Crystallography Open Database

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7132578 CIFC56 H64 N6 O7P -111.244; 12.917; 17.778
86.525; 87.331; 75.394		2492.7Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132579 CIFC106 H110 Cl18 F6 N12 O20 S2 ZnP -116.0885; 20.1668; 21.6212
103.611; 101.577; 109.328		6129.8Hokimoto, Yuya; Nakamura, Takashi
Synthesis of a macrocyclic oligomer of pyridylbenzoxazole utilizing dynamic covalent bonds and its unsymmetric conversion.
Chemical communications (Cambridge, England), 2024, 60, 1281-1284
7132580 CIFC19 H17 N3 SP 1 21/c 17.7135; 22.94; 9.6284
90; 100.29; 90		1676.3Zhang, Xiaoxiang; Liu, Chenrui; Wei, Wanxing; Zhang, Zhuan; Liang, Taoyuan
Iodine-dependent oxidative regioselective aminochalcogenation of indolines.
Chemical communications (Cambridge, England), 2024, 60, 1152-1155
7132581 CIFC25 H26 O5P -110.1019; 10.718; 11.1905
64.873; 69.562; 83.168		1027.3Wu, Shu-Yi; Li, Yang; Shen, Peng; Yang, Xin-Han; Ran, Guang-Yao
Palladium-catalysed fragmentary esterification-induced allylic alkylation of allyl carbonates and cyclic vinylogous anhydrides.
Chemical communications (Cambridge, England), 2024, 60, 1416-1419
7132582 CIFC25 H21 Co F O4 PC 1 2/c 120.3694; 11.8516; 19.7496
90; 106.855; 90		4562.9Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132583 CIFC22 H33 Co F O4 PP n m a16.5748; 13.6875; 10.2341
90; 90; 90		2321.79Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132584 CIFC16 H27 Co F O4 PP b c a14.9882; 15.8456; 16.4634
90; 90; 90		3910Pietraru, Marie-Hélène; Ponsard, Louise; Lentz, Nicolas; Thuéry, Pierre; Nicolas, Emmanuel; Cantat, Thibault
Fluorophosphoniums as Lewis acids in organometallic catalysis: application to the carbonylation of β-lactones.
Chemical communications (Cambridge, England), 2024, 60, 1043-1046
7132585 CIFC116 H128 N8 O24 S8P 1 21/c 115.6273; 11.1454; 21.3411
90; 104.896; 90		3592.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132586 CIFC31 H42 N2 O7 S2P 21 21 2111.1123; 11.2096; 24.9678
90; 90; 90		3110.1Ho, An T.; Vanable, Evan P.; Miguel, Chelsea San; Hull, Kami L.
Iridium-catalysed hydroamination of internal homoallylic amines.
Chemical communications (Cambridge, England), 2024, 60, 1615-1618
7132587 CIFC25.5 H31 Cl N5C 1 2/c 129.863; 9.4396; 17.2974
90; 101.266; 90		4782.1Mohanty, Aisa; Rout, Smruti Rekha; Dandela, Rambabu; Daw, Prosenjit
Ammonia synthesis by the reductive N-N bond cleavage of hydrazine using an air-stable, phosphine-free ruthenium catalyst.
Chemical communications (Cambridge, England), 2024, 60, 416-419
7132588 CIFC14 H19 N O6P c a 2117.469; 7.599; 11.007
90; 90; 90		1461.1Zheng, Peng Xuan; Ou, Song Lin; Qu, Lei Yu; Zhang, Ying; Jiang, Shi Qing; Li, Xiang; Wan, Jun Xiong; Zhang, Min; Bao, Xin
Enriched switching in a donor-acceptor Stenhouse adduct <i>via</i> reversible covalent bonding.
Chemical communications (Cambridge, England), 2024, 60, 1333-1336
7132589 CIFC151.5 H201 Au14 Cl F3 P4.5 S9P -115.8928; 20.0176; 29.1486
75.045; 78.775; 78.621		8681.3Liu, Dong; Gao, Guiqi; Zhang, Yongyu; Li, Qinzhen; Yang, Sha; Chai, Jinsong; Yu, Haizhu; Zhu, Manzhou
[Au<sub>14</sub>(2-SAdm)<sub>9</sub>(Dppe)<sub>2</sub>]<sup>+</sup>: a gold nanocluster with a crystallization-induced emission enhancement phenomenon.
Chemical communications (Cambridge, England), 2024, 60, 1337-1340
7132590 CIFC24 H21 N3 O3 SP -18.0853; 10.9301; 13.3531
104.791; 92.638; 111.152		1051.52Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132591 CIFC24 H20 Br3 N3 O3 SP -110.8989; 11.4714; 11.6523
66.814; 72.69; 71.71		1246Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132592 CIFC26 H25 N3 O4 SP 21 21 2110.5361; 17.81; 26.2442
90; 90; 90		4924.67Tang, Yi; Zhang, Rulei; Dong, Yujie; Yu, Songcheng; Wu, Yongjun; Xiao, Yumei; Guo, Hongchao
4-Vinylbenzodioxinones as a new type of precursor for palladium-catalyzed (4+3) cycloaddition of azomethine imines.
Chemical communications (Cambridge, England), 2024, 60, 1436-1439
7132593 CIFC96 H72 Ag24 N48 O24F d d 245.975; 37.787; 3.754
90; 90; 90		6521.7Peng, Shuyin; Sun, Yuqian; Li, Qingqing; Jiang, Zhongwen; Rao, Yin; Wu, Yichen; Li, Qiaowei
Stepwise construction of coordinative linkages and dynamic covalent linkages for a porous metal-organic framework.
Chemical communications (Cambridge, England), 2024, 60, 1488-1491
7132594 CIFC27 H30 N2 O3 SP 21 21 219.7941; 11.2385; 23.348
90; 90; 90		2569.9Cui, Chen-Chang; Lin, Feng; Wang, Lu-Yao; Liu, Yin-Ping; Tu, Shu-Jiang; Tu, Man-Su; Hao, Wen-Juan; Jiang, Bo
Olefin skeletal rearrangement enabling access to multiarylated <i>N</i>-sulfonyl amidines.
Chemical communications (Cambridge, England), 2024, 60, 1492-1495
7132595 CIFC24 H22 I2 N4 O4 SP 14.7109; 5.1887; 25.0379
84.32; 88.126; 87.821		608.31Cao, Jinlian; Weng, Peimin; Qi, Yuanwei; Lin, Kexin; Yan, Xiaosheng
Noncovalent interaction network of chalcogen, halogen and hydrogen bonds for supramolecular β-sheet organization.
Chemical communications (Cambridge, England), 2024, 60, 1484-1487
7132596 CIFC73 H55 Cl3 N6 O3P c a 2124.6915; 14.7339; 15.6091
90; 90; 90		5678.6Chen, Lihua; Li, Chenfei; Liu, Zheng-Fei; Kuboi, Yoshiaki; Fu, Enguang; Vargas, Lydia Sosa; Adachi, Chihaya; Mathevet, Fabrice; Zhang, Shaodong
A donor-acceptor cage for circularly polarized TADF emission.
Chemical communications (Cambridge, England), 2024, 60, 1758-1761
7132597 CIFC60 H82 B3 K N6 OC 1 2/c 125.1162; 13.2745; 18.3072
90; 110.891; 90		5702.5Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132598 CIFC67 H86 B3 Br N6 O2 SiP 1 21 111.4979; 20.9867; 13.7765
90; 104.384; 90		3220.1Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132599 CIFC54 H76 B3 Br N6P 1 21/c 113.321; 20.663; 19.283
90; 100.62; 90		5217Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132600 CIFC108 H152 B6 Cl6 N12 O2 Si2P 21 21 2119.4723; 23.1794; 24.8889
90; 90; 90		11233.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132601 CIFC61.5 H83.5 B3 Cl Ge N6 OP -116.4864; 16.4582; 44.137
95.16; 97.087; 89.93		11835.7Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132602 CIFC108 H152 B6 Br6 N12 O2 Si2P 21 21 2119.5876; 23.2994; 24.9438
90; 90; 90		11383.8Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132603 CIFC162 H228 B9 Cl3 N18 O3 Sn3P 1 21/n 130.8728; 16.2163; 33.9145
90; 106.314; 90		16295.4Guthardt, Robin; Jones, Cameron
A bromo(boryloxy) silylene and its heavier analogues.
Chemical communications (Cambridge, England), 2024, 60, 1583-1586
7132604 CIFC23 H22 N2P 1 21/c 110.8961; 18.4187; 9.4952
90; 111.962; 90		1767.3Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132605 CIFC22 H19 F N2P 1 21/c 110.454; 20.0412; 9.0834
90; 106.374; 90		1825.9Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132606 CIFC22 H20 N2P 1 21/c 110.0309; 19.6236; 9.0074
90; 104.371; 90		1717.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132607 CIFC23 H20 N2 OP -17.4394; 10.1901; 13.5234
98.505; 92.733; 110.436		944.63Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132608 CIFC44 H43 Cl2 N3 O6 SP -18.7541; 15.3319; 15.5807
82.471; 85.577; 81.058		2044.53Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132609 CIFC48 H43 Cl O P2 PdC 1 2/m 119.3124; 18.4281; 12.7741
90; 103.027; 90		4429.2Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132610 CIFC49 H41 F3 O4 P2 Pd SP 1 21/m 19.2641; 18.7713; 12.8967
90; 101.38; 90		2198.6Liang, Qianqian; Cai, Yan; Jiang, Wenjun; Pang, Mengdi; Fan, Liming; Zhang, Guoying
Palladium-catalyzed allylation and carbonylation: access to allylhydrazones and allyl acylhydrazones.
Chemical communications (Cambridge, England), 2024, 60, 1638-1641
7132611 CIFC4 H6 N8 O2P n a 216.744; 11.212; 9.487
90; 90; 90		717.3Kumar, Parasar; Kumar, Navaneet; Ghule, Vikas D.; Dharavath, Srinivas
Zwitterionic fused pyrazolo-triazole based high performing energetic materials.
Chemical communications (Cambridge, England), 2024, 60, 1646-1649
7132612 CIFC52 H50 N2 O4C 1 2/c 119.961; 14.527; 16.049
90; 118.68; 90		4082.8Gentile, Giuseppe; Bartolomei, Beatrice; Dosso, Jacopo; Demitri, Nicola; Filippini, Giacomo; Prato, Maurizio
Synthesis of a novel tetra-phenol π-extended phenazine and its application as an organo-photocatalyst.
