Crystallography Open Database

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7134623 CIFC56 H40 N4P n a 2115.903; 28.781; 8.8898
90; 90; 90
4068.9Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134624 CIFC55 H38 N4C m c 2130.1235; 14.8515; 8.8086
90; 90; 90
3940.78Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134625 CIFC66 H48 N4P 1 21/c 129.0124; 9.1087; 19.0026
90; 107.111; 90
4799.45Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134626 CIFC56 H40 N4P 1 21 115.4109; 8.6328; 16.4219
90; 111.528; 90
2032.34Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134627 CIFC56 H64 O12P 1 21/n 110.0684; 17.5734; 26.7319
90; 96.356; 90
4700.8Gharpure, Santosh J.; Gupta, Krishna S.; Yadav, Rakhi
Lewis acid-promoted cascade reactions of cyclopropenes: a unified approach to stereoselective synthesis of cyclic ethers and oxaspirolactones
Chemical Communications, 2025, 61, 9705-9708
7134628 CIFC10 H15 N11 O5P -16.616; 9.4274; 12.6888
81.897; 87.036; 79.394
769.86Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134629 CIFC21 H39 N23 O8P 1 21/n 113.9342; 14.6464; 16.6514
90; 98.281; 90
3362.88Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134630 CIFC8 H10 N10 O7P 1 21/c 15.1692; 19.0438; 13.7975
90; 96.071; 90
1350.63Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134631 CIFC5 H10 Cl2 N10 O8P -18.2784; 9.1672; 9.3028
92.785; 90.887; 103.678
684.89Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134632 CIFC81 H119 I S2 UP -113.4289; 14.022; 21.405
85.41; 73.355; 80.472
3806.1Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134633 CIFC72 H98 K S2 UP 1 21/n 114.272; 19.9414; 24.2485
90; 98.185; 90
6830.9Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134634 CIFC72 H98 S2 UP -19.864; 17.52; 20.169
87.762; 84.587; 85.962
3460Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134635 CIFC92 H124 N2 O2 S2 UC 1 2/c 130.491; 18.735; 18.433
90; 113.138; 90
9683Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134636 CIFC26 H25 Cl2 Cu N3 O6P -19.1916; 11.5805; 13.772
70.993; 85.658; 72.744
1323.3Dutta, Lesa; Das, Avijit; Hasan, Babar; Paria, Sayantan; Mondal, Dhrubajyoti
Comparing electrocatalytic and chemical oxygen reduction reaction by a molecular copper complex
Chemical Communications, 2025, 61, 10158-10161
7134637 CIFC52 H51 Cl6 Cu2 N6 O22C 1 c 112.8921; 16.3316; 29.441
90; 96.406; 90
6160.1Dutta, Lesa; Das, Avijit; Hasan, Babar; Paria, Sayantan; Mondal, Dhrubajyoti
Comparing electrocatalytic and chemical oxygen reduction reaction by a molecular copper complex
Chemical Communications, 2025, 61, 10158-10161
7134638 CIFC25 H23 N O SeP -19.2189; 10.9073; 11.3585
97.835; 101.293; 106.079
1053.97MohanaKrishna, Silari; Prasad, Vadla Shiva; Ranga Rao, Vadithya; Ravi, Dharavath; Kumar, Chelukalapally Anil; Adiyala, Praveen Reddy
Stereoselective synthesis of chalcogen-tethered <i>γ</i>-lactams <i>via</i> 5-<i>exo-dig</i> cyclisation under visible-light irradiation.
Chemical communications (Cambridge, England), 2025, 61, 10363-10366
7134639 CIFC36 H55 Al N2P 1 21/n 110.4055; 25.6624; 12.8303
90; 103.621; 90
3329.7Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134640 CIFC30 H43 Al N2A e m 215.6163; 22.5091; 7.737
90; 90; 90
2719.6Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134641 CIFC28 H39 Al N2P 21 21 2116.5787; 20.7155; 29.815
90; 90; 90
10239.5Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134642 CIFC50 H54 O4 P2P 1 21 15.7275; 20.7047; 17.3578
90; 91.347; 90
2057.8Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134643 CIFC15 H13 N O2 SC 1 2/c 113.5806; 13.6; 14.5161
90; 101.264; 90
2629.4Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134644 CIFC21 H19 N O5P 1 21/c 118.065; 7.471; 13.402
90; 97.245; 90
1794.34Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134645 CIFC21 H17 N O3 SP -19.7767; 13.9453; 14.5788
103.754; 99.474; 108.72
1764.7Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134646 CIFC82 H78 Fe2 N2 P6P 1 21/c 122.7264; 15.2574; 21.1376
90; 108.97; 90
6931.3Smythe, Nathan C.; Mondal, Joydeb; Duque, Juan G.; Feller, Russell K.; Flores, Marco; Gordon, John C.; Henson, Neil J.; Paz-Pasternak, Moshe; Rein, Francisca N.; Scott, Brian L.; Taylor, R. Dean; Trovitch, Ryan J.
Historical account of dinitrogen-bridged diiron complex synthesis using a commercial tripodal ligand
Chemical Communications, 2025, 61, 9908-9911
7134647 CIFC9 H19 B11 Cl11 F6 N O4 S2 Si2P -115.9754; 16.3642; 17.2574
71.799; 72.239; 62.887
3743.54Daum, Joshua H.; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Structure and reactivity of a triflimide-bridged bis(trimethylsilyl) cation.
Chemical communications (Cambridge, England), 2025, 61, 10816-10818
7134648 CIFC29 H39 Mo N3 O3 P2C 1 c 112.2585; 21.027; 11.8947
90; 102.628; 90
2991.8Benedict, Rory J.; Heiden, Zachariah M.; Stephens, David N.; Arulsamy, Navamoney; Mock, Michael T.
Catalytic NH<sub>3</sub> oxidation to N<sub>2</sub> by hydrogen atom abstraction using a low-valent molybdenum complex.
Chemical communications (Cambridge, England), 2025, 61, 10315-10318
7134649 CIFC33 H44 F Mo N3 O3 P2P 1 21/c 114.868; 13.21; 18.026
90; 108.924; 90
3349.1Benedict, Rory J.; Heiden, Zachariah M.; Stephens, David N.; Arulsamy, Navamoney; Mock, Michael T.
Catalytic NH<sub>3</sub> oxidation to N<sub>2</sub> by hydrogen atom abstraction using a low-valent molybdenum complex.
Chemical communications (Cambridge, England), 2025, 61, 10315-10318
7134650 CIFC30 H21 N OP 1 21/c 19.762; 19.29; 13.15
90; 110.326; 90
2322.1Ghosh, Suman; Rooj, Arnab; Deb, Shreya; Ganesh, Venkataraman
Cu<sup>(I)</sup>/Pd<sup>(0)</sup> cooperative catalysis enabled regioselective C(sp<sup>2</sup>)-carboboration of 1,3-diynes.
Chemical communications (Cambridge, England), 2025, 61, 10323-10326
7134651 CIFC20 H20 Cl In N2 O4P 1 21/c 113.5529; 7.6912; 19.3672
90; 106.088; 90
1939.74Baumeyer, Oliver; Wu, Andrew; Pandya, Aastha; Nelson, Peter; Hillesheim, Patrick C.; Zeller, Matthias; Carignan, Gia M.; Li, Jing; Ki, Daniel W.
Aggregation-induced emission-active indium complex as fluorescent turn-off chemosensor for perfluoroalkyl substances
Chemical Communications, 2025, 61, 10170-10173
7134652 CIFC28 H34 I2 N2 O2C 1 2/c 131.5672; 4.6473; 18.6492
90; 101.217; 90
2683.62Skonieczny, Kamil; Kielesiński, Łukasz; Grzybowski, Marek; Gryko, Daniel T.
Polysubstitution of dipyrrolonaphthyridinediones as a potent strategy towards strongly emitting fluorophores
Chemical Communications, 2025, 61, 10178-10181
7134653 CIFC28 H34 Br2 N2 O2P -14.5767; 9.1416; 16.102
74.174; 89.89; 76.786
629.67Skonieczny, Kamil; Kielesiński, Łukasz; Grzybowski, Marek; Gryko, Daniel T.
Polysubstitution of dipyrrolonaphthyridinediones as a potent strategy towards strongly emitting fluorophores
Chemical Communications, 2025, 61, 10178-10181
7134654 CIFC16 H20 Li N2 O2C 1 2/c 128.5128; 11.9757; 20.7828
90; 118.145; 90
6257.4Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134655 CIFC16 H20 Li N2 O2C 1 2/c 114.939; 5.9609; 18.837
90; 101.844; 90
1641.7Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134656 CIFC12 H12 N2 Na OC 1 2/c 120.749; 9.4724; 11.9937
90; 101.2; 90
2312.4Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134657 CIFC12 H32 Ag5 I7 N2P 3212.1737; 12.1737; 19.4498
90; 90; 120
2496.3Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134658 CIFC12 H32 Ag5 I7 N2P 3212.0472; 12.0472; 19.178
90; 90; 120
2410.5Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134659 CIFC12 H32 Ag5 I7 N2P 3112.0456; 12.0456; 19.1296
90; 90; 120
2403.8Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134660 CIFC31 H17 Br Cl2 O2C 1 2 143.9803; 8.1757; 14.3605
90; 105.417; 90
4977.8Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134661 CIFC35 H36 N O7P 4316.7397; 16.7397; 10.5216
90; 90; 90
2948.34Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134662 CIFC32 H31 N O7P 1 21/c 18.2745; 33.3961; 10.3175
90; 104.258; 90
2763.27Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134663 CIFC32 H29 N O7P -110.3074; 10.562; 12.7619
102.425; 99.324; 101.043
1301.4Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134664 CIFC32 H29 Cl2 N O6P 1 21 17.0286; 19.9167; 10.5748
90; 103.574; 90
1438.98Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134665 CIFC33 H29 Cl2 N O4P 17.2896; 9.999; 10.356
90.903; 104.271; 97.532
724.321Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134666 CIFC32 H29 F O5P 1 21/c 110.7735; 28.0445; 8.8667
90; 104.427; 90
2594.48Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134667 CIFC62 H58 N2 O16P 1 21/n 122.0372; 9.6693; 26.7286
90; 110.983; 90
5317.76Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134668 CIFC32 H29 N O7P 21 21 2110.51673; 11.3459; 22.2044
90; 90; 90
2649.47Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134669 CIFC31 H28 Br2 O5P 1 21/c 114.4532; 14.9913; 12.6854
90; 101.185; 90
2696.37Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134670 CIFC35 H25 N O4P -18.6029; 12.5447; 12.7442
75.647; 81.569; 89.219
1317.67Yu, Rongjing; Xia, Ting; Shen, Ruwei; Zhu, Shugao
Diastereoselective synthesis of succinimide-fused polycycles <i>via</i> intermolecular interception of indanone-allene intermediates with maleimides.
Chemical communications (Cambridge, England), 2025, 61, 10335-10338
7134671 CIFC45 H32 N2 O6P 1 21/c 112.264; 25.385; 13.1328
90; 93.156; 90
4082.3Yu, Rongjing; Xia, Ting; Shen, Ruwei; Zhu, Shugao
Diastereoselective synthesis of succinimide-fused polycycles <i>via</i> intermolecular interception of indanone-allene intermediates with maleimides.
Chemical communications (Cambridge, England), 2025, 61, 10335-10338
7134672 CIFC100 H107 Si4P 1 21 112.922; 20.382; 16.403
90; 92.435; 90
4316.3Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134673 CIFC216 H253.84 N8 Si8P 1 21/n 115.836; 14.482; 21.301
90; 91.927; 90
4882Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134674 CIFC105.49 H114.49 Cl2.7 O4.26 Si4P 112.6006; 14.1684; 15.1207
71.243; 73.484; 75.284
2411Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134675 CIFC111.05 H112.8 Cl11.07 O4 Si4P -110.9872; 13.9513; 18.9119
72.067; 86.454; 81.331
2726.2Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134676 CIFC8 H5 Cl4 FP 1 21/n 19.8894; 6.0908; 16.5497
90; 96.434; 90
990.58Miele, Margherita; Castiglione, Davide; Prado-Roller, Alexander; Castoldi, Laura; Pace, Vittorio
Geminal homologative fluorination of carbonyl derivatives <i>en route</i> to 1-fluoro-2-haloethyl skeletons.
Chemical communications (Cambridge, England), 2025, 61, 10792-10795
7134677 CIFC14 H36 Cl4 Cu N2P -17.1278; 7.5; 20.0179
96.906; 91.564; 90.184
1061.94Kusumoto, Sotaro; Nagasawa, Sakura; Suzuki, Ryo; Tachibana, Masaru; Tsuji, Yuta; Zenno, Hikaru; Nakashima, Yuto; Hayami, Shinya; Kim, Yang; Koide, Yoshihiro
Ferromagnetic and plastically deformable organic-inorganic hybrid crystal: (C<sub>7</sub>H<sub>9</sub>NH<sub>3</sub>)<sub>2</sub>CuCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10303-10306
7134678 CIFC12 H32 Cl6 N2 SnP n m a12.3494; 7.306; 26.6362
90; 90; 90
2403.24Kusumoto, Sotaro; Nagasawa, Sakura; Suzuki, Ryo; Tachibana, Masaru; Tsuji, Yuta; Zenno, Hikaru; Nakashima, Yuto; Hayami, Shinya; Kim, Yang; Koide, Yoshihiro
Ferromagnetic and plastically deformable organic-inorganic hybrid crystal: (C<sub>7</sub>H<sub>9</sub>NH<sub>3</sub>)<sub>2</sub>CuCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10303-10306
7134679 CIFC28 H23 N O3P 1 21/c 113.893; 20.91; 7.841
90; 100.45; 90
2240Hu, Kai; Wu, Haijian; Sun, Manman; Zhang, Jing; Wang, Zhiming; Yang, Jianguo; Zhu, Gangguo; Huang, Guo-Bo
HFIP-promoted synthesis of bicyclo[2.1.1]-hexanes through formal [2π+2σ] cycloaddition of bicyclo[1.1.0]butanes with α-cyano chalcones.
Chemical communications (Cambridge, England), 2025, 61, 10375-10378
7134680 CIFC37 H64 O8 SiP 21 21 217.3169; 13.642; 38.8677
90; 90; 90
3879.7Sennari, Goh; Watanabe, Akito; Ōno, Takanori; Oshita, Jun; Noguchi, Yoshihiko; Hirose, Tomoyasu; Sunazuka, Toshiaki
Macrocyclic skeletal modification approach to the anti-trypanosomal macrolides, actinoallolides.
Chemical communications (Cambridge, England), 2025, 61, 10367-10370
7134681 CIFC49 H74 Cu N12 O10P 1 21 17.0448; 24.6484; 15.2708
90; 94.92; 90
2641.9Kieninger, Christoph; Wurst, Klaus; Leitner, Daniel; Peters, Luis P.; Dinu, Dennis F.; Wiedemair, Markus; Zaretzke, Marc-Kevin; Bröring, Martin; Hohloch, Stephan; Liedl, Klaus R.; Kräutler, Bernhard
Encasing the paramagnetic copper(II)-ion by the ring-contracted corrin ligand of vitamin B<sub>12</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10606-10609
7134682 CIFC14 H14 Cl N5 Pt SP 1 21/n 111.3054; 8.7072; 15.9931
90; 101.726; 90
1541.48Sheernaly, Nandan; Steinbrueck, Axel; Ochs, Jasmine; Peeters, Frank; Fiedler, Ronja; Narberhaus, Franz; Heinen-Weiler, Jacqueline; Metzler-Nolte, Nils
Design and application of a non-toxic platinum derivative of the metal chelator Dp44mT for use as a long-term stable lysosome tracker
Chemical Communications, 2025, 61, 9964-9967
7134683 CIFC25 H42 O3 SiP 21 21 219.6772; 10.2693; 24.1618
90; 90; 90
2401.15Chen, Louxi; Zhang, Chao-Han; Liu, Junyang; Li, Chuang-Chuang
Asymmetric synthesis of venezuelaene's core with a <i>trans</i>-fused [5-5] ring system.
Chemical communications (Cambridge, England), 2025, 61, 10823-10826
7134684 CIFC26 H44 O3 SiP 111.0269; 11.0409; 12.3804
75.509; 65.961; 67.425
1263.2Chen, Louxi; Zhang, Chao-Han; Liu, Junyang; Li, Chuang-Chuang
Asymmetric synthesis of venezuelaene's core with a <i>trans</i>-fused [5-5] ring system.
Chemical communications (Cambridge, England), 2025, 61, 10823-10826
7134685 CIFC54 H55 B2 FP 1 21/n 18.4189; 21.0396; 12.3265
90; 92.698; 90
2180.98Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134686 CIFC56 H56 B2 Cl6 F2P -18.5609; 12.651; 13.4008
64.065; 78.326; 88.076
1275.71Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134687 CIFC54 H52 B2 F4P -18.8671; 9.2255; 14.6132
73.047; 76.892; 77.113
1097.76Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134688 CIFC28 H22 F2 N2 S2P 1 21/c 111.294; 22.7558; 9.1549
90; 92.8389; 90
2349.96Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134689 CIFC32 H30 F2 N2 S2C 1 2/c 119.0612; 12.1912; 13.5755
90; 121.113; 90
2700.86Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134690 CIFC34 H34 F2 N2 S2P 1 21/n 114.523; 10.6398; 19.0421
90; 91.6399; 90
2941.21Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134691 CIFC30 H26 F2 N2 S2C 1 2/c 119.4157; 10.9681; 13.8257
90; 121.068; 90
2521.9Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134692 CIFC30 H26 F2 N2 S2P b c n21.4133; 13.7635; 8.963
90; 90; 90
2641.59Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134693 CIFC44 H54 F2 N2 S2P -111.6733; 13.4099; 13.521
76.6459; 74.539; 85.3589
1984.37Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134694 CIFC15 H20 N2 O2 SiP 1 21/c 16.99957; 18.62104; 12.07918
90; 90.6114; 90
1574.3Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134695 CIFC18 H16 N2 O2I 1 2/a 113.24004; 11.03585; 20.65862
90; 91.2541; 90
3017.81Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134696 CIFC20 H21 N3 O2P -112.27152; 12.39856; 12.5695
90.248; 91.2744; 109.745
1799.41Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134697 CIFC18 H15 N3 O4P 1 21/c 119.7442; 6.9809; 11.8207
90; 93.323; 90
1626.53Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134698 CIFC15 H19 N3 O4 SiP 1 21/c 115.2895; 10.2141; 10.8354
90; 93.648; 90
1688.72Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134699 CIFC20 H20 N4 O4I 1 2/a 112.63828; 12.14363; 24.6829
90; 90.3855; 90
3788.11Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134700 CIFC16 H15 N OP b c n10.8676; 11.428; 41.042
90; 90; 90
5097.21Li, Wenguang; Yu, Yongqi; Sheng, Heyun; Cao, Man; Chen, Ming; Gao, Wenchao; Zhang, Xu; Su, Fengyun; Li, Ting
Synthesis of cyclopropanes <i>via</i> palladium-catalyzed [2+1] annulations of sulfoxonium ylides and norbornenes.
Chemical communications (Cambridge, England), 2025, 61, 10835-10838
7134701 CIFC70 H40 O18 Th3P -110.1687; 11.9584; 25.02
91.179; 95.315; 90.783
3028.4Yang, Junpu; Bai, Yaoyao; Zhang, Guangtao; Ma, Jingqi; Lin, Jian
From separation to photothermal conversion: selective crystallization of thorium from lanthanides.
Chemical communications (Cambridge, England), 2025, 61, 10776-10779
7134702 CIFC13 H9 N3 O2P -17.2977; 13.0084; 13.3204
63.202; 85.744; 78.104
1104.22Ishu, Km; Singh, Krishna Nand
Copper(II)-mediated metalloradical activation: denitrogenative/decarboxylative annulation to 3-arylimidazo[1,2-<i>a</i>]pyridines using tetrazolo[1,5-<i>a</i>]pyridines and cinnamic acids.
Chemical communications (Cambridge, England), 2025, 61, 10847-10850
7134703 CIFC101 H191.49 Cr7 F8 N2 Ni O33.24P 21 21 2119.4235; 21.7382; 31.1018
90; 90; 90
13132.2Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134704 CIFC134 H128 Cr7 F8 N Ni O32C 1 2/c 124.0332; 24.0911; 23.763
90; 94.616; 90
13713.8Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134705 CIFC102 H88 Cr7 F8 N9 Ni O48P n m a26.8743; 27.944; 16.9778
90; 90; 90
12749.9Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134706 CIFC206 H176 Cr7 F8 N Ni O40P 21 21 231.9625; 17.1553; 16.9723
90; 90; 90
9306.4Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134707 CIFC251 H343.5 Cr7 F8 N19.5 Ni O80P 4/n c c :226.7607; 26.7607; 40.561
90; 90; 90
29047Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134708 CIFC86 H160 Cr7 F8 N Ni O32P 1 21/c 119.1697; 29.3283; 20.8382
90; 104.138; 90
11360.7Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134709 CIFC102 H188 Cr7 F8 N Ni O32P -119.0912; 22.0288; 30.5452
90.1198; 90.1205; 106.277
12331Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134710 CIFC73 H90 N4 O18 S2P -113.938; 16.892; 18.001
77.27; 68.987; 75.532
3790.6Zhang, Ting; Wang, Lulu; Li, Hui; Sun, Mingxia; Chen, Jia; Guan, Shuzhe; Qiu, Hongdeng
Pillar[5]arene-based ionic single crystals formed by dual self-assemblies through host-guest and ionic interactions for iodine capture.
Chemical communications (Cambridge, England), 2025, 61, 10843-10846
7134711 CIFC64 H54 Cu4 N2 O4 P4 S2P n a 2118.91; 21.16; 14.44
90; 90; 90
5778Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134712 CIFC15 H52 B40 Cu4 S4P -112.25; 13.32; 16.05
97.18; 110.76; 99.99
2361.8Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134713 CIFC8 H44 B40 Cu4 S4P 32 2 111.3; 11.3; 29.05
90; 90; 120
3212.4Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134714 CIFC8 H44 B40 Cu4 S4P 32 2 111.31; 11.31; 29.08
90; 90; 120
3221.4Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134715 CIFC3 H3 Ga I3 N O2P c a 2124.5086; 6.6842; 6.5526
90; 90; 90
1073.45He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134716 CIFC14 H22 I6 In2 N2 O4P -18.2731; 11.0036; 17.2172
104.905; 90.308; 94.684
1508.99He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134717 CIFC16 H17 Cl9 Ga3 N3 O6C 1 2/c 143.189; 6.5024; 30.529
90; 134.875; 90
6075.6He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134718 CIFC25 H11 B F15 N O2P 1 21/c 115.7995; 9.9144; 19.6671
90; 111.532; 90
2865.7He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134719 CIFC7 H11 Br3 In N O2P 1 21/c 18.0413; 20.3742; 8.1155
90; 100.43; 90
1307.63He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134720 CIFC26.88 H27.38 N1.62 O7.62I 1 2/c 124.5252; 7.1491; 30.553
90; 106.418; 90
5138.5Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Fan, Weidong; Sun, Daofeng
Steric hindrance regulation in hydrogen-bonded organic frameworks: from nonporous to microporous.
Chemical communications (Cambridge, England), 2025, 61, 10538-10541
7134721 CIFC25 H23 N O8P 1 21/c 112.0307; 22.7887; 8.6147
90; 100.092; 90
2325.3Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Fan, Weidong; Sun, Daofeng
Steric hindrance regulation in hydrogen-bonded organic frameworks: from nonporous to microporous.
Chemical communications (Cambridge, England), 2025, 61, 10538-10541
7134722 CIFC28 H23 N5P 1 21/c 111.901; 8.437; 23.343
90; 95.41; 90
2333.4Kumari, Akanksha; Jain, Anshul; Sharma, Himani; Sermadurai, Selvakumar; Rana, Nirmal K.
Catalyst-free efficient synthesis of functionalized 1,2,4-triazole <i>via</i> ring opening/cyclization of arylidene thiazolone with aryl/alkyl-hydrazine.
Chemical communications (Cambridge, England), 2025, 61, 11029-11032
7134723 CIFC21 H27 F3 N2 O7 SP 1 21/n 19.6415; 10.1608; 24.945
90; 95.477; 90
2432.6Liu, Shuai; Ge, Yongqi; Li, Jianan; Sheng, Xiaoyu; Zhang, Tian-Shu; Wu, Qiong; Ding, Weijie; Cheng, Xu
Electrochemical site-selective C(sp<sup>3</sup>)-H amination of alkyl substituted indoles and pyrroles.
Chemical communications (Cambridge, England), 2025, 61, 11045-11048
7134724 CIFC21 H27 Br O3P 1 21 110.3749; 8.4178; 11.3443
90; 100.01; 90
975.66Roy, Nanda Kishore; Murmu, Ranjit; Munda, Mintu; Niyogi, Sovan; Bisai, Alakesh
Asymmetric total syntheses of immunosuppressive diterpenoids triptobenzenes N and R <i>via</i> a remote Csp<sup>3</sup>-H functionalization.
Chemical communications (Cambridge, England), 2025, 61, 11053-11056
7134725 CIFC21 H26 O3P 1 21 18.3186; 10.0507; 10.7125
90; 99.133; 90
884.29Roy, Nanda Kishore; Murmu, Ranjit; Munda, Mintu; Niyogi, Sovan; Bisai, Alakesh
Asymmetric total syntheses of immunosuppressive diterpenoids triptobenzenes N and R <i>via</i> a remote Csp<sup>3</sup>-H functionalization.
Chemical communications (Cambridge, England), 2025, 61, 11053-11056
7134726 CIFC108 H84 Eu2 N2 O20P -111.8861; 15.3328; 19.6363
91.069; 94.535; 103.539
3465.77Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134727 CIFC107 H81 Ce2 N2 O20P -112.0155; 15.2802; 19.6685
91.682; 94.913; 102.427
3509.32Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134728 CIFC105.1 H75.9 N2 O19.6 Tb2P -111.7036; 15.2043; 19.7918
91.859; 94.475; 103.284
3412.6Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134729 CIFC17 H14 F N O4 SP -19.4933; 9.7205; 9.7983
89.993; 77.842; 70.533
830.96Zhang, Sen; Fayad, Eman; Katouah, Hanadi A.; Huang, Yi-Yong; Qin, Hua-Li
Oxidative [3+2] annulation of activated pyridines for the synthesis of indolizinyl sulfonyl fluorides: a class of important pharmacophores.
Chemical communications (Cambridge, England), 2025, 61, 10586-10589
7134730 CIFC108 H108 Cl6 N24 Zn6P -115.458; 19.827; 22.137
97.02; 106.2; 99.82
6316Kim, Jisu; Jeong, Hye Jin; Min, Sein; Kim, Sarah; Baek, Juhee; Kim, Jaelim; Lee, Eunsung; Oh, Sangwon; Jeong, Keunhong
Parahydrogen-induced hyperpolarization of a Zn(II) complex using NMR signal amplification by reversible exchange (SABRE).
Chemical communications (Cambridge, England), 2025, 61, 11061-11064
7134731 CIFC69 H102 B2 Cl2 N16P 1 21/c 17.6519; 18.4389; 28.0176
90; 95.393; 90
3935.58Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134732 CIFC64 H109 B N5 PP 1 21/n 112.1405; 27.056; 20.237
90; 95.591; 90
6615.7Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134733 CIFC218.75 H318 B6 Mg3 N48 O6R -3 :H41.4755; 41.4755; 11.7891
90; 90; 120
17562.8Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134734 CIFC104 H164 B3 Cl2 N8P 1 c 114.1177; 18.5164; 20.8008
90; 104.244; 90
5270.3Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134735 CIFC160 H98 Ag10 Cl2 Cu4 F60 O15 P4 S12P -118.7192; 19.3113; 25.7905
89.531; 89.166; 85.539
9293.6Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134736 CIFC159.73 H96.91 Ag14 Cl2 F60 O14.73 P4 S12P 1 21/c 119.3202; 19.1149; 49.181
90; 95.395; 90
18082.3Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134737 CIFC165.5 H116 Ag12 Cl6 Cu2 F60 O18.5 P4 S12P -118.7706; 19.9187; 25.5916
89.783; 88.666; 87.693
9558Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134738 CIFC19 H16 N2 O4P 21 21 216.0468; 13.3298; 19.6186
90; 90; 90
1581.3Paul, Pratap; Dash, Jyotirmayee
Palladium-catalysed carbonylation of aryl diazonium salts to access bioconjugation-ready esters.
Chemical communications (Cambridge, England), 2025, 61, 10977-10980
7134739 CIFC300 H224 Cl8 O8 P16 Rh8F d d d :211.6257; 22.2356; 46.905
90; 90; 90
12125.1Mandal, Dipendu; Esposito, Madison R.; Griffin, Samuel E.; Domecus, Grant P.; Cohen, Seth M.
Selective hydrosilylation of olefins by a two-dimensional Rh(I) low-valent metal-organic framework.
Chemical communications (Cambridge, England), 2025, 61, 10526-10529
7134740 CIFC300 H224 Cl8 Ir8 O8 P16F d d d :211.573; 22.229; 46.579
90; 90; 90
11983Mandal, Dipendu; Esposito, Madison R.; Griffin, Samuel E.; Domecus, Grant P.; Cohen, Seth M.
Selective hydrosilylation of olefins by a two-dimensional Rh(I) low-valent metal-organic framework.
Chemical communications (Cambridge, England), 2025, 61, 10526-10529
7134741 CIFC27 H47 F6 N4 O P RuP 1 2/n 112.1425; 10.9767; 24.5384
90; 99.738; 90
3223.5Preston, Andrew Z.; Phearman, Alexander S.; Quiroz, Manuel; Flowers, Sarah E.; Devi, Nilakshi; Zall, Christopher M.; Wiedner, Eric S.; Appel, Aaron M.; Linehan, John C.
DBU as base and ligand in phosphine-free ruthenium complexes for hydrogenation of CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2025, 61, 11247-11250
7134742 CIFC24 H18 Fe N4 S2P n a 2123.582; 7.927; 11.326
90; 90; 90
2117.2Yan, Rong; Li, Zi-Han; Luo, Qian-Cheng; Sun, Na-Na; Ho, Johnny C.; Zheng, Yan-Zhen
Nuclearity effect on water oxidation: a comparative study of dinuclear and mononuclear iron complexes.
Chemical communications (Cambridge, England), 2025, 61, 11601-11604
7134743 CIFC50 H38 Cl2 Fe2 N8 O11 S4P -19.0102; 11.9133; 25.039
84.209; 86.646; 85.619
2662.7Yan, Rong; Li, Zi-Han; Luo, Qian-Cheng; Sun, Na-Na; Ho, Johnny C.; Zheng, Yan-Zhen
Nuclearity effect on water oxidation: a comparative study of dinuclear and mononuclear iron complexes.
Chemical communications (Cambridge, England), 2025, 61, 11601-11604
7134744 CIFC10 H4 S2C 1 2/c 113.036; 9.2577; 12.7472
90; 105.591; 90
1481.77Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134745 CIFC20 H12 S6I 1 2/a 113.9881; 11.6422; 22.2132
90; 92.097; 90
3615.05Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134746 CIFC24 H16 S4P 1 2/n 112.0579; 7.6145; 21.3949
90; 105.709; 90
1891Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134747 CIFC11 H9 Br F3 N OP 21 21 217.084; 10.507; 16.18
90; 90; 90
1204.3Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134748 CIFC11 H10 Br F2 N OP 21 21 217.2114; 8.6463; 17.6697
90; 90; 90
1101.74Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134749 CIFC11 H10 F2 I N OC 1 2/c 120.4768; 11.5083; 14.185
90; 132.601; 90
2460.5Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134750 CIFC31 H24 O4P 1 21/n 19.7595; 14.8506; 16.2013
90; 93.249; 90
2344.35Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134751 CIFC25 H20 O3P -19.1486; 10.1141; 11.1933
76.519; 83.021; 69.176
940.54Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134752 CIFC25 H18 Cl2 O2P -19.6407; 9.9098; 12.2951
97.191; 112.732; 106.874
998.56Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134753 CIFC23 H16 O3P 1 21/c 17.961; 15.645; 13.67
90; 105.538; 90
1640.4Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134754 CIFC2.88 H1.88 Br0.25 O0.62P -14.725; 13.22; 17.69
112.5; 92.17; 89.8
1020Londhe, Gokul S.; Mondal, Shankhajit; Gnanaprakasam, Boopathy
A Mn(III)-catalysed domino process for C-3 substituted dihydrocoumarins from 2-hydroxybenzyl alcohols and 4-hydroxy-2<i>H</i>-chromen-2-ones.
Chemical communications (Cambridge, England), 2025, 61, 11617-11620
7134755 CIFC16 H16 N2 SP b c a7.9502; 15.00228; 22.48379
90; 90; 90
2681.67Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134756 CIFC64 H60 Ag2 F12 N8 Ni2 S4 Sb2F d d d :211.5021; 32.2956; 41.3195
90; 90; 90
15348.8Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134757 CIFC32 H30 N4 Ni S2P -111.23947; 11.63264; 12.08649
94.9271; 109.939; 107.106
1388.98Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134758 CIFC50.2 H52.96 Cl3.06 N2P -19.4575; 13.1091; 17.8161
83.827; 84.966; 86.326
2184.22Zhang, Zhiyu; Xu, Zhenxun; Zhang, Aihui; Bai, Fenghua; Hashikawa, Yoshifumi; Chaolumen, ?
Synthesis of a twisted azananographene featuring a diquinoxaline-fused pyrene.
Chemical communications (Cambridge, England), 2025, 61, 11401-11404
7134759 CIFC24 H36 Bi Cl Ni P2P 1 21/n 17.9299; 15.7754; 20.8624
90; 90.502; 90
2609.73Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134760 CIFC34 H54 Bi Cl N2 Ni P2P b c a19.49554; 17.5937; 21.22369
90; 90; 90
7279.7Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134761 CIFC35 H54 Bi N Ni O3 P2P -110.7706; 12.3565; 15.647
93.308; 109.812; 106.535
1850.5Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134762 CIFC58 H74 B Bi N2 Ni P2P 1 21/c 111.0192; 50.5458; 29.036
90; 91.575; 90
16166.2Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134763 CIFC43 H72 Bi N3 Ni O P2P 1 21/n 113.6212; 20.8338; 16.5044
90; 92.171; 90
4680.3Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134764 CIFC52 H72 Bi2 Cl2 Ni2 O4 P4P -111.7379; 11.8444; 20.9031
86.791; 77.237; 89.535
2829.8Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134765 CIFC30 H18 Cd N4 O8P 1 21/c 120.341; 13.506; 21.538
90; 121.24; 90
5059Li, Kuixiang; Qin, Jin; Hao, Pengfei; Xu, Yi; Zhang, Shimin; Shen, Junju; Fu, Yunlong
Linear-light-controlled reverse electron transfer in a 3-D pyromelliticdiimide-based photo-/thermochromic cadmium(II) coordination polymer.
Chemical communications (Cambridge, England), 2025, 61, 11822-11825
7134766 CIFC34 H39 N O2P 21 21 219.1352; 16.5171; 17.9335
90; 90; 90
2705.9Zhu, Yanren; Yang, Shaoxiong; Chen, Huiyu; Zhang, Fang; Pu, Enfan; Jiang, Piaopiao; Jin, Yi; Zhang, Hongbin; Chen, Jingbo
Cycloaddition of bicyclo[1.1.0]butanes with enamides for the efficient synthesis of 2-amino-bicyclo[2.1.1]hexanes.
