Crystallography Open Database

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7133755 CIFC266 H288 Co2 N20 O18P n -3 n :237.9704; 37.9704; 37.9704
90; 90; 90		54743.9Stamos, Nikolaos-Angelos; McMonagle, Charles J.; Turner, Gemma F.; Allan, David R.; Warren, Mark R.; Warren, Anna J.; McKeown, Neil B.; Moggach, Stephen A.
Ligand effects on gas adsorption in nanoporous phthalocyanine crystals.
Chemical communications (Cambridge, England), 2024, 60, 11508-11511
7133756 CIFC266 H288 Co2 N18 O16P n -3 n :237.8533; 37.8533; 37.8533
90; 90; 90		54238.9Stamos, Nikolaos-Angelos; McMonagle, Charles J.; Turner, Gemma F.; Allan, David R.; Warren, Mark R.; Warren, Anna J.; McKeown, Neil B.; Moggach, Stephen A.
Ligand effects on gas adsorption in nanoporous phthalocyanine crystals.
Chemical communications (Cambridge, England), 2024, 60, 11508-11511
7133757 CIFC23 H43 F N6 O7 S2P n m a17.2223; 7.2801; 12.1354
90; 90; 90		1521.54Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133758 CIFC21 H27 F N6 O7 S2P n n m7.9767; 21.0642; 7.4827
90; 90; 90		1257.3Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133759 CIFC21 H27 Cl N6 O7 S2P 1 21/n 17.6588; 20.9928; 8.031
90; 90.117; 90		1291.22Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133760 CIFC21 H27 Br N6 O7 S2P 1 21 17.7603; 21.0415; 7.9327
90; 99.55; 90		1277.37Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133761 CIFC37 H77 Br N12 O13 S4P 1 n 117.462; 8.6851; 19.081
90; 99.365; 90		2855.24Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133762 CIFC23 H29 F N6 O7 S2P -17.3252; 12.7523; 30.161
96.337; 94.485; 93.536		2784.6Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133763 CIFC23 H33 Br N6 O9 S2C 1 c 131.674; 11.6225; 8.2592
90; 101.032; 90		2984.3Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133764 CIFC37 H77 Cl N12 O13 S4P 1 n 117.5076; 8.6683; 19.0441
90; 99.021; 90		2854.4Dillon, Alexandra M.; Shtukenberg, Alexander G.; Demkiw, Krystyna M.; Woerpel, K. A.; Ward, Michael D.
Hydrogen-bonded frameworks for conformational analysis of reactive substrates.
Chemical communications (Cambridge, England), 2024, 60, 11770-11773
7133765 CIFC21 H26 N4 O5 SP 1 21/c 15.6438; 35.5926; 11.0653
90; 95.787; 90		2211.44Hanna, Fergal E.; Hunter, Christopher A.
Polarisation effects on the H-bond acceptor properties of sulfonamides.
Chemical communications (Cambridge, England), 2024, 60, 11750-11753
7133766 CIFC23 H17 F6 N O2P 1 21/n 111.4138; 11.294; 15.5406
90; 97.968; 90		1984Priyanka, Chiliveru; Madhu, Desagoni; Gangadhar, Palivela Siva; Giribabu, Lingamallu; Punna, Nagender
Cross-conjugated vinylogous annulation of π-CF<sub>3</sub>-allyl Pd-complexes with 4-methyl-3-trifluoroacetyl-quinolones.
Chemical communications (Cambridge, England), 2024, 60, 12233-12236
7133767 CIFC44 H30 Cl2 Ir N3 O3 S2P 1 21/c 111.1502; 24.938; 14.546
90; 100.657; 90		3975Tidma, Sirawit; Sutton, Gregory D.; Dang, Linh T. M.; Jiang, Chenggang; Teets, Thomas S.
Dual-emitting cyclometalated Ir(III) complexes with salicylaldimine-bound fluorophores for ratiometric oxygen sensing.
Chemical communications (Cambridge, England), 2024, 60, 11572-11575
7133768 CIFC43 H29 Ir N4 O3 S2P 1 21/n 115.564; 14.1664; 15.798
90; 100.365; 90		3426.4Tidma, Sirawit; Sutton, Gregory D.; Dang, Linh T. M.; Jiang, Chenggang; Teets, Thomas S.
Dual-emitting cyclometalated Ir(III) complexes with salicylaldimine-bound fluorophores for ratiometric oxygen sensing.
Chemical communications (Cambridge, England), 2024, 60, 11572-11575
7133769 CIFC47 H32 Ir N3 O3P 1 21/n 117.873; 10.022; 19.645
90; 100.26; 90		3462.6Tidma, Sirawit; Sutton, Gregory D.; Dang, Linh T. M.; Jiang, Chenggang; Teets, Thomas S.
Dual-emitting cyclometalated Ir(III) complexes with salicylaldimine-bound fluorophores for ratiometric oxygen sensing.
Chemical communications (Cambridge, England), 2024, 60, 11572-11575
7133770 CIFC19 H17 N O2 SP -18.7535; 9.7512; 11.0588
108.448; 99.312; 107.231		820.53Malo, Sidhartha; Santra, Supriyo; Saha, Jayanta; Ghosh, Debashree; Das, Indrajit
External photocatalyst-free photocycloaddition between triplet vinylnitrenes with 1,3-biradical character and activated olefins under 420 nm LEDs.
Chemical communications (Cambridge, England), 2024, 60, 12545-12548
7133771 CIFC23 H17 N O2 SP 21 21 217.4754; 9.5803; 25.2169
90; 90; 90		1805.9Malo, Sidhartha; Santra, Supriyo; Saha, Jayanta; Ghosh, Debashree; Das, Indrajit
External photocatalyst-free photocycloaddition between triplet vinylnitrenes with 1,3-biradical character and activated olefins under 420 nm LEDs.
Chemical communications (Cambridge, England), 2024, 60, 12545-12548
7133772 CIFC63 H62 Cl3 N2 SC 1 c 127.701; 17.066; 11.137
90; 105.043; 90		5085Kumar, Viksit; Dongre, Sangram D.; Venugopal, Geethu; Narayanan, Aswini; Babu, Sukumaran Santhosh
Tailoring helical ends of π-extended [6]heterohelicenes to control optical, and electrochemical features.
Chemical communications (Cambridge, England), 2024, 60, 11944-11947
7133773 CIFC63 H59 Cl3 N2 SeP 111.0594; 16.3603; 16.3749
62.846; 76.886; 76.976		2542Kumar, Viksit; Dongre, Sangram D.; Venugopal, Geethu; Narayanan, Aswini; Babu, Sukumaran Santhosh
Tailoring helical ends of π-extended [6]heterohelicenes to control optical, and electrochemical features.
Chemical communications (Cambridge, England), 2024, 60, 11944-11947
7133774 CIFC363 H434.5 Cu8 N20.5 O76.5P 1 21/c 128.7693; 53.899; 31.4036
90; 97.109; 90		48321.2Tsoukatos, Steven; Maibam, Ashakiran; Babarao, Ravichandar; Bloch, Witold M.
Topological control in paddlewheel metal-organic cages <i>via</i> ligand length variation.
Chemical communications (Cambridge, England), 2024, 60, 13183-13186
7133775 CIFC195 H223 N17 O74 Rh8P 1 21/m 119.541; 30.103; 19.898
90; 114.14; 90		10681Tsoukatos, Steven; Maibam, Ashakiran; Babarao, Ravichandar; Bloch, Witold M.
Topological control in paddlewheel metal-organic cages <i>via</i> ligand length variation.
Chemical communications (Cambridge, England), 2024, 60, 13183-13186
7133776 CIFC195 H223 Cu8 N17 O69P 1 21/m 119.34; 29.811; 19.575
90; 113.53; 90		10347Tsoukatos, Steven; Maibam, Ashakiran; Babarao, Ravichandar; Bloch, Witold M.
Topological control in paddlewheel metal-organic cages <i>via</i> ligand length variation.
Chemical communications (Cambridge, England), 2024, 60, 13183-13186
7133777 CIFC456 H645 N46 O100.5 Rh8C 1 2/c 159.811; 20.955; 50.565
90; 121.04; 90		54300Tsoukatos, Steven; Maibam, Ashakiran; Babarao, Ravichandar; Bloch, Witold M.
Topological control in paddlewheel metal-organic cages <i>via</i> ligand length variation.
Chemical communications (Cambridge, England), 2024, 60, 13183-13186
7133778 CIFC309 H377 Cu6 N35 O83P -4 3 n41.178; 41.178; 41.178
90; 90; 90		69823Tsoukatos, Steven; Maibam, Ashakiran; Babarao, Ravichandar; Bloch, Witold M.
Topological control in paddlewheel metal-organic cages <i>via</i> ligand length variation.
Chemical communications (Cambridge, England), 2024, 60, 13183-13186
7133779 CIFC7 H18 Cl4 Ga NP b c m6.8857; 13.748; 14.6331
90; 90; 90		1385.24Yang, Zhao; Zeng, Yiyi; Chen, Guoyong; Sun, Xiao; Zhang, Haina; Cai, Hu; Wei, Zhenhong
An organic-inorganic hybrid perovskite material [Me<sub>3</sub>NCMe<sub>3</sub>]GaCl<sub>4</sub> exhibits a two-step off-on-off SHG response with a large temperature interval.
Chemical communications (Cambridge, England), 2024, 60, 11992-11995
7133780 CIFC6 Cl4 Ga NP m -3 m7.2333; 7.2333; 7.2333
90; 90; 90		378.45Yang, Zhao; Zeng, Yiyi; Chen, Guoyong; Sun, Xiao; Zhang, Haina; Cai, Hu; Wei, Zhenhong
An organic-inorganic hybrid perovskite material [Me<sub>3</sub>NCMe<sub>3</sub>]GaCl<sub>4</sub> exhibits a two-step off-on-off SHG response with a large temperature interval.
Chemical communications (Cambridge, England), 2024, 60, 11992-11995
7133781 CIFC7 H18 Cl4 Ga NP m c 217.3448; 7.0749; 14.0244
90; 90; 90		728.76Yang, Zhao; Zeng, Yiyi; Chen, Guoyong; Sun, Xiao; Zhang, Haina; Cai, Hu; Wei, Zhenhong
An organic-inorganic hybrid perovskite material [Me<sub>3</sub>NCMe<sub>3</sub>]GaCl<sub>4</sub> exhibits a two-step off-on-off SHG response with a large temperature interval.
Chemical communications (Cambridge, England), 2024, 60, 11992-11995
7133782 CIFC79 H100 Al2 N4P -113.1124; 13.4322; 21.3152
75.831; 82.021; 75.106		3506.2Squire, Imogen; Tritto, Michelangelo; Morell, Juliana; Bakewell, Clare
Probing the reactivity of a transient Al(I) species with substituted arenes.
