Crystallography Open Database

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7125907 CIFC20 H17.27 Cl N O2P 21 21 2110.0005; 15.089; 23.6172
90; 90; 90
3563.78Lu, Fo-Yun; Chen, Yu-Jue; Chen, Yuan; Ding, Xuan; Guan, Zhi; He, Yan-Hong
Highly enantioselective electrosynthesis of C2-quaternary indolin-3-ones.
Chemical communications (Cambridge, England), 2020, 56, 623-626
7125908 CIFC65.96 H95.17 Br0.76 Mg2 O12C 1 2/c 120.51; 12.667; 26.498
90; 108.671; 90
6522Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125909 CIFC186 H228 O33C 1 2/c 140.636; 12.2639; 36.165
90; 113.845; 90
16485Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125910 CIFC67.57 H98.78 Br0.36 Mg2 O12P 1 21 113.565; 12.45; 20.554
90; 107.915; 90
3302.9Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125911 CIFC72.34 H107.54 Br0.14 Mg2 O12P -111.959; 13.536; 22.775
75.943; 88.27; 73.195
3420Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125912 CIFC251.55 H351.03 Br0.06 Mg4 O44P -114.01; 17.806; 25.7096
95.703; 103.75; 102.801
5996.2Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125913 CIFC69 H101 Mg2 O12P 1 21/c 113.392; 21.18; 23.936
90; 96.985; 90
6739Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125914 CIFC122 H165 Br2 Mg2 O24P 1 21/c 111.973; 26.293; 39.008
90; 97.456; 90
12176Shen, Lingyi; Zhao, Yanxia; Dai, Dihua; Yang, Ying-Wei; Wu, Biao; Yang, Xiao-Juan
Stabilization of Grignard reagents by a pillar[5]arene host - Schlenk equilibria and Grignard reactions.
Chemical communications (Cambridge, England), 2020, 56, 1381-1384
7125915 CIFC39 H0 Ce N11 O0 S7P m -3 m11.3981; 11.3981; 11.3981
90; 90; 90
1480.8Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125916 CIFC39 H0 Lu N11 O0 S7I 4/m m m11.3929; 11.3929; 22.386
90; 90; 90
2905.7Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125917 CIFC39 H0 Gd N11 O S7I 4/m m m11.418; 11.418; 22.504
90; 90; 90
2933.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125918 CIFC39 H0 N11 O0 Pr S7P m -3 m11.4242; 11.4242; 11.4242
90; 90; 90
1491Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125919 CIFC39 H0 N11 O0 S7 TbI 4/m m m11.3933; 11.3933; 22.4759
90; 90; 90
2917.5Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125920 CIFC39 H0 Eu N11 S7I 4/m m m11.3876; 11.3876; 22.5539
90; 90; 90
2924.7Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125921 CIFC39 H0 La N11 O0 S7P m -3 m11.4263; 11.4263; 11.4263
90; 90; 90
1491.82Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125922 CIFC39 Am N11 S7P m -3 m11.3641; 11.3641; 11.3641
90; 90; 90
1467.6Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125923 CIFC39 H0 N11 Nd O0 S7P m -3 m11.3976; 11.3976; 11.3976
90; 90; 90
1480.61Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125924 CIFC39 H0 Ho N11 O0 S7I 4/m m m11.4039; 11.4039; 22.5714
90; 90; 90
2935.39Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125925 CIFC39 H0 N11 O0 S7 TmI 4/m m m11.3875; 11.3875; 22.478
90; 90; 90
2914.8Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125926 CIFC39 H0 Dy N11 O0 S7I 4/m m m11.4134; 11.4134; 22.6144
90; 90; 90
2945.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125927 CIFC39 H0 Er N11 O0 S7I 4/m m m11.4093; 11.4093; 22.577
90; 90; 90
2938.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125928 CIFC39 H0 N11 O0 S7 SmP m -3 m11.3772; 11.3772; 11.3772
90; 90; 90
1472.67Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125929 CIFC39 H0 N11 O0 S7 YbI 4/m m m11.3736; 11.3736; 22.495
90; 90; 90
2909.93Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125930 CIFC39 H0 Cm N11 O3 S7P m -3 m11.3752; 11.3752; 11.3752
90; 90; 90
1471.9Wilson, Richard E.; Carter, Tyler J.; Autillo, Matthieu; Stegman, Samantha
Thiocyanate complexes of the lanthanides, Am and Cm.
Chemical communications (Cambridge, England), 2020, 56, 2622-2625
7125931 CIFC60 H80 B2 F4 I4 N4 O23 V6P 1 21 110.02302; 22.8571; 15.9505
90; 91.5838; 90
3652.82Gu, Yaqi; Li, Qi; Huang, Yichao; Zhu, Yingting; Wei, Yongge; Ruhlmann, Laurent
Polyoxovanadate-iodobodipy supramolecular assemblies: new agents for high efficiency cancer photochemotherapy.
Chemical communications (Cambridge, England), 2020, 56, 2869-2872
7125932 CIFC38 H26 O5 S2C 1 2/c 118.6651; 9.1102; 18.3035
90; 108.224; 90
2956.26Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125933 CIFC21 H14 N2 O7P -16.914; 10.6; 13.029
99.77; 96.31; 92.38
933.6Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125934 CIFC21 H15 N O5P -111.02; 11.052; 16.364
106.83; 104.08; 100.237
1783Zeng, Linwei; Chen, Renjie; Zhang, Chen; Xie, Hujun; Cui, Sunliang
Iridium(i)-catalyzed hydration/esterification of 2-alkynylphenols and carboxylic acids.
Chemical communications (Cambridge, England), 2020, 56, 3093-3096
7125935 CIFC16 H16 N2C 1 2/c 120.126; 7.6043; 19.1043
90; 114.182; 90
2667.2Roy, Subhra Kanti; Purkait, Anisha; Aziz, Sk Md Tarik; Jana, Chandan K.
Acid mediated coupling of aliphatic amines and nitrosoarenes to indoles.
Chemical communications (Cambridge, England), 2020, 56, 3167-3170
7125936 CIFC15 H14 N2P c c n20.3252; 17.4919; 7.6118
90; 90; 90
2706.2Roy, Subhra Kanti; Purkait, Anisha; Aziz, Sk Md Tarik; Jana, Chandan K.
Acid mediated coupling of aliphatic amines and nitrosoarenes to indoles.
Chemical communications (Cambridge, England), 2020, 56, 3167-3170
7125937 CIFC30 H42 O3P 21 21 217.6085; 18.276; 18.693
90; 90; 90
2599.3Wang, Wen-Li; Liu, Xiao-Qin; Zhang, Mei-Hui; Lin, Bin; Zhu, Dong-Rong; Li, Ling-Nan; Chen, Chen; Han, Chao; Luo, Jian-Guang; Kong, Ling-Yi
Taxodisones A and B: bioactive C<sub>30</sub>-terpenes with new skeletons from Taxodium distichum and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 3329-3332
7125938 CIFC30 H42 O3P 1 21 110.264; 12.5469; 20.5284
90; 101.807; 90
2587.74Wang, Wen-Li; Liu, Xiao-Qin; Zhang, Mei-Hui; Lin, Bin; Zhu, Dong-Rong; Li, Ling-Nan; Chen, Chen; Han, Chao; Luo, Jian-Guang; Kong, Ling-Yi
Taxodisones A and B: bioactive C<sub>30</sub>-terpenes with new skeletons from Taxodium distichum and their biosynthetic origin.
Chemical communications (Cambridge, England), 2020, 56, 3329-3332
7125939 CIFC76 H74 Cl2 Cr2 F10 N4P -115.8112; 18.2465; 23.607
78.927; 87.544; 81.311
6606.4Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125940 CIFC44 H50 Cr F8 N2 O5 SP -111.3653; 17.4031; 21.1322
93.966; 102.004; 96.269
4045.7Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125941 CIFC54 H67 Cr F5 N3 OP -111.4314; 13.7772; 15.3492
104.593; 91.816; 93.766
2331.44Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125942 CIFC59 H70 Cr F5 N4P b c a15.3902; 22.0785; 29.9364
90; 90; 90
10172.2Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125943 CIFC44 H45 Cl Cr F5 N3P 1 21/c 118.229; 20.427; 10.3857
90; 105.421; 90
3728Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125944 CIFC49 H53 Cr F8 N3 O4 SP 1 21 117.0256; 17.8637; 17.9461
90; 112.061; 90
5058.5Dong, Yuyang; Clarke, Ryan M.; Zheng, Shao-Liang; Betley, Theodore A.
Synthesis and electronic structure studies of a Cr-imido redox series.
Chemical communications (Cambridge, England), 2020, 56, 3163-3166
7125945 CIFC360 H312 N58 O90 Pd6 S12P -126.739; 26.793; 29.537
64.09; 77.3; 86.34
18556Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125946 CIFC396 H378 N48 O78 Pd6 S12R -3 :H29.802; 29.802; 68.496
90; 90; 120
52685Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125947 CIFC336 H240 N48 O48 Pd6I 4/m35.325; 35.325; 49.962
90; 90; 90
62345Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125948 CIFC420 H426 N48 O78 Pd6 S12R -3 :H29.879; 29.879; 68.309
90; 90; 120
52813Lee, Haeri; Kim, Dongwon; Oh, Hyejin; Jung, Ok-Sang
Molecular balloon, Pd<sub>6</sub>L<sub>8</sub> cages: recognition of alkyl sulfate surfactants.
Chemical communications (Cambridge, England), 2020, 56, 2841-2844
7125949 CIFC8 H9 N OP -16.5511; 6.9192; 8.0265
93.73; 102.78; 91.769
353.68Zhai, Shengxian; Zhang, Xinping; Cheng, Bin; Li, Hui; Li, Yuntong; He, Yixuan; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of tetrasubstituted thiophenes via a [3+2] cascade cyclization reaction of pyridinium 1,4-zwitterionic thiolates and activated allenes.
Chemical communications (Cambridge, England), 2020, 56, 3085-3088
7125950 CIFC22 H16 O5 SP 1 21/c 118.903; 7.1434; 14.656
90; 100.898; 90
1943.3Zhai, Shengxian; Zhang, Xinping; Cheng, Bin; Li, Hui; Li, Yuntong; He, Yixuan; Li, Yun; Wang, Taimin; Zhai, Hongbin
Synthesis of tetrasubstituted thiophenes via a [3+2] cascade cyclization reaction of pyridinium 1,4-zwitterionic thiolates and activated allenes.