Chemical communications (Cambridge, England), 2025, 61, 11493-11496
7134767 CIFC22 H17 Br N O3P 1 21 17.4907; 15.9278; 7.9606
90; 101.271; 90
931.46Zhu, Yanren; Yang, Shaoxiong; Chen, Huiyu; Zhang, Fang; Pu, Enfan; Jiang, Piaopiao; Jin, Yi; Zhang, Hongbin; Chen, Jingbo
Cycloaddition of bicyclo[1.1.0]butanes with enamides for the efficient synthesis of 2-amino-bicyclo[2.1.1]hexanes.
Chemical communications (Cambridge, England), 2025, 61, 11493-11496
7134768 CIFC46 H82 Bi Cl Fe N2 P2 Si2P -112.114; 21.416; 21.921
89.666; 74.179; 80.249
5388Zurakowski, Joseph A.; MacEachern, Mitchell A. Z.; Durfy, Connor S.; Boyle, Paul D.; Chitnis, Saurabh S.; Drover, Marcus W.
Hydro- and chloroelementation reactions across an iron-carbon bond using heavy group 15 reagents.
Chemical communications (Cambridge, England), 2025, 61, 10969-10972
7134769 CIFC112 H106 N6 S4P 1 21/n 124.5514; 15.9391; 34.932
90; 101.616; 90
13389.9Naniyil, Athira; Kumar, Arun; Edwin, Aathira; Gokulnath, Sabapathi
A carbazole-embedded cyclodimer adopting a helical conformation and metal-ion sensing.
Chemical communications (Cambridge, England), 2025, 61, 11633-11636
7134770 CIFC24 H26 Mn3 N16P 1 21/c 110.7686; 12.9029; 10.664
90; 91.158; 90
1481.42León-Alcaide, Luis; Fernández-Alarcón, Alberto; Calbo, Joaquín; Keen, David A.; Mínguez Espallargas, Guillermo
Melt-quenched synthesis of a manganese ZIF glass.
Chemical communications (Cambridge, England), 2025, 61, 11641-11644
7134771 CIFC121 H98 Cl2 Cu8 F12 N8 P4 S8P -112.2639; 16.0411; 17.8781
74.241; 88.232; 74.805
3263.5Chang, Mengfan; Xu, Ying; Lv, Ying; Yu, Haizhu; Li, Hao; Kang, Xi; Zhu, Manzhou
Controlling the photoluminescence chromaticity of emissive copper nanoclusters <i>via</i> ligand engineering.
Chemical communications (Cambridge, England), 2025, 61, 11215-11218
7134772 CIFC27 H20 O3P -18.4872; 10.3122; 11.7926
96.838; 107.111; 99.692
956.65Maharana, Priyanka; Sankar, Raman Vijaya; Sankaralingam, Muniyandi; Gunanathan, Chidambaram
Synthesis of functionalized lactones: catalytic cross-coupling of 1,2-diols and allylic alcohols.
Chemical communications (Cambridge, England), 2025, 61, 11947-11950
7134773 CIFC23 H23 N OP 1 21/c 18.6833; 7.9494; 25.996
90; 99.594; 90
1769.3Li, Juncheng; Adelakun, Ibrahim O.; Wei, Zheng; Wang, Ting
Metal-free photocatalytic oxidative coupling of cyclic ethers and alcohols.
Chemical communications (Cambridge, England), 2025, 61, 11818-11821
7134774 CIFC79 H110 Mg N6 OP -112.6188; 14.4351; 39.6972
87.74; 84.081; 88.177
7184.04Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134775 CIFC43 H58 N2 OP -19.9907; 17.0201; 23.3184
103.355; 102.238; 103.661
3596.71Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134776 CIFC80 H110 Mg N2 O3P 1 21 117.5; 17.78; 22.86
90; 104.86; 90
6875Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134777 CIFC58 H80 N2 OP 1 21/c 112.707; 28.0723; 14.6372
90; 98.653; 90
5161.87Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134778 CIFC19 H24 N2 OP 1 21/c 116.4224; 26.1026; 17.6208
90; 117.172; 90
6719.9Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134779 CIFC110 H138 Mg2 N4 O2C 1 2/c 129.1; 11.07; 29.06
90; 97.9; 90
9272Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134780 CIFC164 H202 K6 Mg2 N4 O2P -113.65; 16.68; 24.09
103.86; 104.61; 93.9
5105Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134781 CIFC62.5 H80 N2 OP -112.4386; 19.1066; 21.5188
89.669; 87.336; 89.355
5108.22Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134782 CIFC93 H86 Cl2 N6P 43 21 215.8363; 15.8363; 58.867
90; 90; 90
14763.2Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134783 CIFC78 H56 Cl4 N6P 1 21/c 113.5469; 23.814; 19.642
90; 108.456; 90
6010.7Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134784 CIFC93 H86 Cl2 N6P 41 21 215.8075; 15.8075; 58.762
90; 90; 90
14683.3Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134785 CIFC16 H21 Li O4P -15.8667; 8.571; 16.0568
86.246; 82.777; 81.975
792.2Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134786 CIFC28 H36 Li4 O4P -110.0389; 12.4597; 13.0418
61.824; 74.874; 82.866
1388.2Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134787 CIFC5.71 H9.42 Li N O0.35F m -3 c25.9396; 25.9396; 25.9396
90; 90; 90
17453.8Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134788 CIFC36 H68 Li4 O8 Si4P 1 21/c 110.809; 27.6823; 16.7998
90; 105.552; 90
4842.76Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134789 CIFC8 H4 Li4 O4P 1 21/n 18.4602; 5.14; 16.5862
90; 99.445; 90
711.48Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134790 CIFC6 H3 Li2 O2P 1 21/c 19.7425; 5.9515; 8.3569
90; 105.758; 90
466.34Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134791 CIFC4 H2 Li O2P 1 21/c 18.35839; 5.13401; 8.4796
90; 93.187; 90
363.314Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134792 CIFC6 H3 Li O2P 1 21/c 110.2674; 5.3379; 8.6255
90; 98.721; 90
467.267Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134793 CIFC38 H38 N4 OP -110.6572; 12.3917; 12.825
105.741; 95.3783; 104.429
1554.92Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134794 CIFC40 H38 B F2 N5P n a 2122.8308; 19.6331; 7.717
90; 90; 90
3459.06Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134795 CIFC160 H160 N16P -119.232; 19.9165; 19.9108
68.127; 74.0072; 73.9936
6674.3Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134796 CIFCl2 Cs18 O83 Pu2 W20P -114.025; 17.2738; 22.2406
100.814; 102.411; 99.105
5056.81Colliard, Ian; Stavila, Vitalie; Deblonde, Gauthier J.-P.
Isolation of a new polyoxometalate complex of plutonium.
Chemical communications (Cambridge, England), 2025, 61, 11858-11861
7134797 CIFC46 H55 N2 O2 SbP b c a18.4576; 16.232; 27.3781
90; 90; 90
8202.6Agou, Tomohiro; Kuroiwa, Shunsuke; Moriyama, Ryo; Kuroda, Takuma; Kubo, Kazuya; Fukumoto, Hiroki; Morita, Masato; Inoue, Ryo; Nabeshima, Tatsuya
Synthesis and structural characterization of Sb(iii) and Bi(iii) complexes with an N2O2-type tetradentate dipyrrin ligand
Chemical Communications, 2025, 61, 7141-7144
7134798 CIFC47 H57 Bi Cl2 N2 O2P -113.8968; 14.1548; 14.2678
62.515; 80.924; 62.258
2197.8Agou, Tomohiro; Kuroiwa, Shunsuke; Moriyama, Ryo; Kuroda, Takuma; Kubo, Kazuya; Fukumoto, Hiroki; Morita, Masato; Inoue, Ryo; Nabeshima, Tatsuya
Synthesis and structural characterization of Sb(iii) and Bi(iii) complexes with an N2O2-type tetradentate dipyrrin ligand
Chemical Communications, 2025, 61, 7141-7144
7134799 CIFC84 H54 N8P -110.8437; 25.2054; 37.5571
73.902; 83.492; 77.695
9619.9Li, Jiajia; Yang, Yanping; Hii, Shan Shiang; Zhu, Xinyuan; Wang, Youfu
Structural isomers of imine-linked covalent organic cages with divergent photocatalytic properties
Chemical Communications, 2025, 61, 7281-7284
7134800 CIFC84 H54 N8P 1 21/n 123.0146; 9.9226; 36.4335
90; 95.329; 90
8284.2Li, Jiajia; Yang, Yanping; Hii, Shan Shiang; Zhu, Xinyuan; Wang, Youfu
Structural isomers of imine-linked covalent organic cages with divergent photocatalytic properties
Chemical Communications, 2025, 61, 7281-7284
7134801 CIFC68 H90 Au2 F12 N8 P2 Sb2P 1 21/n 120.424; 11.606; 32.783
90; 107.44; 90
7414Urvashi,; Patil, Nitin T.
Bidentate (P^N) Au(iii)–azide complexes: synthesis and reductive elimination studies
Chemical Communications, 2025, 61, 7297-7300
7134802 CIFC23 H17 FP 1 21/c 111.689; 17.293; 8.4188
90; 102.698; 90
1660.1Sun, Jie; Zhang, Shaojie; Wang, Ruixue; Lv, Zeng; Wu, Xin-Xing
Palladium-catalyzed sequential [3+2] cyclization/C–H activation of o-iodostyrenes with cyclopropenones as C2 synthons
Chemical Communications, 2025, 61, 8200-8203
7134803 CIFC39 H44 Cl2 P2 Ru S2C 1 2/c 138.852; 14.8412; 18.368
90; 90.004; 90
10591.2Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134804 CIFC43.75 H61 O P2 Ru S4P n a 2117.6021; 12.8281; 17.294
90; 90; 90
3905Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134805 CIFC53.25 H80.2 P2 Ru S2P 1 21/n 110.0461; 25.5274; 17.2498
90; 97.0994; 90
4389.8Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134806 CIFC94 H158 Ca2 N4 O3P -112.7723; 12.8615; 16.5534
71.5478; 72.2458; 62.332
2243.75Thum, Stefan; Schmidt, Marcel A.; Langer, Jens; Harder, Sjoerd
Low-coordinate calcium peroxide and oxide complexes.
Chemical communications (Cambridge, England), 2025, 61, 12127-12130
7134807 CIFC96 H162 Ca2 N4 O4P -112.822; 12.859; 16.6221
71.9328; 71.5933; 62.498
2262.16Thum, Stefan; Schmidt, Marcel A.; Langer, Jens; Harder, Sjoerd
Low-coordinate calcium peroxide and oxide complexes.
Chemical communications (Cambridge, England), 2025, 61, 12127-12130
7134808 CIFC20 H16 Cl O PP 21 21 218.9934; 9.8046; 18.7482
90; 90; 90
1653.15Zhang, Zhaoqi; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical phosphorylation of α,β-unsaturated carboxylic acids <i>via</i> decarboxylative cross-coupling reaction.
Chemical communications (Cambridge, England), 2025, 61, 12034-12037
7134809 CIFC20 H15 O PP b c a11.7526; 16.3049; 16.4854
90; 90; 90
3159Zhang, Zhaoqi; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical phosphorylation of α,β-unsaturated carboxylic acids <i>via</i> decarboxylative cross-coupling reaction.
Chemical communications (Cambridge, England), 2025, 61, 12034-12037
7134810 CIFC24 H17 Br N2 O2P 21 21 214.6907; 12.763; 31.449
90; 90; 90
1882.8Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134811 CIFC24 H15 Br N2 OP 1 c 124.7055; 4.9654; 25.0076
90; 118.895; 90
2685.8Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134812 CIFC24 H17 Br N2 O2P 21 21 214.723; 12.844; 32.01
90; 90; 90
1942Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134813 CIFC24 H21 Br O2P 17.815; 7.9476; 8.2858
70.783; 77.901; 89.307
474.26Zhang, Ke-Feng; Zhou, Lin-Hui; Chen, Yan-Xi; Chen, Wei-Wei; Feng, Yuan-Mei; Ma, Fang
Catalytic Asymmetric Construction of Planarly and Centrally Chiral [2.2]paracyclophanes by Merging Photochemical and Cobalt Catalyzed Desymmetrization
Chemical Communications, 2025
7134814 CIFC18 H22 N2 O5P 1 21 19.1504; 19.6553; 9.7569
90; 102.207; 90
1715.14Liu, Deng-Yin; Hu, Xin-Yue; Zhang, Cong-Zhen; Wen, Miao-Miao; Ren, Xiao-Xi; Liu, Xu-Ge
Switchable synthesis of benzimidazole/quinoxaline <i>C</i>-glycosides with <i>o</i>-phenylenediamines and sulfoxonium ylide glyco-reagents.
Chemical communications (Cambridge, England), 2025, 61, 12131-12134
7134815 CIFC11 H9 Co2 O7 PI 1 2/a 110.652; 5.4984; 42.3062
90; 95.802; 90
2465.14Xu, Yan; Su, Qian-Qian; Liu, Bei; Sun, Wen-Tao; Bao, Song-Song; Li, Su-Zhi; Zheng, Li-Min
Metal-organic framework containing Co<sub>3</sub>(μ<sub>3</sub>-OH)-based kagomé layers showing long-range weak ferromagnetic ordering.
Chemical communications (Cambridge, England), 2025, 61, 12211-12214
7134816 CIFC55 H65 Co8 O43 P5P n m a26.3066; 21.2796; 13.9084
90; 90; 90
7785.8Xu, Yan; Su, Qian-Qian; Liu, Bei; Sun, Wen-Tao; Bao, Song-Song; Li, Su-Zhi; Zheng, Li-Min
Metal-organic framework containing Co<sub>3</sub>(μ<sub>3</sub>-OH)-based kagomé layers showing long-range weak ferromagnetic ordering.
Chemical communications (Cambridge, England), 2025, 61, 12211-12214
7134817 CIFC15 H14 N2 O2 SP 1 21/c 18.3477; 22.4967; 7.7113
90; 106.006; 90
1392.01Zhou, Pengfei; Wan, Guibin; Yuan, Zhihan; Guan, Aoran; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Cobalt(III)-catalyzed C-H functionalization of 2-arylthiazoles with maleimides or allyl acetate.
Chemical communications (Cambridge, England), 2025, 61, 12171-12174
7134818 CIFC38 H44 N4 O2P n a 2117.6633; 8.3253; 21.863
90; 90; 90
3215Bhatt, Tarun; Dutta, Tonmoy; Yaswanth, Kokkiripati; Kalevaru, Venkata Narayana; Wohlrab, Sebastian; Natte, Kishore
Chemoselective transfer hydrogenation and transfer deuteration of substituted quinolines using Hantzsch ester and D<sub>2</sub>O.
Chemical communications (Cambridge, England), 2025, 61, 12305-12308
7134819 CIFC27.5 H27 N O2 PP -18.5764; 9.5269; 15.3568
100.161; 100.588; 102.767
1171.67Bhatt, Tarun; Dutta, Tonmoy; Yaswanth, Kokkiripati; Kalevaru, Venkata Narayana; Wohlrab, Sebastian; Natte, Kishore
Chemoselective transfer hydrogenation and transfer deuteration of substituted quinolines using Hantzsch ester and D<sub>2</sub>O.
Chemical communications (Cambridge, England), 2025, 61, 12305-12308
7134820 CIFC24 H26P 1 21/c 111.615; 10.921; 15.107
90; 111.302; 90
1785.4Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134821 CIFC13 H13 Br2 N3 O ZnP 1 21/c 113.4493; 15.5797; 7.6731
90; 106.091; 90
1544.8Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134822 CIFC14 H18 Br2 N4 O S ZnP 1 21/c 19.9413; 13.4749; 14.3357
90; 98.261; 90
1900.46Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134823 CIFC17 H18 OP -18.972; 13.053; 13.269
63.504; 86.68; 85.485
1386Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134824 CIFC19 H18 Cl2P -18.297; 9.0505; 11.4465
93.075; 97.902; 111.839
785.13Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134825 CIFC15 H19 Br2 N3 O2 ZnP -17.4524; 10.4775; 13.0859
101.879; 94.101; 108.999
934.77Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134826 CIFC21 H18 Cl N O3P 1 21 15.905; 10.3232; 14.2771
90; 96.286; 90
865.08Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134827 CIFC21 H19 N O4P 1 21 17.4802; 13.004; 17.2546
90; 92.2247; 90
1677.13Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134828 CIFC21 H21 N O3P 21 21 216.7817; 8.2331; 31.286
90; 90; 90
1746.84Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134829 CIFC6 H10 N8 OP 1 21/c 13.6169; 19.782; 11.752
90; 94.717; 90
838Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134830 CIFC6 H9 Cl N8C 1 2/c 127.527; 3.8158; 21.717
90; 128.059; 90
1796.1Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134831 CIFC6 H9 Cl N8 O4P 1 21/n 16.8415; 15.8632; 9.8345
90; 92.574; 90
1066.24Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134832 CIFC18 H18 Cl N O2P b c a12.3189; 8.9755; 28.721
90; 90; 90
3175.6Xian, Ning; Yin, Jiang; Ji, Xiaochen; Huang, Huawen
Sulfoxonium ylides as carbon radical precursors in three-component carbohalogenation of alkenes
Chemical Communications, 2025
7134833 CIFC30 H21 Cl N2 O2P 1 21/n 19.1913; 23.5634; 11.1335
90; 101.65; 90
2361.6Bhumij, Mandweep; Ahamed, Rehan; Kant, Ruchir; Mudedla, Sathish Kumar; Srivastava, Ajay Kumar
Regioselective construction of pyrido[1,2,3-<i>de</i>]quinoxaline-2,5-diones through acid-mediated post-Ugi rearrangements.
Chemical communications (Cambridge, England), 2025, 61, 12757-12760
7134834 CIFC26 H16 B2 F4 N4P b c a8.1088; 14.0314; 36.966
90; 90; 90
4205.91Nakano, Takeo; Yamada, Haruki; Inaba, Ryoto; Hamasaki, Atom; Takeda, Takashi; Ohta, Akira
Dimeric boron complexes bearing isoquinolyl-pyrrole ligands.
Chemical communications (Cambridge, England), 2025, 61, 11943-11946
7134835 CIFC25 H17 N O2C 1 2/c 114.5261; 10.9889; 24.318
90; 109.877; 90
3650.52Suresh, Vavilapalli; Reddy, T. Mahipal; Nanubolu, Jagadeesh Babu; Reddy, Maddi Sridhar
Pd-catalyzed electrophilic cyclization/C-H annulation cascade of 1,8-diyne oxime ethers to access fused oxepines.
Chemical communications (Cambridge, England), 2025, 61, 12353-12356
7134836 CIFC34 H25 Br N2 O3P -110.8312; 11.1661; 12.4253
101.941; 98.68; 112.734
1310.87Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134837 CIFC35 H27 Br N2 O4P -110.1577; 10.7731; 13.5579
99.196; 98.716; 109.233
1349.24Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134838 CIFC32 H24 Br N2 O3 SP 1 21/n 110.8268; 11.8871; 20.0235
90; 91.459; 90
2576.17Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134839 CIFC35 H27 Br N2 O3P 1 21 112.1417; 8.895; 12.7012
90; 99.012; 90
1354.8Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134840 CIFC24 H19 N3 O3 SP 19.1403; 9.6457; 11.8785
102.168; 101.295; 90.935
1002.09Dybowska, Joanna; Przydacz, Artur; Olczyk, Weronika; Sieroń, Lesław; Skrzyńska, Anna; Albrecht, Łukasz
Divergent hetero-[8+<i>n</i>] higher order cycloadditions of tropothione and enals catalyzed by <i>N</i>-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 12119-12122
7134841 CIFC24 H19 N3 O3 SP 1 21 111.5801; 5.9732; 15.349
90; 107.687; 90
1011.51Dybowska, Joanna; Przydacz, Artur; Olczyk, Weronika; Sieroń, Lesław; Skrzyńska, Anna; Albrecht, Łukasz
Divergent hetero-[8+<i>n</i>] higher order cycloadditions of tropothione and enals catalyzed by <i>N</i>-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 12119-12122
7134842 CIFC21 H19 Fe N S2P 1 21/c 113.9164; 6.0808; 22.0969
90; 104.013; 90
1814.26Sharma, Deepak; Tomar, Vijesh; Joshi, Raj K.
Synthesis of ferrocenyl/phenyl isothiazole-3-thione and isoselenazole-3-selenone as new heterocycles.
Chemical communications (Cambridge, England), 2025, 61, 13964-13967
7134843 CIFCo H16 N10 O8F m m m6.4648; 12.1663; 17.1617
90; 90; 90
1349.81Zhao, Feng; Gu, Ziyan; Song, Bin; Ju, Xuehai; Hu, Bingcheng; Zhang, Chong
Electrosynthesis of a <i>cyclo</i>-N<sub>5</sub><sup>-</sup> anion <i>via</i> TEMPO-mediated selective C-N bond cleavage in aryl-pentazole.
Chemical communications (Cambridge, England), 2025, 61, 12725-12728
7134844 CIFC17 H14 N2 O3P 1 21/c 114.2794; 4.2726; 22.8872
90; 100.816; 90
1371.55Basak, Soumya Jyoti; Dash, Jyotirmayee
KOtBu-Mediated Annulation for the Pot-Economical Synthesis of Quinazolinobenzoxazepines
Chemical Communications, 2025
7134845 CIFC20 H14 N2 O2P n a 2115.052; 22.635; 4.2116
90; 90; 90
1434.9Basak, Soumya Jyoti; Dash, Jyotirmayee
KOtBu-Mediated Annulation for the Pot-Economical Synthesis of Quinazolinobenzoxazepines
Chemical Communications, 2025
7134846 CIFC108 H78 F36 N6 P6P 1 21/n 16.6796; 34.3789; 48.7726
90; 90.958; 90
11198.4Yu, Yang; Song, Xiaowen; Li, Yawen; Wang, Pingxia; Cheng, Lin; Yang, Ying; He, Gang; Cao, Liping
Angle-controlled synthesis and redox properties of a tetraphenylethene-based hexacationic triangular macrocycle.
Chemical communications (Cambridge, England), 2025, 61, 13193-13196
7134847 CIFC6 H4 N4P 1 21/c 13.6563; 7.4254; 10.3507
90; 94.82; 90
280.02Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134848 CIFC18 H28 K N4 O6P -18.2265; 8.5426; 9.0649
74.121; 65.614; 66.262
526.7Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134849 CIFC54 H94 K2 N12 O15P -113.1139; 14.3079; 19.8832
93.405; 108.729; 111.474
3220.98Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134850 CIFC32 H38 Cl2 N2 O RuP -18.9258; 10.9738; 18.096
98.894; 99.456; 96.569
1709.5Casalta, Clément; Roisnel, Thierry; Jazzar, Rodolphe; Doppiu, Angelino; Mauduit, Marc
<i>N</i>-hydrazine cyclic(amino)(alkyl)carbene ruthenium complexes: synthesis and reactivity in olefin metathesis.
Chemical communications (Cambridge, England), 2025, 61, 13169-13172
7134851 CIFC55 H52 Cl2 N2P -110.1271; 15.252; 15.567
106.892; 100.26; 100.908
2188.5Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134852 CIFC55 H51 Cl3 N2P -110.004; 15.3041; 16.1113
107.88; 102.522; 99.296
2221.55Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134853 CIFC55 H51 Cl3 N2P -19.8151; 15.4638; 16.0395
105.292; 91.583; 107.284
2227.33Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134854 CIFC29 H29 N OP -19.6914; 15.3962; 16.3741
105.062; 90.118; 107.315
2243.97Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134855 CIFC54 H50 N2P 1 21/c 111.033; 16.7127; 22.0929
90; 95.145; 90
4057.32Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134856 CIFC55 H52 Cl2 N2P -19.752; 15.4169; 15.7126
103.388; 92.384; 106.529
2188.48Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134857 CIFC54.05 H50.1 Cl0.1 N2P -19.8175; 15.0293; 15.4757
100.086; 106.629; 93.275
2140.17Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134858 CIFC54 H50 N2P -111.288; 11.9759; 15.6694
74.666; 84.43; 85.549
2030.22Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134859 CIFC58 H58 N2 O2P -19.7222; 15.4668; 16.2481
75.227; 89.808; 72.19
2241.9Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134860 CIFC54 H50 N2P 1 21/c 111.0179; 16.7178; 22.0057
90; 95.442; 90
4035.07Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134861 CIFC56 H54 N2 OP -19.7849; 15.3986; 15.4296
101.789; 92.489; 106.18
2173.17Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134862 CIFC122.5 H136 Ag4 Cl2 F12 O1.5 P8 Pt Sb2P 1 21 114.5881; 15.94377; 26.82398
90; 102.209; 90
6097.85Zhang, Yujie; Jia, Hongli; Yan, Bingzheng; Hou, Jian; Guo, Huifang; Li, Qi; Xin, Chengrui; Li, Simin; Dong, Jinrun; Shen, Hui
One-pot synthesis of atomically precise chiral PtAg<sub>4</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 13691-13694
7134863 CIFC122.5 H136 Ag4 Cl2 F12 O1.5 P8 Pt Sb2P 1 21 114.5524; 15.9421; 26.8018
90; 102.05; 90
6080.9Zhang, Yujie; Jia, Hongli; Yan, Bingzheng; Hou, Jian; Guo, Huifang; Li, Qi; Xin, Chengrui; Li, Simin; Dong, Jinrun; Shen, Hui
One-pot synthesis of atomically precise chiral PtAg<sub>4</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 13691-13694
7134864 CIFC22.8 H39.2 N4 O14.8 ZrI -4 2 d8.9734; 8.9734; 41.816
90; 90; 90
3367.1Shao, Zhen-Wu; Qiu, Yuqing; Xiong, Chaozhi; Liu, Chong
Isomerism and transformation of Zr-hydroxamate metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 12960-12963
7134865 CIFC21.8 H32.2 Cl2 N6.6 O8.6 ZrC c c a :225.7241; 38.687; 17.6068
90; 90; 90
17522Shao, Zhen-Wu; Qiu, Yuqing; Xiong, Chaozhi; Liu, Chong
Isomerism and transformation of Zr-hydroxamate metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 12960-12963
7134866 CIFC61 H50 Co N4 O6 PP 1 21/n 121.2453; 13.3608; 36.5986
90; 95.41; 90
10342.4Kumar, Sachin; Fernández, Sergio; Saltsman, Irena; Fridman, Natalia; Mahammed, Atif; Miller, Alexander J. M.; Gross, Zeev
Substituents effects on the electrocatalytic CO<sub>2</sub> reduction by cobalt corroles in solution.
Chemical communications (Cambridge, England), 2025, 61, 12924-12927
7134867 CIFC157 H82 Cl2 F40 N16 O8P b c a23.9044; 10.7288; 26.6966
90; 90; 90
6846.8Kumar, Sachin; Fernández, Sergio; Saltsman, Irena; Fridman, Natalia; Mahammed, Atif; Miller, Alexander J. M.; Gross, Zeev
Substituents effects on the electrocatalytic CO<sub>2</sub> reduction by cobalt corroles in solution.
Chemical communications (Cambridge, England), 2025, 61, 12924-12927
7134868 CIFC10 H14 F2 Fe K N8C 1 2/c 113.6776; 8.8101; 14.5699
90; 113.281; 90
1612.7Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134869 CIFC10 H14 F2 Fe K N8P a -311.715; 11.715; 11.715
90; 90; 90
1607.78Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134870 CIFC20 H28 F4 Fe2 K2 N16F m -3 m11.8392; 11.8392; 11.8392
90; 90; 90
1659.46Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134871 CIFC10 H14 F2 Fe K N8P a -311.7509; 11.7509; 11.7509
90; 90; 90
1622.61Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134872 CIFC31 H34 N2 O4P 1 21/n 110.52568; 20.80933; 12.23495
90; 96.5124; 90
2662.56Li, Xin-Yu; Xiao, Mei-Qiu; Zhou, Li-Juan; Zhang, Jia-Qi; Zhao, Meng-Yan; Wang, Shuo-Wen; Tang, Shi
Nickel-catalyzed sequential 1,2-<i>N</i>-migration/BCBs ring-opening to access spirocyclobutyl β-amino acid esters.
Chemical communications (Cambridge, England), 2025, 61, 13473-13476
7134873 CIFC23 H19 N O2P 1 21/c 118.3859; 8.7208; 11.3513
90; 101.037; 90
1786.4Wu, Qing; Han, Yingna; Tang, Tian; Zhang, Shuwei; Yu, Xiuzhao; Zhao, Guofeng; Hu, Weiming; Wang, Lei
Palladium-catalyzed tandem cyclization reaction: access to isoxazoline-benzofuran bis-heterocycles.
Chemical communications (Cambridge, England), 2025, 61, 12928-12931
7134874 CIFC29 H29 N3 O4P -15.7514; 10.0954; 22.139
101.995; 91.679; 102.73
1222.7Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134875 CIFC20 H17 Cl3 N2 O2P 21 21 219.0344; 10.3333; 21.6961
90; 90; 90
2025.44Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134876 CIFC32 H35 N3 O4P 1 21/c 114.0792; 20.6051; 9.7661
90; 98.84; 90
2799.52Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134877 CIFC70 H98 N9 O10 PP 1 21/c 114.0616; 16.111; 32.035
90; 96.228; 90
7214.58Oh, Ju Hyun; Shin, Sang Kyu; Kim, Sung Kuk
A calix[4]pyrrole functionalized with an amidoindole ester for the selective recognition of the dihydrogen phosphate anion.
Chemical communications (Cambridge, England), 2025, 61, 13425-13428
7134878 CIFC9 H11 N OR -3 :H24.2502; 24.2502; 7.1744
90; 90; 120
3653.82Cheng, Long; Nian, Cuicui; Han, Zhengyu; Sun, Jianwei; Huang, Hai
Diastereoselective synthesis of 1,4-diaryl piperazines through the dimerization of 3-aminooxetanes with cooperative indium-diphenyl phosphate catalysis.
Chemical communications (Cambridge, England), 2025, 61, 13477-13480
7134879 CIFC26 H33 O4 PP 1 21/n 115.887; 9.64; 16.117
90; 106.397; 90
2368Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134880 CIFC24 H24 OP -16.6003; 12.096; 12.1302
73.196; 79.641; 83.733
910.3Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134881 CIFC39 H58 O6 P2C 1 2/c 112.477; 11.949; 26.368
90; 98.411; 90
3888.9Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134882 CIFC16 H14 N2 O2P -15.9207; 8.0892; 15.695
77.953; 85.273; 68.989
686.2Huang, Jie; Ren, Weijie; Chen, Jiehao; Xiao, Xiangrong; Li, Jiaqi; Wang, Dongyi; Yu, Wanyue; Zhao, Juan; Chen, Xiuwen; Zhu, Zhongzhi
Three-component reaction of isocyanates and 3-aminoacrylates: selective synthesis of <i>N</i>-2-aryl-1,2,3-triazoles and hydrazones.
Chemical communications (Cambridge, England), 2025, 61, 13667-13670
7134883 CIFC22 H16 F6 N2 O6 S2 SeP -17.6925; 8.6622; 20.1522
87.959; 87.081; 70.209
1261.63Kuczmera, Thomas J.; Puylaert, Pim; Wirth, Thomas; Nachtsheim, Boris J.
Imidazopyridine substituted cyclic selenonium(IV) salts as chalcogen bond catalysts.
Chemical communications (Cambridge, England), 2025, 61, 14169-14172
7134884 CIFC4 H8 N2 O2 SP n m a8.7805; 7.6704; 9.7607
90; 90; 90
657.38Ali, Rojan; Matsui, Kai; Šadauskis, Jānis; Catherall, Amanda; Wirth, Thomas
Flow electrochemical oxidation of <i>N</i>-nitrosamines to <i>N</i>-nitramines.
Chemical communications (Cambridge, England), 2025, 61, 13671-13674
7134885 CIFC12 H22 N2 O2P 1 21/n 16.0192; 19.1943; 11.0092
90; 92.078; 90
1271.1Ali, Rojan; Matsui, Kai; Šadauskis, Jānis; Catherall, Amanda; Wirth, Thomas
Flow electrochemical oxidation of <i>N</i>-nitrosamines to <i>N</i>-nitramines.
Chemical communications (Cambridge, England), 2025, 61, 13671-13674
7134886 CIFC38 H32 B0.91 F15 Ga1.09P -110.03; 12.141; 15.017
77.99; 80.13; 78.22
1735Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134887 CIFC17 H29 B Ga I3C 1 2/c 134.509; 8.886; 15.894
90; 111.02; 90
4549.5Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134888 CIFC35 H59 B Br4 GaC 1 2/c 116.896; 13.081; 35.577
90; 101.91; 90
7694Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134889 CIFC29 H30.5 B2 Fe N7.5 OP 1 21/n 112.4656; 17.4511; 13.1482
90; 95.936; 90
2844.9Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134890 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.4966; 17.6717; 13.4291
90; 94.771; 90
2955.36Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134891 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.4828; 17.4584; 13.1586
90; 96.006; 90
2851.91Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134892 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.509; 17.4132; 13.1212
90; 95.783; 90
2843.54Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134893 CIFC29 H29.5 B2 Fe N7.5 OP 1 21/n 112.5019; 17.6496; 13.4172
90; 94.69; 90
2950.64Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134894 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.5324; 17.6041; 13.3803
90; 94.564; 90
2942.62Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134895 CIFC25 H18 F3 N O3 S SeP -110.6587; 10.7075; 11.815
78.288; 74.899; 61.067
1134.63Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134896 CIFC25 H26 F3 N O4 S SeP -110.3394; 10.4055; 11.5682
83.126; 88.202; 79.76
1215.89Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134897 CIFC38 H29 B2 F8 N3 Se2P 1 21/c 112.7389; 12.6882; 21.5602
90; 97.428; 90
3455.6Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134898 CIFC24 H30 Cl2 Cu2 N4 O12P 1 21/c 116.4287; 12.3488; 14.368
90; 105.507; 90
2808.8Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134899 CIFC24 H30 Cl2 Cu N4 Ni O12P 1 c 116.7242; 12.3653; 14.6102
90; 105.631; 90
2909.65Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134900 CIFC21 H20 Cu N2 O4F d d d :26.9285; 31.8012; 34.4133
90; 90; 90
7582.4Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134901 CIFC25 H32 Cl2 Co Cu N4 O12P 19.6012; 11.2838; 14.0602
79.812; 85.501; 84.317
1488.98Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134902 CIFC67 H60 F12 N12 O3 P2 RuP 1 21/n 115.521; 23.4518; 20.2925
90; 91; 90
7385.3Mercier, Gabriel M.; Rousset, Elodie; Oubaha, Ilyes; Bandyopadhyay, Kamalika; Pal, Amlan K.; Ciofini, Ilaria; Chamoreau, Lise-Marie; Marvaud, Valérie; Hanan, Garry S.
A ruthenium terpyridine complex showing stable photocatalytic hydrogen evolution under red light.
Chemical communications (Cambridge, England), 2025, 61, 14911-14914
7134903 CIFC69 H73 B2 Cl2 F4 Ir N4P 1 21/c 124.023; 13.643; 19.181
90; 100.954; 90
6172Fukumoto, Ryo; Yokoo, Takuya; Sakuda, Eri; Omoto, Kenichiro; Horiuchi, Shinnosuke; Arikawa, Yasuhiro; Umakoshi, Keisuke
Covalently linked triarylborane-iridium(III) complex as a photocatalyst for CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 14943-14946
7134904 CIFC17 H13 PC m c 2124.0423; 7.61; 7.1438
90; 90; 90
1307.04Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134905 CIFC31 H37 P Si2C 1 c 118.6524; 14.8278; 10.6662
90; 105.222; 90
2846.5Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134906 CIFC25 H21 PP 1 21/n 17.008; 16.5827; 16.2271
90; 91.776; 90
1884.9Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134907 CIFC27 H25 O P SeC 1 2/c 115.385; 13.0349; 22.32
90; 98.157; 90
4430.8Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134908 CIFC51 H44 Cl2 P2P -111.7787; 12.1311; 15.4644
74.53; 89.83; 72.66
2025.8Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134909 CIFC28 H24 N O2 PP 1 n 16.0125; 12.501; 15.039
90; 96.181; 90
1123.8Thondur, Jagadeesh Reddy; Gowda, Punith S.; Sharada, Duddu S.; Satyanarayana, Gedu
Electrochemical synthesis of phosphorylated oxazolines from <i>N</i>-allylamides.
