Crystallography Open Database

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Searching year of publication is 2022

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1566499 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566500 CIFC5 H12 O5P 21 21 218.264; 8.901; 8.9223
90; 90; 90
656.3Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566501 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566502 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566503 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566504 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566505 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566506 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566507 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566508 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566509 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566510 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566511 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566512 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566513 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566514 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566515 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566516 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566517 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566518 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566519 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566520 CIFC H4 N2 OP -4 21 m5.578; 5.578; 4.686
90; 90; 90
145.8Ruth, Paul Niklas; Herbst-Irmer, Regine; Stalke, Dietmar
Hirshfeld atom refinement based on projector augmented wave densities with periodic boundary conditions
IUCrJ, 2022, 9, 286-297
1566521 CIFC64 H86 Cl2 N6 O6P 3120.2894; 20.2894; 13.6577
90; 90; 120
4869.1Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566522 CIFC69 H96 N6 O6R 3 :H20.366; 20.366; 13.791
90; 90; 120
4953.79Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566523 CIFC66 H90 N6 O6R 3 :H20.3338; 20.3338; 13.7372
90; 90; 120
4918.88Ding, Yanjun; Alimi, Lukman O.; Du, Jing; Hua, Bin; Dey, Avishek; Yu, Pei; Khashab, Niveen M.
Pillar[3]trianglamines: deeper cavity triangular macrocycles for selective hexene isomer separation
Chemical Science, 2022
1566524 CIFC74 H104 Ga2 N8 Sb2P -110.4552; 11.9732; 14.9227
93.2189; 97.3354; 107.995
1753.06Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566525 CIFC66 H102 Ga2 N4 O2 Sb2 SiC 1 2/c 159.557; 11.8135; 21.011
90; 108.078; 90
14053Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566526 CIFC78 H116 Ga2 N6 Sb2 SiP -110.919; 14.343; 26.014
83.994; 78.718; 88.053
3973Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566527 CIFC64.5 H98 Cl2 Ga2 N4 Sb2 SiP 1 21/c 119.7547; 10.5843; 33.512
90; 96.97; 90
6955.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566528 CIFC71.5 H103 Ga2 N7 Sb2P 1 21/c 119.9634; 12.5667; 29.4717
90; 109.028; 90
6989.7Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566529 CIFC65 H103 Ga2 N7 Sb2 SiP 1 21 110.7967; 21.163; 15.164
90; 96.979; 90
3439.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566530 CIFC79 H117 Ga2 N7 Sb2P 1 21/n 110.9672; 45.894; 15.2335
90; 94.502; 90
7643.8Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566531 CIFC72.5 H102 F3 Ga2 N7 Sb2P -110.6581; 12.7136; 27.5744
102.129; 92.993; 98.869
3595.5Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566532 CIFC78 H119 F3 Ga2 N7 Sb2P 1 21/n 112.1758; 27.211; 24.248
90; 99.805; 90
7916.4Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566533 CIFC68 H110 Ga2 N8 Sb2 Si2P 1 21/n 111.889; 18.46; 33.366
90; 96.36; 90
7278Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566534 CIFC81 H112 Ga2 N8 Sb2P -111.6222; 17.8727; 19.5796
108.099; 90.076; 93.817
3856.2Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566535 CIFC77 H110 Ga2 N8 Sb2P 1 21/c 113.6969; 28.763; 20.711
90; 94.587; 90
8133.3Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566536 CIFC84 H108 Ga2 N6 Sb4P -112.0886; 12.3645; 14.1831
86.028; 75.849; 74.786
1983.54Weinert, Hanns Micha; Wölper, Christoph; Schulz, Stephan
Synthesis of Distibiranes and Azadistibiranes by Cycloaddition Reactions of Distibenes with Diazomethanes and Azides
Chemical Science, 2022
1566537 CIFC44 H45 F6 N6 P Ru2P 1 21/n 112.6141; 12.2041; 27.463
90; 98.846; 90
4177.47Bellini, Marco; Bösken, Jonas; Bartoli, Francesco; Miller, Hamish; Thöny, Debora; Poggini, Lorenzo; Wörle, Michael; Oberhauser, Werner; Gamboa-Carballo, Juan José; Lavacchi, Alessandro; Krumeich, Frank; Grützmacher, Hansjörg; Vizza, Francesco
Remarkable Stability of a Molecular Ruthenium Complex in PEM Water Electrolysis
Chemical Science, 2022
1566538 CIFC36 H35 B F4 N2 O Ru2P -19.5469; 10.1082; 17.4002
78.96; 76.819; 85.773
1603.87Bellini, Marco; Bösken, Jonas; Bartoli, Francesco; Miller, Hamish; Thöny, Debora; Poggini, Lorenzo; Wörle, Michael; Oberhauser, Werner; Gamboa-Carballo, Juan José; Lavacchi, Alessandro; Krumeich, Frank; Grützmacher, Hansjörg; Vizza, Francesco
Remarkable Stability of a Molecular Ruthenium Complex in PEM Water Electrolysis
Chemical Science, 2022
1566539 CIFC37 H33 NC 1 2/c 135.402; 9.1778; 17.961
90; 110.844; 90