Chemical communications (Cambridge, England), 2020, 56, 3085-3088
7125951 CIFC25 H28 B Br Cl2 N6 O2 WP 1 21/c 116.371; 10.3034; 17.1373
90; 94.539; 90
2881.6Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125952 CIFC50 H52 B2 N12 O4 W2P 1 21/c 113.8341; 10.1106; 20.5773
90; 106.771; 90
2755.75Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125953 CIFC72 H108 B2 N12 O4 W2P 1 21/c 113.2449; 18.7892; 16.1898
90; 107.336; 90
3846Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125954 CIFC34 H34 B N7 O2 WP 1 21/n 110.2667; 23.1598; 13.5771
90; 92.406; 90
3225.4Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125955 CIFC32.5 H32 B Cl N6 O2 WI 1 2/a 137.593; 10.4555; 32.1962
90; 96.483; 90
12573.9Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125956 CIFC28 H29 B N6 O2 WP 1 21/c 17.9501; 17.9153; 19.455
90; 100.437; 90
2725.1Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125957 CIFC28 H29 B N6 O2 WP 1 21/n 17.9431; 17.7548; 19.9617
90; 99.821; 90
2773.9Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125958 CIFC106 H130 B4 N24 O8 W4I 1 2/m 123.8078; 25.26; 25.4589
90; 114.84; 90
13894.1Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125959 CIFC60 H69 B3 N18 O6 W3P 1 21/n 114.1626; 36.3631; 14.8716
90; 90.019; 90
7658.8Frogley, Benjamin J.; Hill, Anthony F.; Seitz, Antonia
Bi- and poly(carbyne) functionalised polycyclic aromatics.
Chemical communications (Cambridge, England), 2020, 56, 3265-3268
7125960 CIFC26 H32 N4P b c n14.844; 9.534; 16.867
90; 90; 90
2387Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125961 CIFC42 H64 N4 Na O4C 1 2/c 118.399; 14.6911; 15.7048
90; 103.277; 90
4131.6Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125962 CIFC42 H64 K N4 O4C 1 2/c 118.731; 15.129; 15.467
90; 104.882; 90
4236Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125963 CIFC112 H184 K4 N8 O27P -113.5116; 14.2386; 17.4578
84.41; 68.71; 86.045
3112.5Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125964 CIFC64 H104 K2 N4 O19P 1 21/n 112.996; 26.8623; 22.322
90; 101.922; 90
7624.6Wang, Wenqing; Tan, Gengwen; Feng, Rui; Fang, Yong; Chen, Chao; Ruan, Huapeng; Zhao, Yue; Wang, Xinping
Stable, yet "naked", azo radical anion ArNNAr<sup>-</sup> and dianion ArNNAr<sup>2-</sup> (Ar = 4-CN-2,6-<sup>i</sup>Pr<sub>2</sub>-C<sub>6</sub>H<sub>2</sub>) with selective CO<sub>2</sub> activation.
Chemical communications (Cambridge, England), 2020, 56, 3285-3288
7125965 CIFC79 H191.2 N24 O74.1 P6C 1 2/c 149.267; 14.9082; 39.726
90; 100.616; 90
28679Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125966 CIFC82 H171.4 N26 O59.6 P6R -3 :H18.3819; 18.3819; 35.5789
90; 90; 120
10411.3Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125967 CIFC36 H56 N12 O10P -110.6732; 12.999; 16.3255
75.5241; 85.8338; 71.3608
2078Pramanik, Subhamay; Day, Victor W.; Bowman-James, Kristin
Supramolecular traps for highly phosphorylated inositol sources of phosphorus.
Chemical communications (Cambridge, England), 2020, 56, 3269-3272
7125968 CIFC100 H50 Cu10 N20P -110.3306; 12.1908; 16.1323
92.418; 107.283; 91.169
1937.06Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125969 CIFC110 H50 Cu10 N20P -110.8822; 12.4297; 16.2388
96.008; 108.765; 90.917
2065.44Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125970 CIFC100 H50 Cu10 N20C 1 2/m 110.3986; 30.8174; 12.2534
90; 91.742; 90
3924.88Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125971 CIFC110 H50 Cu10 N20P -110.8776; 12.4524; 16.2822
95.7; 108.748; 91.392
2074.41Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125972 CIFC100 H50 Cu10 N20P -110.3877; 12.2263; 16.1951
90.741; 107.985; 91.592
1955.07Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125973 CIFC110 H50 Cu10 N20P -116.3006; 16.5127; 16.5388
98.05; 98.473; 108.223
4099.39Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125974 CIFC100 H50 Cu10 N20C 1 2/m 110.4531; 30.8052; 12.2818
90; 91.966; 90
3952.53Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125975 CIFC110 H50 Cu10 N20P -116.2846; 16.3744; 16.5641
98.035; 98.566; 108.306
4063.83Zhan, Shun-Ze; Li, Jing-Hong; Zhang, Guo-Hui; Li, Ming-De; Sun, Shanshan; Zheng, Ji; Ning, Guo-Hong; Li, Mian; Kuang, Dai-Bin; Wang, Xu-Dong; Li, Dan
Coordination disk-type nano-Saturn complexes.
Chemical communications (Cambridge, England), 2020, 56, 3325-3328
7125976 CIFC90 H82 F24 N18 P4P 42 21 219.429; 19.429; 12.057
90; 90; 90
4551.3Nian, Hao; Li, Aisen; Li, Yawen; Cheng, Lin; Wang, Ling; Xu, Weiqing; Cao, Liping
Tetraphenylethene-based tetracationic dicyclophanes: synthesis, mechanochromic luminescence, and photochemical reactions.
Chemical communications (Cambridge, England), 2020, 56, 3195-3198
7125977 CIFC61.5 H74 Cl4 N8 O7.5P -111.8059; 14.764; 19.268
78.553; 73.274; 75
3078.7Nian, Hao; Li, Aisen; Li, Yawen; Cheng, Lin; Wang, Ling; Xu, Weiqing; Cao, Liping
Tetraphenylethene-based tetracationic dicyclophanes: synthesis, mechanochromic luminescence, and photochemical reactions.
Chemical communications (Cambridge, England), 2020, 56, 3195-3198
7125978 CIFC61 H92 F6 Fe N4 O12 S2P 42 21 228.876; 28.876; 11.5084
90; 90; 90
9596Wang, Fang; Feng, Lili; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
Chiral N,N'-dioxide-iron(iii)-catalyzed asymmetric sulfoxidation with hydrogen peroxide.
Chemical communications (Cambridge, England), 2020, 56, 3233-3236
7125979 CIFC27.5 H44.5 Br Cr N4 O14.25P -19.8426; 12.5393; 16.1571
75.374; 79.253; 72.06
1822.8Ruan, Wenqing; Mao, Jiatao; Yang, Shida; Shi, Chuan; Jia, Guochen; Chen, Qing
Designing Cr complexes for a neutral Fe-Cr redox flow battery.
Chemical communications (Cambridge, England), 2020, 56, 3171-3174
7125980 CIFB4 Ba F6 H4 O6C 1 2/m 16.803; 7.008; 9.588
90; 92.96; 90
456.5Gai, Minqiang; Wang, Ying; Tong, Tinghao; Wang, Liying; Yang, Zhihua; Zhou, Xin; Pan, Shilie
Ba(B<sub>2</sub>OF<sub>3</sub>(OH)<sub>2</sub>)<sub>2</sub> with well-ordered OH/F anions and a unique B<sub>2</sub>OF<sub>3</sub>(OH)<sub>2</sub> dimer.
Chemical communications (Cambridge, England), 2020, 56, 3301-3304
7125981 CIFC30 H23 N3 O2 SP 21 21 2110.313; 14.7947; 15.8422
90; 90; 90
2417.17Ni, Qijian; Wang, Xuyang; Xu, Fangfang; Chen, Xiaoyun; Song, Xiaoxiao
Organocatalytic asymmetric [4+2] cyclization of 2-benzothiazolimines with azlactones: access to chiral benzothiazolopyrimidine derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3155-3158
7125982 CIFC21 H23 Cl F3 N5 OP 1 21/n 111.0699; 23.359; 16.6594
90; 96.992; 90
4275.8Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125983 CIFC24 H35 Cl2 N5 O3P -17.9219; 9.5881; 19.0533
99.49; 91.0584; 110.626
1331.31Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125984 CIFC17 H17 Cl2 N5 OP 1 21/c 15.7035; 20.182; 15.891
90; 96.478; 90
1817.5Carreira-Barral, Israel; Mielczarek, Marcin; Alonso-Carrillo, Daniel; Capurro, Valeria; Soto-Cerrato, Vanessa; Pérez Tomás, Ricardo; Caci, Emanuela; García-Valverde, María; Quesada, Roberto
Click-tambjamines as efficient and tunable bioactive anion transporters.
Chemical communications (Cambridge, England), 2020, 56, 3218-3221
7125985 CIFC14 H19 N0 O2P b c a9.026; 11.173; 23.919
90; 90; 90
2412.2Zhai, Shengxian; Qiu, Shuxian; Chen, Lunjian; Niu, Yongsheng; Yu, Youzhu; Yang, Bo; Zhang, Beining; Han, Chuchu; Yang, Liguo; Zhai, Hongbin
Synthesis of cyclobutane-fused oxygen-containing tricyclic framework via thermally promoted intramolecular cycloaddition of cyclohexadienone-tethered allenes.
Chemical communications (Cambridge, England), 2020, 56, 3405-3408
7125986 CIFC27 H29 N3 SeP 1 21/c 115.3492; 13.4033; 11.3497
90; 92.454; 90
2332.8Zhu, Li-Li; Tian, Lifang; Cai, Bin; Liu, Guanglu; Zhang, Hui; Wang, Yahui
Diamine-mediated N<sup>2</sup>-selective β-selenoalkylation of triazoles with alkenes.
Chemical communications (Cambridge, England), 2020, 56, 2979-2982
7125987 CIFC20 H23 N3 SeP 1 21 111.6605; 5.8592; 13.2196
90; 92.925; 90
902Zhu, Li-Li; Tian, Lifang; Cai, Bin; Liu, Guanglu; Zhang, Hui; Wang, Yahui
Diamine-mediated N<sup>2</sup>-selective β-selenoalkylation of triazoles with alkenes.
Chemical communications (Cambridge, England), 2020, 56, 2979-2982
7125988 CIFC29 H42 F6 N4 O6 S2P b c a14.61721; 17.96113; 27.42571
90; 90; 90
7200.39Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125989 CIFC31.5 H47 Cl2 F3 N4 O3 Pd SP -18.9948; 12.5902; 17.7787
78.6427; 82.2769; 88.4754
1956.04Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125990 CIFC28 H41 Au Cl F3 N4 O3 SP 1 21/n 115.1363; 8.9448; 26.1314
90; 103.763; 90
3436.4Barthes, Cécile; Duhayon, Carine; Canac, Yves; César, Vincent
N-Cyclopropenio-imidazol-2-ylidene: An N-heterocyclic carbene bearing an N-cationic substituent.
Chemical communications (Cambridge, England), 2020, 56, 3305-3308
7125991 CIFC30 H28 Cl2 N6 Ni O8 S2C 1 c 121.948; 8.33062; 20.7006
90; 115.404; 90
3418.9Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125992 CIFC24 H16 Cl2 N4 Ni S2P -18.9125; 12.1348; 12.2295
67.774; 69.928; 87.213
1144.97Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125993 CIFC29 H22 F6 N4 Ni O S2P -110.3997; 12.7078; 13.3086
114.49; 111.726; 92.4482
1446.31Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125994 CIFC26 H24 Cl2 N4 Ni O8 S2P 21 21 218.5516; 10.2011; 33.0145
90; 90; 90
2880.04Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125995 CIFC27 H25 N5 Ni O S2P 1 21/c 111.3962; 18.9231; 12.9723
90; 114.313; 90
2549.38Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125996 CIFC46 H50 Cl6 Co N4 Ni S2P -110.1761; 12.4123; 19.1814
96.674; 91.868; 96.713
2387.24Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125997 CIFC46 H52 Cl4 Co N4 Ni S2P 1 21/n 112.3345; 22.2711; 18.1248
90; 109.54; 90
4692.2Inoue, Satoshi; Yan, Yin-Nan; Yamanishi, Katsunori; Kataoka, Yusuke; Kawamoto, Tatsuya
Photocatalytic and electrocatalytic hydrogen production using nickel complexes supported by hemilabile and non-innocent ligands.