Chemical communications (Cambridge, England), 2025, 61, 14717-14720
7134910 CIFC30 H16 F6 N4 O2P n a 2110.7693; 29.918; 7.4885
90; 90; 90
2412.8Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134911 CIFC74 H54 N12 O6P 3217.1456; 17.1456; 16.9139
90; 90; 120
4306.06Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134912 CIFC43 H31 N6 O2C 1 2/c 128.494; 12.5982; 21.951
90; 105.585; 90
7590.1Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134913 CIFC9 H10 B F2 N O2P n m a13.463; 6.954; 10.056
90; 90; 90
941.5Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134914 CIFC13 H9 B F2 O2P 1 21/c 116.243; 7.2371; 20.146
90; 108.343; 90
2247.9Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134915 CIFC14 H11 B F2 O3P 21 21 217.865; 10.808; 14.417
90; 90; 90
1225.5Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134916 CIFC8 H7 B F2 O3P 1 21/c 19.09; 11.297; 8.038
90; 96.756; 90
819.7Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134917 CIFC18 H15 Cl0.15 N0.85 O1.7 SiP 1 21/n 19.4177; 18.4095; 9.9867
90; 106.888; 90
1656.8Dahmani, Houari; Poulin, Louis-Philippe; Fecteau, Charles-Émile; Harter, Lara; Johnson, Paul Andrew; Bélanger-Chabot, Guillaume
Nitro and nitritosilanes: do they and can they exist?
Chemical communications (Cambridge, England), 2025, 61, 15814-15817
7134918 CIFC36 H30 N2P 1 21/c 15.3157; 34.868; 16.652
90; 94.617; 90
3076.4Jaiswal, Gaurav; Pan, Subhas Chandra
Iridium catalyzed intramolecular cyclization of allyl alcohol-indole hybrids: rapid access to photoluminescent 5<i>H</i>-benzo[<i>b</i>]carbazoles.
Chemical communications (Cambridge, England), 2025, 61, 15011-15014
7134919 CIFC26 H26 Cl2 O6P -18.5461; 11.5957; 13.2007
72.926; 87.247; 81.392
1236.41Dan Xu, ?; Li, Xiaoxuan; Cai, Yifei; Chen, Yushuang; Xin, Yu; Chen, Jing; Yao, Hui; Huang, Nianyu; Wang, Nengzhong
Additive-controlled chemodivergent multi-component domino reaction between salicylaldehydes and Morita-Baylis-Hillman (MBH) carbonates.
Chemical communications (Cambridge, England), 2025, 61, 15433-15436
7134920 CIFC16 H14 O4P -17.0689; 11.6245; 15.613
93.973; 90.876; 92.978
1277.9Dan Xu, ?; Li, Xiaoxuan; Cai, Yifei; Chen, Yushuang; Xin, Yu; Chen, Jing; Yao, Hui; Huang, Nianyu; Wang, Nengzhong
Additive-controlled chemodivergent multi-component domino reaction between salicylaldehydes and Morita-Baylis-Hillman (MBH) carbonates.
Chemical communications (Cambridge, England), 2025, 61, 15433-15436
7134921 CIFC19 H23 N O2P 21 21 219.65189; 12.52806; 12.83597
90; 90; 90
1552.12Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134922 CIFC26 H32 Fe N2 O4I 1 2 112.2589; 5.803; 17.0375
90; 99.601; 90
1195.04Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134923 CIFC46 H56 Fe N2 O4I 1 2 119.6453; 14.5148; 31.1666
90; 100.673; 90
8733.4Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134924 CIFC26 H32 Fe N2 O4I 1 2 112.23289; 5.80595; 17.0105
90; 99.7213; 90
1190.8Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134925 CIFC32 H24 Fe N2 O4I 1 2 114.66217; 5.0273; 16.98028
90; 94.3034; 90
1248.11Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134926 CIFC38 H44 Fe N2 O4I 1 2 112.2867; 6.39098; 20.0622
90; 106.711; 90
1508.84Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134927 CIFC43 H32 N2 O4 SP 21 21 219.682; 17.405; 21.044
90; 90; 90
3546Ghosh, Suman; Saha, Partha Sarathi; Saha, Shib Nath; Chandrasekharan, Sanoop P.; Koner, Mainak; Baidya, Mahiuddin
Cobalt-catalyzed regio- and stereoselective synthesis of atropisomers with vicinal C-C and C-N diaxes.
Chemical communications (Cambridge, England), 2025, 61, 15231-15234
7134928 CIFC38 H33 B N2 OP -110.5016; 11.4289; 13.5999
104.793; 93.4087; 114.921
1405.02Tan, Ji-Hua; Liu, Xiao-Long; Su, Yao-Zu; Xing, Longjiang; Huo, Yanping; Chen, Jia-Xiong; Zhao, Zujin; Chen, Wen-Cheng
Incorporating hybrid charge transfer within a boron/nitrogen/oxygen-embedded scaffold for efficient yellow electroluminescence.
Chemical communications (Cambridge, England), 2025, 61, 14975-14978
7134929 CIFC8 H15 N6 O5.5 S Zn2C 1 2/c 117.4653; 9.737; 9.8807
90; 114.166; 90
1533.05Tian, Wen-Jiang; Hu, Ding-Yi; Fang, Zi-Luo; Zhong, Xiao-Feng; Xue, Ming; Zhou, Hao-Long; Zhou, Dong-Dong; Chen, Xiao-Ming
A stable sulfate-pillared metal triazolate framework with a gating effect for highly efficient dehydration of bioethanol.
Chemical communications (Cambridge, England), 2025, 61, 15461-15464
7134930 CIFC26 H19 N OP 1 21/c 110.2995; 14.7508; 13.5318
90; 106.895; 90
1967.1Yadav, Nisha; Ramasastry, S. S. V.
Creating skeletal complexity through an interrupted Corey-Chaykovsky reaction of activated alkynes.
Chemical communications (Cambridge, England), 2025, 61, 15179-15182
7134931 CIFC32 H22 N2P 42/n :215.539; 15.539; 9.7031
90; 90; 90
2342.9Lijina, M. P.; Sujilkumar, Suvarna; Jadhav, Sohan D.; Hariharan, Mahesh
Exciton interactions in crystalline crossed diazapentacene.
Chemical communications (Cambridge, England), 2025, 61, 15397-15400
7134932 CIFC25 H20 O3P -18.797; 10.718; 11.047
97.418; 90.078; 110.84
964Wu, Hao-Ze; Zhai, Jing-Qi; Sun, Jun-Xi; Liu, Ying-Pin; Tu, Man-Su; Hao, Wen-Juan; Jiang, Bo
Electrochemical dehydrogenative α-vinylation and α-allylation of cyclic β-ketoesters.
Chemical communications (Cambridge, England), 2025, 61, 15187-15190
7134933 CIFC49 H60 Cl3 O2 P TiP 1 21/c 115.782; 24.6362; 12.3944
90; 106.631; 90
4617.46Toda, Tomoyuki; Cheng, Yu; Takenaka, Katsuhiko
Synthesis and structure of titanium complexes with phosphonium-bisphenolate ligands "{P<sup>+</sup>[O<sub>2</sub>]}H<sub>2</sub>" and their catalytic trimerization of 1-octene.
Chemical communications (Cambridge, England), 2025, 61, 15594-15597
7134934 CIFC56 H53.5 B Cl0.5 F15 N2 Na O2P 1 21/c 110.4137; 21.394; 23.4007
90; 95.631; 90
5188.3Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134935 CIFC55.15 H55.58 B F15 K N2 O2.36P 1 21/c 110.4085; 21.402; 23.6416
90; 95.876; 90
5238.8Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134936 CIFC49 H43 B F15 N2 O RbP 1 21/n 110.5897; 19.8422; 22.0049
90; 102.005; 90
4522.61Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134937 CIFC58.79 H59 B F15 N2 O2.4 RbP 1 21/c 112.6204; 20.9998; 22.0018
90; 103.79; 90
5663Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134938 CIFC56 H53.5 B Cl0.5 F15 K N2 O2P 1 21/c 110.4148; 21.3092; 23.9266
90; 96.291; 90
5278.1Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134939 CIFC55.5 H57 B F15 N2 O2 RbP 1 21/c 110.4449; 21.3951; 23.6633
90; 95.879; 90
5260.2Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134940 CIFC57 H59 B Cs F15 N2 O3P n a 2124.4226; 10.8098; 20.7892
90; 90; 90
5488.42Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134941 CIFC57 H59 B Cs F15 N2 O3P 1 21/c 119.7357; 15.5295; 36.8929
90; 91.4071; 90
11303.7Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134942 CIFC57 H59 B Cs F15 N2 O3P 1 21/n 110.658; 36.1409; 43.421
90; 96.705; 90
16610.9Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134943 CIFC40 H42 F6 Li N7 Ni O7 S2P 21 21 2119.0891; 19.1789; 23.9828
90; 90; 90
8780.29Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134944 CIFC43 H48 Co F3 N7 Ni O8 SP 1 21/c 110.4885; 21.9395; 19.6735
90; 96.268; 90
4500.05Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134945 CIFC42 H45 Cu F6 N7 Ni O9 S2P 1 21/n 113.3133; 21.6731; 16.4955
90; 96.1; 90
4732.67Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134946 CIFC75 H64.5 B F24 N6 Ni2 O5.75P -112.952; 17.1844; 35.8757
80.209; 80.119; 75.351
7543.3Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134947 CIFC22 H14 Cl2 F3 NP -18.8332; 10.9154; 11.1884
103.17; 93.958; 111.325
964.66Song, Mengda; Leng, Yuting; Xu, Zhiwei; Wu, Yusheng; Wu, Yangjie
Photocatalytic cyclization reaction of 2-vinylarylamines with CF<sub>3</sub>SO<sub>2</sub>Na and arylaldehydes to access 3-(2,2,2-trifluoroethyl)-3<i>H</i>-indoles.
Chemical communications (Cambridge, England), 2025, 61, 15626-15629
7134948 CIFC25 H19 F6 N O2P 1 21/n 112.2122; 13.7141; 14.0849
90; 112.262; 90
2183.1Song, Mengda; Leng, Yuting; Xu, Zhiwei; Wu, Yusheng; Wu, Yangjie
Photocatalytic cyclization reaction of 2-vinylarylamines with CF<sub>3</sub>SO<sub>2</sub>Na and arylaldehydes to access 3-(2,2,2-trifluoroethyl)-3<i>H</i>-indoles.
Chemical communications (Cambridge, England), 2025, 61, 15626-15629
7134949 CIFC14 H13 F2 N7 O5P n a 2138.4123; 3.6758; 23.4287
90; 90; 90
3308.04Grabowski, Szymon; Wojdyła-Parat, Julianna; Tyszka-Czochara, Małgorzata; Kozieł, Marcin; Chmylak, Michał; Lalik, Sebastian; Gryl, Marlena
The whole is greater than the sum of its parts: binary and ternary 5-fluorouracil co-crystals with enhanced selectivity towards metastatic cancer cells.
Chemical communications (Cambridge, England), 2025, 61, 16770-16773
7134950 CIFC19 H18 F N5 O7P -110.0127; 10.3322; 11.01547
92.4573; 97.6809; 118.558
984.47Grabowski, Szymon; Wojdyła-Parat, Julianna; Tyszka-Czochara, Małgorzata; Kozieł, Marcin; Chmylak, Michał; Lalik, Sebastian; Gryl, Marlena
The whole is greater than the sum of its parts: binary and ternary 5-fluorouracil co-crystals with enhanced selectivity towards metastatic cancer cells.
Chemical communications (Cambridge, England), 2025, 61, 16770-16773
7134951 CIFC10 H18 I2 N2 O4 PbC 1 2 118.4916; 5.0168; 10.5385
90; 121.698; 90
831.81Cheng, Juan; Yi, Gangji; Zhong, Qinglan; Huang, Ling; Zeng, Hongmei; Zou, Guohong; Lin, Zhien
Enhanced second-harmonic generation response in a chiral lead iodide induced by amino acid coordination.
Chemical communications (Cambridge, England), 2025, 61, 15682-15685
7134952 CIFC26 H42 N3 P SnP 1 21/c 116.042; 9.1284; 19.28
90; 99.505; 90
2784.6Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134953 CIFC29 H42 N3 P Si SnP 21 21 216.5953; 17.4977; 10.4421
90; 90; 90
3032.2Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134954 CIFC26 H46 N3 P Si2 SnP 1 21/n 111.485; 17.028; 15.977
90; 90.319; 90
3124.5Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134955 CIFC35 H54 N3 P Si SnP -110.7809; 12.7284; 14.9033
72.507; 82.446; 69.563
1826.93Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134956 CIFC27 H46 N3 P Si SnP 1 21/n 111.3458; 16.8337; 15.6145
90; 90.519; 90
2982.12Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134957 CIFC37 H31 N O4 S2P -111.1541; 11.8712; 12.7603
64.127; 81.601; 81.316
1496.72Yadav, Pooja; Varma, A. Anagha; Gopinath, Purushothaman
Accessing [6,6,5,6] tetracyclic indeno-quinolines <i>via</i> a photomediated cascade reaction of electron-rich 1,7-enynes.
Chemical communications (Cambridge, England), 2025, 61, 16440-16443
7134958 CIFC19 H23 Br N O6 PP 43 21 210.3187; 10.3187; 38.654
90; 90; 90
4115.7Savoskin, Alexander E.; Efremov, Andrey N.; Murashkina, Arina V.; Gontcharenko, Victoriya E.; Bogdanov, Andrei V.; Mitrofanov, Alexander Yu; Beletskaya, Irina P.
Base-promoted cascade annulation and annulation/carboxylation of α-enolizable phosphoryl substituted ynones and isatins with CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2025, 61, 16230-16233
7134959 CIFC45 H57 N4 O10 ZnP 1 21/c 114.7895; 18.2516; 19.007
90; 111.191; 90
4783.7Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134960 CIFC44.5 H48.5 N4 O6.5 ZnC 1 2/c 128.556; 13.118; 24.817
90; 113.023; 90
8556Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134961 CIFC31 H31.94 F N3 O8 ZnP -113.273; 13.274; 18.456
85.563; 77.044; 79.9
3117Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134962 CIFC53 H53 Cl2 O4 Si3C 1 2/c 116.5351; 15.4526; 19.1218
90; 102.301; 90
4773.6Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134963 CIFC52 H50 O4 Si3I 1 2/c 117.857; 11.106; 23.4549
90; 91.262; 90
4650.4Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134964 CIFC28 H38 O2 Si3P -110.5394; 12.0173; 12.3813
82.86; 68.217; 82.581
1439.02Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134965 CIFC38 H42 O2 Si3P 1 21/c 118.8918; 16.4124; 11.5152
90; 101.755; 90
3495.5Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134966 CIFC27 H34 O2 Si3P 1 21/c 110.8977; 18.3039; 13.5149
90; 91.29; 90
2695.14Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134967 CIFC38 H42 O2 Si3P -19.5424; 10.5382; 18.3347
78.61; 82.78; 76.832
1753.6Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134968 CIFC64 H54 O5.25 SiC 1 2/c 129.764; 14.7485; 25.3341
90; 117.338; 90
9878.9Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134969 CIFC39 H34 Cl3 D O4 SiP 1 n 111.0558; 13.5926; 23.5001
90; 102.655; 90
3445.73Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134970 CIFC6 H17 Cl N6 O4P 1 21/c 110.4474; 10.2793; 12.6679
90; 100.902; 90
1335.88Pan, Yu-Ming; An, Xin-You; Fang, Zhi
[C(NH<sub>2</sub>)<sub>3</sub>]<sub>2</sub>[C<sub>2</sub>H<sub>5</sub>(C<sub>2</sub>O<sub>4</sub>)]Cl: rational design of a metal-free UV birefringent crystal through the synergistic assembly of three distinct motifs.
Chemical communications (Cambridge, England), 2025, 61, 15894-15897
7134971 CIFC32 H32 Co N2 O2P b c a16.768; 16.0675; 20.0092
90; 90; 90
5390.88Robaszkiewicz, Jakub; Szarłan, Bartłomiej; Pawluć, Piotr; Kubicki, Maciej; Zaranek, Maciej
Sustainable synthesis of hydrosilanes and alkoxysilanes in a sequential one-pot olefin hydrosilylation and dehydrogenative coupling with alcohol under phenoxyiminato cobalt(II) catalysis.
Chemical communications (Cambridge, England), 2025, 61, 16046-16049
7134972 CIFC98.53 H111.06 N2 O11.84P -116.74959; 24.61558; 24.87337
64.6808; 70.8779; 74.2696
8655Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134973 CIFC92 H100 N2 O9C 1 2 119.5858; 21.7012; 20.0122
90; 113.871; 90
7778.3Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134974 CIFC93.62 H101.24 N2 O9.54C 1 2/c 143.0399; 24.2273; 61.0404
90; 99.47; 90
62781.9Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134975 CIFCa6 Mn2 N6 OR -3 :H8.92557; 8.92557; 9.23716
90; 90; 120
637.296Buschmann, Niklas; Werhahn, Dominik; Steinberg, Simon; Ritter, Clemens; Attfield, J. Paul; Kloß, Simon D
Multiple bonding in unbridged Mn-Mn dimers of solid-state nitridomanganate(IV) oxide Ca<sub>6</sub>[Mn<sub>2</sub>N<sub>6</sub>]O.
Chemical communications (Cambridge, England), 2025, 61, 15662-15665
7134976 CIFCa6 Mn2 N6 OR -3 :H8.95635; 8.95635; 9.25969
90; 90; 120
643.264Buschmann, Niklas; Werhahn, Dominik; Steinberg, Simon; Ritter, Clemens; Attfield, J. Paul; Kloß, Simon D
Multiple bonding in unbridged Mn-Mn dimers of solid-state nitridomanganate(IV) oxide Ca<sub>6</sub>[Mn<sub>2</sub>N<sub>6</sub>]O.
Chemical communications (Cambridge, England), 2025, 61, 15662-15665
7134977 CIFC64 H98 Cl4 Ir2 Li2 O3 P2P 1 21/c 110.52239; 18.32736; 17.04898
90; 99.046; 90
3246.96Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134978 CIFC46 H82 K N4 O9 PP 1 2/n 111.2324; 11.8181; 36.8937
90; 95.713; 90
4873.2Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134979 CIFC26 H54 K N4 O7 PP 1 21/c 117.2179; 8.7318; 21.9955
90; 103.469; 90
3215.92Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134980 CIFC57 H86 Au N2 O3.5 PP 1 21/c 117.92474; 22.02986; 15.23246
90; 114.707; 90
5464.35Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134981 CIFC129 H228 B4 K4 N8 O10.25 P4P -116.8002; 17.1154; 24.435
96.603; 106.698; 92.909
6659.2Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134982 CIFC46 H52 Si2P -19.869; 12.442; 32.249
82.407; 81.941; 74.764
3764Espineira-Gutierrez, Adrian; Caro-Noakes, Ines; Zhang, Min; Mas-Torrent, Marta; Regulska, Elzbieta; Romero-Nieto, Carlos
The role of main group elements in shaping the properties of linearly-fused heterohexaarenes.
Chemical communications (Cambridge, England), 2025, 61, 15590-15593
7134983 CIFC12 H23 Fe3 N2 O19P 1 21/n 114.2657; 8.2582; 21.5884
90; 102.732; 90
2480.8Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134984 CIFC13 H23 Fe3 N2 O18P 1 21/n 114.2147; 8.3281; 21.3984
90; 102.558; 90
2472.6Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134985 CIFC15 H27 Fe3 N2 O18P 1 21/n 114.3325; 8.4968; 21.8494
90; 102.465; 90
2598.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134986 CIFC12 H23 Fe3 N2 O19R -3 c :H8.2548; 8.2548; 63.391
90; 90; 120
3740.9Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134987 CIFC15 H27 Fe3 N2 O18R -3 c :H8.4183; 8.4183; 63.025
90; 90; 120
3868.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134988 CIFC13 H23 Fe3 N2 O18R -3 c :H8.2967; 8.2967; 62.793
90; 90; 120
3743.3Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134989 CIFC9 H9 F O3C 1 2/c 118.7223; 11.2619; 8.6284
90; 109.598; 90
1713.9Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134990 CIFC7 H5 F O3P -17.6681; 8.3643; 11.4816
76.068; 77.79; 64.382
639.61Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134991 CIFC58 H34 N4 O2P 18.8479; 11.4027; 11.4991
86.241; 72.076; 68.194
1023.29Yin, Xiaojun; Chen, Xuefeng; Mo, Xuechao; Chen, Junjin; Huang, Mengyu; Ma, Jiacheng; Li, Yulan; Li, Nengquan; Yang, Chuluo
Charge-transfer modulated chiroptical azacyclooctatetraene-fused [5]helicenes with AIE features.
Chemical communications (Cambridge, England), 2025, 61, 16448-16451
7134992 CIFC28.5 H21 Br Cl O4P 19.0354; 11.1067; 13.6619
106.141; 96.303; 107.287
1229.51Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134993 CIFC28 H22 O4P 21 21 218.8073; 12.1366; 20.0872
90; 90; 90
2147.13Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134994 CIFC28 H22 O4P 1 21 111.628; 15.6621; 12.0951
90; 97.484; 90
2183.98Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134995 CIFC27 H22 N2 O2I 1 a 15.8439; 38.1781; 9.1909
90; 94.124; 90
2045.26Kumar, Pravin; Dash, Om Prakash; Volla, Chandra M. R.
Cobalt-catalyzed regioselective (4+2)-annulation of benzamides with allenyl carbinol acetates: access to 3-vinylisoquinolinones.
Chemical communications (Cambridge, England), 2025, 61, 16962-16965
7134996 CIFC48 H38 Ag P3 SP -110.8475; 12.0536; 15.9663
72.057; 88.8299; 81.512
1963.63Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134997 CIFC48 H38 Ag P3 SP -110.8455; 12.0698; 15.9133
72.271; 88.798; 81.388
1961.13Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134998 CIFC21 H21 Br N2 OP 1 21/c 112.9547; 10.2165; 16.1046
90; 113.338; 90
1957.1Kar, Subarna; Ramachandran, Arya; Rit, Arnab
Efficient synthetic approach to <i>m</i>-terphenyl derivatives <i>via</i> arylation of azolium salts.
Chemical communications (Cambridge, England), 2025, 61, 16802-16805
7134999 CIFC21 H16 N O2 PP -18.71; 10.081; 11.048
99.774; 106.774; 100.943
885.5Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135000 CIFC21 H18 N O2 PP 1 21/c 111.6354; 11.6264; 13.4546
90; 91.652; 90
1819.35Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135001 CIFC106 H58 N18 O17 Pd2 Zn5P 1 21/n 19.9191; 32.4889; 38.6916
90; 95.533; 90
12410.7Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135002 CIFC56 H36 N10 O9 Pd Zn2C 1 2/c 133.103; 10.1085; 43.6
90; 98.346; 90
14435Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135003 CIFC56 H36 N10 O9 Pd Zn2P 1 21/c 122.815; 9.9064; 31.625
90; 95.495; 90
7114.9Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135004 CIFC58 H33 N14 O8.5 Pd Zn3C c c a :233.8282; 10.4006; 43.8964
90; 90; 90
15444.2Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135005 CIFC32 H34 Ag Cl Fe N12 O6C 1 2/c 113.4233; 16.051; 17.725
90; 95.291; 90
3802.7Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135006 CIFC32 H34 Ag Cl Fe N12 O6.16C 1 2/c 113.2411; 15.6597; 17.3891
90; 97.325; 90
3576.2Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135007 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.8631; 25.8631; 20.8337
90; 90; 120
12068.6Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135008 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.546; 25.546; 20.356
90; 90; 120
11504.5Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135009 CIFC28 H27 N O6 SP 1 21/c 110.2849; 24.4179; 10.3397
90; 105.642; 90
2500.5Zheng, Jianfeng; Xiong, Dong; Ye, Yongqi; Tang, Luhao; Yang, Jiajin; Yang, Zeyu; Cai, Yunfei
Efficient syntheses of 2-amino-4<i>H</i>-pyrans <i>via</i> gold-catalyzed cyclization of diester-tethered ynamides.
Chemical communications (Cambridge, England), 2025, 61, 16858-16861
7135010 CIFC18 H15 Br I N OP -16.3543; 8.4335; 16.8759
98.77; 99.305; 90.041
881.73Chen, Chen; Wang, Zi-Yi; Zhang, Xiao-Xu; Wang, Kui; Zhu, Bolin
Pd-catalyzed electrophilic cross-coupling of pyridylphosphonium salts with arylthianthrenium salts to access C4-arylated pyridines.
Chemical communications (Cambridge, England), 2025, 61, 17185-17188
7135011 CIFC33 H51 Al N2 ZnP n m a15.9848; 20.213; 9.8381
90; 90; 90
3178.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135012 CIFC83 H114 Ga2 N4 O2 Zn2P -19.7057; 14.4604; 14.9677
87.7489; 72.9148; 73.06
1918.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135013 CIFC64 H94 N4 Si2P -110.9267; 11.6874; 12.7613
93.932; 104.6; 111.522
1443.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135014 CIFC62 H53 B F20 N2 Si ZnP -111.1667; 12.7101; 21.923
98.644; 101.458; 102.212
2919.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135015 CIFC74 H115 Ga N4 Si ZnP 1 21/n 112.1549; 32.569; 18.1556
90; 101.686; 90
7038.3Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135016 CIFC74 H113.5 Ga N4 Si ZnC 1 2/c 117.5328; 19.9362; 20.5665
90; 93.366; 90
7176.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135017 CIFC33 H51 Ga N2 ZnP 21 21 219.876; 16.0049; 20.269
90; 90; 90
3203.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135018 CIFC74 H120 Ga2 N4 ZnC 1 2/c 117.5441; 20.0646; 20.5353
90; 93.8778; 90
7212.2Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135019 CIFC74 H120 Al Ga N4 ZnC 1 2/c 117.6429; 20.0099; 20.5546
90; 92.706; 90
7248.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135020 CIFC74 H102 Ga N4 Si ZnC 1 2/c 116.4935; 17.0584; 24.336
90; 92.0203; 90
6842.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135021 CIFC78 H78 O12P -16.0018; 16.2806; 16.8345
107.589; 97.731; 95.825
1536.1Yamini, Pokhriyal; Duklan, Bhoomika; Nirmal, Mukesh; Yadagiri, Dongari
Light-induced intramolecular carbene C(sp<sup>3</sup>)-H insertion of <i>N</i>-tosylhydrazones; synthesis of functionalized coumarans and indolines.
Chemical communications (Cambridge, England), 2025, 61, 17017-17020
7135022 CIFC8 H9 N3 O2P b c a12.8099; 7.7737; 18.5183
90; 90; 90
1844.06Kumar, Prashant; Kant, Ruchir; Rastogi, Namrata
Nitrogen atom insertion into NN double bonds: straightforward access to triazenes.
Chemical communications (Cambridge, England), 2025, 61, 16632-16635
7135023 CIFC21 H17 N O2P n m a15.204; 6.943; 15.282
90; 90; 90
1613Bai, Fang; Liu, Pengpeng; Xu, Hongyan; Li, Mengjie; Liu, Binghui; Xu, Miaomiao; Gao, Qinghe
Auto-oxidation-driven vicinal C(sp<sup>3</sup>)-H desaturative cyclization of tertiary alkylamines for the synthesis of pyrido[3,2-<i>c</i>]coumarins.
Chemical communications (Cambridge, England), 2025, 61, 16818-16821
7135024 CIFC20 H20 Dy2 O20P 1 21/n 17.6415; 15.8785; 21.8456
90; 97.457; 90
2628.23Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135025 CIFC60 H50 Cl1.5 Dy8.5 O86P 4/m21.7419; 21.7419; 7.7397
90; 90; 90
3658.64Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135026 CIFC60 H52 Cl1.5 Gd8.5 O86P 4/m21.8854; 21.8854; 7.7744
90; 90; 90
3723.71Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135027 CIFC11 H11 N O2P 1 21/n 113.1083; 6.8867; 21.4225
90; 92.066; 90
1932.61Shi, Yaolian; Gong, Yuchen; Li, Ganpeng; Zhao, Xiao-Jing; He, Yonghui
Cobalt-salen complexes/organic photoredox-cocatalyzed selective oxidative formylation of enaminones.
Chemical communications (Cambridge, England), 2025, 61, 17173-17176
7135028 CIFC68 H92 N4 O P4P 1 c 19.94331; 17.65986; 18.49899
90; 99.9045; 90
3199.96Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135029 CIFC44 H51 N2 P Se2P -19.845; 10.4186; 21.0183
82.912; 80.297; 71.16
2005.68Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135030 CIFC48 H57 F6 N2 O3 P2 SP 1 21/n 112.1447; 29.8408; 13.06799
90; 94.1461; 90
4723.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135031 CIFC67.76 H90.76 N4 P2P -112.0999; 14.6052; 41.8681
85.433; 87.238; 68.411
6856.66Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135032 CIFC33 H41 F3 N2 O3 P2 SP 1 21/c 112.1104; 13.7238; 20.3093
90; 97.664; 90
3345.27Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135033 CIFC76 H102 N4 P4P b c a22.3323; 21.5645; 29.5421
90; 90; 90
14227Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135034 CIFC45 H51 F3 N2 O3 P2 S3P -110.4857; 13.3395; 16.2297
94.945; 99.955; 94.997
2215.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135035 CIFC21 H17 Cl N4 O2P 1 21/c 121.4394; 13.9197; 12.5913
90; 105.292; 90
3624.6Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135036 CIFC21 H21 Cl N4 O4P 1 21/c 19.5672; 35.984; 5.9462
90; 95.563; 90
2037.4Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135037 CIFC14 H14 N4 OP 1 21/n 110.6661; 4.919; 23.7529
90; 102.205; 90
1218.06Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135038 CIFC36 H37 N OP b c a9.7987; 20.5217; 28.652
90; 90; 90
5761.5Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135039 CIFC57 H61 N O3P 1 21 111.4318; 11.308; 18.3289
90; 93.843; 90
2364.1Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135040 CIFC H9 B3 F2 N4 O5P -17.2945; 7.969; 8.237
107.653; 101.435; 95.312
441.19Shen, Chunjie; Zhou, Huan; Hu, Chenhui; Yang, Zhihua; Zhang, Feng; Pan, Shilie
CN<sub>4</sub>H<sub>7</sub>B<sub>3</sub>O<sub>3</sub>F<sub>2</sub>(OH)<sub>2</sub>: short-wave UV hydroxyfluorooxyborate crystals with large birefringence.
Chemical communications (Cambridge, England), 2025, 61, 16997-17000
7135041 CIFC8 H20 Cd3 Cl7 NP -17.818; 11.1147; 13.4404
66.714; 82.325; 70.712
1012.55Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135042 CIFC8 H20 Cd3 Cl7 NP -17.855; 11.1928; 13.5318
67.72; 81.919; 69.603
1031.81Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135043 CIFC20 H22 N2 O3P 21 21 219.8569; 13.5366; 13.7081
90; 90; 90
1829.06Huang, Yinghong; Zheng, Renhua; Cheng, Xiaomeng; Geng, Xiao; Wang, Lei; Zhu, Bihong
Dehalogenation hydrolysis of CF<sub>2</sub>Br<sub>2</sub> enables four-component aminocarbonylation <i>via</i> photocatalytic radical-polar crossover.
Chemical communications (Cambridge, England), 2025, 61, 17033-17036
7135044 CIFC19 H14 F3 N OP 1 21/c 18.33; 17.1545; 11.1957
90; 97.513; 90
1586.1Sachin, ?; Sharma, Tamanna; Rav, Shourabh; Sharma, Upendra
Ru(II)-catalysed, inherent-directing-group-enabled site-selective C-H vinyl trifluoromethylation of isoquinolones and benzamides.
Chemical communications (Cambridge, England), 2025, 61, 17416-17419
7135045 CIFC27 H27 Dy N4 O3P 1 21/c 116.7777; 19.0804; 7.7909
90; 97.375; 90
2473.4Hasegawa, Natsuki; Yanai, Akiho; Masaki, Hinako; Kirishima, Akira; Tsunashima, Ryo; Masuya-Suzuki, Atsuko
Stepwise selective crystallization of Fe and Dy complexes from a Fe/Nd/Dy mixture: separation despite charge and solubility similarity.
Chemical communications (Cambridge, England), 2025, 61, 17384-17387
7135046 CIFC23 H17 O2 PP 1 21/c 112.0273; 5.9723; 24.2673
90; 91.698; 90
1742.37Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135047 CIFC46 H32 O3 P2P 21 21 2111.0559; 16.5376; 18.8101
90; 90; 90
3439.2Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135048 CIFC12 H20 O S Si2P 1 21/n 110.7711; 9.923; 15.3315
90; 110.531; 90
1534.57An, Kun; Liu, Mengqing; Wang, Jingxia; Nishiura, Masayoshi; Cong, Xuefeng; Hou, Zhaomin
Synthesis of [1,3]-thiasilolanes <i>via</i> rare-earth-catalysed intramolecular α-C(sp<sup>3</sup>)-H silylation of alkyl sulphides with hydrosilanes.
Chemical communications (Cambridge, England), 2025, 61, 17181-17184
7135049 CIFC21 H19 N O2P -17.208; 9.749; 12.523
73.203; 76.884; 78.341
811.6Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135050 CIFC24 H19 N O4 SP -111.3303; 14.1464; 14.8702
97.934; 108.308; 112.348
2000.8Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135051 CIFC25 H18 O3C 1 2/c 123.6123; 9.4715; 17.1625
90; 100.183; 90
3777.83Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135052 CIFC25 H17 F O3C 1 2/c 128.2559; 13.6584; 10.0502
90; 91.917; 90
3876.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135053 CIFC36 H22 O2P -110.2845; 16.121; 17.626
98.505; 98.503; 106.719
2711.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135054 CIFC12 H11.5 Cl N1.5 O1.5P -19.0938; 11.5029; 12.1234
111.969; 98.763; 94.676
1149Thakur, Rekha; Luxami, Vijay; Paul, Kamaldeep
Ruthenium(II)-catalyzed C-2 alkenylation of indole with olefins <i>via</i> a quinazolin-4(3<i>H</i>)-one directing group: a platform for selective fluorescent anion sensors.
Chemical communications (Cambridge, England), 2025, 61, 14374-14377
7135055 CIFC21 H25 N3 O3P -18.5658; 10.1115; 23.1709
96.106; 98.963; 101.388
1923.78Paul, Subhankar; Chaudhuri, Debangshu
Side-chain dependent direct <i>vs.</i> indirect photoresponse in hydrazone-based supramolecular polymers.
Chemical communications (Cambridge, England), 2025, 61, 14366-14369
7135056 CIFC38 H22 F6 N4P 1 21/c 117.1; 17.498; 13.593
90; 112.31; 90
3762.8Panua, Anirban; Velmurugan, Gunasekaran; Comba, Peter; Rath, Harapriya
Targeted synthesis of a positional isomer of aromatic <i>N</i>-methyl <i>N</i>-confused corrole and its organocopper(III) complex.
Chemical communications (Cambridge, England), 2025, 61, 17436-17439
7135057 CIFC21 H25 N OP 21 21 219.4002; 10.6999; 17.6147
90; 90; 90
1771.71Ghosh, Subhadeep; Biswas, Sumit; Das, Indrajit
Electro-carbo-cyclization of alkyne-, alkene-, and nitrile-tethered α-halocarbonyls.