Chemical communications (Cambridge, England), 2024, 60, 12908-12911
7133783 CIFC78 H101.91 Al2 N4C 1 2/c 122.1421; 16.4913; 19.8962
90; 103.435; 90		7066.32Squire, Imogen; Tritto, Michelangelo; Morell, Juliana; Bakewell, Clare
Probing the reactivity of a transient Al(I) species with substituted arenes.
Chemical communications (Cambridge, England), 2024, 60, 12908-12911
7133784 CIFC78 H106 Al2 N4I 1 2/a 116.5835; 16.83; 51.4307
90; 96.723; 90		14255.6Squire, Imogen; Tritto, Michelangelo; Morell, Juliana; Bakewell, Clare
Probing the reactivity of a transient Al(I) species with substituted arenes.
Chemical communications (Cambridge, England), 2024, 60, 12908-12911
7133785 CIFC72.5 H93.5 Al2 N4P 1 21/n 115.2755; 20.21; 24.2085
90; 105.824; 90		7190.38Squire, Imogen; Tritto, Michelangelo; Morell, Juliana; Bakewell, Clare
Probing the reactivity of a transient Al(I) species with substituted arenes.
Chemical communications (Cambridge, England), 2024, 60, 12908-12911
7133786 CIFC56 H45 Ni P3P 1 21/n 19.5744; 23.4453; 21.3424
90; 100.245; 90		4714.4Sansores-Paredes, María L G; Lutz, Martin; Moret, Marc-Etienne
Carbene transfer reactivity from a nickelacyclobutane.
Chemical communications (Cambridge, England), 2024, 60, 12397-12400
7133787 CIFC11 H13 N O2 S2P 1 21/n 15.7014; 9.6716; 21.86
90; 92.246; 90		1204.47Hoque, Injamam Ul; Debnath, Saradindu; Lo, Rabindranath; Maity, Soumitra
A chromatographic relay conjugated photoredox strategy: <i>S</i>, <i>Se</i>-pharmacophore from alkenes <i>via</i> formal [2+2+1] heteroannulation.
Chemical communications (Cambridge, England), 2024, 60, 12429-12432
7133788 CIFC13 H13 Cl2 N O2 SP 1 21/c 114.9528; 9.7498; 10.455
90; 108.082; 90		1448.9Hoque, Injamam Ul; Debnath, Saradindu; Lo, Rabindranath; Maity, Soumitra
A chromatographic relay conjugated photoredox strategy: <i>S</i>, <i>Se</i>-pharmacophore from alkenes <i>via</i> formal [2+2+1] heteroannulation.
Chemical communications (Cambridge, England), 2024, 60, 12429-12432
7133789 CIFC59 H90 N3 P Si5P -113.1621; 13.9425; 17.0349
93.904; 102.733; 96.997		3011.9Doleschal, Martin Ernst; Kostenko, Arseni; Liu, Jin Yu; Inoue, Shigeyoshi
Silicon-aryl cooperative activation of ammonia.
Chemical communications (Cambridge, England), 2024, 60, 13020-13023
7133790 CIFC27 H36 Bi F N6 Na O15P -110.1737; 12.4225; 15.0689
68.938; 85.221; 79.107		1744.95Kanagasundaram, Thines; Sun, Yang; Lee, Kevin K.; MacMillan, Samantha N.; Brugarolas, Pedro; Wilson, Justin J.
Fluorine-18 incorporation and radiometal coordination in macropa ligands for PET imaging and targeted alpha therapy.
Chemical communications (Cambridge, England), 2024, 60, 11940-11943
7133791 CIFC13.967 H19 N2 O PP 1 21/n 18.23898; 10.497; 18.2476
90; 97.9891; 90		1562.82Dong, Likun; Zhong, Bing; Zhang, Yu-Shan; Yang, Jin-Dong; Cheng, Jin-Pei
Phosphination of aryl/alkyl bromides <i>via</i> Mn-mediated reductive C-P coupling.
Chemical communications (Cambridge, England), 2024, 60, 12549-12552
7133792 CIFC11 H6 F3 N3 OP 1 21/c 112.0758; 12.1758; 6.8549
90; 97.473; 90		999.33Wang, Huamin; Meng, Li-Qin; Niu, Wenjing; Yang, Wan-Qi; Ou, Yu; Lin, Ying-Wu
The [3+2] annulation of <i>in situ</i> formed trifluorodiazoethane with 4-nitroisoxazoles: access to trifluoromethylpyrazolo[3,4-<i>d</i>]isoxazoles.
Chemical communications (Cambridge, England), 2024, 60, 12425-12428
7133793 CIFC20 H12 F6 N8 OP -17.5837; 8.1452; 16.1468
95.204; 93.854; 90.608		990.9Wang, Huamin; Meng, Li-Qin; Niu, Wenjing; Yang, Wan-Qi; Ou, Yu; Lin, Ying-Wu
The [3+2] annulation of <i>in situ</i> formed trifluorodiazoethane with 4-nitroisoxazoles: access to trifluoromethylpyrazolo[3,4-<i>d</i>]isoxazoles.
Chemical communications (Cambridge, England), 2024, 60, 12425-12428
7133794 CIFC12 H7 Cl F3 N3 O2P b c a7.0457; 23.6493; 30.637
90; 90; 90		5104.9Wang, Huamin; Meng, Li-Qin; Niu, Wenjing; Yang, Wan-Qi; Ou, Yu; Lin, Ying-Wu
The [3+2] annulation of <i>in situ</i> formed trifluorodiazoethane with 4-nitroisoxazoles: access to trifluoromethylpyrazolo[3,4-<i>d</i>]isoxazoles.
Chemical communications (Cambridge, England), 2024, 60, 12425-12428
7133795 CIFC37 H15 B F15 N2 PP 1 21/n 111.6295; 11.5884; 24.2727
90; 98.225; 90		3237.52Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133796 CIFC81 H38 Al2 F30 N4 P2P -111.2784; 17.5791; 20.1614
94.334; 99.002; 100.389		3861.1Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133797 CIFC62 H50 Cl3 F4 In N4 P2C 1 c 124.0532; 20.9341; 11.6059
90; 102.431; 90		5706.94Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133798 CIFC82 H65 Cl12 F Ga4 N8 P4P -117.4641; 17.7994; 17.8166
79.202; 62.982; 61.288		4323.8Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133799 CIFC50 H25 B2 F20 N2 PP -111.9853; 12.0437; 18.347
93.329; 104.396; 115.728		2268.7Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133800 CIFC81.3 H50.2 Al2 Cl2 F21 N4 P2P 1 21/c 115.3044; 25.9421; 19.9557
90; 109.49; 90		7469Tang, Beili; Ju, Shaoying; Yan, Weili; Chen, Ting; Stephan, Douglas W.; Wu, Yile
Reactivity of <i>N</i>-(isocyanoimino)triphenylphosphorane toward group 13 Lewis acids.
Chemical communications (Cambridge, England), 2024, 60, 12932-12935
7133801 CIFBa2 F2 Ge Se3P n m a12.8823; 19.118; 6.4566
90; 90; 90		1590.2Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence.
Chemical communications (Cambridge, England), 2024, 60, 12734-12737
7133802 CIFBa3 F2 Ge Se4P 1 21/n 19.3777; 9.4571; 12.3301
90; 91.668; 90		1093.04Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence.
Chemical communications (Cambridge, England), 2024, 60, 12734-12737
7133803 CIFBa2 F2 Ge S3P n m a12.626; 18.669; 6.316
90; 90; 90		1489Li, Kaixuan; Wu, Hongping; Yu, Hongwei; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng
Ba<sub>2</sub>GeF<sub>2</sub>Q<sub>3</sub> (Q = S, Se) and Ba<sub>3</sub>GeF<sub>2</sub>Se<sub>4</sub>: new F-based chalcohalides with enhanced birefringence.
Chemical communications (Cambridge, England), 2024, 60, 12734-12737
7133804 CIFC26 H25 Cl N4 OP 1 21/n 17.6248; 10.9476; 26.8702
90; 90.753; 90		2242.75Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan
A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril.
Chemical communications (Cambridge, England), 2024, 60, 12852-12855
7133805 CIFC30 H24 F6 N2 O4P 1 21/c 110.4972; 20.641; 12.7749
90; 106.847; 90		2649.18Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan
A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril.
Chemical communications (Cambridge, England), 2024, 60, 12852-12855
7133806 CIFC27 H26.5 Cl N2.5 OP 1 21/c 110.0721; 19.0557; 23.2446
90; 94.802; 90		4445.7Qiu, Xujun; Cai, Qianyu; Pohl, Eric; Jung, André; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan
A simple method to modulate the selectivity of aryl azide photolysis using cucurbit[8]uril.
Chemical communications (Cambridge, England), 2024, 60, 12852-12855
7133807 CIFC24 H26 Eu N3 O14P b c a14.0075; 18.751; 20.4381
90; 90; 90		5368.2Wang, Hao; Sun, Xiao-Han; Wang, Tian-Tian; Li, Yu-Xin; Xu, Ying-Ming; Sun, Wen-Bin
Two-dimensional viologen-based lanthanide coordination polymers as multi-stimuli responsive materials to light and amines with a fluorescence response.
Chemical communications (Cambridge, England), 2024, 60, 12413-12416
7133808 CIFC24 H26 N3 O14 TbP b c a14.6366; 18.5358; 19.7866
90; 90; 90		5368.13Wang, Hao; Sun, Xiao-Han; Wang, Tian-Tian; Li, Yu-Xin; Xu, Ying-Ming; Sun, Wen-Bin
Two-dimensional viologen-based lanthanide coordination polymers as multi-stimuli responsive materials to light and amines with a fluorescence response.
Chemical communications (Cambridge, England), 2024, 60, 12413-12416
7133809 CIFC3.5 H2.83 Cl0.17 N0 O0.5 S0.33P -18.2512; 11.5639; 11.6055
117.324; 97.055; 94.082		966.08Barik, Dinabandhu; Chakraborty, Nikita; Sahoo, Ashish K.; Dhara, Hirendra Nath; Patel, Bhisma K.
Electron-donor-acceptor (EDA) complex-driven regioselective vicinal and oxidative geminal functionalization of alkynes.
Chemical communications (Cambridge, England), 2024, 60, 12577-12580
7133810 CIFC3.33 H2.83 N0.17 O0.33 S0.33P n a 2111.753; 8.71; 17.811
90; 90; 90		1823.3Barik, Dinabandhu; Chakraborty, Nikita; Sahoo, Ashish K.; Dhara, Hirendra Nath; Patel, Bhisma K.
Electron-donor-acceptor (EDA) complex-driven regioselective vicinal and oxidative geminal functionalization of alkynes.
Chemical communications (Cambridge, England), 2024, 60, 12577-12580
7133811 CIFC24 H22 Cl N5 O2P 1 21/c 116.3613; 6.8967; 19.5442
90; 103.785; 90		2141.83Qiu, Xujun; Pohl, Eric; Jung, André; Cai, Qianyu; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan
Modulating the photolysis of aryl azides in a supramolecular host to develop photoactivatable fluorophores.
