Lin; Lei, Jian; Hsieh, Chia-Min; Chen, Yi-Kuan; Huang, Pei-Yun; Lai, Po-Ting; Chou, Tsu-Yu; Lin, Wei-Chen; Chen, Wei; Yu, Chi-Hua; Hsu, Liang-Yan; Lin, Hao-Wu; Cheng, Chien-Hong
Substituent engineering of the diboron molecular architecture for a nondoped and ultrathin emitting layer.
Chemical science, 2022, 13, 12996-13005
1567895 CIFC60 H56 B2 N2P 1 21/c 127.7304; 9.0103; 18.61
90; 98.171; 90
4602.7Wu, Tien-Lin; Lei, Jian; Hsieh, Chia-Min; Chen, Yi-Kuan; Huang, Pei-Yun; Lai, Po-Ting; Chou, Tsu-Yu; Lin, Wei-Chen; Chen, Wei; Yu, Chi-Hua; Hsu, Liang-Yan; Lin, Hao-Wu; Cheng, Chien-Hong
Substituent engineering of the diboron molecular architecture for a nondoped and ultrathin emitting layer.
Chemical science, 2022, 13, 12996-13005
1567896 CIFC68 H72 B2 N2P -19.5981; 11.916; 25.0597
85.521; 89.469; 89.876
2857.2Wu, Tien-Lin; Lei, Jian; Hsieh, Chia-Min; Chen, Yi-Kuan; Huang, Pei-Yun; Lai, Po-Ting; Chou, Tsu-Yu; Lin, Wei-Chen; Chen, Wei; Yu, Chi-Hua; Hsu, Liang-Yan; Lin, Hao-Wu; Cheng, Chien-Hong
Substituent engineering of the diboron molecular architecture for a nondoped and ultrathin emitting layer.
Chemical science, 2022, 13, 12996-13005
1567901 CIFC132 H56 N4 Ni ThC 1 2/m 125.3169; 15.0051; 19.9071
90; 94.325; 90
7540.8Shen, Yi; Yu, Xiaojuan; Meng, Qingyu; Yao, Yang-Rong; Autschbach, Jochen; Chen, Ning
ThC<sub>2</sub>@C<sub>82</sub> <i>versus</i> Th@C<sub>84</sub>: unexpected formation of triangular thorium carbide cluster inside fullerenes.
Chemical science, 2022, 13, 12980-12986
1567902 CIFC132 H56 N4 Ni ThC 1 2/m 125.261; 14.9722; 19.9879
90; 94.646; 90
7534.8Shen, Yi; Yu, Xiaojuan; Meng, Qingyu; Yao, Yang-Rong; Autschbach, Jochen; Chen, Ning
ThC<sub>2</sub>@C<sub>82</sub> <i>versus</i> Th@C<sub>84</sub>: unexpected formation of triangular thorium carbide cluster inside fullerenes.
Chemical science, 2022, 13, 12980-12986
1567964 CIFC21 H20 Br PP 1 21/c 110.8668; 9.9356; 17.4186
90; 105.376; 90
1813.3Hui, Jiwen; Wang, Xiaowu; Yao, Xiaoqian; Li, Zhibo
A one-component phosphonium borane Lewis pair serves as a dual initiator and catalyst in the ring-opening alternating copolymerization of anhydrides and epoxides
Polymer Chemistry, 2022, 13, 6551-6563
1567965 CIFC22 H22 Br PP 1 21/c 111.3364; 10.3332; 18.1348
90; 104.699; 90
2054.8Hui, Jiwen; Wang, Xiaowu; Yao, Xiaoqian; Li, Zhibo
A one-component phosphonium borane Lewis pair serves as a dual initiator and catalyst in the ring-opening alternating copolymerization of anhydrides and epoxides
Polymer Chemistry, 2022, 13, 6551-6563
1567995 CIFC45 H61 Cl4 N O3 P RhP 1 21 110.862; 19.566; 12.2
90; 111.654; 90
2409.8Rieg, Carolin; Kirchhof, Manuel; Gugeler, Katrin; Beurer, Ann-Katrin; Stein, Lukas; Dirnberger, Klaus; Frey, Wolfgang; Bruckner, Johanna R.; Traa, Yvonne; Kästner, Johannes; Ludwigs, Sabine; Laschat, Sabine; Dyballa, Michael
Determination of accessibility and spatial distribution of chiral Rh diene complexes immobilized on SBA-15 via phosphine-based solid-state NMR probe molecules
Catalysis Science & Technology, 2023, 13, 410-425
1568329 CIFC12 H18 Br NP 1 21/c 18.1655; 10.6042; 14.4716
90; 102.495; 90
1223.4Stroek, Wowa; Hoareau, Lilian; Albrecht, Martin
From the bottle: simple iron salts for the efficient synthesis of pyrrolidines <i>via</i> catalytic C-H bond amination.
Catalysis science & technology, 2023, 13, 958-962
1568382 CIFC60 H64 B F24 Fe N3 O2 P2P 1 21/c 113.6976; 23.8148; 20.2227
90; 98.742; 90
6520.1Schlenker, Kevin; Casselman, Lillee K.; VanderLinden, Ryan T.; Saouma, Caroline T.