Chemical communications (Cambridge, England), 2024, 60, 602-605
7132613 CIFC56 H95 Mo6 N7 O18P 1 21/c 112.4406; 29.2646; 18.9032
90; 92.548; 90		6875.27Jones, Claire F.; Hood, Bethany R.; de Coene, Yovan; Lopez-Poves, Ivan; Champagne, Benoît; Clays, Koen; Fielden, John
Bridge improvement work: maximising non-linear optical performance in polyoxometalate derivatives.
Chemical communications (Cambridge, England), 2024, 60, 1731-1734
7132614 CIFC30 H33 O3 PP 1 21 110.97433; 9.78846; 11.7517
90; 102.023; 90		1234.7Huang, Yu; Zhang, Yulong; Pan, Li; Wu, Qian; Li, Ning; Shi, Enxue; Xiao, Junhua
CAMDOL-enabled diastereoselective synthesis of α-substituted phosphonates.
Chemical communications (Cambridge, England), 2024, 60, 1924-1927
7132615 CIFC27 H34 N3 O3 PP 1 21 111.2201; 8.4447; 13.8792
90; 98.303; 90		1301.28Chen, Zi-Jia; Fan, Ling-Jie; Xie, Pei-Pei; Qian, Pu-Fan; Hu, Xinquan; Zhou, Tao; Shi, Bing-Feng
Pd(II)-Catalyzed enantioselective C-H olefination toward the synthesis of <i>P</i>-stereogenic phosphinamides.
Chemical communications (Cambridge, England), 2024, 60, 1623-1626
7132616 CIFC44 H54 B N3 Ni PP 1 21/c 114.5193; 29.0183; 9.5279
90; 103.894; 90		3896.89Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132617 CIFC26 H36 N3 Ni O PP 42/n :221.355; 21.355; 11.6688
90; 90; 90		5321.4Bermejo, José; Ortega-Lepe, Isabel; Santos, Laura L.; Rendón, Nuria; López-Serrano, Joaquín; Álvarez, Eleuterio; Suárez, Andrés
Nitrous oxide activation by picoline-derived Ni-CNP hydrides.
Chemical communications (Cambridge, England), 2024, 60, 1575-1578
7132618 CIFC10 H32 Bi I9 N4C m c m11.8846; 11.8525; 23.941
90; 90; 90		3372.4Wang, Yu-Yin; Kang, Huai-Yuan; Zhang, Shao-Ya; Qu, Hao; Zhu, Lin; Zhao, Dan; Li, Xian-Feng; Lei, Xiao-Wu; Yue, Cheng-Yang
Exploring 0D lead-free metal halide with highly efficient blue light emission and high-sensitivity photodetection.
Chemical communications (Cambridge, England), 2024, 60, 2784-2787
7132619 CIFC52 H98 N4 O6 Si6P -111.9643; 16.5858; 17.5688
90.529; 98.876; 109.35		3243.16Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132620 CIFC70 H134 N4 O6 Si6P -115.9929; 16.1504; 17.3188
79.449; 65.041; 78.584		3950.26Kim, Junghwan; Kim, Chungryeol; Lee, Dongwhan
Fluoride-triggered phase transition of metallogels for on-demand <i>in situ</i> containment of fluids.
Chemical communications (Cambridge, England), 2024, 60, 1762-1765
7132621 CIFC36 H26 N8 Ni O4P b c n12.655; 15.538; 17.066
90; 90; 90		3355.7Nogita, Kohei; Sugahara, Takaya; Miki, Koji; Mu, Huiying; Kobayashi, Minoru; Harada, Hiroshi; Ohe, Kouichi
A reductively convertible nickel phthalocyanine precursor as a biological thiol-responsive turn-on photoacoustic contrast agent.
Chemical communications (Cambridge, England), 2024, 60, 1472-1475
7132622 CIFC18 H17 Cl N2 O2P c c n21.1441; 11.5844; 12.8398
90; 90; 90		3145Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132623 CIFC18 H18 N2 O3 SP 1 21/c 113.7896; 9.0412; 13.8981
90; 108.87; 90		1639.61Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132624 CIFC19 H18 N2 O2P 1 21/n 19.1979; 15.6759; 10.7636
90; 95.704; 90		1544.27Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132625 CIFC40 H34 Cl2 N4 O4P n a 2110.2787; 11.9147; 27.5592
90; 90; 90		3375.1Yadav, Dharmendra K.; Tiwari, Sona; Senthil, Sathyapriya; Vechalapu, Sai Kumari; Duraisamy, Santhosh; Rawat, Viral; Rahman, Mohammed Isfahur; Khanna, Shweta; Allimuthu, Dharmaraja
Diazepam-based covalent modifiers of GPX4 induce ferroptosis in liver cancer cells.
Chemical communications (Cambridge, England), 2024, 60, 1928-1931
7132626 CIFC2.6 H1.8 N0.2 O0.6P 21 21 213.8378; 8.6367; 29.4303
90; 90; 90		975.49Chand, Tapasi; Gupta, Princi; Oza, Nehali; Kapur, Manmohan
Cobalt(II)-catalyzed <i>peri</i>-C(sp<sup>2</sup>)-H selective hydroxylation of naphthalene monoimides.
Chemical communications (Cambridge, England), 2024, 60, 1770-1773
7132627 CIFC38.49 H30.98 Cl3.98 P2 SbF d d 228.25; 31.29; 15.7735
90; 90; 90		13943Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132628 CIFC38.5 H31 Br Cl3 P2 SbF d d 227.674; 31.304; 16.183
90; 90; 90		14019Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132629 CIFC39 H32 Cl4 F6 P2 Sb2P 1 21/n 114.6987; 15.5168; 17.522
90; 93.975; 90		3986.7Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132630 CIFC40 H34 Au Bi Cl8 P2P 1 21/c 111.6409; 23.1633; 15.8194
90; 97.161; 90		4232.3Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132631 CIFC141 H87.9 B2 Br2 Cl5.9 F48.05 P4 Sb2P -112.135; 16.6073; 18.5495
107.079; 95.331; 99.299		3487.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132632 CIFC41 H37 Br F6 O P2 Sb2P 1 21/c 110.3202; 20.6841; 18.508
90; 92.122; 90		3948.1Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132633 CIFC40 H34 Au Cl8 P2 SbP 1 21/c 111.6084; 23.1906; 15.8524
90; 97.164; 90		4234.2Obi, Akachukwu D.; Deng, Chun-Lin; Alexis, Andrew J.; Dickie, Diane A.; Gilliard, Jr, Robert J
Geminal bimetallic coordination of a carbone to main-group and transition metals.
Chemical communications (Cambridge, England), 2024, 60, 1880-1883
7132634 CIFC27 H21 In N6P 1 21/c 116.1797; 15.4641; 9.7077
90; 99.032; 90		2398.8Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132635 CIFC33 H33 In N6P -19.9431; 10.4086; 14.78
83.547; 80.299; 74.885		1451.83Fu, Li-Zhi; He, Piao; Wang, Jia-Wei; Ma, Fan; Liu, Chao; Chen, Guo; Yi, Xiao-Yi
Mononuclear indium(III) photosensitizers for photo-dehalogenation and olefin reduction.
Chemical communications (Cambridge, England), 2024, 60, 1595-1598
7132636 CIFC54 H72 B2 N4 SiP 1 21/c 112.4737; 14.971; 26.1547
90; 92.786; 90		4878.5Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132637 CIFC52 H68 B2 N4 SiP 1 21/c 122.4231; 11.6708; 19.4398
90; 113.005; 90		4682.72Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132638 CIFC110 H142 B4 N8 Si2P -111.641; 12.3141; 17.9847
95.791; 101.108; 104.877		2414.05Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132639 CIFC54 H72 B2 N4 SiI 1 2/a 124.18452; 11.44862; 68.9173
90; 90.4985; 90		19081.1Brückner, Tobias; Duwe, Dario; Fantuzzi, Felipe; Heß, Merlin; Dewhurst, Rian D.; Radacki, Krzysztof; Braunschweig, Holger
Hydrosilylation of BB triple bonds: catalyst- and reductant-free construction of B-Si bonds and B<sub>2</sub>Si heterocycles.
Chemical communications (Cambridge, England), 2024, 60, 3259-3262
7132640 CIFC18 H37 BrP -15.561; 7.204; 46.69
87.22; 87.14; 89.974		1865.9Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132641 CIFC35 H69 Br2 N S2P -18.7215; 9.0562; 25.5173
93.301; 91.998; 106.02		1931.3Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132642 CIFC21 H40 Br N S2P -18.6976; 9.0477; 15.3351
96.503; 101.075; 100.606		1150.16Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132643 CIFC35 H73 N O4 S3P 1 21 15.0644; 7.3853; 51.831
90; 90.179; 90		1938.58Musozoda, Muhammadiqboli; Muller, 2nd, Joseph E; Anderson, Grace I.; Boucher, Mairead; Zeller, Matthias; Raymond, Casey C.; Hillesheim, Patrick C.; Mirjafari, Arsalan
Alkyl-templated cocrystallization of long-chain 1-bromoalkanes by lipid-like ionic liquids.
Chemical communications (Cambridge, England), 2024, 60, 1723-1726
7132644 CIFC17 H16 N2P 1 21/c 112.0756; 8.8912; 12.87
90; 92.604; 90		1380.4Zhao, Mi-Na; Yang, Zi-Mo; Li, Lian-Qing
DMF as an amine source: iron-catalyzed cyclization of 2<i>H</i>-azirines to imidazoles.
Chemical communications (Cambridge, England), 2024, 60, 1904-1907
7132645 CIFC39 H27 N3 SP -110.2867; 12.154; 12.446
79.931; 88.875; 74.591		1476.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132646 CIFC39 H27 N3 OP 1 21/c 114.239; 8.5693; 23.345
90; 102.743; 90		2778.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132647 CIFC40 H29 Cl2 N3 O SP -110.8035; 11.2186; 15.653
69.437; 83.85; 70.803		1677.4Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132648 CIFC39 H27 N3 O SP 1 21/c 117.993; 17.184; 9.741
90; 103.718; 90		2925.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132649 CIFC39 H27 N3 SP -110.141; 10.944; 15.802
90.812; 103.552; 114.74		1535.9Chen, Jianai; Wang, Haiyang; Yu, Yue; Liu, Jin; Zhao, Fengyi; Li, Weijun; Dong, Yujie
Sulphur-induced structural rearrangement in the self-sensitization photo-oxidation behaviour of phenothiazine-imidazole molecules.