Chemical communications (Cambridge, England), 2025, 61, 17448-17451
7135058 CIFC46 H76 O2 P2C 1 2/c 115.876; 14.4684; 20.2954
90; 104.386; 90
4515.68Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135059 CIFC22 H28 P2 Se2I 1 2/a 114.989; 8.3205; 18.148
90; 95.024; 90
2254.65Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135060 CIFC14 H36 Cl6 Mn N4P 21 21 218.4441; 16.7468; 17.4329
90; 90; 90
2465.22Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135061 CIFC14 H36 Br6 Mn N4P 21 21 218.6152; 17.2628; 18.0558
90; 90; 90
2685.3Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135062 CIFC14 H36 Cl10 Mn3 N4P 1 21/n 19.5893; 8.8686; 16.9149
90; 90.355; 90
1438.48Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135063 CIFC14 H36 I6 Mn N4P 21 21 218.9096; 18.141; 18.976
90; 90; 90
3067.1Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135064 CIFC88.5 H47 Cu N12 OP -113.047; 13.52; 21.777
79.204; 73.104; 77.349
3554.7Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135065 CIFC88 H44 Cu N12P -113.329; 15.694; 21.415
78.765; 75.079; 68.029
3990Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135066 CIFC25 H31 N O2C 1 c 145.525; 7.0641; 6.6022
90; 94.133; 90
2117.7Xiao, Yao; Pan, Xue-Lan; Cao, Xiang-Jian; Qi, Xin; Qiu, Sheng-Qi; Yu, Zhen-Qiang
A room temperature nematic luminescent liquid crystal: a FRET donor for amplified circularly polarized luminescence.
Chemical communications (Cambridge, England), 2025, 61, 17922-17925
7135067 CIFC29 H29 N3 O4P 1 21/n 111.4876; 12.9087; 17.8682
90; 106.868; 90
2535.67Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135068 CIFC29 H29 N3 O4P 1 2/n 111.9144; 11.0129; 20.0815
90; 97.27; 90
2613.75Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135069 CIFC20 H25.69 Mn2 N8 O8.85P 1 21/c 113.7898; 12.1567; 17.2696
90; 103.019; 90
2820.6Howlett, Thomas; Wang, Ziqi; Tang, Wendy; Arora, Nyati; Shende, Prapti M.; Liu, Phillip; Kumari, Sneha; Joy, Monu; Wriedt, Mario; Smaldone, Ronald A.; Gassensmith, Jeremiah J.
From Spontaneous Ligand Evolution to High-Throughput Water-Based Synthesis: Scalable Access to CO2 Selective Mixed-Ligand Metal Organic Frameworks
Chemical Communications, 2025
7135070 CIFC68 H137.5 Al I Mo6 N Na3 O94.25P 1 21 114.6954; 34.3474; 25.064
90; 105.154; 90
12211.1Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135071 CIFC208 H400 Al2 I2 Mo12 N2 O223P 1 21/n 128.963; 17.363; 37.324
90; 109.111; 90
17735Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135072 CIFC30 H28P c c n16.2667; 16.4045; 18.0519
90; 90; 90
4817.1Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135073 CIFC30 H28P 1 2/n 113.061; 6.7745; 13.079
90; 91.233; 90
1157Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135074 CIFC30 H28P 1 21/c 121.3224; 5.817; 19.767
90; 109.562; 90
2310.2Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135075 CIFC42 H38 N2 O9P -15.9506; 11.9443; 13.0049
83.657; 78.757; 84.862
898.85Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135076 CIFC38 H30 N2 O8P -14.7799; 11.7694; 14.1229
94.792; 91.588; 93.494
789.83Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135077 CIFC13 H9 SP 1 21/n 112.122; 5.585; 14.566
90; 107.22; 90
941.9Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135078 CIFC26 H8 F10 S2P 1 21/c 113.016; 4.9514; 17.4745
90; 102.038; 90
1101.42Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135079 CIFC26 H16 Br2 S2P 1 21/n 18.9039; 5.6737; 22.1636
90; 101.035; 90
1098.96Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135080 CIFC28 H24 N2 O6P -19.9897; 11.2443; 12.144
108.063; 102.688; 90.502
1260.85Tang, Shou-Yang; Sang, Qian-Qian; Chen, Ze-Le; Cai, Bao-Gui; Xuan, Jun
Visible-light-promoted synthesis of imidazo[1,5-<i>a</i>]indole-3-ones <i>via</i> cascade carbene N-H insertion and oxidative cyclization.
Chemical communications (Cambridge, England), 2025, 61, 17870-17873
7135081 CIFC2.21 H2.34 N0.28 O0.62P 1 21/c 121.4354; 9.9487; 15.1153
90; 104.054; 90
3126.92Biswas, Sourabh; Srinivasu, Vinjamuri; Mallick, Manasi; Chandu, Palasetty; Sureshkumar, Devarajulu
Photoredox-driven tandem ring-opening and vinylation: a route to distal alkenyl ketones from cyclopropenes.
Chemical communications (Cambridge, England), 2025, 61, 18388-18391
7135082 CIFC16 H11 F3 O6P -19.1458; 9.3792; 10.2964
86.62; 77.558; 63.535
771.41Ni, Tongtong; Xu, Xuefeng; Li, Wenguang; Li, Shiyuan; Sheng, Heyun; Zhang, Xu
Nickel-catalyzed [4+2] cycloadditions of β-ketoesters and alkynes.
Chemical communications (Cambridge, England), 2025, 61, 17645-17648
7135083 CIFC22 H23 N O2P 21 21 218.541; 12.2915; 17.0269
90; 90; 90
1787.51Manna, Sabyasachi; Sreedhara, Rahul Halanuru; Punesh, Thanay Umesh; Prabhu, Kandikere Ramaiah
Use of tailored boronic acids both as a radical donor and acceptor in a visible light-mediated di-functionalization of maleimides: rapid access to fused benzo[<i>e</i>]isoindole-1,3-diones.
Chemical communications (Cambridge, England), 2025, 61, 17669-17672
7135084 CIFC8 H24 Cl6 Mo N2 NaP 1 21/n 19.0726; 6.8264; 15.7029
90; 90.066; 90
972.53Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135085 CIFC8 H24 Ag Cl6 Mo N2P 63/m m c9.054; 9.054; 6.7638
90; 90; 120
480.18Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135086 CIFC71 H133 Fe K N7 O11 Si4P 1 21/c 118.115; 19.364; 25.348
90; 106.419; 90
8528.9Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135087 CIFC39 H83 Fe K N5 O6 Si4P -112.6097; 13.1708; 17.6115
110.391; 93.952; 93.322
2724.6Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135088 CIFC44 H96 Fe K N5 O6 Si4P -112.6019; 13.1359; 17.7179
110.508; 93.368; 93.329
2732.63Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135089 CIFC72 H152 F4 Fe2 K2 N8 O12 S4 Si8P -111.8028; 15.389; 29.1949
103.183; 92.864; 99.764
5066.5Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135090 CIFC28.6 H22.9 Cl Cu N6.3C 1 2/c 123.24; 30.2; 7.495
90; 97.687; 90
5213.1David, A. John; Seethapathy, Logeshwari; Kumar, S. Vijay; Das, Rajorshi; Das, Anjan
Photocatalytic carboxylation of aryl halides/alkenes with a copper(I) complex bypassing the demand for dual catalysts.
Chemical communications (Cambridge, England), 2025, 61, 17677-17680
7135091 CIFC17 H16 N2 OP 1 21/n 18.8248; 13.1914; 11.6734
90; 102.126; 90
1328.6Liu, Xiang; Wu, Wen-Rong; Ma, Shaohong; Chen, Juan; Meng, Yuan-Jie; Yang, Zi-Feng; Zhang, Shang-Shi; Feng, Pengju
Base-promoted [3+2] annulation of <i>N</i>-aminoisoquinolinium derivatives with cyclic iodonium ylide/2,2-difluorovinyl tosylate.
Chemical communications (Cambridge, England), 2025, 61, 17673-17676
7135092 CIFC16 H17 N3 SP 1 21/c 17.8135; 27.8711; 13.276
90; 90.854; 90
2890.8Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135093 CIFC39 H22 B Cl2 F10 N3 SP -112.0186; 12.5059; 13.7414
95.301; 106.618; 113.936
1756.94Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135094 CIFC27 H13 B F10 N2 O SP -19.6678; 10.2025; 13.9028
104.522; 95.869; 111.606
1205.04Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135095 CIFC28 H16 B F10 N3 SP -19.8457; 10.564; 13.7846
105.553; 90.551; 113.918
1251.18Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135096 CIFC17 H19 F6 O P SiP -18.9992; 10.1647; 11.3907
99.1849; 91.1844; 112.8
944.31Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135097 CIFC18 H21 F6 O P SiP -110.0771; 10.5675; 11.3486
92.695; 109.345; 114.43
1014.09Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135098 CIFC44 H88 Cl4 Cu4 Si4P -17.4937; 13.8967; 27.206
100.646; 91.838; 91.599
2781.3Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135099 CIFC88 H168 Cu8 Si8P 21 21 2114.9963; 22.5357; 30.877
90; 90; 90
10434.9Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135100 CIFC34 H20 F4 N2 SC 1 2/c 129.3094; 14.7807; 6.9665
90; 98.9151; 90
2981.5Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135101 CIFC22 H16 N2 SP 1 21/c 19.5987; 15.087; 11.7651
90; 101.039; 90
1672.25Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135102 CIFC13 H9 B F2 N2 SP 1 21/c 112.1127; 9.1231; 11.7692
90; 113.578; 90
1191.98Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135103 CIFC15 H13 B F2 N2 SP 1 21/c 16.9891; 13.5514; 14.4026
90; 95.392; 90
1358.06Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135104 CIFC105 H102 Cl6 N18 Se3P 3119.6339; 19.6339; 26.1675
90; 90; 120
8735.9Liu, Chao; Du, Ziwei; Ding, Xu; Wang, Zhixuan; Cao, Lili; Zhou, Ziwen; Chen, Jia; Zhang, Ning
Precise heteroatom engineering for iodine capture promotion in porous organic cages.
Chemical communications (Cambridge, England), 2025, 61, 19076-19079
7135105 CIFC27 H26 N O2 SeP 1 21 15.4585; 20.644; 21.236
90; 93.871; 90
2387.5Reddy, Chada Raji; Vinaya, Puthiya Purayil; Ajaykumar, Uprety; Nagendraprasad, Thallamapuram
Electrophilic aryl migration of <i>N</i>-benzyl propiolamides to functionalized-acrylamides.
Chemical communications (Cambridge, England), 2025, 61, 18669-18672
7135106 CIFC34 H52 B2 F2 O10 S2P -18.7369; 10.5221; 11.1567
69.401; 88.06; 71.327
905.93Wang, Shuting; Tang, Shuai; Han, Xiao-Le; Zhang, Hua
Regioselective postmodification of aryl sulfonyl fluorides <i>via</i> iridium(I)-catalysed C-H borylation.
Chemical communications (Cambridge, England), 2025, 61, 18830-18833
7135107 CIFC52 H52 Ag2 F6 N12 O8 S4P 18.38282; 13.97902; 14.3924
115.939; 100.085; 95.7768
1462.99Sawant, Diksha U.; Halat, Peter; McKay, Alasdair I.; Izgorodina, Ekaterina I.; Turner, David R.
Dependence of an anion template on amino acid binding in DMSO/H<sub>2</sub>O by a chiral Ag/urea-based tweezer.
Chemical communications (Cambridge, England), 2025, 61, 18846-18849
7135108 CIFC23 H25 Cl N2 O2P 21 21 2110.5633; 10.5879; 18.4454
90; 90; 90
2062.99Clark, Paul; Keenan, Thomas; Liu, Shiqi; Huang, Jingjun; Ma, Yao-Rui; Hasija, Avantika; Huang, Pei-Qiang; Jean, Alexandre; Leitch, David C.; Arseniyadis, Stellios
Palladium-catalysed asymmetric allylic alkylation of hydantoins using bench-stable chiral palladium precatalysts.
Chemical communications (Cambridge, England), 2025, 61, 19064-19067
7135109 CIFC29 H20 N2 O3 S2 Se2P 1 21/c 15.7891; 14.1638; 32.308
90; 94.605; 90
2640.6Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135110 CIFC14 H4 Cl2 N2 Se2P -17.8604; 8.7632; 11.4837
93.4629; 106.53; 112.541
687.45Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135111 CIFC36 H34 N2 O4 S2P 1 21/n 15.9391; 23.454; 23.02
90; 93.477; 90
3200.7Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135112 CIFC28 H18 N2 O4 S2P 1 21/c 111.6031; 16.6534; 12.2098
90; 96.077; 90
2346.1Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135113 CIFC28 H18 N2 O2 S4P 1 n 16.1558; 16.8897; 12.1311
90; 103.961; 90
1224Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135114 CIFC36 H34 N2 O2 S2 Se2P -15.6312; 17.0766; 17.206
86.595; 81.468; 87.677
1632.5Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135115 CIFC31.5 H26 N2 O2 S2 Se2P -16.2952; 11.3991; 20.6848
104.048; 91.718; 99.82
1414.88Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135116 CIFC32 H27 F O2 SC 1 2/c 135.9609; 12.6981; 11.4122
90; 91.584; 90
5209.2Yu, Tianxin; Shi, Tingchang; Zhang, Zhilei; Xu, Hai-Bing; He, Zikai; Jiang, Lang; Gu, Xinggui; Wang, Erjing
Boosting aggregation-induced emission of hydroxylated tetraphenylthiophene via biogenic amine entangling
Chemical Communications, 2025
7135117 CIFC31 H29 I O3P 1 21/c 120.985; 10.746; 12.2193
90; 102.749; 90
2687.57Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-catalyzed stereoselective desymmetrization of prochiral cyclopentane-1,3-diones <i>via</i> alkoxyallylation.
Chemical communications (Cambridge, England), 2025, 61, 19108-19111
7135118 CIFC25 H28 O3P 1 21 18.4261; 11.7773; 11.2319
90; 107.842; 90
1061.01Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-catalyzed stereoselective desymmetrization of prochiral cyclopentane-1,3-diones <i>via</i> alkoxyallylation.
Chemical communications (Cambridge, England), 2025, 61, 19108-19111
7135119 CIFC25 H18 N2 O4P -18.1541; 8.182; 15.3186
103.249; 101.047; 92.876
971.63Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135120 CIFC47 H32 N4 O2P 1 21/c 114.78458; 16.90271; 14.64273
90; 108.139; 90
3477.36Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135121 CIFC13 H10 N4 O7P -17.4442; 9.0095; 10.8263
88.03; 76.686; 87.558
705.721Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135122 CIFC6 H6 N2 OP 1 21/c 115.999; 8.007; 9.943
90; 105.312; 90
1228.5Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135123 CIFC19 H16 N6 O8P -18.1848; 10.8341; 12.2177
71.159; 81.7; 89.974
1013.38Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135124 CIFC14 H11 N3 O8P 1 21/n 18.4196; 13.3701; 13.4639
90; 101.402; 90
1485.7Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135125 CIFC31 H23 N7 O14C 1 2/c 117.8367; 12.2586; 13.8777
90; 90.554; 90
3034.26Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135126 CIFC19 H19 N5 O4P -17.9234; 8.7843; 13.3922
92.797; 101.022; 95.147
909.16Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135127 CIFC20 H17 N5 O9P -17.2524; 8.8044; 16.4118
93.805; 91.218; 94.787
1041.61Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135128 CIFC46 H45 Cl2 Fe2 N O6 S4P 21 21 2110.6274; 13.5606; 31.507
90; 90; 90
4540.6Li, Shiguang; Wang, Jiang; Lv, Ya; Chi, Yonggui Robin; Gan, Xiuhai; Wu, Xingxing
N-Heterocyclic carbene-catalyzed asymmetric synthesis of bis-ferrocene derivatives bearing two stereogenic planes.
Chemical communications (Cambridge, England), 2025, 61, 19036-19039
7135129 CIFC22 H18 F N O3P 1 21/n 111.0201; 7.3436; 21.6386
90; 94.376; 90
1746.05Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135130 CIFC11 H9 F0.5 N0.5 O1.5P 1 21/n 17.3449; 9.4651; 25.5608
90; 93.017; 90
1774.53Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135131 CIFF K1.999 Na0.501 O4 P Sc0.5P -3 m 111.2963; 11.2963; 7.1996
90; 90; 120
795.63Zhao, Huijian; Li, Conggang; Ye, Ning; Hu, Zhanggui
Tailoring UV waveplate materials <i>via</i> rational assembly of functional motifs in scandium fluoride phosphate.
Chemical communications (Cambridge, England), 2025, 61, 17145-17148
7135132 CIFC25 H19 N O5P 1 21/c 19.51124; 15.99027; 12.44468
90; 101.867; 90
1852.23Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135133 CIFC20 H16 O5P 1 21/c 110.2969; 9.8246; 14.8656
90; 93.018; 90
1501.76Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135134 CIFC20.5 H16.98 Cl O6C 1 2/c 120.9727; 8.1208; 20.9626
90; 100.685; 90
3508.34Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135135 CIFC19 H14 O5P 1 21/c 18.3627; 10.9839; 16.0035
90; 97.525; 90
1457.34Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135136 CIFC20 H18 O3P -17.8446; 8.6853; 11.0599
77.008; 83.439; 81.312
723.3Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135137 CIFC16 H11 N O3 SP 1 21/c 110.3033; 16.8149; 7.3464
90; 92.449; 90
1271.59Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135138 CIFC22 H21 I O6P -19.0209; 9.603; 13.967
73.695; 71.448; 66.6
1036.01Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135139 CIFC56 H119 Au Cl N Sb2 Si9P 1 21/n 118.0962; 23.3405; 18.1023
90; 100.648; 90
7514.29Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa M.; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au-Sb bimetallic linkage.
Chemical communications (Cambridge, England), 2025, 61, 19309-19312
7135140 CIFC106 H224 Au2 Cl2 N2 O Sb4 Si18P 1 21/n 112.5283; 36.1287; 17.215
90; 109.18; 90
7359.5Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa M.; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au-Sb bimetallic linkage.
Chemical communications (Cambridge, England), 2025, 61, 19309-19312
7135141 CIFC40.5 H30 Cl6 Ir N5 S2P 1 21/c 113.353; 15.201; 20.751
90; 91.064; 90
4211.3Morales-Pioz, Eva; Redrado, Marta; Benedi, Andrea; de Aquino, Araceli; García-Orduña, Pilar; Royo-Cañas, María; Godino, Javier; Marzo, I.; Rodríguez, Laura; Gimeno, M Concepción; Fernández-Moreira, Vanesa
Cyclometallated iridium(III) complexes: ligand-driven selectivity for chemotherapy and photodynamic therapy.
Chemical communications (Cambridge, England), 2025, 61, 19237-19240
7135142 CIFC27 H19 BP -111.7047; 11.9303; 13.8652
98.8114; 95.4596; 94.8484
1894.93Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135143 CIFC26 H16 B FP 1 21/c 13.8479; 25.12; 18.2066
90; 92.161; 90
1758.6Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135144 CIFC46 H28 B2C 1 2/c 159.4616; 9.983; 21.9645
90; 105.428; 90
12568.4Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135145 CIFC48 H38 B2P 1 21/n 127.7844; 3.9198; 32.0442
90; 103.451; 90
3394.2Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135146 CIFC38 H26 B NP 1 21/c 19.2605; 31.4635; 10.1892
90; 116.391; 90
2659.39Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135147 CIFC29 H23 BP 1 21/c 111.4924; 4.8929; 36.2021
90; 97.4308; 90
2018.59Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135148 CIFC24 H21 BP -17.4166; 12.7823; 19.1202
79.8121; 89.9142; 85.4566
1778.29Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135149 CIFC32 H26 N2 OP -18.8121; 10.1918; 13.9891
99.49; 97.145; 103.344
1188.33Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 19281-19284
7135150 CIFC32 H26 N2 OP 21 21 2111.6092; 12.2172; 16.4574
90; 90; 90
2334.2Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 19281-19284
7135151 CIFC59 H56 Cl6 N8 O3P -115.1639; 18.904; 20.266
89.732; 74.207; 89.827
5590Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular engineering of porous organic cages for iodine capture and fluorescence detection.
Chemical communications (Cambridge, England), 2025, 61, 19124-19127
7135152 CIFC73 H64 Cl12 N6 O3P -110.502; 17.367; 38.68
93.004; 90.221; 92.104
7040.2Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular engineering of porous organic cages for iodine capture and fluorescence detection.
Chemical communications (Cambridge, England), 2025, 61, 19124-19127
7135153 CIFC43 H40 F10 N4 O9 ZnP 1 21 110.981; 14.833; 13.238
90; 90.05; 90
2156.2Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically interlocked porphyrinoids: self-assembly of metal-stabilised catenaphyrins.
Chemical communications (Cambridge, England), 2026, 62, 148-151
7135154 CIFC76 H64 N12 O8 Zn2P 31 2 123.123; 23.123; 16.184
90; 90; 120
7494Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically interlocked porphyrinoids: self-assembly of metal-stabilised catenaphyrins.
Chemical communications (Cambridge, England), 2026, 62, 148-151
7135155 CIFC46 H59 Br Cl2 N2 PdP 1 21/c 113.0408; 15.0939; 21.6308
90; 95.267; 90
4239.75Tzouras, Nikolaos V.; Fleischer, Ruben; Satta, Pierpaolo; Manna, Sourav; Doppiu, Angelino; Goossen, Lukas J.
Mild cross-coupling of tertiary alkoxides with aryl chlorides enabled by a shelf-stable methylnaphthyl palladium NHC complex
Chemical Communications, 2025
7135156 CIFC20 H17 Br N4 O3P 1 21/c 120.707; 6.5276; 13.766
90; 95.222; 90
1853Shivpuje, Umesh; Ahmad, Manzoor; Roy, Naveen Joseph; Talukdar, Pinaki
Ligand-responsive ON-OFF anion transport using copper-caged acylhydrazone transporters
Chemical Communications, 2025
7135157 CIFC64 H84 O4 S4I 41/a :228.37523; 28.37523; 14.57079
90; 90; 90
11731.7Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135158 CIFC52 H72 O4 S4P -110.7957; 11.4363; 12.1971
68.795; 86.611; 62.936
1240.07Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135159 CIFC52 H72 O4 S4P c c n13.5017; 24.9584; 14.6029
90; 90; 90
4920.9Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135160 CIFC257 H205 Co4 N11 O45P -122.5652; 22.5982; 30.2731
77.825; 85.366; 65.661
13748.6Ma, Li-Li; Liu, Shengjin; Yang, Feinian; Cao, Jian; Ding, Longyi; Li, Yang; Yuan, Guozan
Integration of perylene diimide into a two-dimensional cobalt-organic framework for enhanced photocatalysis
Chemical Communications, 2025
7135161 CIFC29 H27 N3 O4 S2I 1 2/a 121.6291; 8.6367; 30.4166
90; 94.806; 90
5661.97Yadav, Anup Kumar; Kumar, Vipin; Singh, Saurabh; Samai, Subhasis; Singh, Maya Shankar
Synthesis of pyrrolo[3,4-c]pyridines via metal-free cross-coupling/cyclization cascades of β-ketothioamides with 2aroylmalononitrile at room temperature
Chemical Communications, 2025
7135162 CIFC20 H20 N2 OP c a 2112.718; 6.6198; 20.0762
90; 90; 90
1690.2Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135163 CIFC23 H26 N2 OP 1 21/n 114.5518; 7.7103; 18.9048
90; 110.142; 90
1991.4Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135164 CIFC316 H654 N34 O236 P16 V52C 1 2/c 139.393; 29.71; 48.245
90; 103.779; 90
54839Han, Shicheng; Liu, Fangcheng; Fu, Gang; Guo, Ji; Lin, Jiaheng; Wu, Hongyu; Mu, Chengyi; Fang, Xikui
Diphosphonate Functionalization of a Polyoxometalate-Organic Cage Enhances Proton Conductivity
Chemical Communications, 2025
7135165 CIFC H N OP -19.7302; 10.877; 11.3278
108.364; 92.134; 90.464
1136.79Saikia, Anil Kumar; Arandhara, Pallav Jyoti; Chutia, Archana
Leveraging cascade annulation of 2-alkynylcyclopropanes with substituted azides to access fused N-heterocyclic scaffolds
Chemical Communications, 2025
7135166 CIFB8 F12 K4 Na8 O24 Y8P 41 21 26.674; 6.674; 19.991
90; 90; 90
890.4Zhao, Huijian; Liu, Mengru; Nan, Weina; Yang, Ning; Li, Conggang; Ye, Ning; Hu, Zhanggui
KNa<sub>2</sub>Y<sub>2</sub>B<sub>2</sub>O<sub>6</sub>F<sub>3</sub>: a beryllium free deep-UV nonlinear optical crystal with well-balanced properties.
Chemical communications (Cambridge, England), 2025, 61, 17878-17881
7135167 CIFC78 H100 Cl2 Cu2 N6 P2 Si2P b c a13.856; 18.909; 33.767
90; 90; 90
8847Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135168 CIFC48 H61 Cu N3 P SiP 1 21/c 111.1435; 21.864; 18.789
90; 104.38; 90
4434.4Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135169 CIFC42 H65 Cu N3 P SiP 1 21 110.0396; 19.1146; 11.968
90; 114.685; 90
2086.8Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135170 CIFC19 H13 N O2P 1 21/c 127.591; 8.5988; 12.4
90; 100.846; 90
2889.3Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135171 CIFC19 H13 N O2P 1 21/c 127.509; 8.6819; 12.636
90; 101.062; 90
2961.8Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135172 CIFC21 H19 N O3P 1 21/c 18.52527; 26.3892; 15.8287
90; 100.735; 90
3498.74Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135173 CIFC22 H21 N O3P 1 21/c 18.50169; 27.8458; 8.1178
90; 103.313; 90
1870.13Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135174 CIFC20 H17 N O3P 1 21/n 18.1669; 26.4699; 15.7893
90; 104.465; 90
3305.1Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135175 CIFC102 H63.43 Mn4 N10 O26.71P b c a22.7346; 13.7881; 26.2173
90; 90; 90
8218.3Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135176 CIFC75.7 H62.42 Mn4 N7 O30.91C 1 2/c 124.6796; 13.604; 21.497
90; 91.574; 90
7214.7Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135177 CIFC23 H21 N O2 SP 21 21 216.4453; 14.9945; 20.1091
90; 90; 90
1943.42Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135178 CIFC18 H18 I N3 O2 SP 1 21/c 17.6989; 13.6394; 17.7709
90; 98.755; 90
1844.35Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135179 CIFC22 H19 N O3 SP c a 2115.1706; 11.7513; 21.1278
90; 90; 90
3766.5Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135180 CIFC26 H19 Br2 N O SP -18.2318; 10.8621; 13.1254
78.435; 79.26; 79.268
1116.05Chen, Jiahong; Huang, Yuanyuan; Wang, Nan; Wang, Mengke; Huang, Weichun; Wu, Xin-Xing; Xu, Xiao-Ping; Zi, You
Regioselective Functionalization of Sulfenamides: S-Arylation with Cyclic Diaryl λ3 -Bromanes and λ3 -Chloranes
Chemical Communications, 2025
7135181 CIFC40 H60 Mo2 O4 UC 1 2/c 116.2375; 13.6368; 17.8447
90; 95.875; 90
3930.55Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135182 CIFC40 H60 Cl Mo2 O4 UP n m a18.2457; 16.2988; 13.5222
90; 90; 90
4021.27Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135183 CIFC26 H30 N2 O6 S2P b c a10.405; 10.958; 23.3754
90; 90; 90
2665.2Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135184 CIFC17 H17 N O4P -16.6452; 9.1816; 12.2867
81.324; 80.372; 85.557
729.59Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135185 CIFC22 H21 Cl2 N O3P 1 21/n 15.9876; 29.771; 11.4497
90; 97.157; 90
2025.1Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135186 CIFC23 H23 Cl2 N O4P b c a14.2188; 10.3324; 29.7421
90; 90; 90
4369.5Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135187 CIFC60 H65 Cl2 O5 P3 Re2P 1 21/n 112.2713; 15.3656; 30.0068
90; 97.177; 90
5613.6Li, Lei; Fu, Bingjie; Zhao, Yue; Sun, Yue; Li, Yang; Jiang, Wenfeng; Bai, Wei
Synthesis and characterization of rhena-phenalenyl complexes.
Chemical communications (Cambridge, England), 2025, 61, 15858-15861
7135188 CIFC41 H35 Cl4 O2 P2 ReP 1 21/n 112.6366; 10.614; 28.7173
90; 95.677; 90
3832.8Li, Lei; Fu, Bingjie; Zhao, Yue; Sun, Yue; Li, Yang; Jiang, Wenfeng; Bai, Wei
Synthesis and characterization of rhena-phenalenyl complexes.
Chemical communications (Cambridge, England), 2025, 61, 15858-15861
7135189 CIFC10 H10 Fe I3 PbC 1 2/c 119.1013; 18.1903; 13.8623
90; 92.82; 90
4810.74Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135190 CIFC9.99 Fe I3 PbP 63/m m c10.9271; 10.9271; 8.1291
90; 90; 120
840.59Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135191 CIFC10 Fe I3R -3 m :H8.5305; 8.5305; 17.0548
90; 90; 120
1074.8Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135192 CIFC48 H73 N3 S4P 1 21/c 114.444; 17.6533; 18.4027
90; 96.711; 90
4660.2Lim, Gayeong; Cha, Jaegeum; Kim, Youngsuk
Reversible cyclodimerization of cyclic (alkyl)(amino)carbene-carbon disulfide adduct.
Chemical communications (Cambridge, England), 2025, 61, 18384-18387
7135193 CIFC29.03 H42.41 B N2 SP -4 21 c23.7578; 23.7578; 10.4931
90; 90; 90
5922.65Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135194 CIFC46 H60 B2 N2 SP 1 21/c 114.2244; 26.2529; 11.4501
90; 92.246; 90
4272.55Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135195 CIFC46 H60 B2 N2 SP -110.0786; 15.1951; 15.3131
75.107; 70.973; 75.478
2106.45Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135196 CIFC47 H65 B2 N2 S2P -113.8574; 18.3602; 20.3029
64.529; 80.521; 79.824
4567.2Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135197 CIFC19 H46 Au B10 F3 N4 P2P 110.1568; 11.9327; 13.4874
98.078; 92.088; 91.572
1616.48Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135198 CIFC31 H24 Au F3 P2P b c a15.0808; 18.4456; 19.4861
90; 90; 90
5420.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135199 CIFC19 H47 Au B10 F2 N4 P2P 21 21 2110.2254; 16.748; 18.788
90; 90; 90
3217.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135200 CIFC25 H40 Au B F3 PP -18.6619; 9.6434; 17.4721
79.094; 85.397; 67.85
1327.3Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135201 CIFC18 H29 Au F3 P SP 1 21/n 18.2996; 25.654; 10.1969
90; 105.659; 90
2090.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135202 CIFC17 H28 Au F3 N PP 1 21/c 115.643; 8.8608; 15.3181
90; 111.893; 90
1970.1Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135203 CIFC22 H19 Bi FeP -18.2785; 9.4737; 12.7844
97.188; 101.459; 110.864
896.98Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135204 CIFC34 H28 Bi2 FeP 1 21/n 114.2965; 12.9935; 15.2543
90; 91.357; 90
2832.9Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135205 CIFC22 H9 F10 Fe SbP 1 21/n 17.3495; 19.1515; 14.5035
90; 99.657; 90
2012.5Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135206 CIFC34 H31 B Fe P SbP -18.9845; 16.3617; 20.0366
82.755; 82.306; 86.952
2893.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135207 CIFC36 H28 Bi Fe O2 P W0.5P -19.1002; 10.1731; 16.7783
98.928; 97.552; 92.666
1517.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135208 CIFC38 H28 Bi Fe O4 P WP 1 21/n 19.7245; 15.1827; 22.7398
90; 101.645; 90
3288.3Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135209 CIFC24 H23 Fe SbP 1 21/n 113.5485; 8.7852; 17.4796
90; 106.904; 90
1990.64Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135210 CIFC24 H17 F6 Fe SbP 1 21/c 111.2444; 20.5216; 9.9176
90; 103.895; 90
2221.55Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135211 CIFC34 H18 F10 Fe P SbP -111.2557; 11.3367; 13.0357
101.126; 96.212; 110.747
1497.76Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135212 CIFC34 H18 F10 Fe P SbP 1 21/n 19.0076; 15.7671; 20.942
90; 94.116; 90
2966.59Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135213 CIFC34 H31 B Bi Fe PP 1 21/n 18.8411; 29.7793; 11.1614
90; 101.634; 90
2878.22Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135214 CIFC34 H31 B Bi Fe PP 1 21/c 19.1589; 16.358; 19.491
90; 96.875; 90
2899.2Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135215 CIFC58 H84 Bi Fe O4 P WP 1 21/c 116.3885; 15.0042; 29.725
90; 92.94; 90
7299.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135216 CIFC18 H22 O5P 1 21/c 18.1345; 10.4932; 20.272
90; 95.961; 90
1721Luo, Xue-Ling; Lv, Yu; Luo, Di-Jing; Qin, Lu-Lu; Li, Shu-Hui; Ye, Zhi-Peng; Xie, Zhen-Zhen; Xia, Peng-Ju
Photoinduced [3+2] cycloaddition <i>via</i> HFIP-promoted <i>in situ</i> formation of isobutylene from the Boc group.
Chemical communications (Cambridge, England), 2025, 61, 18180-18183
7135217 CIFC27 H21 F N2P 1 21/c 113.68938; 17.62391; 8.08
90; 92.3948; 90
1947.68Liu, Xingwang; Xiao, Shunli; Huang, Hao; Bai, Lele; Lai, Wenze; Wu, Gaorong
Ru(II)-catalyzed stereoselective C(7)-H α-fluoroalkenylation of indolines.
Chemical communications (Cambridge, England), 2025, 61, 18850-18853
7135218 CIFC31 H41 N6P 1 21/n 113.9813; 15.2468; 15.1459
90; 112.159; 90
2990.2Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135219 CIFC44 H72 N5P -111.0521; 13.746; 15.6376
69.62; 76.6492; 89.3974
2160.43Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135220 CIFC30 H44 N5P -111.9464; 14.9849; 17.3068
67.949; 89.902; 84.01
2853.52Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135221 CIFC33 H24 N6 Ni O3R -3 :H18.4326; 18.4326; 19.6463
90; 90; 120
5780.8Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135222 CIFC66 H48 N12 NiR -3 :H18.959; 18.959; 20.322
90; 90; 120
6326Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135223 CIFC66 H48 N12 Ni O8 Re2R -3 :H18.7166; 18.7166; 23.4717
90; 90; 120
7120.8Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135224 CIFC64 H46 N14 NiR -3 :H18.651; 18.651; 23.358
90; 90; 120
7037Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135225 CIFC8 H10 Cl2 N SbP 1 21/c 19.0035; 7.6161; 16.2664
90; 97.081; 90
1106.9Benny, Annabel; Vijayan, Devika; Thayalan, Rajeshkumar; Maron, Laurent; Venugopal, Ajay
An aldehyde-stabilised alkoxyaluminium dication.
Chemical communications (Cambridge, England), 2025, 61, 16074-16077
7135226 CIFC76 H40 Al3 F81 O14P -115.8741; 15.9964; 22.6
84.126; 82.511; 63.971
5106.2Benny, Annabel; Vijayan, Devika; Thayalan, Rajeshkumar; Maron, Laurent; Venugopal, Ajay
An aldehyde-stabilised alkoxyaluminium dication.