Large changes in hydricity as a function of charge and not metal in (PNP)M–H (de)hydrogenation catalysts that undergo metal–ligand cooperativity
Catalysis Science & Technology, 2023, 13, 1358-1368
1568383 CIFC36 H68 K N O4 P2 RuP 21 21 2112.158; 17.5241; 19.0088
90; 90; 90
4050Schlenker, Kevin; Casselman, Lillee K.; VanderLinden, Ryan T.; Saouma, Caroline T.
Large changes in hydricity as a function of charge and not metal in (PNP)M–H (de)hydrogenation catalysts that undergo metal–ligand cooperativity
Catalysis Science & Technology, 2023, 13, 1358-1368
1568404 CIFC74 H48.4 Cl15.6 Fe1.6 I2.4 N12P -120.6469; 23.6627; 24.8965
64.38; 69.27; 68.88
9942.9Yamada, Yasuyuki; Miwa, Yusuke; Toyoda, Yuka; Phung, Quan Manh; Oyama, Kin-ichi; Tanaka, Kentaro
Evaluation of CH4 oxidation activity of high-valent iron-oxo species of a μ-nitrido-bridged heterodimer of iron porphycene and iron phthalocyanine
Catalysis Science & Technology, 2023, 13, 1725-1734
1568560 CIFC16 H24 I N3 O5 RuP b c a14.031; 14.473; 19.564
90; 90; 90
3973Colaiezzi, Roberta; Saviozzi, Chiara; di Nicola, Nicola; Zacchini, Stefano; Pampaloni, Guido; Crucianelli, Marcello; Marchetti, Fabio; Di Giuseppe, Andrea; Biancalana, Lorenzo
Ruthenium(ii) arene complexes bearing simple dioxime ligands: effective catalysts for the one-pot transfer hydrogenation/N-methylation of nitroarenes with methanol
Catalysis Science & Technology, 2023, 13, 2160-2183
1568561 CIFC16 H28 Cl N3 O6 RuP c a 2110.1596; 11.7047; 16.363
90; 90; 90
1945.8Colaiezzi, Roberta; Saviozzi, Chiara; di Nicola, Nicola; Zacchini, Stefano; Pampaloni, Guido; Crucianelli, Marcello; Marchetti, Fabio; Di Giuseppe, Andrea; Biancalana, Lorenzo
Ruthenium(ii) arene complexes bearing simple dioxime ligands: effective catalysts for the one-pot transfer hydrogenation/N-methylation of nitroarenes with methanol
Catalysis Science & Technology, 2023, 13, 2160-2183
1568562 CIFC16 H28 Cl N2 O3.5 RuP 1 21/c 115.4589; 13.1592; 17.7332
90; 98.356; 90
3569.1Colaiezzi, Roberta; Saviozzi, Chiara; di Nicola, Nicola; Zacchini, Stefano; Pampaloni, Guido; Crucianelli, Marcello; Marchetti, Fabio; Di Giuseppe, Andrea; Biancalana, Lorenzo
Ruthenium(ii) arene complexes bearing simple dioxime ligands: effective catalysts for the one-pot transfer hydrogenation/N-methylation of nitroarenes with methanol
Catalysis Science & Technology, 2023, 13, 2160-2183
1568580 CIFC30 H28 N2P -18.916; 11.0941; 12.5663
94.783; 103.724; 107.064
1138.58Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568581 CIFC63 H52 B Cl2 Cu F4 N2 P2P b c a17.4954; 23.7716; 26.188
90; 90; 90
10891.4Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568582 CIFC63 H50 Cu F3 N2 O3 P2 SP -115.2564; 16.0253; 23.0757
90.355; 93.137; 98.235
5574.6Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568583 CIFC63 H51 Cl3 Cu N3 O3 P2P 1 21/c 116.7053; 14.7608; 22.8229
90; 95.361; 90
5603.1Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568584 CIFC67 H59 Cl3 Cu N3 O3 P2P b c a17.979; 24.99; 27.167
90; 90; 90
12206Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568585 CIFC69 H61 Cl9 Cu N3 O3 P2P 4113.2253; 13.2253; 40.325
90; 90; 90
7053.2Viana, Maria S.; Gomes, Clara S. B.; Rosa, Vitor
Heteroleptic Copper Complexes as Catalysts for the CuAAC Reaction: Counter-Ion Influence in Catalyst Efficiency
Catalysts, 2023, 13, 386
1568586 CIFIn O3 TbP 63 c m6.3088; 6.3088; 12.3067
90; 90; 120
424.195Min, Chang; Wu, You; Li, Yanbin; Zhou, Chunming; Cheong, Sang-Wook; Lu, Xiaosong; Zhou, Tianyuan; Zhang, Le
Structural and Improper Ferroelectric Properties of TbInO3 Single Crystal Grown by Laser Floating Zone
Crystals, 2023, 13, 287
1568587 CIFCl2 Cu H4 O2P m n a8.0553; 3.7295; 7.3674
90; 90; 90
221.333Boeré, René T.
Crystal Structures of CuCl2·2H2O (Eriochalcite) and NiCl2∙6H2O (Nickelbischofite) at Low Temperature: Full Refinement of Hydrogen Atoms Using Non-Spherical Atomic Scattering Factors
Crystals, 2023, 13, 293
1568588 CIFCl2 Cu H4 O2P m n a8.0405; 3.7238; 7.3585
90; 90; 90
220.32Boeré, René T.