Chemical communications (Cambridge, England), 2024, 60, 12856-12859
7133812 CIFC24 H25 Cl N5 O2.5P -19.5693; 10.1473; 24.8566
101.497; 93.876; 103.476		2283.56Qiu, Xujun; Pohl, Eric; Jung, André; Cai, Qianyu; Su, Haopu; Fuhr, Olaf; Schepers, Ute; Bräse, Stefan
Modulating the photolysis of aryl azides in a supramolecular host to develop photoactivatable fluorophores.
Chemical communications (Cambridge, England), 2024, 60, 12856-12859
7133813 CIFC21 H22 Cl Cu N2 SP 21 21 218.5644; 9.6993; 23.7155
90; 90; 90		1970.02Saha, Ratnakar; Maharana, Suraj Kumar; Jana, Narayan Ch; Bagh, Bidraha
Copper-catalyzed C(sp<sup>3</sup>)-H alkylation of fluorene with primary and secondary alcohols using a borrowing hydrogen method.
Chemical communications (Cambridge, England), 2024, 60, 10144-10147
7133814 CIFC325 H504 Cr14 Cu4 F16 N6 Ni2 O86 S2P -116.506; 34.2036; 35.1533
80.444; 88.909; 85.438		19508.6Lockyer, Selena J.; Whitehead, George F. S.; Timco, Grigore A.; McInnes, Eric J. L.; Winpenny, Richard E. P.
One-, two- and three-dimensional interlocked polymers based on hybrid inorganic-organic rotaxanes.
Chemical communications (Cambridge, England), 2024, 60, 10124-10127
7133815 CIFC170.2 H290.65 Cr7 Cu4 F8 N5 Ni O61.2P 1 21/n 126.8191; 19.6641; 43.9326
90; 104.391; 90		22441.9Lockyer, Selena J.; Whitehead, George F. S.; Timco, Grigore A.; McInnes, Eric J. L.; Winpenny, Richard E. P.
One-, two- and three-dimensional interlocked polymers based on hybrid inorganic-organic rotaxanes.
Chemical communications (Cambridge, England), 2024, 60, 10124-10127
7133816 CIFC178 H302.48 Cr7 Cu4 F8 N6 Ni O59.88P 1 21/n 135.2731; 16.6464; 37.7375
90; 94.682; 90		22084.4Lockyer, Selena J.; Whitehead, George F. S.; Timco, Grigore A.; McInnes, Eric J. L.; Winpenny, Richard E. P.
One-, two- and three-dimensional interlocked polymers based on hybrid inorganic-organic rotaxanes.
Chemical communications (Cambridge, England), 2024, 60, 10124-10127
7133817 CIFC16 H21.5 N3.5 O3.5 ZnP 41 21 218.1052; 18.1052; 13.2724
90; 90; 90		4350.67Fu, Hong-Ru; Zhang, Ruo-Yu; Li, Ting; Wei, Chen-Ying; Liu, Shuang; Xu, Jia-Yi; Zhu, Xueli; Wei, Jiaojiao; Ding, Qing-Rong; Ma, Lu-Fang
Color-tunable and white circularly polarized luminescence through confining guests into chiral MOFs.
Chemical communications (Cambridge, England), 2024, 60, 10212-10215
7133818 CIFC16 H22.5 N3.5 O4 ZnP 43 21 218.1042; 18.1042; 13.2792
90; 90; 90		4352.42Fu, Hong-Ru; Zhang, Ruo-Yu; Li, Ting; Wei, Chen-Ying; Liu, Shuang; Xu, Jia-Yi; Zhu, Xueli; Wei, Jiaojiao; Ding, Qing-Rong; Ma, Lu-Fang
Color-tunable and white circularly polarized luminescence through confining guests into chiral MOFs.
Chemical communications (Cambridge, England), 2024, 60, 10212-10215
7133819 CIFC27 H20 Br O PP 1 21/n 17.9801; 17.8286; 15.0481
90; 102.601; 90		2089.38Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133820 CIFC27 H20 F O PP 1 21/n 112.1019; 13.6934; 12.1992
90; 91.695; 90		2020.72Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133821 CIFC23 H27 Cl3 F3 O4 P SP 1 21/c 110.2309; 22.3914; 12.3597
90; 106.861; 90		2709.69Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133822 CIFC29 H25 O PP 1 21/n 111.1653; 15.513; 13.4254
90; 109.732; 90		2188.84Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133823 CIFC26 H25 O PP 1 21/c 116.0883; 6.3238; 21.618
90; 109.454; 90		2073.83Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133824 CIFC29 H24 F3 O5 P SP 1 21/c 110.5096; 15.4521; 16.5422
90; 90.04; 90		2686.4Qin, Yunlong; Zhang, Jianing; Zhang, Congcong; Wang, Qilin
Substituent-dependent [4+2] or [2+2] cycloadditions of phenylallenyl phosphine oxides with arynes.
Chemical communications (Cambridge, England), 2024, 60, 11343-11346
7133825 CIFC39 H38 B Cl2 N2 O6 Rh Si2P 21 21 218.5875; 22.565; 40.397
90; 90; 90		7828Prieto-Pascual, Unai; Bustos, Itxaso; Salcedo-Abraira, Pablo; Vitorica-Yrezabal, Iñigo J; Landa, Aitor; Freixa, Zoraida; Huertos, Miguel A.
Unsaturated chiral-only-at-metal rhodium(III) complexes bearing SiN-type ligands.
Chemical communications (Cambridge, England), 2024, 60, 11299-11302
7133826 CIFC38 H36 B N2 O6 Rh Si2P 1 21 110.208; 8.5609; 21.3464
90; 101.94; 90		1825.1Prieto-Pascual, Unai; Bustos, Itxaso; Salcedo-Abraira, Pablo; Vitorica-Yrezabal, Iñigo J; Landa, Aitor; Freixa, Zoraida; Huertos, Miguel A.
Unsaturated chiral-only-at-metal rhodium(III) complexes bearing SiN-type ligands.
Chemical communications (Cambridge, England), 2024, 60, 11299-11302
7133827 CIFC22 H24 O2P 1 21 17.857; 10.6978; 11.0526
90; 105.428; 90		895.52Chang, Chi-Hao; Yen, Chao-Ting; Goncalves, Théo P; Lin, Yu-Sheng; Wang, Yu-Chun; Basha, R. Sidick; Chen, Bo-Yan; Fu, Cheng-Hao; Chen, Liang-Wei; Jhou, Meng-Li; Huang, Kuo-Wei; Chou, Chih-Ming
Substrate-directed regioselective alkene functionalizations of (<i>E</i>)-β,γ-unsaturated carboxylic acids.
Chemical communications (Cambridge, England), 2024, 60, 11339-11342
7133828 CIFC23 H23 F3 O2P 1 21/c 111.4578; 22.1975; 8.4627
90; 109.64; 90		2027.1Chang, Chi-Hao; Yen, Chao-Ting; Goncalves, Théo P; Lin, Yu-Sheng; Wang, Yu-Chun; Basha, R. Sidick; Chen, Bo-Yan; Fu, Cheng-Hao; Chen, Liang-Wei; Jhou, Meng-Li; Huang, Kuo-Wei; Chou, Chih-Ming
Substrate-directed regioselective alkene functionalizations of (<i>E</i>)-β,γ-unsaturated carboxylic acids.
Chemical communications (Cambridge, England), 2024, 60, 11339-11342
7133829 CIFC31 H35 O3 PP 1 21/c 112.4838; 21.18; 10.3247
90; 96.69; 90		2711.3Gurram, Durga Prasad; Marri, Gangababu; Jothimani, Naveen; Chen, Yi-Ru; Lin, Wenwei
Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and <i>C</i>-acylated chromone adducts <i>via</i> allylic phosphorus ylides.
Chemical communications (Cambridge, England), 2024, 60, 9817-9820
7133830 CIFC26 H14 O5P 1 21/c 119.4485; 6.3637; 15.7718
90; 105.28; 90		1882.98Gurram, Durga Prasad; Marri, Gangababu; Jothimani, Naveen; Chen, Yi-Ru; Lin, Wenwei
Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and <i>C</i>-acylated chromone adducts <i>via</i> allylic phosphorus ylides.
Chemical communications (Cambridge, England), 2024, 60, 9817-9820
7133831 CIFC31 H37 O3 PP 1 21/n 111.3575; 11.1326; 21.2159
90; 97.976; 90		2656.6Gurram, Durga Prasad; Marri, Gangababu; Jothimani, Naveen; Chen, Yi-Ru; Lin, Wenwei
Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and <i>C</i>-acylated chromone adducts <i>via</i> allylic phosphorus ylides.
Chemical communications (Cambridge, England), 2024, 60, 9817-9820
7133832 CIFC31 H36 O4 PP 1 21/n 19.6734; 14.613; 19.9002
90; 101.356; 90		2758Gurram, Durga Prasad; Marri, Gangababu; Jothimani, Naveen; Chen, Yi-Ru; Lin, Wenwei
Diversity-oriented synthesis of chromone inden-1-one-fused cyclopentadienylides and <i>C</i>-acylated chromone adducts <i>via</i> allylic phosphorus ylides.
Chemical communications (Cambridge, England), 2024, 60, 9817-9820
7133833 CIFC23 H23 N3 O2P -19.4621; 9.9741; 11.4369
71.12; 86.589; 79.453		1004Srinivasu, Vinjamuri; Pattanaik, Swadhin; Sureshkumar, Devarajulu
Photoredox cross-dehydrogenative C(sp<sup>2</sup>)-C(sp<sup>3</sup>) coupling of heteroarenes with secondary amines through 1,5-HAT.
Chemical communications (Cambridge, England), 2024, 60, 9757-9760
7133834 CIFC54.25 H60.5 Cl2.5 Dy F6 N6 O2 P Si2P 1 n 120.8869; 11.3031; 23.5314
90; 98.892; 90		5488.7Armenis, Alexandros S.; Mondal, Arpan; Giblin, Sean R.; Raptopoulou, Catherine P.; Psycharis, Vassilis; Alexandropoulos, Dimitris I.; Tang, Jinkui; Layfield, Richard A.; Stamatatos, Theocharis C.
Unveiling new [1+1] Schiff-base macrocycles towards high energy-barrier hexagonal bipyramidal Dy(III) single-molecule magnets.
Chemical communications (Cambridge, England), 2024, 60, 12730-12733
7133835 CIFC53 H55 Dy F6 N3 O5 P Si2P 1 21/c 116.895; 14.733; 20.76
90; 97.425; 90		5124.1Armenis, Alexandros S.; Mondal, Arpan; Giblin, Sean R.; Raptopoulou, Catherine P.; Psycharis, Vassilis; Alexandropoulos, Dimitris I.; Tang, Jinkui; Layfield, Richard A.; Stamatatos, Theocharis C.
Unveiling new [1+1] Schiff-base macrocycles towards high energy-barrier hexagonal bipyramidal Dy(III) single-molecule magnets.
