Crystallography Open Database

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7134684 CIFC26 H44 O3 SiP 111.0269; 11.0409; 12.3804
75.509; 65.961; 67.425
1263.2Chen, Louxi; Zhang, Chao-Han; Liu, Junyang; Li, Chuang-Chuang
Asymmetric synthesis of venezuelaene's core with a <i>trans</i>-fused [5-5] ring system.
Chemical communications (Cambridge, England), 2025, 61, 10823-10826
7134685 CIFC54 H55 B2 FP 1 21/n 18.4189; 21.0396; 12.3265
90; 92.698; 90
2180.98Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134686 CIFC56 H56 B2 Cl6 F2P -18.5609; 12.651; 13.4008
64.065; 78.326; 88.076
1275.71Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134687 CIFC54 H52 B2 F4P -18.8671; 9.2255; 14.6132
73.047; 76.892; 77.113
1097.76Wang, Zhen; Yang, Yuxuan; Fang, Luohan; Xie, Yangbin; Ma, Wenming; Zhang, Yahui; Sun, Chun-Lin; Zhang, Baoxin; Zhang, Xiaoxiang; Pan, Xiaobo
Efficient UV-matchable light-converting agent based on a space-conjugated di-triarylboron structure.
Chemical communications (Cambridge, England), 2025, 61, 11255-11258
7134688 CIFC28 H22 F2 N2 S2P 1 21/c 111.294; 22.7558; 9.1549
90; 92.8389; 90
2349.96Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134689 CIFC32 H30 F2 N2 S2C 1 2/c 119.0612; 12.1912; 13.5755
90; 121.113; 90
2700.86Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134690 CIFC34 H34 F2 N2 S2P 1 21/n 114.523; 10.6398; 19.0421
90; 91.6399; 90
2941.21Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134691 CIFC30 H26 F2 N2 S2C 1 2/c 119.4157; 10.9681; 13.8257
90; 121.068; 90
2521.9Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134692 CIFC30 H26 F2 N2 S2P b c n21.4133; 13.7635; 8.963
90; 90; 90
2641.59Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134693 CIFC44 H54 F2 N2 S2P -111.6733; 13.4099; 13.521
76.6459; 74.539; 85.3589
1984.37Fukata, Oka; Kitagawa, Daichi; Mutoh, Katsuya; Kobatake, Seiya
Twisting of aryl groups affects thermal back reactivity of diarylbenzene photoswitches.
Chemical communications (Cambridge, England), 2025, 61, 11057-11060
7134694 CIFC15 H20 N2 O2 SiP 1 21/c 16.99957; 18.62104; 12.07918
90; 90.6114; 90
1574.3Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134695 CIFC18 H16 N2 O2I 1 2/a 113.24004; 11.03585; 20.65862
90; 91.2541; 90
3017.81Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134696 CIFC20 H21 N3 O2P -112.27152; 12.39856; 12.5695
90.248; 91.2744; 109.745
1799.41Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134697 CIFC18 H15 N3 O4P 1 21/c 119.7442; 6.9809; 11.8207
90; 93.323; 90
1626.53Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134698 CIFC15 H19 N3 O4 SiP 1 21/c 115.2895; 10.2141; 10.8354
90; 93.648; 90
1688.72Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134699 CIFC20 H20 N4 O4I 1 2/a 112.63828; 12.14363; 24.6829
90; 90.3855; 90
3788.11Sosnin, Daniil; Aprahamian, Ivan
Alkyne hydrazones for Raman scattering spectroscopy
Chemical Communications, 2025, 61, 10119-10121
7134700 CIFC16 H15 N OP b c n10.8676; 11.428; 41.042
90; 90; 90
5097.21Li, Wenguang; Yu, Yongqi; Sheng, Heyun; Cao, Man; Chen, Ming; Gao, Wenchao; Zhang, Xu; Su, Fengyun; Li, Ting
Synthesis of cyclopropanes <i>via</i> palladium-catalyzed [2+1] annulations of sulfoxonium ylides and norbornenes.
Chemical communications (Cambridge, England), 2025, 61, 10835-10838
7134701 CIFC70 H40 O18 Th3P -110.1687; 11.9584; 25.02
91.179; 95.315; 90.783
3028.4Yang, Junpu; Bai, Yaoyao; Zhang, Guangtao; Ma, Jingqi; Lin, Jian
From separation to photothermal conversion: selective crystallization of thorium from lanthanides.
Chemical communications (Cambridge, England), 2025, 61, 10776-10779
7134702 CIFC13 H9 N3 O2P -17.2977; 13.0084; 13.3204
63.202; 85.744; 78.104
1104.22Ishu, Km; Singh, Krishna Nand
Copper(II)-mediated metalloradical activation: denitrogenative/decarboxylative annulation to 3-arylimidazo[1,2-<i>a</i>]pyridines using tetrazolo[1,5-<i>a</i>]pyridines and cinnamic acids.
Chemical communications (Cambridge, England), 2025, 61, 10847-10850
7134703 CIFC101 H191.49 Cr7 F8 N2 Ni O33.24P 21 21 2119.4235; 21.7382; 31.1018
90; 90; 90
13132.2Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134704 CIFC134 H128 Cr7 F8 N Ni O32C 1 2/c 124.0332; 24.0911; 23.763
90; 94.616; 90
13713.8Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134705 CIFC102 H88 Cr7 F8 N9 Ni O48P n m a26.8743; 27.944; 16.9778
90; 90; 90
12749.9Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134706 CIFC206 H176 Cr7 F8 N Ni O40P 21 21 231.9625; 17.1553; 16.9723
90; 90; 90
9306.4Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134707 CIFC251 H343.5 Cr7 F8 N19.5 Ni O80P 4/n c c :226.7607; 26.7607; 40.561
90; 90; 90
29047Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134708 CIFC86 H160 Cr7 F8 N Ni O32P 1 21/c 119.1697; 29.3283; 20.8382
90; 104.138; 90
11360.7Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134709 CIFC102 H188 Cr7 F8 N Ni O32P -119.0912; 22.0288; 30.5452
90.1198; 90.1205; 106.277
12331Geue, Niklas; Renningholtz, Tim; Whitehead, George F. S.; Timco, Grigore A.; Trujillo, Cristina; Barran, Perdita E.; Winpenny, Richard E. P.
Energetics of carboxylate-metal bonds in polymetallic rings.
Chemical communications (Cambridge, England), 2025, 61, 11049-11052
7134710 CIFC73 H90 N4 O18 S2P -113.938; 16.892; 18.001
77.27; 68.987; 75.532
3790.6Zhang, Ting; Wang, Lulu; Li, Hui; Sun, Mingxia; Chen, Jia; Guan, Shuzhe; Qiu, Hongdeng
Pillar[5]arene-based ionic single crystals formed by dual self-assemblies through host-guest and ionic interactions for iodine capture.
Chemical communications (Cambridge, England), 2025, 61, 10843-10846
7134711 CIFC64 H54 Cu4 N2 O4 P4 S2P n a 2118.91; 21.16; 14.44
90; 90; 90
5778Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134712 CIFC15 H52 B40 Cu4 S4P -112.25; 13.32; 16.05
97.18; 110.76; 99.99
2361.8Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134713 CIFC8 H44 B40 Cu4 S4P 32 2 111.3; 11.3; 29.05
90; 90; 120
3212.4Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134714 CIFC8 H44 B40 Cu4 S4P 32 2 111.31; 11.31; 29.08
90; 90; 120
3221.4Nagar, Harshita; Duary, Subrata; Yadav, Vivek; Kini, Amoghavarsha Ramachandra; Antharjanam, Sudhadevi; Base, Tomas; Som, Anirban; Nannenga, Brent L.; Pradeep, Thalappil
Mechanochromic luminescence in copper nanoclusters: resolving structural transitions through microcrystal electron diffraction.
Chemical communications (Cambridge, England), 2025, 61, 10764-10767
7134715 CIFC3 H3 Ga I3 N O2P c a 2124.5086; 6.6842; 6.5526
90; 90; 90
1073.45He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134716 CIFC14 H22 I6 In2 N2 O4P -18.2731; 11.0036; 17.2172
104.905; 90.308; 94.684
1508.99He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134717 CIFC16 H17 Cl9 Ga3 N3 O6C 1 2/c 143.189; 6.5024; 30.529
90; 134.875; 90
6075.6He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134718 CIFC25 H11 B F15 N O2P 1 21/c 115.7995; 9.9144; 19.6671
90; 111.532; 90
2865.7He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134719 CIFC7 H11 Br3 In N O2P 1 21/c 18.0413; 20.3742; 8.1155
90; 100.43; 90
1307.63He, Zhou; Ju, Shaoying; Chen, Ting; Zhang, Xinghua; Stephan, Douglas W.; Wu, Yile
Group 13 Lewis acid-mediated formation of 5-oxazolone derivatives from <i>tert</i>-butyl isocyanoacetate.
Chemical communications (Cambridge, England), 2025, 61, 10582-10585
7134720 CIFC26.88 H27.38 N1.62 O7.62I 1 2/c 124.5252; 7.1491; 30.553
90; 106.418; 90
5138.5Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Fan, Weidong; Sun, Daofeng
Steric hindrance regulation in hydrogen-bonded organic frameworks: from nonporous to microporous.
Chemical communications (Cambridge, England), 2025, 61, 10538-10541
7134721 CIFC25 H23 N O8P 1 21/c 112.0307; 22.7887; 8.6147
90; 100.092; 90
2325.3Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Fan, Weidong; Sun, Daofeng
Steric hindrance regulation in hydrogen-bonded organic frameworks: from nonporous to microporous.
Chemical communications (Cambridge, England), 2025, 61, 10538-10541
7134722 CIFC28 H23 N5P 1 21/c 111.901; 8.437; 23.343
90; 95.41; 90
2333.4Kumari, Akanksha; Jain, Anshul; Sharma, Himani; Sermadurai, Selvakumar; Rana, Nirmal K.
Catalyst-free efficient synthesis of functionalized 1,2,4-triazole <i>via</i> ring opening/cyclization of arylidene thiazolone with aryl/alkyl-hydrazine.
Chemical communications (Cambridge, England), 2025, 61, 11029-11032
7134723 CIFC21 H27 F3 N2 O7 SP 1 21/n 19.6415; 10.1608; 24.945
90; 95.477; 90
2432.6Liu, Shuai; Ge, Yongqi; Li, Jianan; Sheng, Xiaoyu; Zhang, Tian-Shu; Wu, Qiong; Ding, Weijie; Cheng, Xu
Electrochemical site-selective C(sp<sup>3</sup>)-H amination of alkyl substituted indoles and pyrroles.
Chemical communications (Cambridge, England), 2025, 61, 11045-11048
7134724 CIFC21 H27 Br O3P 1 21 110.3749; 8.4178; 11.3443
90; 100.01; 90
975.66Roy, Nanda Kishore; Murmu, Ranjit; Munda, Mintu; Niyogi, Sovan; Bisai, Alakesh
Asymmetric total syntheses of immunosuppressive diterpenoids triptobenzenes N and R <i>via</i> a remote Csp<sup>3</sup>-H functionalization.
Chemical communications (Cambridge, England), 2025, 61, 11053-11056
7134725 CIFC21 H26 O3P 1 21 18.3186; 10.0507; 10.7125
90; 99.133; 90
884.29Roy, Nanda Kishore; Murmu, Ranjit; Munda, Mintu; Niyogi, Sovan; Bisai, Alakesh
Asymmetric total syntheses of immunosuppressive diterpenoids triptobenzenes N and R <i>via</i> a remote Csp<sup>3</sup>-H functionalization.
Chemical communications (Cambridge, England), 2025, 61, 11053-11056
7134726 CIFC108 H84 Eu2 N2 O20P -111.8861; 15.3328; 19.6363
91.069; 94.535; 103.539
3465.77Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134727 CIFC107 H81 Ce2 N2 O20P -112.0155; 15.2802; 19.6685
91.682; 94.913; 102.427
3509.32Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134728 CIFC105.1 H75.9 N2 O19.6 Tb2P -111.7036; 15.2043; 19.7918
91.859; 94.475; 103.284
3412.6Zhang, Jinli; Xi, Xiao-Juan; Xu, Lin; Lang, Feifan; Yang, Yan; Pang, Jiandong
Rare-earth-pentacene-octacarboxylate frameworks for highly efficient urinary 1-HP fluorescence sensing.
Chemical communications (Cambridge, England), 2025, 61, 11195-11198
7134729 CIFC17 H14 F N O4 SP -19.4933; 9.7205; 9.7983
89.993; 77.842; 70.533
830.96Zhang, Sen; Fayad, Eman; Katouah, Hanadi A.; Huang, Yi-Yong; Qin, Hua-Li
Oxidative [3+2] annulation of activated pyridines for the synthesis of indolizinyl sulfonyl fluorides: a class of important pharmacophores.
Chemical communications (Cambridge, England), 2025, 61, 10586-10589
7134730 CIFC108 H108 Cl6 N24 Zn6P -115.458; 19.827; 22.137
97.02; 106.2; 99.82
6316Kim, Jisu; Jeong, Hye Jin; Min, Sein; Kim, Sarah; Baek, Juhee; Kim, Jaelim; Lee, Eunsung; Oh, Sangwon; Jeong, Keunhong
Parahydrogen-induced hyperpolarization of a Zn(II) complex using NMR signal amplification by reversible exchange (SABRE).
Chemical communications (Cambridge, England), 2025, 61, 11061-11064
7134731 CIFC69 H102 B2 Cl2 N16P 1 21/c 17.6519; 18.4389; 28.0176
90; 95.393; 90
3935.58Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134732 CIFC64 H109 B N5 PP 1 21/n 112.1405; 27.056; 20.237
90; 95.591; 90
6615.7Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134733 CIFC218.75 H318 B6 Mg3 N48 O6R -3 :H41.4755; 41.4755; 11.7891
90; 90; 120
17562.8Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134734 CIFC104 H164 B3 Cl2 N8P 1 c 114.1177; 18.5164; 20.8008
90; 104.244; 90
5270.3Huerfano, I. J.; Gorobets, Evgueni; Zhou, Wen; Piers, Warren E.; Van Humbeck, Jeffrey F.; Derksen, Darren J.