Crystal Structures of CuCl2·2H2O (Eriochalcite) and NiCl2∙6H2O (Nickelbischofite) at Low Temperature: Full Refinement of Hydrogen Atoms Using Non-Spherical Atomic Scattering Factors
Crystals, 2023, 13, 293
1568589 CIFCl2 H12 Ni O6I 1 2/m 16.5628; 7.033; 8.7326
90; 96.723; 90
400.29Boeré, René T.
Crystal Structures of CuCl2·2H2O (Eriochalcite) and NiCl2∙6H2O (Nickelbischofite) at Low Temperature: Full Refinement of Hydrogen Atoms Using Non-Spherical Atomic Scattering Factors
Crystals, 2023, 13, 293
1568590 CIFCl2 H12 Ni O6I 1 2/m 16.5579; 7.0244; 8.7291
90; 96.702; 90
399.36Boeré, René T.
Crystal Structures of CuCl2·2H2O (Eriochalcite) and NiCl2∙6H2O (Nickelbischofite) at Low Temperature: Full Refinement of Hydrogen Atoms Using Non-Spherical Atomic Scattering Factors
Crystals, 2023, 13, 293
1568591 CIFC10 H18 Ca O5P -15.8633; 6.8363; 16.0587
79.338; 81.318; 82.834
622.21Lopresti, Mattia; Milanesio, Marco; Palin, Luca
The Crystal Structure of Calcium Sebacate by X-ray Powder Diffraction Data
Crystals, 2023, 13, 261
1568592 CIFC6 H5 N O2C 1 2/c 121.211; 3.7625; 13.9555
90; 107.653; 90
1061.29Baptista, Diogo S.; Piedade, M. Fátima M.; Esteves, Catarina V.
Solubility and Crystallization Studies of Picolinic Acid
Crystals, 2023, 13, 392
1568598 CIFFe16 O128 P12 S4P 113.3722; 13.3488; 21.585
92.345; 90.153; 120.34
3321.3Mauro, Daniela; Biagioni, Cristian
New Crystal-Structure Data on Bohuslavite, Fe3+4(PO4)3(SO4)(OH)(H2O)10·nH2O
Minerals, 2023, 13, 286
1568626 CIFC27 H20 Co O5 P2F d d 241.7016; 15.1215; 19.8592
90; 90; 90
12523Huang, Weiheng; Jackstell, Ralf; Spannenberg, Anke; Beller, Matthias
An improved cobalt-catalysed alkoxycarbonylation of olefins using secondary phosphine oxide promotors
Catalysis Science & Technology, 2023, 13, 2475-2479
1568705 CIFC21 H18 Cl4 N4 Ni O2P n a 2119.3515; 10.4522; 11.307
90; 90; 90
2287Bansal, Sadhna; Gonnade, Rajesh G.; Punji, Benudhar
Chemodivergent coupling of azoarenes with benzyl alcohols via a borrowing hydrogen strategy using a well-defined nickel catalyst
Catalysis Science & Technology, 2023, 13, 2705-2713
1568723 CIFC18 H27 B N2 O4 SP -16.4445; 11.458; 13.656
80.205; 85.649; 82.844
984.4Choi, Hyoju; Wang, Ruibin; Kim, Suyeon; Kim, Dongwook; Baik, Mu-Hyun; Park, Sehoon
Rhodium-catalyzed double hydroboration of pyridine: the origin of the chemo- and regioselectivities
Catalysis Science & Technology, 2023, 13, 2735-2747
1568724 CIFC18 H27 B N2 O4 SP 1 21/c 112.029; 14.49; 11.877
90; 95.143; 90
2061.8Choi, Hyoju; Wang, Ruibin; Kim, Suyeon; Kim, Dongwook; Baik, Mu-Hyun; Park, Sehoon
Rhodium-catalyzed double hydroboration of pyridine: the origin of the chemo- and regioselectivities
Catalysis Science & Technology, 2023, 13, 2735-2747
1568765 CIFC17 H19 N O2 SP 1 21/c 112.8925; 7.8461; 15.2747
90; 100.851; 90
1517.5Tokareva, Marina A.; Pernik, Indrek; Messerle, Barbara A.; Glukhareva, Tatiana V.; Keaveney, Sinead T.
The effect of the C5-substituent on regioselectivity in the Rh(i)-catalyzed intermolecular transannulation of 1,2,3-thiadiazoles with phenylacetylene
Catalysis Science & Technology, 2023, 13, 2772-2782
1568766 CIFC9 H7 N O2 S0.5P -18.8717; 8.9788; 10.5747
100.966; 100.107; 93.879
809.68Tokareva, Marina A.; Pernik, Indrek; Messerle, Barbara A.; Glukhareva, Tatiana V.; Keaveney, Sinead T.
The effect of the C5-substituent on regioselectivity in the Rh(i)-catalyzed intermolecular transannulation of 1,2,3-thiadiazoles with phenylacetylene
Catalysis Science & Technology, 2023, 13, 2772-2782
1568767 CIFC16 H18 N2 O2 SP 1 21/n 111.0494; 10.37004; 26.5033
90; 100.257; 90
2988.28Tokareva, Marina A.; Pernik, Indrek; Messerle, Barbara A.; Glukhareva, Tatiana V.; Keaveney, Sinead T.