Chemical communications (Cambridge, England), 2025, 61, 16074-16077
7135227 CIFC39 H31 Cl4 N3 O3 SP 1 21 112.1261; 9.8525; 15.413
90; 92.231; 90
1840Li, Wenkai; Fu, Liling; Xu, Yongqiang; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Atroposelective synthesis of isoquinolinone bearing two distinct C−N axes via cobalt-catalyzed enantioselective C−H activation/annulation
Chemical Communications, 2025
7135228 CIFC23 H21 N O4 SP 1 21/n 19.927; 15.272; 13.8
90; 100.295; 90
2058.5Li, Wenkai; Fu, Liling; Xu, Yongqiang; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Atroposelective synthesis of isoquinolinone bearing two distinct C−N axes via cobalt-catalyzed enantioselective C−H activation/annulation
Chemical Communications, 2025
7135229 CIFC12 H10 Cl N O2P 1 21/n 114.959; 5.3671; 15.422
90; 108.397; 90
1174.9Parthasarathy, Thiyagaraj; Bhowmik, Aritra; Bhattacharya, Biswajit; Mishra, Manish Kumar; Ghosh, Soumyajit
Reversible Twisting-Induced Crystalline–Polycrystalline Transformation in Cyanoacrylate Crystals
Chemical Communications, 2025
7135230 CIFC12 H10 Cl N O2P 1 21/n 114.959; 5.3671; 15.422
90; 108.397; 90
1174.9Parthasarathy, Thiyagaraj; Bhowmik, Aritra; Bhattacharya, Biswajit; Mishra, Manish Kumar; Ghosh, Soumyajit
Reversible Twisting-Induced Crystalline–Polycrystalline Transformation in Cyanoacrylate Crystals
Chemical Communications, 2025
7135231 CIFC42 H32 N4 O4P 1 21/n 112.5542; 14.0614; 18.8278
90; 96.095; 90
3304.9Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135232 CIFC42 H32 N4 O4P 1 21/c 114.0567; 12.8429; 19.1088
90; 111.022; 90
3220.1Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135233 CIFC39 H26 Cl2 N4 OP 1 21/n 111.101; 10.5875; 26.8424
90; 96.405; 90
3135.14Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135234 CIFC42 H32 N4 O4P -110.268; 11.7261; 14.837
104.156; 106.691; 100.305
1598.4Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135235 CIFC40 H32 N4 O3P 1 2/c 112.1304; 10.3755; 25.2295
90; 102.918; 90
3094.99Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135236 CIFC62 H42 N4 O2 P2P b c a14.0167; 23.1649; 32.3543
90; 90; 90
10505.3Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135237 CIFC460 H476 N40 O45P -117.8141; 20.6055; 28.5357
98.149; 104.186; 104.628
9591.7Huang, Jiaming; Martínez-Belmonte, Marta; Ballester, Pablo
Reducing rotatable bonds in one substrate accelerates a bimolecular Diels-Alder reaction in a bis-calix[4]pyrrole cage.
Chemical communications (Cambridge, England), 2025
7135238 CIFC22 H20 N O2P 1 21/c 18.7902; 31.2988; 7.0352
90; 110.298; 90
1815.35Ghosh, Abhipsa; Panda, Asutosh; Mahulkar, Pranav Shridhar; Ravikumar, Ponneri C.
Cobalt(III)-catalysed annulation of indoles with phenylethynyl ether for the synthesis of the ABC ring system of ergot alkaloids.
Chemical communications (Cambridge, England), 2025
7135239 CIFC102 H124 N10 S2 Zn2P -110.9369; 13.6261; 16.2574
98.636; 93.497; 109.826
2236.97Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135240 CIFC42 H55 N5 S6 ZnP 1 21/c 116.7048; 14.9584; 17.0574
90; 92.938; 90
4256.7Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135241 CIFC62 H81 N5 S ZnP -113.5911; 14.3769; 15.09
100.512; 92.232; 96.334
2876.1Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135242 CIFC96 H122 N10 O2 Zn2P -112.0595; 12.8394; 15.0633
106.138; 108.774; 91.802
2102.42Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135243 CIFC48 H59 N5 Te ZnP 1 21/n 117.2703; 27.8793; 18.1885
90; 92.174; 90
8751.2Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135244 CIFC63 H83 N5 Se ZnP -113.6388; 14.3737; 15.113
99.88; 92.266; 96.26
2896.27Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135245 CIFC96 H118 N10 Se2 Zn2P 1 21/n 115.7525; 14.9627; 19.4718
90; 112.101; 90
4252.3Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135246 CIFC102 H124 N10 O2 Zn2P -111.9496; 13.6798; 15.5151
113.349; 103.698; 94.74
2217.57Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135247 CIFC68 H87 N5 Te ZnP -112.3684; 12.4059; 21.7277
91.49; 90.601; 111.293
3104.57Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135248 CIFC126.1 H154.9 Cl6.9 Cu14 O37.2 P8 Si16P -114.2336; 16.6267; 18.4779
94.817; 94.588; 94.845
4325.19Arteev, Ivan S.; Khrustalev, Victor N.; Shul'pina, Lidia S.; Rodionov, Alexey N.; Shubina, Elena S.; Ragimov, Karim; Wang, Zhi; Bilyachenko, Alexey N.
High-nuclearity Cu<sub>14</sub> ionic complex featuring 1,3-bis(diphenylphosphino)propane and methylsilsesquioxane ligands: highly efficient catalysis of mild peroxidative alkane fuctionalizations.
Chemical communications (Cambridge, England), 2025
7135249 CIFC35 H57 Al Fe N2 P2 SiP -110.8871; 11.7522; 16.8494
75.091; 80.271; 71.666
1968.4Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135250 CIFC43.25 H74 Al Fe N4 P2 SiP -111.9256; 12.237; 18.8626
85.197; 81.93; 61.139
2386.51Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135251 CIFC37 H59 Al Fe N4 O P2P 1 21 112.7184; 17.9691; 17.6796
90; 90.455; 90
4040.34Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135252 CIFC33 H62 Al Fe N2 O P3P 1 21/n 115.2649; 14.4485; 17.2914
90; 91.259; 90
3812.78Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135253 CIFC41.5 H73 Al Fe N2 O P2 SiP 1 21/c 117.6664; 11.4726; 22.7577
90; 95.962; 90
4587.57Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135254 CIFC51 H82 Al Fe N3 O P2 SiP 1 21/c 114.59351; 10.0249; 35.96271
90; 94.4545; 90
5245.4Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135255 CIFC41.5 H73 Al Fe N2 O P2 SiP 1 21/c 117.6664; 11.4726; 22.7577
90; 95.962; 90
4587.57Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135256 CIFC21 H32 Al N3P 1 21/n 110.931; 9.974; 19.421
90; 91.464; 90
2116.7Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135257 CIFC33 H68 Al Mg N5 Si4P 1 21/c 19.9558; 17.0612; 24.8384
90; 100.093; 90
4153.71Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135258 CIFC33 H66 Al Ca N5 Si4P c a 2112.6499; 15.8975; 20.806
90; 90; 90
4184.1Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135259 CIFC54 H96 Al2 Ca N8 Si4P 1 21/c 111.6207; 25.9517; 21.1162
90; 100.348; 90
6264.58Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135260 CIFC33 H68 Al Mg N5 Si4P b c a12.85853; 20.3422; 32.09584
90; 90; 90
8395.33Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135261 CIFC40.3 H83.7 Al Ca N5 O Si4P 1 21/n 111.049; 19.6928; 23.4848
90; 98.614; 90
5052.32Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135262 CIFC23 H19 Br2 N O Se2P 1 21/n 18.4802; 8.4836; 30.641
90; 90.366; 90
2204.3Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135263 CIFC17 H16 Br N O SeP 1 21/c 17.9325; 19.3831; 10.3168
90; 100.504; 90
1559.7Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135264 CIFC17 H16 Br N O SP 1 21/c 18.0318; 19.4472; 10.3438
90; 101.538; 90
1583.01Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135265 CIFC3.4 H3.4 N0.2 O0.2 S0.2P -17.929; 9.6466; 10.3599
76.164; 68.361; 71.046
690.17Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135266 CIFC4 H1.5 Cu0.12 F0.75 N Si0.12I 4/m m m15.391; 15.391; 8.068
90; 90; 90
1911.17Huang, Yun-Tao; Song, Zi-Meng; Zhao, Xin-Ye; Li, Bei-Bei; Di, Zhengyi; Li, Cheng-Peng
A stable amino-functionalized fluorinated metal-organic framework for efficient separation of propyne/propylene
Chemical Communications, 2025
7135267 CIFC114 H75 N3 O6C 1 2/c 121.5241; 26.661; 42.4881
90; 100.448; 90
23977.7Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135268 CIFC46 H78 B2 N14 O4 Ti2P 43 21 214.9943; 14.9943; 29.2
90; 90; 90
6565.01Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135269 CIFC29 H49 B N7 O Si2 TiP -111.9183; 12.1325; 14.2731
79.695; 71.091; 65.428
1773.34Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135270 CIFC27 H39 B Cl N6 O2 TiP 1 21/n 110.5793; 15.3351; 18.0389
90; 94.362; 90
2918.06Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135271 CIFC31 H47 B Cl N6 O2 TiP 1 21/n 110.8294; 15.1747; 20.4317
90; 94.178; 90
3348.68Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135272 CIFC62 H94 B2 N14 O4 Ti2P 1 21/n 122.5766; 14.9516; 23.4386
90; 105.686; 90
7617.19Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135273 CIFC58 H86 B2 N14 O2 Ti2P 1 21/n 115.2132; 17.9147; 26.801
90; 91.589; 90
7301.5Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135274 CIFC29 H43 B Cl N6 O TiP 1 21/n 18.7343; 21.1361; 16.4149
90; 91.354; 90
3029.49Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135275 CIFC30 H48 B N7 O2 Si TiP -111.3501; 11.8716; 13.3789
85.07; 72.758; 80.766
1697.99Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135276 CIFC38 H60 B2 I2 N14 O2 Ti2P 1 21/n 110.9341; 15.8235; 32.5097
90; 95.991; 90
5593.97Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135277 CIFC54 H78 B2 N14 O4 Ti2P -114.5243; 15.2715; 20.314
102.862; 110.431; 101.972
3910.78Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135278 CIFC236 H317 F30 N20 O89.5 Pd5 S10P 1 21/a 133.1133; 45.6826; 41.2995
90; 92.8019; 90
62399Sakata, Yoko; Nakamura, Ryosuke; Saito, Takuho; Ogoshi, Tomoki; Tashiro, Shohei; Akine, Shigehisa
Size-selective formation of metallonanobelts <i>via</i> tethering-template-directed self-assembly.
Chemical communications (Cambridge, England), 2025
7135279 CIFC26 H32 O4 SP 1 21/c 121.4284; 10.2324; 11.5649
90; 105.207; 90
2447Samantaray, Swati; Saha, Sharajit; Punniyamurthy, Tharmalingam
Rh-catalyzed chemodivergent [4+1]-annulation/allylation of sulfoxonium ylides with α-methylene-β-lactones: access to α-indanonyl/α-benzyl acrylates
Chemical Communications, 2026
7135280 CIFC17 H18 O3P -18.4589; 9.2758; 9.7016
93.006; 108.39; 93.186
719.26Samantaray, Swati; Saha, Sharajit; Punniyamurthy, Tharmalingam
Rh-catalyzed chemodivergent [4+1]-annulation/allylation of sulfoxonium ylides with α-methylene-β-lactones: access to α-indanonyl/α-benzyl acrylates
Chemical Communications, 2026
7135281 CIFC16 H17 N OP 21 21 215.5367; 7.7309; 29.9149
90; 90; 90
1280.47Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135282 CIFC24 H21 NP 1 21/n 18.1945; 21.1; 11.376
90; 107.258; 90
1878.4Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135283 CIFC18 H21 NP 1 21/c 18.355; 16.065; 11.289
90; 108.475; 90
1437.2Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135284 CIFC6 N1.5 O11.917 P0.333 W3 Zr0.5R -3 m :H22.6915; 22.6915; 39.2399
90; 90; 120
17497.9Liang, Zhijie; Yao, Yiqing; Ding, Yuyang; Wang, Haifeng; Li, Huafeng; Feng, Gang
Stable Zr-based polyoxometalate as a green catalyst for selective oxidation of aniline
Chemical Communications, 2026
7135285 CIFC34 H36 N4 O6P -19.0582; 11.4917; 16.1874
102.344; 104.774; 102.029
1528.74Luan, Yu-Yong; Li, Jin-Ye; Liu, Xue-Yuan; Liang, Yong-Min
Ru-Catalyzed C-H Annulation: Accessing Quinazolinone-BCP Hybrids from Stable Precursors
Chemical Communications, 2026
7135286 CIFC40 H59 Cl2 N2 P RuP 1 21/n 112.2189; 18.2929; 17.8873
90; 103.89; 90
3881.24Pontavatchai, Apicha; Schwedtmann, Kevin; Royla, Philipp; Schwedtmann, Kai; Khamnaen, Tossapol; Schwarzenbolz, Uwe; Henle, Thomas; Somsook, Ekasith; Weigand, Jan J.
Chain-length-dependent reactivity of alkenyl phosphates in ruthenium-catalyzed cross-metathesis
Chemical Communications, 2026
7135287 CIFC37 H45 Fe N O2 SnP 21 21 2110.7163; 14.799; 21.254
90; 90; 90
3370.7Cao, Phuong Anh; Phung, Alice C.; Schwirzke, Ella L.; Fettinger, James C.; Rusmore, Theo A. H.; Mears, Kristian L.; Vasko, Petra; Power, Philip P.
Ammonia reactivity with ferriotetrylenes: a structural snapshot of a highly dynamic process.
Chemical communications (Cambridge, England), 2025, 61, 19092-19095
7135288 CIFC37 H42 Fe O2 PbP 21 21 218.3897; 18.0566; 21.6854
90; 90; 90
3285.1Cao, Phuong Anh; Phung, Alice C.; Schwirzke, Ella L.; Fettinger, James C.; Rusmore, Theo A. H.; Mears, Kristian L.; Vasko, Petra; Power, Philip P.
Ammonia reactivity with ferriotetrylenes: a structural snapshot of a highly dynamic process.
Chemical communications (Cambridge, England), 2025, 61, 19092-19095
7135289 CIFC9 H18 B9 N O2P -17.035; 9.707; 11.99
97.167; 102.787; 102.826
765.4Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135290 CIFC13 H19 B9 N2 O2P 1 21/n 19.3624; 15.562; 12.4785
90; 106.649; 90
1741.9Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135291 CIFC14 H20 B9 N O2P -16.5542; 10.0432; 14.4842
79.901; 79.8; 74.684
896.7Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135292 CIFC7 H15 B9 Cl NC 1 2/c 120.3463; 6.4323; 20.4209
90; 103.65; 90
2597.1Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135293 CIFC7 H14 B9 Cl2 NC 1 2/c 120.226; 7.0287; 19.947
90; 96.446; 90
2817.8Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135294 CIFC31 H36 Cl3 N O4P -17.3825; 10.0528; 20.4633
100.577; 90.989; 99.932
1468.62Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135295 CIFC33 H30 Cl3 N O5P -110.1653; 11.261; 13.4588
76.983; 77.769; 87.169
1466.98Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135296 CIFC27 H27 Cl3 N2 O6P -17.4109; 9.9848; 18.796
96.494; 99.614; 104.201
1312.01Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135297 CIFC26.25 H21.25 Cl0.75 N SP -19.4521; 14.7452; 14.7989
101.038; 95.116; 97.429
1993.62Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135298 CIFC27 H29 N O5P 1 21/c 17.6653; 32.012; 9.0652
90; 99.477; 90
2194.07Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135299 CIFC32 H29.34 N O4.17 SP 1 21/n 110.2097; 12.1202; 21.9452
90; 100.603; 90
2669.21Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135300 CIFC27 H20 O5 SP 1 21/c 114.2771; 37.754; 17.4551
90; 107.017; 90
8996.7Yang, Zhi-Yuan; Li, Xue-Song; Zhang, Ming-Li; You, Zi-Xin; Liang, Yong-Min; Zhou, Ming-Dong
Lewis Acid Catalysed Cyclization of Pyridinium 1,4-Zwitterionic Thiolates with Propargyl Alcohols and Fluorescence Applications
Chemical Communications, 2026
7135301 CIFC36 H23 F3 I N OP 1 21/n 16.9559; 28.73; 14.9096
90; 96.72; 90
2959.1Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135302 CIFC38 H29 I N2 O2P 1 21 114.085; 7.2681; 15.308
90; 97.143; 90
1554.9Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135303 CIFC35 H24 I N OC 1 2/c 125.9967; 13.28; 17.7015
90; 93.282; 90
6101.2Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135304 CIFC75.87 H107.61 La S2C 1 2/c 121.1776; 18.2359; 36.0813
90; 91.179; 90
13931.4Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135305 CIFC75.63 H106.89 La S2C 1 2/c 121.1136; 18.2758; 36.158
90; 91.79; 90
13945.4Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135306 CIFC75.53 H106.59 La S2C 1 2/c 121.0895; 18.2926; 36.1914
90; 92.017; 90
13953.3Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135307 CIFC75.73 H107.19 La S2C 1 2/c 121.1388; 18.2563; 36.118
90; 91.482; 90
13933.9Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135308 CIFC27 H25 N2 RbP 1 21/c 114.3566; 11.8396; 26.4983
90; 101.79; 90
4409.06Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135309 CIFC46 H69 Cs2 Li N4 Si4P c a 2125.3737; 12.0154; 17.5574
90; 90; 90
5352.82Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135310 CIFC27 H25 Cs N2P 1 21/c 114.4348; 12.0323; 26.6844
90; 100.598; 90
4555.59Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135311 CIFC44 H28 F18 N6 P2 RuP -19.0051; 11.4959; 22.2845
86.46; 80.555; 74.909
2196.74Mandal, Arif Ali; Kumar, Saurav; Singh, Srijan; Mandal, Apurba; Banerjee, Samya; Dhar, Prodyut
Novel Ru(II)-Photo-antibiotics for Development of Infection-Resistant Mask Coatings
Chemical Communications, 2026
7135312 CIFC31 H24 Br N2 O4P 1 21 19.214; 14.22; 11.153
90; 111.181; 90
1362.6Devi, Manju; Jain, Gyanshree; Gupta, Navya; Ansari, Najmuddin; Singh, Ravi Prakash
Atroposelective Synthesis of Barbiturate Substituted Chiral Styrenes
Chemical Communications, 2026
7135313 CIFC4.09 H3.74 N0.17 O0.61 P0.09C 1 2 119.0074; 11.0694; 18.0225
90; 110.883; 90
3542.9Devi, Manju; Jain, Gyanshree; Gupta, Navya; Ansari, Najmuddin; Singh, Ravi Prakash
Atroposelective Synthesis of Barbiturate Substituted Chiral Styrenes
Chemical Communications, 2026
7135314 CIFC108 H35 Co N5C 1 2/c 125.189; 22.7748; 24.3234
90; 96.945; 90
13851Wang, Tao; Song, Yupeng; Wang, Chong; Wang, Hongyi; Zhang, Youpeng; Jiang, Ying; Dong, Tianyang; Wu, Bo; Wang, Chun-Ru
Fullerene–Porphyrin Nanosheet as an Efficient Catalyst Enables Solar-Light-Driven Ammonia Synthesis
Chemical Communications, 2026
7135315 CIFC16 H10 N4 SC 1 c 111.947; 17.077; 7.029
90; 111.18; 90
1337.2Nakamura, Ryo; Sawamura, Yuta; Nakada, Kazushi; Mizoguchi, Ryusuke; Ishii, Ayumi; Yamashita, Tomohiro; Yokota, Hiroko; Richards, Gary James; Hori, Akiko
Red-fluorescence under UV and green-SHG under NIR dual-mode emission in yellow crystal of 1,2,5-thiadiazole derivative
Chemical Communications, 2026
7135316 CIFC40 H28 N6 SP 1 21/c 125.61; 7.253; 17.715
90; 106.797; 90
3150Nakamura, Ryo; Sawamura, Yuta; Nakada, Kazushi; Mizoguchi, Ryusuke; Ishii, Ayumi; Yamashita, Tomohiro; Yokota, Hiroko; Richards, Gary James; Hori, Akiko
Red-fluorescence under UV and green-SHG under NIR dual-mode emission in yellow crystal of 1,2,5-thiadiazole derivative
Chemical Communications, 2026
7135317 CIFC33.5 H15 B F15 O SbP 1 21/n 110.1599; 15.9561; 19.0317
90; 99.943; 90
3038.9NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135318 CIFC39 H20 B F15 O SbP -113.4947; 15.3391; 19.1866
76.297; 81.376; 68.207
3574.3NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135319 CIFC36 H33 B F15 O PR 3 :H17.232; 17.232; 9.882
90; 90; 120
2541.2NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135320 CIFC4 H4 Cl2 Fe N2C m m m12.015; 7.2065; 3.5729
90; 90; 90
309.36Lassoued, Mohamed Saber; Huang, Xue-Qi; Hussain, Abid; Zheng, Yan-Zhen
A Stable Narrow-Bandgap 2D Iron–Pyrazine Framework Exhibiting High Photoconductivity and Spin–Charge Coupling
Chemical Communications, 2026
7135321 CIFC43 H63 Cl Fe N7 O4P 19.0318; 13.1643; 17.9475
88.547; 81.094; 88.722
2107.14Dey Biswas, Doyel; Das, Soumadip; Pal, Debraj; Sen Gupta, Sayam
Enantioselective C-H Bond Oxidation using Bio-Inspired Chiral Fe-TAML Catalyst
Chemical Communications, 2026
7135322 CIFC43 H63 Cl Fe N7 O4P 19.0356; 13.1688; 17.9549
88.5; 81.057; 88.78
2109.4Dey Biswas, Doyel; Das, Soumadip; Pal, Debraj; Sen Gupta, Sayam
Enantioselective C-H Bond Oxidation using Bio-Inspired Chiral Fe-TAML Catalyst
Chemical Communications, 2026
7135323 CIFC19 H14 B F2 N3 OP 1 21/c 111.1316; 18.2559; 8.0791
90; 99.445; 90
1619.56Figliola, Carlotta; Chériaux, Camille; Oppé, Nicolas; Estaque, Lilian; Retailleau, Pascal; Vanthuyne, Nicolas; Pieters, Gregory; Jacquemin, Denis; Ulrich, Gilles
Design of Heavy-Atom Free Dipyridomethene Boron Complexes for Singlet Oxygen Emission with Induced Chirality
Chemical Communications, 2026
7135324 CIFC22 H13 B F N3 OP -17.5432; 8.0975; 14.2914
95.85; 95.816; 103.652
836.72Figliola, Carlotta; Chériaux, Camille; Oppé, Nicolas; Estaque, Lilian; Retailleau, Pascal; Vanthuyne, Nicolas; Pieters, Gregory; Jacquemin, Denis; Ulrich, Gilles
Design of Heavy-Atom Free Dipyridomethene Boron Complexes for Singlet Oxygen Emission with Induced Chirality
Chemical Communications, 2026
7135325 CIFC28 H22 Fe O2P 21 21 218.2412; 11.3911; 21.879
90; 90; 90
2053.9Parganiha, Devendra; Upadhyay, Yagya Dutt; Khevariya, Sumit; Patil, Pruthviraj Amar; Jaiswal, Svastik; Dhasmana, Yogesh; Kumar, Sangit
Native Carboxylate-Assisted Enantioselective C-H Annulations with Allenes and 1,3-Dienes on Ferrocene
Chemical Communications, 2026
7135326 CIFC24 H14 F3 NP 1 21/c 14.6753; 36.904; 10.6315
90; 100.522; 90
1803.49Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135327 CIFC23 H13 F2 NC 1 2/c 117.2254; 7.4849; 26.994
90; 107.221; 90
3324.32Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135328 CIFC23 H15 NP 1 21/c 118.3518; 5.289; 17.3164
90; 109.188; 90
1587.4Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135329 CIFC108 H155 Cs2 O12 P7 Pd6P n a 2130.981; 14.8646; 25.5815
90; 90; 90
11780.8Krämer, Felix; Kennedy, Alan; Fernandez, Israel; Mulvey, Robert E.
A Palladium Inverse Crown: Synthesis and Characterisation
Chemical Communications, 2026
7135330 CIFC15 H8 O2 S2I 1 2/a 113.5461; 3.8602; 46.3601
90; 95.505; 90
2413.02Ueda, Masafumi; Uehara, Asuka; Usui, Kazuteru; Hasegawa, Masashi
A Folded Mechanochromic Organic Fluorophore Based on Thianthrene-Fused Coumarin
Chemical Communications, 2026
7135331 CIFC15 H8 O2 S2P 1 21/n 16.8001; 14.5918; 12.0415
90; 94.287; 90
1191.48Ueda, Masafumi; Uehara, Asuka; Usui, Kazuteru; Hasegawa, Masashi
A Folded Mechanochromic Organic Fluorophore Based on Thianthrene-Fused Coumarin
Chemical Communications, 2026
7135332 CIFC32 H47 Au B21 PP 1 21/c 115.4148; 16.6168; 15.9182
90; 97.988; 90
4037.8Thornton, Ragene; French, Kirk; Shuford, Kevin; Martin, Caleb Daniel
Reactivity of Gold and Copper Acetylide with a Secondary Borane
Chemical Communications, 2026
7135333 CIFC32 H47 B21 Cu PP 1 21/c 112.6977; 13.7024; 23.9248
90; 103.948; 90
4039.9Thornton, Ragene; French, Kirk; Shuford, Kevin; Martin, Caleb Daniel
Reactivity of Gold and Copper Acetylide with a Secondary Borane
Chemical Communications, 2026
7135334 CIFC42 H25 N3 SP 1 c 121.659; 19.2095; 7.3318
90; 97.873; 90
3021.7Liu, Minglun; Zheng, Xiaoxue; Zhang, Min; Yao, Shankun; Zhang, Pan; Liang, Lili; Chen, Yuncong
Construction of a pyrene based AIEgen for ratiometric detection of trace water in organic solvents
Chemical Communications, 2026
7135335 CIFC24 H23 N3 O3 SP b c n35.6279; 7.9727; 15.4012
90; 90; 90
4374.7Hu, Chunyang; Liu, Zuquan; Li, Chenxing; Feng, Jianquan; Zhu, Yiwei; Du, Ding
Enantioselective Synthesis of N-Arylpyrrole Aldehydes via NHC-Organocatalytic Atroposelective Desymmetrization Followed by Kinetic Resolution
Chemical Communications, 2026
7135336 CIFC25 H18 Br N OP -19.9195; 10.2361; 10.9376
106.469; 105.026; 103.433
970.91Cui, Zhiyang; Sun, Honghao; Jin, Jingrong; Tang, Yi; Wang, Bo; Zhou, Leijie; Zheng, Bing; Zheng, Li; Guo, Hongchao
Tandem [2+4] annulation/aromatization reaction of yne-enones with <i>o</i>-sulfonamidobenzaldehydes.
Chemical communications (Cambridge, England), 2026, 62, 4774-4777
7135337 CIFC22 H24 N2 O2P -19.1227; 9.6393; 12.1
103.32; 93.697; 117.161
903.37Wang, Jian; Chen, Shenglin; Sun, Daokuan; Shen, Yirui; Zhao, Yufen; Wu, Ju
Alternating current polarity for electrochemical <i>de novo</i> synthesis of 3,3'-bisoxindoles.
Chemical communications (Cambridge, England), 2026, 62, 5312-5316
7135338 CIFC20 H16 F4 N2 O2P -17.4607; 8.2686; 14.3732
79.31; 87.117; 86.788
869.2Wang, Jian; Chen, Shenglin; Sun, Daokuan; Shen, Yirui; Zhao, Yufen; Wu, Ju
Alternating current polarity for electrochemical <i>de novo</i> synthesis of 3,3'-bisoxindoles.
Chemical communications (Cambridge, England), 2026, 62, 5312-5316
7135339 CIFC48 H96 F15 Ho6 I3 O24I m -3 m18.2616; 18.2616; 18.2616
90; 90; 90
6089.99Li, Yangjuan; He, Miao; Gong, Yu
Synthesis of crown ether-capped highly symmetrical fluoride-centered lanthanide clusters [Ln<sub>6</sub>F<sub>13</sub>(12-crown-4)<sub>6</sub>]I<sub>3</sub>F<sub>2</sub> (Ln = Ho, Er).
Chemical communications (Cambridge, England), 2026, 62, 5433-5437
7135340 CIFC48 H96 Er6 F15 I3 O24I m -3 m18.2915; 18.2915; 18.2915
90; 90; 90
6120Li, Yangjuan; He, Miao; Gong, Yu
Synthesis of crown ether-capped highly symmetrical fluoride-centered lanthanide clusters [Ln<sub>6</sub>F<sub>13</sub>(12-crown-4)<sub>6</sub>]I<sub>3</sub>F<sub>2</sub> (Ln = Ho, Er).
Chemical communications (Cambridge, England), 2026, 62, 5433-5437
7135341 CIFC18 H35 B3 F12 Ho N O8P 21 21 2110.3911; 10.7144; 26.1234
90; 90; 90
2908.43Li, Yangjuan; He, Miao; Gong, Yu
Synthesis of crown ether-capped highly symmetrical fluoride-centered lanthanide clusters [Ln<sub>6</sub>F<sub>13</sub>(12-crown-4)<sub>6</sub>]I<sub>3</sub>F<sub>2</sub> (Ln = Ho, Er).
Chemical communications (Cambridge, England), 2026, 62, 5433-5437
7135342 CIFC55 H65 Be N S2P -110.9982; 14.4252; 15.7174
91.496; 98.37; 108.461
2333.1Tröster, Tobias; Saha, Koushik; Roy, Dipak Kumar; Dewhurst, Rian D.; Braunschweig, Holger
Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles.
Chemical communications (Cambridge, England), 2026, 62, 5032-5036
7135343 CIFC103 H110 Be2 N2 S4P -112.06; 13.36; 15.212
95.952; 111.349; 101.372
2196.3Tröster, Tobias; Saha, Koushik; Roy, Dipak Kumar; Dewhurst, Rian D.; Braunschweig, Holger
Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles.
Chemical communications (Cambridge, England), 2026, 62, 5032-5036
7135344 CIFC77 H76 Be Br4 N7P -114.361; 15.539; 18.59
82.622; 67.945; 64.377
3464Tröster, Tobias; Saha, Koushik; Roy, Dipak Kumar; Dewhurst, Rian D.; Braunschweig, Holger
Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles.
Chemical communications (Cambridge, England), 2026, 62, 5032-5036
7135345 CIFC36 H36 Be O2 S2P 1 21/n 116.2072; 10.3142; 19.731
90; 111.967; 90
3058.9Tröster, Tobias; Saha, Koushik; Roy, Dipak Kumar; Dewhurst, Rian D.; Braunschweig, Holger
Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles.
Chemical communications (Cambridge, England), 2026, 62, 5032-5036
7135346 CIFC54 H60 B2 Be N2C 1 2/c 120.2312; 12.8953; 16.6996
90; 94.553; 90
4342.97Tröster, Tobias; Saha, Koushik; Roy, Dipak Kumar; Dewhurst, Rian D.; Braunschweig, Holger
Ring expansion of an antiaromatic beryllole: synthesis of novel five-, seven- and nine-membered beryllacycles.
Chemical communications (Cambridge, England), 2026, 62, 5032-5036
7135347 CIFC45 H44 N2 O2 S2P 1 21/c 120.2872; 20.8753; 9.1499
90; 102.409; 90
3784.5Kurek, Eléonore; Dal Pra, Ophélie; Skrzypczak, Aliocha; Massip, Stéphane; Daniel, Jonathan; Blanchard-Desce, Mireille; Grazon, Chloé
One spiro to shift them all: tuning fluorescent organic nanoparticles emission <i>via</i> steric design.
Chemical communications (Cambridge, England), 2026, 62, 5271-5274
7135348 CIFC55 H64 N2 O2 S2P b c a30.466; 9.8067; 31.955
90; 90; 90
9547Kurek, Eléonore; Dal Pra, Ophélie; Skrzypczak, Aliocha; Massip, Stéphane; Daniel, Jonathan; Blanchard-Desce, Mireille; Grazon, Chloé
One spiro to shift them all: tuning fluorescent organic nanoparticles emission <i>via</i> steric design.
Chemical communications (Cambridge, England), 2026, 62, 5271-5274
7135349 CIFC8 H2 N18 O6P -16.479; 11.334; 11.614
105.371; 96.16; 97.443
806.4Kukreja, Sonali; Yadav, Abhishek Kumar; Dharavath, Srinivas
4,5-Diazido-6-nitropyridazin-3(2<i>H</i>)-one: a versatile nitrogen-rich compound for multifaceted energetic applications.
Chemical communications (Cambridge, England), 2026, 62, 4986-4990
7135350 CIFC49 H35 Cl3 N4P -110.2442; 10.4061; 19.7416
85.184; 80.187; 68.756
1932.23Zhang, Ying; Sha, Renmanduhu; Gong, Jianye; Liu, Lingxiu; Feng, Lina; Zhang, Weijing; Jiang, Guoyu; Wang, Jianguo
The anion-π<sup>+</sup> interaction strategy enhances the PDT antibacterial performance of AIE-active photosensitizers.
Chemical communications (Cambridge, England), 2026, 62, 5326-5330
7135351 CIFC57 H54 Br0.92 N4 O4P 1 2/c 120.1429; 10.8615; 22.1765
90; 109.655; 90
4569.1Zhang, Ying; Sha, Renmanduhu; Gong, Jianye; Liu, Lingxiu; Feng, Lina; Zhang, Weijing; Jiang, Guoyu; Wang, Jianguo
The anion-π<sup>+</sup> interaction strategy enhances the PDT antibacterial performance of AIE-active photosensitizers.
Chemical communications (Cambridge, England), 2026, 62, 5326-5330
7135352 CIFC54 H54 Br2 N4 O4P 1 21/n 111.0375; 8.4725; 48.75
90; 90.538; 90
4558.7Zhang, Ying; Sha, Renmanduhu; Gong, Jianye; Liu, Lingxiu; Feng, Lina; Zhang, Weijing; Jiang, Guoyu; Wang, Jianguo
The anion-π<sup>+</sup> interaction strategy enhances the PDT antibacterial performance of AIE-active photosensitizers.
Chemical communications (Cambridge, England), 2026, 62, 5326-5330
7135353 CIFC74 H104 La2 N6 Ni2 O2 P4P -111.5616; 11.8002; 16.2436
75.419; 70.756; 66.803
1904He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135354 CIFC48 H69 La N4 Ni P2P -110.1638; 12.7284; 20.816
104.653; 104.046; 96.32
2484.9He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135355 CIFC39 H59 La N4 Ni P2P -110.7419; 12.0017; 17.493
98.31; 91.12; 113.988
2031.1He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135356 CIFC76 H100 I2 La2 N4 P4P -110.29; 11.7435; 16.775
77.377; 84.43; 84.471
1962.9He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135357 CIFC76 H100 I2 La2 N4 Ni2 P4P -111.364; 13.293; 14.6
79.748; 71.941; 67.907
1938He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135358 CIFC78 H106 La2 N4 Ni2 P4P 1 21/n 112.8479; 20.5016; 14.9962
90; 112.053; 90
3661He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135359 CIFC36 H52 I La N2 O P2P 1 21/n 111.0776; 17.6945; 19.544
90; 91.566; 90
3829.4He, Xiuyan; Wu, Changjiang; Hong, Dongjing; Fang, Huayi; Cui, Peng
A tetranuclear lanthanum-nickel hydrido complex supported by an arene-anchored bis(phosphinomethylamido) ligand.
Chemical communications (Cambridge, England), 2026, 62, 3807-3810
7135360 CIFC14 H2 N28 O2P 1 21/n 112.339; 6.4087; 14.207
90; 102.801; 90
1095.5Jujam, Manojkumar; Ghule, Vikas D.; Dharavath, Srinivas
Catenated nitrogen-rich triazine-tetrazole molecules for advanced explosives and gas-generator applications.