Chemical communications (Cambridge, England), 2024, 60, 1888-1891
7132650 CIFC32 H41 F6 N PP -111.0504; 11.3069; 13.576
112.089; 90.039; 102.919		1525.21Inoue, Takeru; Matsuura, Yuuka; Horii, Koki; Konishi, Akihito; Nishida, Jun-Ichi; Yasuda, Makoto; Kawase, Takeshi
<i>N</i>-2,6-Di(isopropyl)phenyl-2-azaphenalenyl radical cations.
Chemical communications (Cambridge, England), 2024, 60, 1735-1738
7132651 CIFC17 H14 N3 O2P -17.1044; 10.0383; 10.7169
102.103; 109.324; 102.128		672.07Kuroda, Yusuke; Krell, Maya; Kurokawa, Kazuma; Takasu, Kiyosei
Synthesis of mesoionic triazolones <i>via</i> a formal [3+2] cycloaddition between 4-phenyl-1,2,4-triazoline-3,5-dione and alkynes.
Chemical communications (Cambridge, England), 2024, 60, 1719-1722
7132652 CIFC46 H38 N2 O3 PtP -110.8643; 11.6179; 14.5758
77.263; 82.321; 84.958		1775.15Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132653 CIFC30 H24 N2 O PtP 1 21/n 111.8288; 15.4199; 12.409
90; 98.051; 90		2241.08Ikeshita, Masahiro; Watanabe, Shinya; Suzuki, Seika; Tanaka, Shota; Hattori, Shingo; Shinozaki, Kazuteru; Imai, Yoshitane; Tsuno, Takashi
Circularly polarized phosphorescence with a large dissymmetry factor from a helical platinum(II) complex.
Chemical communications (Cambridge, England), 2024, 60, 2413-2416
7132654 CIFC20 H40 N6 ZnC 1 2/c 115.4081; 10.2686; 15.6427
90; 99.301; 90		2442.44Zhang, Xiaofeng; Li, Yinghua; Fan, Weibin; Huang, Deguang
Direct transformation of nitriles to cyanide using chloride anion as catalyst.
Chemical communications (Cambridge, England), 2024, 60, 2058-2061
7132655 CIFC57 H34 Cl Co N6 O5P -110.5787; 13.3611; 18.6693
73.222; 89.394; 84.62		2514.9Bulbul, Amir Sohel; Rathour, Vikram; Ganesan, Vellaichamy; Sankar, Muniappan
π-Extended nonplanar cobalt porphyrins immobilized on MWCNTs as efficient electrocatalysts for selective oxygen reduction reaction.
Chemical communications (Cambridge, England), 2024, 60, 3146-3149
7132656 CIFC36 H48 Cl2 Cu2 N10 O12P -111.652; 13.232; 16.02
106.82; 96.99; 110.12		2151.7De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132657 CIFC12 H20 Cu F6 N4 O8 S2P 1 21/c 110.686; 14.011; 8.0619
90; 110.87; 90		1127.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132658 CIFC40 H52 Cu2 F6 N10 O10 S2P n m a13.529; 20.929; 16.907
90; 90; 90		4787.2De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132659 CIFC37.12 H54.51 B2 Cl0.37 Cu2 F8 N10.38 O6.26P -111.5059; 15.193; 15.47
76.645; 73.531; 68.4		2386.8De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132660 CIFC15 H20 N4 O7P 1 21/c 111.301; 23.093; 6.9978
90; 105.89; 90		1756.5De Tovar, Jonathan; Philouze, Christian; Thibon-Pourret, Aurore; Belle, Catherine
Insights into non-covalent interactions in dicopper(II,II) complexes bearing a naphthyridine scaffold: anion-dictated electrochemistry.
Chemical communications (Cambridge, England), 2024, 60, 2228-2231
7132661 CIFC126 H102 N6 S6I a -333.06; 33.06; 33.06
90; 90; 90		36133.4Yamamoto, Koji; Tsutsui, Kanta; Tanuma, Miho; Ito, Kaname; Wakamatsu, Kan; Yamamoto, Koji; Nakamura, Yosuke
Phenothiazine cyclic hexamers: synthesis, properties, and complexation behavior with C<sub>60</sub>.
Chemical communications (Cambridge, England), 2024, 60, 2220-2223
7132662 CIFC84 H98 N13 O24 Sc3P 1 21/n 115.847; 16.418; 34.089
90; 101.579; 90		8689Wang, Hao; Shi, Le; Xiong, Zhangyi; Ma, Si; Cao, Honghao; Cai, Shijia; Qiao, Zhiwei; Pan, Jun; Chen, Zhijie
A two-dimensional metal-organic framework assembled from scandium-based cages for the selective capture of sulfur hexafluoride.
Chemical communications (Cambridge, England), 2024, 60, 2397-2400
7132663 CIFC25 H16 F3 N3 O2P 1 21/c 111.571; 21.464; 8.872
90; 107.385; 90		2102.8Lai, Dipti; Bhattacharjee, Suvam; Mandal, Saurodeep; Ghosh, Sumit; Sahoo, Prithidipa; Sinha, Subrata; Hajra, Alakananda
Iodine(III)-promoted oxidative carbotrifluoromethylation of maleimides with imidazopyridines and Langlois' reagent.
Chemical communications (Cambridge, England), 2024, 60, 2232-2235
7132664 CIFC38 H20 Co N6I 41/a :213.6416; 13.6416; 14.5402
90; 90; 90		2705.83Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132665 CIFC38 H20 Fe N6I 41/a :213.7275; 13.7275; 14.5027
90; 90; 90		2732.95Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132666 CIFC36 H20 Cl2 Mn N4I 41/a :213.789; 13.789; 14.4334
90; 90; 90		2744.32Mine, Kosuke; Arae, Sachie; Murakawa, Hiroshi; Tsuchiizu, Masahisa; Hanasaki, Noriaki; Matsuda, Masaki
Diamond lattice in single-component molecular crystals comprising tetrabenzoporphyrin neutral radicals.
Chemical communications (Cambridge, England), 2024, 60, 3019-3022
7132667 CIFC360 H380 B2 Cu58 F8 O12 P4 S36I 41/a c d :250.9312; 50.9312; 64.4799
90; 90; 90		167260Zhang, Qian; Zheng, Hao; Zhou, Jie; Yang, Jia-Ji; Xu, Kai-Yue; Shen, Lian-Yun; Guan, Zong-Jie; Yang, Yang
A bowl-shaped phosphangulene-protected cubic Cu<sub>58</sub> nanocluster.
Chemical communications (Cambridge, England), 2024, 60, 2389-2392
7132668 CIFC32 H34 Cl2 N2 O4P 21 21 2110.2222; 10.4342; 27.3088
90; 90; 90		2912.77Qiu, Xujun; Seibert, Jasmin; Fuhr, Olaf; Biedermann, Frank; Bräse, Stefan
Reversing the stereoselectivity of intramolecular [2+2] photocycloaddition utilizing cucurbit[8]uril as a molecular flask.
Chemical communications (Cambridge, England), 2024, 60, 3267-3270
7132669 CIFC38 H46 N10 O8 P4P -19.9127; 12.0311; 17.7893
96.019; 99.704; 95.561		2065.42Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132670 CIFC15 H18.8 N5 O2 PP -19.0435; 10.15596; 10.73364
108.653; 99.9637; 113.648		802.4Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132671 CIFC52 H80 N20 O12 P4 Zn2P 1 21/n 117.7137; 10.1405; 18.5083
90; 92.467; 90		3321.49Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132672 CIFC46 H66 Co2 N18 O10 P4P 1 21/n 112.2983; 10.2366; 22.8341
90; 94.766; 90		2864.7Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132673 CIFC52 H80 Co2 N20 O12 P4P 1 21/n 117.5968; 10.1687; 18.3843
90; 92.14; 90		3287.3Shayan, Mohsen; Abdollahi, Maryam F.; Lawrence, Mason Chester; Guinand, Etienne C.; Goulet, Maxime; George, Tanner; Masuda, Jason D.; Katz, Michael J.; Laventure, Audrey; Werner-Zwanziger, Ulrike; Chitnis, Saurabh S.
Rigid PN cages as 3-dimensional building blocks for crystalline or amorphous networked materials.
Chemical communications (Cambridge, England), 2024, 60, 2629-2632
7132674 CIFB2 F O4 SbP -14.3436; 6.3169; 7.0009
92.888; 95.126; 104.803		184.44Hu, Chenhui; Wu, Mengfan; Han, Jian; Yang, Zhihua; Han, Shujuan; Pan, Shilie
New antimony fluorooxoborates with strong birefringence and unprecedented structural characterisation.
Chemical communications (Cambridge, England), 2024, 60, 2653-2656
7132675 CIFC19 H16 F2 O2P c a 217.534; 12.716; 15.945
90; 90; 90		1527.6Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132676 CIFC27 H24 N4 OI 41/a :224.3936; 24.3936; 16.9622
90; 90; 90		10093.3Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132677 CIFC27 H24 N4 OP b c n26.264; 9.4519; 18.6059
90; 90; 90		4618.8Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132678 CIFC27 H22 Cl2 N4 OP 1 21 110.1692; 9.7507; 23.6934
90; 101.686; 90		2300.67Yu, Jiulong; Wu, Jinyu; Zhu, Yu; Xiong, Dong; Yang, Lin; Li, Jun; Zheng, Jianfeng
Chiral phosphoric acid-catalyzed enantioselective [5+1] cycloaddition reaction of <i>C</i>,<i>N</i>-cyclic azomethine imines with isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2637-2640
7132679 CIFC23 H18 Br N3 O2P 1 21/c 17.8608; 18.2829; 13.4885
90; 96.3335; 90		1926.7Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132680 CIFC23 H18 Br N3 OP 1 21/n 19.9612; 15.0034; 13.3232
90; 99.6334; 90		1963.1Aghaie, Kimia; Amiri, Kamran; Rezaei-Gohar, Mohammad; Rominger, Frank; Dar'in, Dmitry; Sapegin, Alexander; Balalaie, Saeed
Transition-metal-free intramolecular double hydrofunctionalization of alkyne to access 6/7/5-fused heterocyclic skeletons.