The effect of the C5-substituent on regioselectivity in the Rh(i)-catalyzed intermolecular transannulation of 1,2,3-thiadiazoles with phenylacetylene
Catalysis Science & Technology, 2023, 13, 2772-2782
1568768 CIFC17 H21 N O2 SP 1 21/n 19.7409; 7.7066; 21.1913
90; 91.38; 90
1590.35Tokareva, Marina A.; Pernik, Indrek; Messerle, Barbara A.; Glukhareva, Tatiana V.; Keaveney, Sinead T.
The effect of the C5-substituent on regioselectivity in the Rh(i)-catalyzed intermolecular transannulation of 1,2,3-thiadiazoles with phenylacetylene
Catalysis Science & Technology, 2023, 13, 2772-2782
1568782 CIFC51 H47 N9 O14 ZnP b c a14.6426; 20.0946; 32.345
90; 90; 90
9517.1Pook, Niels-Patrick
Supramolecular Structure of Tris(1,10-phenanthroline)zinc(II)-Cation and N,N′,N″-tris(carboxymethyl)-1,3,5-benzenetricarboxamide-Anion: Synthesis, Crystal Structure, Vibrational Spectra, and Theoretical Investigations
Crystals, 2023, 13, 569
1568783 CIFC22 H28 Cl Cu Ho N6 O10P 1 21/n 18.8038; 16.3659; 19.8889
90; 91.557; 90
2864.6Zhang, Shaoliang; Du, Ruili; Fan, Xiufang; Zhao, Xinhua; Wang, Yanlan; Li, Shanshan
Self-Assembly Heterometallic Cu-Ln Complexes: Synthesis, Crystal Structures and Magnetic Characterization
Crystals, 2023, 13, 535
1568784 CIFC22 H28 Cl Cu Gd N6 O10P 1 21/n 18.8191; 16.5598; 20.0787
90; 91.748; 90
2931Zhang, Shaoliang; Du, Ruili; Fan, Xiufang; Zhao, Xinhua; Wang, Yanlan; Li, Shanshan
Self-Assembly Heterometallic Cu-Ln Complexes: Synthesis, Crystal Structures and Magnetic Characterization
Crystals, 2023, 13, 535
1568826 CIFC8 H17 Li O2I 41/a :219.3447; 19.3447; 10.3928
90; 90; 90
3889.2Deglmann, Peter; Machleit, Sara; Gallizioli, Cesare; Rupf, Susanne M.; Plajer, Alex J.
Lithium catalysed sequence selective ring opening terpolymerisation: a mechanistic study
Catalysis Science & Technology, 2023, 13, 2937-2945
1568827 CIFC8 H17 Li O SP -18.1843; 11.066; 13.037
113.372; 102.438; 98.398
1022.5Deglmann, Peter; Machleit, Sara; Gallizioli, Cesare; Rupf, Susanne M.; Plajer, Alex J.
Lithium catalysed sequence selective ring opening terpolymerisation: a mechanistic study
Catalysis Science & Technology, 2023, 13, 2937-2945
1568859 CIFC32 H26 N3 O P Pd SP -19.848; 11.6412; 14.0807
71.591; 74.372; 75.139
1448.83Clinton, Savarimuthu Selvan; Ramesh, Rengan; Malecki, Jan Grzegorz
Orthometallated Pd(ii) C^N^S pincer complex catalyzed sustainable synthesis of bis(indolyl)methanes via acceptorless dehydrogenative coupling of alcohols
Catalysis Science & Technology, 2023, 13, 3358-3365
1568889 CIFC12 H18 N4 O4 ZnP 1 21 19.374; 8.2061; 10.172
90; 90.621; 90
782.4Sahoo, Sangita; Manna, Subarna; Rit, Arnab
N-Heterocyclic carbene supported zinc catalysed N-formylation of diverse N–H functionalities with carbon dioxide under ambient conditions
Catalysis Science & Technology, 2023, 13, 3344-3350
1569035 CIFC10 H4 Br4 N2P -17.8725; 10.9122; 15.6053
103.034; 96.915; 92.46
1293.15Sakhapov, Ilyas F.; Zagidullin, Almaz A.; Dobrynin, Alexey B.; Litvinov, Igor A.; Yakhvarov, Dmitry G.; Bondarenko, Mikhail A.; Novikov, Alexander S.; Fedin, Vladimir P.; Adonin, Sergey A.
Crystal Structures of 3,3′,5,5′-Tetrabromo-4,4′-bipyridine and Co(II) Coordination Polymer Based Thereon
Crystals, 2023, 13, 704
1569036 CIFC12 H12 Br4 Co N4 O8C 1 2/c 118.3716; 11.4111; 13.2287
90; 132.282; 90
2051.8Sakhapov, Ilyas F.; Zagidullin, Almaz A.; Dobrynin, Alexey B.; Litvinov, Igor A.; Yakhvarov, Dmitry G.; Bondarenko, Mikhail A.; Novikov, Alexander S.; Fedin, Vladimir P.; Adonin, Sergey A.