Chemical communications (Cambridge, England), 2020, 56, 2829-2832
7125998 CIFC17 H16 Br N O2P 1 21/c 115.7754; 8.5582; 11.6197
90; 107.162; 90
1498.91Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7125999 CIFC20 H14 Br N O3P 21 21 214.2743; 15.4368; 24.939
90; 90; 90
1645.5Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126000 CIFC18 H18 Br N O2P c a 2111.5591; 7.965; 17.2106
90; 90; 90
1584.55Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126001 CIFC18 H14 Br N O2P b c a8.3242; 12.6129; 28.2407
90; 90; 90
2965.06Li, Xingjun; Wang, Jiang; Xie, Xiong; Dai, Wenhao; Han, Xu; Chen, Kaixian; Liu, Hong
Ir(iii)-Catalyzed direct C-H functionalization of N-phenylacetamide with α-diazo quinones: a novel strategy for producing 2-hydroxy-2'-amino-1,2'-biaryl scaffolds.
Chemical communications (Cambridge, England), 2020, 56, 3441-3444
7126002 CIFC18 H18 F3 N O2P 1 21 111.25978; 5.81649; 12.31963
90; 94.0216; 90
804.855Sun, Xi-Shang; Ou-Yang, Qiu; Xu, Shi-Ming; Wang, Xing-Heng; Tao, Hai-Yan; Chung, Lung Wa; Wang, Chun-Jiang
Asymmetric synthesis of quaternary α-trifluoromethyl α-amino acids by Ir-catalyzed allylation followed by kinetic resolution.
Chemical communications (Cambridge, England), 2020, 56, 3333-3336
7126003 CIFC18 H18 F3 N O2P 21 21 215.7902; 8.6739; 32.4787
90; 90; 90
1631.2Sun, Xi-Shang; Ou-Yang, Qiu; Xu, Shi-Ming; Wang, Xing-Heng; Tao, Hai-Yan; Chung, Lung Wa; Wang, Chun-Jiang
Asymmetric synthesis of quaternary α-trifluoromethyl α-amino acids by Ir-catalyzed allylation followed by kinetic resolution.
Chemical communications (Cambridge, England), 2020, 56, 3333-3336
7126004 CIFC22 H19 Cl N2 O2 SP 1 21/c 16.7878; 22.1588; 13.8692
90; 96.581; 90
2072.31Zhang, Jun; Yang, Min; Liu, Jin-Biao; He, Fu-Sheng; Wu, Jie
A copper-catalyzed insertion of sulfur dioxide via radical coupling.
Chemical communications (Cambridge, England), 2020, 56, 3225-3228
7126005 CIFC14 H17 N3 O5P 1 21/c 17.1763; 28.9373; 7.067
90; 92.186; 90
1466.48Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126006 CIFC9 H9 N3 O5P 21 21 215.4911; 10.5173; 18.2619
90; 90; 90
1054.65Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126007 CIFC12 H13 N3 O5P 1 21 16.6674; 16.3925; 11.6108
90; 101.031; 90
1245.56Fellowes, Thomas; Harris, Benjamin L.; White, Jonathan M.
Experimental evidence of chalcogen bonding at oxygen.
Chemical communications (Cambridge, England), 2020, 56, 3313-3316
7126008 CIFC33 H16 B F9 O2P -19.717; 10.2493; 15.4586
85.283; 75.672; 66.463
1367.33Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126009 CIFC23 H12 B F9 O4P -17.8452; 10.557; 15.699
71.33; 75.721; 84.401
1193.5Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126010 CIFC23 H6 B F15 O4P 1 21/n 113.314; 10.1081; 18.044
90; 111.202; 90
2264Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126011 CIFC24 H14 B F9 O3P 1 21/c 19.0378; 17.4814; 14.4485
90; 96.721; 90
2267.1Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126012 CIFC32 H15 B F15 I O2P 1 21/n 116.1557; 37.6672; 16.7091
90; 104.564; 90
9841.4Gazis, Theodore A.; Mohajeri Thaker, Bayan A. J.; Willcox, Darren; Ould, Darren M. C.; Wenz, Jan; Rawson, Jeremy M.; Hill, Michael S.; Wirth, Thomas; Melen, Rebecca L.
1,3-Carboboration of iodonium ylides.
Chemical communications (Cambridge, England), 2020, 56, 3345-3348
7126013 CIFC34 H36 N4 O8C 1 2/c 118.896; 15.0948; 22.5368
90; 103.389; 90
6253.5Johnson, Stuart; Kovács, Ervin; Greaney, Michael F.
Arylation and alkenylation of activated alkyl halides using sulfonamides.
Chemical communications (Cambridge, England), 2020, 56, 3222-3224
7126014 CIFC22 H29 N3P 1 21/n 116.2354; 5.8866; 20.5287
90; 93.513; 90
1958.3Sarkar, Tanumay; Talukdar, Kangkan; Roy, Subhasish; Punniyamurthy, Tharmalingam
Expedient iron-catalyzed stereospecific synthesis of triazines via cycloaddition of aziridines with diaziridines.
Chemical communications (Cambridge, England), 2020, 56, 3381-3384
7126015 CIFC28 H33 N3 O2P -16.1688; 10.0037; 20.56
103.548; 91.18; 95.599
1226.3Sarkar, Tanumay; Talukdar, Kangkan; Roy, Subhasish; Punniyamurthy, Tharmalingam
Expedient iron-catalyzed stereospecific synthesis of triazines via cycloaddition of aziridines with diaziridines.
Chemical communications (Cambridge, England), 2020, 56, 3381-3384
7126016 CIFC18 H16 N5 O2C 1 2/c 128.46; 4.932; 24.318
90; 112.81; 90
3146.4Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126017 CIFC68 H94 N10 O6 Ti2P 1 21/n 112.3192; 17.5994; 14.9947
90; 96.71; 90
3228.7Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126018 CIFC68 H94 N10 O6 Ti2P -19.9438; 12.8964; 13.5489
86.435; 79.518; 74.129
1643.23Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126019 CIFC88 H114 N14 O6 Ti2P -112.7936; 18.121; 19.6033
98.602; 108.452; 101.429
4113.9Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126020 CIFC90.5 H116.5 N14.5 O6 V2P -112.807; 18.384; 20.411
73.022; 72.779; 70.673
4230Borilovic, Ivana; Alonso, Pablo J.; Roubeau, Olivier; Aromí, Guillem
A bis-vanadyl coordination complex as a 2-qubit quantum gate.
Chemical communications (Cambridge, England), 2020, 56, 3139-3142
7126021 CIFC12 H48 In6 N6 S12P 1 21/n 19.742; 14.4225; 28.1311
90; 93.409; 90
3945.54Wang, Kai-Yao; Sun, Meng; Ding, Dong; Liu, Hua-Wei; Cheng, Lin; Wang, Cheng
Di-lacunary [In<sub>6</sub>S<sub>15</sub>]<sup>12-</sup> cluster: the building block of a highly negatively charged framework for superior Sr<sup>2+</sup> adsorption capacities.
Chemical communications (Cambridge, England), 2020, 56, 3409-3412
7126022 CIFC2 H5 Na OP -4 21 m4.41084; 4.41084; 9.06779
90; 90; 90
176.418Beske, Maurice; Tapmeyer, Lukas; Schmidt, Martin U.
Crystal structure of sodium ethoxide (C<sub>2</sub>H<sub>5</sub>ONa), unravelled after 180 years.
Chemical communications (Cambridge, England), 2020, 56, 3520-3523
7126023 CIFC6 H17 Na O3P 1 21/n 111.622; 5.1926; 17.682
90; 104.08; 90
1035Beske, Maurice; Tapmeyer, Lukas; Schmidt, Martin U.
Crystal structure of sodium ethoxide (C<sub>2</sub>H<sub>5</sub>ONa), unravelled after 180 years.
Chemical communications (Cambridge, England), 2020, 56, 3520-3523
7126024 CIFC10 H17 Au Cl3 N3 OP 1 21/c 17.0041; 15.654; 16.326
90; 115.405; 90
1616.9Terrón, Angel; Buils, Jordi; Mooibroek, Tiddo J.; Barceló-Oliver, Miquel; García-Raso, Angel; Fiol, Juan J.; Frontera, Antonio
Synthesis, X-ray characterization and regium bonding interactions of a trichlorido(1-hexylcytosine)gold(iii) complex.
Chemical communications (Cambridge, England), 2020, 56, 3524-3527
7126025 CIFC42 H40 Cu2 N8C 1 2/c 125.3657; 9.9388; 29.1779
90; 92.788; 90
7347.2Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126026 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.115; 9.2099; 26.461
90; 83.888; 90
5843.5Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126027 CIFC42 H40 Cu2 N8C 1 2/c 124.808; 9.6971; 27.648
90; 92.073; 90
6646.8Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126028 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.215; 9.2391; 26.599
90; 84.042; 90
5919Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126029 CIFC42 H40 Cu2 N8C 1 2/c 125.1863; 9.9249; 28.57
90; 91.745; 90
7138.4Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126030 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 124.259; 9.2882; 26.841
90; 84.039; 90
6015Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126031 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 123.997; 9.1398; 26.116
90; 83.75; 90
5693.9Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126032 CIFC42 H40 Cu2 N8 Ne3.5C 1 2/c 123.811; 9.0709; 25.766
90; 83.532; 90
5530Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126033 CIFC42 H40 Cu2 N8C 1 2/c 124.281; 9.4519; 26.2355
90; 91.553; 90
6018.9Giordano, Nico; Beavers, Christine M.; Kamenev, Konstantin V.; Love, Jason B.; Pankhurst, James R.; Teat, Simon J.; Parsons, Simon
Pressure-induced inclusion of neon in the crystal structure of a molecular Cu<sub>2</sub>(pacman) complex at 4.67 GPa.
Chemical communications (Cambridge, England), 2020, 56, 3449-3452
7126034 CIFC18 H26 Eu F4 N5 O9 S4P 4/n :212.782; 12.782; 8.4363
90; 90; 90
1378.32Zeng, Qi; Wang, Lei; Huang, Yitao; Zheng, Sai-Li; He, Yonghe; He, Jun; Liao, Wei-Ming; Xu, Gang; Zeller, Matthias; Xu, Zhengtao
An air-stable anionic two-dimensional semiconducting metal-thiolate network and its exfoliation into ultrathin few-layer nanosheets.