Chemical communications (Cambridge, England), 2024, 60, 2661-2664
7132681 CIFC26 H19 Mo O6 PP 1 21/c 19.4364; 30.672; 24.941
90; 94.189; 90		7199.5Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132682 CIFC24 H24 Br O3 PP -19.5566; 10.874; 12.1513
97.716; 112.057; 109.43		1054.03Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132683 CIFC21 H19 O PP -18.1143; 8.9827; 12.4136
94.652; 90.566; 113.742		824.6Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132684 CIFC24 H24 Br O2 PP -18.8789; 9.5863; 13.4826
84.831; 87.383; 65.062		1036.32Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132685 CIFC28 H23 Mo O6 PP -19.4957; 18.3164; 22.5419
99.296; 92.701; 95.011		3846.9Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132686 CIFC29 H26 Br O2 PP -18.9276; 10.5777; 14.307
69.469; 84.259; 72.909		1209.4Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer
Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Chemical communications (Cambridge, England), 2024, 60, 2625-2628
7132687 CIFC20 H15 F OP b c a16.4099; 10.0684; 18.6788
90; 90; 90		3086.1Zhang, Zhou; Li, Jin; Cai, Zhiwei; Kang, Songyao; Wang, Jian; Cui, Yue; Han, Siyuan; Sheng, Lei; Yin, Qing; Dai, Ang; Zhao, Weining; Zhao, Fangyuan
Electrochemical aerobic Wacker-type oxygenation of triaryl substituted alkenes to 1,2,2-triarylethanones.
Chemical communications (Cambridge, England), 2024, 60, 3035-3038
7132688 CIFC23 H18 N2 OP 21 21 216.2987; 7.8754; 36.641
90; 90; 90		1817.57Wang, Mingxu; Gao, Ying; Zhao, Xiao-Jing; Gao, Lu; He, Yonghui
Electrochemical multicomponent [2+2+1] cascade cyclization of enaminones and primary amines towards the synthesis of 4-acylimidazoles.
Chemical communications (Cambridge, England), 2024, 60, 2677-2680
7132689 CIFC56 H71 Cl Ga Ge N2P -111.3222; 12.2948; 20.0701
98.212; 91.794; 114.236		2508.9Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132690 CIFC53 H66 Cl Ga Ge N2 P4C 1 2/c 145.016; 10.0401; 23.339
90; 102.56; 90		10296Bücker, Anna; Gehlhaar, Alexander; Wölper, Christoph; Schulz, Stephan
Activation of non-polar bonds by an electron-rich gallagermylene.
Chemical communications (Cambridge, England), 2024, 60, 2902-2905
7132691 CIFC33 H21 F OP 21 21 218.733; 16.125; 16.631
90; 90; 90		2342Hore, Soumyadip; Singh, Abhijeet; Singh, Ravi P.
Asymmetric 1,2-diaxial synthesis of bi-(hetero)aryl benzofulvene atropisomers <i>via</i> transient directing group-assisted dehydrogenative coupling.
Chemical communications (Cambridge, England), 2024, 60, 2524-2527
7132692 CIFC44 H36 Br Cl2 N3P 1 21/c 115.5477; 14.2729; 16.1793
90; 92.941; 90		3585.6Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132693 CIFC57 H46 Au Br Cl8 N2P 1 21/m 110.2999; 14.4369; 17.7726
90; 98.815; 90		2611.5Bernt, Felix; Leonhardt, Christopher M.; Schatz, Dominic; Wegner, Hermann A.
Synthesis and investigation of a <i>meta</i>[6]cycloparaphenylene gold(I) <i>N</i>-heterocyclic carbene complex.
Chemical communications (Cambridge, England), 2024, 60, 3055-3058
7132694 CIFC78 H102 O2 P2 Si2P -114.1352; 15.4491; 19.4502
85.75; 69.641; 64.337		3574.6Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132695 CIFC46 H32 Cl6 O2 P2 SP -114.0465; 14.1358; 14.4268
118.189; 92.506; 114.771		2185.5Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132696 CIFC29 H21 O2 PP 1 21/c 19.475; 18.8265; 12.489
90; 109.249; 90		2103.26Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132697 CIFC58 H44 N6 O2 P2P -19.9714; 10.8463; 22.5248
77.043; 86.915; 82.273		2351.83Tokura, Yu; Xu, Shibo; Yasui, Kosuke; Nishii, Yuji; Hirano, Koji
Pd-catalysed C-H alkynylation of benzophospholes.
Chemical communications (Cambridge, England), 2024, 60, 2792-2795
7132698 CIFC24 H26 O5 SP 1 21/n 110.416; 19.09; 11.659
90; 113.372; 90		2128.1Mishra, Manmath; Verma, Kshitiz; Banerjee, Sonbidya; Punniyamurthy, Tharmalingam
Iron-catalyzed cascade C-C/C-O bond formation of 2,4-dienals with donor-acceptor cyclopropanes: access to functionalized hexahydrocyclopentapyrans.
Chemical communications (Cambridge, England), 2024, 60, 2788-2791
7132699 CIFC14 H19 N O3P 1 21/c 18.4622; 17.4106; 10.0167
90; 109.344; 90		1392.47Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132700 CIFC17 H17 N O3P 1 21/n 110.8048; 10.1624; 14.3028
90; 110.088; 90		1474.95Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132701 CIFC13 H16 Cl N O3P 1 21/c 18.5014; 16.7568; 10.0698
90; 105.68; 90		1381.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132702 CIFC16 H14 Cl N O3P 1 21/c 110.9337; 9.852; 14.5888
90; 111.998; 90		1457.08Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132703 CIFC27 H35 Cl N2 O6P 1 21 18.5052; 16.9899; 10.0551
90; 107.507; 90		1385.69Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132704 CIFC30 H33 Cl N2 O6P 1 21 110.7599; 9.7943; 14.5273
90; 111.649; 90		1422.98Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132705 CIFC29 H30 Cl2 N2 O6P 1 21 110.7438; 9.7103; 14.4644
90; 110.923; 90		1409.5Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132706 CIFC16 H15 N O3P 1 21/c 111.2259; 9.0079; 14.0101
90; 107.097; 90		1354.12Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132707 CIFC31 H36 N2 O6P 1 21 110.6827; 9.9438; 14.441
90; 110.66; 90		1435.37Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132708 CIFC33 H31 Cl N2 O6P 1 21 110.8824; 10.0217; 14.4325
90; 111.003; 90		1469.44Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132709 CIFC13 H17 N O3P 1 21/c 110.7023; 9.0828; 13.337
90; 103.692; 90		1259.61Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132710 CIFC30 H33 Cl N2 O6P 1 21 110.7094; 9.8205; 14.5002
90; 111.286; 90		1420.97Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132711 CIFC31 H30 F6 N2 O6P 1 21 113.8243; 9.1832; 13.8585
90; 117.871; 90		1555.27Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132712 CIFC33 H29 F3 N2 O6P 1 21 112.9498; 9.6063; 13.1925
90; 117.118; 90		1460.7Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132713 CIFC29 H32 N2 O6P 1 21 110.9173; 9.1344; 14.1599
90; 108.014; 90		1342.85Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132714 CIFC30 H31 F3 N2 O6P 1 21 111.4316; 9.5763; 14.2272
90; 111.456; 90		1449.55Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132715 CIFC14 H16 F3 N O3P 1 21/c 18.966; 17.0296; 10.0714
90; 107.371; 90		1467.64Koch, Katelyn N.; Teo, Aaron J.; Wheeler, Kraig A.
Dual space divergence in small molecule quasiracemates: benzoyl leucine and phenylalanine assemblies.
Chemical communications (Cambridge, England), 2024, 60, 2800-2803
7132716 CIFC20 H38 K16 N2 Na10.5 O218 P7 W39 Zr3P 31 2 122.6518; 22.6518; 75.9558
90; 90; 120		33751.8Yang, Dongsheng; Liu, Lihua; Zhang, Yunfan; Zhang, Miao; Ma, Pengtao; Wang, Jingping; Niu, Jingyang
A wheel-shaped Zr-substituted phosphotungstate [{Zr(C<sub>2</sub>O<sub>4</sub>)<sub>2</sub>}<sub>3</sub> (PO<sub>4</sub>)(P<sub>6</sub>W<sub>39</sub>O<sub>150</sub>)]<sup>39-</sup> with tunable proton conduction properties.
Chemical communications (Cambridge, England), 2024, 60, 3043-3046
7132717 CIFC20 H48 N10 P2 UP 1 21/n 19.909; 10.674; 14.833
90; 104.484; 90		1519Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132718 CIFC40 H98 N10 P4 U2P -110.769; 13.579; 20.817
82.853; 79.684; 69.571		2800.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132719 CIFC40 H96 N20 P4 U2P 21 21 210.5753; 27.797; 10.3786
90; 90; 90		3050.9Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132720 CIFC40 H96 N20 P4 U2C 1 2/c 125.24; 10.392; 25.465
90; 110.915; 90		6239Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132721 CIFC40 H96 N20 P4 U2C 1 2/c 125.206; 10.392; 25.457
90; 110.647; 90		6240Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132722 CIFC20 H48 N10 P2 UC 1 2/c 125.309; 10.4218; 25.538
90; 110.799; 90		6297.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132723 CIFC40 H96 N20 P4 U2C 1 2/c 125.279; 10.4213; 25.477
90; 110.786; 90		6274.8Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132724 CIFC40 H96 N20 P4 U2P 21 21 210.5761; 27.7942; 10.3688
90; 90; 90		3048Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132725 CIFC80 H192 N40 P8 U4P 1 2/n 124.9458; 10.2858; 25.3172
90; 111.158; 90		6058.2Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132726 CIFC20 H48 N10 P2 UP 1 21/n 110.1931; 10.6719; 14.9477
90; 102.736; 90		1586Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132727 CIFC20 H48 N10 P2 UP 1 21/n 19.8845; 10.6539; 14.7678
90; 104.838; 90		1503.32Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132728 CIFC40 H96 N20 P4 U2P 21 21 210.5757; 27.8005; 10.3708
90; 90; 90		3049.1Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132729 CIFC40 H96 N20 P4 U2P 1 2/n 124.9421; 10.2665; 25.3542
90; 111.169; 90		6054.3Li, Kai; Rajeshkumar, Thayalan; Zhao, Yue; Wang, Tianwei; Maron, Laurent; Zhu, Congqing
Temperature induced single-crystal to single-crystal transformation of uranium azide complexes.