Chemical communications (Cambridge, England), 2024, 60, 12730-12733
7133836 CIFC28 H44 Br8 Mn2 N8P 21 21 233.1106; 16.5169; 7.9113
90; 90; 90		4326.57Qi, Zhikai; Zhang, Ke; Zhao, Xingxing; Zhang, Nan; Li, Shi-Li; Zhang, Xian-Ming
Promoting structural distortion to enhance the crystal field strength of Mn(II) in tetrahedral bromide for near-unity yellow emission.
Chemical communications (Cambridge, England), 2024, 60, 12880-12883
7133837 CIFC12 H38 Br10 N6 O Pb2P 1 21/c 113.7743; 17.5198; 13.7748
90; 96.25; 90		3304.42Tian, Dongjie; Lin, Jie; Mesbah, Adel; Zhou, Jiajing; Yang, Mianji; Gautier, Romain; Chen, Xi
A core-shell model of polymetallic hybrid metal halides.
Chemical communications (Cambridge, England), 2024, 60, 12924-12927
7133838 CIFC25 H26 Cl2 F N3 O3P -19.8105; 10.5343; 13.5571
109.987; 96.545; 110.033		1193.91Dhake, Kushal; Woelk, Kyla J.; Krueckl, Liam D. N.; Alberts, Faith; Mutter, James; Pohl, Matthew O.; Thomas, Gilian T.; Sharma, Muskan; Bjornerud-Brown, Jaelyn; Fernández, Nahiane Pipaón; Schley, Nathan D.; Leitch, David C.
Diastereoselective dearomative cycloaddition of bicyclobutanes with pyridinium ylides: a modular approach to multisubstituted azabicyclo[3.1.1]heptanes.
Chemical communications (Cambridge, England), 2024, 60, 13008-13011
7133839 CIFC20 H23 N O4P -15.8883; 10.8918; 14.0443
75.094; 88.484; 89.578		870.1Dhake, Kushal; Woelk, Kyla J.; Krueckl, Liam D. N.; Alberts, Faith; Mutter, James; Pohl, Matthew O.; Thomas, Gilian T.; Sharma, Muskan; Bjornerud-Brown, Jaelyn; Fernández, Nahiane Pipaón; Schley, Nathan D.; Leitch, David C.
Diastereoselective dearomative cycloaddition of bicyclobutanes with pyridinium ylides: a modular approach to multisubstituted azabicyclo[3.1.1]heptanes.
Chemical communications (Cambridge, England), 2024, 60, 13008-13011
7133840 CIFC60 H46 Cl Ga P4P 1 21/c 125.641; 10.5252; 19.2556
90; 109.104; 90		4910.4Meyer, Fabio; Puylaert, Pim; Duvinage, Daniel; Hupf, Emanuel; Beckmann, Jens
Cationic dinuclear complexes [M<sub>2</sub>(PCP)<sub>2</sub><i>μ</i>-Cl][GaCl<sub>4</sub>] of the group 10 elements. metallophilic interactions and catalytic dehydrogenation of Me<sub>2</sub>NHBH<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12912-12915
7133841 CIFC60 H46 Cl5 Ga Ni2 P4P -114.839; 15.097; 15.823
100.633; 98.985; 111.337		3147Meyer, Fabio; Puylaert, Pim; Duvinage, Daniel; Hupf, Emanuel; Beckmann, Jens
Cationic dinuclear complexes [M<sub>2</sub>(PCP)<sub>2</sub><i>μ</i>-Cl][GaCl<sub>4</sub>] of the group 10 elements. metallophilic interactions and catalytic dehydrogenation of Me<sub>2</sub>NHBH<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12912-12915
7133842 CIFC60 H46 Cl5 Ga P4 Pt2P -113.4598; 15.8581; 16.9458
70.12; 86.263; 89.413		3393.97Meyer, Fabio; Puylaert, Pim; Duvinage, Daniel; Hupf, Emanuel; Beckmann, Jens
Cationic dinuclear complexes [M<sub>2</sub>(PCP)<sub>2</sub><i>μ</i>-Cl][GaCl<sub>4</sub>] of the group 10 elements. metallophilic interactions and catalytic dehydrogenation of Me<sub>2</sub>NHBH<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12912-12915
7133843 CIFC60 H46 Cl5 Ga P4 Pd2P -115.1433; 15.3082; 15.6366
77.139; 61.775; 89.651		3092.9Meyer, Fabio; Puylaert, Pim; Duvinage, Daniel; Hupf, Emanuel; Beckmann, Jens
Cationic dinuclear complexes [M<sub>2</sub>(PCP)<sub>2</sub><i>μ</i>-Cl][GaCl<sub>4</sub>] of the group 10 elements. metallophilic interactions and catalytic dehydrogenation of Me<sub>2</sub>NHBH<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12912-12915
7133844 CIFC61 H48 Cl5 Ga P4 PtP -110.9998; 12.2209; 21.688
89.922; 83.531; 69.049		2703Meyer, Fabio; Puylaert, Pim; Duvinage, Daniel; Hupf, Emanuel; Beckmann, Jens
Cationic dinuclear complexes [M<sub>2</sub>(PCP)<sub>2</sub><i>μ</i>-Cl][GaCl<sub>4</sub>] of the group 10 elements. metallophilic interactions and catalytic dehydrogenation of Me<sub>2</sub>NHBH<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12912-12915
7133846 CIFC53 H89 Fe K2 N5 O12P 1 21/c 121.8155; 9.8873; 27.5274
90; 90.332; 90		5937.46Zars, Ethan; Pick, Lisa; Kankanamge, Achala; Gau, Michael R.; Meyer, Karsten; Mindiola, Daniel J.
C<sub>sp<sup>2</sup></sub>-H/F bond activation and borylation with iron.
Chemical communications (Cambridge, England), 2024, 60, 14415-14418
7133847 CIFC53 H89 Cl Fe K N3 O9P 1 21/n 114.8545; 23.4401; 16.8987
90; 103.34; 90		5725.21Zars, Ethan; Pick, Lisa; Kankanamge, Achala; Gau, Michael R.; Meyer, Karsten; Mindiola, Daniel J.
C<sub>sp<sup>2</sup></sub>-H/F bond activation and borylation with iron.
Chemical communications (Cambridge, England), 2024, 60, 14415-14418
7133848 CIFC59 H82 Fe K N3 O6P 1 21/c 110.6531; 23.67132; 22.34027
90; 95.7507; 90		5605.26Zars, Ethan; Pick, Lisa; Kankanamge, Achala; Gau, Michael R.; Meyer, Karsten; Mindiola, Daniel J.
C<sub>sp<sup>2</sup></sub>-H/F bond activation and borylation with iron.
Chemical communications (Cambridge, England), 2024, 60, 14415-14418
7133849 CIFC24 H49 B2 K O10P 1 21/n 110.1611; 19.448; 15.5969
90; 95.925; 90		3065.69Zars, Ethan; Pick, Lisa; Kankanamge, Achala; Gau, Michael R.; Meyer, Karsten; Mindiola, Daniel J.
C<sub>sp<sup>2</sup></sub>-H/F bond activation and borylation with iron.
Chemical communications (Cambridge, England), 2024, 60, 14415-14418
7133850 CIFC21 H13 B F2 N2 SP 1 21/n 15.9057; 15.6724; 17.7952
90; 97.537; 90		1632.83Ohashi, Fumika; Takano, Hideaki; Shinokubo, Hiroshi
Zig-zag-fused π-extended BODIPYs <i>via</i> gold-catalysed cycloisomerisation.
Chemical communications (Cambridge, England), 2024, 60, 12892-12895
7133851 CIFC21 H13 B F2 N2 SP 1 21/n 111.6699; 10.8486; 14.0687
90; 111.763; 90		1654.18Ohashi, Fumika; Takano, Hideaki; Shinokubo, Hiroshi
Zig-zag-fused π-extended BODIPYs <i>via</i> gold-catalysed cycloisomerisation.
Chemical communications (Cambridge, England), 2024, 60, 12892-12895
7133852 CIFC23 H15 B F2 N2P 1 21/n 15.8694; 16.1821; 17.7533
90; 97.915; 90		1670.13Ohashi, Fumika; Takano, Hideaki; Shinokubo, Hiroshi
Zig-zag-fused π-extended BODIPYs <i>via</i> gold-catalysed cycloisomerisation.
Chemical communications (Cambridge, England), 2024, 60, 12892-12895
7133853 CIFC40 H24 B2 F4 N4P -111.2443; 12.5476; 23.0507
94.375; 92.406; 112.285		2991.65Ohashi, Fumika; Takano, Hideaki; Shinokubo, Hiroshi
Zig-zag-fused π-extended BODIPYs <i>via</i> gold-catalysed cycloisomerisation.
Chemical communications (Cambridge, England), 2024, 60, 12892-12895
7133854 CIFC22 H21 N3 O3P 1 21/n 110.6241; 20.0539; 18.4446
90; 92.354; 90		3926.39Bao, Mei-Zhu; Pan, Xiao-Ying; Wu, Wen-Rong; Xiao, Lin; Liu, Jidan; Liu, Xu-Ge; Zhang, Shang-Shi; Zhao, Limin
Metal-catalyzed divergent synthesis from ylides with 3-arylbenzo[<i>d</i>][1,2,3]triazin-4(3<i>H</i>)-ones.
Chemical communications (Cambridge, England), 2024, 60, 12928-12931
7133855 CIFC20 H18 Cl3 N3 O3P -110.2448; 14.5349; 14.7931
70.151; 89.702; 85.415		2064.74Bao, Mei-Zhu; Pan, Xiao-Ying; Wu, Wen-Rong; Xiao, Lin; Liu, Jidan; Liu, Xu-Ge; Zhang, Shang-Shi; Zhao, Limin
Metal-catalyzed divergent synthesis from ylides with 3-arylbenzo[<i>d</i>][1,2,3]triazin-4(3<i>H</i>)-ones.
Chemical communications (Cambridge, England), 2024, 60, 12928-12931
7133856 CIFC34 H22 N4P 1 21/n 112.5223; 12.3066; 15.2608
90; 90.707; 90		2351.6Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133857 CIFC28 H18 N4 O2P n a 2117.8407; 8.7838; 13.7388
90; 90; 90		2153Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133858 CIFC38 H36 Cl2 N4 O3P -19.1994; 13.5661; 14.2548
93.7; 100.621; 107.105		1657.77Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133859 CIFC36 H36 N4 OP 1 21/c 110.4599; 24.1253; 11.7099
90; 96.396; 90		2936.58Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133860 CIFC46 H46 Cl6 F6 N3 O8 Pd2P -111.1926; 14.311; 15.3221
74.279; 75.916; 69.724		2185.49Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133861 CIFC39.5 H36 N4 O3C 1 2/c 125.5909; 14.0921; 20.263
90; 120.791; 90		6277.4Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133862 CIFC33 H28 N4 O3P 1 21/n 113.2208; 16.2811; 13.317
90; 115.094; 90		2595.9Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133863 CIFC66 H66 F9 N6 O10.5 Pd3 S1.5P 1 21/n 115.9963; 21.8997; 20.1858
90; 90.029; 90		7071.4Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133864 CIFC34 H30 N4 O2C 1 2/c 117.7407; 11.1622; 27.225
90; 90.328; 90		5391.1Vijaykumar, Muniyappa; Pradhan, Chandini; Gonnade, Rajesh G.; Punji, Benudhar
Chelation-assisted and steric-controlled selectivity in the Pd-catalyzed C-H/C-H oxidative coupling of indoles.