Chemical communications (Cambridge, England), 2026, 62, 4991-4995
7135361 CIFC11 H15 N11 O4 S2P -15.12; 13.3302; 13.9482
80.226; 88.777; 80.059
924.04Jujam, Manojkumar; Ghule, Vikas D.; Dharavath, Srinivas
Catenated nitrogen-rich triazine-tetrazole molecules for advanced explosives and gas-generator applications.
Chemical communications (Cambridge, England), 2026, 62, 4991-4995
7135362 CIFB15 Na2.89 O30 Rb4.11 Sc2.01 Sr0.99R 3 2 :H12.924; 12.924; 15.1974
90; 90; 120
2198.33Liu, Zelong; Zhao, Huijian; Xu, Longyun; Jia, Ning; Ye, Ning; Hu, Zhanggui; Li, Conggang
Two scandium borate UV NLO crystals designed through chemical element substitution.
Chemical communications (Cambridge, England), 2026, 62, 4610-4614
7135363 CIFB15 Na4.01 O30 Rb2.99 Sc2.22 Sr0.78R 3 2 :H12.8969; 12.8969; 14.891
90; 90; 120
2145Liu, Zelong; Zhao, Huijian; Xu, Longyun; Jia, Ning; Ye, Ning; Hu, Zhanggui; Li, Conggang
Two scandium borate UV NLO crystals designed through chemical element substitution.
Chemical communications (Cambridge, England), 2026, 62, 4610-4614
7135364 CIFC H N O ZnC 1 2/c 117.5131; 8.7986; 9.6977
90; 105.755; 90
1438.2Song, Ping; Wilkins, Nicholas Stiles; Taheri-Qazvini, Omid; Adeleke, Adebayo A.; Moghaddam, Alireza Lotfollahzade; Amirani, Morteza Chehel; Srinivasan, Karthik; Masoumifard, Nima; Ramanathan, Vaidhyanathan
Understanding the potential of a new zinc-triazolato-carbonate metal-organic framework for humid CO<sub>2</sub> capture processes.
Chemical communications (Cambridge, England), 2026, 62, 5523-5526
7135365 CIFC7 H10 N8 O3 Zn2C 1 2/c 117.5097; 8.9985; 9.905
90; 108.729; 90
1478Song, Ping; Wilkins, Nicholas Stiles; Taheri-Qazvini, Omid; Adeleke, Adebayo A.; Moghaddam, Alireza Lotfollahzade; Amirani, Morteza Chehel; Srinivasan, Karthik; Masoumifard, Nima; Ramanathan, Vaidhyanathan
Understanding the potential of a new zinc-triazolato-carbonate metal-organic framework for humid CO<sub>2</sub> capture processes.
Chemical communications (Cambridge, England), 2026, 62, 5523-5526
7135366 CIFC29 H23.4 B F8.6 RhP -18.2646; 9.3254; 17.716
88.548; 77.438; 69.538
1246.7Addison, Emily J.; Zurakowski, Joseph A.; Boyle, Paul D.; Nelson, David J.; Drover, Marcus W.
From borane to metal-bound boraindene: a cascade of bond breaking and making at rhodium.
Chemical communications (Cambridge, England), 2026, 62, 5871-5874
7135367 CIFC18 H15 N O SP 21 21 215.5223; 8.7061; 29.2709
90; 90; 90
1407.28Ahashan, Sk Jubayar; Maji, Kousik; Kabir, Syed Ramizul; Dash, Jyotirmayee
Synthesis of thieno[2,3-<i>b</i>]indoles by Cloke-Wilson rearrangement of spiro donor-acceptor cyclopropanes.
Chemical communications (Cambridge, England), 2026, 62, 3861-3865
7135368 CIFC80 H53 B2 N3 O2P 1 21/n 118.576; 13.694; 24.8877
90; 111.155; 90
5904.27Song, Yunyi; Yokoyama, Hiromichi; Shoji, Yoshiaki; Sakai, Hayato; Hasobe, Taku; Fukushima, Takanori
Gate-opening cooperative methanol binding to multi-bladed benzenes bearing 1,2-diboryl functionality.
Chemical communications (Cambridge, England), 2026, 62, 3889-3892
7135369 CIFC31 H33 F N2 Ni O SP 1 21/n 111.9419; 12.3816; 18.7832
90; 92.574; 90
2774.48Lindenmaier, Ivo H.; Richter, Robert C.; Renz, Liesa; Vochezer, Mattis T.; Schier, Marius; Faßnacht, Pascal; Ströbele, Markus; Fleischer, Ivana
Nickel-catalyzed cross-electrophile-coupling of thioesters with alkyl bromides to form ketones under mechanochemical conditions.
Chemical communications (Cambridge, England), 2026, 62, 5284-5288
7135370 CIFC18 H25 Cl2 N OP 1 21 113.1647; 9.6045; 15.8224
90; 113.961; 90
1828.18Asano, Ren; Nonami, Reina; Hamasaki, Hina; Kanemoto, Kazuya; Fujita, Harunori; Yamamoto, Kaisei; Seki, Tomohiro; Shibatomi, Kazutaka; Kuwahara, Shunsuke; Shirai, Tomohiko
Cationic iridium-catalyzed enantioselective decarboxylative aryl addition of aromatic carboxylic acids to bicyclic alkenes.
Chemical communications (Cambridge, England), 2026, 62, 6096-6100
7135371 CIFC39 H37 B F15 PP 1 21/c 115.7197; 14.6804; 16.6983
90; 95.935; 90
3832.8Goraya, Armaan; Ajithkumar, V. S.; Ruhlandt, Karin; Stephan, Douglas W.; McCahill, Jenny SJ; Bedi, Vaibhav
Beyond FLP additions: FLP deprotonation and C-O bond cleavage of aliphatic, aryl and ester derived olefins
Chemical Communications, 2026
7135372 CIFC55 H39 B2 Cl2 F30 O2 PP -112.5198; 12.5678; 18.6747
81.71; 81.998; 88.438
2879.3Goraya, Armaan; Ajithkumar, V. S.; Ruhlandt, Karin; Stephan, Douglas W.; McCahill, Jenny SJ; Bedi, Vaibhav
Beyond FLP additions: FLP deprotonation and C-O bond cleavage of aliphatic, aryl and ester derived olefins
Chemical Communications, 2026
7135373 CIFC46 H61 B F15 PC 1 2/c 131.918; 11.1232; 25.038
90; 100.385; 90
8743.6Goraya, Armaan; Ajithkumar, V. S.; Ruhlandt, Karin; Stephan, Douglas W.; McCahill, Jenny SJ; Bedi, Vaibhav
Beyond FLP additions: FLP deprotonation and C-O bond cleavage of aliphatic, aryl and ester derived olefins
Chemical Communications, 2026
7135374 CIFC36.65 H36.9 B Cl5.7 F15 O2 PP -113.1112; 13.1605; 15.0066
99.437; 91.072; 118.514
2230.4Goraya, Armaan; Ajithkumar, V. S.; Ruhlandt, Karin; Stephan, Douglas W.; McCahill, Jenny SJ; Bedi, Vaibhav
Beyond FLP additions: FLP deprotonation and C-O bond cleavage of aliphatic, aryl and ester derived olefins
Chemical Communications, 2026
7135375 CIFC62 H45 B2 Cl6 F30 O2 PC 1 2/c 135.508; 16.827; 23.878
90; 105.967; 90
13717Goraya, Armaan; Ajithkumar, V. S.; Ruhlandt, Karin; Stephan, Douglas W.; McCahill, Jenny SJ; Bedi, Vaibhav
Beyond FLP additions: FLP deprotonation and C-O bond cleavage of aliphatic, aryl and ester derived olefins
Chemical Communications, 2026
7135376 CIFC19 H23 N O2 S2C 1 2/c 134.921; 5.8632; 24.09
90; 131.034; 90
3720.6Dalai, Pallaba Ganjan; Barik, Dinabandhu; Manna, Supriya; Lokesh, Allu; Patel, Bhisma K.
Visible-light-mediated β,β-thio- and selenosulfonylation of <i>N</i>-ethyl tertiary amines.
Chemical communications (Cambridge, England), 2026, 62, 4076-4079
7135377 CIFC84 H91 Cl3 Co N10 O4P 1 21/c 119.623; 14.1656; 32.426
90; 101.462; 90
8833.7Maji, Subrata; Gupta, Prachi; Clowes, Rob; Matsushita, Yoshitaka; Shrestha, Lok Kumar; Slater, Anna G.; Hill, Jonathan P.; Chahal, Mandeep K.
Central-metal-cation-based modulation of gas adsorption selectivity in porous tetrapyrrolic materials.
Chemical communications (Cambridge, England), 2026, 62, 5227-5231
7135378 CIFC84.85 H91.85 Cl5.55 Cu N10 O4P 1 21/c 119.665; 13.997; 32.546
90; 100.624; 90
8805Maji, Subrata; Gupta, Prachi; Clowes, Rob; Matsushita, Yoshitaka; Shrestha, Lok Kumar; Slater, Anna G.; Hill, Jonathan P.; Chahal, Mandeep K.
Central-metal-cation-based modulation of gas adsorption selectivity in porous tetrapyrrolic materials.
Chemical communications (Cambridge, England), 2026, 62, 5227-5231
7135379 CIFC39 H52 N2 O5 RuP -111.144; 12.154; 12.562
83.54; 87.11; 86.504
1685.9Casalta, Clément; Morvan, Fanny; Colombel-Rouen, Sophie; Roisnel, Thierry; Jazzar, Rodolphe; Doppiu, Angelino; Mauduit, Marc
Design, synthesis and reactivity of <i>N</i>-adamantyl cyclometalated cyclic(alkyl)(amino)carbene ruthenium complexes in <i>Z</i>-selective olefin metathesis.
Chemical communications (Cambridge, England), 2026, 62, 4099-4102
7135380 CIFC36 H46 Cl5 N O RuP b c a11.2496; 20.1871; 29.943
90; 90; 90
6800Casalta, Clément; Morvan, Fanny; Colombel-Rouen, Sophie; Roisnel, Thierry; Jazzar, Rodolphe; Doppiu, Angelino; Mauduit, Marc
Design, synthesis and reactivity of <i>N</i>-adamantyl cyclometalated cyclic(alkyl)(amino)carbene ruthenium complexes in <i>Z</i>-selective olefin metathesis.
Chemical communications (Cambridge, England), 2026, 62, 4099-4102
7135381 CIFC26 H27 N O4 SP 21 21 217.36; 10.914; 28.239
90; 90; 90
2268.4Khaitan, Bhavya; Panda, Sangram Keshari; Gandhi, Shikha
Diastereoselective intramolecular <i>O</i>-allylation with alkynes using palladium/Brønsted acid combined catalysis: access to substituted chiral oxazolidines.
Chemical communications (Cambridge, England), 2026, 62, 5289-5292
7135382 CIFC29 H28 Cl3 N O8 SP -110.9319; 12.8338; 13.0162
118.405; 108.271; 94.015
1471.87Tang, Zhicheng; Liu, Mingyang; Yang, Xiuran; Zhong, Zhuang; Liu, Sensheng; Zhou, Haifeng
Photochemical HAT-mediated site-selective C(sp<sup>3</sup>)-H aminoalkylation of cubanes catalyzed by TBADT.
Chemical communications (Cambridge, England), 2026, 62, 4059-4062
7135383 CIFC22 H19 Cl2 Cu2 N3 O3 SiP -19.8896; 14.2302; 17.4646
89.113; 88.283; 76.202
2385.72Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 1): americium and curium.
Chemical communications (Cambridge, England), 2026, 62, 4018-4022
7135384 CIFC18 H22 N2 O3 SP 21 21 218.7877; 8.8493; 23.306
90; 90; 90
1812.39Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 1): americium and curium.
Chemical communications (Cambridge, England), 2026, 62, 4018-4022
7135385 CIFC334.5 H392.5 Cl19.5 N14 O12 S2 Se2P 119.264; 21.682; 22.237
99.146; 105.5; 97.73
8682Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 1): americium and curium.
Chemical communications (Cambridge, England), 2026, 62, 4018-4022
7135386 CIFC169 H218 I N3 O9 SeP 21 21 2113.062; 33.4078; 36.9123
90; 90; 90
16107.5Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 1): americium and curium.
Chemical communications (Cambridge, England), 2026, 62, 4018-4022
7135387 CIFC163 H194.5 N9.5 O5 SeP 21 21 2113.53; 27.651; 42.347
90; 90; 90
15843Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 1): americium and curium.
Chemical communications (Cambridge, England), 2026, 62, 4018-4022
7135388 CIFC30 H27 N3 O3R 3 c :H12.828; 12.828; 25.5324
90; 90; 120
3638.6Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135389 CIFC25 H23 Cl3 N3 O6.5P n a 2112.3523; 13.3248; 15.9694
90; 90; 90
2628.4Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135390 CIFC30 H33 N3 O3R -3 c :H15.983; 15.983; 18.6933
90; 90; 120
4135.5Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135391 CIFC27 H18 F3 N3 O3P 1 21/c 117.846; 16.4283; 7.7056
90; 94.458; 90
2252.3Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135392 CIFC24 H21 N3 O3P m n 2118.741; 4.507; 11.291
90; 90; 90
953.7Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135393 CIFC24 H13 N6 O3.5P -110.2262; 12.4749; 17.7971
102.205; 92.512; 104.981
2132Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135394 CIFC46 H40 Cl3 N3 O3P -112.4889; 13.5583; 13.632
61.128; 78.86; 85.886
1982.7Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135395 CIFC28 H40 B N3P 1 21/n 125.0088; 8.8029; 25.0143
90; 109.169; 90
5201.6Koh, An-Ping; Vernezoul, Gaël; Fan, Jun; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
Bis(<i>N</i>-heterocyclic carbene)-borylene-mediated heteroallene activation.
Chemical communications (Cambridge, England), 2026, 62, 5980-5984
7135396 CIFK17 O125 P4 Pr W34P -114.6606; 22.5777; 24.8922
95.446; 102.747; 99.329
7856.6Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 2): californium.
Chemical communications (Cambridge, England), 2026, 62, 4023-4027
7135397 CIFCf4 K68 O492 P16 W136P 1 21/n 112.3745; 23.4607; 51.819
90; 90.635; 90
15042.9Colliard, Ian; Deblonde, Gauthier J.-P.
Actinide complexes with Wells-Dawson polyoxometalates (part 2): californium.
Chemical communications (Cambridge, England), 2026, 62, 4023-4027
7135398 CIFC57 H43 N4P -112.5314; 13.3027; 14.2917
68.818; 70.202; 66.085
1978.4Singh, Hemant K.; Punjani, Vidhika; Rybáček, Jiří; Pietrzak, Anna; Bednárová, Lucie; Kaszyński, Piotr
Azahelicene-fused Blatter radicals: chiral paramagnetic NIR absorbers.
Chemical communications (Cambridge, England), 2026, 62, 5046-5050
7135399 CIFC28 H29 Cd Cl0.644 N4.356 O8.067P 1 21/c 19.2171; 29.385; 11.2508
90; 106.903; 90
2915.6Cui, Jing-Wang; Ma, Shuai; Chen, Yun-Rui; Pan, Jia-Qi; Tan, Bin; Zhang, Jie
Controlled ROS generation in pyridinium-functionalized nanocatalysts for selective photooxidation.
Chemical communications (Cambridge, England), 2026, 62, 4122-4126
7135400 CIFC44 H26 F4 N6 O2 Pd2P -110.403; 14.4561; 15.3486
66.517; 82.651; 71.201
2004.1Fan, Weixue; Liu, Hua-Chao; Zhang, Yi; Zhang, Qizheng; Guo, Xiaoyu; Miao, Jingsheng; Yang, Chuluo; Li, Kai
Shortening the intramolecular Pd-Pd distances for photoactive dinuclear Pd(II) complexes.
Chemical communications (Cambridge, England), 2026, 62, 5687-5690
7135401 CIFC42 H24 F4 N8 O2 Pd2C 1 2/c 120.7115; 26.5389; 22.1807
90; 106.922; 90
11664Fan, Weixue; Liu, Hua-Chao; Zhang, Yi; Zhang, Qizheng; Guo, Xiaoyu; Miao, Jingsheng; Yang, Chuluo; Li, Kai
Shortening the intramolecular Pd-Pd distances for photoactive dinuclear Pd(II) complexes.
Chemical communications (Cambridge, England), 2026, 62, 5687-5690
7135402 CIFC44 H28 F4 N8 O2 Pd2P -110.9051; 13.026; 16.5638
81.142; 78.462; 67.062
2115.5Fan, Weixue; Liu, Hua-Chao; Zhang, Yi; Zhang, Qizheng; Guo, Xiaoyu; Miao, Jingsheng; Yang, Chuluo; Li, Kai
Shortening the intramolecular Pd-Pd distances for photoactive dinuclear Pd(II) complexes.
Chemical communications (Cambridge, England), 2026, 62, 5687-5690
7135403 CIFC16 H14 Ge0.5 N3C 1 2/c 118.5498; 7.608; 18.5459
90; 93.523; 90
2612.4Barik, Jogendrananda; Rit, Arnab
Anilido-pyrazole ligand supported germylenes: synthesis, structure, and catalytic <i>N</i>-formylation of amines using CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2026, 62, 4131-4134
7135404 CIFC3.38 H4.92 Ge0.15 N0.62 Si0.31P 1 21/n 19.2899; 13.6579; 19.1626
90; 102.816; 90
2370.8Barik, Jogendrananda; Rit, Arnab
Anilido-pyrazole ligand supported germylenes: synthesis, structure, and catalytic <i>N</i>-formylation of amines using CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2026, 62, 4131-4134
7135405 CIFC258 H452.92 B4 F16 Fe2 N64 O20.46P -113.001; 18.757; 33.217
77.55; 85.89; 72.53
7545Tołoczko, Aleksandra; Kaźmierczak, Marcin; Maliuzhenko, Vladyslav; Siczek, Miłosz; Weselski, Marek; Bronisz, Robert
"Inverted" hysteresis in a bilayer Fe(II) spin crossover system.
Chemical communications (Cambridge, England), 2026, 62, 6110-6113
7135406 CIFC25 H44 N6 O2P -15.376; 8.035; 31.164
85.73; 88.55; 74.99
1296.6Tołoczko, Aleksandra; Kaźmierczak, Marcin; Maliuzhenko, Vladyslav; Siczek, Miłosz; Weselski, Marek; Bronisz, Robert
"Inverted" hysteresis in a bilayer Fe(II) spin crossover system.
Chemical communications (Cambridge, England), 2026, 62, 6110-6113
7135407 CIFC258 H452.92 B4 F16 Fe2 N64 O20.46P -113.046; 18.844; 33.352
78.27; 86.54; 72.34
7650Tołoczko, Aleksandra; Kaźmierczak, Marcin; Maliuzhenko, Vladyslav; Siczek, Miłosz; Weselski, Marek; Bronisz, Robert
"Inverted" hysteresis in a bilayer Fe(II) spin crossover system.
Chemical communications (Cambridge, England), 2026, 62, 6110-6113
7135408 CIFC62 H48 Al F36 N2 O4P -111.5239; 15.1374; 19.9082
106.186; 100.095; 96.151
3238.53Yang, Jiayao; Yang, Linlin; Li, Tao; Zhao, Wanxiang
Stable radical cations based on indolo[3,2,1-<i>jk</i>]carbazole: synthesis, characterization, and theoretical calculation.
Chemical communications (Cambridge, England), 2026, 62, 5536-5539
7135409 CIFC108 H96 Al F36 N4 O4C 1 2/c 148.7724; 13.9285; 39.1474
90; 124.354; 90
21955Yang, Jiayao; Yang, Linlin; Li, Tao; Zhao, Wanxiang
Stable radical cations based on indolo[3,2,1-<i>jk</i>]carbazole: synthesis, characterization, and theoretical calculation.
Chemical communications (Cambridge, England), 2026, 62, 5536-5539
7135410 CIFC96 H174 K2 N8 O68I 431.0665; 31.0665; 30.9131
90; 90; 90
29835.1Feng, Ning; Cai, Xinyi; Ding, Boxin; Meng, Hong; Li, Hongguang
Red CPL from water insoluble achiral carbon dots assisted by cyclodextrin MOF Templating
Chemical Communications, 2026
7135411 CIFC96 H56 K2 N8 O68I 431.0665; 31.0665; 30.9131
90; 90; 90
29835.1Feng, Ning; Cai, Xinyi; Ding, Boxin; Meng, Hong; Li, Hongguang
Red CPL from water insoluble achiral carbon dots assisted by cyclodextrin MOF Templating
Chemical Communications, 2026
7135412 CIFC88.5 H75 B Cl3 O4 Os P3P 1 21/c 113.0065; 24.5208; 23.9619
90; 96.58; 90
7591.8Deng, Zhihong; Zhang, Hong; Luo, Ming; Xia, Haiping
Tuning the reactivity of an osmium-peroxo unit by modulating metallacycle aromaticity.
Chemical communications (Cambridge, England), 2026, 62, 5914-5918
7135413 CIFC66 H57 Cl6.25 O4.5 Os P3P 1 21/n 113.0692; 23.4824; 20.1169
90; 96.239; 90
6137.2Deng, Zhihong; Zhang, Hong; Luo, Ming; Xia, Haiping
Tuning the reactivity of an osmium-peroxo unit by modulating metallacycle aromaticity.
Chemical communications (Cambridge, England), 2026, 62, 5914-5918
7135414 CIFH O4 Rb SeP 14.6181; 7.5724; 10.617
69.154; 77.963; 89.597
338.43Chi, Yang; Xin, Mei-Ling
Strong second-harmonic generation and wide temperature range switching behavior coexisting in an ultrawide-bandgap selenate.
Chemical communications (Cambridge, England), 2026, 62, 4333-4336
7135415 CIFH O4 Rb SeC 1 2 119.9401; 7.6068; 4.6292
90; 102.751; 90
684.84Chi, Yang; Xin, Mei-Ling
Strong second-harmonic generation and wide temperature range switching behavior coexisting in an ultrawide-bandgap selenate.
Chemical communications (Cambridge, England), 2026, 62, 4333-4336
7135416 CIFH O4 Rb SeP 14.6245; 7.5938; 10.6496
69.145; 78.003; 89.743
340.86Chi, Yang; Xin, Mei-Ling
Strong second-harmonic generation and wide temperature range switching behavior coexisting in an ultrawide-bandgap selenate.
Chemical communications (Cambridge, England), 2026, 62, 4333-4336
7135417 CIFC19 H18 O4 P ReP c a 2115.0665; 12.9576; 19.5981
90; 90; 90
3826.05Pan, Xiong; Fang, Zi-Luo; Guo, Ming-Yu; Yang, Hao; Zhang, Wei-Xiong
A new polar glass-ceramic built from monovalent perrhenate anions and large methyltriphenylphosphonium cations.
Chemical communications (Cambridge, England), 2026, 62, 4302-4305
7135418 CIFC21 H16 F3 N O2P b c a7.3884; 17.41; 27.1385
90; 90; 90
3490.88Ye, Shasha; Zou, Jiayi; Yang, Xueying; Xu, Haiyun; Ma, Chunhua; Zhang, Xinying; Fan, Xuesen
Synthesis of CF<sub>3</sub>-indene-1-ol-fused pyridones possessing potent anticancer activities through C-H activation-initiated cascade annulation under redox-neutral conditions.
Chemical communications (Cambridge, England), 2026, 62, 4354-4357
7135419 CIFC19 H10 Cl2 F3 N O2P 1 21/n 16.3061; 16.2896; 17.1248
90; 98.141; 90
1741.4Ye, Shasha; Zou, Jiayi; Yang, Xueying; Xu, Haiyun; Ma, Chunhua; Zhang, Xinying; Fan, Xuesen
Synthesis of CF<sub>3</sub>-indene-1-ol-fused pyridones possessing potent anticancer activities through C-H activation-initiated cascade annulation under redox-neutral conditions.
Chemical communications (Cambridge, England), 2026, 62, 4354-4357
7135420 CIFC17 H29 Cl2 N3 O3 RuP 1 21/n 111.395; 17.1279; 11.6609
90; 110.596; 90
2130.4M, Thillai Natarajan; Padhi, Sumanta Kumar
Hydride-mediated ammonia borane dehydrogenation in water by arene-Ru(II) catalysts revealed through real-time gas evolution.
Chemical communications (Cambridge, England), 2026, 62, 5880-5884
7135421 CIFC34 H40 Cl2 F12 N4 P2 Ru2P 1 21/c 19.4601; 15.895; 26.358
90; 94.147; 90
3953M, Thillai Natarajan; Padhi, Sumanta Kumar
Hydride-mediated ammonia borane dehydrogenation in water by arene-Ru(II) catalysts revealed through real-time gas evolution.
Chemical communications (Cambridge, England), 2026, 62, 5880-5884
7135422 CIFC16 H20 Cl F6 N2 O P RuP 1 21/n 111.3484; 15.5897; 11.7304
90; 110.02; 90
1949.92M, Thillai Natarajan; Padhi, Sumanta Kumar
Hydride-mediated ammonia borane dehydrogenation in water by arene-Ru(II) catalysts revealed through real-time gas evolution.
Chemical communications (Cambridge, England), 2026, 62, 5880-5884
7135423 CIFC25 H15 N OP 1 21/n 18.95059; 11.1282; 17.174
90; 101.952; 90
1673.52Nakamura, Shuto; Kawaguchi, Soki; Nishimura, Yuta; Harimoto, Takashi; Hasegawa, Jun-Ya; Suzuki, Takanori; Ishigaki, Yusuke
Nitrogen-centred helical acridiniums with a 6-7-6-6 fused ring skeleton.
Chemical communications (Cambridge, England), 2026, 62, 4268-4271
7135424 CIFC25 H16 B F4 NP 1 21/n 19.75691; 7.33195; 26.2699
90; 96.4206; 90
1867.49Nakamura, Shuto; Kawaguchi, Soki; Nishimura, Yuta; Harimoto, Takashi; Hasegawa, Jun-Ya; Suzuki, Takanori; Ishigaki, Yusuke
Nitrogen-centred helical acridiniums with a 6-7-6-6 fused ring skeleton.
Chemical communications (Cambridge, England), 2026, 62, 4268-4271
7135425 CIFC34 H26 B F4 NP 21 21 2111.24384; 13.79725; 17.01571
90; 90; 90
2639.72Nakamura, Shuto; Kawaguchi, Soki; Nishimura, Yuta; Harimoto, Takashi; Hasegawa, Jun-Ya; Suzuki, Takanori; Ishigaki, Yusuke
Nitrogen-centred helical acridiniums with a 6-7-6-6 fused ring skeleton.
Chemical communications (Cambridge, England), 2026, 62, 4268-4271
7135426 CIFC34 H26 B F4 N OP 21 21 2111.5153; 13.2614; 17.5945
90; 90; 90
2686.84Nakamura, Shuto; Kawaguchi, Soki; Nishimura, Yuta; Harimoto, Takashi; Hasegawa, Jun-Ya; Suzuki, Takanori; Ishigaki, Yusuke
Nitrogen-centred helical acridiniums with a 6-7-6-6 fused ring skeleton.
Chemical communications (Cambridge, England), 2026, 62, 4268-4271
7135427 CIFC33 H24 B Cl2 F4 N OI 1 2/a 124.5693; 8.47276; 26.6677
90; 93.9884; 90
5538Nakamura, Shuto; Kawaguchi, Soki; Nishimura, Yuta; Harimoto, Takashi; Hasegawa, Jun-Ya; Suzuki, Takanori; Ishigaki, Yusuke
Nitrogen-centred helical acridiniums with a 6-7-6-6 fused ring skeleton.
Chemical communications (Cambridge, England), 2026, 62, 4268-4271
7135428 CIFC28 H25 N O2 P2 S2P 1 21/n 113.0525; 9.021; 22.2487
90; 101.178; 90
2570.01Duari, Prakash; Jörges, Mike; Mondal, Sunita; Feichtner, Kai-Stephan; Gessner, Viktoria H.
Reactivity of ketenyl anions towards ammonia.
Chemical communications (Cambridge, England), 2026, 62, 4293-4297
7135429 CIFC116 H130 K6 N2 O14 P6 Se6P 1 21/c 127.5782; 14.6756; 31.7159
90; 113.102; 90
11806.9Duari, Prakash; Jörges, Mike; Mondal, Sunita; Feichtner, Kai-Stephan; Gessner, Viktoria H.
Reactivity of ketenyl anions towards ammonia.
Chemical communications (Cambridge, England), 2026, 62, 4293-4297
7135430 CIFC108 H114 K6 N2 O12 P6 S6C 1 c 124.33755; 22.84495; 23.04768
90; 98.1107; 90
12686.1Duari, Prakash; Jörges, Mike; Mondal, Sunita; Feichtner, Kai-Stephan; Gessner, Viktoria H.
Reactivity of ketenyl anions towards ammonia.
Chemical communications (Cambridge, England), 2026, 62, 4293-4297
7135431 CIFC29 H31 N O2 SeP -16.6419; 11.9656; 17.5698
107.138; 90.007; 100.861
1308.14Luo, Xian-Bing; Wu, Xia-Die; Wang, Lei; Li, Zhifang; Hou, Zhong-Wei
Regioselective electrochemical 7-<i>endo-dig</i> selenocyclization of <i>N</i>-benzyl propiolamides to access selenated benzo[<i>c</i>]azepinones.
Chemical communications (Cambridge, England), 2026, 62, 4346-4349
7135432 CIFC35 H23 N O SeC 1 2/c 119.5813; 8.5064; 32.0053
90; 98.372; 90
5274.2Luo, Xian-Bing; Wu, Xia-Die; Wang, Lei; Li, Zhifang; Hou, Zhong-Wei
Regioselective electrochemical 7-<i>endo-dig</i> selenocyclization of <i>N</i>-benzyl propiolamides to access selenated benzo[<i>c</i>]azepinones.
Chemical communications (Cambridge, England), 2026, 62, 4346-4349
7135433 CIFC27 H27 N O2 SeC 1 2/c 124.2397; 6.654; 30.0658
90; 100.312; 90
4771.01Luo, Xian-Bing; Wu, Xia-Die; Wang, Lei; Li, Zhifang; Hou, Zhong-Wei
Regioselective electrochemical 7-<i>endo-dig</i> selenocyclization of <i>N</i>-benzyl propiolamides to access selenated benzo[<i>c</i>]azepinones.
Chemical communications (Cambridge, England), 2026, 62, 4346-4349
7135434 CIFC24 H26 N O2 PP 1 21/n 117.6262; 13.7083; 19.441
90; 116.945; 90
4187.5Kaste, Malte; Heilmann, Tobias; Kircher, Johannes; Golz, Christopher; Mata, Ricardo A.; Alcarazo, Manuel
Synthesis and reactivity of a strongly pyramidalized P(III)-compound embedded into a pyrrolide (ONO)<sup>3-</sup> pincer ligand.
Chemical communications (Cambridge, England), 2026, 62, 5696-5700
7135435 CIFC29 H39 N2 O2 PP 1 21/c 111.1848; 11.1217; 21.2471
90; 93.249; 90
2638.8Kaste, Malte; Heilmann, Tobias; Kircher, Johannes; Golz, Christopher; Mata, Ricardo A.; Alcarazo, Manuel
Synthesis and reactivity of a strongly pyramidalized P(III)-compound embedded into a pyrrolide (ONO)<sup>3-</sup> pincer ligand.
Chemical communications (Cambridge, England), 2026, 62, 5696-5700
7135436 CIFC32 H26 Fe2 Sb2P 1 21/c 112.44; 21.792; 10.3344
90; 113.814; 90
2563.1Thakur, Arunabha; Murphy, Brendan L.; Jiang, You; Bhuvanesh, Nattamai; Gabbaï, François P
Fluoride ion chelation <i>via</i> pnictogen bonding using a distibora[1.1]ferrocenophane.
Chemical communications (Cambridge, England), 2026, 62, 5293-5296
7135437 CIFC45 H28 Cl10 Fe2 O4 Sb2P -111.9378; 12.3613; 16.8723
69.563; 79.623; 78.431
2269.2Thakur, Arunabha; Murphy, Brendan L.; Jiang, You; Bhuvanesh, Nattamai; Gabbaï, François P
Fluoride ion chelation <i>via</i> pnictogen bonding using a distibora[1.1]ferrocenophane.
Chemical communications (Cambridge, England), 2026, 62, 5293-5296
7135438 CIFC32 H26 Fe2 Sb2P -17.5974; 8.8039; 10.737
111.794; 92.182; 105.042
636.71Thakur, Arunabha; Murphy, Brendan L.; Jiang, You; Bhuvanesh, Nattamai; Gabbaï, François P
Fluoride ion chelation <i>via</i> pnictogen bonding using a distibora[1.1]ferrocenophane.
Chemical communications (Cambridge, England), 2026, 62, 5293-5296
7135439 CIFC63.34 H72.02 Cl8 F Fe2 N O5.67 S1.67 Sb2C 1 c 113.3688; 36.463; 14.5282
90; 107.355; 90
6759.6Thakur, Arunabha; Murphy, Brendan L.; Jiang, You; Bhuvanesh, Nattamai; Gabbaï, François P
Fluoride ion chelation <i>via</i> pnictogen bonding using a distibora[1.1]ferrocenophane.
Chemical communications (Cambridge, England), 2026, 62, 5293-5296
7135440 CIFC16 H19 N O4 SP 1 21/n 16.9274; 21.8077; 20.0653
90; 95.639; 90
3016.6Liu, Bifu; Zhang, Qiaoya; Zhang, Jun; Huang, Aidong; Zhong, Hulin; Feng, Kejun; Gao, Yang; Huo, Yanping; Chen, Qian; Li, Xianwei
Tunable regioselectivity for C-H alkynylation of weakly coordinating amides that tolerated strongly coordinating heterocycles.
Chemical communications (Cambridge, England), 2026, 62, 6373-6377
7135441 CIFB4 La O12 V3C 1 2/c 17.5691; 9.6753; 11.606
90; 104.937; 90
821.23Wei, Yu-Long; Yao, Wen-Dong; Lv, Yi-Lei; Ma, Liang; Tang, Ru-Ling
REV<sub>3</sub>(BO<sub>3</sub>)<sub>4</sub> (RE = La-Nd): a series of rare earth vanadoborates exhibit large birefringence induced by distorted V<sup>III</sup>O<sub>6</sub> groups.
Chemical communications (Cambridge, England), 2026
7135442 CIFB4 Ce O12 V3C 1 2/c 17.5498; 9.6596; 11.5824
90; 104.918; 90
816.21Wei, Yu-Long; Yao, Wen-Dong; Lv, Yi-Lei; Ma, Liang; Tang, Ru-Ling
REV<sub>3</sub>(BO<sub>3</sub>)<sub>4</sub> (RE = La-Nd): a series of rare earth vanadoborates exhibit large birefringence induced by distorted V<sup>III</sup>O<sub>6</sub> groups.
Chemical communications (Cambridge, England), 2026
7135443 CIFB4 Nd O12 V3C 1 2/c 17.5261; 9.6411; 11.5559
90; 104.807; 90
810.65Wei, Yu-Long; Yao, Wen-Dong; Lv, Yi-Lei; Ma, Liang; Tang, Ru-Ling
REV<sub>3</sub>(BO<sub>3</sub>)<sub>4</sub> (RE = La-Nd): a series of rare earth vanadoborates exhibit large birefringence induced by distorted V<sup>III</sup>O<sub>6</sub> groups.