Chemical communications (Cambridge, England), 2020, 56, 3645-3648
7126035 CIFC12 H36 Ag Bi I12 N4P -18.6582; 9.3734; 12.1489
90.286; 95.226; 90.478
981.82Yao, Yunpeng; Kou, Bo; Peng, Yu; Wu, Zhenyue; Li, Lina; Wang, Sasa; Zhang, Xinyuan; Liu, Xitao; Luo, Junhua
(C<sub>3</sub>H<sub>9</sub>NI)<sub>4</sub>AgBiI<sub>8</sub>: a direct-bandgap layered double perovskite based on a short-chain spacer cation for light absorption.
Chemical communications (Cambridge, England), 2020, 56, 3206-3209
7126036 CIFC52 H38 F5 N3P -112.1765; 13.0482; 15.231
111.513; 112.548; 93.946
2016.53Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126037 CIFC400 H344 Cl F72 N80 Pt8C 1 2/c 131.6392; 8.7956; 37.084
90; 93.548; 90
10300.2Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126038 CIFC54 H39 F5 N3 O2 RhC 2 2 2112.7471; 24.2024; 35.7587
90; 90; 90
11031.9Das, Mainak; Chitranshi, Sangya; Murugavel, M.; Adinarayana, B.; Suresh, Cherumuttathu H.; Srinivasan, A.
Isosmaragdyrin with an N<sub>3</sub>C<sub>2</sub> core: stabilization of Rh(i) and organo-Pt(ii) complexes.
Chemical communications (Cambridge, England), 2020, 56, 3551-3554
7126039 CIFC36 H21 N5 O2 SI 1 2/a 117.1162; 7.7907; 42.35
90; 90.551; 90
5647Bui, Anh Thy; Philippe, Clotilde; Beau, Maxime; Richy, Nicolas; Cordier, Marie; Roisnel, Thierry; Lemiègre, Loïc; Mongin, Olivier; Paul, Frédéric; Trolez, Yann
Synthesis, characterization and unusual near-infrared luminescence of 1,1,4,4-tetracyanobutadiene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3571-3574
7126040 CIFC32 H19 N5 O2 SP 1 21/n 18.766; 26.272; 11.5682
90; 109.987; 90
2503.7Bui, Anh Thy; Philippe, Clotilde; Beau, Maxime; Richy, Nicolas; Cordier, Marie; Roisnel, Thierry; Lemiègre, Loïc; Mongin, Olivier; Paul, Frédéric; Trolez, Yann
Synthesis, characterization and unusual near-infrared luminescence of 1,1,4,4-tetracyanobutadiene derivatives.
Chemical communications (Cambridge, England), 2020, 56, 3571-3574
7126045 CIFC54 H72 As N3P 1 21/n 112.59029; 15.93625; 23.78509
90; 93.231; 90
4764.7Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126046 CIFC54 H72 As Cl4 Ga N3P -111.4502; 19.3524; 25.1018
76.229; 89.254; 88.856
5401.1Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126047 CIFC57 H76 As N3P 1 21/c 118.8381; 11.9051; 22.8999
90; 101.668; 90
5029.6Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126048 CIFC57 H76 As Cl8 Ga2 N3P -113.7117; 24.2939; 24.861
100.452; 98.045; 98.408
7937.7Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126049 CIFC57 H76 As Cl4 Ga N3P 1 21/n 112.6066; 23.8366; 18.7085
90; 98.41; 90
5561.4Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126050 CIFC54 H72 As Cl8 Ga2 N3P b c a18.8893; 26.1136; 24.2536
90; 90; 90
11963.5Sharma, Mahendra K.; Blomeyer, Sebastian; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-arsa-1,3-butadiene radical cations and dications.
Chemical communications (Cambridge, England), 2020, 56, 3575-3578
7126051 CIFBa3 Cl3 F6 InP 63/m10.131; 10.131; 5.9315
90; 90; 120
527.23Jiang, Xiaoqing; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
In[Ba<sub>3</sub>Cl<sub>3</sub>F<sub>6</sub>]: a novel infrared-transparent molecular sieve constructed by halides.
Chemical communications (Cambridge, England), 2020, 56, 3297-3300
7126052 CIFC16 H15 N3 O3P 1 21/c 17.053; 18.102; 11.924
90; 106.894; 90
1456.7Pal, Pranesh; Mainkar, Prathama S.; Nayani, Kiranmai; Chandrasekhar, Srivari
Mn-catalyzed radical initiated domino transformation of alkynylated cyclohexadienones with TMSN<sub>3</sub> and O<sub>2</sub> to bicyclic azido alcohols.
Chemical communications (Cambridge, England), 2020, 56, 3453-3456
7126053 CIFC90 H100 Ag12 F36 N12 O26 S6P b c a20.9281; 22.1548; 28.9986
90; 90; 90
13445.4Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126054 CIFC84 H92 Ag12 F36 N8 O26 S6C 1 2/c 130.2957; 20.8495; 22.4448
90; 114.615; 90
12888.9Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126055 CIFC82 H84 Ag12 F36 N8 O24 S6P 1 21/c 113.8315; 29.7018; 16.2995
90; 94.93; 90
6671.4Chen, Xu-Ran; Yang, Ling; Tan, Yu-Ling; Yu, Hong; Ni, Chun-Yan; Niu, Zheng; Lang, Jian-Ping
The solvent-induced isomerization of silver thiolate clusters with symmetry transformation.
Chemical communications (Cambridge, England), 2020, 56, 3649-3652
7126056 CIFC41 H54 Ag F6 N4 PI 49.6472; 9.6472; 21.411
90; 90; 90
1992.7Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126057 CIFC37 H46 Ag B F4 N4C 1 2 113.8399; 13.5554; 18.233
90; 100.627; 90
3361.9Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126058 CIFC41 H54 Ag F6 N4 PI 49.614; 9.614; 21.337
90; 90; 90
1972.2Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126059 CIFC43 H62 N6 O8 ZnP 1 21 18.7797; 19.0092; 12.9597
90; 90.5449; 90
2162.8Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126060 CIFC37 H42 Ag F10 N4 PC 2 2 2113.8896; 14.0055; 37.666
90; 90; 90
7327.2Lee, Eunji; Hosoi, Yasuhiro; Temma, Honoka; Ju, Huiyeong; Ikeda, Mari; Kuwahara, Shunsuke; Habata, Yoichi
Silver ion-induced chiral enhancement by argentivorous molecules.
Chemical communications (Cambridge, England), 2020, 56, 3373-3376
7126061 CIFC16 H12 B NP 1 21/c 19.493; 8.9361; 13.533
90; 96.47; 90
1140.7Abengózar, Alberto; Valencia, Isabel; Otárola, Guillermo G; Sucunza, David; García-García, Patricia; Pérez-Redondo, Adrián; Mendicuti, Francisco; Vaquero, Juan J.
Expanding the BN-embedded PAH family: 4a-aza-12a-borachrysene.
Chemical communications (Cambridge, England), 2020, 56, 3669-3672
7126062 CIFC154 H122 Cl6 O16P -111.895; 13.566; 21.429
89.762; 74.368; 73.348
3180Shimoyama, Daisuke; Sekiya, Ryo; Haino, Takeharu
Upper-rim functionalization and supramolecular polymerization of a feet-to-feet-connected biscavitand.
Chemical communications (Cambridge, England), 2020, 56, 3733-3736
7126063 CIFC50 H128 N25 Nd O88 Si2 W22P -113.4923; 19.9659; 24.448
102.869; 97.74; 94.707
6319.1Nie, Yan-Mei; Li, Sang-Hao; Lin, Ming-Yuan; Yan, Jun
A micro-environment tuning approach for enhancing the catalytic capabilities of lanthanide containing polyoxometalate in the cyanosilylation of ketones.
Chemical communications (Cambridge, England), 2020, 56, 3809-3812
7126064 CIFC94 H46 Ag13 F36 N12P -115.3728; 15.4794; 15.4872
61.894; 68.689; 61.905
2819.87Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126065 CIFC94 H46 Ag11.5 Cu1.5 F36 N12P -115.4952; 15.5896; 15.5997
61.283; 67.64; 61.42
2846.14Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126066 CIFC94 H46 Ag11.96 Cu F36 N12P -115.5019; 15.7093; 15.9495
60.608; 65.701; 61.289
2888.52Peng, Su-Kao; Lu, Zhou; Xie, Mo; Huang, Yong-Liang; Luo, Dong; Wang, Jia-Nan; Zhu, Xiao-Wei; Li, Xue; Zhou, Xiao-Ping; Li, Dan
Unexpected structural transformation into noria-like Ag<sub>13</sub> metal clusters and a copper-doping induced boost in photoluminescence.
Chemical communications (Cambridge, England), 2020, 56, 4789-4792
7126067 CIFC14 H10 Cl N SP 1 21/n 17.994; 5.8548; 25.946
90; 92.333; 90
1213.4Reddy, Mandapati Bhargava; Anandhan, Ramasamy
Visible light initiated amino group ortho-directed copper(i)-catalysed aerobic oxidative C(sp)-S coupling reaction: synthesis of substituted 2-phenylbenzothiazoles via thia-Wolff rearrangement.
Chemical communications (Cambridge, England), 2020, 56, 3781-3784
7126068 CIFC37 H36 F3 N O6P 1 21/n 16.4039; 49.826; 9.4014
90; 90.163; 90
2999.8Matsuhashi, Chihiro; Ueno, Takuya; Uekusa, Hidehiro; Sato-Tomita, Ayana; Ichiyanagi, Kouhei; Maki, Shojiro; Hirano, Takashi
Isomeric difference in the crystalline-state chemiluminescence property of an adamantylideneadamantane 1,2-dioxetane with a phthalimide chromophore.
Chemical communications (Cambridge, England), 2020, 56, 3369-3372
7126069 CIFC37 H36 F3 N O6P -16.847; 9.989; 23.661
81.861; 81.721; 71.02
1506.6Matsuhashi, Chihiro; Ueno, Takuya; Uekusa, Hidehiro; Sato-Tomita, Ayana; Ichiyanagi, Kouhei; Maki, Shojiro; Hirano, Takashi
Isomeric difference in the crystalline-state chemiluminescence property of an adamantylideneadamantane 1,2-dioxetane with a phthalimide chromophore.
Chemical communications (Cambridge, England), 2020, 56, 3369-3372
7126070 CIFC47 H40 Cl2 Co2 N10 O16C 1 2/c 116.718; 13.417; 22.998
90; 101.935; 90
5047.1Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126071 CIFC46 H40 Cl2 Fe2 N10 O12C 1 2/c 115.885; 13.472; 23.262
90; 100.741; 90
4891Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126072 CIFC24 H23 Cl Mn N5 O6P 21 21 219.033; 11.082; 24.474
90; 90; 90
2449.9Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126073 CIFC24 H20 Cl Cu N5 O6P -113.82; 14.61; 14.99
62.12; 76.15; 71.48
2522Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126074 CIFC23 H20 Cl N5 Ni O6P 1 21/n 112.15; 13.633; 14.455
90; 107.636; 90
2282Chai, Xiaomin; Huang, Hai-Hua; Liu, Huiping; Ke, Zhuofeng; Yong, Wen-Wen; Zhang, Ming-Tian; Cheng, Yuan-Sheng; Wei, Xian-Wen; Zhang, Liyan; Yuan, Guozan
Highly efficient and selective photocatalytic CO<sub>2</sub> to CO conversion in aqueous solution.