Chemical communications (Cambridge, England), 2024, 60, 13028-13031
7133865 CIFC53 H64 Al F15 O2 P4 WP 1 21/n 113.8441; 11.8025; 34.6152
90; 99.341; 90		5581Escomel, Léon; Le Dé, Quentin; Benonie, Maxime; Vendier, Laure; Simonneau, Antoine
Low-valent group 6 metals/Al(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> donor-acceptor systems for CO<sub>2</sub> activation and cleavage.
Chemical communications (Cambridge, England), 2024, 60, 13235-13238
7133866 CIFC58 H48 Al2 F30 Mo O4 P4P 1 2/n 113.8498; 14.1073; 21.9884
90; 107.491; 90		4097.5Escomel, Léon; Le Dé, Quentin; Benonie, Maxime; Vendier, Laure; Simonneau, Antoine
Low-valent group 6 metals/Al(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> donor-acceptor systems for CO<sub>2</sub> activation and cleavage.
Chemical communications (Cambridge, England), 2024, 60, 13235-13238
7133867 CIFC54 H62 Al F15 Mo N O P4I 1 2/a 124.8425; 20.3105; 27.5805
90; 113.272; 90		12783.9Escomel, Léon; Le Dé, Quentin; Benonie, Maxime; Vendier, Laure; Simonneau, Antoine
Low-valent group 6 metals/Al(C<sub>6</sub>F<sub>5</sub>)<sub>3</sub> donor-acceptor systems for CO<sub>2</sub> activation and cleavage.
Chemical communications (Cambridge, England), 2024, 60, 13235-13238
7133868 CIFC26 H25 F Fe N5 O5P -110.2719; 11.296; 12.0615
68.508; 65.942; 81.917		1189.02Fan, Zi-Xuan; Lian, Kai-Ting; Liao, Pei-Yu; Ruan, Ze-Yu; Ni, Zhao-Ping; Tong, Ming-Liang
Synergetic spin crossover and fluorescence in a mononuclear iron(III) complex.
Chemical communications (Cambridge, England), 2024, 60, 13227-13230
7133869 CIFC26 H25 Cl Fe N5 O5P -110.1942; 12.1461; 12.1213
66.188; 65.374; 83.184		1245.99Fan, Zi-Xuan; Lian, Kai-Ting; Liao, Pei-Yu; Ruan, Ze-Yu; Ni, Zhao-Ping; Tong, Ming-Liang
Synergetic spin crossover and fluorescence in a mononuclear iron(III) complex.
Chemical communications (Cambridge, England), 2024, 60, 13227-13230
7133870 CIFC26 H25 Cl Fe N5 O5P -110.306; 12.235; 12.191
66.11; 65.439; 82.87		1276.5Fan, Zi-Xuan; Lian, Kai-Ting; Liao, Pei-Yu; Ruan, Ze-Yu; Ni, Zhao-Ping; Tong, Ming-Liang
Synergetic spin crossover and fluorescence in a mononuclear iron(III) complex.
Chemical communications (Cambridge, England), 2024, 60, 13227-13230
7133871 CIFC26 H25 F Fe N5 O5P -110.3263; 11.723; 12.4752
66.229; 65.108; 81.559		1253.2Fan, Zi-Xuan; Lian, Kai-Ting; Liao, Pei-Yu; Ruan, Ze-Yu; Ni, Zhao-Ping; Tong, Ming-Liang
Synergetic spin crossover and fluorescence in a mononuclear iron(III) complex.
Chemical communications (Cambridge, England), 2024, 60, 13227-13230
7133872 CIFC28 H27 N O3P 1 21/c 18.8507; 29.1696; 9.5087
90; 113.46; 90		2252Yang, Peng; Brockmann, Till; Wu, Xiao-Feng
Copper-catalyzed strain-enabled reaction of bicyclobutanes with diazo compounds to synthesize penta-1,4-dienes.
Chemical communications (Cambridge, England), 2024, 60, 13048-13050
7133873 CIFC17 H12 N2 O2P 1 21 15.65731; 5.62441; 20.6396
90; 93.064; 90		655.79Li, Xinyue; Fang, Yuhua; Zhao, Yuanyuan; Luo, Shenshen; Xue, Yuhui; Yong, Tingting; Wang, Bin
Employing a PhI(OAc)<sub>2</sub>-mediated domino reaction to assemble nitrogen-containing heterocyclic derivatives and assessing their anti-inflammatory activity.
Chemical communications (Cambridge, England), 2024, 60, 13352-13355
7133874 CIFC46 H32 N4I 1 2 116.6067; 5.4254; 20.6546
90; 93.326; 90		1857.8Meng, Li; Li, Zhong-Qiu; Shao, Jiang-Yang; Chen, Zili; Zhong, Yu-Wu
An organic polarized photonic heterostructure based on tetra(4-pyridylphenyl)ethylene.
Chemical communications (Cambridge, England), 2024, 60, 13199-13202
7133875 CIFC15 H22.33 N1.33 O1.33 Tb0.33R -3 :H13.9426; 13.9426; 39.401
90; 90; 120		6633.2Shirai, Sora; Muratsugu, Satoshi; Matsui, Hisaki; Harada, Kazuhiro; Ehara, Masahiro; Nakai, Hidetaka; Tada, Mizuki
Circularly polarized luminescence induction on a Tb(III) complex with a tris(<i>o-tert</i>-butylaryloxide)-functionalized 1,4,7-triazacyclononane ligand coordinating chiral 1-phenylethylamine.
Chemical communications (Cambridge, England), 2024, 60, 14180-14183
7133876 CIFC108 H153 N9 O6 Tb2P 1 21 112.552; 36.55; 21.8477
90; 100.864; 90		9843.5Shirai, Sora; Muratsugu, Satoshi; Matsui, Hisaki; Harada, Kazuhiro; Ehara, Masahiro; Nakai, Hidetaka; Tada, Mizuki
Circularly polarized luminescence induction on a Tb(III) complex with a tris(<i>o-tert</i>-butylaryloxide)-functionalized 1,4,7-triazacyclononane ligand coordinating chiral 1-phenylethylamine.
Chemical communications (Cambridge, England), 2024, 60, 14180-14183
7133877 CIFC31 H45 N3 O2 SiI 41/a :227.23555; 27.23555; 17.39351
90; 90; 90		12902.1Wang, Jingyan; Hwang, Gi Byoung; Knapp, Caroline E.; Wilson, Daniel W. N.
Reversible CO<sub>2</sub> insertion into the silicon-nitrogen σ-bond of an N-heterocyclic iminosilane.
Chemical communications (Cambridge, England), 2024, 60, 13051-13054
7133878 CIFC7 Cl6 N PP m -3 m7.2009; 7.2009; 7.2009
90; 90; 90		373.39Ernst, Moritz J.; Kleoff, Merlin; Voßnacker, Patrick; Thiele, Günther; Müller, Christian; Riedel, Sebastian
A polychloride-enabled synthesis of [NEt<sub>3</sub>Me][PCl<sub>6</sub>] serving as a potential PCl<sub>3</sub>-storage and PCl<sub>5</sub>-reagent.
Chemical communications (Cambridge, England), 2024, 60, 13372-13375
7133879 CIFC19 H14 F2 O5 S2P -17.2477; 9.2848; 14.6674
99.987; 97.544; 105.341		920.97Kumawat, Sandeep; Natte, Kishore
Accessing structurally diverse aryl difluoromethyl ethers with bromo(difluoro)acetic acid.
Chemical communications (Cambridge, England), 2024, 60, 13935-13938
7133880 CIFC13 H16 N2 O4P 1 21/c 113.5013; 11.448; 9.0667
90; 100.556; 90		1377.7Naveen, Kumar; Rawat, Vishesh Singh; Verma, Rahul; Gnanamani, Elumalai
Catalyst-free ring opening of azlactones in water microdroplets.
Chemical communications (Cambridge, England), 2024, 60, 13263-13266
7133881 CIFC27 H25 N O5P c a 2118.656; 9.9609; 12.339
90; 90; 90		2293Verma, Kshitiz; Bhattacharyya, Hemanga; Saha, Sharajit; Punniyamurthy, Tharmalingam
Expedient (3+3)-annulation of carbonyl ylides with azaoxyallyl cations: formal access to oxa-benzo[<i>c</i>]azepin-3-ones.
Chemical communications (Cambridge, England), 2024, 60, 13368-13371
7133882 CIFC18 H17 I N PP b c a12.63127; 12.19906; 22.48435
90; 90; 90		3464.6Fayafrou, Oussama; Lognon, Elise; Duhayon, Carine; Sortais, Jean-Baptiste; Monari, Antonio; Baslé, Olivier; Canac, Yves
Photoluminescent ruthenium(II) bipyridyl complexes containing phosphonium ylide ligands.
Chemical communications (Cambridge, England), 2024, 60, 13602-13605
7133883 CIFC18 H17 F6 N P2C 1 2/c 124.3853; 12.6612; 13.1682
90; 98.506; 90		4020.92Fayafrou, Oussama; Lognon, Elise; Duhayon, Carine; Sortais, Jean-Baptiste; Monari, Antonio; Baslé, Olivier; Canac, Yves
Photoluminescent ruthenium(II) bipyridyl complexes containing phosphonium ylide ligands.
Chemical communications (Cambridge, England), 2024, 60, 13602-13605
7133884 CIFC28 H30 Cl F6 N P2 RuP 1 21/n 110.9068; 15.3075; 17.2234
90; 92.768; 90		2872.19Fayafrou, Oussama; Lognon, Elise; Duhayon, Carine; Sortais, Jean-Baptiste; Monari, Antonio; Baslé, Olivier; Canac, Yves
Photoluminescent ruthenium(II) bipyridyl complexes containing phosphonium ylide ligands.
Chemical communications (Cambridge, England), 2024, 60, 13602-13605
7133885 CIFC27 H30.5 F12 N5.5 O0.5 P3 RuP -111.9873; 12.2991; 13.4048
100.976; 100.112; 106.324		1806.06Fayafrou, Oussama; Lognon, Elise; Duhayon, Carine; Sortais, Jean-Baptiste; Monari, Antonio; Baslé, Olivier; Canac, Yves
Photoluminescent ruthenium(II) bipyridyl complexes containing phosphonium ylide ligands.
Chemical communications (Cambridge, England), 2024, 60, 13602-13605
7133886 CIFC39 H34 Cl2 F12 N5 P3 RuP -111.9812; 13.8864; 14.5882
95.3; 110.311; 92.43		2259.26Fayafrou, Oussama; Lognon, Elise; Duhayon, Carine; Sortais, Jean-Baptiste; Monari, Antonio; Baslé, Olivier; Canac, Yves
Photoluminescent ruthenium(II) bipyridyl complexes containing phosphonium ylide ligands.