Development of electronically tuneable N-heterocyclic borates.
Chemical communications (Cambridge, England), 2025, 61, 10610-10613
7134735 CIFC160 H98 Ag10 Cl2 Cu4 F60 O15 P4 S12P -118.7192; 19.3113; 25.7905
89.531; 89.166; 85.539
9293.6Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134736 CIFC159.73 H96.91 Ag14 Cl2 F60 O14.73 P4 S12P 1 21/c 119.3202; 19.1149; 49.181
90; 95.395; 90
18082.3Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134737 CIFC165.5 H116 Ag12 Cl6 Cu2 F60 O18.5 P4 S12P -118.7706; 19.9187; 25.5916
89.783; 88.666; 87.693
9558Ma, Along; Ren, Yonggang; Zuo, Yang; Zhao, Jiaqi; Zhang, Shuo; Ma, Xiaoshuang; Wang, Shuxin
Regulating Ag-Cu synergy effect <i>via</i> Cu doping numbers to boost CO<sub>2</sub> electroreduction on Ag<sub>14</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 10772-10775
7134738 CIFC19 H16 N2 O4P 21 21 216.0468; 13.3298; 19.6186
90; 90; 90
1581.3Paul, Pratap; Dash, Jyotirmayee
Palladium-catalysed carbonylation of aryl diazonium salts to access bioconjugation-ready esters.
Chemical communications (Cambridge, England), 2025, 61, 10977-10980
7134739 CIFC300 H224 Cl8 O8 P16 Rh8F d d d :211.6257; 22.2356; 46.905
90; 90; 90
12125.1Mandal, Dipendu; Esposito, Madison R.; Griffin, Samuel E.; Domecus, Grant P.; Cohen, Seth M.
Selective hydrosilylation of olefins by a two-dimensional Rh(I) low-valent metal-organic framework.
Chemical communications (Cambridge, England), 2025, 61, 10526-10529
7134740 CIFC300 H224 Cl8 Ir8 O8 P16F d d d :211.573; 22.229; 46.579
90; 90; 90
11983Mandal, Dipendu; Esposito, Madison R.; Griffin, Samuel E.; Domecus, Grant P.; Cohen, Seth M.
Selective hydrosilylation of olefins by a two-dimensional Rh(I) low-valent metal-organic framework.
Chemical communications (Cambridge, England), 2025, 61, 10526-10529
7134741 CIFC27 H47 F6 N4 O P RuP 1 2/n 112.1425; 10.9767; 24.5384
90; 99.738; 90
3223.5Preston, Andrew Z.; Phearman, Alexander S.; Quiroz, Manuel; Flowers, Sarah E.; Devi, Nilakshi; Zall, Christopher M.; Wiedner, Eric S.; Appel, Aaron M.; Linehan, John C.
DBU as base and ligand in phosphine-free ruthenium complexes for hydrogenation of CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2025, 61, 11247-11250
7134742 CIFC24 H18 Fe N4 S2P n a 2123.582; 7.927; 11.326
90; 90; 90
2117.2Yan, Rong; Li, Zi-Han; Luo, Qian-Cheng; Sun, Na-Na; Ho, Johnny C.; Zheng, Yan-Zhen
Nuclearity effect on water oxidation: a comparative study of dinuclear and mononuclear iron complexes.
Chemical communications (Cambridge, England), 2025, 61, 11601-11604
7134743 CIFC50 H38 Cl2 Fe2 N8 O11 S4P -19.0102; 11.9133; 25.039
84.209; 86.646; 85.619
2662.7Yan, Rong; Li, Zi-Han; Luo, Qian-Cheng; Sun, Na-Na; Ho, Johnny C.; Zheng, Yan-Zhen
Nuclearity effect on water oxidation: a comparative study of dinuclear and mononuclear iron complexes.
Chemical communications (Cambridge, England), 2025, 61, 11601-11604
7134744 CIFC10 H4 S2C 1 2/c 113.036; 9.2577; 12.7472
90; 105.591; 90
1481.77Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134745 CIFC20 H12 S6I 1 2/a 113.9881; 11.6422; 22.2132
90; 92.097; 90
3615.05Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134746 CIFC24 H16 S4P 1 2/n 112.0579; 7.6145; 21.3949
90; 105.709; 90
1891Nagase, Mai; Yoshida, Ryu; Nakano, Sachiko; Hirose, Takashi; Segawa, Yasutomo
Synthesis, structure, and properties of twisted π-conjugated molecules featuring three-dimensional π-π interactions in solid states.
Chemical communications (Cambridge, England), 2025, 61, 11187-11190
7134747 CIFC11 H9 Br F3 N OP 21 21 217.084; 10.507; 16.18
90; 90; 90
1204.3Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134748 CIFC11 H10 Br F2 N OP 21 21 217.2114; 8.6463; 17.6697
90; 90; 90
1101.74Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134749 CIFC11 H10 F2 I N OC 1 2/c 120.4768; 11.5083; 14.185
90; 132.601; 90
2460.5Sihag, Naveen; Bhartiya, Hemaang; Jain, Swati; Singh, Jitendra; Reddy, S. Rajagopala; Yadav, M. Ramu
Pd-catalyzed enantioselective reductive Heck reaction of mono-fluoro, <i>gem</i>-difluoro, and trifluoromethyl tethered-alkenes.
Chemical communications (Cambridge, England), 2025, 61, 11413-11416
7134750 CIFC31 H24 O4P 1 21/n 19.7595; 14.8506; 16.2013
90; 93.249; 90
2344.35Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134751 CIFC25 H20 O3P -19.1486; 10.1141; 11.1933
76.519; 83.021; 69.176
940.54Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134752 CIFC25 H18 Cl2 O2P -19.6407; 9.9098; 12.2951
97.191; 112.732; 106.874
998.56Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134753 CIFC23 H16 O3P 1 21/c 17.961; 15.645; 13.67
90; 105.538; 90
1640.4Goel, Komal; Shree V, Divya; Satyanarayana, Gedu
Acid-triggered cascade cyclization pathways of enynes: A rapid access to fused polycyclic products.
Chemical communications (Cambridge, England), 2025, 61, 11457-11460
7134754 CIFC2.88 H1.88 Br0.25 O0.62P -14.725; 13.22; 17.69
112.5; 92.17; 89.8
1020Londhe, Gokul S.; Mondal, Shankhajit; Gnanaprakasam, Boopathy
A Mn(III)-catalysed domino process for C-3 substituted dihydrocoumarins from 2-hydroxybenzyl alcohols and 4-hydroxy-2<i>H</i>-chromen-2-ones.
Chemical communications (Cambridge, England), 2025, 61, 11617-11620
7134755 CIFC16 H16 N2 SP b c a7.9502; 15.00228; 22.48379
90; 90; 90
2681.67Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134756 CIFC64 H60 Ag2 F12 N8 Ni2 S4 Sb2F d d d :211.5021; 32.2956; 41.3195
90; 90; 90
15348.8Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134757 CIFC32 H30 N4 Ni S2P -111.23947; 11.63264; 12.08649
94.9271; 109.939; 107.106
1388.98Marquardt, Michael; Vendier, Laure; Sournia-Saquet, Alix; Maurel, Vincent; Mouesca, Jean-Marie; Bastin, Stéphanie; Castillo, Ivan; César, Vincent
A non-innocent, π-extended N-heterobicyclic carbene-thiolate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11437-11440
7134758 CIFC50.2 H52.96 Cl3.06 N2P -19.4575; 13.1091; 17.8161
83.827; 84.966; 86.326
2184.22Zhang, Zhiyu; Xu, Zhenxun; Zhang, Aihui; Bai, Fenghua; Hashikawa, Yoshifumi; Chaolumen, ?
Synthesis of a twisted azananographene featuring a diquinoxaline-fused pyrene.
Chemical communications (Cambridge, England), 2025, 61, 11401-11404
7134759 CIFC24 H36 Bi Cl Ni P2P 1 21/n 17.9299; 15.7754; 20.8624
90; 90.502; 90
2609.73Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134760 CIFC34 H54 Bi Cl N2 Ni P2P b c a19.49554; 17.5937; 21.22369
90; 90; 90
7279.7Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134761 CIFC35 H54 Bi N Ni O3 P2P -110.7706; 12.3565; 15.647
93.308; 109.812; 106.535
1850.5Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134762 CIFC58 H74 B Bi N2 Ni P2P 1 21/c 111.0192; 50.5458; 29.036
90; 91.575; 90
16166.2Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134763 CIFC43 H72 Bi N3 Ni O P2P 1 21/n 113.6212; 20.8338; 16.5044
90; 92.171; 90
4680.3Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134764 CIFC52 H72 Bi2 Cl2 Ni2 O4 P4P -111.7379; 11.8444; 20.9031
86.791; 77.237; 89.535
2829.8Yoo, Dagyum; Brannan, Alexander C.; Lim, Soohyun; Lee, Heui Beom; Lee, Yunho
Reversible CO binding at a nickel complex supported by an ambiphilic PBiP tridentate ligand.
Chemical communications (Cambridge, England), 2025, 61, 11453-11456
7134765 CIFC30 H18 Cd N4 O8P 1 21/c 120.341; 13.506; 21.538
90; 121.24; 90
5059Li, Kuixiang; Qin, Jin; Hao, Pengfei; Xu, Yi; Zhang, Shimin; Shen, Junju; Fu, Yunlong
Linear-light-controlled reverse electron transfer in a 3-D pyromelliticdiimide-based photo-/thermochromic cadmium(II) coordination polymer.
Chemical communications (Cambridge, England), 2025, 61, 11822-11825
7134766 CIFC34 H39 N O2P 21 21 219.1352; 16.5171; 17.9335
90; 90; 90
2705.9Zhu, Yanren; Yang, Shaoxiong; Chen, Huiyu; Zhang, Fang; Pu, Enfan; Jiang, Piaopiao; Jin, Yi; Zhang, Hongbin; Chen, Jingbo
Cycloaddition of bicyclo[1.1.0]butanes with enamides for the efficient synthesis of 2-amino-bicyclo[2.1.1]hexanes.
Chemical communications (Cambridge, England), 2025, 61, 11493-11496
7134767 CIFC22 H17 Br N O3P 1 21 17.4907; 15.9278; 7.9606
90; 101.271; 90
931.46Zhu, Yanren; Yang, Shaoxiong; Chen, Huiyu; Zhang, Fang; Pu, Enfan; Jiang, Piaopiao; Jin, Yi; Zhang, Hongbin; Chen, Jingbo
Cycloaddition of bicyclo[1.1.0]butanes with enamides for the efficient synthesis of 2-amino-bicyclo[2.1.1]hexanes.
Chemical communications (Cambridge, England), 2025, 61, 11493-11496
7134768 CIFC46 H82 Bi Cl Fe N2 P2 Si2P -112.114; 21.416; 21.921
89.666; 74.179; 80.249
5388Zurakowski, Joseph A.; MacEachern, Mitchell A. Z.; Durfy, Connor S.; Boyle, Paul D.; Chitnis, Saurabh S.; Drover, Marcus W.
Hydro- and chloroelementation reactions across an iron-carbon bond using heavy group 15 reagents.
Chemical communications (Cambridge, England), 2025, 61, 10969-10972
7134769 CIFC112 H106 N6 S4P 1 21/n 124.5514; 15.9391; 34.932
90; 101.616; 90
13389.9Naniyil, Athira; Kumar, Arun; Edwin, Aathira; Gokulnath, Sabapathi
A carbazole-embedded cyclodimer adopting a helical conformation and metal-ion sensing.
Chemical communications (Cambridge, England), 2025, 61, 11633-11636
7134770 CIFC24 H26 Mn3 N16P 1 21/c 110.7686; 12.9029; 10.664
90; 91.158; 90
1481.42León-Alcaide, Luis; Fernández-Alarcón, Alberto; Calbo, Joaquín; Keen, David A.; Mínguez Espallargas, Guillermo
Melt-quenched synthesis of a manganese ZIF glass.
Chemical communications (Cambridge, England), 2025, 61, 11641-11644
7134771 CIFC121 H98 Cl2 Cu8 F12 N8 P4 S8P -112.2639; 16.0411; 17.8781
74.241; 88.232; 74.805
3263.5Chang, Mengfan; Xu, Ying; Lv, Ying; Yu, Haizhu; Li, Hao; Kang, Xi; Zhu, Manzhou
Controlling the photoluminescence chromaticity of emissive copper nanoclusters <i>via</i> ligand engineering.
Chemical communications (Cambridge, England), 2025, 61, 11215-11218
7134772 CIFC27 H20 O3P -18.4872; 10.3122; 11.7926
96.838; 107.111; 99.692
956.65Maharana, Priyanka; Sankar, Raman Vijaya; Sankaralingam, Muniyandi; Gunanathan, Chidambaram
Synthesis of functionalized lactones: catalytic cross-coupling of 1,2-diols and allylic alcohols.
Chemical communications (Cambridge, England), 2025, 61, 11947-11950
7134773 CIFC23 H23 N OP 1 21/c 18.6833; 7.9494; 25.996
90; 99.594; 90
1769.3Li, Juncheng; Adelakun, Ibrahim O.; Wei, Zheng; Wang, Ting
Metal-free photocatalytic oxidative coupling of cyclic ethers and alcohols.
Chemical communications (Cambridge, England), 2025, 61, 11818-11821
7134774 CIFC79 H110 Mg N6 OP -112.6188; 14.4351; 39.6972
87.74; 84.081; 88.177
7184.04Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134775 CIFC43 H58 N2 OP -19.9907; 17.0201; 23.3184
103.355; 102.238; 103.661
3596.71Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134776 CIFC80 H110 Mg N2 O3P 1 21 117.5; 17.78; 22.86
90; 104.86; 90
6875Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134777 CIFC58 H80 N2 OP 1 21/c 112.707; 28.0723; 14.6372
90; 98.653; 90
5161.87Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134778 CIFC19 H24 N2 OP 1 21/c 116.4224; 26.1026; 17.6208
90; 117.172; 90
6719.9Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134779 CIFC110 H138 Mg2 N4 O2C 1 2/c 129.1; 11.07; 29.06
90; 97.9; 90
9272Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134780 CIFC164 H202 K6 Mg2 N4 O2P -113.65; 16.68; 24.09
103.86; 104.61; 93.9
5105Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134781 CIFC62.5 H80 N2 OP -112.4386; 19.1066; 21.5188
89.669; 87.336; 89.355
5108.22Evans, Matthew J.; Jones, Cameron
Unsymmetrical bis(anilido)xanthene ligands: development and use in the preparation of magnesium diamide complexes.