Chemical communications (Cambridge, England), 2026
7135444 CIFB4 O12 Pr V3C 1 2/c 17.5419; 9.6567; 11.5679
90; 104.864; 90
814.3Wei, Yu-Long; Yao, Wen-Dong; Lv, Yi-Lei; Ma, Liang; Tang, Ru-Ling
REV<sub>3</sub>(BO<sub>3</sub>)<sub>4</sub> (RE = La-Nd): a series of rare earth vanadoborates exhibit large birefringence induced by distorted V<sup>III</sup>O<sub>6</sub> groups.
Chemical communications (Cambridge, England), 2026
7135445 CIFC24 H45 B3 N2P 1 21/n 16.539; 35.084; 10.245
90; 94.713; 90
2342.4Bedi, Vaibhav; Ocampochua, Andrew Niles L.; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactions of phosphazines with primary and secondary boranes: adducts, rings and reduction.
Chemical communications (Cambridge, England), 2026, 62, 6123-6127
7135446 CIFC60 H75 B3 F17 N2 P2P 1 21/n 110.598; 42.394; 13.4643
90; 92.053; 90
6045.5Bedi, Vaibhav; Ocampochua, Andrew Niles L.; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactions of phosphazines with primary and secondary boranes: adducts, rings and reduction.
Chemical communications (Cambridge, England), 2026, 62, 6123-6127
7135447 CIFC60 H32 B2 F20 N2 P2P -112.882; 18.1764; 22.7716
89.856; 87.89; 78.647
5224Bedi, Vaibhav; Ocampochua, Andrew Niles L.; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactions of phosphazines with primary and secondary boranes: adducts, rings and reduction.
Chemical communications (Cambridge, England), 2026, 62, 6123-6127
7135448 CIFC53 H41 B F10 N2 P2P 1 21/n 113.1429; 25.7801; 13.7285
90; 98.058; 90
4605.6Bedi, Vaibhav; Ocampochua, Andrew Niles L.; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactions of phosphazines with primary and secondary boranes: adducts, rings and reduction.
Chemical communications (Cambridge, England), 2026, 62, 6123-6127
7135449 CIFC51 H38 B F8 N2 P2P -111.6875; 19.101; 21.623
113.71; 99.873; 91.176
4332.8Bedi, Vaibhav; Ocampochua, Andrew Niles L.; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
Reactions of phosphazines with primary and secondary boranes: adducts, rings and reduction.
Chemical communications (Cambridge, England), 2026, 62, 6123-6127
7135450 CIFC15 H12 Br O2 S1.5I 1 2/a 116.6288; 9.5465; 19.9075
90; 107.989; 90
3005.8Tiwari, Shashikant; Kumar, Nitin; Rawat, Diwan S.
Stereoselective thiosulfonylation of alkynes using sodium thiosulfate as a sulfur transfer agent to access <i>bis</i>-(<i>Z</i>)-vinyl sulfones.
Chemical communications (Cambridge, England), 2026, 62, 6751-6754
7135451 CIFC38 H42 O4 S3P 1 21/c 16.9287; 24.5829; 20.8338
90; 93.895; 90
3540.4Tiwari, Shashikant; Kumar, Nitin; Rawat, Diwan S.
Stereoselective thiosulfonylation of alkynes using sodium thiosulfate as a sulfur transfer agent to access <i>bis</i>-(<i>Z</i>)-vinyl sulfones.
Chemical communications (Cambridge, England), 2026, 62, 6751-6754
7135452 CIFC19 H17 N O SP 1 21/c 111.2703; 9.7437; 17.104
90; 94.312; 90
1872.9Xu, Yongqiang; Li, Wenkai; Gu, Xiaoli; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Construction of oxindole spiro medium-sized S-heterocycles <i>via</i> ring expansion [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2026, 62, 4545-4548
7135453 CIFC20 H18 Br N O SP 1 21/c 116.64; 13.25; 7.717
90; 95.778; 90
1692.8Xu, Yongqiang; Li, Wenkai; Gu, Xiaoli; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Construction of oxindole spiro medium-sized S-heterocycles <i>via</i> ring expansion [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2026, 62, 4545-4548
7135454 CIFC20 H17 N O SP 1 21/c 18.0368; 14.1257; 14.1169
90; 95.904; 90
1594.1Xu, Yongqiang; Li, Wenkai; Gu, Xiaoli; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Construction of oxindole spiro medium-sized S-heterocycles <i>via</i> ring expansion [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2026, 62, 4545-4548
7135455 CIFC20 H18 Br N O SP -17.0549; 15.033; 17.847
65.113; 87.985; 89.238
1716Xu, Yongqiang; Li, Wenkai; Gu, Xiaoli; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Construction of oxindole spiro medium-sized S-heterocycles <i>via</i> ring expansion [2,3]-sigmatropic rearrangement.
Chemical communications (Cambridge, England), 2026, 62, 4545-4548
7135456 CIFC40 H28 B2 F4 N4 O4P 1 21/c 17.5341; 14.4259; 16.8748
90; 92.484; 90
1832.3Campillo-Alvarado, Gonzalo; Vargas-Olvera, Eva C; Swenson, Dale C.; Morales-Rojas, Hugo; Höpfl, Herbert; MacGillivray, Leonard R.
Rotisserie-like motion enables guest transport in a nonporous organic crystal involving a diboron host.
Chemical communications (Cambridge, England), 2026, 62, 4519-4522
7135457 CIFC34 H22 B2 F4 N4 O4P 1 21/n 17.3611; 13.623; 15.855
90; 102.723; 90
1550.9Campillo-Alvarado, Gonzalo; Vargas-Olvera, Eva C; Swenson, Dale C.; Morales-Rojas, Hugo; Höpfl, Herbert; MacGillivray, Leonard R.
Rotisserie-like motion enables guest transport in a nonporous organic crystal involving a diboron host.
Chemical communications (Cambridge, England), 2026, 62, 4519-4522
7135458 CIFC37 H25 B2 F4 N4 O4P 1 21/c 112.6124; 15.3927; 17.4936
90; 105.945; 90
3265.5Campillo-Alvarado, Gonzalo; Vargas-Olvera, Eva C; Swenson, Dale C.; Morales-Rojas, Hugo; Höpfl, Herbert; MacGillivray, Leonard R.
Rotisserie-like motion enables guest transport in a nonporous organic crystal involving a diboron host.
Chemical communications (Cambridge, England), 2026, 62, 4519-4522
7135459 CIFC27 H20 F N3 O3P -19.5015; 10.5542; 12.0742
68.976; 87.437; 76.468
1097.8Boruah, Deepjyoti; Ghosh, Subhendu; Mandal, Raju; Patel, Bhisma K.
Photosensitizer-free polarity-mismatched electrophilic α,α-bis-functionalization of acetone with quinoxaline and maleimide.
Chemical communications (Cambridge, England), 2026, 62, 4561-4564
7135460 CIFC32 H23 N5P -19.9729; 10.3862; 12.3764
94.304; 98.744; 102.558
1228.95Perumal, Karuppaiah; Shanthi, Markabandhu; Hemamalini, Vijayakumar; Shankar, Bhaskaran; Ramesh, Subburethinam
Metal-Free, Iodine-Mediated Multicomponent Synthesis of Bis-Pyrazolo-Pyridine Derivatives
Chemical Communications, 2026
7135461 CIFC26 H34 Cl2 Mn N4 Ni O14P -18.4801; 13.367; 16.142
100.569; 104.558; 105.991
1638.5Bhadauriya, Kiran; Goyal, Ayusie; Kumar, Rakesh; Singh, Baghendra; Draksharapu, Apparao
Heterometallic molecular Ni-salen catalysts for efficient electrocatalytic oxygen evolution reaction.
Chemical communications (Cambridge, England), 2026, 62, 6396-6399
7135462 CIFC66 H78 Cl2 Co N6 Ni3 O23P -112.1492; 15.5959; 18.6011
89.457; 78.403; 76.541
3355.15Bhadauriya, Kiran; Goyal, Ayusie; Kumar, Rakesh; Singh, Baghendra; Draksharapu, Apparao
Heterometallic molecular Ni-salen catalysts for efficient electrocatalytic oxygen evolution reaction.
Chemical communications (Cambridge, England), 2026, 62, 6396-6399
7135463 CIFC44 H47 Cl2 Fe N4 Ni2 O16C 1 2 118; 20.4; 12.978
90; 108.789; 90
4511.6Bhadauriya, Kiran; Goyal, Ayusie; Kumar, Rakesh; Singh, Baghendra; Draksharapu, Apparao
Heterometallic molecular Ni-salen catalysts for efficient electrocatalytic oxygen evolution reaction.
Chemical communications (Cambridge, England), 2026, 62, 6396-6399
7135464 CIFC66 H71 N11 O16 S4P -113.6618; 14.754; 19.1796
72.997; 71.086; 88.933
3484.94Yang, Yi; Zhou, Bin; Dai, Yu-Ying; Cao, Li-Hui
Solvent-induced structural transformation in luminescence-enhanced polymorphic ionic HOFs.
Chemical communications (Cambridge, England), 2026, 62, 5691-5695
7135465 CIFC131 H152 N20 O37 S8P -113.9046; 14.577; 19.1732
96.614; 111.196; 101.551
3474.23Yang, Yi; Zhou, Bin; Dai, Yu-Ying; Cao, Li-Hui
Solvent-induced structural transformation in luminescence-enhanced polymorphic ionic HOFs.
Chemical communications (Cambridge, England), 2026, 62, 5691-5695
7135466 CIFC24 H16 Cu2 O10P -3 m 119.057; 19.057; 7.058
90; 90; 120
2219.8Takahara, Teppei; Usuba, Junichi; Kusaka, Shinpei; Hijikata, Yuh; Iguchi, Hiroaki; Kato, Kenichi; Matsuda, Ryotaro
Expansion of Pore Size and Interlayer Distance in a Kagomé-Type MOF Engineered through the Geometric Features of Azulene
Chemical Communications, 2026
7135467 CIFC18 H15 Fe N O4P 21 21 217.6243; 10.6505; 19.4172
90; 90; 90
1576.73Gupta, Princi; Patel, Brijesh; Waske, Shivam; Madhavan, Suchithra; Kapur, Manmohan
Native carboxylate-assisted palladium/norbornene-mediated distal C-H functionalization of ferrocene.
Chemical communications (Cambridge, England), 2026, 62, 6364-6367
7135468 CIFC44 H67 Cl6 K N9 O16.25 U3P -113.9789; 14.6991; 17.4435
74.253; 87.805; 69.205
3218.28Singh, Mukesh K.; Sproules, Stephen; Love, Jason B.
Stabilisation and characterisation of a trinuclear uranyl complex by ligand-radical formation.
Chemical communications (Cambridge, England), 2026, 62, 5660-5664
7135469 CIFC29 H23 O3 PP 1 21/n 113.7395; 10.4643; 16.2174
90; 98.524; 90
2305.9Khantong, Adisorn; Chemin, Alexandre; Galangau, Olivier; Le Guennic, Boris; Jacquemin, Denis; Bouit, Pierre-Antoine
Make the ylides shine: synthesis and structure-property relationships of phospha-squaraines.
Chemical communications (Cambridge, England), 2026, 62, 6563-6566
7135470 CIFC174 H178 Ag14 O18 Pt S12P -119.759; 20.696; 22.251
88.498; 88.172; 84.406
9049Yu, Linlin; Ren, Yonggang; Han, Yue; Ma, Along; Zhang, Shuo; Zhang, Linwen; Wang, Shuxin
Modulation of the surface active site number in Pt1Ag14 nanoclusters by ligand engineering to boost photocatalytic H<sub>2</sub> production.
Chemical communications (Cambridge, England), 2026, 62, 3373-3377
7135471 CIFC71 H51 B2 Cl N2 O7P n m a8.2913; 42.949; 25.2756
90; 90; 90
9000.7Wang, Yan-Fang; Cai, Youlie; Du, Zhenglin; Xiao, Ding; Wang, Mengbin; Liu, Ming; Li, Guangfeng
Rigid arc-shaped ligands for the fabrication of dative B-N-bonded crystalline porous polymers.
Chemical communications (Cambridge, England), 2026, 62, 3313-3316
7135472 CIFC105 H96 B2 N2 O7P 1 21/c 143.8807; 24.9175; 8.3149
90; 94.544; 90
9062.9Wang, Yan-Fang; Cai, Youlie; Du, Zhenglin; Xiao, Ding; Wang, Mengbin; Liu, Ming; Li, Guangfeng
Rigid arc-shaped ligands for the fabrication of dative B-N-bonded crystalline porous polymers.
Chemical communications (Cambridge, England), 2026, 62, 3313-3316
7135473 CIFC86 H110 O6P 17.1333; 12.758; 20.093
102.376; 90.215; 94.854
1779.2Wang, Meng; Song, Yuxuan; Wang, Zhixuan; Xu, Bin; Tian, Wenjing
Solvent-dependent self-assemblies with multi-inverted circularly polarized luminescence based on 9,10-distyrylanthracene.
Chemical communications (Cambridge, England), 2026, 62, 3334-3337
7135474 CIFC21 H22 N6 OP 1 21/n 119.1428; 10.6392; 19.4801
90; 101.946; 90
3881.5Jiang, Jingjing; Zhang, Jinghan; Huang, Nan; Xu, Haocheng; Liu, Xintao; Li, Jiayin; Zhou, Xinlong; Zhao, Jingjing; Li, Pan
Lewis acid-switched regiodivergent <i>N</i><sup>1</sup>/<i>N</i><sup>2</sup>-alkylation of ben-zotriazoles with α-hydroxyl diazo compounds.
Chemical communications (Cambridge, England), 2026, 62, 3279-3282
7135475 CIFC17 H21 N5 O2I 1 2/a 119.85; 9.741; 19.851
90; 112.07; 90
3557.1Jiang, Jingjing; Zhang, Jinghan; Huang, Nan; Xu, Haocheng; Liu, Xintao; Li, Jiayin; Zhou, Xinlong; Zhao, Jingjing; Li, Pan
Lewis acid-switched regiodivergent <i>N</i><sup>1</sup>/<i>N</i><sup>2</sup>-alkylation of ben-zotriazoles with α-hydroxyl diazo compounds.
Chemical communications (Cambridge, England), 2026, 62, 3279-3282
7135476 CIFC42 H42 N2 O2P -17.5529; 14.0354; 16.8483
110.038; 98.621; 90.387
1655.73Zwaihed, Walaa; Maurel, François; Allain, Magali; Pauli, Guido F.; Cabanetos, Clément; Kobeissi, Marwan; Schmaltz, Bruno
From benzyl to fluorenyl: enhancing photostability and modulating optoelectronic properties of <i>para</i>-azaquinodimethanes.
Chemical communications (Cambridge, England), 2026, 62, 3347-3351
7135477 CIFC25 H16 Br N O2 SP -17.374; 8.7891; 16.2598
92.277; 94.132; 103.09
1022.05Pal, Satyajit; Sarkar, Subhankar; Pramanik, Tanmay; Santra, Sougata; Majee, Adinath
PhI(OCOCF<sub>3</sub>)<sub>2</sub>-mediated metal-free 2,3-difunctionalization of indoles: direct access to carbochalcogenated scaffolds.
Chemical communications (Cambridge, England), 2026, 62, 3326-3329
7135478 CIFC90 H90 N6 O4P -19.708; 14.094; 14.845
73.353; 84.16; 70.601
1835.5Herman, Robert J.; Jalife, Said; LeBlanc, Abigail G.; Khan, Muhammad Usama Gul; Stewart, Marvin L.; Njoroge, Sheila W.; Tanha, Sajila Riman; Fronczek, Frank R.; Wu, Judy; Lee, Semin
Selective strain-promoted reactivity of a fluorene-derived [6]cycloparaphenyleneacetylene carbon nanohoop.
Chemical communications (Cambridge, England), 2026, 62, 243-246
7135479 CIFC98 H88 Cl6 N6P 1 21/c 118.272; 25.467; 9.441
90; 103.359; 90
4274Herman, Robert J.; Jalife, Said; LeBlanc, Abigail G.; Khan, Muhammad Usama Gul; Stewart, Marvin L.; Njoroge, Sheila W.; Tanha, Sajila Riman; Fronczek, Frank R.; Wu, Judy; Lee, Semin
Selective strain-promoted reactivity of a fluorene-derived [6]cycloparaphenyleneacetylene carbon nanohoop.
Chemical communications (Cambridge, England), 2026, 62, 243-246
7135480 CIFC91.3 H90.6 O2.33P -110.825; 18.566; 19.147
107.809; 100.919; 93.994
3564Herman, Robert J.; Jalife, Said; LeBlanc, Abigail G.; Khan, Muhammad Usama Gul; Stewart, Marvin L.; Njoroge, Sheila W.; Tanha, Sajila Riman; Fronczek, Frank R.; Wu, Judy; Lee, Semin
Selective strain-promoted reactivity of a fluorene-derived [6]cycloparaphenyleneacetylene carbon nanohoop.
Chemical communications (Cambridge, England), 2026, 62, 243-246
7135481 CIFC66 H18 N6 O41 Zn5F m -3 m38.578; 38.578; 38.578
90; 90; 90
57414Lin, Lin; Wang, Zihao; Zhao, Xinhui; Alezi, Dalal; Jia, Jiangtao
A reticular chemistry approach to constructing metal-organic frameworks with <i>hmc</i> topology using organic cage building blocks.
Chemical communications (Cambridge, England), 2026, 62, 2603-2606
7135482 CIFC20 H36 N6 O14 S3P 15.34785; 9.40623; 14.69319
83.7804; 88.77; 89.4031
734.57Yazaki, Masana; Zhang, Yaozhuo; Zhou, Lin; Morise, Ryo; Akaike, Takaaki; Arisawa, Mieko
Acid-catalyzed esterification and biotin/fluorescent labeling of glutathione polysulfides based on stability under heating and pH change.
Chemical communications (Cambridge, England), 2026, 62, 2668-2671
7135483 CIFC80 H136 Ag8 S8I 1 2 116.9196; 12.7575; 20.1848
90; 91.289; 90
4355.82Hao, Jingbin; Wu, Shenao; Cao, Jiayun; Li, Qinzhen; Chai, Jinsong; Gao, Guiqi; Xiong, Lin; Yang, Sha; Zhu, Manzhou
Exploring the origin of chirality in Ag<sub>8</sub> clusters based on modular disassembly.
Chemical communications (Cambridge, England), 2026, 62, 2572-2575
7135484 CIFC80 H136 Ag8 S8I 1 2 116.9038; 12.7806; 20.1609
90; 91.331; 90
4354.4Hao, Jingbin; Wu, Shenao; Cao, Jiayun; Li, Qinzhen; Chai, Jinsong; Gao, Guiqi; Xiong, Lin; Yang, Sha; Zhu, Manzhou
Exploring the origin of chirality in Ag<sub>8</sub> clusters based on modular disassembly.
Chemical communications (Cambridge, England), 2026, 62, 2572-2575
7135485 CIFC27 H21 N O4 SP n a 2116.0438; 20.1986; 14.2693
90; 90; 90
4624.1Su, Yin; Sun, Ziyi; Zhao, Quansheng; Fu, Liang
Facile synthesis of multisubstituted 2,3-dihydrofurans <i>via</i> intermolecular cyclization of enals or alkyl/aryl aldehydes with acyl-stabilized sulfur ylides.
Chemical communications (Cambridge, England), 2026, 62, 2585-2588
7135486 CIFC24 H17 Br O2 SP -19.778; 14.662; 15.35
89.547; 78.444; 73.771
2067.4Su, Yin; Sun, Ziyi; Zhao, Quansheng; Fu, Liang
Facile synthesis of multisubstituted 2,3-dihydrofurans <i>via</i> intermolecular cyclization of enals or alkyl/aryl aldehydes with acyl-stabilized sulfur ylides.
Chemical communications (Cambridge, England), 2026, 62, 2585-2588
7135487 CIFCe8 K5 O336 Te8 W88I 41/a :238.599; 38.599; 27.82
90; 90; 90
41449Lin, Xiao-Ling; Cao, Jia-Wei; Li, Shi-Xiong; Liu, Yu-Feng; Yang, Guo-Ping
Self-assembly of a tellurotungstate skeleton inlaid with Ce(III) for efficient photocatalytic synthesis of quinazolines.
Chemical communications (Cambridge, England), 2026, 62, 2619-2623
7135488 CIFC34 H28 Cd N4 O5 S2P c c n20.5528; 14.096; 11.5518
90; 90; 90
3346.7Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135489 CIFC68 H36 Cd2 F20 N8 O10 S4P 1 21/c 18.9359; 34.849; 23.558
90; 99.623; 90
7232.9Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135490 CIFC68 H36 Cd2 F20 N8 O10 S4P 1 21/c 18.41379; 36.0269; 23.0429
90; 95.148; 90
6956.7Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135491 CIFC34 H28 Cd N4 O5 S2P c c n13.7335; 20.0531; 12.0778
90; 90; 90
3326.2Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135492 CIFC34 H20 Cd F6 N4 O4 S2P 1 21/c 120.89; 4.033; 21.32
90; 115.964; 90
1614.9Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135493 CIFC34 H20 Cd F6 N4 O4 S2P 1 21/c 120.94; 4.0627; 21.764
90; 117.167; 90
1647.3Song, Wei-Chao; Niu, Zi-Yi; Ding, Bo; Wang, Xiu-Guang; Yang, En-Cui
Photosalient Cd(II) complexes by visible-light-driven single-crystal-to-single-crystal [2+2] stereoselective cycloaddition.
Chemical communications (Cambridge, England), 2026, 62, 2589-2593
7135494 CIFC19 H15 N O3P c a 2121.5147; 5.6766; 24.744
90; 90; 90
3022Meena, Shivam A.; Thakur, Deepika; Tripathi, Surya P.; Ranjan, Rahul; Verma, Akhilesh K.
Photocatalytic oxidative cyclopropanation of aza-1,6-enynes: construction of 3-aza-bicyclo[3.1.0]hexane derivatives.
Chemical communications (Cambridge, England), 2026, 62, 2641-2645
7135495 CIFC20 H15 N O5P 1 21/c 19.51; 23.244; 7.6943
90; 105.888; 90
1635.9Meena, Shivam A.; Thakur, Deepika; Tripathi, Surya P.; Ranjan, Rahul; Verma, Akhilesh K.
Photocatalytic oxidative cyclopropanation of aza-1,6-enynes: construction of 3-aza-bicyclo[3.1.0]hexane derivatives.
Chemical communications (Cambridge, England), 2026, 62, 2641-2645
7135496 CIFC14 H12 Br N O3P 1 21/n 111.2247; 7.7018; 15.9626
90; 97.502; 90
1368.16Meena, Shivam A.; Thakur, Deepika; Tripathi, Surya P.; Ranjan, Rahul; Verma, Akhilesh K.
Photocatalytic oxidative cyclopropanation of aza-1,6-enynes: construction of 3-aza-bicyclo[3.1.0]hexane derivatives.
Chemical communications (Cambridge, England), 2026, 62, 2641-2645
7135497 CIFC25 H19 N O3 SP 1 21/c 129.481; 6.8544; 15.489
90; 138.05; 90
2092.3Meena, Shivam A.; Thakur, Deepika; Tripathi, Surya P.; Ranjan, Rahul; Verma, Akhilesh K.
Photocatalytic oxidative cyclopropanation of aza-1,6-enynes: construction of 3-aza-bicyclo[3.1.0]hexane derivatives.
Chemical communications (Cambridge, England), 2026, 62, 2641-2645
7135498 CIFC17 H12 N2 OP b c a5.1777; 19.0358; 24.8301
90; 90; 90
2447.3Zhang, Ziyi; Li, Xi; Feng, Yilin; Gao, Xin; Qi, Yong; Yan, Jiaying; Zhang, Nuonuo
A facile strategy for π-extended BOPYINs: transformation into six-membered BODIPY analogues and their optical properties.
Chemical communications (Cambridge, England), 2026, 62, 2659-2663
7135499 CIFC4.25 H2.5 B0.25 Cl0.25 F0.5 N0.5P 1 21/c 18.72703; 7.5733; 21.4926
90; 90.3969; 90
1420.46Zhang, Ziyi; Li, Xi; Feng, Yilin; Gao, Xin; Qi, Yong; Yan, Jiaying; Zhang, Nuonuo
A facile strategy for π-extended BOPYINs: transformation into six-membered BODIPY analogues and their optical properties.
Chemical communications (Cambridge, England), 2026, 62, 2659-2663
7135500 CIFC17 H11 B F2 N2 OP 1 21/c 19.6144; 8.748; 16.3991
90; 105.208; 90
1330.97Zhang, Ziyi; Li, Xi; Feng, Yilin; Gao, Xin; Qi, Yong; Yan, Jiaying; Zhang, Nuonuo
A facile strategy for π-extended BOPYINs: transformation into six-membered BODIPY analogues and their optical properties.
Chemical communications (Cambridge, England), 2026, 62, 2659-2663
7135501 CIFC4.6 H3 B0.2 F0.4 N0.4 O0.2P -110.1116; 11.6324; 30.3083
94.567; 97.121; 90.226
3525.85Zhang, Ziyi; Li, Xi; Feng, Yilin; Gao, Xin; Qi, Yong; Yan, Jiaying; Zhang, Nuonuo
A facile strategy for π-extended BOPYINs: transformation into six-membered BODIPY analogues and their optical properties.
Chemical communications (Cambridge, England), 2026, 62, 2659-2663
7135502 CIFC17 H13 N O2 SP 1 21/c 19.5107; 14.457; 11.245
90; 111.41; 90
1439.4Wang, Cheng; Zhang, Qiang; Qin, Sisi; Lai, Zhimin; Liang, Taoyuan; Huang, Guan; Zhao, Shuangliang; Zhang, Zhuan
Time-dependent Rh(III)-catalyzed chemodivergent reactions of 2-pyridylthiophenes with nitroalkenes.
Chemical communications (Cambridge, England), 2026, 62, 1614-1617
7135503 CIFC17 H13 F N2 O2 SP -19.8276; 11.1008; 15.5044
103.401; 106.506; 98.916
1532.72Wang, Cheng; Zhang, Qiang; Qin, Sisi; Lai, Zhimin; Liang, Taoyuan; Huang, Guan; Zhao, Shuangliang; Zhang, Zhuan
Time-dependent Rh(III)-catalyzed chemodivergent reactions of 2-pyridylthiophenes with nitroalkenes.
Chemical communications (Cambridge, England), 2026, 62, 1614-1617
7135504 CIFC25 H30 N2 O4P 21 21 2110.2722; 10.9298; 20.1804
90; 90; 90
2265.72Li, Shan-Shan; Wu, Xiao-Guang; Li, Zhen; Tian, Jin-Rui; Ma, Ai-Jun; Tu, Yong-Qiang
Biosynthesis inspired asymmetric total synthesis of camptothecin.
Chemical communications (Cambridge, England), 2026, 62, 1276-1279
7135505 CIFC28 H38 N2 O6 SiP 1 21 112.0055; 18.7238; 40.9353
90; 95.11; 90
9165.22Li, Shan-Shan; Wu, Xiao-Guang; Li, Zhen; Tian, Jin-Rui; Ma, Ai-Jun; Tu, Yong-Qiang
Biosynthesis inspired asymmetric total synthesis of camptothecin.
Chemical communications (Cambridge, England), 2026, 62, 1276-1279
7135506 CIFC101.4 H134.8 Cl2 N4 O40.7 Zr6P 1 21/n 123.1003; 14.9053; 27.912
90; 92.428; 90
9601.9Yang, Shungang; Wu, Zhengyang; Wang, Kang; Wei, Nan; Feng, Yanyan; Cui, Peng; Jiang, Yao
Enhancing iodine capture through a zirconium-based metal-organic cage featuring functionalized indole units.
Chemical communications (Cambridge, England), 2026, 62, 1927-1931
7135507 CIFC21 H24 Cl N O6C 1 2/c 120.5201; 8.6569; 22.7664
90; 90.366; 90
4044.15Mao, Zhuo-Ya; Yan, De-Xiang; Zhou, Su-Fan; Liu, Meng-En; Li, You-Zherui; Liang, Tai-Gang; Wei, Bang-Guo
Chloride-incorporating cascade dearomatization of isoquinolines with chloroformate and DMAD achieving 100% atom economy.
Chemical communications (Cambridge, England), 2026, 62, 1860-1863
7135508 CIFC70 H60 Br2 N6P 1 21 114.7393; 8.7872; 22.5044
90; 89.995; 90
2914.71Xiang, Mei; Huang, Cong; Gao, Jie; Chen, Kai; Xie, Zhen-Zhen; Yang, Hua
EnT-catalysis-enabled, radical-relay cascade cyclization to access multisubstituted cyclohexane/cyclohexene.
Chemical communications (Cambridge, England), 2026, 62, 1941-1944
7135509 CIFC39 H37 N O4 S2P -111.1879; 12.0483; 16.967
109.2; 98.081; 104.655
2025.94Xiang, Mei; Huang, Cong; Gao, Jie; Chen, Kai; Xie, Zhen-Zhen; Yang, Hua
EnT-catalysis-enabled, radical-relay cascade cyclization to access multisubstituted cyclohexane/cyclohexene.
Chemical communications (Cambridge, England), 2026, 62, 1941-1944
7135510 CIFC17 H10 Br F O2P 1 21/c 110.2785; 14.3225; 9.823
90; 105.808; 90
1391.39Sharma, Manvi; Thakur, Deepika; Meena, Shivam A.; Nandy, Abhijit; Banerjee, Shibdas; Verma, Akhilesh K.
Unlocking reactivity potential of <i>gem</i>-dihaloolefins: access to Halo-functionalized 1,4-naphthoquinones <i>via</i> intramolecular radical oxidative cyclization.
Chemical communications (Cambridge, England), 2026, 62, 1954-1958
7135511 CIFC41 H71 B9 Co4 Fe OP -115.677; 17.2637; 19
82.268; 78.144; 89.95
4984.9Giri, Soumen; Bairagi, Subhash; Shyamal, Sampad; Ghosh, Sundargopal
Expanding icosahedral frameworks: structure and bonding of bicapped icosahedral cluster [(Cp*Co)<sub>4</sub>Fe(CO)B<sub>9</sub>H<sub>11</sub>].
Chemical communications (Cambridge, England), 2026, 62, 1981-1985
7135512 CIFC30 H54 B7 Co3P 1 21/m 18.3355; 18.415; 11.3221
90; 108.9; 90
1644.2Giri, Soumen; Bairagi, Subhash; Shyamal, Sampad; Ghosh, Sundargopal
Expanding icosahedral frameworks: structure and bonding of bicapped icosahedral cluster [(Cp*Co)<sub>4</sub>Fe(CO)B<sub>9</sub>H<sub>11</sub>].
Chemical communications (Cambridge, England), 2026, 62, 1981-1985
7135513 CIFC8 H6 N4 O4P 1 21/c 16.5856; 20.0958; 6.9138
90; 96.051; 90
909.89Shanmugapriya, V.; Panda, Pradeepta K.
A bipyrrole scaffold as an emerging Frontier in robust design of high energy materials.
Chemical communications (Cambridge, England), 2026, 62, 1936-1940
7135514 CIFC40 H28 N28 O40P 110.309; 11.351; 12.68
89.771; 89.807; 89.955
1483.8Shanmugapriya, V.; Panda, Pradeepta K.
A bipyrrole scaffold as an emerging Frontier in robust design of high energy materials.
Chemical communications (Cambridge, England), 2026, 62, 1936-1940
7135515 CIFC10 H8 N6 O8P 1 21/c 18.5497; 13.502; 12.107
90; 97.392; 90
1386Shanmugapriya, V.; Panda, Pradeepta K.
A bipyrrole scaffold as an emerging Frontier in robust design of high energy materials.
Chemical communications (Cambridge, England), 2026, 62, 1936-1940
7135516 CIFC10 H10 N4 O4C 1 2/c 120.286; 8.192; 13.64
90; 100.804; 90
2226.6Shanmugapriya, V.; Panda, Pradeepta K.
A bipyrrole scaffold as an emerging Frontier in robust design of high energy materials.
Chemical communications (Cambridge, England), 2026, 62, 1936-1940
7135517 CIFC10 H6 N8 O12P 1 21/c 112.1882; 9.3309; 14.4003
90; 99.528; 90
1615.1Shanmugapriya, V.; Panda, Pradeepta K.
A bipyrrole scaffold as an emerging Frontier in robust design of high energy materials.
Chemical communications (Cambridge, England), 2026, 62, 1936-1940
7135518 CIFC35 H39 PP 1 21/n 117.72878; 6.21523; 25.4446
90; 97.0692; 90
2782.39Deka, Rajesh; Bhowmick, Toma; Orthaber, Andreas
Expect the unexpected - Li<sup>+</sup> migration governing the substitution of 7<i>H</i>-benzo[<i>de</i>]anthracene with main-group fragments.
Chemical communications (Cambridge, England), 2026, 62, 1900-1904
7135519 CIFC29 H21 O PP 1 21/c 118.8945; 5.60435; 19.3173
90; 94.74; 90
2038.54Deka, Rajesh; Bhowmick, Toma; Orthaber, Andreas
Expect the unexpected - Li<sup>+</sup> migration governing the substitution of 7<i>H</i>-benzo[<i>de</i>]anthracene with main-group fragments.
Chemical communications (Cambridge, England), 2026, 62, 1900-1904
7135520 CIFC312 H304 Cl24 Co16 N8 O100 S16P 1 21 125.191; 43.168; 24.625
90; 109.29; 90
25275Shutilov, Ilia D.; Volodin, Pavel A.; Ovsyannikov, Alexander S.; Zinoviev, Ilya M.; Guskov, Vladimir Yu; Islamov, Daut R.; Mukhametzyanov, Timur A.; Lin, Meijin; Dorovatovskii, Pavel V.; Peters, Georgy S.; Kulikova, Elizaveta S.; Burilov, Vladimir A.; Solovieva, Svetlana E.; Antipin, Igor S.
Edge-centred chirality-induced enantiopure square-like sulfonylcalix[4]arene-{Co<sup>II</sup><sub>16</sub>} cages for selective (+)-/(-)-α-pinene adsorption.
Chemical communications (Cambridge, England), 2026, 62, 1986-1990
7135521 CIFC21 H23 N O5C 1 2/c 137.342; 6.4577; 15.8102
90; 95.294; 90
3796.3Alharthi, Asma A.; Kariuki, Benson M.; Morrill, Louis C.; Browne, Duncan L.
Mechanochemical one-pot Barbier/Simmons-Smith reaction <i>via</i> sequential zinc activation.
Chemical communications (Cambridge, England), 2026, 62, 1864-1868
7135522 CIFC21 H18 N2P 21 21 216.466; 12.77; 19.58
90; 90; 90
1617Chouhan, Raju; Kumar Das, Sajal
Synthesis of indoline-2,3-fused tetrahydroquinolines bearing two free N-H groups using a protecting-group-free approach.
Chemical communications (Cambridge, England), 2026, 62, 2322-2325
7135523 CIFC42 H50 I2 N4 Zn2P -18.6589; 10.4497; 12.2569
113.997; 91.188; 98.88
996.74Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135524 CIFC42 H52 N4 Zn2P 1 21/n 112.9672; 8.7179; 17.1328
90; 105.754; 90
1864.05Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135525 CIFC42 H50 N4 ZnP 1 21/n 110.9819; 17.5081; 18.8427
90; 95.554; 90
3605.92Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135526 CIFC36 H51 N3 Si ZnP -111.1288; 11.8347; 13.5265
83.517; 79.388; 74.63
1684.56Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135527 CIFC38 H54 N2 O ZnP n m a16.592; 20.0498; 10.2782
90; 90; 90
3419.21Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135528 CIFC34 H58 Zn2P -110.6973; 11.7395; 14.1251
107.827; 91.855; 100.722
1651.6Pitz, Benjamin; Danés, Sergi; Morgenstern, Bernd; Schäfer, André
Accessing zinc(I) <i>via</i> reductive elimination of cyclopentadienes.