Chemical communications (Cambridge, England), 2024, 60, 13602-13605
7133887 CIFC2.4 H2.67 F0.13 N0.13 O0.93P 21 21 215.1122; 13.527; 26.011
90; 90; 90		1798.7Zargar, Irshad Ahmad; Rasool, Bisma; Bappa, S. K.; Mukherjee, Debaraj
Anomeric oxyacetamide assisted site-selective C-2 arylation and its application in <i>O</i>/<i>S</i> glycosylation of 2,3 eno-pyranoside.
Chemical communications (Cambridge, England), 2024, 60, 13040-13043
7133888 CIFC6 H4 Cl2 N2 Ni SP m m a12.67; 3.55; 8.87
90; 90; 90		399Myatt, Emily; Lata, Simrun; Pitcairn, Jem; Daisenberger, Dominik; Kronawitter, Silva M.; Hallweger, Sebastian A.; Kieslich, Gregor; Argent, Stephen P.; Tidey, Jeremiah P.; Cliffe, Matthew J.
Ligand solid-solution tuning of magnetic and mechanical properties of the van der Waals metal-organic magnet NiCl<sub>2</sub>(btd)<sub>1-<i>x</i></sub>(bod)<sub><i>x</i></sub>.
Chemical communications (Cambridge, England), 2024, 60, 14427-14430
7133889 CIFC12 H8 Cl2 N4 Ni O2P 42 b c14.1275; 14.1275; 6.862
90; 90; 90		1369.6Myatt, Emily; Lata, Simrun; Pitcairn, Jem; Daisenberger, Dominik; Kronawitter, Silva M.; Hallweger, Sebastian A.; Kieslich, Gregor; Argent, Stephen P.; Tidey, Jeremiah P.; Cliffe, Matthew J.
Ligand solid-solution tuning of magnetic and mechanical properties of the van der Waals metal-organic magnet NiCl<sub>2</sub>(btd)<sub>1-<i>x</i></sub>(bod)<sub><i>x</i></sub>.
Chemical communications (Cambridge, England), 2024, 60, 14427-14430
7133890 CIFC6 H4 Cl2 N2 Ni OP 1 2/c 13.52; 8.96; 12.17
90; 93.05; 90		383Myatt, Emily; Lata, Simrun; Pitcairn, Jem; Daisenberger, Dominik; Kronawitter, Silva M.; Hallweger, Sebastian A.; Kieslich, Gregor; Argent, Stephen P.; Tidey, Jeremiah P.; Cliffe, Matthew J.
Ligand solid-solution tuning of magnetic and mechanical properties of the van der Waals metal-organic magnet NiCl<sub>2</sub>(btd)<sub>1-<i>x</i></sub>(bod)<sub><i>x</i></sub>.
Chemical communications (Cambridge, England), 2024, 60, 14427-14430
7133891 CIFC22 H26 Br N2 PP 1 21/c 19.4539; 16.8444; 13.8253
90; 109.865; 90		2070.6Clark, Ella F.; Dunstan, Estelle; Kociok-Köhn, Gabriele; Buchard, Antoine
Aminophosphonium organocatalysts for the ring-opening copolymerisation of epoxide and cyclic anhydride.
Chemical communications (Cambridge, England), 2024, 60, 13067-13070
7133892 CIFC25 H23 Br N PP b c a11.1188; 18.1495; 21.2078
90; 90; 90		4279.7Clark, Ella F.; Dunstan, Estelle; Kociok-Köhn, Gabriele; Buchard, Antoine
Aminophosphonium organocatalysts for the ring-opening copolymerisation of epoxide and cyclic anhydride.
Chemical communications (Cambridge, England), 2024, 60, 13067-13070
7133893 CIFC2 H3 B K2 O7P n m a13.1577; 7.0592; 7.8332
90; 90; 90		727.57Wang, Xiao; Han, Tingwen; Poeppelmeier, Kenneth R.; Hou, Xueling; Pan, Shilie; Zhang, Fangfang
Exploring short-wavelength birefringent crystals <i>via</i> triggering cooperative arrangement between different π-conjugated groups.
Chemical communications (Cambridge, England), 2024, 60, 13566-13569
7133894 CIFC6 H8 B2 Cs4 O18P b a m11.2578; 24.484; 3.9326
90; 90; 90		1084Wang, Xiao; Han, Tingwen; Poeppelmeier, Kenneth R.; Hou, Xueling; Pan, Shilie; Zhang, Fangfang
Exploring short-wavelength birefringent crystals <i>via</i> triggering cooperative arrangement between different π-conjugated groups.
Chemical communications (Cambridge, England), 2024, 60, 13566-13569
7133895 CIFC34 H20P 1 21/n 19.8987; 21.3915; 20.2646
90; 96.076; 90		4266.9Bharathi, Kabali Divya; Mohanakrishnan, Arasambattu K.
Serendipitous synthesis of phenanthrene derivatives by exploiting electrocyclization during thermolysis of Diels-Alder intermediate dihydrodibenzothiophene-<i>S</i>,<i>S</i>-dioxides.
Chemical communications (Cambridge, England), 2024, 60, 13590-13593
7133896 CIFC24 H14 O2 SP 1 21/c 110.7358; 7.263; 22.198
90; 95.021; 90		1724.2Bharathi, Kabali Divya; Mohanakrishnan, Arasambattu K.
Serendipitous synthesis of phenanthrene derivatives by exploiting electrocyclization during thermolysis of Diels-Alder intermediate dihydrodibenzothiophene-<i>S</i>,<i>S</i>-dioxides.
Chemical communications (Cambridge, England), 2024, 60, 13590-13593
7133897 CIFC76 H56 O4P -112.1839; 13.885; 16.4844
91.638; 102.362; 91.987		2720.6Bharathi, Kabali Divya; Mohanakrishnan, Arasambattu K.
Serendipitous synthesis of phenanthrene derivatives by exploiting electrocyclization during thermolysis of Diels-Alder intermediate dihydrodibenzothiophene-<i>S</i>,<i>S</i>-dioxides.
Chemical communications (Cambridge, England), 2024, 60, 13590-13593
7133898 CIFC32 H20 O2 S2P n a 2112.8414; 18.5591; 10.0685
90; 90; 90		2399.6Bharathi, Kabali Divya; Mohanakrishnan, Arasambattu K.
Serendipitous synthesis of phenanthrene derivatives by exploiting electrocyclization during thermolysis of Diels-Alder intermediate dihydrodibenzothiophene-<i>S</i>,<i>S</i>-dioxides.
Chemical communications (Cambridge, England), 2024, 60, 13590-13593
7133899 CIFC36 H24P 1 21/c 111.434; 22.093; 9.934
90; 96.97; 90		2491Bharathi, Kabali Divya; Mohanakrishnan, Arasambattu K.
Serendipitous synthesis of phenanthrene derivatives by exploiting electrocyclization during thermolysis of Diels-Alder intermediate dihydrodibenzothiophene-<i>S</i>,<i>S</i>-dioxides.
Chemical communications (Cambridge, England), 2024, 60, 13590-13593
7133900 CIFC17 H15 N O S2C 1 c 17.2278; 22.429; 9.66
90; 98.99; 90		1546.8Nguyen, Le Anh; Ngo, Quoc Anh; Retailleau, Pascal; Nguyen, Thanh Binh
Room temperature dithiocarbamation of 2-tetralones with elemental sulfur and isothiocyanates S<sub>8</sub>/R-NCS: atom-efficient access to 4-hydroxythiazolidine-2-thiones.
Chemical communications (Cambridge, England), 2024, 60, 13586-13589
7133901 CIFC18 H15 N O S2P 1 21/c 111.1398; 14.0582; 10.5753
90; 106.341; 90		1589.2Nguyen, Le Anh; Ngo, Quoc Anh; Retailleau, Pascal; Nguyen, Thanh Binh
Room temperature dithiocarbamation of 2-tetralones with elemental sulfur and isothiocyanates S<sub>8</sub>/R-NCS: atom-efficient access to 4-hydroxythiazolidine-2-thiones.
Chemical communications (Cambridge, England), 2024, 60, 13586-13589
7133902 CIFC25 H28 N2 O2 S2P c a 2131.023; 8.7121; 17.796
90; 90; 90		4809.8Lee, Minji; Noh, Hyunju; Kim, Youngsuk
Diamidocarbene-derived palladium and nickel-sulfur clusters.
Chemical communications (Cambridge, England), 2024, 60, 13867-13870
7133903 CIFC106.75 H125.53 N9.68 Ni3 O8.85 S8P -114.1896; 16.1897; 25.073
89.342; 89.718; 66.28		5273Lee, Minji; Noh, Hyunju; Kim, Youngsuk
Diamidocarbene-derived palladium and nickel-sulfur clusters.
Chemical communications (Cambridge, England), 2024, 60, 13867-13870
7133904 CIFC102 H115 N9 O8 Pd4 S8P -115.1195; 15.562; 21.9749
89.159; 83.597; 76.313		4991.9Lee, Minji; Noh, Hyunju; Kim, Youngsuk
Diamidocarbene-derived palladium and nickel-sulfur clusters.
Chemical communications (Cambridge, England), 2024, 60, 13867-13870
7133905 CIFC102 H115 N9 Ni4 O8 S8P -115.1288; 15.5209; 21.5815
89.171; 84.225; 76.607		4904.6Lee, Minji; Noh, Hyunju; Kim, Youngsuk
Diamidocarbene-derived palladium and nickel-sulfur clusters.
Chemical communications (Cambridge, England), 2024, 60, 13867-13870
7133906 CIFC12 H18 Cl4 Cu N4C 1 2/c 111.344; 12.2584; 14.3901
90; 112.637; 90		1846.9Deng, Xin; Zhou, Lin; Yan, Xin; Wang, Yan-Juan; Yang, Wen-Li; Lv, Hui-Peng; Tang, Yuan-Yuan
Hydrogen-bond engineering induced ferroelastic phase transition in copper-based organic-inorganic hybrid thermochromic materials.
Chemical communications (Cambridge, England), 2024, 60, 14766-14769
7133907 CIFC12 H18 Cl4 Cu N4C 1 2/c 113.3776; 8.3515; 15.9482
90; 93.345; 90		1778.75Deng, Xin; Zhou, Lin; Yan, Xin; Wang, Yan-Juan; Yang, Wen-Li; Lv, Hui-Peng; Tang, Yuan-Yuan
Hydrogen-bond engineering induced ferroelastic phase transition in copper-based organic-inorganic hybrid thermochromic materials.
Chemical communications (Cambridge, England), 2024, 60, 14766-14769
7133908 CIFC12 H18 Cl4 Cu N4C 1 2/c 111.3689; 12.3269; 14.343
90; 113.26; 90		1846.7Deng, Xin; Zhou, Lin; Yan, Xin; Wang, Yan-Juan; Yang, Wen-Li; Lv, Hui-Peng; Tang, Yuan-Yuan
Hydrogen-bond engineering induced ferroelastic phase transition in copper-based organic-inorganic hybrid thermochromic materials.