Chemical communications (Cambridge, England), 2020, 56, 3851-3854
7126075 CIFC84 H138 Cl16 Dy6 K4 O6P -113.9788; 16.4794; 37.2813
85.933; 84.334; 70.868
8067.4Wu, Jianfeng; Demeshko, Serhiy; Dechert, Sebastian; Meyer, Franc
Hexanuclear [Cp*Dy]<sub>6</sub> single-molecule magnet.
Chemical communications (Cambridge, England), 2020, 56, 3887-3890
7126076 CIFC112 H80 Cl2P 1 21/c 125.9806; 24.253; 26.5964
90; 97.253; 90
16624.5Yu, Jie; Tang, Chunlin; Gu, Xinggui; Zheng, Xiaoyan; Yu, Zhen-Qiang; He, Zikai; Li, Xin-Gui; Tang, Ben Zhong
Highly emissive phenylene-expanded [5]radialene.
Chemical communications (Cambridge, England), 2020, 56, 3911-3914
7126077 CIFC129 H56 N4 Ni Sc1.75 U0.88C 1 2/c 125.2486; 15.0232; 39.512
90; 95.365; 90
14921.8Li, Xiaomeng; Yao, Yang-Rong; Yang, Wei; Zhuang, Jiaxin; Echegoyen, Luis; Chen, Ning
Crystallographic and spectroscopic characterization of a mixed actinide-lanthanide carbide cluster stabilized inside an I<sub>h</sub>(7)-C<sub>80</sub> fullerene cage.
Chemical communications (Cambridge, England), 2020, 56, 3867-3870
7126078 CIFC11 H10 F3 N3 O2P -16.1114; 8.7281; 20.9657
80.025; 89.183; 88.02
1100.73Wagner, Shana; Sudhamalla, Babu; Mannes, Philip; Sappa, Sushma; Kavoosi, Sam; Dey, Debasis; Wang, Sinan; Islam, Kabirul
Engineering bromodomains with a photoactive amino acid by engaging 'Privileged' tRNA synthetases.
Chemical communications (Cambridge, England), 2020, 56, 3641-3644
7126079 CIFC23 H19 F3 N2 Ni O2 SP 1 21/n 16.9629; 27.163; 11.1046
90; 96.72; 90
2085.8Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126080 CIFC30 H30 F N2 Ni O2P 1 2/c 114.4635; 6.9797; 25.786
90; 100.159; 90
2562.3Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126081 CIFC28 H37 N3 Ni O Si2P 1 21/c 111.9534; 13.7247; 17.1253
90; 93.572; 90
2804.1Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126082 CIFC42 H55.5 N4.5 Ni1.5 Si3P 1 21/c 123.5957; 13.6797; 26.9113
90; 101.433; 90
8514.1Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126083 CIFC62 H70 F6 N4 Ni2 O11 S2P -112.8801; 14.0913; 17.4958
81.586; 77.019; 84.657
3055Berkefeld, Andreas; Fröhlich, Markus; Kordan, Mike; Hörner, Gerald; Schubert, Hartmut
Selective metalation of phenol-type proligands for preparative organometallic chemistry.
Chemical communications (Cambridge, England), 2020, 56, 3987-3990
7126084 CIFC55 H63 B N5 O2 Si2 YP 1 21/c 112.054; 22.253; 20.28
90; 93.554; 90
5429Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126085 CIFC70 H68 B Ho N6 O2P 21 21 221.104; 25.522; 11.123
90; 90; 90
5991Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126086 CIFC67 H75 B Ho N8 O2 Si2P -113.665; 14.335; 17.329
95.521; 108.465; 90.85
3201.2Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126087 CIFC75 H73.5 B Ho N7 O2P -115.645; 15.651; 28.55
101.047; 93.207; 90.009
6850Ma, Yan; Zhai, Yuan-Qi; Ding, You-Song; Han, Tian; Zheng, Yan-Zhen
Understanding a pentagonal-bipyramidal holmium(iii) complex with a record energy barrier for magnetisation reversal.
Chemical communications (Cambridge, England), 2020, 56, 3979-3982
7126088 CIFC24 H14 Br N O2P -16.7672; 9.2017; 15.1089
81.431; 82.868; 80.818
913.54Liu, Jing; Ba, Dan; Chen, Yanhui; Wen, Si; Cheng, Guolin
Synthesis of 3-(2-quinolyl) chromones from ynones and quinoline N-oxides via tandem reactions under transition metal- and additive-free conditions.
Chemical communications (Cambridge, England), 2020, 56, 4078-4081
7126089 CIFC22 H16 N2 O2P 1 21/c 19.3098; 10.3197; 18.503
90; 91.529; 90
1777Zhang, Cong-Hai; Huang, Rong; Qing, Xia; Lin, Jun; Yan, Sheng-Jiao
Cascade reaction of isatins with nitro-substituted enamines: highly selective synthesis of functionalized (Z)-3-(1-(arylamino)-2-oxoarylidene)indolin-2-ones.
Chemical communications (Cambridge, England), 2020, 56, 3488-3491
7126090 CIFC72 H94 Mn2 N6P 1 21/n 112.3092; 12.735; 20.557
90; 92.955; 90
3218.2Nguyen, Thao T.; Kim, Jun-Hyeong; Kim, Suyeon; Oh, Changjin; Flores, Marco; Groy, Thomas L.; Baik, Mu-Hyun; Trovitch, Ryan J.
Scope and mechanism of nitrile dihydroboration mediated by a β-diketiminate manganese hydride catalyst.
Chemical communications (Cambridge, England), 2020, 56, 3959-3962
7126091 CIFC40 H30 N2P 1 21/n 113.1968; 17.0333; 19.6066
90; 101.946; 90
4311.82Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126092 CIFC62 H53 Cl6 N3P -113.119; 15.227; 15.449
106.247; 109.671; 101.252
2643.3Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126093 CIFC63 H54 Cl9 N3P -111.337; 20.266; 26.705
71.662; 84.799; 86.827
5798Zhang, Chi; Jiao, Tianyu; Tong, Lu; Wang, Hongye; Pan, Yuanjiang; Li, Hao
High yielding self-assembly favored by preorganization.
Chemical communications (Cambridge, England), 2020, 56, 3903-3906
7126094 CIFC26 H48 Co8 K N8 O12 S2R -3 :H13.4577; 13.4577; 20.3224
90; 90; 120
3187.48Yu, You-Zhu; Guo, Yu-Hua; Zhang, Yan-Ru; Tian, Xiu-Juan; Zhang, Xian-Ming
Tetrahedral μ<sub>4</sub>-chloride and in situ generated octahedral μ<sub>6</sub>-sulfide templating Co<sub>8</sub> complexes with different distortions of the cube.
Chemical communications (Cambridge, England), 2020, 56, 4236-4239
7126095 CIFC26 H51 Cl4 Co8 N5 O12R 3 m :H14.8782; 14.8782; 16.9496
90; 90; 120
3249.3Yu, You-Zhu; Guo, Yu-Hua; Zhang, Yan-Ru; Tian, Xiu-Juan; Zhang, Xian-Ming
Tetrahedral μ<sub>4</sub>-chloride and in situ generated octahedral μ<sub>6</sub>-sulfide templating Co<sub>8</sub> complexes with different distortions of the cube.
Chemical communications (Cambridge, England), 2020, 56, 4236-4239
7126096 CIFC58 H71 Ce F12 K N6 O8P 1 21/c 125.0707; 15.4308; 16.9537
90; 105.921; 90
6307.1Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126097 CIFC109 H124.5 Ce2 Cs2 F12 N14.5 O10P -111.233; 14.495; 20.522
70.871; 75.802; 72.404
2969.3Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126098 CIFC118 H160 Ce2 F12 N12 O10 Rb2P b c n32.651; 17.14; 23.603
90; 90; 90
13209Lapsheva, Ekaterina N.; Cheisson, Thibault; Álvarez Lamsfus, Carlos; Carroll, Patrick J.; Gau, Michael R.; Maron, Laurent; Schelter, Eric J.
Reactivity of Ce(iv) imido compounds with heteroallenes.
Chemical communications (Cambridge, England), 2020, 56, 4781-4784
7126099 CIFC35 H47 N2 O ReP 1 21/n 110.1864; 25.6639; 12.2342
90; 106.406; 90
3068.08Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126100 CIFC34 H47 N4 ReP 1 21/n 113.0017; 17.4412; 13.855
90; 98.992; 90
3103.22Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126101 CIFC43 H56 N3 ReP 1 21/m 19.4458; 19.0455; 10.9694
90; 106.664; 90
1890.52Lohrey, Trevor D.; Fostvedt, Jade I.; Bergman, Robert G.; Arnold, John
Electron acceptors promote proton-hydride tautomerism in low valent rhenium β-diketiminates.
Chemical communications (Cambridge, England), 2020, 56, 3761-3764
7126102 CIFC78 H76 Cu F6 N4 O6 S2P -110.1269; 13.1476; 29.1917
97.319; 96.976; 111.49
3527.03Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126103 CIFC78 H76 Cu F6 N4 O6 S2P -110.249; 13.097; 15.188
72.156; 73.95; 68.985
1779.4Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126104 CIFC46 H36 Cu F6 N4 O6 S2P 111.743; 13.021; 15.225
72.071; 85.436; 89.509
2207.6Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126105 CIFC78 H76 Cu F6 N4 O6 S2P -110.166; 13.051; 15.236
72.382; 74.26; 69.168
1770.1Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126106 CIFC78 H76 Cu F6 N4 O6 S2P -110.2443; 13.0741; 15.129
72.449; 73.851; 69.024
1770.7Kałuża, Adrianna M; Mukherjee, Soumya; Wang, Shi-Qiang; O'Hearn, Daniel J; Zaworotko, Michael J.
[Cu(4-phenylpyridine)<sub>4</sub>(trifluoromethanesulfonate)<sub>2</sub>], a Werner complex that exhibits high selectivity for o-xylene.
Chemical communications (Cambridge, England), 2020, 56, 1940-1943
7126107 CIFC12 H18 Ag3 F2 O2 S2I 21 21 2111.3195; 22.5808; 23.2576
90; 90; 90
5944.7Wang, Jia-Yin; Li, Wen-Hua; Wei, Zhong; Zhang, Chong; Li, Ya-Hui; Dong, Xi-Yan; Xu, Gang; Zang, Shuang-Quan
A hydrophobic semiconducting metal-organic framework assembled from silver chalcogenide wires.
Chemical communications (Cambridge, England), 2020, 56, 2091-2094
7126108 CIFC46 H38 N4P 1 21/c 122.5463; 7.4089; 22.2178
90; 109.269; 90
3503.4Chai, Danyang; Zeng, Xuan; Su, Xiaoxuan; Zhou, Changjiang; Zou, Yang; Zhong, Cheng; Gong, Shaolong; Yang, Chuluo
A simple and effective strategy to lock the quasi-equatorial conformation of acridine by H-H repulsion for highly efficient thermally activated delayed fluorescence emitters.