Chemical communications (Cambridge, England), 2025, 61, 11814-11817
7134782 CIFC93 H86 Cl2 N6P 43 21 215.8363; 15.8363; 58.867
90; 90; 90
14763.2Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134783 CIFC78 H56 Cl4 N6P 1 21/c 113.5469; 23.814; 19.642
90; 108.456; 90
6010.7Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134784 CIFC93 H86 Cl2 N6P 41 21 215.8075; 15.8075; 58.762
90; 90; 90
14683.3Xiao, Xiong; Liang, Jia-Qi; Hu, Jia-Jun; Yuan, Li; Zhu, Jia-Zhen; Chen, Zong-Ju; Song, You; Li, Cheng-Hui; Zheng, You-Xuan
Planar chiral orange-red TADF materials with AIE properties for efficient circularly polarized OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 11766-11769
7134785 CIFC16 H21 Li O4P -15.8667; 8.571; 16.0568
86.246; 82.777; 81.975
792.2Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134786 CIFC28 H36 Li4 O4P -110.0389; 12.4597; 13.0418
61.824; 74.874; 82.866
1388.2Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134787 CIFC5.71 H9.42 Li N O0.35F m -3 c25.9396; 25.9396; 25.9396
90; 90; 90
17453.8Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134788 CIFC36 H68 Li4 O8 Si4P 1 21/c 110.809; 27.6823; 16.7998
90; 105.552; 90
4842.76Zhang, Ruichen; O'Brien, Tom; Abdilah, Fauzi; White, Andrew J. P.; Lickiss, Paul D.; Davies, Robert P.
Organometallic and zeolitic ultralight MOFs from lithium alkynyl building blocks.
Chemical communications (Cambridge, England), 2025, 61, 11637-11640
7134789 CIFC8 H4 Li4 O4P 1 21/n 18.4602; 5.14; 16.5862
90; 99.445; 90
711.48Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134790 CIFC6 H3 Li2 O2P 1 21/c 19.7425; 5.9515; 8.3569
90; 105.758; 90
466.34Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134791 CIFC4 H2 Li O2P 1 21/c 18.35839; 5.13401; 8.4796
90; 93.187; 90
363.314Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134792 CIFC6 H3 Li O2P 1 21/c 110.2674; 5.3379; 8.6255
90; 98.721; 90
467.267Griffiths, Kieran; Cook, Chris; Seymour, Valerie R.; Bragg, Ryan J.; Halcovitch, Nathan R.; Griffin, John M.
Chemical lithiation reveals the structures of conjugated tetralithium dicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 11991-11994
7134793 CIFC38 H38 N4 OP -110.6572; 12.3917; 12.825
105.741; 95.3783; 104.429
1554.92Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134794 CIFC40 H38 B F2 N5P n a 2122.8308; 19.6331; 7.717
90; 90; 90
3459.06Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134795 CIFC160 H160 N16P -119.232; 19.9165; 19.9108
68.127; 74.0072; 73.9936
6674.3Alkaş, Adil; Diaz-Rodriguez, Roberto M; Sequeira, Steve O.; Hilborn, James W.; Atansi, Mmasinachi; Sullivan, Em C.; Brown, Emily B.; Gapare, Rosinah Liandrah; Mutus, Bulent; Robertson, Katherine N.; Thompson, Alison
Introducing the substituted azobispyrrole framework: synthesis and properties.
Chemical communications (Cambridge, England), 2025, 61, 11649-11652
7134796 CIFCl2 Cs18 O83 Pu2 W20P -114.025; 17.2738; 22.2406
100.814; 102.411; 99.105
5056.81Colliard, Ian; Stavila, Vitalie; Deblonde, Gauthier J.-P.
Isolation of a new polyoxometalate complex of plutonium.
Chemical communications (Cambridge, England), 2025, 61, 11858-11861
7134797 CIFC46 H55 N2 O2 SbP b c a18.4576; 16.232; 27.3781
90; 90; 90
8202.6Agou, Tomohiro; Kuroiwa, Shunsuke; Moriyama, Ryo; Kuroda, Takuma; Kubo, Kazuya; Fukumoto, Hiroki; Morita, Masato; Inoue, Ryo; Nabeshima, Tatsuya
Synthesis and structural characterization of Sb(iii) and Bi(iii) complexes with an N2O2-type tetradentate dipyrrin ligand
Chemical Communications, 2025, 61, 7141-7144
7134798 CIFC47 H57 Bi Cl2 N2 O2P -113.8968; 14.1548; 14.2678
62.515; 80.924; 62.258
2197.8Agou, Tomohiro; Kuroiwa, Shunsuke; Moriyama, Ryo; Kuroda, Takuma; Kubo, Kazuya; Fukumoto, Hiroki; Morita, Masato; Inoue, Ryo; Nabeshima, Tatsuya
Synthesis and structural characterization of Sb(iii) and Bi(iii) complexes with an N2O2-type tetradentate dipyrrin ligand
Chemical Communications, 2025, 61, 7141-7144
7134799 CIFC84 H54 N8P -110.8437; 25.2054; 37.5571
73.902; 83.492; 77.695
9619.9Li, Jiajia; Yang, Yanping; Hii, Shan Shiang; Zhu, Xinyuan; Wang, Youfu
Structural isomers of imine-linked covalent organic cages with divergent photocatalytic properties
Chemical Communications, 2025, 61, 7281-7284
7134800 CIFC84 H54 N8P 1 21/n 123.0146; 9.9226; 36.4335
90; 95.329; 90
8284.2Li, Jiajia; Yang, Yanping; Hii, Shan Shiang; Zhu, Xinyuan; Wang, Youfu
Structural isomers of imine-linked covalent organic cages with divergent photocatalytic properties
Chemical Communications, 2025, 61, 7281-7284
7134801 CIFC68 H90 Au2 F12 N8 P2 Sb2P 1 21/n 120.424; 11.606; 32.783
90; 107.44; 90
7414Urvashi,; Patil, Nitin T.
Bidentate (P^N) Au(iii)–azide complexes: synthesis and reductive elimination studies
Chemical Communications, 2025, 61, 7297-7300
7134802 CIFC23 H17 FP 1 21/c 111.689; 17.293; 8.4188
90; 102.698; 90
1660.1Sun, Jie; Zhang, Shaojie; Wang, Ruixue; Lv, Zeng; Wu, Xin-Xing
Palladium-catalyzed sequential [3+2] cyclization/C–H activation of o-iodostyrenes with cyclopropenones as C2 synthons
Chemical Communications, 2025, 61, 8200-8203
7134803 CIFC39 H44 Cl2 P2 Ru S2C 1 2/c 138.852; 14.8412; 18.368
90; 90.004; 90
10591.2Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134804 CIFC43.75 H61 O P2 Ru S4P n a 2117.6021; 12.8281; 17.294
90; 90; 90
3905Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134805 CIFC53.25 H80.2 P2 Ru S2P 1 21/n 110.0461; 25.5274; 17.2498
90; 97.0994; 90
4389.8Mondragón-Díaz, Alexander; Kelley, Steven P.; Hazari, Nilay; Bernskoetter, Wesley H.
A highly active sulfur based pincer ruthenium catalyst for CO2 hydrogenation
Chemical Communications, 2025, 61, 6957-6960
7134806 CIFC94 H158 Ca2 N4 O3P -112.7723; 12.8615; 16.5534
71.5478; 72.2458; 62.332
2243.75Thum, Stefan; Schmidt, Marcel A.; Langer, Jens; Harder, Sjoerd
Low-coordinate calcium peroxide and oxide complexes.
Chemical communications (Cambridge, England), 2025, 61, 12127-12130
7134807 CIFC96 H162 Ca2 N4 O4P -112.822; 12.859; 16.6221
71.9328; 71.5933; 62.498
2262.16Thum, Stefan; Schmidt, Marcel A.; Langer, Jens; Harder, Sjoerd
Low-coordinate calcium peroxide and oxide complexes.
Chemical communications (Cambridge, England), 2025, 61, 12127-12130
7134808 CIFC20 H16 Cl O PP 21 21 218.9934; 9.8046; 18.7482
90; 90; 90
1653.15Zhang, Zhaoqi; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical phosphorylation of α,β-unsaturated carboxylic acids <i>via</i> decarboxylative cross-coupling reaction.
Chemical communications (Cambridge, England), 2025, 61, 12034-12037
7134809 CIFC20 H15 O PP b c a11.7526; 16.3049; 16.4854
90; 90; 90
3159Zhang, Zhaoqi; Shen, Yirui; Zhao, Yufen; Wu, Ju
Electrochemical phosphorylation of α,β-unsaturated carboxylic acids <i>via</i> decarboxylative cross-coupling reaction.
Chemical communications (Cambridge, England), 2025, 61, 12034-12037
7134810 CIFC24 H17 Br N2 O2P 21 21 214.6907; 12.763; 31.449
90; 90; 90
1882.8Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134811 CIFC24 H15 Br N2 OP 1 c 124.7055; 4.9654; 25.0076
90; 118.895; 90
2685.8Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134812 CIFC24 H17 Br N2 O2P 21 21 214.723; 12.844; 32.01
90; 90; 90
1942Manoharan, Deepak; Bhowmik, Aritra; Mishra, Manish Kumar; Ghosh, Soumyajit
Water-driven modulation of multiresponsive properties in acylhydrazone-based crystals.
Chemical communications (Cambridge, England), 2025, 61, 12139-12142
7134813 CIFC24 H21 Br O2P 17.815; 7.9476; 8.2858
70.783; 77.901; 89.307
474.26Zhang, Ke-Feng; Zhou, Lin-Hui; Chen, Yan-Xi; Chen, Wei-Wei; Feng, Yuan-Mei; Ma, Fang
Catalytic Asymmetric Construction of Planarly and Centrally Chiral [2.2]paracyclophanes by Merging Photochemical and Cobalt Catalyzed Desymmetrization
Chemical Communications, 2025
7134814 CIFC18 H22 N2 O5P 1 21 19.1504; 19.6553; 9.7569
90; 102.207; 90
1715.14Liu, Deng-Yin; Hu, Xin-Yue; Zhang, Cong-Zhen; Wen, Miao-Miao; Ren, Xiao-Xi; Liu, Xu-Ge
Switchable synthesis of benzimidazole/quinoxaline <i>C</i>-glycosides with <i>o</i>-phenylenediamines and sulfoxonium ylide glyco-reagents.
Chemical communications (Cambridge, England), 2025, 61, 12131-12134
7134815 CIFC11 H9 Co2 O7 PI 1 2/a 110.652; 5.4984; 42.3062
90; 95.802; 90
2465.14Xu, Yan; Su, Qian-Qian; Liu, Bei; Sun, Wen-Tao; Bao, Song-Song; Li, Su-Zhi; Zheng, Li-Min
Metal-organic framework containing Co<sub>3</sub>(μ<sub>3</sub>-OH)-based kagomé layers showing long-range weak ferromagnetic ordering.
Chemical communications (Cambridge, England), 2025, 61, 12211-12214
7134816 CIFC55 H65 Co8 O43 P5P n m a26.3066; 21.2796; 13.9084
90; 90; 90
7785.8Xu, Yan; Su, Qian-Qian; Liu, Bei; Sun, Wen-Tao; Bao, Song-Song; Li, Su-Zhi; Zheng, Li-Min
Metal-organic framework containing Co<sub>3</sub>(μ<sub>3</sub>-OH)-based kagomé layers showing long-range weak ferromagnetic ordering.
Chemical communications (Cambridge, England), 2025, 61, 12211-12214
7134817 CIFC15 H14 N2 O2 SP 1 21/c 18.3477; 22.4967; 7.7113
90; 106.006; 90
1392.01Zhou, Pengfei; Wan, Guibin; Yuan, Zhihan; Guan, Aoran; Wei, Zongwu; Liang, Taoyuan; Jiang, Jun; Zhang, Zhuan
Cobalt(III)-catalyzed C-H functionalization of 2-arylthiazoles with maleimides or allyl acetate.
Chemical communications (Cambridge, England), 2025, 61, 12171-12174
7134818 CIFC38 H44 N4 O2P n a 2117.6633; 8.3253; 21.863
90; 90; 90
3215Bhatt, Tarun; Dutta, Tonmoy; Yaswanth, Kokkiripati; Kalevaru, Venkata Narayana; Wohlrab, Sebastian; Natte, Kishore
Chemoselective transfer hydrogenation and transfer deuteration of substituted quinolines using Hantzsch ester and D<sub>2</sub>O.
Chemical communications (Cambridge, England), 2025, 61, 12305-12308
7134819 CIFC27.5 H27 N O2 PP -18.5764; 9.5269; 15.3568
100.161; 100.588; 102.767
1171.67Bhatt, Tarun; Dutta, Tonmoy; Yaswanth, Kokkiripati; Kalevaru, Venkata Narayana; Wohlrab, Sebastian; Natte, Kishore
Chemoselective transfer hydrogenation and transfer deuteration of substituted quinolines using Hantzsch ester and D<sub>2</sub>O.
Chemical communications (Cambridge, England), 2025, 61, 12305-12308
7134820 CIFC24 H26P 1 21/c 111.615; 10.921; 15.107
90; 111.302; 90
1785.4Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134821 CIFC13 H13 Br2 N3 O ZnP 1 21/c 113.4493; 15.5797; 7.6731
90; 106.091; 90
1544.8Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134822 CIFC14 H18 Br2 N4 O S ZnP 1 21/c 19.9413; 13.4749; 14.3357
90; 98.261; 90
1900.46Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134823 CIFC17 H18 OP -18.972; 13.053; 13.269
63.504; 86.68; 85.485
1386Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134824 CIFC19 H18 Cl2P -18.297; 9.0505; 11.4465
93.075; 97.902; 111.839
785.13Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134825 CIFC15 H19 Br2 N3 O2 ZnP -17.4524; 10.4775; 13.0859
101.879; 94.101; 108.999
934.77Samanta, Arup; Phukan, Hirak Jyoti; Tripathi, Ujjwal Kumar; Srimani, Dipankar
Merging metal-ligand cooperation and redox promoted strategy for tailored synthesis of alkylated 9<i>H</i>-fluorenes.