5453.8Duan, Shengzu; Zi, Yujin; Wang, Lingling; Cong, Jielun; Chen, Wen; Li, Minyan; Zhang, Hongbin; Yang, Xiaodong; Walsh, Patrick
α-Branched Amines through Radical Coupling with 2-Azaallyl Anions, Redox Active Esters and Alkenes
Chemical Science, 2022
1566540 CIFC21 H15 Cl F3 N3 O2P 1 21/n 115.287; 15.859; 17.629
90; 114.523; 90
3888Yang, Hefei; Wang, Le-Cheng; Zhang, Yu; Zheng, Dongling; Chen, Zhengkai; Wu, Xiao-Feng
Controllable access to trifluoromethyl-containing indoles and indolines: Palladium-catalyzed regioselective functionalization of unactivated alkenes with trifluoroacetimidoyl chlorides
Chemical Science, 2022
1566541 CIFC22 H15 F3 N3 OP 1 21/c 115.6657; 33.014; 7.2436
90; 98.651; 90
3703.7Yang, Hefei; Wang, Le-Cheng; Zhang, Yu; Zheng, Dongling; Chen, Zhengkai; Wu, Xiao-Feng
Controllable access to trifluoromethyl-containing indoles and indolines: Palladium-catalyzed regioselective functionalization of unactivated alkenes with trifluoroacetimidoyl chlorides
Chemical Science, 2022
1566542 CIFC492 H528 N48 O60P 3 c 132.5182; 32.5182; 51.424
90; 90; 120
47092Xu, Ning; Su, Kongzhao; M. El-Sayed, El-Sayed; Ju, Zhanfeng; Yuan, Daqiang
Chiral Proline-Substituted Porous Organic Cages in Asymmetric Organocatalysis
Chemical Science, 2022
1566543 CIFC280 H320 N32 O40P 128.4101; 30.2731; 32.7364
82.444; 81.795; 63.273
24818Xu, Ning; Su, Kongzhao; M. El-Sayed, El-Sayed; Ju, Zhanfeng; Yuan, Daqiang
Chiral Proline-Substituted Porous Organic Cages in Asymmetric Organocatalysis
Chemical Science, 2022
1566544 CIFC28 H28 Br Cl Cu N6 O2P 1 21/c 116.1127; 8.9758; 19.2463
90; 103.825; 90
2702.85Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566545 CIFC28 H28 Cl Cu N6 O1.5P 1 21/c 115.0147; 34.2629; 10.2999
90; 107.565; 90
5051.7Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566546 CIFC32 H39 Cl3 Cu N8 O3P 17.2313; 9.2604; 14.1201
78.16; 77.214; 70.423
859.9Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566547 CIFC60 H63 Br2 Cl N14 Ni O4P -19.7632; 15.6735; 19.622
87.172; 75.925; 85.319
2901.4Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566548 CIFC33 H39 Cl Cu N8 O3C 1 2/c 137.667; 10.5159; 19.22
90; 118.948; 90
6661.9Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566549 CIFC26 H23 Br N6 OP -112.22; 12.7328; 16.424
76.485; 82.598; 67.698
2296.6Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566550 CIFC12 H16 N2 O2P -17.7366; 7.9072; 10.7395
99.872; 102.594; 113.64
562.21Wittmann, Christopher; Bacher, Felix; Enyedy, Eva A.; Dömötör, Orsolya; Spengler, Gabriella; Madejski, Christian; Reynisson, Jóhannes; Arion, Vladimir B.
Highly Antiproliferative Latonduine and Indolo[2,3-<i>c</i>]quinoline Derivatives: Complex Formation with Copper(II) Markedly Changes the Kinase Inhibitory Profile.
Journal of medicinal chemistry, 2022, 65, 2238-2261
1566551 CIFC17 H29 N OP 1 21 17.18; 4.628; 48.944
90; 92.55; 90
1624.8Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566552 CIFC17 H31 N O3P 1 21 112.37896; 5.01515; 13.9105
90; 99.1891; 90
852.51Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566553 CIFC16 H27 N OP 21 21 215.1556; 9.493; 31.8376
90; 90; 90
1558.2Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566554 CIFC16 H25 N OP 21 21 215.0809; 9.5095; 31.1268
90; 90; 90
1503.95Wu, Zhen-Long; Zhang, Wei-Yan; Zhong, Jin-Cheng; Huang, Xiao-Jun; Xu, Wei; Chen, Min-Feng; Weng, Shao-Quan; Zhang, Dong-Mei; Che, Chun-Tao; Ye, Wen-Cai; Wang, Ying
Angiogenesis-Inhibitory Piperidine Alkaloids from the Leaves of <i>Microcos paniculata</i>.
Journal of natural products, 2022, 85, 375-383
1566555 CIFC21 H22 O8 SP 1 21/c 19.3577; 25.184; 9.0558
90; 96.873; 90
2118.8Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566556 CIFC9 H9 N O3 SP 21 21 218.2204; 8.5993; 13.4964
90; 90; 90
954.06Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566557 CIFC19 H20 O8 SP -18.1509; 10.0095; 12.0777
106.945; 90.36; 90.567
942.51Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566558 CIFC21 H22 O9 SP -18.1167; 9.0623; 15.8947
86.54; 87.286; 65.417
1060.92Xu, Yanchao; Liu, Wen; Wu, Dan; He, Wenwen; Zuo, Mingxing; Wang, Dongyang; Fu, Peng; Wang, Liping; Zhu, Weiming
Sulfur-Containing Phenolic Compounds from the Cave Soil-Derived <i>Aspergillus fumigatus</i> GZWMJZ-152.
Journal of natural products, 2022, 85, 433-440
1566559 CIFBi O2P 1 21/m 111.6212; 3.4067; 7.3247
90; 99.9889; 90
285.589Feng, Xuezhen; Zou, Haiyuan; Zheng, Renji; Wei, Wenfei; Wang, Ranhao; Zou, Wensong; Lim, Gukhyun; Hong, Jihyun; Duan, Lele; Chen, Hong
Bi<sub>2</sub>O<sub>3</sub>/BiO<sub>2</sub> Nanoheterojunction for Highly Efficient Electrocatalytic CO<sub>2</sub> Reduction to Formate.
Nano letters, 2022, 22, 1656-1664
1566560 CIF
HKL
Paper
C6 H13 Cl6 N3 O2 SnP -17.4224; 7.4518; 8.4986
105.726; 97.426; 112.383
403.85Ghallab, Rochdi; Bougueria, Hassiba; Merazig, Hocine
4-Amidinopyridinium hexachloridostannate(IV) dihydrate
IUCrData, 2022, 7, x220195
1566561 CIF
HKL
Paper
C10 H14 Cl10 N4 O2 SnP -17.4624; 8.4715; 10.1324
101.434; 90.043; 107.554
597.34Ghallab, Rochdi; Bougueria, Hassiba; Merazig, Hocine
Bis(2-amino-3,5-dichloropyridinium) hexachloridostannate(IV) dihydrate
IUCrData, 2022, 7, x220191
1566562 CIFC34 H38 Au2 O4 P2 S2P 1 21/n 111.7462; 39.197; 15.6529
90; 107.882; 90
6858.7Duminy, Welni; Pillay, Michael N.; van Zyl, Werner E.