Chemical communications (Cambridge, England), 2024, 60, 14766-14769
7133909 CIFC19 H22 O S SiP 21 21 216.013; 16.5709; 17.6278
90; 90; 90		1756.45Ding, Yang; Ke, Jie; Zhang, Wenbin; Li, Bin; He, Chuan
Rhodium-catalyzed synthesis of Si-stereogenic alkoxysilanes and silyl enol ethers <i>via</i> hydrosilylation of carbonyl compounds.
Chemical communications (Cambridge, England), 2024, 60, 13734-13737
7133910 CIFC121 H150 O23C 1 2/c 121.429; 20.658; 12.85
90; 97.93; 90		5634Wang, Aopu; Zhao, Xueru; Zhang, Hui; Ding, Yanjun; Xue, Min; Shao, Li
Charge-transfer host-guest complexes based on pillar[<i>n</i>]arenes and quinonoid compounds for near-infrared photothermal conversion.
Chemical communications (Cambridge, England), 2024, 60, 13722-13725
7133911 CIFC244 H322 Cl4 O42P 1 c 146.908; 15.5822; 16.4942
90; 94.71; 90		12015.4Wang, Aopu; Zhao, Xueru; Zhang, Hui; Ding, Yanjun; Xue, Min; Shao, Li
Charge-transfer host-guest complexes based on pillar[<i>n</i>]arenes and quinonoid compounds for near-infrared photothermal conversion.
Chemical communications (Cambridge, England), 2024, 60, 13722-13725
7133913 CIFC7 H6 N2 O4P 1 21/c 19.4038; 10.9694; 7.4547
90; 100.726; 90		755.55Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133914 CIFC7 H6 N2 O4P 1 21/c 19.4072; 10.9721; 7.5088
90; 100.453; 90		762.17Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133915 CIFC7 H6 N2 O4P 1 21/c 19.3773; 10.9848; 7.5143
90; 100.458; 90		761.17Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133916 CIFC7 H6 N2 O4P 1 21/c 19.3808; 10.9778; 7.5597
90; 100.221; 90		766.15Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133917 CIFC7 H6 N2 O4P 1 21/c 19.4094; 10.9728; 7.5549
90; 100.201; 90		767.69Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133918 CIFC7 H6 N2 O4P 1 21/c 19.3883; 10.9737; 7.6099
90; 99.955; 90		772.2Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133919 CIFC7 H6 N2 O4P 1 21/c 17.264; 21.365; 9.973
90; 100.19; 90		1523.3Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133920 CIFC7 H6 N2 O4P 1 21/c 19.4017; 10.963; 7.6527
90; 99.639; 90		777.63Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133921 CIFC7 H6 N2 O4P 1 21/c 19.427; 10.9529; 7.6965
90; 99.34; 90		784.15Harsha, Priyasha; Das, Dinabandhu
Bidirectional strain release in a thermosalient organic salt crystal induced by anisotropic thermal expansion and phase transformation.
Chemical communications (Cambridge, England), 2024, 60, 14105-14108
7133922 CIFC136 H108 Cl3 N9 O RuP -115.3821; 16.7184; 23.3719
102.612; 104.135; 93.651		5644.16Yoneda, Akira; Watanabe, Taito; Kosugi, Kento; Takahara, Teppei; Kusaka, Shinpei; Matsuda, Ryotaro; Saga, Yutaka; Kambe, Tetsuya; Kondo, Mio; Masaoka, Shigeyuki
Development of a Ru-porphyrin-based supramolecular framework catalyst for styrene epoxidation.
Chemical communications (Cambridge, England), 2024, 60, 13939-13942
7133923 CIFC125 H92 N4 O2 RuP -17.886; 16.7298; 19.9827
112.717; 94.736; 95.806		2398Yoneda, Akira; Watanabe, Taito; Kosugi, Kento; Takahara, Teppei; Kusaka, Shinpei; Matsuda, Ryotaro; Saga, Yutaka; Kambe, Tetsuya; Kondo, Mio; Masaoka, Shigeyuki
Development of a Ru-porphyrin-based supramolecular framework catalyst for styrene epoxidation.
Chemical communications (Cambridge, England), 2024, 60, 13939-13942
7133924 CIFC64 H48 Cl8 F8 OC 1 2/c 118.3396; 12.3007; 28.775
90; 110.005; 90		6099.7Imoto, Daiki; Shudo, Hiroki; Mizukami, Kiichi; Kimizuka, Nobuo; Yagi, Akiko; Itami, Kenichiro
Synthesis and size-dependent properties of multiple sizes of chlorinated fluorocycloparaphenylenes.
Chemical communications (Cambridge, England), 2024, 60, 12585-12588
7133925 CIFC37 H14 Cl8 F6P 61 2 211.9887; 11.9887; 39.3782
90; 90; 120		4901.5Imoto, Daiki; Shudo, Hiroki; Mizukami, Kiichi; Kimizuka, Nobuo; Yagi, Akiko; Itami, Kenichiro
Synthesis and size-dependent properties of multiple sizes of chlorinated fluorocycloparaphenylenes.
Chemical communications (Cambridge, England), 2024, 60, 12585-12588
7133926 CIFC45 H33 N3 O4P -19.5254; 11.8656; 17.5066
86.314; 80.905; 81.884		1932.4Wang, Yue; Wei, Xingfu; Xue, Aiqi; Huang, Yue; Qu, Jingping; Wang, Baomin
Construction of atropisomeric benzoxepinone-embedded styrenes <i>via</i> intramolecular [3+2] cycloaddition and catalytic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 12864-12867
7133927 CIFC39 H30 N2 O4P 1 21/c 113.0367; 15.1484; 17.888
90; 96.818; 90		3507.6Wang, Yue; Wei, Xingfu; Xue, Aiqi; Huang, Yue; Qu, Jingping; Wang, Baomin
Construction of atropisomeric benzoxepinone-embedded styrenes <i>via</i> intramolecular [3+2] cycloaddition and catalytic kinetic resolution.
Chemical communications (Cambridge, England), 2024, 60, 12864-12867
7133928 CIFC1.891 H1.239 N0.152 O0.022P -112.669; 14.2191; 17.5161
90.205; 92.857; 98.28		3118.4Tu, Zhen-Long; Hu, Li-Yuan; Wang, Jun-Yi; Wang, Cong; Xiao, Xunwen; Luo, Xu-Feng
Ring-extended carbazole modification to activate efficient phosphorescent OLED performance of traditional host materials.
Chemical communications (Cambridge, England), 2024, 60, 12421-12424
7133929 CIFC8 H3 Cu N2.2 O4R -3 m :H18.8651; 18.8651; 23.6734
90; 90; 120		7296.4Lu, Wanpeng; Chen, Yinlin; Wang, Zi; Guo, Lixia; Chen, Jin; Ma, Yujie; Li, Weiyao; Li, Jiangnan; He, Meng; Fan, Mengtian; Sheveleva, Alena M.; Tuna, Floriana; McInnes, Eric J. L.; Frogley, Mark D.; Chater, Philip A.; Dejoie, Catherine; Schröder, Martin; Yang, Sihai
High ammonia adsorption in copper-carboxylate materials: host-guest interactions and crystalline-amorphous-crystalline phase transitions.
Chemical communications (Cambridge, England), 2024, 60, 12385-12388
7133930 CIFC47 H85 Ir O0.5 Si UP -112.0803; 12.3459; 16.9963
105.679; 96.253; 96.29		2400.3Ye, Christopher Z.; Del Rosal, Iker; Ouellette, Erik T.; Hohloch, Stephan; Maron, Laurent; Camp, Clément; Arnold, John
Reduction of CS2 to an ethanetetrathiolate by a hydride-bridged uranium–iridium heterobimetallic complex
Chemical Communications, 2024, 60, 12377-12380
7133931 CIFC96 H166 Ir2 S4 U2C 1 2/c 129.472; 18.083; 17.948
90; 99.352; 90		9438.1Ye, Christopher Z.; Del Rosal, Iker; Ouellette, Erik T.; Hohloch, Stephan; Maron, Laurent; Camp, Clément; Arnold, John
Reduction of CS2 to an ethanetetrathiolate by a hydride-bridged uranium–iridium heterobimetallic complex
Chemical Communications, 2024, 60, 12377-12380
7133932 CIFC6 H18 B3 F12 N5I 41/a :214.3261; 14.3261; 28.6549
90; 90; 90		5881Moriguchi, Jumpei; Koga, Tomoe; Tsunoji, Nao; Nishihara, Sadafumi; Akutagawa, Tomoyuki; Masuya-Suzuki, Atsuko; Tsunashima, Ryo
Solvent-assisted mechanochemical crystallization of the metal-free perovskite solid solution (H<sub>2</sub>dabco, H<sub>2</sub>hmta)NH<sub>4</sub>(BF<sub>4</sub>)<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12181-12184
7133933 CIFC10.73 B3 F12 NF m -3 c14.6769; 14.6769; 14.6769
90; 90; 90		3161.6Moriguchi, Jumpei; Koga, Tomoe; Tsunoji, Nao; Nishihara, Sadafumi; Akutagawa, Tomoyuki; Masuya-Suzuki, Atsuko; Tsunashima, Ryo
Solvent-assisted mechanochemical crystallization of the metal-free perovskite solid solution (H<sub>2</sub>dabco, H<sub>2</sub>hmta)NH<sub>4</sub>(BF<sub>4</sub>)<sub>3</sub>.
Chemical communications (Cambridge, England), 2024, 60, 12181-12184
7133934 CIFC13 H11 N3 O2P -18.252; 10.694; 12.745
81.615; 82.031; 80.082		1088.6Yadav, Pushpendra; Chatterjee, Deblina; Bhowmick, Suman; Tiwari, Khushboo; Awasthi, Annapurna; Tiwari, Dharmendra Kumar
Autocatalytic and DMSO-promoted regioselective synthesis of pyrimidine-fused quinolines from anilines and barbituric acids.
Chemical communications (Cambridge, England), 2024, 60, 12746-12749
7133935 CIFC60 H38 N5 O25 Zn5.5I -4 2 d38.8022; 38.8022; 12.8725
90; 90; 90		19381Yang, Mei; Yuan, Wenke; Li, Xiu-Yuan; Liu, Bo; Zhou, Huifang
Metal-organic framework with pore contraction and modification by diethylammonium cations for record SO<sub>2</sub>/CO<sub>2</sub> separation.
Chemical communications (Cambridge, England), 2024, 60, 12754-12757
7133936 CIFC100 H180 K4 Lu2 N10 O14P -112.4692; 16.0421; 16.7103
113.745; 95.077; 102.135		2934.75Chen, Xiao; Xu, Hanhua; Xi, Zhenfeng; Wei, Junnian
A (C<sub>5</sub>Me<sub>5</sub>)/enolamido lutetium dinitrogen complex promoted by deprotonation on the amidinate ligand.