Chemical communications (Cambridge, England), 2020, 56, 2308-2311
7126109 CIFC45 H37 N5P -16.0216; 15.6695; 18.6718
99.624; 90.21; 95.366
1729Chai, Danyang; Zeng, Xuan; Su, Xiaoxuan; Zhou, Changjiang; Zou, Yang; Zhong, Cheng; Gong, Shaolong; Yang, Chuluo
A simple and effective strategy to lock the quasi-equatorial conformation of acridine by H-H repulsion for highly efficient thermally activated delayed fluorescence emitters.
Chemical communications (Cambridge, England), 2020, 56, 2308-2311
7126110 CIFC26 H25 Br N2 O6 S2P 1 21 18.6142; 15.2562; 10.0113
90; 93.761; 90
1312.9Wu, Ju; Abou-Hamdan, Hussein; Guillot, Régis; Kouklovsky, Cyrille; Vincent, Guillaume
Electrochemical synthesis of 3a-bromofuranoindolines and 3a-bromopyrroloindolines mediated by MgBr<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 1713-1716
7126111 CIFC6 H21 Bi Cl9 N3P -18.181; 11.7216; 11.8724
104.188; 93.217; 108.402
1036.24Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126112 CIFC6 H21 Bi Br6 Cl3 N3P -18.3218; 12.1968; 12.2353
104.697; 108.11; 93.253
1129.25Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126113 CIFC6 H24 Bi Cl6 N3C 1 2/m 121.162; 7.9735; 11.8046
90; 104.186; 90
1931.1Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126114 CIFC6 H21 Bi Cl9 N3C 1 2/m 122.52; 8.2945; 12.1353
90; 106.123; 90
2177.6Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126115 CIFC6 H24 Bi Br6 N3P 1 2/c 111.773; 8.0673; 22.7281
90; 103.72; 90
2097.04Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126116 CIFC6 H24 Bi Br6 N3C 1 2/m 122.444; 8.1886; 11.9852
90; 104.248; 90
2134.9Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126117 CIFC6 H24 Bi I6 N3P 1 21/c 18.952; 29.5398; 11.8481
90; 93.269; 90
3128.02Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126118 CIFC6 Bi Cl3 I6 N3C 1 2/m 126.2181; 8.6303; 13.2652
90; 110.247; 90
2816.1Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126119 CIFC6 Bi Cl3 I6 N3P -18.5701; 12.4903; 12.9228
103.943; 108.815; 93.035
1257.88Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126120 CIFC6 H24 Bi Cl6 N3P 1 2/c 111.5267; 7.8653; 21.5333
90; 103.831; 90
1895.62Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126121 CIFC6 H21 Bi Br6 Cl3 N3C 1 2/m 124.29; 8.274; 12.4821
90; 108.894; 90
2373.4Li, Hui-Hui; Wang, Chang-Feng; Wu, Ya-Xing; Jiang, Fan; Shi, Chao; Ye, Heng-Yun; Zhang, Yi
Halogen substitution regulates the phase transition temperature and band gap of semiconductor compounds.
Chemical communications (Cambridge, England), 2020, 56, 1697-1700
7126122 CIFC25 H24 Cl N SiP -18.346; 9.916; 13.969
86.705; 77.173; 71.341
1067.8Zeng, Ya-Li; Chen, Bo; Wang, Ya-Ting; He, Cheng-Yu; Mu, Zi-Yuan; Du, Ji-Yuan; He, Long; Chu, Wen-Dao; Liu, Quan-Zhong
Copper-catalyzed asymmetric silyl addition to alkenyl-substituted N-heteroarenes.
Chemical communications (Cambridge, England), 2020, 56, 1693-1696
7126123 CIFIn3 La3 O3 S6P m c n3.985; 20.546; 14.8477
90; 90; 90
1215.67Kabbour, Houria; Sayede, Adlane; Saitzek, Sébastien; Lefèvre, Gauthier; Cario, Laurent; Trentesaux, Martine; Roussel, Pascal
Structure of the water-splitting photocatalyst oxysulfide α-LaOInS<sub>2</sub> and ab initio prediction of new polymorphs.
Chemical communications (Cambridge, England), 2020, 56, 1645-1648
7126124 CIFC18 H13 NF d d 238.272; 12.8163; 10.858
90; 90; 90
5325.9Liu, Xiaobing; Sheng, Heyun; Zhou, Yao; Song, Qiuling
Palladium-catalyzed C-H bond activation for the assembly of N-aryl carbazoles with aromatic amines as nitrogen sources.
Chemical communications (Cambridge, England), 2020, 56, 1665-1668
7126125 CIFC30 H20 N2P 21 21 219.0542; 12.4973; 18.9834
90; 90; 90
2148.03Liu, Xiaobing; Sheng, Heyun; Zhou, Yao; Song, Qiuling
Palladium-catalyzed C-H bond activation for the assembly of N-aryl carbazoles with aromatic amines as nitrogen sources.
Chemical communications (Cambridge, England), 2020, 56, 1665-1668
7126126 CIFC42 H36 O2I 1 2/a 112.3667; 16.1708; 15.3924
90; 108.863; 90
2912.85Lin, Wei-Bin; He, Dong-Qiang; Lu, Hai-Yan; Hu, Zhi-Qiang; Chen, Chuan-Feng
Sign inversions of circularly polarized luminescence for helical compounds by chemically fine-tuning operations.
Chemical communications (Cambridge, England), 2020, 56, 1863-1866
7126127 CIFC40 H30 Cl2 O2I 1 2/a 112.4619; 16.5737; 15.2124
90; 103.676; 90
3052.89Lin, Wei-Bin; He, Dong-Qiang; Lu, Hai-Yan; Hu, Zhi-Qiang; Chen, Chuan-Feng
Sign inversions of circularly polarized luminescence for helical compounds by chemically fine-tuning operations.
Chemical communications (Cambridge, England), 2020, 56, 1863-1866
7126128 CIFC108 H68 N4 O40 Zr6C m m m20.7974; 34.3196; 24.2844
90; 90; 90
17333.2Mallick, Arijit; Liang, Hanfeng; Shekhah, Osama; Jia, Jiangtao; Mouchaham, Georges; Shkurenko, Aleksander; Belmabkhout, Youssef; Alshareef, Husam N.; Eddaoudi, Mohamed
Made-to-order porous electrodes for supercapacitors: MOFs embedded with redox-active centers as a case study.
Chemical communications (Cambridge, England), 2020, 56, 1883-1886
7126129 CIFC49 H65 Cl9 N14 O2P -112.9113; 13.8869; 16.5533
102.178; 91.521; 97.504
2871.85Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126130 CIFC56 H54 F6 N12 O2P -110.8092; 14.1679; 17.2034
78.408; 86.646; 86.284
2572.64Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126131 CIFC44 H54 Cl2 N12 O2P -110.7643; 14.0058; 15.9242
89.704; 78.054; 67.659
2165.3Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126132 CIFC25 H30 Cl4 N6 OP -110.3164; 15.7661; 18.2979
68.115; 89.376; 87.542
2759.08Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126133 CIFC22 H31 N7 OP b c a9.8856; 10.418; 42.5525
90; 90; 90
4382.4Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126134 CIFC34 H36 N6 OP -111.2953; 11.412; 13.0664
70.404; 73.213; 70.603
1466.5Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126135 CIFC33 H33 Cl N6 OP -19.1544; 10.8644; 15.5035
72.725; 84.894; 83.984
1461.55Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126136 CIFC32 H35 N7 OP 1 21 16.7885; 7.9643; 26.039
90; 94.113; 90
1404.19Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126137 CIFC32 H37 N7 OP -16.3741; 9.3723; 24.838
83.121; 85.819; 79.949
1448.5Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126138 CIFC33 H33 Cl N6 OP 1 21/n 19.0985; 10.3538; 30.3383
90; 97.525; 90
2833.38Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126139 CIFC30 H32 Cl N7 OP 1 21/n 19.8002; 15.121; 19.4804
90; 90.374; 90
2886.72Abdelraheem, Eman M. M.; Goodwin, Imogen; Shaabani, Shabnam; de Haan, Michel P.; Kurpiewska, Katarzyna; Kalinowska-TÅ‚uÅ›cik, Justyna; Dömling, Alexander
'Atypical Ugi' tetrazoles.
Chemical communications (Cambridge, England), 2020, 56, 1799-1802
7126140 CIFC42 H58 N4P -16.449; 10.347; 13.623
85.979; 84.125; 82.722
895.5Guo, Jing; Cheong, Odelia; Bamford, Karlee L.; Zhou, Jiliang; Stephan, Douglas W.
Frustrated Lewis pair-catalyzed double hydroarylation of alkynes with N-substituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 1855-1858
7126141 CIFC48 H62 Br2 N4P 1 21/n 110.782; 13.431; 15.604
90; 97.24; 90
2241.6Guo, Jing; Cheong, Odelia; Bamford, Karlee L.; Zhou, Jiliang; Stephan, Douglas W.
Frustrated Lewis pair-catalyzed double hydroarylation of alkynes with N-substituted pyrroles.
Chemical communications (Cambridge, England), 2020, 56, 1855-1858
7126142 CIFC23 H23 I N2P 1 21/c 19.759; 14.912; 14.143
90; 104.115; 90
1996Elhussin, Imad Elddin Haj; Zhang, Sijing; Liu, Jiejie; Li, Dandan; Zhang, Qiong; Li, Shengli; Tian, Xiaohe; Wu, Jieying; Tian, Yupeng
A novel water-soluble quinoline-indole derivative as a three-photon fluorescent probe for identifying nucleolus RNA and mitochondrial DNA.
Chemical communications (Cambridge, England), 2020, 56, 1859-1862
7126143 CIFC23 H24 N2 O4 SP 1 21/c 110.532; 13.748; 14.154
90; 92.091; 90
2048Elhussin, Imad Elddin Haj; Zhang, Sijing; Liu, Jiejie; Li, Dandan; Zhang, Qiong; Li, Shengli; Tian, Xiaohe; Wu, Jieying; Tian, Yupeng
A novel water-soluble quinoline-indole derivative as a three-photon fluorescent probe for identifying nucleolus RNA and mitochondrial DNA.
Chemical communications (Cambridge, England), 2020, 56, 1859-1862
7126144 CIFC14 H8 Cl N OP b c a14.7356; 5.75805; 24.963
90; 90; 90
2118.07Shan, Xiang-Huan; Yang, Bo; Qu, Jian-Ping; Kang, Yan-Biao
CuSO<sub>4</sub>-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes.
Chemical communications (Cambridge, England), 2020, 56, 4063-4066
7126145 CIFC14 H8 Br N OP c a 218.28779; 5.59996; 24.2843
90; 90; 90
1127.07Shan, Xiang-Huan; Yang, Bo; Qu, Jian-Ping; Kang, Yan-Biao
CuSO<sub>4</sub>-Catalyzed dual annulation to synthesize O, S or N-containing tetracyclic heteroacenes.
Chemical communications (Cambridge, England), 2020, 56, 4063-4066
7126146 CIFC28 H29 N2 O2 PP 21 21 219.1724; 11.6412; 22.267
90; 90; 90
2377.62Lundrigan, Travis; Tien, Chieh-Hung; Robertson, Katherine N.; Speed, Alexander W. H.