Silver(I) and Gold(I) Monothiocarbonate Complexes: Synthesis, Structure, Luminescence
Inorganics, 2022, 10, 19
1566563 CIFC17 H22 O10P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566564 CIFC1.21 H1.21 O0.6P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566565 CIFC13.25 H13.25 O13.25P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566566 CIFC17 H22 O10P 21 21 217.776; 8.6993; 26.8196
90; 90; 90
1814.23Chen, Jianwei; Chen, Jun; Wang, Siqi; Bao, Xiaoze; Li, Songwei; Wei, Bin; Zhang, Huawei; Wang, Hong
Amycolachromones A–F, Isolated from a Streptomycin-Resistant Strain of the Deep-Sea Marine Actinomycete Amycolatopsis sp. WP1
Marine Drugs, 2022, 20, 162
1566567 CIFC36 H31 N5 OP -17.8563; 9.2517; 21.803
95.923; 98.136; 96.538
1547.1Guillon, Jean; Savrimoutou, Solène; Albenque-Rubio, Sandra; Pinaud, Noël; Moreau, Stéphane; Desplat, Vanessa
Synthesis, Crystal Structure and Anti-Leukemic Activity of 1,3-Dihydro-1-{1-[4-(4-phenylpyrrolo[1,2-a]quinoxalin-3-yl)benzyl]piperidin-4-yl}-2H-benzimidazol-2-one
Molbank, 2022, 2022, M1333
1566568 CIFC80 H110 Cu4 O2 P6P 1 21/n 117.127; 19.946; 23.841
90; 105.715; 90
7840Dannenberg, Steven G.; Waterman, Rory
Cyclo-Tetrakis(μ-diphenylphosphido)-1,5-bis(tri-tert-butylphosphine)-Tetracopper
Molbank, 2022, 2022, M1334
1566569 CIFC28 H37 Cl4 I N2 SP 1 21/n 110.5912; 18.7089; 16.071
90; 102.093; 90
3113.8Saab, Marina; Nahra, Fady; Van Hecke, Kristof
Charge-Transfer Adducts of Chalcogenourea Derivatives of N-Heterocyclic Carbenes with Iodine Monochloride
Molbank, 2022, 2022, M1344
1566570 CIFC30 H42 Cl3 I N2 SeP 1 21/n 19.741; 16.9218; 19.8068
90; 97.399; 90
3237.67Saab, Marina; Nahra, Fady; Van Hecke, Kristof
Charge-Transfer Adducts of Chalcogenourea Derivatives of N-Heterocyclic Carbenes with Iodine Monochloride
Molbank, 2022, 2022, M1344
1566571 CIFC20 H24 N6 O4P -19.6243; 9.859; 12.5952
68.645; 72.467; 75.23
1047.06Lopes, Susana M. M.; Lemos, Américo; Paixão, José A.; Pinho e Melo, Teresa M. V. D.
Ethyl 7-Acetyl-8a-methyl-3-(1-phenyl-1H-tetrazol-5-yl)-1,4,4a,5,6,8a-hexahydro-7H-pyrano[2,3-c]pyridazine-1-carboxylate
Molbank, 2022, 2022, M1338
1566572 CIFC26 H31 N O12P 1 21 110.1989; 8.7455; 15.8721
90; 99.068; 90
1398.01Fitzgerald, Liam S.; O’Malley, Ciaran; Murphy, Paul V.
(1R,2R,3S,4R)-1-(Acetylamino)-2,4,5-tris(acetyloxy)-1-((2S)-4-(benzyloxy)-5-oxo-2,5-dihydrofuran-2-yl)pentan-3-yl Acetate
Molbank, 2022, 2022, M1337
1566573 CIFC13 H13 Cl N2P 1 21/c 19.4547; 16.2237; 7.9004
90; 104.169; 90
1174.98Adeleke, Adesola A.; Omondi, Bernard
Crystal Structure of a Chiral Sec-Amine, 4-Chloro-N-(1-(pyridin-2-yl)ethyl)aniline
Molbank, 2022, 2022, M1335
1566574 CIFC11 H10 N4 O3C 1 c 123.794; 5.347; 8.9367
90; 96.216; 90
1130.3Pokhodylo, Nazariy T.; Slyvka, Yuriy I.; Goreshnik, Evgeny A.; Obushak, Mykola D.
Ethyl 5-Formyl-1-(pyridin-3-yl)-1H-1,2,3-triazole-4-carboxylate: Synthesis, Crystal Structure, Hirshfeld Surface Analysis, and DFT Calculation
Molbank, 2022, 2022, M1340
1566575 CIFC14 H16 Co N2 O12P 1 21/n 16.9863; 23.7443; 10.6564
90; 100.456; 90
1738.38Xia, Zhengyao; Li, Yan; Ji, Cheng; Jiang, Yucheng; Ma, Chunlan; Gao, Ju; Zhang, Jinlei
Slow-Relaxation Behavior of a Mononuclear Co(II) Complex Featuring Long Axial Co-O Bond.
Nanomaterials (Basel, Switzerland), 2022, 12, 707
1566576 CIFC70 H81 B N2 O4P 1 21/c 125.398; 21.296; 11.522
90; 96.49; 90
6192Han, Jianmei; Huang, Zhongyan; Miao, Jingsheng; Qiu, Yuntao; Xie, Ziyang; Yang, Chuluo
Narrowband blue emission with insensitivity to the doping concentration from an oxygen-bridged triarylboron-based TADF emitter: nondoped OLEDs with a high external quantum efficiency up to 21.4%
Chemical Science, 2022
1566577 CIFC20 H46 Cl N2 P2 ReP 1 21/n 18.5852; 23.581; 12.2292
90; 92.515; 90
2473.39Connor, Gannon P.; Delony, Daniel; Weber, Jeremy E.; Mercado, Brandon Q.; Curley, Julia B.; Schneider, Sven; Mayer, James M.; Holland, Patrick L.
Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen
Chemical Science, 2022
1566578 CIFC54 H67 B Cl F24 N3 O0.5 P2 ReP -112.2681; 15.3208; 17.9247
92.777; 109.357; 97.022
3140.5Connor, Gannon P.; Delony, Daniel; Weber, Jeremy E.; Mercado, Brandon Q.; Curley, Julia B.; Schneider, Sven; Mayer, James M.; Holland, Patrick L.
Facile conversion of ammonia to a nitride in a rhenium system that cleaves dinitrogen
Chemical Science, 2022
1566579 CIFC14 H22 OP 4110.0087; 10.0087; 12.7456
90; 90; 90
1276.78Pan, Aaron; Chojnacka, Maja; Crowley, Robert; Göttemann, Lucas; Haines, Brandon E.; Kou, Kevin G. M.