Chemical communications (Cambridge, England), 2025, 61, 12582-12585
7134826 CIFC21 H18 Cl N O3P 1 21 15.905; 10.3232; 14.2771
90; 96.286; 90
865.08Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134827 CIFC21 H19 N O4P 1 21 17.4802; 13.004; 17.2546
90; 92.2247; 90
1677.13Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134828 CIFC21 H21 N O3P 21 21 216.7817; 8.2331; 31.286
90; 90; 90
1746.84Xiao, Yu-Qing; Li, Zi-Qing; Hu, Fang; Li, Tian-Yu; Zhou, Zheng-Xin; Zhang, Zhihan; Tan, Ying; Xiao, Wen-Jing; Gavrilov, Konstantin Nikolaevich; Lu, Liang-Qiu
Pd-catalyzed asymmetric (6+2) dipolar cyclization for medium-sized spirooxindoles.
Chemical communications (Cambridge, England), 2025, 61, 12030-12033
7134829 CIFC6 H10 N8 OP 1 21/c 13.6169; 19.782; 11.752
90; 94.717; 90
838Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134830 CIFC6 H9 Cl N8C 1 2/c 127.527; 3.8158; 21.717
90; 128.059; 90
1796.1Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134831 CIFC6 H9 Cl N8 O4P 1 21/n 16.8415; 15.8632; 9.8345
90; 92.574; 90
1066.24Wang, Yaxi; Liu, Junliang; He, Jinxuan; Ren, Xiaoting; Hu, Lu; Pang, Siping
Tetraamino-driven hydrogen-bonded networks: selective self-assembly of energetic materials.
Chemical communications (Cambridge, England), 2025, 61, 13433-13436
7134832 CIFC18 H18 Cl N O2P b c a12.3189; 8.9755; 28.721
90; 90; 90
3175.6Xian, Ning; Yin, Jiang; Ji, Xiaochen; Huang, Huawen
Sulfoxonium ylides as carbon radical precursors in three-component carbohalogenation of alkenes
Chemical Communications, 2025
7134833 CIFC30 H21 Cl N2 O2P 1 21/n 19.1913; 23.5634; 11.1335
90; 101.65; 90
2361.6Bhumij, Mandweep; Ahamed, Rehan; Kant, Ruchir; Mudedla, Sathish Kumar; Srivastava, Ajay Kumar
Regioselective construction of pyrido[1,2,3-<i>de</i>]quinoxaline-2,5-diones through acid-mediated post-Ugi rearrangements.
Chemical communications (Cambridge, England), 2025, 61, 12757-12760
7134834 CIFC26 H16 B2 F4 N4P b c a8.1088; 14.0314; 36.966
90; 90; 90
4205.91Nakano, Takeo; Yamada, Haruki; Inaba, Ryoto; Hamasaki, Atom; Takeda, Takashi; Ohta, Akira
Dimeric boron complexes bearing isoquinolyl-pyrrole ligands.
Chemical communications (Cambridge, England), 2025, 61, 11943-11946
7134835 CIFC25 H17 N O2C 1 2/c 114.5261; 10.9889; 24.318
90; 109.877; 90
3650.52Suresh, Vavilapalli; Reddy, T. Mahipal; Nanubolu, Jagadeesh Babu; Reddy, Maddi Sridhar
Pd-catalyzed electrophilic cyclization/C-H annulation cascade of 1,8-diyne oxime ethers to access fused oxepines.
Chemical communications (Cambridge, England), 2025, 61, 12353-12356
7134836 CIFC34 H25 Br N2 O3P -110.8312; 11.1661; 12.4253
101.941; 98.68; 112.734
1310.87Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134837 CIFC35 H27 Br N2 O4P -110.1577; 10.7731; 13.5579
99.196; 98.716; 109.233
1349.24Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134838 CIFC32 H24 Br N2 O3 SP 1 21/n 110.8268; 11.8871; 20.0235
90; 91.459; 90
2576.17Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134839 CIFC35 H27 Br N2 O3P 1 21 112.1417; 8.895; 12.7012
90; 99.012; 90
1354.8Raza, Mohammad Saim; Roshani, K. M.; Peddinti, Rama Krishna
(4 + 3) Annulation of Enone-Tethered Indoles with α-Alkylidene Succinimides: Access to Seven-Membered Azepino[3,2,1-hi]Indole Scaffolds
Chemical Communications, 2025
7134840 CIFC24 H19 N3 O3 SP 19.1403; 9.6457; 11.8785
102.168; 101.295; 90.935
1002.09Dybowska, Joanna; Przydacz, Artur; Olczyk, Weronika; Sieroń, Lesław; Skrzyńska, Anna; Albrecht, Łukasz
Divergent hetero-[8+<i>n</i>] higher order cycloadditions of tropothione and enals catalyzed by <i>N</i>-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 12119-12122
7134841 CIFC24 H19 N3 O3 SP 1 21 111.5801; 5.9732; 15.349
90; 107.687; 90
1011.51Dybowska, Joanna; Przydacz, Artur; Olczyk, Weronika; Sieroń, Lesław; Skrzyńska, Anna; Albrecht, Łukasz
Divergent hetero-[8+<i>n</i>] higher order cycloadditions of tropothione and enals catalyzed by <i>N</i>-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 12119-12122
7134842 CIFC21 H19 Fe N S2P 1 21/c 113.9164; 6.0808; 22.0969
90; 104.013; 90
1814.26Sharma, Deepak; Tomar, Vijesh; Joshi, Raj K.
Synthesis of ferrocenyl/phenyl isothiazole-3-thione and isoselenazole-3-selenone as new heterocycles.
Chemical communications (Cambridge, England), 2025, 61, 13964-13967
7134843 CIFCo H16 N10 O8F m m m6.4648; 12.1663; 17.1617
90; 90; 90
1349.81Zhao, Feng; Gu, Ziyan; Song, Bin; Ju, Xuehai; Hu, Bingcheng; Zhang, Chong
Electrosynthesis of a <i>cyclo</i>-N<sub>5</sub><sup>-</sup> anion <i>via</i> TEMPO-mediated selective C-N bond cleavage in aryl-pentazole.
Chemical communications (Cambridge, England), 2025, 61, 12725-12728
7134844 CIFC17 H14 N2 O3P 1 21/c 114.2794; 4.2726; 22.8872
90; 100.816; 90
1371.55Basak, Soumya Jyoti; Dash, Jyotirmayee
KOtBu-Mediated Annulation for the Pot-Economical Synthesis of Quinazolinobenzoxazepines
Chemical Communications, 2025
7134845 CIFC20 H14 N2 O2P n a 2115.052; 22.635; 4.2116
90; 90; 90
1434.9Basak, Soumya Jyoti; Dash, Jyotirmayee
KOtBu-Mediated Annulation for the Pot-Economical Synthesis of Quinazolinobenzoxazepines
Chemical Communications, 2025
7134846 CIFC108 H78 F36 N6 P6P 1 21/n 16.6796; 34.3789; 48.7726
90; 90.958; 90
11198.4Yu, Yang; Song, Xiaowen; Li, Yawen; Wang, Pingxia; Cheng, Lin; Yang, Ying; He, Gang; Cao, Liping
Angle-controlled synthesis and redox properties of a tetraphenylethene-based hexacationic triangular macrocycle.
Chemical communications (Cambridge, England), 2025, 61, 13193-13196
7134847 CIFC6 H4 N4P 1 21/c 13.6563; 7.4254; 10.3507
90; 94.82; 90
280.02Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134848 CIFC18 H28 K N4 O6P -18.2265; 8.5426; 9.0649
74.121; 65.614; 66.262
526.7Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134849 CIFC54 H94 K2 N12 O15P -113.1139; 14.3079; 19.8832
93.405; 108.729; 111.474
3220.98Deshapriya, Saroshan; Demir, Selvan
Isolation of 1,4,5,8-tetraazanaphthalene radicals.
Chemical communications (Cambridge, England), 2025, 61, 12301-12304
7134850 CIFC32 H38 Cl2 N2 O RuP -18.9258; 10.9738; 18.096
98.894; 99.456; 96.569
1709.5Casalta, Clément; Roisnel, Thierry; Jazzar, Rodolphe; Doppiu, Angelino; Mauduit, Marc
<i>N</i>-hydrazine cyclic(amino)(alkyl)carbene ruthenium complexes: synthesis and reactivity in olefin metathesis.
Chemical communications (Cambridge, England), 2025, 61, 13169-13172
7134851 CIFC55 H52 Cl2 N2P -110.1271; 15.252; 15.567
106.892; 100.26; 100.908
2188.5Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134852 CIFC55 H51 Cl3 N2P -110.004; 15.3041; 16.1113
107.88; 102.522; 99.296
2221.55Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134853 CIFC55 H51 Cl3 N2P -19.8151; 15.4638; 16.0395
105.292; 91.583; 107.284
2227.33Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134854 CIFC29 H29 N OP -19.6914; 15.3962; 16.3741
105.062; 90.118; 107.315
2243.97Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134855 CIFC54 H50 N2P 1 21/c 111.033; 16.7127; 22.0929
90; 95.145; 90
4057.32Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134856 CIFC55 H52 Cl2 N2P -19.752; 15.4169; 15.7126
103.388; 92.384; 106.529
2188.48Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134857 CIFC54.05 H50.1 Cl0.1 N2P -19.8175; 15.0293; 15.4757
100.086; 106.629; 93.275
2140.17Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134858 CIFC54 H50 N2P -111.288; 11.9759; 15.6694
74.666; 84.43; 85.549
2030.22Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134859 CIFC58 H58 N2 O2P -19.7222; 15.4668; 16.2481
75.227; 89.808; 72.19
2241.9Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134860 CIFC54 H50 N2P 1 21/c 111.0179; 16.7178; 22.0057
90; 95.442; 90
4035.07Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134861 CIFC56 H54 N2 OP -19.7849; 15.3986; 15.4296
101.789; 92.489; 106.18
2173.17Yang, Wenyan; Li, Lele; Xue, Xinlei; Deng, Shengyong; Wei, Peifa
Positional isomerism-directed formation of hydrogen-bonded organic frameworks with distinct single-crystal transformation pathways.
Chemical communications (Cambridge, England), 2025, 61, 13113-13116
7134862 CIFC122.5 H136 Ag4 Cl2 F12 O1.5 P8 Pt Sb2P 1 21 114.5881; 15.94377; 26.82398
90; 102.209; 90
6097.85Zhang, Yujie; Jia, Hongli; Yan, Bingzheng; Hou, Jian; Guo, Huifang; Li, Qi; Xin, Chengrui; Li, Simin; Dong, Jinrun; Shen, Hui
One-pot synthesis of atomically precise chiral PtAg<sub>4</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 13691-13694
7134863 CIFC122.5 H136 Ag4 Cl2 F12 O1.5 P8 Pt Sb2P 1 21 114.5524; 15.9421; 26.8018
90; 102.05; 90
6080.9Zhang, Yujie; Jia, Hongli; Yan, Bingzheng; Hou, Jian; Guo, Huifang; Li, Qi; Xin, Chengrui; Li, Simin; Dong, Jinrun; Shen, Hui
One-pot synthesis of atomically precise chiral PtAg<sub>4</sub> nanoclusters.
Chemical communications (Cambridge, England), 2025, 61, 13691-13694
7134864 CIFC22.8 H39.2 N4 O14.8 ZrI -4 2 d8.9734; 8.9734; 41.816
90; 90; 90
3367.1Shao, Zhen-Wu; Qiu, Yuqing; Xiong, Chaozhi; Liu, Chong
Isomerism and transformation of Zr-hydroxamate metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 12960-12963
7134865 CIFC21.8 H32.2 Cl2 N6.6 O8.6 ZrC c c a :225.7241; 38.687; 17.6068
90; 90; 90
17522Shao, Zhen-Wu; Qiu, Yuqing; Xiong, Chaozhi; Liu, Chong
Isomerism and transformation of Zr-hydroxamate metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 12960-12963
7134866 CIFC61 H50 Co N4 O6 PP 1 21/n 121.2453; 13.3608; 36.5986
90; 95.41; 90
10342.4Kumar, Sachin; Fernández, Sergio; Saltsman, Irena; Fridman, Natalia; Mahammed, Atif; Miller, Alexander J. M.; Gross, Zeev
Substituents effects on the electrocatalytic CO<sub>2</sub> reduction by cobalt corroles in solution.
Chemical communications (Cambridge, England), 2025, 61, 12924-12927
7134867 CIFC157 H82 Cl2 F40 N16 O8P b c a23.9044; 10.7288; 26.6966
90; 90; 90
6846.8Kumar, Sachin; Fernández, Sergio; Saltsman, Irena; Fridman, Natalia; Mahammed, Atif; Miller, Alexander J. M.; Gross, Zeev
Substituents effects on the electrocatalytic CO<sub>2</sub> reduction by cobalt corroles in solution.
Chemical communications (Cambridge, England), 2025, 61, 12924-12927
7134868 CIFC10 H14 F2 Fe K N8C 1 2/c 113.6776; 8.8101; 14.5699
90; 113.281; 90
1612.7Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134869 CIFC10 H14 F2 Fe K N8P a -311.715; 11.715; 11.715
90; 90; 90
1607.78Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134870 CIFC20 H28 F4 Fe2 K2 N16F m -3 m11.8392; 11.8392; 11.8392
90; 90; 90
1659.46Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134871 CIFC10 H14 F2 Fe K N8P a -311.7509; 11.7509; 11.7509
90; 90; 90
1622.61Ji, Luan-Ying; Zhou, Jun-Si; Liu, Shu-Yi; Qin, Yan; Lv, Hui-Peng; Chen, Xiao-Gang
Effective enhancement of mechanical properties <i>via</i> H/F substitution in 3D cyanide hybrid perovskites.