Chemical communications (Cambridge, England), 2024, 60, 2966-2969
7132730 CIFC16 H14 Cl2 N2 O2 SnC 1 c 110.7059; 14.2716; 10.8582
90; 101.977; 90		1622.91Žáková, Andrea; Saha, Pritha; Paparakis, Alexandros; Zábranský, Martin; Gastelu, Gabriela; Kukla, Jaroslav; Uranga, Jorge G.; Hulla, Martin
Hexacoordinated tin complexes catalyse imine hydrogenation with H<sub>2</sub>.
Chemical communications (Cambridge, England), 2024, 60, 3287-3290
7132731 CIFC51 H40 B Cl4 N OP -19.2148; 13.8751; 16.7722
74.99; 87.948; 80.579		2043.28Huang, Yong; Jia, Mengjiao; Li, Chuan; Yang, Yang; He, Yuling; Luo, Yanju; Huang, Yan; Zhou, Liang; Lu, Zhiyun
A spiroacridine-based thermally activated delayed fluorescence emitter for high-efficiency and narrow-band deep-blue OLEDs.
Chemical communications (Cambridge, England), 2024, 60, 3194-3197
7132732 CIFC194 H142 Ag14 Cl4 F36 P8 Pd S6P 1 21/c 117.46; 36.131; 18.471
90; 110.07; 90		10945Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132733 CIFC183 H171 Ag14 O21 P7 Pd S6P -119.457; 20.805; 27.84
82.006; 74.854; 84.149		10747Ma, Along; Ren, Yonggang; Zuo, Yang; Wang, Jiawei; Huang, Shutong; Ma, Xiaoshuang; Wang, Shuxin
Ligand-controlled exposure of active sites on the Pd<sub>1</sub>Ag<sub>14</sub> nanocluster surface to boost electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 3162-3165
7132734 CIFC18 H15 Br O3P 1 21 17.2004; 6.8661; 16.0022
90; 100.88; 90		776.91Sarkar, Rahul; Korell, Alexander; Schneider, Christoph
Organocatalytic enantioselective oxa-Piancatelli rearrangement.
Chemical communications (Cambridge, England), 2024, 60, 3063-3066
7132735 CIFC66 H58 Hg O P4 S2C 1 2/c 124.571; 14.09; 20.038
90; 122.893; 90		5825Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132736 CIFC31 H26 P2 SP 1 21/n 19.72967; 15.22975; 16.93649
90; 91.2641; 90		2509.05Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132737 CIFC58 H63 Cl P2 S UP -112.0774; 14.1627; 14.3748
94.016; 90.702; 93.297		2448.4Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132738 CIFC43 H49 K O6 P2 SP -19.4692; 10.8945; 21.4146
77.036; 83.374; 73.667		2062.75Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132739 CIFC58 H63 Cl P2 S ThP -112.1389; 14.1799; 14.3984
94.193; 90.436; 93.016		2468.15Jörges, Mike; Gremillion, Alexander J.; Knyszek, Daniel; Kelley, Steven P.; Walensky, Justin R.; Gessner, Viktoria H.
From a mercury(II) bis(yldiide) complex to actinide yldiides.
Chemical communications (Cambridge, England), 2024, 60, 3190-3193
7132740 CIFC19 H20 N2 OP 1 21/c 18.637; 13.293; 29.631
90; 96.679; 90		3378.9Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132741 CIFC26 H28 N4C 1 2/c 115.2301; 10.2357; 28.4109
90; 95.828; 90		4406.1Zhang, Min; Zheng, Yongpeng; Jin, Yangbin; Jiang, Huanfeng; Wu, Wanqing
Palladium-catalyzed ligand-regulated divergent synthesis of pyrrole[2,3-<i>b</i>]indoles and ureas from 2-ethynylanilines and isocyanides.
Chemical communications (Cambridge, England), 2024, 60, 2950-2953
7132742 CIFC34 H28 B2 F6 N4P -18.4898; 11.7179; 16.2792
90.732; 99.945; 95.106		1588.18McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132743 CIFC17 H15 B F4 N2P 1 21 110.3062; 7.7018; 10.3247
90; 101.056; 90		804.326McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132744 CIFC34 H28 B2 F6 N4P -18.359; 11.6452; 16.1214
90.762; 100.271; 94.709		1538.31McDonald, Peter W.; Ritchie, Chris
A multi-chromic boron trifluoride-pyridyl Lewis adduct.
Chemical communications (Cambridge, England), 2024, 60, 3051-3054
7132745 CIFC5 H8 Er N3 O8P c c a8.2526; 6.5427; 19.313
90; 90; 90		1042.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132746 CIFC5 H8 Er N3 O8P c c a8.1956; 6.534; 19.322
90; 90; 90		1034.7Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132747 CIFC5 H8 Er N3 O8P c c a8.4551; 6.584; 19.2134
90; 90; 90		1069.58Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132748 CIFC5 H8 Er N3 O8P c c a7.8462; 6.5142; 19.58
90; 90; 90		1000.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132749 CIFC5 H8 Er N3 O8P c c a8.3154; 6.549; 19.234
90; 90; 90		1047.44Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132750 CIFC5 H8 Er N3 O8P c c a8.3583; 6.5585; 19.218
90; 90; 90		1053.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132751 CIFC5 H8 Er N3 O8P c c a7.801; 6.5107; 19.64
90; 90; 90		997.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132752 CIFC5 H8 Er N3 O8P c c a8.4958; 6.5946; 19.201
90; 90; 90		1075.76Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132753 CIFC5 H8 Er N3 O8P c c a7.736; 6.479; 19.71
90; 90; 90		988Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132754 CIFC5 H8 Er N3 O8P c c a8.4154; 6.5724; 19.21
90; 90; 90		1062.49Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132755 CIFC6 H10 Er N O8P 1 2/n 19.1183; 8.948; 13.1042
90; 96.446; 90		1062.4Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132756 CIFC6 H10 Er N O8P 1 2/n 19.1326; 8.974; 13.1405
90; 96.41; 90		1070.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132757 CIFC6 H10 Er N O8P 1 2/n 19.1263; 8.963; 13.1305
90; 96.44; 90		1067.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132758 CIFC6 H10 Er N O8P 1 2/a 19.0759; 8.863; 6.4822
90; 96.228; 90		518.3Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132759 CIFC6 H10 Er N O8P 1 2/a 19.0907; 8.903; 6.5091
90; 96.38; 90		523.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132760 CIFC6 H10 Er N O8P 1 2/n 19.1539; 8.9987; 13.1797
90; 96.604; 90		1078.5Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132761 CIFC6 H10 Er N O8P 1 2/a 19.0471; 8.792; 6.4339
90; 96.131; 90		508.8Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132762 CIFC6 H10 Er N O8P 1 2/n 19.1533; 8.9945; 13.1812
90; 96.747; 90		1077.68Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132763 CIFC6 H10 Er N O8P 1 2/a 19.1025; 8.913; 6.5273
90; 96.442; 90		526.2Hitchings, Thomas J.; Scatena, Rebecca; Allan, David R.; Cairns, Andrew B.; Saines, Paul J.
Negative linear compressibility exhibited by the hybrid perovskite [(NH<sub>2</sub>)<sub>3</sub>C]Er(HCO<sub>2</sub>)<sub>2</sub>(C<sub>2</sub>O<sub>4</sub>).
Chemical communications (Cambridge, England), 2024, 60, 3271-3274
7132764 CIFC141 H123 Ag4 Cd6 N7 O2 S16I 1 2/m 115.6408; 26.8262; 40.7797
90; 90.156; 90		17110.4Li, Yan-Ling; Liu, Yu-Dong; Li, Wei-Li; Li, Fu-An; Feng, Yun-Xiao; Luo, Xiao-Qiang; Han, Yong-Jun
Ligand engineering to achieve synergistic properties in a 2D bilayer supertetrahedral chalcogenide cluster-based assembled material.
Chemical communications (Cambridge, England), 2024, 60, 3279-3282
7132765 CIFC35 H36 N2 O9P -110.6256; 14.683; 20.9217
110.478; 90.035; 90.542		3057.7Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132766 CIFC71 H73 Cl3 N4 O16 S2P -110.084; 15.1221; 22.373
100.593; 94.039; 95.97		3321.3Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132767 CIFC124 H120 N8 O24P 1 21/n 117.0682; 11.8271; 27.346
90; 106.721; 90		5286.9Emenike, Bright U.; Shinn, David W.; Spinelle, Ronald A.; Yoo, Barney; Rosario, Ambar M.
Quantifying macrocyclization-induced strain utilizing <i>N</i>-phenylimides as conformational reporters.
Chemical communications (Cambridge, England), 2024, 60, 4040-4043
7132768 CIFC23 H18 Cl3 N O2P 21 21 215.5787; 13.2751; 27.4431
90; 90; 90		2032.4Wei, Jian; Du, Zhongjian; Wang, Xu; Ji, Chenlei; Li, Longji; You, Yang'en
Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors.
Chemical communications (Cambridge, England), 2024, 60, 3303-3306
7132769 CIFC29 H31 N3 O6 SP -18.2702; 12.562; 13.769
89.503; 79.822; 87.707		1406.8Samantaray, Swati; Maharana, Prabhat Kumar; Kar, Subhradeep; Saha, Sharajit; Punniyamurthy, Tharmalingam
Redox-neutral zinc-catalyzed cascade [1,4]-H shift/annulation of diaziridines with donor-acceptor aziridines.
Chemical communications (Cambridge, England), 2024, 60, 3441-3444
7132770 CIFC13 H14 Cl N O4 SP 1 21 15.5934; 10.4137; 12.5612
90; 97.969; 90		724.6Wan, Chuan; Yang, Dongyan; Guo, Xiaochun; Zhang, Tuanjie; Ruan, Zhijun; Dai, Chuan; Xing, Yun; Yin, Feng; Wang, Rui; Li, Zigang
β-Carbonyl sulfonium enables cysteine-specific bioconjugation for activity-based protein profiling in live cells.