Synergistic Brønsted/Lewis acid catalyzed aromatic alkylation with unactivated tertiary alcohols or di-tert-butylperoxide to synthesize quaternary carbon centers
Chemical Science, 2022
1566580 CIFC261 H476 Ag55 Cu3 F3 Mo8 O38 S43P -123.3674; 23.7497; 38.3998
73.33; 75.236; 73.633
19233.6Gao, Jin-Ping; Qi, Zhikai; Zhang, Fu-Qiang; Zhang, Xian-Ming
In situ insertion of copper to form heteroanionic D3h-symmetric [Cu3Mo8O32]10− for a templated Ag55 nanocluster
Nanoscale, 2022
1566581 CIF
Paper
C68.39 H67.65 Cl6 N12 O4 Zn3C 1 2/c 133.3132; 14.4948; 31.7714
90; 102.245; 90
14992.4Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566582 CIFC68.62 H68.92 Cl6 N12 O4 Zn3C 1 2/c 133.306; 14.488; 31.8026
90; 102.247; 90
14996.7Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566583 CIFC54.5 H43 I6 N12 O4 Zn3C 1 2/c 134.4866; 14.9746; 31.0009
90; 101.933; 90
15663.6Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566584 CIFC55 H42 I6 N12 O4 Zn3C 1 2/c 134.4862; 15.0052; 31.125
90; 101.958; 90
15756.8Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566585 CIFC63 H78 I6 N12 Zn3C 1 2/c 134.5713; 15.1587; 29.5198
90; 100.649; 90
15203.6Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566586 CIFC64.69 H81.39 I6 N12 Zn3C 1 2/c 134.595; 15.1725; 29.535
90; 100.647; 90
15235.8Meurer, Florian; von Essen, Carolina; Kühn, Clemens; Puschmann, Horst; Bodensteiner, Michael
The benefits of Cu Kβ radiation for the single-crystal X-ray structure determination of crystalline sponges
IUCrJ, 2022, 9
1566587 CIFC25 H21 F3 N2 O3 SP 1 21/c 115.2479; 19.58181; 16.7407
90; 116.095; 90
4488.95Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566588 CIFC36 H32 F3 N O5 SC 1 2 129.3277; 7.49483; 18.2663
90; 124.382; 90
3313.6Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566589 CIFC33 H34 Cl N O2P 1 21 111.1324; 7.5493; 16.7445
90; 90.526; 90
1407.18Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566590 CIFC30 H29 Cl N2 O3P 21 21 2112.3663; 16.7129; 25.3786
90; 90; 90
5245.17Dai, Yating; Liang, Shuangshuang; Zeng, Guangkuo; Huang, Hongchun; Zhao, Xiaowei; Cao, Shanshan; Jiang, Zhiyong
Asymmetric [3 + 2] photocycloadditions of cyclopropylamines with electron-rich and electron-neutral olefins
Chemical Science, 2022
1566591 CIFC25 H25 O2 PP 21 21 215.89107; 16.00327; 22.3169
90; 90; 90
2103.96Zhang, Ya-Qian; Zhang, Qingwei; Han, Xue-Yu; Wu, Yue; Qi, Peng-Jia; Zhang, Qing
Ni-Catalyzed Asymmetric Hydrophosphinylation of Conjugated Enynes and Mechanistic Studies
Chemical Science, 2022
1566592 CIFC23 H22 O3 SP 17.2748; 12.2905; 12.5063
63.599; 79.446; 75.302
965.6Li, Yanjun; Liou, Yan-Cheng; Chen, Xinran; Ackermann, Lutz
Thioether-enabled palladium-catalyzed atroposelective C–H olefination for N−C and C−C axial chirality
Chemical Science, 2022
1566593 CIFC20 H20 N2 O SP 1 21 111.0831; 6.8389; 12.0729
90; 109.142; 90
864.48Li, Yanjun; Liou, Yan-Cheng; Chen, Xinran; Ackermann, Lutz
Thioether-enabled palladium-catalyzed atroposelective C–H olefination for N−C and C−C axial chirality
Chemical Science, 2022
1566594 CIF
HKL
Paper
C15 H26 I N3 O6P 1 21 110.816; 7.0106; 13.169
90; 106.833; 90
955.8Lambrecht, Sina; Villinger, Alexander; Jopp, Stefan
1-(Methyl-α-<small>D</small>-glucopyranosid-6-yl)-3-vinylimidazolium iodide dimethylformamide monosolvate
IUCrData, 2022, 7, x220265
1566595 CIF
HKL
Paper
C77 H83 Cl4 K Mn N6 O8 SP b c a19.5585; 24.7224; 29.8538
90; 90; 90
14435.3Yuan, Yiwen; Li, Jianfeng
([2.2.2]Cryptand)potassium (4-methylbenzenethiolato)[5,10,15,20-tetrakis(4-chlorophenyl)porphyrinato]manganate(II) tetrahydrofuran disolvate
IUCrData, 2022, 7, x220241
1566596 CIF
HKL
Paper
C17 H15 B F4 N2P 1 21/n 111.426; 9.0735; 15.5434
90; 102.118; 90
1575.54Welton, Claire E.; Nesterov, Vladimir N.; Smucker, Bradley W.