Air and water stable secondary phosphine oxides as diazaphospholene precatalysts.
Chemical communications (Cambridge, England), 2020, 56, 8027-8030
7126147 CIFC H N OP 1 21 114.2375; 4.3802; 15.0293
90; 104.466; 90
907.56Hossain, Munshi Sahid; Rahaman, Sk Atiur; Hatai, Joydev; Saha, Monochura; Bandyopadhyay, Subhajit
Switching the recognition ability of a photoswitchable receptor towards phosphorylated anions.
Chemical communications (Cambridge, England), 2020, 56, 4172-4175
7126148 CIFC2.933 H3.067 Cl0.133 N0.4 O0.867P -111.7556; 13.9168; 14.9786
97.472; 106.582; 110.609
2124.5Hossain, Munshi Sahid; Rahaman, Sk Atiur; Hatai, Joydev; Saha, Monochura; Bandyopadhyay, Subhajit
Switching the recognition ability of a photoswitchable receptor towards phosphorylated anions.
Chemical communications (Cambridge, England), 2020, 56, 4172-4175
7126149 CIFC18 H14 N2 O4P 21 21 218.8208; 11.9769; 14.7126
90; 90; 90
1554.3Zhao, Sihan; Cheng, Shaobing; Liu, Hui; Zhang, Jiayan; Liu, Min; Yuan, Weicheng; Zhang, Xiaomei
Synthesis of chiral [2,3]-fused indolines through enantioselective dearomatization inverse-electron-demand Diels-Alder reaction/oxidation of indoles with 2-(2-nitrovinyl)-1,4-benzoquinone.
Chemical communications (Cambridge, England), 2020, 56, 4200-4203
7126150 CIFC18 H14 N2 O4P 21 21 218.8208; 11.9769; 14.7126
90; 90; 90
1554.3Zhao, Sihan; Cheng, Shaobing; Liu, Hui; Zhang, Jiayan; Liu, Min; Yuan, Weicheng; Zhang, Xiaomei
Synthesis of chiral [2,3]-fused indolines through enantioselective dearomatization inverse-electron-demand Diels-Alder reaction/oxidation of indoles with 2-(2-nitrovinyl)-1,4-benzoquinone.
Chemical communications (Cambridge, England), 2020, 56, 4200-4203
7126151 CIFC19 H33 F6 N2 O9 PP c c n17.7788; 19.721; 15.0786
90; 90; 90
5286.79Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126152 CIFC19 H33 F6 N2 O9 PP c c n16.774; 20; 15.122
90; 90; 90
5073.1Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126153 CIFC20 H33 F3 N2 O12 SP 1 21/c 110.0129; 18.4433; 14.9448
90; 98.44; 90
2729.98Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126154 CIFC20 H33 F3 N2 O12 SP 1 21/c 120.31807; 17.85897; 14.6402
90; 96.2561; 90
5280.7Huang, Rui-Kang; Chen, Xiao-Xian; Xiao, Zhi-Feng; Liu, De-Xuan; Zhang, Wei-Xiong; Chen, Xiao-Ming
Enhancing switchable dielectric property for crystalline supramolecular rotor compounds by adding polar components.
Chemical communications (Cambridge, England), 2020, 56, 4114-4117
7126155 CIFBi Cu O Se2 SrP 1 21/m 17.6529; 4.0559; 9.1405
90; 113.758; 90
259.67Luo, Mengjia; Bu, Kejun; Zhang, Xian; Huang, Jian; Wang, Ruiqi; Huang, Fuqiang
Intrinsically low thermal conductivity in a p-type semiconductor SrOCuBiSe<sub>2</sub> with a [SrO]-intercalated CuBiSe<sub>2</sub> structure.
Chemical communications (Cambridge, England), 2020, 56, 4356-4359
7126156 CIFC29 H27 Cl Mn N5 O3P b c a13.4901; 13.2578; 30.134
90; 90; 90
5389.4Liu, Yi; Guo, Jin-Han; Dao, Xiao-Yao; Zhang, Xiu-Du; Zhao, Yue; Sun, Wei-Yin
Coordination polymers with a pyridyl-salen ligand for photocatalytic carbon dioxide reduction.
Chemical communications (Cambridge, England), 2020, 56, 4110-4113
7126157 CIFC29 H27 Cl Fe N5 O3P b c a13.4819; 13.3393; 30.1323
90; 90; 90
5419Liu, Yi; Guo, Jin-Han; Dao, Xiao-Yao; Zhang, Xiu-Du; Zhao, Yue; Sun, Wei-Yin
Coordination polymers with a pyridyl-salen ligand for photocatalytic carbon dioxide reduction.
Chemical communications (Cambridge, England), 2020, 56, 4110-4113
7126158 CIFC14 H26 Cl O6 P Si3 WP 1 21/c 19.3757; 10.4164; 25.134
90; 93.912; 90
2448.9Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126159 CIFC17 H34 N O6 P Si4 WP 1 21/c 115.8672; 16.5104; 22.0806
90; 91.193; 90
5783.3Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126160 CIFC19 H34 N O7 P Si3 WP 21 21 219.9978; 13.3597; 21.3413
90; 90; 90
2850.5Kunzmann, Robert; Omatsu, Yamato; Schnakenburg, Gregor; Espinosa Ferao, Arturo; Yanagisawa, Tatsuya; Tokitoh, Norihiro; Streubel, Rainer
A synthetic equivalent for unknown 1,3-zwitterions? - A K/OR phosphinidenoid complex with an additional Si-Cl function.
Chemical communications (Cambridge, England), 2020, 56, 3899-3902
7126161 CIFC25 H17 Cd N2 O6P -19.7751; 11.1664; 11.1677
109.183; 114.745; 90.306
1030.98Yang, Xiao-Dong; Ma, Mei-Jing; Pang, Xin-Zhu; Chen, Yun-Rui; Rooney, David; Zhang, Jie
Synergism of photocycloaddition and photoinduced electron transfer for multi-state responsive materials with high-stability and reversibility.
Chemical communications (Cambridge, England), 2020, 56, 4126-4129
7126162 CIFC25 H17 Cd N2 O6P -19.7751; 11.1664; 11.1677
109.183; 114.745; 90.306
1030.98Levine, Andrew M.; Bu, Guanhong; Biswas, Sankarsan; Tsai, Esther H. R.; Braunschweig, Adam B.; Nannenga, Brent L.
Crystal structure and orientation of organic semiconductor thin films by microcrystal electron diffraction and grazing-incidence wide-angle X-ray scattering.
Chemical communications (Cambridge, England), 2020, 56, 4204-4207
7126163 CIFC55 H82 Au B2 K O8 P2P 1 21/c 119.9307; 14.7178; 20.3785
90; 110.812; 90
5587.7Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126164 CIFC61 H88 Au B2 K O7 P2P -111.3469; 13.0442; 21.464
103.942; 95.7811; 101.004
2990.5Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126165 CIFC79.12 H112.34 Au B2 K O11.15 P2P 1 21/c 114.6392; 45.535; 23.842
90; 96.0286; 90
15805Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126166 CIFC50 H72 Au B2 K O8 P2P -110.0837; 14.1067; 18.4824
81.7553; 84.4017; 73.8383
2494.48Taylor, Jordan W.; Harman, W. Hill
C[double bond, length as m-dash]O scission and reductive coupling of organic carbonyls by a redox-active diboraanthracene.
Chemical communications (Cambridge, England), 2020, 56, 4480-4483
7126167 CIFC6 H6 Co3 O12P 1 21/n 111.269; 9.848; 14.466
90; 91.16; 90
1605.1Song, Yoodae; Khudozhitkov, Alexander E.; Lee, Jihyun; Kang, Hyosik; Kolokolov, Daniil I.; Stepanov, Alexander G.; Yoon, Minyoung
Transformation of a proton insulator to a conductor via reversible amorphous to crystalline structure transformation of MOFs.
Chemical communications (Cambridge, England), 2020, 56, 4468-4471
7126168 CIFC6 H6 Mg3 O12P 1 21/n 111.35; 9.864; 14.566
90; 91.4; 90
1630.3Song, Yoodae; Khudozhitkov, Alexander E.; Lee, Jihyun; Kang, Hyosik; Kolokolov, Daniil I.; Stepanov, Alexander G.; Yoon, Minyoung
Transformation of a proton insulator to a conductor via reversible amorphous to crystalline structure transformation of MOFs.
Chemical communications (Cambridge, England), 2020, 56, 4468-4471
7126169 CIFC28 H19 PP 1 21/c 19.0803; 21.343; 21.376
90; 99.849; 90
4081.6Xing, Chang; Liu, Jianxun; Chen, Fang; Li, Yuanyuan; Lv, Changjian; Peng, Qiuchen; Hou, Hongwei; Li, Kai
Diphenyl-1-pyrenylphosphine: photo-triggered AIE/ACQ transition with remarkable third-order nonlinear optical signal change.
Chemical communications (Cambridge, England), 2020, 56, 4220-4223
7126170 CIFC28 H19 O PP 1 21/c 19.042; 21.62; 21.34
90; 100.14; 90
4107Xing, Chang; Liu, Jianxun; Chen, Fang; Li, Yuanyuan; Lv, Changjian; Peng, Qiuchen; Hou, Hongwei; Li, Kai
Diphenyl-1-pyrenylphosphine: photo-triggered AIE/ACQ transition with remarkable third-order nonlinear optical signal change.
Chemical communications (Cambridge, England), 2020, 56, 4220-4223
7126171 CIFC60 H41 F8 N5 O RuP 21 21 2110.8463; 20.3999; 21.4989
90; 90; 90
4756.92Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126172 CIFC64 H54 F8 N6 RuC 1 2/c 128.865; 12.4422; 18.7711
90; 128.307; 90
5290.1Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126173 CIFC66 H44 F8 N6 RuP n n m12.6211; 12.9645; 17.2046
90; 90; 90
2815.12Shing, Ka-Pan; Wan, Qingyun; Chang, Xiao-Yong; Che, Chi-Ming
The first crystallographically characterised ruthenium(vi) alkylimido porphyrin competent for aerobic epoxidation and hydrogen atom abstraction.
Chemical communications (Cambridge, England), 2020, 56, 4428-4431
7126174 CIFC648 H540 Cl0 Eu8 N96 O48P 4/n :238.2; 38.2; 46.77
90; 90; 90
68249Li, Xiao-Zhen; Zhou, Li-Peng; Hu, Shao-Jun; Cai, Li-Xuan; Guo, Xiao-Qing; Wang, Zhuo; Sun, Qing-Fu
Metal ion adaptive self-assembly of photoactive lanthanide-based supramolecular hosts.
Chemical communications (Cambridge, England), 2020, 56, 4416-4419
7126175 CIFC18 H14 F6 N2 O2C 2 2 2110.8529; 12.6448; 13.8015
90; 90; 90
1894Breising, Valentina M.; Kayser, Jacob M.; Kehl, Anton; Schollmeyer, Dieter; Liermann, Johannes C.; Waldvogel, Siegfried R.