Chemical communications (Cambridge, England), 2024, 60, 3725-3728
7132771 CIFC26.68 H32.49 N6 O1.56R -3 :H37.3204; 37.3204; 9.7227
90; 90; 120		11727.6Kang, Xiang; Zhang, Mingtao; Tang, Weiwei; Gong, Junbo
Growth "self-inhibition" of irbesartan desmotrope: surface intra-annular tautomer inter-conversion is the culprit.
Chemical communications (Cambridge, England), 2024, 60, 3511-3514
7132772 CIFC12 H14 Cl4 N2 O4 Pb S2P 1 21/c 14.3263; 18.5138; 12.3948
90; 97.504; 90		984.27Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132773 CIFC12 H12 Br4 N2 O4 Pb S2P 1 21/c 14.4621; 19.0334; 12.5804
90; 98.489; 90		1056.73Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132774 CIFC12 H12 I4 N2 O4 Pb S2P 1 21/c 14.6903; 19.9065; 12.82
90; 99.393; 90		1180.92Wang, Jing; Yang, Jin-Hai; Chen, Jie; Wang, Shuai-Hua; Chen, Yong-Jun; Xu, Gang
1D Pb halide perovskite-like materials for high performance X-ray detection.
Chemical communications (Cambridge, England), 2024, 60, 3311-3314
7132775 CIFC62 H66 N10 O14 S4C 1 2/c 137.954; 10.748; 24.5839
90; 93.542; 90		10009.3Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132776 CIFC42 H48 N8 O16 S4P 1 21/c 112.9205; 27.6064; 15.3072
90; 113.718; 90		4998.72Huang, Ming-Feng; Cao, Li-Hui; Zhou, Bin
A solvent-controlled photoresponsive ionic hydrogen-bonded organic framework for encryption applications.
Chemical communications (Cambridge, England), 2024, 60, 3437-3440
7132777 CIFC41 H33 N O7 SP 1 21 19.1592; 17.6405; 10.2784
90; 94.192; 90		1656.27Barik, Shilpa; Sankar, Ganga; Biju, Akkattu T.
Enantioselective synthesis of tricyclic oxoquinolines <i>via</i> NHC-catalyzed Michael-aldol-lactamization-dehydration cascade.
Chemical communications (Cambridge, England), 2024, 60, 4290-4293
7132778 CIFC18 H14 Ca F9 N3 O8P 1 21/n 124.1213; 8.1633; 24.2668
90; 98.981; 90		4719.8Baudet, Judith; Lesur, Emilie; Ribéraud, Maxime; Chevalier, Arnaud; D'Anfray, Timothée; Thuéry, Pierre; Audisio, Davide; Taran, Frédéric
Synthesis of sydnonimines from sydnones and their use for bioorthogonal release of isocyanates in cells.
Chemical communications (Cambridge, England), 2024, 60, 3657-3660
7132779 CIFC36 H92 I2 K O10 Si8 UP -113.4213; 15.8641; 16.3965
104.442; 102.934; 96.066		3246.4Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132780 CIFC36 H98 I2 K O11 Si8 UP 1 2/c 114.8717; 15.8095; 28.9025
90; 103.785; 90		6599.7Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132781 CIFC40 H98 I2 K O10 Si8 UC 1 2/c 149.049; 13.108; 21.124
90; 90.054; 90		13581Lin, Nathan J.; Zeller, Matthias; Bart, Suzanne C.
Solution and solid-state characterization of rare silyluranium(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3954-3957
7132782 CIFC27 H15 B F N5P -18.0536; 8.9238; 15.0934
79.306; 85.035; 65.599		970.63Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132783 CIFC34 H22 B Cl2 N5P -19.3419; 10.0645; 14.7904
91.141; 105.751; 90.019		1338.11Kage, Yuto; Jiang, Yuchuan; Minakuchi, Namiki; Mori, Shigeki; Shimizu, Soji
One-pot synthesis of azabora[6]helicene by a Schiff base forming reaction.
Chemical communications (Cambridge, England), 2024, 60, 3543-3546
7132784 CIFC16 H13 F2 N OP 1 21/n 110.169; 10.856; 12.0502
90; 102.79; 90		1297.27Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132785 CIFC16 H13 F2 N OP -19.7065; 11.7198; 12.029
77.71; 89.322; 71.433		1265.13Wang, Xuan; Li, Jianlong; Du, Haifang; Liang, Weihong; Luo, Cheng; Wu, Yunshan; Liu, Bo
Synthesis of 1,4-epoxy-2-aryltetrahydro-1-benzazepines <i>via</i> rhodium(III)-catalyzed C-H allylation/intramolecular 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2024, 60, 2401-2404
7132786 CIFC210 H228 Ag3 B F4 N36 O24R 3 2 :H38.1751; 38.1751; 37.5163
90; 90; 120		47349Bajpayee, Nikhil; Pophali, Salil; Vijayakanth, Thangavel; Nandi, Shyamapada; Desai, Aamod V.; Kumar, Vinod; Jain, Rahul; Bera, Santu; Shimon, Linda J. W.; Misra, Rajkumar
Metal-driven folding and assembly of a minimal β-sheet into a 3D-porous honeycomb framework.
Chemical communications (Cambridge, England), 2024, 60, 2621-2624
7132787 CIFC76 H65 Cu2 N20 O16.5P 4319.7601; 19.7601; 19.9303
90; 90; 90		7782Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132788 CIFC40 H33 Cl4 Cu2 N9 OP 1 21/n 115.805; 9.323; 27.137
90; 99.835; 90		3939.9Qiu, Zhao-Feng; Wang, Peng; Zhang, Xiao-Yu; Chen, Jia-Qi; Zhang, Kai-Yang; Lu, Xiang-Yu; Zhao, Yue; Sun, Wei-Yin
Supramolecular assemblies of Cu(II) with a tetraphenylethene-imidazole ligand for tuning photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2024, 60, 2204-2207
7132789 CIFC41.5 H45.5 N6.5 O18 Tb TiP m -3 n25.9298; 25.9298; 25.9298
90; 90; 90		17434Yao, Qingxia; Pan, Xuze; Si, Xuezhen; Wang, Xin; Zhang, Xiaoying; Hou, Jinle; Su, Jie; Qiu, Yi; Li, Jun
A porous and photoactive Ti-MOF based on a novel tetranuclear [Ti<sub>2</sub>Tb<sub>2</sub>] cluster.
Chemical communications (Cambridge, England), 2024, 60, 2188-2191
7132790 CIFC29 H32 N2 O5P -111.4759; 11.5363; 19.7187
85.779; 79.152; 85.444		2551.2Lai, Jingxiong; Huang, You
A highly diastereoselective (5+1) annulation of allenoates and pyrazolones catalyzed by CH<sub>3</sub>OK.
Chemical communications (Cambridge, England), 2024, 60, 2066-2069
7132791 CIFC10 H19 N O3P 1 21 15.4153; 11.2753; 9.4479
90; 98.633; 90		570.34Zhang, Qiuxin; Zhang, Heng; Geng, Senbai; Zhao, Xian; Liu, Shucheng; Hong, Kun; Pan, Jianming; Yan, Xingchen
Green transformation of CO<sub>2</sub> into γ-amino alcohols with continuous stereocenters.
Chemical communications (Cambridge, England), 2024, 60, 2062-2065
7132792 CIFC52 H52 B2 Hg N14 O4 Se2 W2P -113.7335; 21.8752; 22.673
117.984; 91.487; 103.84		5764.1Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132793 CIFC20 H23 B N6 O2 Se WP 1 21/c 17.9715; 18.2689; 19.7379
90; 101.415; 90		2817.58Onn, Chee S.; Hill, Anthony F.; Ward, Jas S.
Spodium bonding in bis(alkynyl)mecurials.
Chemical communications (Cambridge, England), 2024, 60, 2552-2555
7132794 CIFC29 H43 B N6 O2 Si Te WP -110.6281; 11.0432; 15.1354
84.687; 87.521; 75.938		1715.38Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132795 CIFC21 H30 Au B Cl6 N6 O2 S Te WP -111.1523; 11.161; 14.3505
89.093; 89.186; 77.275		1742.02Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132796 CIFC64 H100 B2 Cl4 Cu4 N12 O4 Si2 Te2 W2P 1 21/n 110.9539; 18.7716; 20.4333
90; 102.63; 90		4099.87Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132797 CIFC24 H27 B N8 O2 Te WP 1 21 17.9095; 18.2594; 9.7522
90; 99.742; 90		1388.13Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132798 CIFC23 H31 Au B Cl N6 O2 S Si WP 1 21/m 112.3181; 24.9472; 16.5061
90; 108.592; 90		4807.6Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132799 CIFC26 H27 B N6 O2 Te WP 1 21/n 120.5319; 14.2779; 21.6073
90; 117.804; 90		5602.9Onn, Chee S.; Hill, Anthony F.
Carbon-chalcogen wires: alkynyltellurolatocarbynes.
Chemical communications (Cambridge, England), 2024, 60, 3555-3558
7132800 CIFC33 H28 F3 N3 O2P 21 21 218.2405; 13.6044; 25.8384
90; 90; 90		2896.67Wang, Lan; Lu, Mengxi; Li, Kuan; Yang, Sen; Wang, Lei; Guo, Hongchao
Palladium-catalyzed enantioselective umpolung allylation of amido-tethered allylic carbonates with isatin-derived ketimines.
Chemical communications (Cambridge, England), 2024, 60, 3729-3732
7132801 CIFC22 H17 F N2P 1 21/c 16.2418; 18.1094; 15.2988
90; 96.701; 90		1717.49Qin, Jiaze; Jiang, Shixuan; Luo, Xiaofeng; Wang, Tianqiang; Liu, Peihua; Yuan, Bingxiang; Yan, Rulong
I<sub>2</sub>-catalyzed synthesis of 3-aminopyrrole with homopropargylic amines and nitrosoarenes.
Chemical communications (Cambridge, England), 2024, 60, 3701-3704
7132802 CIFC38 H28 N8P 1 21/n 111.5521; 9.4107; 32.526
90; 95.722; 90		3518.39Zhang, Li; Luo, Yu-Ting; Xiao, Sai-Jin; Fan, Jia-Qi; Tan, Quan-Gen; Sun, Chen; Song, An-Min; Liang, Ru-Ping; Qiu, Jian-Ding
The construction of a stable hydrogen-bonded organic framework for the photocatalytic reduction and removal of uranium.