1-(2-Methylphenyl)-4,4'-bipyridin-1-ium tetrafluoridoborate
IUCrData, 2022, 7, x220248
1566597 CIFC28 H24 O6 S2P 21 21 219.2608; 14.3014; 18.9339
90; 90; 90
2507.65Hu, Linfeng; Li, Jinzhao; Zhang, Yongyan; Feng, Xiaoming; Liu, Xiaohua
Enantioselective [1,2]-Stevens Rearrangement of Thiosulfonates to Construct Dithio-Substituted Quaternary Carbon Centers
Chemical Science, 2022
1566598 CIFC33 H43 Cl2 Cr N2 O2P -116.326; 16.389; 16.464
70.953; 89.935; 71.859
3932.2Tian, Jiliang; Zhang, Xingwang; Liu, Shaofeng; Li, Zhibo
Chromium complexes supported by NNO-tridentate ligands: an unprecedented activity with the requirement of a small amount of MAO
Polymer Chemistry, 2022, 13, 1852-1860
1566599 CIFC31 H37 Cl2 Cr F2 N2 O2P 1 21/c 114.4764; 14.5398; 15.5208
90; 109.539; 90
3078.75Tian, Jiliang; Zhang, Xingwang; Liu, Shaofeng; Li, Zhibo
Chromium complexes supported by NNO-tridentate ligands: an unprecedented activity with the requirement of a small amount of MAO
Polymer Chemistry, 2022, 13, 1852-1860
1566600 CIFC36 H48 Ca Gd K O3P 1 21/c 19.2772; 13.9703; 26.2056
90; 90.079; 90
3396.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566601 CIFC36 H48 Ca Er K O3P 1 21/c 19.2555; 13.9514; 26.113
90; 90.709; 90
3371.6Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566602 CIFC36 H48 Ca Dy K O3P 1 21/c 19.2628; 13.9533; 26.1417
90; 90.377; 90
3378.7Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566603 CIFC36 H48 Ca Ho K O3P 1 21/c 19.2613; 13.9568; 26.1226
90; 90.566; 90
3376.4Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566604 CIFC36 H48 Ca K O3 TmP 1 21/c 19.2649; 13.9648; 26.111
90; 90.8583; 90
3377.9Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566605 CIFC36 H48 Ca K O3 TbP 1 21/c 19.2738; 13.9561; 26.155
90; 90.302; 90
3385.1Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566606 CIFC36 H48 Ca K O3 YbP 1 21/c 19.2602; 13.9561; 26.1046
90; 90.935; 90
3373.2Zhou, Zheng; McNeely, James; Greenough, Joshua; Wei, Zheng; Han, Haixiang; Rouzières, Mathieu; Rogachev, Andrey Yu.; Clérac, Rodolphe; Petrukhina, Marina A.
Lanthanide-mediated tuning of electronic and magnetic properties in heterotrimetallic cyclooctatetraenyl multidecker self-assemblies
Chemical Science, 2022
1566607 CIFC92 H166 Fe N4 O28 Si16P 21 21 2116.2474; 17.2899; 46.6858
90; 90; 90
13114.8Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566608 CIFC92 H182 Fe N4 O32 Si16P 1 21 116.9205; 17.5657; 21.7093
90; 90.98; 90
6451.5Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566609 CIFC76.5 Fe N4 O27.5 S2 Si16I 1 2 137.4731; 17.2234; 42.6209
90; 103.053; 90
26797.4Zong, Zhaohui; Hao, Aiyou; Xing, Pengyao; Zhao, Yanli
Chiral Molecular Nanosilicas
Chemical Science, 2022
1566610 CIFCl Ga6 K3 Mn2 S12P 3 1 c10.9208; 10.9208; 6.1774
90; 90; 120
638.04Liu, Bin-Wen; Pei, Shao-Min; Jiang, Xiao-Ming; Guo, Guo-Cong
Broad transparency and wide band gap achieved in a magnetic infrared nonlinear optical chalcogenide by suppressing d-d transitions.
Materials horizons, 2022, 9, 1513-1517
1566611 CIFC28 H41 F O4P 1 21 110.3779; 7.2974; 33.47
90; 98.797; 90
2504.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566612 CIFC26 H39 F O4C 1 2 114.7648; 6.0876; 26.974
90; 96.281; 90
2409.9Jiang, Liyin; Sarró, Pau; Teo, Wei Jie; Llop, Jordi; Suero, Marcos
Catalytic alkene skeletal modification for the construction of fluorinated tertiary stereocenters
Chemical Science, 2022
1566613 CIFC227 H209 Ag6 Au19 B2 F8 O17 P6 S17P -120.4536; 20.7898; 33.6586
72.945; 82.104; 63.917
12289Shi, Wan-Qi; Guan, Zong-Jie; Li, Jiao-Jiao; Han, Xu-Shuang; Wang, Quan-Ming
Site-Specified Doping of Silver Atoms into Au25 Nanocluster as Directed by Ligand Binding Preference
Chemical Science, 2022
1566614 CIFC66 H72 N4 Ni Si4P -111.7807; 11.8079; 22.9033
80.502; 78.053; 71.215
2934.25Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566615 CIFC34 H29 N2 Si2P -110.31; 12.326; 12.941
77.219; 79.312; 79.801
1560Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566616 CIFC83 H103 N7 Ni5 Si4P -113.9645; 14.7686; 24.4091
89.5959; 79.412; 63.052
4394.3Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566617 CIFC73 H85 N5 Ni2 Si4P -114.392; 22.272; 22.51
97.75; 95.438; 102.855
6912Shimamoto, Kento; Sunada, Yusuke
Metalation-Induced Denitrogenative Reductive Coupling of Isocyanides on a Silylene-Bridged Nickel Cluster
Chemical Science, 2022
1566618 CIFC35 H48 N PP -110.677; 11.8045; 12.4452
96.831; 101.037; 111.157
1405.1Chen, Zicong; Gu, Changxue; Yuen, On Ying; So, Chau Ming
Palladium-catalyzed chemoselective direct α-arylation of carbonyl compounds with chloroaryl triflates at the C–Cl site
Chemical Science, 2022
1566619 CIFC42 H34 B F3 P2 SeP -19.6724; 12.8821; 14.5407
84.961; 77.687; 74.085
1701.43Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566620 CIFC43 H39 B F3 O3 P2 RhP -19.1533; 13.0253; 33.273
83.172; 88.634; 79.181
3868.8Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566621 CIFC36.96 H31.91 B0.95 F2.87 I0.05 P2 Se0.95P n a 2114.5444; 19.8328; 11.0256
90; 90; 90
3180.4Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566622 CIFC15 H16 B F3 K O0.5 PP -15.6907; 21.5917; 26.847
78.455; 89.976; 89.948
3232Kelty, Margaret L.; McNeece, Andrew J.; Kurutz, Josh W.; Filatov, Alexander S.; Anderson, John S.