Chemical communications (Cambridge, England), 2025, 61, 13165-13168
7134872 CIFC31 H34 N2 O4P 1 21/n 110.52568; 20.80933; 12.23495
90; 96.5124; 90
2662.56Li, Xin-Yu; Xiao, Mei-Qiu; Zhou, Li-Juan; Zhang, Jia-Qi; Zhao, Meng-Yan; Wang, Shuo-Wen; Tang, Shi
Nickel-catalyzed sequential 1,2-<i>N</i>-migration/BCBs ring-opening to access spirocyclobutyl β-amino acid esters.
Chemical communications (Cambridge, England), 2025, 61, 13473-13476
7134873 CIFC23 H19 N O2P 1 21/c 118.3859; 8.7208; 11.3513
90; 101.037; 90
1786.4Wu, Qing; Han, Yingna; Tang, Tian; Zhang, Shuwei; Yu, Xiuzhao; Zhao, Guofeng; Hu, Weiming; Wang, Lei
Palladium-catalyzed tandem cyclization reaction: access to isoxazoline-benzofuran bis-heterocycles.
Chemical communications (Cambridge, England), 2025, 61, 12928-12931
7134874 CIFC29 H29 N3 O4P -15.7514; 10.0954; 22.139
101.995; 91.679; 102.73
1222.7Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134875 CIFC20 H17 Cl3 N2 O2P 21 21 219.0344; 10.3333; 21.6961
90; 90; 90
2025.44Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134876 CIFC32 H35 N3 O4P 1 21/c 114.0792; 20.6051; 9.7661
90; 98.84; 90
2799.52Guo, Jing; Yan, Maying; Xiao, Lei; Li, Jiajie; Qu, Zheng-Wang; Grimme, Stefan; Stephan, Douglas W.
C(sp<sup>3</sup>)-H functionalization of <i>N</i>-protected dialkylpyrrole derivatives with azodicarboxylates.
Chemical communications (Cambridge, England), 2025, 61, 13659-13662
7134877 CIFC70 H98 N9 O10 PP 1 21/c 114.0616; 16.111; 32.035
90; 96.228; 90
7214.58Oh, Ju Hyun; Shin, Sang Kyu; Kim, Sung Kuk
A calix[4]pyrrole functionalized with an amidoindole ester for the selective recognition of the dihydrogen phosphate anion.
Chemical communications (Cambridge, England), 2025, 61, 13425-13428
7134878 CIFC9 H11 N OR -3 :H24.2502; 24.2502; 7.1744
90; 90; 120
3653.82Cheng, Long; Nian, Cuicui; Han, Zhengyu; Sun, Jianwei; Huang, Hai
Diastereoselective synthesis of 1,4-diaryl piperazines through the dimerization of 3-aminooxetanes with cooperative indium-diphenyl phosphate catalysis.
Chemical communications (Cambridge, England), 2025, 61, 13477-13480
7134879 CIFC26 H33 O4 PP 1 21/n 115.887; 9.64; 16.117
90; 106.397; 90
2368Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134880 CIFC24 H24 OP -16.6003; 12.096; 12.1302
73.196; 79.641; 83.733
910.3Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134881 CIFC39 H58 O6 P2C 1 2/c 112.477; 11.949; 26.368
90; 98.411; 90
3888.9Zheng, Yiyi; Wu, Mingxia; Sun, Shiyue; Zi, You; Sun, Fei; Wu, Xin-Xing
Divergent synthesis of alkylphosphonate-containing indanes and indenes <i>via</i> norbornene derivative-controlled palladium-catalyzed three-component systems.
Chemical communications (Cambridge, England), 2025, 61, 13687-13690
7134882 CIFC16 H14 N2 O2P -15.9207; 8.0892; 15.695
77.953; 85.273; 68.989
686.2Huang, Jie; Ren, Weijie; Chen, Jiehao; Xiao, Xiangrong; Li, Jiaqi; Wang, Dongyi; Yu, Wanyue; Zhao, Juan; Chen, Xiuwen; Zhu, Zhongzhi
Three-component reaction of isocyanates and 3-aminoacrylates: selective synthesis of <i>N</i>-2-aryl-1,2,3-triazoles and hydrazones.
Chemical communications (Cambridge, England), 2025, 61, 13667-13670
7134883 CIFC22 H16 F6 N2 O6 S2 SeP -17.6925; 8.6622; 20.1522
87.959; 87.081; 70.209
1261.63Kuczmera, Thomas J.; Puylaert, Pim; Wirth, Thomas; Nachtsheim, Boris J.
Imidazopyridine substituted cyclic selenonium(IV) salts as chalcogen bond catalysts.
Chemical communications (Cambridge, England), 2025, 61, 14169-14172
7134884 CIFC4 H8 N2 O2 SP n m a8.7805; 7.6704; 9.7607
90; 90; 90
657.38Ali, Rojan; Matsui, Kai; Šadauskis, Jānis; Catherall, Amanda; Wirth, Thomas
Flow electrochemical oxidation of <i>N</i>-nitrosamines to <i>N</i>-nitramines.
Chemical communications (Cambridge, England), 2025, 61, 13671-13674
7134885 CIFC12 H22 N2 O2P 1 21/n 16.0192; 19.1943; 11.0092
90; 92.078; 90
1271.1Ali, Rojan; Matsui, Kai; Šadauskis, Jānis; Catherall, Amanda; Wirth, Thomas
Flow electrochemical oxidation of <i>N</i>-nitrosamines to <i>N</i>-nitramines.
Chemical communications (Cambridge, England), 2025, 61, 13671-13674
7134886 CIFC38 H32 B0.91 F15 Ga1.09P -110.03; 12.141; 15.017
77.99; 80.13; 78.22
1735Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134887 CIFC17 H29 B Ga I3C 1 2/c 134.509; 8.886; 15.894
90; 111.02; 90
4549.5Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134888 CIFC35 H59 B Br4 GaC 1 2/c 116.896; 13.081; 35.577
90; 101.91; 90
7694Ding, Yi; Tang, Yongheng; Nazish, Mohd; Ruth, Paul Niklas; Wachendorf, Sophia Luisa; Herbst-Irmer, Regine; Stalke, Dietmar; Roesky, Herbert W.
1,2,4-Tri(<sup><i>t</i></sup>Bu)cyclopentadienyl gallium (Cp'''Ga) as a versatile reagent for the synthesis of Lewis adducts and ionic compounds.
Chemical communications (Cambridge, England), 2025, 61, 13441-13444
7134889 CIFC29 H30.5 B2 Fe N7.5 OP 1 21/n 112.4656; 17.4511; 13.1482
90; 95.936; 90
2844.9Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134890 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.4966; 17.6717; 13.4291
90; 94.771; 90
2955.36Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134891 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.4828; 17.4584; 13.1586
90; 96.006; 90
2851.91Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134892 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.509; 17.4132; 13.1212
90; 95.783; 90
2843.54Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134893 CIFC29 H29.5 B2 Fe N7.5 OP 1 21/n 112.5019; 17.6496; 13.4172
90; 94.69; 90
2950.64Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134894 CIFC58 H61 B4 Fe2 N15 O2P 1 21 112.5324; 17.6041; 13.3803
90; 94.564; 90
2942.62Becker, Jens-Georg; Sundaresan, Sriram; Carrella, Luca M.; Rentschler, Eva
Chirality without compromise: identical spin crossover behavior between the racemate and the enantiopure Fe(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 13389-13392
7134895 CIFC25 H18 F3 N O3 S SeP -110.6587; 10.7075; 11.815
78.288; 74.899; 61.067
1134.63Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134896 CIFC25 H26 F3 N O4 S SeP -110.3394; 10.4055; 11.5682
83.126; 88.202; 79.76
1215.89Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134897 CIFC38 H29 B2 F8 N3 Se2P 1 21/c 112.7389; 12.6882; 21.5602
90; 97.428; 90
3455.6Kurokawa, Takuma; Takahashi, Shintaro; Kano, Naokazu
<i>Se</i>-Aryl-<i>N</i>-phenylphenoselenazinium salts: aryl radical precursors incorporating a photosensitizer unit.
Chemical communications (Cambridge, England), 2025, 61, 14454-14457
7134898 CIFC24 H30 Cl2 Cu2 N4 O12P 1 21/c 116.4287; 12.3488; 14.368
90; 105.507; 90
2808.8Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134899 CIFC24 H30 Cl2 Cu N4 Ni O12P 1 c 116.7242; 12.3653; 14.6102
90; 105.631; 90
2909.65Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134900 CIFC21 H20 Cu N2 O4F d d d :26.9285; 31.8012; 34.4133
90; 90; 90
7582.4Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134901 CIFC25 H32 Cl2 Co Cu N4 O12P 19.6012; 11.2838; 14.0602
79.812; 85.501; 84.317
1488.98Xie, Xin-Ling; Chen, Feng; Wang, Wen-Wen; Lyu, Lei-Yan; Sun, Meng-Jiao; Zhang, Teng; Cao, Rong
Copper-based homometallic and heterometallic binuclear complexes for electrocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 13485-13488
7134902 CIFC67 H60 F12 N12 O3 P2 RuP 1 21/n 115.521; 23.4518; 20.2925
90; 91; 90
7385.3Mercier, Gabriel M.; Rousset, Elodie; Oubaha, Ilyes; Bandyopadhyay, Kamalika; Pal, Amlan K.; Ciofini, Ilaria; Chamoreau, Lise-Marie; Marvaud, Valérie; Hanan, Garry S.
A ruthenium terpyridine complex showing stable photocatalytic hydrogen evolution under red light.
Chemical communications (Cambridge, England), 2025, 61, 14911-14914
7134903 CIFC69 H73 B2 Cl2 F4 Ir N4P 1 21/c 124.023; 13.643; 19.181
90; 100.954; 90
6172Fukumoto, Ryo; Yokoo, Takuya; Sakuda, Eri; Omoto, Kenichiro; Horiuchi, Shinnosuke; Arikawa, Yasuhiro; Umakoshi, Keisuke
Covalently linked triarylborane-iridium(III) complex as a photocatalyst for CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 14943-14946
7134904 CIFC17 H13 PC m c 2124.0423; 7.61; 7.1438
90; 90; 90
1307.04Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134905 CIFC31 H37 P Si2C 1 c 118.6524; 14.8278; 10.6662
90; 105.222; 90
2846.5Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134906 CIFC25 H21 PP 1 21/n 17.008; 16.5827; 16.2271
90; 91.776; 90
1884.9Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134907 CIFC27 H25 O P SeC 1 2/c 115.385; 13.0349; 22.32
90; 98.157; 90
4430.8Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134908 CIFC51 H44 Cl2 P2P -111.7787; 12.1311; 15.4644
74.53; 89.83; 72.66
2025.8Steffen, Leo; Szych, Lilian S.; Franzke, Yannick J.; Kopp, Richard O.; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Di-π-methane rearrangement in 1-phosphabarrelenes: formation and reactivity of an unprecedented 2-phosphasemibullvalene.
Chemical communications (Cambridge, England), 2025, 61, 14907-14910
7134909 CIFC28 H24 N O2 PP 1 n 16.0125; 12.501; 15.039
90; 96.181; 90
1123.8Thondur, Jagadeesh Reddy; Gowda, Punith S.; Sharada, Duddu S.; Satyanarayana, Gedu
Electrochemical synthesis of phosphorylated oxazolines from <i>N</i>-allylamides.
Chemical communications (Cambridge, England), 2025, 61, 14717-14720
7134910 CIFC30 H16 F6 N4 O2P n a 2110.7693; 29.918; 7.4885
90; 90; 90
2412.8Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134911 CIFC74 H54 N12 O6P 3217.1456; 17.1456; 16.9139
90; 90; 120
4306.06Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134912 CIFC43 H31 N6 O2C 1 2/c 128.494; 12.5982; 21.951
90; 105.585; 90
7590.1Benny, Renitta; Andrews, Alex P.; De, Soumen
Foldamer engineering with squaramide and phenanthroline motifs: synthesis, characterisation, and structural insights.
Chemical communications (Cambridge, England), 2025, 61, 14955-14958
7134913 CIFC9 H10 B F2 N O2P n m a13.463; 6.954; 10.056
90; 90; 90
941.5Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134914 CIFC13 H9 B F2 O2P 1 21/c 116.243; 7.2371; 20.146
90; 108.343; 90
2247.9Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134915 CIFC14 H11 B F2 O3P 21 21 217.865; 10.808; 14.417
90; 90; 90
1225.5Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134916 CIFC8 H7 B F2 O3P 1 21/c 19.09; 11.297; 8.038
90; 96.756; 90
819.7Ogoshi, Hikari; Ito, Shunichiro; Tanaka, Kazuo
Regulation of the frontier molecular orbitals and photophysical properties of boron tropolonate complexes by regioselective functionalization.
Chemical communications (Cambridge, England), 2025, 61, 14625-14628
7134917 CIFC18 H15 Cl0.15 N0.85 O1.7 SiP 1 21/n 19.4177; 18.4095; 9.9867
90; 106.888; 90
1656.8Dahmani, Houari; Poulin, Louis-Philippe; Fecteau, Charles-Émile; Harter, Lara; Johnson, Paul Andrew; Bélanger-Chabot, Guillaume
Nitro and nitritosilanes: do they and can they exist?
Chemical communications (Cambridge, England), 2025, 61, 15814-15817
7134918 CIFC36 H30 N2P 1 21/c 15.3157; 34.868; 16.652
90; 94.617; 90
3076.4Jaiswal, Gaurav; Pan, Subhas Chandra
Iridium catalyzed intramolecular cyclization of allyl alcohol-indole hybrids: rapid access to photoluminescent 5<i>H</i>-benzo[<i>b</i>]carbazoles.
Chemical communications (Cambridge, England), 2025, 61, 15011-15014
7134919 CIFC26 H26 Cl2 O6P -18.5461; 11.5957; 13.2007
72.926; 87.247; 81.392
1236.41Dan Xu, ?; Li, Xiaoxuan; Cai, Yifei; Chen, Yushuang; Xin, Yu; Chen, Jing; Yao, Hui; Huang, Nianyu; Wang, Nengzhong
Additive-controlled chemodivergent multi-component domino reaction between salicylaldehydes and Morita-Baylis-Hillman (MBH) carbonates.