Chemical communications (Cambridge, England), 2024, 60, 3583-3586
7132803 CIFC19 H17 Br O2P 21 21 217.1586; 11.9651; 18.845
90; 90; 90		1614.1Li, Zheyao; Zhang, Huiwen; Zhao, Lin; Ma, Yueyue; Wu, Qiufang; Ren, Haosong; Lin, Zhongren; Zheng, Jun; Yu, Xinhong
Metal-free β,γ-C(sp<sup>3</sup>)-H difunctionalization of propanols: DMP-initiated asymmetric spirocyclopropanation.
Chemical communications (Cambridge, England), 2024, 60, 3579-3582
7132804 CIFC29 H19 N O5P -19.9434; 11.2111; 11.3362
100.833; 92.317; 115.863		1106.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132805 CIFC29 H18 O6P 1 21/c 18.5559; 26.5; 9.988
90; 99.097; 90		2236.1Wang, Kai-Kai; Li, Yan-Li; Li, Ya-Fei; Yao, Wei-Wei; Li, Lan-Xin; He, Xiao-Long; Chen, Rongxiang
Substrate-controlled [4+1] and [3+2] annulations of ninhydrin-derived Morita-Baylis-Hillman carbonates to access polysubstituted furans and cyclopentenes.
Chemical communications (Cambridge, England), 2024, 60, 3717-3720
7132806 CIFC27 H23 NP 1 21/n 19.4988; 11.9651; 17.3667
90; 97.139; 90		1958.49Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132807 CIFC16 H14 O2P n a 2116.5657; 5.4295; 14.0697
90; 90; 90		1265.48Shinde, Jivan; Suresh, Sundaram; Kavala, Veerababurao; Yao, Ching-Fa
Pd(II)-catalyzed hydroarylations/hydroalkenylations of terminal alkynes: regioselective synthesis of allylic, homoallylic, and 1,3-diene systems.
Chemical communications (Cambridge, England), 2024, 60, 3790-3793
7132808 CIFC26 H23.62 Cl0.38 N2 O3 SP 1 21/n 110.908; 15.648; 14.141
90; 112.321; 90		2232.8Wang, Bi; Liang, Ren-Xiao; Shen, Zhen-Lu; Jia, Yi-Xia
Copper-catalyzed intramolecular dearomative aza-Wacker reaction of indole.
Chemical communications (Cambridge, England), 2024, 60, 3858-3861
7132809 CIFC20 H22 O2P 1 21 18.546; 6.518; 15.6
90; 105.428; 90		837.7Magham, Lakshmi Revati; Samad, Abdus; Thopate, Satish B.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
Organocatalytic enantioselective desymmetrization of enal-tethered cyclohexane-1,3-diones.
Chemical communications (Cambridge, England), 2024, 60, 3834-3837
7132810 CIFC18 H20 Cl N O2P -18.3513; 13.4596; 15.583
77.965; 76.1; 77.207		1635.64Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132811 CIFC18 H17 Cl F3 N OP 1 21/c 16.2156; 11.1571; 24.7517
90; 92.551; 90		1714.78Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132812 CIFC17 H24 Cl N OP 1 21/n 19.2235; 7.0079; 25.1221
90; 94.528; 90		1618.76Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132813 CIFC14 H18 Cl N OI 1 2/a 118.5653; 6.3699; 23.6434
90; 108.817; 90		2646.61Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132814 CIFC19 H22 Cl N OP 1 21/n 116.7373; 6.1891; 18.0916
90; 110.509; 90		1755.3Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132815 CIFC15 H20 Cl N OC 1 2/c 117.0047; 6.656; 24.757
90; 92.075; 90		2800.24Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132816 CIFC16 H22 Cl N OP 1 21/c 112.6132; 6.8258; 17.3255
90; 93.319; 90		1489.14Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132817 CIFC17 H18 Cl N OP 21 21 217.6345; 9.6295; 20.4737
90; 90; 90		1505.15Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132818 CIFC13 H18 Cl N OP -16.66649; 9.4285; 10.2117
93.58; 96.362; 93.083		635.47Campbell, Aaron D. G.; Roper, Natalie J.; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.; Denton, Ross M.; Ermanis, Kristaps; Armstrong, Roly J.
Synthesis, structure and stereodynamics of atropisomeric <i>N</i>-chloroamides.
Chemical communications (Cambridge, England), 2024, 60, 3818-3821
7132819 CIFC26 H44 B N2 SiP -110.212; 11.708; 12.522
106.885; 100.518; 90.377		1405.7Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132820 CIFC35 H62 B N3 O SiP 1 21/n 110.2572; 18.663; 19.5822
90; 99.642; 90		3695.67Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132821 CIFC66 H96 B2 N4 O2 Si2C 1 2/c 116.1834; 30.376; 17.5363
90; 113.974; 90		7876.9Wang, Hanqiang
Synthesis, structure and reactivity of iminoborane radicals.
Chemical communications (Cambridge, England), 2024, 60, 3806-3809
7132822 CIFC20 H15 Cl3 O2P 1 21/c 110.8147; 9.8903; 16.969
90; 104.319; 90		1758.6Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132823 CIFC24 H16 O2P 1 21/c 112.2366; 17.3994; 8.2782
90; 102.186; 90		1722.8Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132824 CIFC38 H30 Cl2 O2P -19.6677; 12.9019; 13.3368
73.28; 88.509; 71.049		1502.7Zhou, Hongxun; Li, Lijun; Yan, Qinqin; Ma, Jinyue; Wang, Ying; Gao, Yongjun; Liu, Zhong-Quan; Li, Zejiang
Metal-free radical bicyclization/chloroalkylarylation of 1,6-enynes with chloroalkanes.
Chemical communications (Cambridge, England), 2024, 60, 3938-3941
7132825 CIFC12 H11 Br2 N3 ZnP -17.8069; 7.8757; 11.9902
77.783; 85.879; 77.735		703.79Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132826 CIFC14 H17 Br2 N3 S ZnP -17.852; 10.8828; 11.3769
75.796; 74.568; 76.283		892.99Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132827 CIFC15 H19 Br2 N3 O S ZnP -17.5172; 10.647; 13.487
105.076; 92.008; 109.849		971.3Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132828 CIFC15 H17 Br2 N3 O S ZnP 1 21/c 17.3412; 19.033; 13.475
90; 98.398; 90		1862.6Samanta, Arup; Behera, Prativa; Chaubey, Amit; Mondal, Avijit; Pal, Debjyoti; Mohar, Kailash; Roy, Lisa; Srimani, Dipankar
Experimental and theoretical insights for designing Zn<sup>2+</sup> complexes to trigger chemo-selective hetero-coupling of alcohols.
Chemical communications (Cambridge, England), 2024, 60, 4056-4059
7132829 CIFC26 H26 Cl N3 O5P -18.2719; 10.9748; 14.3779
91.073; 98.225; 110.945		1203Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132830 CIFC28.01 H30.01 Br N3 O5P -111.0881; 11.9277; 12.1514
115.124; 105.133; 100.196		1326.22Li, Ming-Jun; Lu, Ming-Ming; Xu, Peng; Chen, Si-Qi; Wu, Luan-Ting; Zhang, Ze; Xu, Hui
Chemodivergent mechanosynthesis of cyclopentenyl and pyrrolinyl spirobarbiturates from unsaturated barbiturates and enamino esters.
Chemical communications (Cambridge, England), 2024, 60, 3958-3961
7132831 CIFC98 H72 Cl4 Cu2 F20 N8P 1 21/c 117.46; 22.68; 14.222
90; 95.69; 90		5604Dong, Yuting; Qian, Long; Chen, Feng; Wang, Yue; Zhang, Tao; Qiu, Fengxian; Teranishi, Toshiharu; Xue, Songlin
Benzene-fused porphyrin(2.1.2.1) array: synthesis, structure, and electrocatalytic hydrogen evolution.
Chemical communications (Cambridge, England), 2024, 60, 3986-3989
7132832 CIFC19 H17 F3 N2 O4 SP b c a19.2019; 13.9245; 28.2926
90; 90; 90		7564.8Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132833 CIFC18 H17 F3 N2 O4 SP b c a19.421; 13.8099; 27.8614
90; 90; 90		7472.49Lou, Mingliang; Liu, Xiaolei; Han, Shoule; Bai, Songlin; Qi, Xiangbing
Total synthesis of (±)-3-demethoxyerythratidinone <i>via</i> Tf<sub>2</sub>O-promoted cascade reaction of enaminone.
Chemical communications (Cambridge, England), 2024, 60, 3842-3845
7132834 CIFC20 H18 N2 O4.5 VP 1 21/c 115.3045; 8.8087; 13.3399
90; 98.687; 90		1777.76Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132835 CIFC55.66 H21.3 Cl3.31 F10 N8 Pd SP 1 21 113.3831; 7.1785; 26.0801
90; 93.166; 90		2501.71Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132836 CIFC45 H29 B Cl3 F4 N3 Pd SP -19.276; 14.42; 15.664
112.75; 91.73; 91.28		1930Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132837 CIFC74 H42 B F20 N3 Pd SP 1 21/n 113.546; 27.1678; 16.8019
90; 99.633; 90		6096.17Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132838 CIFC46 H32 Cl4 F6 N3 P Pd SP 1 21/c 113.77; 16.0819; 19.035
90; 90.479; 90		4215.1Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132839 CIFC55 H29 Cl3 N8 Pd SP -114.7468; 17.6065; 20.521
69.671; 82.618; 65.328		4539.2Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132840 CIFC47 H20.5 Cl0.5 F16 N3 P Pd SP n a 2128.14; 14.513; 20.554
90; 90; 90		8394Fujita, Masaki; Haketa, Yohei; Seki, Shu; Maeda, Hiromitsu
Substitution-pattern- and counteranion-dependent ion-pairing assemblies of heteroporphyrin-based π-electronic cations.