Crystal Structures of 3,3′,5,5′-Tetrabromo-4,4′-bipyridine and Co(II) Coordination Polymer Based Thereon
Crystals, 2023, 13, 704
1569037 CIFC15 H22 Br N S3P -18.0769; 8.5225; 12.5476
99.941; 96.608; 93.121
842.66Caltagirone, Claudia; Aragoni, Maria Carla; Arca, Massimiliano; Blake, Alexander John; Demartin, Francesco; Garau, Alessandra; Podda, Enrico; Pop, Alexandra; Lippolis, Vito; Silvestru, Cristian
Functionalization and Coordination Effects on the Structural Chemistry of Pendant Arm Derivatives of 1,4,7-trithia-10-aza-cyclododecane ([12]aneNS3)
Crystals, 2023, 13, 616
1569038 CIFC16 H23 Cl3 N2 O3 S3P -18.5163; 9.5058; 14.5582
73.29; 89.59; 85.96
1125.9Caltagirone, Claudia; Aragoni, Maria Carla; Arca, Massimiliano; Blake, Alexander John; Demartin, Francesco; Garau, Alessandra; Podda, Enrico; Pop, Alexandra; Lippolis, Vito; Silvestru, Cristian
Functionalization and Coordination Effects on the Structural Chemistry of Pendant Arm Derivatives of 1,4,7-trithia-10-aza-cyclododecane ([12]aneNS3)
Crystals, 2023, 13, 616
1569039 CIFC18 H23 Cl N2 O S3P -18.4811; 9.8093; 11.8739
99.469; 99.016; 93.623
958.31Caltagirone, Claudia; Aragoni, Maria Carla; Arca, Massimiliano; Blake, Alexander John; Demartin, Francesco; Garau, Alessandra; Podda, Enrico; Pop, Alexandra; Lippolis, Vito; Silvestru, Cristian
Functionalization and Coordination Effects on the Structural Chemistry of Pendant Arm Derivatives of 1,4,7-trithia-10-aza-cyclododecane ([12]aneNS3)
Crystals, 2023, 13, 616
1569066 CIFC2 H6 Cu O12 Zn4P -15.2524984878; 6.3202611905; 13.523442891
89.662; 100.131; 91.0107
441.87Santamaría-Pérez, David; Chuliá-Jordán, Raquel; Otero-de-la-Roza, Alberto; Oliva, Robert; Popescu, Catalin
High-Pressure Experimental and DFT Structural Studies of Aurichalcite Mineral
Minerals, 2023, 13, 619
1569186 CIFC46 H37 Br2 Cl2 N Ni O P2 S2P -18.874; 16.683; 16.979
118.128; 102.945; 94.354
2112Chen, Luo; Li, Tao; Xie, Bin; Lai, Chuan; Ji, Run-Wu; He, Jia-Yu; Cao, Jia-Xi; Liu, Meng-Nan; Li, Wei; Zhang, Dong-Liang
Electrocatalytic hydrogen evolution by robust square planar nickel complexes in an S2P2 coordination environment
Catalysis Science & Technology, 2023, 13, 3655-3666
1569187 CIFC47 H41 N Ni O P2 S2P -18.889; 14.156; 16.604
99.93; 100.826; 95.15
2005.2Chen, Luo; Li, Tao; Xie, Bin; Lai, Chuan; Ji, Run-Wu; He, Jia-Yu; Cao, Jia-Xi; Liu, Meng-Nan; Li, Wei; Zhang, Dong-Liang
Electrocatalytic hydrogen evolution by robust square planar nickel complexes in an S2P2 coordination environment
Catalysis Science & Technology, 2023, 13, 3655-3666
1569189 CIFC9 H21 Br3 N4P 43 21 29.9901; 9.9901; 15.6499
90; 90; 90
1561.89Qaroush, Abdussalam K.; Eftaiha, Ala'a F.; Al-Qaisi, Feda'a M.; Assaf, Khaleel I.; Hammad, Suhad B.; Al-Anati, Malak H.; Radwan, Enas S.; Awwadi, Firas F.
Newly synthesized imidazolium precursors for CO2 utilization and sequestration: aprotic versus protic salts
Catalysis Science & Technology, 2023, 13, 3245-3257
1569260 CIFC36 H46 Cl5 N O RuP 1 21/n 110.7816; 16.045; 21.2485
90; 100.265; 90
3617Sytniczuk, Adrian; Struzik, Filip; Purohit, Vishal; Grela, Karol; Kajetanowicz, Anna
Aza-Claisen rearrangement as a key step in synthesis of specialised anilines used in the production of efficient ethenolysis catalysts
Catalysis Science & Technology, 2023, 13, 3682-3688
1569261 CIFC20 H21 Br2 N3 O2P 1 21/c 110.7492; 21.4852; 8.9772
90; 94.765; 90
2066.1Zhang, Xiao; Bai, Fan; Li, Miaomiao; Ru, Huihui; Wang, Lanzhi
NiFe2O4@SiO2@PrNH2–DPA–CeCl3: a cerium-based magnetic nano dual-acid catalyst with high efficacy and recyclability for domino sequential synthesis of lactam ring-fused 1,5-benzodiazepines
Catalysis Science & Technology, 2023, 13, 3987-3999
1569275 CIFB2 Cd Ga O7 TbP -4 21 m7.3487; 7.3487; 4.7247
90; 90; 90
255.15Chen, Xuean; Zhang, Jinyuan; Xiao, Weiqiang; Song, Xiaoyan
A new melilite-type rare-earth borate CdTbGaB2O7 and multicolor tunable emission in the CdTb1−xSmxGaB2O7 (0 ≤ x ≤ 0.2) phosphors
RSC Advances, 2023, 13, 16272-16284
1569279 CIFC42 H28P 1 21/c 116.4311; 8.03; 11.2057
90; 104.651; 90
1430.43Sonina, Alina A.; Cheshkina, Darya S.; Kazantsev, Maxim S.