Electrostatic vs. Inductive Effects in Phosphine Ligand Donor Properties and Reactivity
Chemical Science, 2022
1566623 CIFC91 H144 O10P -111.9787; 17.3956; 22.0177
110.06; 90.8994; 101.377
4207.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566624 CIFC16 H16 F10 O2P 1 21/a 111.164; 5.0419; 15.9267
90; 91.317; 90
896.2Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566625 CIFC108 H108 F60 O12C 1 2/c 169.979; 13.9205; 24.2019
90; 96.4154; 90
23428.5Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566626 CIFC81 H94 F30 O10P 1 21/a 123.6441; 22.5243; 31.147
90; 95.0726; 90
16522.9Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566627 CIFC91 H94 F50 O10P -120.9282; 22.7403; 24.2682
98.976; 98.951; 114.017
10108.6Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566628 CIFC90.65 H93.56 F50 O10P 1 21/n 122.9793; 21.8597; 40.474
90; 102.22; 90
19870Onishi, Katsuto; Ohtani, Shunsuke; Kato, Kenichi; Fa, Shixin; Sakata, Yoko; Akine, Shigehisa; Ogasawara, Moe; Asakawa, Hitoshi; Nagano, Shusaku; Takashima, Yoshinori; Mizuno, Motohiro; Ogoshi, Tomoki
State- and water repellency-controllable molecular glass of pillar[5]arenes with fluoroalkyl groups by guest vapors
Chemical Science, 2022
1566629 CIFC18 H26 Cd N4 O6 P2 S4P -17.2387; 9.6411; 10.4545
81.448; 75.399; 70.165
662.56Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566630 CIFC26 H42 Cd N4 O6 P2 S4P -19.9154; 12.3655; 15.4749
106.08; 99.172; 91.827
1794.03Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566631 CIFC22 H34 Cd N4 O6 P2 S4P -19.0611; 9.2065; 10.5703
82.436; 77.672; 64.113
774.27Tan, Yee Seng; Yeo, Chien Ing; Kwong, Huey Chong; Tiekink, Edward R. T.
Unusual {⋯HNC <sub>2</sub> O⋯HC <sub> <i>n</i> </sub> O}, <i>n</i> = 1 or 2, synthons predominate in the molecular packing of one-dimensional coordination polymers, {Cd[S <sub>2</sub> P(OR) <sub>2</sub> ] <sub>2</sub> ( <sup>3</sup> LH <sub>2</sub> )} <sub> <i>n</i> </sub> , for R = Me and Et, but are precluded when R = i-Pr; <sup>3</sup> LH <sub>2</sub> = <i>N</i> , <i>N</i> ′-bis(3-pyridylmethyl)oxalamide
CrystEngComm, 2022, 24, 2992-3004
1566632 CIFC78 H78 N6 O3P -114.2538; 17.1903; 17.3592
79.038; 72.546; 68.828
3767.7Fang, Lingyi; Zhang, Yuyan; Ren, Ming; Xie, Xinrui; Li, Tianyu; Yuan, Yi; Zhang, Jing; Wang, Peng
A triple helicene based molecular semiconductor characteristic of a fully fused conjugated backbone for perovskite solar cells
Energy & Environmental Science, 2022, 15, 1630-1637
1566633 CIFC15 H15 N3 O SP 1 21/n 16.6492; 13.731; 15.329
90; 101.032; 90
1373.7Kshtriya, Vivekshinh; Koshti, Bharti; Mehmood, Tahir; Singh, Ramesh; Joshi, Khashti Ballabh; Bandyopadhyay, Sujoy; Boukhvalov, Danil W.; Reddy, J. Prakasha; Gour, Nidhi
A new aggregation induced emission enhancement (AIEE) dye which self-assembles to panchromatic fluorescent flowers and has application in sensing dichromate ions.
Soft matter, 2022, 18, 3019-3030
1566663 CIFC36 H37 K N3 O3 P2 Ru SP c a 2112.6529; 18.7504; 15.5836
90; 90; 90
3697.2Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566664 CIFC100 H83 N6 O3 P6 Ru2P 1 21/c 114.8971; 22.753; 28.6172
90; 100.332; 90
9542.6Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566665 CIFC51 H48 Cl N4 O2 P3 RuP b c n25.849; 19.5041; 21.0152
90; 90; 90
10595Tossaint, Alex S.; Rebreyend, Christophe; Sinha, Vivek; Weber, Manuela; Canossa, Stefano; Pidko, Evgeny A.; Filonenko, Georgy A.
Two step activation of Ru-PN3P pincer catalysts for CO2 hydrogenation
Catalysis Science & Technology, 2022, 12, 2972-2977
1566666 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566667 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5Wei, Yu-Bai; Luo, Dong; Xiong, Xiao; Huang, Yong-Liang; Xie, Mo; Lu, Weigang; Li, Dan
Biomimetic Mimicry of Formaldehyde-Induced DNA–Protein Crosslinks in the Confined Space of Metal–Organic Framework
Chemical Science, 2022
1566668 CIFC16 H29 N O6 SP 21 21 215.46991; 10.15896; 34.3303
90; 90; 90
1907.69Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566669 CIFC18 H22 O2 SP n a 219.3374; 6.0661; 28.5106
90; 90; 90
1614.89Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566670 CIFC15 H20 Cl N O3 SP -15.0188; 9.6241; 16.1198
89.487; 85.132; 82.136
768.5Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566671 CIFC10 H18 O4 S2P 1 21/n 16.4691; 11.4368; 8.7387
90; 102.114; 90
632.143Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566672 CIFC11 H14 O3 SP -15.72076; 8.13039; 11.8424
91.8184; 91.4466; 103.412
535.219Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566673 CIFC10 H11 F O3 SP 1 c 15.7165; 12.1828; 14.7356
90; 91.722; 90
1025.77Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566674 CIFC15 H27 N O6 SP 1 21/c 111.1742; 16.6182; 10.3665
90; 116.394; 90
1724.34Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566675 CIFC10 H18 O4 S2P 1 21/c 16.09765; 8.92648; 22.0926
90; 91.4743; 90
1202.11Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566676 CIFC15 H17 N O2 SP 1 21/c 19.0612; 15.82137; 10.2622
90; 114.837; 90
1335.12Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566677 CIFC25 H30 O8 SP 1 21 110.04584; 19.87397; 12.32816
90; 95.9688; 90
2447.98Nguyen, Vu T.; Haug, Graham C.; Nguyen, Viet D.; Vuong, Ngan T. H.; Karki, Guna B.; Arman, Hadi; Larionov, Oleg V.