Chemical communications (Cambridge, England), 2024, 60, 4190-4193
7132841 CIFC20 H26 O4I 1 2/a 110.1083; 14.7871; 22.9034
90; 91.199; 90		3422.68Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132842 CIFC18 H24 O2P -19.864; 9.8656; 16.5931
105.165; 97.065; 105.295		1471Koyama, Ryosei; Anada, Masahiro; Sueki, Shunsuke; Makino, Kosho; Kojima, Tatsuhiro; Kawasaki-Takasuka, Tomoko; Mori, Keiji
Divergent synthesis of multi-substituted phenanthrenes <i>via</i> an internal redox reaction/ring expansion sequence.
Chemical communications (Cambridge, England), 2024, 60, 3822-3825
7132843 CIFC27 H15 Br O2P 1 21/c 117.7637; 15.582; 7.0233
90; 95.518; 90		1935Nishimoto, Mikey; Uetake, Yuta; Yakiyama, Yumi; Sakurai, Hidehiro
Strain-induced carbon-carbon bond cleavage of bowl-shaped sumanenone.
Chemical communications (Cambridge, England), 2024, 60, 3982-3985
7132844 CIFC14 H11 N3 O2P 21 21 218.1213; 11.1938; 13.6325
90; 90; 90		1239.31Bhattacharjee, Suvam; Hajra, Alakananda
Site-selective direct nitration of 2<i>H</i>-indazoles: easy access to 7-nitroindazoles.
Chemical communications (Cambridge, England), 2024, 60, 4076-4079
7132845 CIFC38 H61 N4 P2 Sc SiP 1 21/c 115.5452; 15.3097; 17.8477
90; 97.496; 90		4211.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132846 CIFC73 H110 N10 Ni2 P4 Sc2P -112.49; 12.54; 13.517
65.861; 73.439; 76.945		1837.3Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132847 CIFC46 H59 N6 Ni P2 ScP -110.9882; 11.7463; 18.988
74.157; 89.563; 72.84		2245.6Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132848 CIFC43 H57 N4 Ni P2 ScP -111.122; 11.696; 16.447
101.88; 96.172; 90.996		2079.8Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132849 CIFC48 H68 N5 Ni O1.5 P2 ScP -110.142; 10.213; 23.78
77.96; 79.02; 81.49		2350Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132850 CIFC118 H142 N10 Ni2 O2 P4 Sc2C 1 2/c 128.918; 11.542; 36.001
90; 109.45; 90		11330Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132851 CIFC43 H58 N5 Ni P2 ScP -112.237; 13.83; 15.21
68.64; 72.04; 64.89		2134Ma, Lei; Pan, Xiaowei; Hong, Dongjing; Fang, Huayi; Cui, Peng
A scandium metalloligand supported Ni(0) complex with a heterobimetallocycle: versatile reactivity with unsaturated bonds.
Chemical communications (Cambridge, England), 2024, 60, 4222-4225
7132852 CIFC21 H19 N O2P 1 21/c 110.0187; 15.8815; 10.6953
90; 99.728; 90		1677.28Karjee, Pallab; Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Punniyamurthy, Tharmalingam
One-pot C-N/C-C bond formation and oxidation of donor-acceptor cyclopropanes with tetrahydroisoquinolines: access to benzo-fused indolizines.
Chemical communications (Cambridge, England), 2024, 60, 4068-4071
7132853 CIFC22 H20 O5P 1 21/n 19.08906; 9.90544; 20.1477
90; 92.251; 90		1812.52Nambu, Hisanori; Onuki, Yuta; Aso, Kana; Kanamori, Momoka; Tomohara, Keisuke; Tsuge, Kiyoshi; Yakura, Takayuki
Ring expansion of spirocyclopropanes with stabilized sulfonium ylides: highly diastereoselective synthesis of cyclobutanes.
Chemical communications (Cambridge, England), 2024, 60, 4537-4540
7132854 CIFC21 H14 O2P 1 21/c 18.1483; 18.778; 9.9744
90; 98.77; 90		1508.3Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132855 CIFC21 H18 O4P -18.487; 10.1115; 10.5324
91.975; 93.296; 108.179		856.01Gopalakrishnan, Dinesh Kumar; Bhardwaj, Srashti; Kumar, Sandeep; Karmakar, Tarak; Vaitla, Janakiram
Carbene-mediated stereoselective olefination of vinyl sulfoxonium ylides with diazo compounds and acetals.
Chemical communications (Cambridge, England), 2024, 60, 3846-3849
7132856 CIFC27 H50 Mn3 N6 O53 P W9P 3 1 c18.9481; 18.9481; 29.4882
90; 90; 120		9168.8Liu, Fangcheng; Han, Shicheng; Dong, Liwei; Fang, Xikui
Functionalized polyoxometalates enable fast ion transport in solid-state batteries at room temperature.
Chemical communications (Cambridge, England), 2024, 60, 4198-4201
7132857 CIFC17 H18 OP 1 21 111.5667; 5.2499; 12.1291
90; 117.369; 90		654.08Wang, Kun; Niu, Saisai; Tang, Weijun; Xue, Dong; Xiao, Jianliang; Li, Hongfeng; Wang, Chao
Ru-catalyzed asymmetric hydrogenation of α,β-unsaturated ketones <i>via</i> a hydrogenation/isomerization cascade.
Chemical communications (Cambridge, England), 2024, 60, 4338-4341
7132858 CIFC30 H45 F5 O2P 1 21 112.4586; 9.2797; 13.4386
90; 105.661; 90		1495.99Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132859 CIFC31 H45 F7 O2P 1 21 112.9607; 8.8159; 13.5926
90; 106.421; 90		1489.74Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132860 CIFC32 H45 F9 O2P 1 21 112.299; 9.2607; 14.5611
90; 94.027; 90		1654.38Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132861 CIFC31 H45 F7 O2P 1 21 112.7803; 9.3254; 13.7005
90; 104.745; 90		1579.07Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132862 CIFC33 H45 F11 O2P 21 21 219.236; 12.542; 29.3792
90; 90; 90		3403.2Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132863 CIFC34 H45 F13 O2P 1 21 113.3455; 8.8735; 14.404
90; 90.499; 90		1705.68Jiang, Huan-Huan; Zhang, Nan; Mao, Wei-Xin; Lan, Jin-Fei; Zhou, Long-Xing; Xu, Hua-Ming; Zhang, Han-Yue; Liao, Wei-Qiang
Modulating the ferroelectric phases in cholesteryl-based organic compounds with perfluoroalkyl tail engineering.
Chemical communications (Cambridge, England), 2024, 60, 4322-4325
7132864 CIFC44 H53 Ca I N2 O2P 1 21/c 111.1453; 21.6411; 16.4519
90; 99.62; 90		3912.34Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132865 CIFC44 H53 I N2 O2 SrP 1 21/c 111.1365; 21.9592; 16.4408
90; 99.267; 90		3968.1Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132866 CIFC40 H57 N3 O Si2 SrC 1 2/c 122.9542; 9.945; 37.2321
90; 105.936; 90		8172.69Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132867 CIFC35.99 H48.98 Ca N3 Si2C 1 2/c 121.9451; 9.6032; 35.7576
90; 105.893; 90		7247.62Mondal, Sumana; Sarkar, Subham; Mandal, Chhotan; Mallick, Dibyendu; Mukherjee, Debabrata
Fluorenyl-tethered N-heterocyclic carbene (NHC): an exclusive C-donor ligand for heteroleptic calcium and strontium chemistry.
Chemical communications (Cambridge, England), 2024, 60, 4553-4556
7132868 CIFC88 H64 N16 Pt2C 1 2/m 114.2019; 21.4417; 19.1515
90; 98.888; 90		5761.9van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132869 CIFC100 H80 B4 F16 N16 Pt2P -111.1598; 14.8934; 17.8869
87.192; 75.514; 86.266		2870.67van Hilst, Quinn V. C.; Pearcy, Aston C.; Preston, Dan; Wright, L. James; Hartinger, Christian G.; Brooks, Heather J. L.; Crowley, James D.
A dynamic covalent approach to [Pt<sub><i>n</i></sub>L<sub>2<i>n</i></sub>]<sup>2<i>n</i>+</sup> cages.
Chemical communications (Cambridge, England), 2024, 60, 4302-4305
7132870 CIFC19 H17 Cl N2 O4P -19.6699; 9.6753; 10.4512
76.908; 71.347; 71.318		869.2Porashar, Bikoshita; Behera, Bipin Kumar; Phukon, Hunmoina; Saikia, Anil K.
Synthesis of tetrahydroquinazolines from 2-aminobenzonitriles and alkylidene malonates <i>via</i> 1,4-conjugate addition and an unprecedented rearrangement reaction.
Chemical communications (Cambridge, England), 2024, 60, 4358-4361
7132871 CIFC52 H34.66 Au3 Lu N20 O9.33P b c a19.9815; 23.8662; 23.8919
90; 90; 90		11393.6Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132872 CIFC52 H34.34 Au3 N20 O9.17 TbP b c a20.0668; 23.8472; 23.9197
90; 90; 90		11446.5Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132873 CIFC52 H34.51 Au3 Eu N20 O9.25P b c a20.1041; 23.8591; 23.936
90; 90; 90		11481.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132874 CIFC52 H34.4 Au3 Ce N20 O9.2P b c a20.2203; 23.8559; 23.9799
90; 90; 90		11567.3Karpiuk, Thomas E.; Mahato, Samyadeb; Storr, Tim; Leznoff, Daniel B.
Unusually short unsupported Au(III)⋯Au(III) aurophilic contacts in emissive lanthanide tetracyanoaurate(III) complexes.
Chemical communications (Cambridge, England), 2024, 60, 3914-3917
7132875 CIFC19 H16 O4P 1 21/c 110.9362; 17.792; 8.2146
90; 108.127; 90		1519.04Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132876 CIFC20 H22 O5 SC 1 2/c 121.549; 10.8252; 17.856
90; 113.929; 90		3807.3Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333
7132877 CIFC25 H22 O4P 1 21/c 110.2833; 10.038; 20.688
90; 98.406; 90		2112.6Zhou, Xinlong; Jiang, Jingjing; Zhang, Min; Wu, Qingqing; Zhu, Keyong; Shi, Dongjie; Hou, Sensen; Zhao, Jingjing; Li, Pan
Dioxane promoted photochemical <i>O</i>-alkylation of 1,3-dicarbonyl compounds beyond carbene insertion into C-H and C-C bonds.
Chemical communications (Cambridge, England), 2024, 60, 4330-4333

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