Additive-Assisted Crystallization of 9,10-Diphenylanthracene
Crystals, 2023, 13, 861
1569288 CIFC4 H11 N O4P 1 21 15.8966; 14.2652; 7.4117
90; 98.338; 90
616.85Xu, Xuexia; Yang, Qin; Wang, Lanteng; Zheng, Jie; Gu, Yang; Xing, Xiwen; Zhou, Jiahai
Enzymatic hydrolysis of l-azetidine-2-carboxylate ring opening
Catalysis Science & Technology, 2023, 13, 3953-3962
1569289 CIFC66 H70 Au2 N6 OP -112.4705; 14.3086; 17.1528
103.775; 95.912; 101.539
2875.84Ma, Xinyuan; Voloshkin, Vladislav A.; Martynova, Ekaterina A.; Beliš, Marek; Peng, Min; Villa, Marco; Tzouras, Nikolaos V.; Janssens, Wim; Van Hecke, Kristof; Ceroni, Paola; Nolan, Steven P.
Novel dinuclear NHC–gold(i)-amido complexes and their application in energy transfer photocatalysis
Catalysis Science & Technology, 2023, 13, 4168-4175
1569290 CIFC56 H50 Au2 N6C 1 2/c 127.2565; 17.0998; 52.008
90; 101.377; 90
23763.6Ma, Xinyuan; Voloshkin, Vladislav A.; Martynova, Ekaterina A.; Beliš, Marek; Peng, Min; Villa, Marco; Tzouras, Nikolaos V.; Janssens, Wim; Van Hecke, Kristof; Ceroni, Paola; Nolan, Steven P.
Novel dinuclear NHC–gold(i)-amido complexes and their application in energy transfer photocatalysis
Catalysis Science & Technology, 2023, 13, 4168-4175
1569291 CIFC16 H32 F6 N PP n m a15.201; 9.7668; 13.4419
90; 90; 90
1995.7Killeen, Charles; Liu, Jie; Zijlstra, Harmen S.; Maass, Florian; Piers, James; Adams, Reid; Oliver, Allen; McIndoe, J. Scott
Competitive isomerization and catalyst decomposition during ring-closing metathesis
Catalysis Science & Technology, 2023, 13, 4000-4008
1569292 CIFC14 H28 F6 N PP 1 21/c 19.4663; 13.2301; 14.178
90; 93.998; 90
1771.3Killeen, Charles; Liu, Jie; Zijlstra, Harmen S.; Maass, Florian; Piers, James; Adams, Reid; Oliver, Allen; McIndoe, J. Scott
Competitive isomerization and catalyst decomposition during ring-closing metathesis
Catalysis Science & Technology, 2023, 13, 4000-4008
1569440 CIFC7 H13 N3 SiP 1 21/c 19.4337; 19.5412; 10.7349
90; 100.794; 90
1943.92Herbig, Marcus; Kroke, Edwin; Wagler, Jörg
Molecular Structures and Intermolecular Hydrogen Bonding of Silylated 2-Aminopyrimidines
Crystals, 2023, 13, 990
1569441 CIFC10 H14 N6 SiP -18.6757; 8.874; 9.0989
64.211; 75.463; 79.194
608.08Herbig, Marcus; Kroke, Edwin; Wagler, Jörg
Molecular Structures and Intermolecular Hydrogen Bonding of Silylated 2-Aminopyrimidines
Crystals, 2023, 13, 990
1569442 CIFC30 H38 N18 O Si2P -110.064; 11.1921; 18.6757
72.898; 89; 63.346
1780.7Herbig, Marcus; Kroke, Edwin; Wagler, Jörg
Molecular Structures and Intermolecular Hydrogen Bonding of Silylated 2-Aminopyrimidines
Crystals, 2023, 13, 990
1569443 CIFC23 H24 N12 O SiP 1 21/c 115.9611; 21.1674; 22.6832
90; 97.74; 90
7593.81Herbig, Marcus; Kroke, Edwin; Wagler, Jörg
Molecular Structures and Intermolecular Hydrogen Bonding of Silylated 2-Aminopyrimidines
Crystals, 2023, 13, 990
1569444 CIFC22 H19 Cl N4 SP 1 21/c 111.0242; 16.5074; 11.0507
90; 97.688; 90
1992.94Salama, Eid E.; Youssef, Mohamed F.; Boraei, Ahmed T. A.; Haukka, Matti; Soliman, Saied M.; Barakat, Assem; Sarhan, Ahmed A. M.
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
Crystals, 2023, 13, 992
1569445 CIFC23 H17 Cl N4 SP -112.1537; 12.8679; 15.0994
70.272; 69.417; 67.402
1984.17Salama, Eid E.; Youssef, Mohamed F.; Boraei, Ahmed T. A.; Haukka, Matti; Soliman, Saied M.; Barakat, Assem; Sarhan, Ahmed A. M.