Functional Group Divergence and the Structural Basis of Acridine Photocatalysis Revealed by Direct Decarboxysulfonylation
Chemical Science, 2022
1566678 CIFC23 H27 B O3P n a 2112.912; 10.1397; 15.597
90; 90; 90
2042wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566679 CIFC23 H27 B O3P 1 21/n 112.4943; 9.9586; 16.762
90; 95.6616; 90
2075.5wu, Fu-Peng; Wu, Xiao-Feng
Catalyst-Controlled Selective Borocarbonylation of Benzylidenecyclopropanes: Regiodivergent Synthesis of γ-Vinylboryl Ketones and β-Cyclopropylboryl Ketones
Chemical Science, 2022
1566680 CIFC50.5 H47 Co O3 P2P 1 21/n 19.9652; 18.349; 23.3602
90; 96.462; 90
4244.3Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566681 CIFC45 H32 Co2 O7 P2P -110.8578; 11.6947; 17.4282
106.744; 95.84; 112.496
1900.9Martínez-Carrión, Alicia; Romero-Navarro, Andrés; Núñez-Rico, José Luis; Gutiérrez, Albert; Grabulosa, Arnald; Vidal-Ferran, Anton
Valorisation of mixtures of linear alkenes using cobalt-mediated isomerisation and hydroformylation chemistries
Catalysis Science & Technology, 2022, 12, 3219-3227
1566682 CIFC16 H19 N O6 SP 21 21 218.0346; 12.621; 16.5455
90; 90; 90
1677.79Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566683 CIFC16 H19 N O6 SP 1 21 110.1269; 8.043; 10.8756
90; 114.408; 90
806.66Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566684 CIFC17 H26 F6 N3 O7 S2P 1 21 111.0402; 9.5966; 12.5085
90; 115.079; 90
1200.32Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566685 CIFC16 H20 N2 O6 SP 21 21 218.1051; 14.1921; 15.2659
90; 90; 90
1756.01Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566686 CIFC160 H218 N8 O49 S8P 1 21 113.5261; 12.674; 25.4683
90; 99.78; 90
4302.6Li, Gonglin; Zhang, Yan; Zeng, Hongkun; Feng, Xiaoming; Su, Zhishan; Lin, Lili
Water Enables Diastereodivergency in Bispidine-Based Chiral Amine-Catalyzed Asymmetric Mannich Reaction of Cyclic N-Sulfonyl Ketimines with Ketones
Chemical Science, 2022
1566687 CIFC1220 H968 B11.95 Cu24 F47.82 N52 O104P 1 21/n 118.838; 32.458; 64.439
90; 94.55; 90
39277Domoto, Yuya; Yamamoto, Kidai; Horie, Shumpei; Yu, Zhengsu; Fujita, Makoto
Multiplication of weak chiral inductions for excellent control over the helical orientation of discrete topologically chiral (M3L2)n polyhedra
Chemical Science, 2022
1566688 CIFC29.4 H40.8 Cl8.8 N2 P2 PdP 1 21/n 115.262; 12.8154; 20.9917
90; 108.535; 90
3892.8Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566689 CIFC26 H40 B2 N2 P2P -19.1591; 11.3142; 15.1394
103.273; 102.525; 105.201
1408Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566690 CIFC28 H34 F6 N2 O6 P2 Pd S2P -111.2734; 12.1729; 13.5903
73.9005; 72.8892; 73.6404
1671.4Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Börner, Armin; Franke, Robert; Beller, Matthias
(In situ) spectroscopic studies on state-of-the-art Pd(ii) catalysts in solution for the alkoxycarbonylation of alkenes
Catalysis Science & Technology, 2022, 12, 3175-3189
1566691 CIFC17 H21 B F2 N4 OP 21 21 218.9883; 11.1112; 17.485
90; 90; 90
1746.2Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566692 CIFC15 H19 B F2 N4P 4110.5675; 10.5675; 13.404
90; 90; 90
1496.9Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566693 CIFC16 H17 B F2 N4 OP -16.9141; 9.2485; 12.7582
93.651; 101.649; 97.353
789.08Zeng, Lintao; Chen, Tianhong; Zhu, Beitong; Koo, Seyoung; Tang, Yonghe; Lin, Weiying; James, Tony D.; Kim, Jong Seung
A molecular recognition platform for the simultaneous sensing of diverse chemical weapons
Chemical Science, 2022
1566694 CIFC83 H135 As7 K La2 O6 Si8P -115.7346; 18.2731; 19.7473
106.435; 102.572; 100.222
5139Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566695 CIFC96 H164 As14 Ce2 K2 O12 Si8P -111.223; 16.579; 18.693
72.888; 89.816; 73.008
3166Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566696 CIFC80 H132 As7 K Nd2 O6 Si8P -115.6899; 18.4469; 20.1223
111.299; 104.839; 100.119
5006.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566697 CIFC77 H129 As3 K Nd2 O6 Si8P -111.7764; 17.4676; 26.292
84.855; 79.39; 71.581
5040.7Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566698 CIFC58 H102 As7 K2 Nd O12 Si4P 1 21/n 114.2709; 31.995; 17.4941
90; 98.678; 90
7896.3Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566699 CIFC77 H132 As7 Ce2 K O6 Si8P 1 21/n 120.0117; 18.0444; 27.5019
90; 96.273; 90
9871.5Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566700 CIFC74 H138 As14 K2 Nd2 O12 Si8C 1 2/c 141.591; 13.2497; 19.5306
90; 95.516; 90
10712.9Reinfandt, Niklas; Hauser, Adrian; Münzfeld, Luca; Roesky, Peter W.