Chemical communications (Cambridge, England), 2025, 61, 15433-15436
7134920 CIFC16 H14 O4P -17.0689; 11.6245; 15.613
93.973; 90.876; 92.978
1277.9Dan Xu, ?; Li, Xiaoxuan; Cai, Yifei; Chen, Yushuang; Xin, Yu; Chen, Jing; Yao, Hui; Huang, Nianyu; Wang, Nengzhong
Additive-controlled chemodivergent multi-component domino reaction between salicylaldehydes and Morita-Baylis-Hillman (MBH) carbonates.
Chemical communications (Cambridge, England), 2025, 61, 15433-15436
7134921 CIFC19 H23 N O2P 21 21 219.65189; 12.52806; 12.83597
90; 90; 90
1552.12Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134922 CIFC26 H32 Fe N2 O4I 1 2 112.2589; 5.803; 17.0375
90; 99.601; 90
1195.04Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134923 CIFC46 H56 Fe N2 O4I 1 2 119.6453; 14.5148; 31.1666
90; 100.673; 90
8733.4Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134924 CIFC26 H32 Fe N2 O4I 1 2 112.23289; 5.80595; 17.0105
90; 99.7213; 90
1190.8Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134925 CIFC32 H24 Fe N2 O4I 1 2 114.66217; 5.0273; 16.98028
90; 94.3034; 90
1248.11Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134926 CIFC38 H44 Fe N2 O4I 1 2 112.2867; 6.39098; 20.0622
90; 106.711; 90
1508.84Stroek, Wowa; Rowlinson, Nathalie A. V.; Hudson, Luke A.; Albrecht, Martin
Enantioselective C-H amination catalyzed by homoleptic iron salox complexes.
Chemical communications (Cambridge, England), 2025, 61, 15274-15277
7134927 CIFC43 H32 N2 O4 SP 21 21 219.682; 17.405; 21.044
90; 90; 90
3546Ghosh, Suman; Saha, Partha Sarathi; Saha, Shib Nath; Chandrasekharan, Sanoop P.; Koner, Mainak; Baidya, Mahiuddin
Cobalt-catalyzed regio- and stereoselective synthesis of atropisomers with vicinal C-C and C-N diaxes.
Chemical communications (Cambridge, England), 2025, 61, 15231-15234
7134928 CIFC38 H33 B N2 OP -110.5016; 11.4289; 13.5999
104.793; 93.4087; 114.921
1405.02Tan, Ji-Hua; Liu, Xiao-Long; Su, Yao-Zu; Xing, Longjiang; Huo, Yanping; Chen, Jia-Xiong; Zhao, Zujin; Chen, Wen-Cheng
Incorporating hybrid charge transfer within a boron/nitrogen/oxygen-embedded scaffold for efficient yellow electroluminescence.
Chemical communications (Cambridge, England), 2025, 61, 14975-14978
7134929 CIFC8 H15 N6 O5.5 S Zn2C 1 2/c 117.4653; 9.737; 9.8807
90; 114.166; 90
1533.05Tian, Wen-Jiang; Hu, Ding-Yi; Fang, Zi-Luo; Zhong, Xiao-Feng; Xue, Ming; Zhou, Hao-Long; Zhou, Dong-Dong; Chen, Xiao-Ming
A stable sulfate-pillared metal triazolate framework with a gating effect for highly efficient dehydration of bioethanol.
Chemical communications (Cambridge, England), 2025, 61, 15461-15464
7134930 CIFC26 H19 N OP 1 21/c 110.2995; 14.7508; 13.5318
90; 106.895; 90
1967.1Yadav, Nisha; Ramasastry, S. S. V.
Creating skeletal complexity through an interrupted Corey-Chaykovsky reaction of activated alkynes.
Chemical communications (Cambridge, England), 2025, 61, 15179-15182
7134931 CIFC32 H22 N2P 42/n :215.539; 15.539; 9.7031
90; 90; 90
2342.9Lijina, M. P.; Sujilkumar, Suvarna; Jadhav, Sohan D.; Hariharan, Mahesh
Exciton interactions in crystalline crossed diazapentacene.
Chemical communications (Cambridge, England), 2025, 61, 15397-15400
7134932 CIFC25 H20 O3P -18.797; 10.718; 11.047
97.418; 90.078; 110.84
964Wu, Hao-Ze; Zhai, Jing-Qi; Sun, Jun-Xi; Liu, Ying-Pin; Tu, Man-Su; Hao, Wen-Juan; Jiang, Bo
Electrochemical dehydrogenative α-vinylation and α-allylation of cyclic β-ketoesters.
Chemical communications (Cambridge, England), 2025, 61, 15187-15190
7134933 CIFC49 H60 Cl3 O2 P TiP 1 21/c 115.782; 24.6362; 12.3944
90; 106.631; 90
4617.46Toda, Tomoyuki; Cheng, Yu; Takenaka, Katsuhiko
Synthesis and structure of titanium complexes with phosphonium-bisphenolate ligands "{P<sup>+</sup>[O<sub>2</sub>]}H<sub>2</sub>" and their catalytic trimerization of 1-octene.
Chemical communications (Cambridge, England), 2025, 61, 15594-15597
7134934 CIFC56 H53.5 B Cl0.5 F15 N2 Na O2P 1 21/c 110.4137; 21.394; 23.4007
90; 95.631; 90
5188.3Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134935 CIFC55.15 H55.58 B F15 K N2 O2.36P 1 21/c 110.4085; 21.402; 23.6416
90; 95.876; 90
5238.8Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134936 CIFC49 H43 B F15 N2 O RbP 1 21/n 110.5897; 19.8422; 22.0049
90; 102.005; 90
4522.61Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134937 CIFC58.79 H59 B F15 N2 O2.4 RbP 1 21/c 112.6204; 20.9998; 22.0018
90; 103.79; 90
5663Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134938 CIFC56 H53.5 B Cl0.5 F15 K N2 O2P 1 21/c 110.4148; 21.3092; 23.9266
90; 96.291; 90
5278.1Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134939 CIFC55.5 H57 B F15 N2 O2 RbP 1 21/c 110.4449; 21.3951; 23.6633
90; 95.879; 90
5260.2Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134940 CIFC57 H59 B Cs F15 N2 O3P n a 2124.4226; 10.8098; 20.7892
90; 90; 90
5488.42Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134941 CIFC57 H59 B Cs F15 N2 O3P 1 21/c 119.7357; 15.5295; 36.8929
90; 91.4071; 90
11303.7Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134942 CIFC57 H59 B Cs F15 N2 O3P 1 21/n 110.658; 36.1409; 43.421
90; 96.705; 90
16610.9Groth, Lucie J.; Bockfeld, Dirk; Tamm, Matthias
Heavy alkali metal complexes of N-heterocyclic carbenes.
Chemical communications (Cambridge, England), 2025, 61, 15806-15809
7134943 CIFC40 H42 F6 Li N7 Ni O7 S2P 21 21 2119.0891; 19.1789; 23.9828
90; 90; 90
8780.29Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134944 CIFC43 H48 Co F3 N7 Ni O8 SP 1 21/c 110.4885; 21.9395; 19.6735
90; 96.268; 90
4500.05Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134945 CIFC42 H45 Cu F6 N7 Ni O9 S2P 1 21/n 113.3133; 21.6731; 16.4955
90; 96.1; 90
4732.67Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134946 CIFC75 H64.5 B F24 N6 Ni2 O5.75P -112.952; 17.1844; 35.8757
80.209; 80.119; 75.351
7543.3Patterson, Claire R.; Oyala, Paul H.; Buss, Joshua A.
Synthesis and electronic structure elucidation of bioinspired heterobimetallic nickel complexes.
Chemical communications (Cambridge, England), 2025, 61, 12345-12348
7134947 CIFC22 H14 Cl2 F3 NP -18.8332; 10.9154; 11.1884
103.17; 93.958; 111.325
964.66Song, Mengda; Leng, Yuting; Xu, Zhiwei; Wu, Yusheng; Wu, Yangjie
Photocatalytic cyclization reaction of 2-vinylarylamines with CF<sub>3</sub>SO<sub>2</sub>Na and arylaldehydes to access 3-(2,2,2-trifluoroethyl)-3<i>H</i>-indoles.
Chemical communications (Cambridge, England), 2025, 61, 15626-15629
7134948 CIFC25 H19 F6 N O2P 1 21/n 112.2122; 13.7141; 14.0849
90; 112.262; 90
2183.1Song, Mengda; Leng, Yuting; Xu, Zhiwei; Wu, Yusheng; Wu, Yangjie
Photocatalytic cyclization reaction of 2-vinylarylamines with CF<sub>3</sub>SO<sub>2</sub>Na and arylaldehydes to access 3-(2,2,2-trifluoroethyl)-3<i>H</i>-indoles.
Chemical communications (Cambridge, England), 2025, 61, 15626-15629
7134949 CIFC14 H13 F2 N7 O5P n a 2138.4123; 3.6758; 23.4287
90; 90; 90
3308.04Grabowski, Szymon; Wojdyła-Parat, Julianna; Tyszka-Czochara, Małgorzata; Kozieł, Marcin; Chmylak, Michał; Lalik, Sebastian; Gryl, Marlena
The whole is greater than the sum of its parts: binary and ternary 5-fluorouracil co-crystals with enhanced selectivity towards metastatic cancer cells.
Chemical communications (Cambridge, England), 2025, 61, 16770-16773
7134950 CIFC19 H18 F N5 O7P -110.0127; 10.3322; 11.01547
92.4573; 97.6809; 118.558
984.47Grabowski, Szymon; Wojdyła-Parat, Julianna; Tyszka-Czochara, Małgorzata; Kozieł, Marcin; Chmylak, Michał; Lalik, Sebastian; Gryl, Marlena
The whole is greater than the sum of its parts: binary and ternary 5-fluorouracil co-crystals with enhanced selectivity towards metastatic cancer cells.
Chemical communications (Cambridge, England), 2025, 61, 16770-16773
7134951 CIFC10 H18 I2 N2 O4 PbC 1 2 118.4916; 5.0168; 10.5385
90; 121.698; 90
831.81Cheng, Juan; Yi, Gangji; Zhong, Qinglan; Huang, Ling; Zeng, Hongmei; Zou, Guohong; Lin, Zhien
Enhanced second-harmonic generation response in a chiral lead iodide induced by amino acid coordination.
Chemical communications (Cambridge, England), 2025, 61, 15682-15685
7134952 CIFC26 H42 N3 P SnP 1 21/c 116.042; 9.1284; 19.28
90; 99.505; 90
2784.6Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134953 CIFC29 H42 N3 P Si SnP 21 21 216.5953; 17.4977; 10.4421
90; 90; 90
3032.2Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134954 CIFC26 H46 N3 P Si2 SnP 1 21/n 111.485; 17.028; 15.977
90; 90.319; 90
3124.5Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134955 CIFC35 H54 N3 P Si SnP -110.7809; 12.7284; 14.9033
72.507; 82.446; 69.563
1826.93Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134956 CIFC27 H46 N3 P Si SnP 1 21/n 111.3458; 16.8337; 15.6145
90; 90.519; 90
2982.12Takahashi, Shintaro; Ishii, Akihiko; Nakata, Norio
Iminophosphonamido stannylenes enable quantitative CO<sub>2</sub> conversion to isocyanates.
Chemical communications (Cambridge, England), 2025, 61, 15389-15392
7134957 CIFC37 H31 N O4 S2P -111.1541; 11.8712; 12.7603
64.127; 81.601; 81.316
1496.72Yadav, Pooja; Varma, A. Anagha; Gopinath, Purushothaman
Accessing [6,6,5,6] tetracyclic indeno-quinolines <i>via</i> a photomediated cascade reaction of electron-rich 1,7-enynes.
Chemical communications (Cambridge, England), 2025, 61, 16440-16443
7134958 CIFC19 H23 Br N O6 PP 43 21 210.3187; 10.3187; 38.654
90; 90; 90
4115.7Savoskin, Alexander E.; Efremov, Andrey N.; Murashkina, Arina V.; Gontcharenko, Victoriya E.; Bogdanov, Andrei V.; Mitrofanov, Alexander Yu; Beletskaya, Irina P.
Base-promoted cascade annulation and annulation/carboxylation of α-enolizable phosphoryl substituted ynones and isatins with CO<sub>2</sub>.
Chemical communications (Cambridge, England), 2025, 61, 16230-16233
7134959 CIFC45 H57 N4 O10 ZnP 1 21/c 114.7895; 18.2516; 19.007
90; 111.191; 90
4783.7Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134960 CIFC44.5 H48.5 N4 O6.5 ZnC 1 2/c 128.556; 13.118; 24.817
90; 113.023; 90
8556Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134961 CIFC31 H31.94 F N3 O8 ZnP -113.273; 13.274; 18.456
85.563; 77.044; 79.9
3117Dutta, Abhishek; Ghosh, Subhajit; Dastidar, Parthasarathi
Developing a Zn(II)-metallovesicle for loading and delivering doxorubicin to kill cancer cells-a multi-drug delivery system.
Chemical communications (Cambridge, England), 2025, 61, 15646-15649
7134962 CIFC53 H53 Cl2 O4 Si3C 1 2/c 116.5351; 15.4526; 19.1218
90; 102.301; 90
4773.6Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134963 CIFC52 H50 O4 Si3I 1 2/c 117.857; 11.106; 23.4549
90; 91.262; 90
4650.4Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134964 CIFC28 H38 O2 Si3P -110.5394; 12.0173; 12.3813
82.86; 68.217; 82.581
1439.02Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134965 CIFC38 H42 O2 Si3P 1 21/c 118.8918; 16.4124; 11.5152
90; 101.755; 90
3495.5Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134966 CIFC27 H34 O2 Si3P 1 21/c 110.8977; 18.3039; 13.5149
90; 91.29; 90
2695.14Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134967 CIFC38 H42 O2 Si3P -19.5424; 10.5382; 18.3347
78.61; 82.78; 76.832
1753.6Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134968 CIFC64 H54 O5.25 SiC 1 2/c 129.764; 14.7485; 25.3341
90; 117.338; 90
9878.9Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134969 CIFC39 H34 Cl3 D O4 SiP 1 n 111.0558; 13.5926; 23.5001
90; 102.655; 90
3445.73Szathmári, Balázs; Holczbauer, Tamás; Balterer, Bence; Domján, Attila; Volk, Balázs; Kovács, Ilona; Kelemen, Zsolt
Synthesis and characterization of the first neutral hexacoordinated silole complexes.