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
Crystals, 2023, 13, 992
1569484 CIFC18 H39 Cu N3 O4 SP 1 21/n 110.2913; 16.4105; 13.1029
90; 92.4886; 90
2210.8Nakano, Akiyuki; Raut, Vivek S.; Asao, Naoki; Ando, Akane; Fujisawa, Kiyoshi; Higashimura, Hideyuki
Enzyme-inspired catalysts with high activity and selectivity for oxidative polymerization of 2-phenylphenol
Catalysis Science & Technology, 2023, 13, 4968-4977
1569485 CIFC18 H10 Cl Cu F6 N3 PP -310.9907; 10.9907; 23.1929
90; 90; 120
2426.3Nakano, Akiyuki; Raut, Vivek S.; Asao, Naoki; Ando, Akane; Fujisawa, Kiyoshi; Higashimura, Hideyuki
Enzyme-inspired catalysts with high activity and selectivity for oxidative polymerization of 2-phenylphenol
Catalysis Science & Technology, 2023, 13, 4968-4977
1569547 CIFC32 H31 F3 N4 O3 Ru SP 1 21/c 118.9076; 11.49805; 14.5081
90; 100.559; 90
3100.66Knörr, Pascal; Lentz, Nicolas; Albrecht, Martin
Efficient additive-free formic acid dehydrogenation with a NNN–ruthenium complex
Catalysis Science & Technology, 2023, 13, 5625-5631
1569548 CIFC32 H34 Cl2 F12 N4 P2 RuP 1 21/c 120.26618; 10.02851; 20.44489
90; 101.764; 90
4067.94Knörr, Pascal; Lentz, Nicolas; Albrecht, Martin
Efficient additive-free formic acid dehydrogenation with a NNN–ruthenium complex
Catalysis Science & Technology, 2023, 13, 5625-5631
1569579 CIFC102 H78 Au Cl3 N2P -19.8807; 19.9006; 20.5724
91.843; 101.967; 101.976
3859.18Rahman, Md. Mahbubur; Gao, Pengcheng; Zhao, Qun; Lalancette, Roger; Szostak, Roman; Szostak, Michal
[Au(Np#)Cl]: highly reactive and broadly applicable Au(i)–NHC catalysts for alkyne π-activation reactions
Catalysis Science & Technology, 2023, 13, 5131-5139
1569584 CIFC38 H51 Cl Ir O6 P2P 1 21/c 18.2561; 40.9906; 12.059
90; 109.088; 90
3856.65Chakrabarti, Kaushik; Spangenberg, Alice; Subramaniyan, Vasudevan; Hederstedt, Andreas; Abdelaziz, Omar Y.; Polukeev, Alexey V.; Wallenberg, Reine; Hulteberg, Christian P.; Wendt, Ola F.
Acceptorless dehydrogenation of 4-methylpiperidine by supported pincer-ligated iridium catalysts in continuous flow
Catalysis Science & Technology, 2023, 13, 5113-5119
1569594 CIFC21 H20 Br2 Cu N2 SP 1 21/c 110.9864; 12.8237; 15.4669
90; 90.946; 90
2178.78Jana, Narayan Ch.; Behera, Sourav; Maharana, Suraj Kumar; Behera, Rakesh R.; Bagh, Bidraha
Selective aerobic oxidation of biomass model compound veratryl alcohol catalyzed by air-stable copper(ii) complexes in water
Catalysis Science & Technology, 2023, 13, 5422-5434
1569595 CIFC16 H15 Br2 Cu N3 OP 1 21/n 111.7434; 13.1713; 12.2852
90; 112.638; 90
1753.8Jana, Narayan Ch.; Behera, Sourav; Maharana, Suraj Kumar; Behera, Rakesh R.; Bagh, Bidraha
Selective aerobic oxidation of biomass model compound veratryl alcohol catalyzed by air-stable copper(ii) complexes in water
Catalysis Science & Technology, 2023, 13, 5422-5434
1569596 CIFC21 H22 Br2 Cu N2 SP 1 21/c 116.8022; 9.4781; 13.723
90; 94.977; 90
2177.19Jana, Narayan Ch.; Behera, Sourav; Maharana, Suraj Kumar; Behera, Rakesh R.; Bagh, Bidraha
Selective aerobic oxidation of biomass model compound veratryl alcohol catalyzed by air-stable copper(ii) complexes in water
Catalysis Science & Technology, 2023, 13, 5422-5434
1569606 CIFC67 H56 Cu F6 N2 O3 P3P 1 2/n 112.8402; 19.2826; 25.7915
90; 101.171; 90
6264.79Doettinger, Florian; Kleeberg, Christian; Queffélec, Clémence; Tschierlei, Stefanie; Pellegrin, Yann; Karnahl, Michael
Rich or poor: the impact of electron donation and withdrawal on the photophysical and photocatalytic properties of copper(i) complexes
Catalysis Science & Technology, 2023, 13, 4092-4106
1569607 CIFC48 H49 Cl4 Cu F6 N2 O P3P -19.7521; 15.5514; 16.6886
94.049; 99.373; 100.684
2440.59Doettinger, Florian; Kleeberg, Christian; Queffélec, Clémence; Tschierlei, Stefanie; Pellegrin, Yann; Karnahl, Michael
Rich or poor: the impact of electron donation and withdrawal on the photophysical and photocatalytic properties of copper(i) complexes
Catalysis Science & Technology, 2023, 13, 4092-4106
1569617 CIFC92 H108 Cu12 Mo10 N5 O116 P V2F 2 326.2487; 26.2487; 26.2487
90; 90; 90
18085.2Lu, Xinlin; Cheng, Ting; Geletii, Yurii V.; Bacsa, John; Hill, Craig L.