Chemical communications (Cambridge, England), 2024, 60, 12750-12753
7133937 CIFC108 H196 K4 Lu4 N16 O12C 1 2/c 149.9594; 25.6494; 20.3764
90; 96.014; 90		25967.2Chen, Xiao; Xu, Hanhua; Xi, Zhenfeng; Wei, Junnian
A (C<sub>5</sub>Me<sub>5</sub>)/enolamido lutetium dinitrogen complex promoted by deprotonation on the amidinate ligand.
Chemical communications (Cambridge, England), 2024, 60, 12750-12753
7133938 CIFC90 H78 N2P -112.2461; 17.578; 17.8214
82.377; 88.409; 74.137		3657.4Tong, Zekun; Dong, Shaoqiang
Boat-to-boat conformation inversions of cyclobis[7,8-(<i>para</i>-quinodimethane)-3,7-(9-(<i>p</i>-tolyl)-9<i>H</i>-carbazole)] in the neutral and tetracationic state.
Chemical communications (Cambridge, England), 2024, 60, 12766-12769
7133939 CIFC24 H20 N2 OP 1 21/c 123.0317; 9.3673; 18.4944
90; 112.123; 90		3696.3Yang, Haitao; Pan, Yu; Tian, Yijing; Yu, Kaili; Bai, Yifeng; Jiang, Yonggang; Zhang, Hongbin; Deng, Guogang; Yang, Xiaodong
Intramolecular cyclization of <i>N</i>-aryl amides for the synthesis of 3-amino oxindoles.
Chemical communications (Cambridge, England), 2024, 60, 14125-14128
7133940 CIFC18 H22 N2 O2P 1 21/n 112.7459; 10.4541; 13.475
90; 111.592; 90		1669.51Rogers, Cory H.; Pradeep, Anu; Galiano, Layla A.; Kelley, S. Ariel; Varadharajan, Ramkumar; Belmore, Ken; Whitt, Logan M.; Li, Yanmei; Champagne, Pier Alexandre; Ramamurthy, Vaidhyanathan; Blackstock, Silas C.
Dynamic covalent and noncovalent assembly of <i>o</i>-nitrosocumene in organic solvents and water.
Chemical communications (Cambridge, England), 2024, 60, 13899-13902
7133941 CIFC6 H20 Cl4 Co N2 O2P 1 21/n 18.4749; 12.0762; 15.04
90; 100.772; 90		1512.14Dafonte-Rodríguez, Pedro; Delgado-Ferreiro, Ignacio; García-Ben, Javier; Ferradanes-Martínez, Angel; Gelpi, María; Walker, Julian; McMonagle, Charles James; Castro-García, Socorro; Señarís-Rodríguez, María Antonia; Bermúdez-García, Juan Manuel; Sánchez-Andújar, Manuel
Exploring the effect of pressure on the crystal structure and caloric properties of the molecular ionic hybrid [(CH<sub>3</sub>)<sub>3</sub>NOH]<sub>2</sub>[CoCl<sub>4</sub>].
Chemical communications (Cambridge, England), 2024, 60, 14065-14068
7133942 CIFC6 Cl4 Co N2 O2P n m a12.2008; 8.7001; 15.4434
90; 90; 90		1639.29Dafonte-Rodríguez, Pedro; Delgado-Ferreiro, Ignacio; García-Ben, Javier; Ferradanes-Martínez, Angel; Gelpi, María; Walker, Julian; McMonagle, Charles James; Castro-García, Socorro; Señarís-Rodríguez, María Antonia; Bermúdez-García, Juan Manuel; Sánchez-Andújar, Manuel
Exploring the effect of pressure on the crystal structure and caloric properties of the molecular ionic hybrid [(CH<sub>3</sub>)<sub>3</sub>NOH]<sub>2</sub>[CoCl<sub>4</sub>].
Chemical communications (Cambridge, England), 2024, 60, 14065-14068
7133943 CIFC2 H13 N5 O8P 1 21/c 15.7762; 22.1425; 7.9135
90; 92.015; 90		1011.51Inoue, Kazuki; Nishiwaki, Yosuke; Kumasaki, Mieko; Matsumoto, Shinya; Okada, Ken
Synthesis of environmentally friendly energetic cocrystal derived from commodity chemicals.
Chemical communications (Cambridge, England), 2024, 60, 13963-13966
7133944 CIFC240 H232 Cl16 N8 O8P -114.7048; 23.2163; 32.0917
81.364; 79.536; 89.251		10650.3Mirzaei, M. Saeed; Mirzaei, Saber; Espinoza Castro, Victor M.; Lawrence, Charlotte; Hernández Sánchez, Raúl
Dual molecular tweezers extending from a nanohoop.
Chemical communications (Cambridge, England), 2024, 60, 14236-14239
7133945 CIFC725.6 H557.62 Cl88.8 F192 N48 O24F d -3 :235.673; 35.673; 35.673
90; 90; 90		45396.1David, Tim; Oestreich, Robert; Pausch, Tobias; Wada, Yuki; Fleck-Kunde, Tom; Kawano, Masaki; Janiak, Christoph; Schmidt, Bernd M.
Fluorinated <i>vs.</i> non-fluorinated tetrahedral Tri<sup>4</sup>Tri<sup>4</sup> porous organic cages for H<sub>2</sub>, CO<sub>2</sub>, and CH<sub>4</sub> adsorption.
Chemical communications (Cambridge, England), 2024, 60, 14762-14765
7133946 CIFC350.54 H326.54 Cl45 N24F -4 3 c35.2652; 35.2652; 35.2652
90; 90; 90		43857David, Tim; Oestreich, Robert; Pausch, Tobias; Wada, Yuki; Fleck-Kunde, Tom; Kawano, Masaki; Janiak, Christoph; Schmidt, Bernd M.
Fluorinated <i>vs.</i> non-fluorinated tetrahedral Tri<sup>4</sup>Tri<sup>4</sup> porous organic cages for H<sub>2</sub>, CO<sub>2</sub>, and CH<sub>4</sub> adsorption.
Chemical communications (Cambridge, England), 2024, 60, 14762-14765
7133947 CIFC16 H18 I O4 PP -110.5418; 12.7822; 13.0647
97.395; 95.008; 107.951		1645.7Koch, Jan Rick; Damrath, Mattis; Puylaert, Pim; Nachtsheim, Boris J.
Synthesis of phosphate stabilised iodanes and their application in intramolecular aryl migrations.
Chemical communications (Cambridge, England), 2024, 60, 14653-14655
7133948 CIFC8 H10 I O5 PC 1 2/c 122.585; 4.466; 22.66
90; 99.875; 90		2251.7Koch, Jan Rick; Damrath, Mattis; Puylaert, Pim; Nachtsheim, Boris J.
Synthesis of phosphate stabilised iodanes and their application in intramolecular aryl migrations.
Chemical communications (Cambridge, England), 2024, 60, 14653-14655
7133949 CIFC115.5 H99.5 I4 N10P -122.459; 30.925; 33.796
100.82; 101.36; 91.89		22544Lee, Seungwon; Lee, Byeung Ju; Song, Geunmoo; Jeong, Kyu-Sung
Helical aromatic foldamers with tubular cavities capable of accommodating multiple halide ions.
Chemical communications (Cambridge, England), 2024, 60, 14081-14084
7133950 CIFC258 H123 I8 N22 OP -125.2; 25.207; 29.256
104.05; 103.3; 116.8		14803Lee, Seungwon; Lee, Byeung Ju; Song, Geunmoo; Jeong, Kyu-Sung
Helical aromatic foldamers with tubular cavities capable of accommodating multiple halide ions.
Chemical communications (Cambridge, England), 2024, 60, 14081-14084
7133951 CIFC186 H111.75 I6 N16 O0.75P 1 21/c 138.554; 51.49; 43.138
90; 93.47; 90		85478Lee, Seungwon; Lee, Byeung Ju; Song, Geunmoo; Jeong, Kyu-Sung
Helical aromatic foldamers with tubular cavities capable of accommodating multiple halide ions.
Chemical communications (Cambridge, England), 2024, 60, 14081-14084
7133952 CIFC67 H54 Cl11 Cr3 N12 O P2P n a 2123.746; 17.54; 16.981
90; 90; 90		7073López-Plá, Jessica M; Obies, Mohammed; Zahariou, Georgia; Pissas, Michael; Sanakis, Yiannis; McGrady, John E.; Raptis, Raphael G.
Pyrazolate-supported Cr<sub>3</sub>(μ<sub>3</sub>-O) cores; homovalent CrIII3 and mixed-valent CrIII2Cr<sup>IV</sup>.
Chemical communications (Cambridge, England), 2024, 60, 14117-14120
7133953 CIFC67 H54 Br3 Cl8 Cr3 N12 O P2P n a 2124.0399; 17.8794; 16.9017
90; 90; 90		7264.7López-Plá, Jessica M; Obies, Mohammed; Zahariou, Georgia; Pissas, Michael; Sanakis, Yiannis; McGrady, John E.; Raptis, Raphael G.
Pyrazolate-supported Cr<sub>3</sub>(μ<sub>3</sub>-O) cores; homovalent CrIII3 and mixed-valent CrIII2Cr<sup>IV</sup>.
Chemical communications (Cambridge, England), 2024, 60, 14117-14120
7133954 CIFC24 H10 N2 O2P 1 21/c 110.0418; 14.1923; 10.918
90; 106.166; 90		1494.47Nakagawa, Aoi; Ota, Wataru; Ehara, Takumi; Matsuo, Yusuke; Miyata, Kiyoshi; Onda, Ken; Sato, Tohru; Seki, Shu; Tanaka, Takayuki
Synthesis of substituent-free dioxadiaza[8]circulene to investigate intermolecular interactions and photophysical properties.
Chemical communications (Cambridge, England), 2024, 60, 14770-14773
7133955 CIFC56 H58 N2 O2P 1 21/c 111.8608; 13.4284; 27.874
90; 90.771; 90		4439.13Nakagawa, Aoi; Ota, Wataru; Ehara, Takumi; Matsuo, Yusuke; Miyata, Kiyoshi; Onda, Ken; Sato, Tohru; Seki, Shu; Tanaka, Takayuki
Synthesis of substituent-free dioxadiaza[8]circulene to investigate intermolecular interactions and photophysical properties.
Chemical communications (Cambridge, England), 2024, 60, 14770-14773
7133956 CIFC62 H86 N2 O7.5P -110.2049; 16.5666; 17.5296
109.901; 90.1; 106.501		2655.85Nakagawa, Aoi; Ota, Wataru; Ehara, Takumi; Matsuo, Yusuke; Miyata, Kiyoshi; Onda, Ken; Sato, Tohru; Seki, Shu; Tanaka, Takayuki
Synthesis of substituent-free dioxadiaza[8]circulene to investigate intermolecular interactions and photophysical properties.
Chemical communications (Cambridge, England), 2024, 60, 14770-14773

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