Chemical communications (Cambridge, England), 2025, 61, 16042-16045
7134970 CIFC6 H17 Cl N6 O4P 1 21/c 110.4474; 10.2793; 12.6679
90; 100.902; 90
1335.88Pan, Yu-Ming; An, Xin-You; Fang, Zhi
[C(NH<sub>2</sub>)<sub>3</sub>]<sub>2</sub>[C<sub>2</sub>H<sub>5</sub>(C<sub>2</sub>O<sub>4</sub>)]Cl: rational design of a metal-free UV birefringent crystal through the synergistic assembly of three distinct motifs.
Chemical communications (Cambridge, England), 2025, 61, 15894-15897
7134971 CIFC32 H32 Co N2 O2P b c a16.768; 16.0675; 20.0092
90; 90; 90
5390.88Robaszkiewicz, Jakub; Szarłan, Bartłomiej; Pawluć, Piotr; Kubicki, Maciej; Zaranek, Maciej
Sustainable synthesis of hydrosilanes and alkoxysilanes in a sequential one-pot olefin hydrosilylation and dehydrogenative coupling with alcohol under phenoxyiminato cobalt(II) catalysis.
Chemical communications (Cambridge, England), 2025, 61, 16046-16049
7134972 CIFC98.53 H111.06 N2 O11.84P -116.74959; 24.61558; 24.87337
64.6808; 70.8779; 74.2696
8655Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134973 CIFC92 H100 N2 O9C 1 2 119.5858; 21.7012; 20.0122
90; 113.871; 90
7778.3Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134974 CIFC93.62 H101.24 N2 O9.54C 1 2/c 143.0399; 24.2273; 61.0404
90; 99.47; 90
62781.9Chen, Jin-Fa; Gao, Qing-Xiu; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
Guest-triggered crystallization of π-conjugated pillar[5]arene: from amorphous aggregates to an ordered architecture <i>via</i> solid-state host-guest synergy.
Chemical communications (Cambridge, England), 2025, 61, 15882-15885
7134975 CIFCa6 Mn2 N6 OR -3 :H8.92557; 8.92557; 9.23716
90; 90; 120
637.296Buschmann, Niklas; Werhahn, Dominik; Steinberg, Simon; Ritter, Clemens; Attfield, J. Paul; Kloß, Simon D
Multiple bonding in unbridged Mn-Mn dimers of solid-state nitridomanganate(IV) oxide Ca<sub>6</sub>[Mn<sub>2</sub>N<sub>6</sub>]O.
Chemical communications (Cambridge, England), 2025, 61, 15662-15665
7134976 CIFCa6 Mn2 N6 OR -3 :H8.95635; 8.95635; 9.25969
90; 90; 120
643.264Buschmann, Niklas; Werhahn, Dominik; Steinberg, Simon; Ritter, Clemens; Attfield, J. Paul; Kloß, Simon D
Multiple bonding in unbridged Mn-Mn dimers of solid-state nitridomanganate(IV) oxide Ca<sub>6</sub>[Mn<sub>2</sub>N<sub>6</sub>]O.
Chemical communications (Cambridge, England), 2025, 61, 15662-15665
7134977 CIFC64 H98 Cl4 Ir2 Li2 O3 P2P 1 21/c 110.52239; 18.32736; 17.04898
90; 99.046; 90
3246.96Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134978 CIFC46 H82 K N4 O9 PP 1 2/n 111.2324; 11.8181; 36.8937
90; 95.713; 90
4873.2Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134979 CIFC26 H54 K N4 O7 PP 1 21/c 117.2179; 8.7318; 21.9955
90; 103.469; 90
3215.92Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134980 CIFC57 H86 Au N2 O3.5 PP 1 21/c 117.92474; 22.02986; 15.23246
90; 114.707; 90
5464.35Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134981 CIFC129 H228 B4 K4 N8 O10.25 P4P -116.8002; 17.1154; 24.435
96.603; 106.698; 92.909
6659.2Genoux, Alexandre; Wong, Tak Hin; Fadaei-Tirani, Farzaneh; Severin, Kay
Covalent capture of nitrous oxide by phosphanides.
Chemical communications (Cambridge, England), 2025, 61, 15654-15657
7134982 CIFC46 H52 Si2P -19.869; 12.442; 32.249
82.407; 81.941; 74.764
3764Espineira-Gutierrez, Adrian; Caro-Noakes, Ines; Zhang, Min; Mas-Torrent, Marta; Regulska, Elzbieta; Romero-Nieto, Carlos
The role of main group elements in shaping the properties of linearly-fused heterohexaarenes.
Chemical communications (Cambridge, England), 2025, 61, 15590-15593
7134983 CIFC12 H23 Fe3 N2 O19P 1 21/n 114.2657; 8.2582; 21.5884
90; 102.732; 90
2480.8Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134984 CIFC13 H23 Fe3 N2 O18P 1 21/n 114.2147; 8.3281; 21.3984
90; 102.558; 90
2472.6Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134985 CIFC15 H27 Fe3 N2 O18P 1 21/n 114.3325; 8.4968; 21.8494
90; 102.465; 90
2598.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134986 CIFC12 H23 Fe3 N2 O19R -3 c :H8.2548; 8.2548; 63.391
90; 90; 120
3740.9Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134987 CIFC15 H27 Fe3 N2 O18R -3 c :H8.4183; 8.4183; 63.025
90; 90; 120
3868.1Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134988 CIFC13 H23 Fe3 N2 O18R -3 c :H8.2967; 8.2967; 62.793
90; 90; 120
3743.3Yan, Qin-Yuan; Han, Song-De; Xu, Ting; Ji, Cui-Xian; Lv, Lin-Lin; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
Organic ammonium modulated mixed-valence multiferroics exhibiting large spontaneous strain and exchange bias.
Chemical communications (Cambridge, England), 2025, 61, 16412-16415
7134989 CIFC9 H9 F O3C 1 2/c 118.7223; 11.2619; 8.6284
90; 109.598; 90
1713.9Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134990 CIFC7 H5 F O3P -17.6681; 8.3643; 11.4816
76.068; 77.79; 64.382
639.61Karbalaei, Sana; Franke, Alicja; Zahl, Achim; Pokkuluri, P. Raj; Beyers, Ronald J.; Ivanović-Burmazović, Ivana; Goldsmith, Christian R.
An Fe(II) complex detects hydrogen peroxide with <sup>1</sup>H and <sup>19</sup>F magnetic resonance imaging responses.
Chemical communications (Cambridge, England), 2025, 61, 15898-15901
7134991 CIFC58 H34 N4 O2P 18.8479; 11.4027; 11.4991
86.241; 72.076; 68.194
1023.29Yin, Xiaojun; Chen, Xuefeng; Mo, Xuechao; Chen, Junjin; Huang, Mengyu; Ma, Jiacheng; Li, Yulan; Li, Nengquan; Yang, Chuluo
Charge-transfer modulated chiroptical azacyclooctatetraene-fused [5]helicenes with AIE features.
Chemical communications (Cambridge, England), 2025, 61, 16448-16451
7134992 CIFC28.5 H21 Br Cl O4P 19.0354; 11.1067; 13.6619
106.141; 96.303; 107.287
1229.51Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134993 CIFC28 H22 O4P 21 21 218.8073; 12.1366; 20.0872
90; 90; 90
2147.13Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134994 CIFC28 H22 O4P 1 21 111.628; 15.6621; 12.0951
90; 97.484; 90
2183.98Zhai, Jing-Jing; Lou, Shao-Jie; Zhang, Xiao-Xiao; Lan, Qiu-Yi; Jing, Cheng-Cheng; Mao, Yang-Jie; Wang, Yi-Feng; Chu, Ming-Ming; Xu, Dan-Qian
Remote asymmetric conjugate addition of naphthoquinone methides: constructing adjacent tertiary-quaternary carbon stereocenters.
Chemical communications (Cambridge, England), 2025, 61, 16644-16647
7134995 CIFC27 H22 N2 O2I 1 a 15.8439; 38.1781; 9.1909
90; 94.124; 90
2045.26Kumar, Pravin; Dash, Om Prakash; Volla, Chandra M. R.
Cobalt-catalyzed regioselective (4+2)-annulation of benzamides with allenyl carbinol acetates: access to 3-vinylisoquinolinones.
Chemical communications (Cambridge, England), 2025, 61, 16962-16965
7134996 CIFC48 H38 Ag P3 SP -110.8475; 12.0536; 15.9663
72.057; 88.8299; 81.512
1963.63Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134997 CIFC48 H38 Ag P3 SP -110.8455; 12.0698; 15.9133
72.271; 88.798; 81.388
1961.13Łaski, Piotr; Drapała, Jakub; Kamiński, Radosław; Durka, Krzysztof; Szarejko, Dariusz; Henning, Robert; Jarzembska, Katarzyna N.
Capturing the short-lived excited singlet state in crystals of a TADF silver(I) complex.
Chemical communications (Cambridge, England), 2025, 61, 16560-16563
7134998 CIFC21 H21 Br N2 OP 1 21/c 112.9547; 10.2165; 16.1046
90; 113.338; 90
1957.1Kar, Subarna; Ramachandran, Arya; Rit, Arnab
Efficient synthetic approach to <i>m</i>-terphenyl derivatives <i>via</i> arylation of azolium salts.
Chemical communications (Cambridge, England), 2025, 61, 16802-16805
7134999 CIFC21 H16 N O2 PP -18.71; 10.081; 11.048
99.774; 106.774; 100.943
885.5Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135000 CIFC21 H18 N O2 PP 1 21/c 111.6354; 11.6264; 13.4546
90; 91.652; 90
1819.35Meng, Li-Qin; Zhu, Xinrong; Xing, Qiaoyan; Zhang, Junliang; Wang, Huamin; Lin, Ying-Wu
Concise synthesis of phosphonylated heteroarenes from nitroheteroarenes by dearomatization/elimination.
Chemical communications (Cambridge, England), 2025, 61, 16810-16813
7135001 CIFC106 H58 N18 O17 Pd2 Zn5P 1 21/n 19.9191; 32.4889; 38.6916
90; 95.533; 90
12410.7Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135002 CIFC56 H36 N10 O9 Pd Zn2C 1 2/c 133.103; 10.1085; 43.6
90; 98.346; 90
14435Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135003 CIFC56 H36 N10 O9 Pd Zn2P 1 21/c 122.815; 9.9064; 31.625
90; 95.495; 90
7114.9Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135004 CIFC58 H33 N14 O8.5 Pd Zn3C c c a :233.8282; 10.4006; 43.8964
90; 90; 90
15444.2Kenny, Mitchell S.; Gładysiak, Andrzej; Lessard, Jacob M.; Pyle, Dylan; Stylianou, Kyriakos C.
Stacked, twisted, and porous: structural diversity in photoactive porphyrin-based metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 18906-18909
7135005 CIFC32 H34 Ag Cl Fe N12 O6C 1 2/c 113.4233; 16.051; 17.725
90; 95.291; 90
3802.7Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135006 CIFC32 H34 Ag Cl Fe N12 O6.16C 1 2/c 113.2411; 15.6597; 17.3891
90; 97.325; 90
3576.2Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135007 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.8631; 25.8631; 20.8337
90; 90; 120
12068.6Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135008 CIFC54 H30 Ag6 Fe3 N18 S3P 6525.546; 25.546; 20.356
90; 90; 120
11504.5Yao, Nian-Tao; Jiang, Jiao-Jiao; Qian, Bing-Yuan; Sun, Hui-Ying; Yi, Cheng; Zhao, Liang
Large dielectric modulation triggered by spin crossover in polar Hofmann-type polymers.
Chemical communications (Cambridge, England), 2025, 61, 16640-16643
7135009 CIFC28 H27 N O6 SP 1 21/c 110.2849; 24.4179; 10.3397
90; 105.642; 90
2500.5Zheng, Jianfeng; Xiong, Dong; Ye, Yongqi; Tang, Luhao; Yang, Jiajin; Yang, Zeyu; Cai, Yunfei
Efficient syntheses of 2-amino-4<i>H</i>-pyrans <i>via</i> gold-catalyzed cyclization of diester-tethered ynamides.
Chemical communications (Cambridge, England), 2025, 61, 16858-16861
7135010 CIFC18 H15 Br I N OP -16.3543; 8.4335; 16.8759
98.77; 99.305; 90.041
881.73Chen, Chen; Wang, Zi-Yi; Zhang, Xiao-Xu; Wang, Kui; Zhu, Bolin
Pd-catalyzed electrophilic cross-coupling of pyridylphosphonium salts with arylthianthrenium salts to access C4-arylated pyridines.
Chemical communications (Cambridge, England), 2025, 61, 17185-17188
7135011 CIFC33 H51 Al N2 ZnP n m a15.9848; 20.213; 9.8381
90; 90; 90
3178.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135012 CIFC83 H114 Ga2 N4 O2 Zn2P -19.7057; 14.4604; 14.9677
87.7489; 72.9148; 73.06
1918.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135013 CIFC64 H94 N4 Si2P -110.9267; 11.6874; 12.7613
93.932; 104.6; 111.522
1443.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135014 CIFC62 H53 B F20 N2 Si ZnP -111.1667; 12.7101; 21.923
98.644; 101.458; 102.212
2919.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135015 CIFC74 H115 Ga N4 Si ZnP 1 21/n 112.1549; 32.569; 18.1556
90; 101.686; 90
7038.3Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135016 CIFC74 H113.5 Ga N4 Si ZnC 1 2/c 117.5328; 19.9362; 20.5665
90; 93.366; 90
7176.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135017 CIFC33 H51 Ga N2 ZnP 21 21 219.876; 16.0049; 20.269
90; 90; 90
3203.8Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135018 CIFC74 H120 Ga2 N4 ZnC 1 2/c 117.5441; 20.0646; 20.5353
90; 93.8778; 90
7212.2Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135019 CIFC74 H120 Al Ga N4 ZnC 1 2/c 117.6429; 20.0099; 20.5546
90; 92.706; 90
7248.4Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135020 CIFC74 H102 Ga N4 Si ZnC 1 2/c 116.4935; 17.0584; 24.336
90; 92.0203; 90
6842.7Sahoo, Rajata Kumar; Wölper, Christoph; Möbius, Joost; Schulz, Stephan
Synthesis and reactivity of acyclic heterotrinuclear metal complexes.