Reactivity and stability synergism directed by the electron transfer between polyoxometalates and metal–organic frameworks
Catalysis Science & Technology, 2023, 13, 5094-5103
1569623 CIFC70 H126 Cl4 In10 N20 S16F d -3 m :274.59; 74.59; 74.59
90; 90; 90
414994Yin, Haiyan; Liu, Yifan; Ablez, Abdusalam; Wang, Yanqi; Hu, Qianqian; Huang, Xiaoying
Dispersible Supertetrahedral Chalcogenide T3 Clusters: Photocatalytic Activity and Photogenerated Carrier Dynamics
Catalysts, 2023, 13, 1160
1569624 CIFC4 H11 Cl2 Cu N5P 1 21/n 17.5287; 16.5771; 7.9737
90; 113.925; 90
909.64Pastrana-Dávila, Andrea; Minotta, Gianella; Ellena, Javier; Santiago, Pedro H. O.; D’Vries, Richard F.
Synthesis, Characterization and Structural Analysis of Two New Biguanide Complexes
Crystals, 2023, 13, 1176
1569625 CIFC12 H39 Cl5.01 Co2 N15 O3P 1 21/n 110.3808; 26.2761; 11.3407
90; 101.374; 90
3032.62Pastrana-Dávila, Andrea; Minotta, Gianella; Ellena, Javier; Santiago, Pedro H. O.; D’Vries, Richard F.
Synthesis, Characterization and Structural Analysis of Two New Biguanide Complexes
Crystals, 2023, 13, 1176
1569626 CIFC20 H28 Co O8 PbP 1 21/c 18.7792; 20.142; 13.72
90; 91.957; 90
2424.7Zhang, Yuxuan; Wei, Zheng; Dikarev, Evgeny V.
Synthesis, Structure, and Characterizations of a Heterobimetallic Heptanuclear Complex [Pb2Co5(acac)14]
Crystals, 2023, 13, 1089
1569627 CIFC70 H98 Co5 O28 Pb2P 1 21/c 123.8452; 10.7063; 16.3561
90; 97.096; 90
4143.63Zhang, Yuxuan; Wei, Zheng; Dikarev, Evgeny V.
Synthesis, Structure, and Characterizations of a Heterobimetallic Heptanuclear Complex [Pb2Co5(acac)14]
Crystals, 2023, 13, 1089
1569628 CIFC6 H6 Cl N O3P 1 21/c 112.648; 13.634; 8.574
90; 97.801; 90
1464.8Johnson, Aidan V.; Piedade, M. Fátima M.; Esteves, Catarina V.
pH-Dependent Crystallization of 2-, 4-, 5-, and 6-Hydroxynicotinic Acids in Aqueous Media
Crystals, 2023, 13, 1062
1569629 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5443; 9.5443; 7.5603
90; 90; 120
596.428Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569630 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.543; 9.543; 7.5634
90; 90; 120
596.51Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569631 CIFAl0.25 B4 Bi0.05 Fe2.75 O12 Sm0.95R 3 2 :H9.5435; 9.5435; 7.5628
90; 90; 120
596.525Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569632 CIFAl0.17 B4 Bi0.05 Fe2.83 O12 Sm0.95R 3 2 :H9.5534; 9.5534; 7.5767
90; 90; 120
598.862Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569633 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5329; 9.5329; 7.5553
90; 90; 120
594.61Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569634 CIFB4 Bi0.05 Fe3 O12 Sm0.95R 3 2 :H9.565; 9.565; 7.5869
90; 90; 120
601.125Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569635 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5443; 9.5443; 7.5598
90; 90; 120
596.388Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569636 CIFAl0.07 B4 Bi0.07 Fe2.93 O12 Sm0.93R 3 2 :H9.5595; 9.5595; 7.5816
90; 90; 120
600.015Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569637 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5444; 9.5444; 7.5601
90; 90; 120
596.424Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569638 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5439; 9.5439; 7.5624
90; 90; 120
596.543Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569639 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5443; 9.5443; 7.5632
90; 90; 120
596.657Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569640 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5452; 9.5452; 7.568
90; 90; 120
597.148Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569641 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5438; 9.5438; 7.5616
90; 90; 120
596.468Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569642 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.5441; 9.5441; 7.5621
90; 90; 120
596.545Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128
1569643 CIFAl0.28 B4 Bi0.07 Fe2.72 O12 Sm0.93R 3 2 :H9.544; 9.544; 7.561
90; 90; 120
596.445Smirnova, Ekaterina S.; Alekseeva, Olga A.; Artemov, Vladimir V.; Sorokin, Timofei A.; Khmelenin, Dmitry N.; Sidorova, Ekaterina V.; Frolov, Kirill V.; Gudim, Irina A.
Crystal Structure of Bismuth-Containing Samarium Iron–Aluminium Borates Sm1−xBixFe3−yAly(BO3)4 (x = 0.05–0.07, y = 0–0.28) in the Temperature Range of 25–500 K
Crystals, 2023, 13, 1128

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