Chemical communications (Cambridge, England), 2026, 62, 2204-2207
7135529 CIFC112 H105 N8 O8 S8P -114.0675; 16.7852; 21.3193
89.436; 73.799; 87.024
4827.6Wang, Jie; Xu, Xue-Cen; Gong, Yue; Meng, Yu-Xuan; Zhao, Yu-Long
Visible-light-induced generation of alkenyl radicals from alkenyl sulfonium salts: direct synthesis of 11-alkenyl-substituted dibenzodiazepines.
Chemical communications (Cambridge, England), 2026, 62, 2330-2334
7135530 CIFC34 H25 B Cl3 F5 N2 SP 1 21/c 118.4324; 10.1495; 17.5125
90; 96.661; 90
3254.1Zhai, Ziyu; Cai, Fangjian; Li, Pengfei; Qu, Chulin; Shen, Zhen
Engineering asymmetric D-π-A BODIPYs as high-performance photosensitizers for photodynamic therapy.
Chemical communications (Cambridge, England), 2026, 62, 2230-2233
7135531 CIFC34 H24 B Cl3 F5 I N2 SP -19.4467; 13.6728; 13.7889
104.414; 91.701; 102.953
1674.15Zhai, Ziyu; Cai, Fangjian; Li, Pengfei; Qu, Chulin; Shen, Zhen
Engineering asymmetric D-π-A BODIPYs as high-performance photosensitizers for photodynamic therapy.
Chemical communications (Cambridge, England), 2026, 62, 2230-2233
7135532 CIFC35 H37 N O4 SP 1 21/n 110.4934; 17.6933; 16.8167
90; 99.353; 90
3080.73Tiwari, Shashikant; Sharma, Ritika; Rawat, Diwan S.
Experimental and spectroscopic evidence of the hidden triplet transition state of quinone methide: a new reactivity paradigm.
Chemical communications (Cambridge, England), 2026, 62, 2343-2347
7135533 CIFC31 H35 N O4P 1 21/c 19.2331; 14.1143; 20.5532
90; 97.619; 90
2654.82Tiwari, Shashikant; Sharma, Ritika; Rawat, Diwan S.
Experimental and spectroscopic evidence of the hidden triplet transition state of quinone methide: a new reactivity paradigm.
Chemical communications (Cambridge, England), 2026, 62, 2343-2347
7135534 CIFC20 H24.75 Cl N OP 1 21/c 114.7585; 10.9981; 11.9327
90; 112.781; 90
1785.77Tiwari, Shashikant; Sharma, Ritika; Rawat, Diwan S.
Experimental and spectroscopic evidence of the hidden triplet transition state of quinone methide: a new reactivity paradigm.
Chemical communications (Cambridge, England), 2026, 62, 2343-2347
7135535 CIFC31.99 H32.06 Br N SP -18.016; 12.509; 14.522
80.973; 83.02; 87.953
1427.3Martínez-Núñez, Clara; Arribas-Torrecilla, Carlos; Sanz, Roberto; Suárez-Pantiga, Samuel
Controlled gold-catalyzed 5-<i>exo-dig</i> cyclization of 3-sulfur-substituted 1,3-dien-5-ynes for synthesizing fulvenes and the <i>in situ</i> reaction with indoles.
Chemical communications (Cambridge, England), 2026, 62, 2287-2291
7135536 CIFC31 H31 N OP 1 21/c 110.8475; 18.7319; 13.0573
90; 110.439; 90
2486.1Martínez-Núñez, Clara; Arribas-Torrecilla, Carlos; Sanz, Roberto; Suárez-Pantiga, Samuel
Controlled gold-catalyzed 5-<i>exo-dig</i> cyclization of 3-sulfur-substituted 1,3-dien-5-ynes for synthesizing fulvenes and the <i>in situ</i> reaction with indoles.
Chemical communications (Cambridge, England), 2026, 62, 2287-2291
7135537 CIFC19 H16 F NP b c a14.44; 7.72; 26.4
90; 90; 90
2943Deka, Upasana; Gogoi, Abhijit; Das, Sajal Kumar
Reactivity divergence in the cyclization of terminal epoxides all-carbon-tethered to indoles.
Chemical communications (Cambridge, England), 2026, 62, 2222-2225
7135538 CIFC106 H100 O8P 1 21/c 113.7434; 35.5425; 17.7905
90; 106.626; 90
8326.9Li, Zhenyu; Jiang, Jingxiong; Jia, Xiaoxi; Wang, Ke; Shi, Wenjing; Qu, Wen-Juan; Lin, Qi; Wei, Tai-Bao; Shi, Bingbing
Highly selective separation of toluene/methylcyclohexane using clamparene-based 3D porous crystals.
Chemical communications (Cambridge, England), 2026, 62, 2326-2329
7135539 CIFC17 H17 N O3 PC 1 2/c 121.4243; 13.8932; 11.1722
90; 98.625; 90
3287.82Du, Jiahui; Ruan, Chengkai; Cui, Guifa; Zhao, Hongping; He, Chengyu
Cu-catalyzed tandem cross-coupling/cyclization of aryl diazophosphonates with phenylacetylene derivatives.
Chemical communications (Cambridge, England), 2026, 62, 2268-2271
7135540 CIFC16 H12 Cl N O2 SP -17.5367; 10.6159; 19.4914
100.908; 99.555; 102.92
1456.76Barik, Dinabandhu; Panigrahi, Pritishree; Manna, Supriya; Chakraborty, Nikita; Phouzder, Anushka; Patel, Bhisma K.
DABCO-directed EDA-complex mediated regioselective C4-sulfonylation of quinoline <i>N</i>-oxide.
Chemical communications (Cambridge, England), 2026, 62, 3037-3040
7135541 CIFC17 H15 N O3 SC 1 2/c 126.51; 8.002; 18.352
90; 126.765; 90
3119Barik, Dinabandhu; Panigrahi, Pritishree; Manna, Supriya; Chakraborty, Nikita; Phouzder, Anushka; Patel, Bhisma K.
DABCO-directed EDA-complex mediated regioselective C4-sulfonylation of quinoline <i>N</i>-oxide.
Chemical communications (Cambridge, England), 2026, 62, 3037-3040
7135542 CIFC38 H56 Br N5 O10 SP 1 21 112.1491; 12.2447; 14.3618
90; 100.839; 90
2098.38Nadraws, Jonathan W.; Pokle, Maithili S.; Smith, 3rd, Amos B
A 2nd-generation scalable synthesis of the HIV-1 entry inhibitor CJF-III-288 enabled by photoredox catalysis.
Chemical communications (Cambridge, England), 2026, 62, 2981-2985
7135543 CIFC26 H17 N3P 1 21/n 15.921; 13.6349; 22.0309
90; 96.426; 90
1767.4Dzieszkowski, Krzysztof; Kruczała, Krzysztof; Kijewska, Monika; Pawlicki, Miłosz
Constraint driven modulation of <i>N</i>,<i>N</i>-diarylamine(s) under space limitations imprinted in 7.6.6 defect.
Chemical communications (Cambridge, England), 2026, 62, 2976-2980
7135544 CIFC26 H19 N3P c a 2112.3366; 19.8244; 7.4816
90; 90; 90
1829.74Dzieszkowski, Krzysztof; Kruczała, Krzysztof; Kijewska, Monika; Pawlicki, Miłosz
Constraint driven modulation of <i>N</i>,<i>N</i>-diarylamine(s) under space limitations imprinted in 7.6.6 defect.
Chemical communications (Cambridge, England), 2026, 62, 2976-2980
7135545 CIFC130 H56 Lu N4 NiC 1 2/m 125.2393; 15.1444; 19.8378
90; 94.756; 90
7556.6Zhang, Rui; Yu, Pengwei; Li, Mengyang; Tan, Xiaoxue; Hu, Zhicong; Shen, Wangqiang; Bao, Lipiao; Lu, Xing
Crystallographic determination of Lu@<i>C</i><sub>2v</sub>(9)-C<sub>82</sub>: electronic configuration and encapsulation energy-driven formation preference.
Chemical communications (Cambridge, England), 2026, 62, 2991-2994
7135546 CIFC55 H132 Cu Ge9 K N2 O6 Si12P 1 21/n 118.2014; 25.589; 20.2737
90; 90.1; 90
9442.6Chen, Tianzi; Wang, Xinyue; Han, Yulin; Guo, Chenxi; Duan, Dongyu; Tang, Yu; Pan, Fuxing
Stepwise coordination of {Cu(C<sub>5</sub>Me<sub>5</sub>)} with a tri-silylated Ge<sub>9</sub> cluster.
Chemical communications (Cambridge, England), 2026, 62, 3541-3544
7135547 CIFC78 H210 Cu Ge18 K O6 Si24R -3 :H23.6847; 23.6847; 23.4153
90; 90; 120
11375.4Chen, Tianzi; Wang, Xinyue; Han, Yulin; Guo, Chenxi; Duan, Dongyu; Tang, Yu; Pan, Fuxing
Stepwise coordination of {Cu(C<sub>5</sub>Me<sub>5</sub>)} with a tri-silylated Ge<sub>9</sub> cluster.
Chemical communications (Cambridge, England), 2026, 62, 3541-3544
7135548 CIFC66.25 H149.5 Cu2 Ge9 K N2 O6.31 Si12P 1 21/c 116.4552; 24.525; 28.508
90; 98.022; 90
11392.2Chen, Tianzi; Wang, Xinyue; Han, Yulin; Guo, Chenxi; Duan, Dongyu; Tang, Yu; Pan, Fuxing
Stepwise coordination of {Cu(C<sub>5</sub>Me<sub>5</sub>)} with a tri-silylated Ge<sub>9</sub> cluster.
Chemical communications (Cambridge, England), 2026, 62, 3541-3544
7135549 CIFLa84 O216 Os36R -3 c :H9.8639; 9.8639; 56.3934
90; 90; 120
4751.8Brennan, Ashley T.; Pelly, Maximilian T.; Gibbs, Alexandra S.; Rost, Andreas W.
Unconventional magnetism and residual entropy in La<sub>7</sub>Os<sub>3</sub>O<sub>18</sub>.
Chemical communications (Cambridge, England), 2026, 62, 3508-3511
7135550 CIFC23 H21 Br2 N O6P 1 21/c 110.1233; 26.4151; 8.7332
90; 103.709; 90
2268.8Kar, Subhradeep; Maharana, Prabhat Kumar; Punniyamurthy, Tharmalingam
Cobalt-catalysed (4+3)-annulation of oxiranes with 4-vinyl indoles: stereospecific access to fused oxepinoindoles.
Chemical communications (Cambridge, England), 2026, 62, 3550-3554
7135551 CIFC16 H13 N O3P -18.3684; 8.5801; 8.9751
89.554; 83.754; 84.365
637.5Zhao, Taotao; Liang, Qianyi; Gu, Keying; Huang, Jiangbin; Zhuang, Xiong; Hu, Jinhui; Wu, Jia-Qiang
Synthesis of isoquinolin-1,4-diones <i>via</i> photocatalytic C(sp<sup>2</sup>)-C(sp<sup>3</sup>)-scission/oxidation of 4-(hydroxy(aryl)methyl)-isoquinolin-1(2<i>H</i>)-ones.
Chemical communications (Cambridge, England), 2026, 62, 3522-3525
7135552 CIFC60 H66 S6R -3 :H22.7937; 22.7937; 9.0138
90; 90; 120
4055.7d'Agostino, Simone; Vitale, Andrea; Kapadiya, Yashraj; Gingras, Marc; Negri, Fabrizia; Ceroni, Paola; Fermi, Andrea
Polymorphism-dependent room-temperature phosphorescence of a persulfurated benzene.
Chemical communications (Cambridge, England), 2026, 62, 6567-6571
7135553 CIFC60 H66 S6P 1 21/c 118.6009; 6.3115; 22.523
90; 100.967; 90
2595.9d'Agostino, Simone; Vitale, Andrea; Kapadiya, Yashraj; Gingras, Marc; Negri, Fabrizia; Ceroni, Paola; Fermi, Andrea
Polymorphism-dependent room-temperature phosphorescence of a persulfurated benzene.
Chemical communications (Cambridge, England), 2026, 62, 6567-6571
7135554 CIFC60 H66 S6R -3 :H22.326; 22.326; 8.9976
90; 90; 120
3884d'Agostino, Simone; Vitale, Andrea; Kapadiya, Yashraj; Gingras, Marc; Negri, Fabrizia; Ceroni, Paola; Fermi, Andrea
Polymorphism-dependent room-temperature phosphorescence of a persulfurated benzene.
Chemical communications (Cambridge, England), 2026, 62, 6567-6571
7135555 CIFC60 H66 S6P 1 21/c 118.861; 6.3789; 23.076
90; 100.795; 90
2727d'Agostino, Simone; Vitale, Andrea; Kapadiya, Yashraj; Gingras, Marc; Negri, Fabrizia; Ceroni, Paola; Fermi, Andrea
Polymorphism-dependent room-temperature phosphorescence of a persulfurated benzene.
Chemical communications (Cambridge, England), 2026, 62, 6567-6571
7135556 CIFC195 H173 Cl14 Dy4 N12 O17.5P 21 21 2117.7008; 28.3765; 36.0385
90; 90; 90
18101.7Qin, Haowei; Wang, Tingting; Feng, Tingting; Zhu, Zhenhua; Ying, Xu; Zhang, Peng; Tang, Jinkui
Chiral biphenanthrene-diol-based lanthanide cubanes.
Chemical communications (Cambridge, England), 2026, 62, 6591-6595
7135557 CIFC195 H173 Cl14 Dy4 N12 O17.5P 21 21 2117.5839; 28.4582; 35.8538
90; 90; 90
17941.5Qin, Haowei; Wang, Tingting; Feng, Tingting; Zhu, Zhenhua; Ying, Xu; Zhang, Peng; Tang, Jinkui
Chiral biphenanthrene-diol-based lanthanide cubanes.
Chemical communications (Cambridge, England), 2026, 62, 6591-6595
7135558 CIFC194 H171 Cl12 Er4 N12 O17.5P 21 21 2117.4169; 28.5045; 35.6754
90; 90; 90
17711.4Qin, Haowei; Wang, Tingting; Feng, Tingting; Zhu, Zhenhua; Ying, Xu; Zhang, Peng; Tang, Jinkui
Chiral biphenanthrene-diol-based lanthanide cubanes.
Chemical communications (Cambridge, England), 2026, 62, 6591-6595
7135559 CIFC195 H172 Cl14 Er4 N12 O17P 21 21 2117.5439; 28.4744; 35.6072
90; 90; 90
17787.6Qin, Haowei; Wang, Tingting; Feng, Tingting; Zhu, Zhenhua; Ying, Xu; Zhang, Peng; Tang, Jinkui
Chiral biphenanthrene-diol-based lanthanide cubanes.
Chemical communications (Cambridge, England), 2026, 62, 6591-6595
7135560 CIFC51 H53 F6 N6 SbP -111.0231; 12.611; 15.2281
98.437; 93.659; 92.019
2087.58Wada, Kaito; Tanioka, Yuma; Mori, Shigeki; Uno, Hidemitsu; Takase, Masayoshi
π-Stacked dimerization of an antiaromatic homoHPHAC monocation.
Chemical communications (Cambridge, England), 2026, 62, 6716-6720
7135561 CIFC50 H76 Br2 O P4P 1 21/c 112.5338; 15.7508; 14.4968
90; 115.625; 90
2580.43Senn, Sebastian; Konrad, Nele; Müller, Jens; Ballmann, Joachim; Gade, Lutz H.
Tetracationic phosphonium-bridged ladder stilbenes: redox states and electronic properties of highly charged P-heteropolycyclic materials
Chemical Communications, 2026, 62, 6391-6395
7135562 CIFC56 H78 Br4 O2 P4C 1 2/c 123.0439; 8.5972; 30.0718
90; 102.595; 90
5814.25Senn, Sebastian; Konrad, Nele; Müller, Jens; Ballmann, Joachim; Gade, Lutz H.
Tetracationic phosphonium-bridged ladder stilbenes: redox states and electronic properties of highly charged P-heteropolycyclic materials
Chemical Communications, 2026, 62, 6391-6395
7135563 CIFC46 H82 Br4 O8 P4P 32 2 112.4139; 12.4139; 32.4727
90; 90; 120
4333.77Senn, Sebastian; Konrad, Nele; Müller, Jens; Ballmann, Joachim; Gade, Lutz H.
Tetracationic phosphonium-bridged ladder stilbenes: redox states and electronic properties of highly charged P-heteropolycyclic materials
Chemical Communications, 2026, 62, 6391-6395
7135564 CIFC80 H92 Cl Ir N4 O13P 1 21/c 117.504; 16.409; 29.43
90; 106.308; 90
8113Ogura, Shota; Sugiyama, Kanami; Higashi, Masahiro; Horiuchi, Shinnosuke
Unveiling a host-guest assembly composed of an emissive Ir(III) complex salt and a concave aromatic host at a local minimum state.
Chemical communications (Cambridge, England), 2026, 62, 6577-6581
7135565 CIFC65 H50 Cl4 Ir2 N8 O6I -421.1828; 21.1828; 13.4693
90; 90; 90
6043.8Ogura, Shota; Sugiyama, Kanami; Higashi, Masahiro; Horiuchi, Shinnosuke
Unveiling a host-guest assembly composed of an emissive Ir(III) complex salt and a concave aromatic host at a local minimum state.
Chemical communications (Cambridge, England), 2026, 62, 6577-6581
7135566 CIFC24 H15 Ca O5P b a m21.598; 6.9255; 16.482
90; 90; 90
2465.3Mao, Shanshan; Miao, Jiafeng; Zhou, Kang; Yin, Li; Guo, Fu-An; Hei, Xiuze; Wang, Hao
Hydrophobic Pores in a Calcium-Based MOF Enable One-Step Ethylene Purification from C₂H₂/CO₂/C₂H₄ Mixtures
Chemical Communications, 2026
7135567 CIFC69 H8 Br N S2P -110.0033; 12.9511; 16.0243
97.87; 91.414; 109.58
1931.99Chen, Jun-Shen; Qiu, Wen-Jie; Guo, Li-Feng; Wang, Guan-Wu
Mechanochemical applications of magnesium nitride to fullerene chemistry: synthesis of pyrroline-fused tetra-functionalized [60]fullerene derivatives.
Chemical communications (Cambridge, England), 2026, 62, 6114-6117
7135568 CIFC17 H14 F3 N OP 1 21 15.5451; 23.8249; 32.5396
90; 90.416; 90
4298.7Yu, Xiang; Niu, Mengru; Chen, Huan; Wu, Jiajia; Fang, Fang; Zhai, Xiaoting; Zhang, Guoyu
Enantioselective photoredox- and Cu-catalyzed alkoxycyanation of styrenes to synthesize chiral β-cyanoethers.
Chemical communications (Cambridge, England), 2026, 62, 6132-6136
7135569 CIFC29 H19 F3 N2 O3P 1 21/c 17.7488; 8.7541; 36.3995
90; 95.663; 90
2457.06Yu, Xiaowen; Li, Jinxia; Duan, Jiongjiong; Fan, Feifei; Xie, Huanping; Huang, Yanfan; Shi, Shukui; Kong, Weiguang; Li, Ting
Copper-catalysed decarboxylative alkynylation-cyclization reaction of propargylic cyclic carbonates with nitrile imines to access tetrasubstituted pyrazoles.
Chemical communications (Cambridge, England), 2026, 62, 6600-6603
7135570 CIFC29 H21 Cl N2 O3P n a 2118.3289; 17.9535; 7.4598
90; 90; 90
2454.78Yu, Xiaowen; Li, Jinxia; Duan, Jiongjiong; Fan, Feifei; Xie, Huanping; Huang, Yanfan; Shi, Shukui; Kong, Weiguang; Li, Ting
Copper-catalysed decarboxylative alkynylation-cyclization reaction of propargylic cyclic carbonates with nitrile imines to access tetrasubstituted pyrazoles.
Chemical communications (Cambridge, England), 2026, 62, 6600-6603
7135571 CIFFe5.52 Ge6 Yb Zn0.48C m c m8.1799; 17.541; 5.0739
90; 90; 90
728.02Meduri, Rahul; Wilkinson, Grant R.; Idrees, Muhammad Z.; Wei, Kaya; Stoian, Sebastian A.; La Pierre, Henry S.; McCandless, Gregory T.; Chan, Julia Y.
Zn-flux-enabled synthesis of orthorhombic kagome YbFe<sub>6</sub>Ge<sub>6</sub>: Yb reduction and magnetic behavior.
Chemical communications (Cambridge, England), 2026, 62, 6617-6621
7135572 CIFC40 H43 N3 O5P 1 21 112.5022; 9.4634; 15.5437
90; 111.466; 90
1711.46Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135573 CIFC38 H40 N2 O5P 21 21 219.6446; 14.5699; 23.0364
90; 90; 90
3237.09Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135574 CIFC39 H41 Cl3 N2 O5P 21 21 2110.0076; 12.1774; 29.6416
90; 90; 90
3612.3Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135575 CIFC44 H52 N2 O7P 19.9305; 12.4553; 15.747
87.322; 87.545; 89.705
1943.8Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135576 CIFC40 H46 N2 O6P 1 21 112.3135; 9.8662; 15.529
90; 111.669; 90
1753.3Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135577 CIFC56 H56 N2 O8P 21 21 219.8974; 12.6796; 38.5083
90; 90; 90
4832.6Jiang, Yihua; Souare, Sokhna; Robeyns, Koen; Leng, Fucheng; Collard, Laurent; Leyssens, Tom
Solvent-triggered breakdown of solid solution behaviour enables direct enantioselective crystallization of <i>RS</i>-phenprocoumon.
Chemical communications (Cambridge, England), 2026, 62, 6613-6616
7135578 CIFC20 H21 NP 21 21 216.9325; 11.039; 19.2749
90; 90; 90
1475.07Parui, Nabin; Maji, Kousik; Diasi, Manab; Dash, Jyotirmayee
A concise synthesis of indole-fused azepino- and azocino-indoles <i>via</i> acid-catalyzed 1,2-migration.
Chemical communications (Cambridge, England), 2026, 62, 6746-6750
7135579 CIFC38 H36 F2 N2P -18.155; 12.2573; 14.773
102.43; 95.802; 90.091
1434.3Parui, Nabin; Maji, Kousik; Diasi, Manab; Dash, Jyotirmayee
A concise synthesis of indole-fused azepino- and azocino-indoles <i>via</i> acid-catalyzed 1,2-migration.
Chemical communications (Cambridge, England), 2026, 62, 6746-6750
7135580 CIFCl10 K4 O Tc2I 4/m m m7.0126; 7.0126; 17.5752
90; 90; 90
864.29Bustos, Jenna; Zakharov, Lev N.; Buils, Jordi; Hosseini, Farzaneh; Solé-Daura, Albert; Bo, Carles; Nyman, May
Building block approach to technetium-substituted polyoxotungstates.
Chemical communications (Cambridge, England), 2026, 62, 5875-5879
7135581 CIFNa16 O90 Si2 Tc2 W20P -111.1764; 13.2378; 17.844
105.751; 93.888; 107.964
2383.7Bustos, Jenna; Zakharov, Lev N.; Buils, Jordi; Hosseini, Farzaneh; Solé-Daura, Albert; Bo, Carles; Nyman, May
Building block approach to technetium-substituted polyoxotungstates.
Chemical communications (Cambridge, England), 2026, 62, 5875-5879
7135582 CIFCs14 O100 P2 Tc6 W20P 1 21/m 111.352; 18.3764; 12.9618
90; 105.154; 90
2609.92Bustos, Jenna; Zakharov, Lev N.; Buils, Jordi; Hosseini, Farzaneh; Solé-Daura, Albert; Bo, Carles; Nyman, May
Building block approach to technetium-substituted polyoxotungstates.
Chemical communications (Cambridge, England), 2026, 62, 5875-5879
7135583 CIFC18 H25 Co F5 N4 O6 SP 1 21/c 16.7293; 21.385; 17.178
90; 99.13; 90
2440.7Scott, Kathleen M.; Kadakia, Rahul T.; Hastings, Christopher D.; Barone, Georgia E. F.; Reyna, Jackson A.; Xiong, Jin; Guo, Yisong; Que, Emily L.
A responsive Co(II) <sup>19</sup>F PARAShift probe: activation of Fermi contact interactions triggered by pH-dependent coordination changes.
Chemical communications (Cambridge, England), 2026, 62, 6741-6745
7135584 CIFC21 H34 Co F5 N4 Na O8 SP -110.1113; 11.8024; 13.7663
64.957; 69.304; 75.254
1381.63Scott, Kathleen M.; Kadakia, Rahul T.; Hastings, Christopher D.; Barone, Georgia E. F.; Reyna, Jackson A.; Xiong, Jin; Guo, Yisong; Que, Emily L.
A responsive Co(II) <sup>19</sup>F PARAShift probe: activation of Fermi contact interactions triggered by pH-dependent coordination changes.
Chemical communications (Cambridge, England), 2026, 62, 6741-6745
7135585 CIFC32 H32 B2 N12 Ni O2P 1 21/n 111.696; 8.6183; 16.3091
90; 109.013; 90
1554.27Zhang, Xiang-Ming; Fu, Jiang-Hong; Zhao, Pan-Pan; Chen, Shumei; Zhang, Hai-Xia; Zhang, Jian
Synthesis of hybrid nickel boron-oxo clusters for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2026, 62, 6904-6908
7135586 CIFC9 H14 B9 N6 Ni O16P -317.9513; 17.9513; 7.5178
90; 90; 120
2098.04Zhang, Xiang-Ming; Fu, Jiang-Hong; Zhao, Pan-Pan; Chen, Shumei; Zhang, Hai-Xia; Zhang, Jian
Synthesis of hybrid nickel boron-oxo clusters for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2026, 62, 6904-6908
7135587 CIFC36 H36 B6 N14 Ni2 O10C 1 2/c 118.5281; 16.6027; 14.4927
90; 95.728; 90
4435.9Zhang, Xiang-Ming; Fu, Jiang-Hong; Zhao, Pan-Pan; Chen, Shumei; Zhang, Hai-Xia; Zhang, Jian
Synthesis of hybrid nickel boron-oxo clusters for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2026, 62, 6904-6908
7135588 CIFC16 H12 N2 OP b c a10.9912; 7.7964; 29.0779
90; 90; 90
2491.74Guo, Chengxian; Xing, Qiaoyan; Xie, Hongding; Liu, Jiamiao; Li, Jiahui; Zhang, Junliang; Wang, Huamin
Desulfonylcyanamidation of α,β-unsaturated sulfones with <i>N</i>-tosyl <i>N</i>-aryl cyanamides (NCTS): access to <i>N</i>-cyanoenaminones.
Chemical communications (Cambridge, England), 2026, 62, 6768-6772
7135589 CIFC28 H16 Br2 N8P n a 2114.229; 12.9685; 26.3149
90; 90; 90
4855.9Mboyi, Clève D; Sabbadin, Henri; Penouilh, Marie-José; Bonnin, Quentin; Amardeil, Régine; Cattey, Hélène; Fournier, Sophie; Devillers, Charles H.; Roger, Julien; Hierso, Jean-Cyrille
Small cavitand macrocycles from direct C-C coupling of <i>s</i>-aryl tetrazine units.
Chemical communications (Cambridge, England), 2026, 62, 6987-6991
7135590 CIFC28 H10 Br3.79 F4.21 N8C 1 2/c 127.3462; 7.8804; 25.6877
90; 94.721; 90
5516.9Mboyi, Clève D; Sabbadin, Henri; Penouilh, Marie-José; Bonnin, Quentin; Amardeil, Régine; Cattey, Hélène; Fournier, Sophie; Devillers, Charles H.; Roger, Julien; Hierso, Jean-Cyrille
Small cavitand macrocycles from direct C-C coupling of <i>s</i>-aryl tetrazine units.
Chemical communications (Cambridge, England), 2026, 62, 6987-6991
7135591 CIFC28 H17 Br N8P 1 21/c 112.6054; 13.4378; 15.1105
90; 109.094; 90
2418.7Mboyi, Clève D; Sabbadin, Henri; Penouilh, Marie-José; Bonnin, Quentin; Amardeil, Régine; Cattey, Hélène; Fournier, Sophie; Devillers, Charles H.; Roger, Julien; Hierso, Jean-Cyrille
Small cavitand macrocycles from direct C-C coupling of <i>s</i>-aryl tetrazine units.
Chemical communications (Cambridge, England), 2026, 62, 6987-6991
7135592 CIFC58 H36 Cl4 N16P 1 21/c 112.5323; 26.102; 15.6284
90; 101.219; 90
5014.6Mboyi, Clève D; Sabbadin, Henri; Penouilh, Marie-José; Bonnin, Quentin; Amardeil, Régine; Cattey, Hélène; Fournier, Sophie; Devillers, Charles H.; Roger, Julien; Hierso, Jean-Cyrille
Small cavitand macrocycles from direct C-C coupling of <i>s</i>-aryl tetrazine units.
Chemical communications (Cambridge, England), 2026, 62, 6987-6991
7135593 CIFC46 H26 F6 N12 OP 1 21/c 114.5165; 12.9555; 21.3838
90; 101.202; 90
3945Mboyi, Clève D; Sabbadin, Henri; Penouilh, Marie-José; Bonnin, Quentin; Amardeil, Régine; Cattey, Hélène; Fournier, Sophie; Devillers, Charles H.; Roger, Julien; Hierso, Jean-Cyrille
Small cavitand macrocycles from direct C-C coupling of <i>s</i>-aryl tetrazine units.
Chemical communications (Cambridge, England), 2026, 62, 6987-6991
7135594 CIFC39 H72 Mg N O P SiP -110.13; 20.64; 21.16
112.9; 98.2; 90.4
4024.4Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135595 CIFC80 H126 Mg2 N2 P2 Si2P 1 21/n 117.98; 11.29; 19.38
90; 102.8; 90
3836.3Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135596 CIFC64 H116 Mg2 N2 P2 Si2P -110.35; 13.04; 14.35
65.3; 74.3; 71.3
1645.5Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135597 CIFC39 H60 Mg N O P SiP 1 21/n 115.96; 14.18; 17.72
90; 105.9; 90
3856.8Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135598 CIFC74 H140 Mg4 N2 P2 Si2P 1 21/n 119.19; 10.33; 22.22
90; 115.1; 90
3988.8Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135599 CIFC44 H77 Mg N O P SiP -110.63; 11.19; 19.26
82; 86.5; 73.5
2174.7Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135600 CIFC84 H140 Mg2 N2 O2 P2 Si2P 1 21/c 115.8577; 19.881; 26.5216
90; 90.826; 90
8360.5Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135601 CIFC72 H104 Mg2 N2 O2 P2 Si2P 1 21/c 115.42; 15.39; 30.35
90; 103.2; 90
7012Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135602 CIFC62 H112 Mg2 N2 P2 Si2P 1 21/c 113.433; 12.45; 20.428
90; 106.7; 90
3272.3Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135603 CIFC36.955 H67.886 Br0.023 Mg N O P SiP 1 21/c 120.032; 19.501; 19.921
90; 95.54; 90
7746Kubisz, Malte; Hadlington, Terrance John; Fernandez, Israel
Catalyst-free insertion of carbon monoxide into terminal Mg-C(sp3) bonds
Chemical Communications, 2026
7135604 CIFC12 H5 Cl F9 NP 1 21/n 111.5848; 7.2834; 32.0201
90; 96.31; 90
2685.38Koike, Takashi; Taguchi, Hina; Hirota, Kaori; Kiyatake, Shota; Tatara, Naohiro; Kayaki, Yoshihito; Yamaguchi, Airi; Yajima, Tomoko
Facile generation and reaction of densely trifluoromethylated alkyl radicals by dual photoredox and acid catalysis
Chemical Communications, 2026
7135605 CIFC12 H12 F12 N6P 1 21/n 19.608; 9.0002; 20.4814
90; 95.068; 90
1764.18Wang, Yuehui; Wen, Lele; Ling, Lin; Xing, Chunhui; Lu, Long
Direct NF<sub>2</sub> functionalization of ketones: a mild strategy for accessing high-performance gem-difluoroamino compounds.
Chemical communications (Cambridge, England), 2026, 62, 5429-5432
7135606 CIFC10 H12 F8 N4P 21 21 217.4094; 7.8335; 21.8556
90; 90; 90
1268.53Wang, Yuehui; Wen, Lele; Ling, Lin; Xing, Chunhui; Lu, Long
Direct NF<sub>2</sub> functionalization of ketones: a mild strategy for accessing high-performance gem-difluoroamino compounds.
Chemical communications (Cambridge, England), 2026, 62, 5429-5432
7135607 CIFC22 H24 Cu N8 OP b c a14.8303; 15.7103; 18.4694
90; 90; 90
4303.16Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135608 CIFC18 H10 Cu N6 O2P 1 21 112.1966; 8.964; 15.6705
90; 97.257; 90
1699.54Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135609 CIFC38 H45 Cu2 N7 O7C 1 2/c 132.5141; 13.8003; 19.1607
90; 107.065; 90
8218.96Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135610 CIFC17 H21 Cu N5 OP b c a7.2005; 13.8992; 33.6442
90; 90; 90
3367.15Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135611 CIFC12 H12 Cu N10 O2P 1 21/c 18.0354; 12.7317; 7.4563
90; 96.782; 90
757.47Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135612 CIFC24 H27 Cl3 Cu F3 N5 O3P 21 21 219.7664; 14.5775; 20.2849
90; 90; 90
2887.96Shrivastav, Akash; Bhattacharya, Subrato
iClick reaction of Cu(II) azido complex having Schiff base ligand
Chemical Communications, 2026
7135613 CIFC41 H61 K Mg N2 O2 SC 1 2/c 117.84; 13.453; 36.71
90; 101.14; 90
8644Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135614 CIFC83 H118 K2 Mg2 N4 O2 S2P -114.304; 14.3229; 20.2313
91.745; 92.462; 90.652
4138.8Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135615 CIFC41 H61 K Mg N2 O3 SC 1 2/c 117.3049; 13.2052; 36.1133
90; 95.887; 90
8208.9Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135616 CIFC42 H61 K Mg N2 O4 SP b c a16.1294; 21.3984; 23.591
90; 90; 90
8142.3Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135617 CIFC40 H59 K Mg N2 O2 SP b c a15.971; 22.01; 22.603
90; 90; 90
7945Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135618 CIFC86 H130 K2 Mg2 N4 O6 S2P 1 21/c 117.214; 19.393; 27.132
90; 107.346; 90
8645.6Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135619 CIFC88 H132 K2 Mg2 N4 O6 S2P 1 21/c 118.0904; 13.4627; 20.4918
90; 113.102; 90
4590.5Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135620 CIFC40 H53 K Mg N2 O SC 1 2/c 138.2556; 10.5263; 19.3654
90; 93.559; 90
7783.2Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135621 CIFC42 H63 K Mg N2 O2 SP b c a16.0887; 21.608; 23.849
90; 90; 90
8291Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026
7135622 CIFC41 H61 K Mg N2 O2 SP b c a15.982; 21.314; 23.857
90; 90; 90
8126.7Yang, Li; Sun, Zhenzhou; Wang, Lin; Geng, Jianqi; Wu, Biao; Yang, Xiao-Juan
Direct C-H magnesiation of thiophenes with a Mg-Mg-bonded compound
Chemical Communications, 2026

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