From a nanoparticular solid-state material to molecular organo-f-element-polyarsenides
Chemical Science, 2022
1566701 CIFC43 H40 Au N O6P 21 21 219.9306; 13.2468; 27.4297
90; 90; 90
3608.3Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566702 CIFC38 H24 N O2 PP 21 21 2111.8935; 12.6595; 18.8734
90; 90; 90
2841.7Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566703 CIFC41.17 H29.17 Au Cl3.5 N O3P 21 21 2112.999; 13.954; 22.15
90; 90; 90
4018Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566704 CIFC42 H32 Au Cl4 N O3P 21 21 2112.578; 13.7123; 21.0398
90; 90; 90
3628.8Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566705 CIFC42 H36 Au N O5P 21 21 219.9266; 13.1669; 27.3976
90; 90; 90
3580.9Guo, Jia; Xiong, Wen-Bin; Ma, Hao-Ran; Fan, Luoyi; Zhou, You-Yun; Wong, Henry N. C.; Cui, Jian-Fang
Optical Resolution of 1,16-Dihydroxytetraphenylene by Chiral Gold(III) Complexation and Its Applications as Chiral Ligands in Asymmetric Catalysis
Chemical Science, 2022
1566706 CIFH66 Mo60 Na8 O187I 41/a c d :223.5571; 23.5571; 61.035
90; 90; 90
33870.6Li, xuexin; Ji, Tuo; Gao, Jun-Yang; Chen, Wei-Chao; Yuan, Ye; Sha, Haoyan; Faller, Roland; Shan, Guo-Gang; Shao, Kui-Zhan; Wang, Xinlong; Su, Zhong-Min
An Unprecedented Fully Reduced {MoV60} Polyoxometalate: From All-Inorganic Molecular Light-Absorber Model to Improved Photoelectronic Performance
Chemical Science, 2022
1566707 CIFC54.5 H53 B Cl P2 SP -18.8424; 11.4067; 24.8662
81.957; 80.897; 69.046
2303.2Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566708 CIFC29.25 H31.5 B Cl0.5 F4 P2 Pt SP b a m20.9374; 10.9959; 14.9555
90; 90; 90
3443.14Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566709 CIFC28 H28 Cl O P2 Rh SP 21 21 2110.4581; 14.2792; 17.4031
90; 90; 90
2598.86Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566710 CIFC54 H53 B Cl P2 Rh SP 1 21/n 110.9915; 34.1432; 12.5533
90; 99.76; 90
4642.9Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566711 CIFC45.5 H36 Cl F7 P3 Rh SP -19.1404; 12.3384; 19.4965
102.063; 92.077; 103.656
2080.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566712 CIFC43 H32 F4 O3 P2 S2P 1 21/n 112.4956; 28.031; 12.6611
90; 119.324; 90
3866.48Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566713 CIFC56 H59 B P2 Pt SP 1 21/c 116.6775; 15.3273; 19.3126
90; 102.496; 90
4819.76Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566714 CIFC47 H35 F13 N2 O8 P2 Pt S5P 1 21/c 123.6369; 12.7303; 18.9449
90; 98.297; 90
5640.95Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566715 CIFC32 H39 B2 F8 N O2 P2 Pt SP -110.727; 13.1882; 15.143
65.687; 75.111; 75.546
1861.41Li, Ruiping; Barel, Nitsan; Subramaniyan, Vasudevan; Cohen, Orit; Tibika, Françoise; Tulchinsky, Yuri
Sulfonium cations as versatile strongly π-acidic ligands
Chemical Science, 2022
1566718 CIF
HKL
Paper
C21 H18 N2 OC 1 2/c 130.3989; 8.7177; 14.0581
90; 115.367; 90
3366.3Meenatchi, C. Selva; Athimoolam, S.; Suresh, J.; Priya, R. Vishnu; Rubina, S. Raja; Bhandari, S. R.
(<i>E</i>)-5-(4-Methylbenzylidene)-1-phenyl-4,5,6,7-tetrahydro-1<i>H</i>-indazol-4-one
IUCrData, 2022, 7, x220283
1566719 CIFC20 H56 Bi2 Br10 N4P -112.4378; 13.2166; 14.021
97.835; 93.139; 90.289
2279.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566720 CIFC20 H56 Ag Bi Br8 N4P -18.4797; 8.7683; 13.9411
73.253; 88.908; 87.415
991.56Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566721 CIFC20 Ag Bi Br8 N8C m m m8.774; 27.47; 8.771
90; 90; 90
2114Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566722 CIFC25 H69 Br9 N5 Pb2P -111.996; 13.422; 17.477
72.658; 70.158; 77.179
2503.7Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566723 CIFC25 H70 Br9 N5 Pb2P -111.975; 13.366; 17.472
72.618; 70.213; 77.258
2488.9Su, Chang-Yuan; Yao, Yefeng; Zhang, Zhixu; Wang, Ying; Chen, Ming; Huang, Pei-Zhi; Zhang, Yi; Qiao, Wencheng; Fu, Da-Wei
The construction of a two-dimensional organic-inorganic hybrid double perovskite ferroelastic with high Tc and narrow band gap
Chemical Science, 2022
1566724 CIFC23 H23 Cl N2 O2P 1 21 19.6064; 7.9331; 13.748
90; 101.106; 90
1028.09Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566725 CIFC23 H23 Cl N2 O2P 21 21 219.2992; 18.0846; 24.744
90; 90; 90
4161.26Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566726 CIFC23 H23 Cl N2 O2P 21 21 219.11893; 17.37833; 50.2087
90; 90; 90
7956.66Xiao, Lu; Li, Bo; Xiao, Fan; Fu, Cong; Wei, Liang; Dang, Yanfeng; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent Synthesis of Enantioenriched Azepino[3,4,5-cd]-Indoles via Cooperative Cu/Ir-Catalyzed Asymmetric Allylic Alkylation and Intramolecular Friedel-Crafts Reaction
Chemical Science, 2022
1566727 CIFC23 H30 N4 O2P 1 21/c 116.0767; 12.9097; 10.9767
90; 99.712; 90
2245.51Zhan, Yi-Zhou; Meng, Huan; Shu, Wei
Rapid Access to t-Butylalkylated Olefins Enabled by Ni-Catalyzed Intermolecular Regio- and trans-Selective Cross-Electrophile t-Butylalkylation of Alkynes
Chemical Science, 2022
1566728 CIF
HKL
Paper
C15 H14 Cl N5 O2P 1 21 17.1533; 11.936; 9.004
90; 98.128; 90
761.1Song, Jingjing; Jiang, Xinyu; Wang, Ziyi; Pei, Jingyao; Li, Hongsen
4-Chloro-5-(dimethylamino)-2-[(5-phenyl-1,3,4-oxadiazol-2-yl)methyl]pyridazin-3(2<i>H</i>)-one
IUCrData, 2022, 7, x220342
1566729 CIF
HKL
Paper
C16 H9 N O2 SP 1 21/c 14.60717; 20.7275; 12.6444
90; 91.911; 90
1206.81Abdallah, Amira E. M.; Elgemeie, Galal H.; Jones, Peter G.
3-(Benzo[<i>d</i>]thiazol-2-yl)-2<i>H</i>-chromen-2-one
IUCrData, 2022, 7, x220332

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