Electrochemical formation of N,N'-diarylhydrazines by dehydrogenative N-N homocoupling reaction.
Chemical communications (Cambridge, England), 2020, 56, 4348-4351
7126176 CIFC51 H39 N6 O16 Tb2P n a 2112.071; 33.798; 11.609
90; 90; 90
4736.2Yue, Dan; Wang, Yanyan; Chen, Dong; Wang, Zhenling
Solvent triggering structural changes for two terbium-based metal-organic frameworks and their photoluminescence sensing.
Chemical communications (Cambridge, England), 2020, 56, 4320-4323
7126177 CIFC18 H11 N2 O6 TbP 1 21/c 117.4278; 12.1359; 7.4214
90; 92.644; 90
1567.97Yue, Dan; Wang, Yanyan; Chen, Dong; Wang, Zhenling
Solvent triggering structural changes for two terbium-based metal-organic frameworks and their photoluminescence sensing.
Chemical communications (Cambridge, England), 2020, 56, 4320-4323
7126178 CIFC30 H16 N6I -4 2 d22.3365; 22.3365; 9.9167
90; 90; 90
4947.63Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126179 CIFC16 H10 N4P 1 n 111.6524; 4; 14.3571
90; 92.273; 90
668.65Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126180 CIFC25 H15 Cl3 N4P 21 21 2111.21; 17.1917; 19.618
90; 90; 90
3780.76Otani, Takashi; Sasayama, Takuma; Iwashimizu, Chisaki; Kanyiva, Kyalo Stephen; Kawai, Hidetoshi; Shibata, Takanori
Short-step synthesis and chiroptical properties of polyaza[5]-[9]helicenes with blue to green-colour emission.
Chemical communications (Cambridge, England), 2020, 56, 4484-4487
7126181 CIFC44 H28 N4 S8P -111.4592; 12.9511; 16.7818
67.616; 88.901; 64.349
2044Anderson, Christopher L.; Liang, Jiatao; Teat, Simon J.; Garzón-Ruiz, Andrés; Nenon, David P.; Navarro, Amparo; Liu, Yi
A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 4472-4475
7126182 CIFC22 H16 N2 S4P 1 21/n 15.4963; 10.4093; 17.0568
90; 98.615; 90
964.85Anderson, Christopher L.; Liang, Jiatao; Teat, Simon J.; Garzón-Ruiz, Andrés; Nenon, David P.; Navarro, Amparo; Liu, Yi
A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.
Chemical communications (Cambridge, England), 2020, 56, 4472-4475
7126183 CIFC39 H25 Cl2 N3 O2P -19.4415; 11.5767; 15.2148
91.73; 103.575; 110.232
1505.45Zhang, Liang; Li, Meng; Gao, Qing-Yu; Chen, Chuan-Feng
An ultralong room-temperature phosphorescent material based on the combination of small singlet-triplet splitting energy and H-aggregation.
Chemical communications (Cambridge, England), 2020, 56, 4296-4299
7126184 CIFC38 H23 N3 O2P 4115.82204; 15.82204; 44.7484
90; 90; 90
11202.2Zhang, Liang; Li, Meng; Gao, Qing-Yu; Chen, Chuan-Feng
An ultralong room-temperature phosphorescent material based on the combination of small singlet-triplet splitting energy and H-aggregation.
Chemical communications (Cambridge, England), 2020, 56, 4296-4299
7126185 CIFC59.56 H40 B12 I0.44 N11.57 P2P 1 21/n 114.8599; 14.7377; 15.2073
90; 109.961; 90
3130.3Mayer, Martin; Rohdenburg, Markus; van Lessen, Valentin; Nierstenhöfer, Marc C; Aprà, Edoardo; Grabowsky, Simon; Asmis, Knut R.; Jenne, Carsten; Warneke, Jonas
First steps towards a stable neon compound: observation and bonding analysis of [B<sub>12</sub>(CN)<sub>11</sub>Ne]<sup/>.
Chemical communications (Cambridge, England), 2020, 56, 4591-4594
7126186 CIFC17 H22 B F I N O6P 1 21/c 117.3516; 11.231; 10.6444
90; 106.111; 90
1992.86Zeng, Yao-Fu; Liu, Xu-Ge; Tan, Dong-Hang; Fan, Wen-Xin; Li, Yi-Na; Guo, Yu; Wang, Honggen
Halohydroxylation of alkenyl MIDA boronates: switchable stereoselectivity induced by B(MIDA) substituent.
Chemical communications (Cambridge, England), 2020, 56, 4332-4335
7126187 CIFC14 H17 B Br N O5C 1 2/c 121.4754; 6.47129; 24.0236
90; 114.374; 90
3041.07Zeng, Yao-Fu; Liu, Xu-Ge; Tan, Dong-Hang; Fan, Wen-Xin; Li, Yi-Na; Guo, Yu; Wang, Honggen
Halohydroxylation of alkenyl MIDA boronates: switchable stereoselectivity induced by B(MIDA) substituent.
Chemical communications (Cambridge, England), 2020, 56, 4332-4335
7126188 CIFC150 H130 Cl4 Co3 N24 O24A e a 213.2673; 66.3212; 19.2434
90; 90; 90
16932.3Wang, Hao; Sayed, Sayed Youssef; Zhou, Yuqiao; Olsen, Brian C.; Luber, Erik J.; Buriak, Jillian M.
Water-soluble pH-switchable cobalt complexes for aqueous symmetric redox flow batteries.
Chemical communications (Cambridge, England), 2020, 56, 3605-3608
7126189 CIFC28 H19 N3P 1 21/c 15.182; 16.682; 22.341
90; 95.945; 90
1920.9Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126190 CIFC28 H17 Cl2 N3P 1 21/n 15.421; 15.895; 24.997
90; 94.464; 90
2147Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126191 CIFC28 H17 Br2 N3I 1 2/a 17.5013; 12.4477; 23.8886
90; 95.423; 90
2220.6Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126192 CIFC28 H17 Br2 N3P 1 21/n 15.3634; 15.7657; 25.1499
90; 94.964; 90
2118.64Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126193 CIFC29.75 H19 Br2 N3P 1 21/n 119.6547; 5.3445; 43.593
90; 97.224; 90
4542.9Ishi-I, Tsutomu; Tanaka, Honoka; Park, In Seob; Yasuda, Takuma; Kato, Shin-Ichiro; Ito, Mitsunori; Hiyoshi, Hidetaka; Matsumoto, Taisuke
White-light emission from a pyrimidine-carbazole conjugate with tunable phosphorescence-fluorescence dual emission and multicolor emission switching.
Chemical communications (Cambridge, England), 2020, 56, 4051-4054
7126194 CIFC12 H22 N10 O18 ThP b c n9.8581; 18.755; 14.3424
90; 90; 90
2651.75Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126195 CIFC8 H12 N6 O8 UP -17.5785; 7.5951; 7.6538
117.032; 102.909; 92.179
377.53Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126196 CIFC6 H8 N6 O8 UP 1 21/n 19.1942; 5.8616; 12.1915
90; 91.678; 90
656.75Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126197 CIFC16 H25 N13 O15 ThC 1 2/c 115.7287; 12.981; 14.2585
90; 98.8468; 90
2876.6Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126198 CIFC6 H11 N5 O11 UP 1 21/c 18.5201; 9.1476; 20.323
90; 97.003; 90
1572.1Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126199 CIFC12 H22 N10 O18 ThP c c n9.7722; 11.8036; 23.0503
90; 90; 90
2658.79Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126200 CIFC21 H23 N10 O19 U2P -111.52; 12.224; 12.375
88.974; 72.739; 85.516
1659.1Kelley, Steven P.; Smetana, Volodymyr; Emerson, Stephen D.; Mudring, Anja-Verena; Rogers, Robin D.
Benchtop access to anhydrous actinide N-donor coordination complexes using ionic liquids.
Chemical communications (Cambridge, England), 2020, 56, 4232-4235
7126201 CIFC16 H13 Br Fe N4 O3P -18.045; 8.9535; 12.195
96.322; 91.386; 92.148
872.11Wright, Mark A.; Wooldridge, Tyler; O'Connell, Maria A; Wright, Joseph A.
Ferracyclic carbonyl complexes as anti-inflammatory agents.
Chemical communications (Cambridge, England), 2020, 56, 4300-4303
7126202 CIFC39 H51 Fe2 N4 O20.5 S2C 1 2 123.8608; 13.3771; 15.4092
90; 101.705; 90
4816.2Wright, Mark A.; Wooldridge, Tyler; O'Connell, Maria A; Wright, Joseph A.
Ferracyclic carbonyl complexes as anti-inflammatory agents.
Chemical communications (Cambridge, England), 2020, 56, 4300-4303
7126203 CIFC39 H24 Cl4 N2 OI b a 238.6912; 13.8512; 12.528
90; 90; 90
6714Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126204 CIFC20 H26 Br Cl2 N2 O2 RhP b c n29.056; 9.526; 33.069
90; 90; 90
9153Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126205 CIFC38 H25 Br N2P b c a21.018; 10.048; 27.166
90; 90; 90
5737Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126206 CIFC20 H21 Br Cl N2 RhP -18.968; 11.141; 11.249
65.119; 83.659; 80.437
1004.4Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126207 CIFC34 H31 Br Cl N2 RhP 1 21/c 111.4817; 20.8558; 14.978
90; 111.615; 90
3334.4Wu, Shaonan; Wang, Zhuo; Bao, Yinwei; Chen, Chen; Liu, Kun; Zhu, Bolin
A novel approach for rhodium(iii)-catalyzed C-H functionalization of 2,2'-bipyridine derivatives with alkynes: a significant substituent effect.
Chemical communications (Cambridge, England), 2020, 56, 4408-4411
7126208 CIFC3 H10 N4 O3P 1 21/c 19.1606; 9.7305; 7.8691
90; 102.839; 90
683.89Guan, Ruifang; Dong, Baoli; Xu, Cui; Zhang, Hao; Cao, Duxia; Lin, Weiying
A strategy to construct fluorescent non-aromatic small-molecules: hydrogen bonds contributing to the unexpected fluorescence.
Chemical communications (Cambridge, England), 2020, 56, 4424-4427
7126209 CIFC14 H16 O2P 21 21 218.4235; 10.6627; 12.6898
90; 90; 90
1139.76Zhou, Pan; Xu, Tao
Nickel-catalyzed intramolecular desymmetrization addition of aryl halides to 1,3-diketones.
Chemical communications (Cambridge, England), 2020, 56, 8194-8197
7126210 CIFC44 H46 Fe N2 O2P 1 21/c 117.7; 10.2249; 20.534
90; 101.099; 90
3646.7Kephart, Jonathan A.; Hecht, Zachary; Livesay, Brooke N.; Bhowmick, Indrani; Shores, Matthew P.; Popescu, V. Codrina; Arulsamy, Navamoney; Hulley, Elliott B.
Self-assembly of an organometallic Fe<sub>9</sub>O<sub>6</sub> cluster from aerobic oxidation of (tmeda)Fe(CH<sub>2</sub><sup>t</sup>Bu)<sub>2</sub>.
Chemical communications (Cambridge, England), 2020, 56, 4994-4997

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