Chemical communications (Cambridge, England), 2025, 61, 16774-16777
7135021 CIFC78 H78 O12P -16.0018; 16.2806; 16.8345
107.589; 97.731; 95.825
1536.1Yamini, Pokhriyal; Duklan, Bhoomika; Nirmal, Mukesh; Yadagiri, Dongari
Light-induced intramolecular carbene C(sp<sup>3</sup>)-H insertion of <i>N</i>-tosylhydrazones; synthesis of functionalized coumarans and indolines.
Chemical communications (Cambridge, England), 2025, 61, 17017-17020
7135022 CIFC8 H9 N3 O2P b c a12.8099; 7.7737; 18.5183
90; 90; 90
1844.06Kumar, Prashant; Kant, Ruchir; Rastogi, Namrata
Nitrogen atom insertion into NN double bonds: straightforward access to triazenes.
Chemical communications (Cambridge, England), 2025, 61, 16632-16635
7135023 CIFC21 H17 N O2P n m a15.204; 6.943; 15.282
90; 90; 90
1613Bai, Fang; Liu, Pengpeng; Xu, Hongyan; Li, Mengjie; Liu, Binghui; Xu, Miaomiao; Gao, Qinghe
Auto-oxidation-driven vicinal C(sp<sup>3</sup>)-H desaturative cyclization of tertiary alkylamines for the synthesis of pyrido[3,2-<i>c</i>]coumarins.
Chemical communications (Cambridge, England), 2025, 61, 16818-16821
7135024 CIFC20 H20 Dy2 O20P 1 21/n 17.6415; 15.8785; 21.8456
90; 97.457; 90
2628.23Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135025 CIFC60 H50 Cl1.5 Dy8.5 O86P 4/m21.7419; 21.7419; 7.7397
90; 90; 90
3658.64Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135026 CIFC60 H52 Cl1.5 Gd8.5 O86P 4/m21.8854; 21.8854; 7.7744
90; 90; 90
3723.71Shao, Xueying; Yang, Yue; Dong, Xiaofang; Wang, Shen; Liang, Yulu; Liu, Zhongyi; Min, Hui; Wang, Yu-Xia; Cheng, Peng
Magnetic modulation and magnetocaloric effect of lanthanide porous organic frameworks with croconic acid.
Chemical communications (Cambridge, England), 2025, 61, 16862-16865
7135027 CIFC11 H11 N O2P 1 21/n 113.1083; 6.8867; 21.4225
90; 92.066; 90
1932.61Shi, Yaolian; Gong, Yuchen; Li, Ganpeng; Zhao, Xiao-Jing; He, Yonghui
Cobalt-salen complexes/organic photoredox-cocatalyzed selective oxidative formylation of enaminones.
Chemical communications (Cambridge, England), 2025, 61, 17173-17176
7135028 CIFC68 H92 N4 O P4P 1 c 19.94331; 17.65986; 18.49899
90; 99.9045; 90
3199.96Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135029 CIFC44 H51 N2 P Se2P -19.845; 10.4186; 21.0183
82.912; 80.297; 71.16
2005.68Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135030 CIFC48 H57 F6 N2 O3 P2 SP 1 21/n 112.1447; 29.8408; 13.06799
90; 94.1461; 90
4723.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135031 CIFC67.76 H90.76 N4 P2P -112.0999; 14.6052; 41.8681
85.433; 87.238; 68.411
6856.66Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135032 CIFC33 H41 F3 N2 O3 P2 SP 1 21/c 112.1104; 13.7238; 20.3093
90; 97.664; 90
3345.27Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135033 CIFC76 H102 N4 P4P b c a22.3323; 21.5645; 29.5421
90; 90; 90
14227Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135034 CIFC45 H51 F3 N2 O3 P2 S3P -110.4857; 13.3395; 16.2297
94.945; 99.955; 94.997
2215.54Wieneke, Jan; Cirigliano, Francesco; Schorpp, Marcel
A diazadiphospholenium cation featuring a reactive PP bond: synthesis and reversible main-group bond activation.
Chemical communications (Cambridge, England), 2025, 61, 17601-17604
7135035 CIFC21 H17 Cl N4 O2P 1 21/c 121.4394; 13.9197; 12.5913
90; 105.292; 90
3624.6Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135036 CIFC21 H21 Cl N4 O4P 1 21/c 19.5672; 35.984; 5.9462
90; 95.563; 90
2037.4Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135037 CIFC14 H14 N4 OP 1 21/n 110.6661; 4.919; 23.7529
90; 102.205; 90
1218.06Guo, Ting-Ting; Zhao, Qing-Sheng; Yang, Shu; Chen, Tian-Tian; Liu, Jin; Yan, Sheng-Jiao
Rh(III)-catalyzed cyclization of 5-amino-pyrazoles with maleimides to pyrazoloquinazolines.
Chemical communications (Cambridge, England), 2025, 61, 16846-16849
7135038 CIFC36 H37 N OP b c a9.7987; 20.5217; 28.652
90; 90; 90
5761.5Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135039 CIFC57 H61 N O3P 1 21 111.4318; 11.308; 18.3289
90; 93.843; 90
2364.1Yu, Yue; Guan, Ning; Zhao, Chunying; Cao, Hua; Ma, Yan-Long
Mechanochemically controllable synthesis of mono- or di-alkenylated indolizines.
Chemical communications (Cambridge, England), 2025, 61, 16834-16837
7135040 CIFC H9 B3 F2 N4 O5P -17.2945; 7.969; 8.237
107.653; 101.435; 95.312
441.19Shen, Chunjie; Zhou, Huan; Hu, Chenhui; Yang, Zhihua; Zhang, Feng; Pan, Shilie
CN<sub>4</sub>H<sub>7</sub>B<sub>3</sub>O<sub>3</sub>F<sub>2</sub>(OH)<sub>2</sub>: short-wave UV hydroxyfluorooxyborate crystals with large birefringence.
Chemical communications (Cambridge, England), 2025, 61, 16997-17000
7135041 CIFC8 H20 Cd3 Cl7 NP -17.818; 11.1147; 13.4404
66.714; 82.325; 70.712
1012.55Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135042 CIFC8 H20 Cd3 Cl7 NP -17.855; 11.1928; 13.5318
67.72; 81.919; 69.603
1031.81Chen, Hui-Ping; Wang, Zhen-Yu; Qi, Jun-Chao; Peng, Hang; Yang, Tian-En; Zhang, Xiao-Xuan; Luo, Xin-Yu; Liao, Wei-Qiang
A five- and six-coordinated two-dimensional metal halide organic-inorganic phase transition material.
Chemical communications (Cambridge, England), 2025, 61, 16636-16639
7135043 CIFC20 H22 N2 O3P 21 21 219.8569; 13.5366; 13.7081
90; 90; 90
1829.06Huang, Yinghong; Zheng, Renhua; Cheng, Xiaomeng; Geng, Xiao; Wang, Lei; Zhu, Bihong
Dehalogenation hydrolysis of CF<sub>2</sub>Br<sub>2</sub> enables four-component aminocarbonylation <i>via</i> photocatalytic radical-polar crossover.
Chemical communications (Cambridge, England), 2025, 61, 17033-17036
7135044 CIFC19 H14 F3 N OP 1 21/c 18.33; 17.1545; 11.1957
90; 97.513; 90
1586.1Sachin, ?; Sharma, Tamanna; Rav, Shourabh; Sharma, Upendra
Ru(II)-catalysed, inherent-directing-group-enabled site-selective C-H vinyl trifluoromethylation of isoquinolones and benzamides.
Chemical communications (Cambridge, England), 2025, 61, 17416-17419
7135045 CIFC27 H27 Dy N4 O3P 1 21/c 116.7777; 19.0804; 7.7909
90; 97.375; 90
2473.4Hasegawa, Natsuki; Yanai, Akiho; Masaki, Hinako; Kirishima, Akira; Tsunashima, Ryo; Masuya-Suzuki, Atsuko
Stepwise selective crystallization of Fe and Dy complexes from a Fe/Nd/Dy mixture: separation despite charge and solubility similarity.
Chemical communications (Cambridge, England), 2025, 61, 17384-17387
7135046 CIFC23 H17 O2 PP 1 21/c 112.0273; 5.9723; 24.2673
90; 91.698; 90
1742.37Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135047 CIFC46 H32 O3 P2P 21 21 2111.0559; 16.5376; 18.8101
90; 90; 90
3439.2Eichhorn, Katharina; Bruhn, Clemens; Pietschnig, Rudolf
β-Carboxyphospholes <i>via</i> carboxylative desilylation: luminophores with a versatile connectivity attached.
Chemical communications (Cambridge, England), 2025, 61, 17129-17132
7135048 CIFC12 H20 O S Si2P 1 21/n 110.7711; 9.923; 15.3315
90; 110.531; 90
1534.57An, Kun; Liu, Mengqing; Wang, Jingxia; Nishiura, Masayoshi; Cong, Xuefeng; Hou, Zhaomin
Synthesis of [1,3]-thiasilolanes <i>via</i> rare-earth-catalysed intramolecular α-C(sp<sup>3</sup>)-H silylation of alkyl sulphides with hydrosilanes.
Chemical communications (Cambridge, England), 2025, 61, 17181-17184
7135049 CIFC21 H19 N O2P -17.208; 9.749; 12.523
73.203; 76.884; 78.341
811.6Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135050 CIFC24 H19 N O4 SP -111.3303; 14.1464; 14.8702
97.934; 108.308; 112.348
2000.8Maiti, Sandip; Roy, Charles Patriot; Kabir, Syed Ramizul; Dash, Jyotirmayee
Rh(II)-catalyzed synthesis of furo[2,3-<i>b</i>]indoles from 3-diazooxindoles and electron-rich arylacetylenes.
Chemical communications (Cambridge, England), 2025, 61, 18649-18652
7135051 CIFC25 H18 O3C 1 2/c 123.6123; 9.4715; 17.1625
90; 100.183; 90
3777.83Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135052 CIFC25 H17 F O3C 1 2/c 128.2559; 13.6584; 10.0502
90; 91.917; 90
3876.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135053 CIFC36 H22 O2P -110.2845; 16.121; 17.626
98.505; 98.503; 106.719
2711.5Begum, Fathima; Bhumannagari, Haripriya; Balasubramanian, Sridhar; Nayani, Kiranmai
Divergent coupling of <i>ortho</i>-alkynylnaphthols and <i>p</i>-quinone monoketals through a Michael addition/intramolecular annulation cascade to access benzofuryl β-naphthols.
Chemical communications (Cambridge, England), 2025, 61, 15003-15006
7135054 CIFC12 H11.5 Cl N1.5 O1.5P -19.0938; 11.5029; 12.1234
111.969; 98.763; 94.676
1149Thakur, Rekha; Luxami, Vijay; Paul, Kamaldeep
Ruthenium(II)-catalyzed C-2 alkenylation of indole with olefins <i>via</i> a quinazolin-4(3<i>H</i>)-one directing group: a platform for selective fluorescent anion sensors.
Chemical communications (Cambridge, England), 2025, 61, 14374-14377
7135055 CIFC21 H25 N3 O3P -18.5658; 10.1115; 23.1709
96.106; 98.963; 101.388
1923.78Paul, Subhankar; Chaudhuri, Debangshu
Side-chain dependent direct <i>vs.</i> indirect photoresponse in hydrazone-based supramolecular polymers.
Chemical communications (Cambridge, England), 2025, 61, 14366-14369
7135056 CIFC38 H22 F6 N4P 1 21/c 117.1; 17.498; 13.593
90; 112.31; 90
3762.8Panua, Anirban; Velmurugan, Gunasekaran; Comba, Peter; Rath, Harapriya
Targeted synthesis of a positional isomer of aromatic <i>N</i>-methyl <i>N</i>-confused corrole and its organocopper(III) complex.
Chemical communications (Cambridge, England), 2025, 61, 17436-17439
7135057 CIFC21 H25 N OP 21 21 219.4002; 10.6999; 17.6147
90; 90; 90
1771.71Ghosh, Subhadeep; Biswas, Sumit; Das, Indrajit
Electro-carbo-cyclization of alkyne-, alkene-, and nitrile-tethered α-halocarbonyls.
Chemical communications (Cambridge, England), 2025, 61, 17448-17451
7135058 CIFC46 H76 O2 P2C 1 2/c 115.876; 14.4684; 20.2954
90; 104.386; 90
4515.68Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135059 CIFC22 H28 P2 Se2I 1 2/a 114.989; 8.3205; 18.148
90; 95.024; 90
2254.65Uttendorfer, Maria K.; Schneider, Lisa M.; Diener, Lukas S.; Hierlmeier, Gabriele; Balázs, Gábor; Wolf, Robert
A radical path to 1,2-diphosphacyclobutenes.
Chemical communications (Cambridge, England), 2025, 61, 17464-17467
7135060 CIFC14 H36 Cl6 Mn N4P 21 21 218.4441; 16.7468; 17.4329
90; 90; 90
2465.22Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135061 CIFC14 H36 Br6 Mn N4P 21 21 218.6152; 17.2628; 18.0558
90; 90; 90
2685.3Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135062 CIFC14 H36 Cl10 Mn3 N4P 1 21/n 19.5893; 8.8686; 16.9149
90; 90.355; 90
1438.48Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135063 CIFC14 H36 I6 Mn N4P 21 21 218.9096; 18.141; 18.976
90; 90; 90
3067.1Li, Xintong; Liu, Junhui; Xiang, Junwei; Lv, Qingsong; Wang, Juan; Guo, Fengwan
New strategy for dimensional control of manganese-based metal halides: feed composition control.
Chemical communications (Cambridge, England), 2025, 61, 18184-18187
7135064 CIFC88.5 H47 Cu N12 OP -113.047; 13.52; 21.777
79.204; 73.104; 77.349
3554.7Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135065 CIFC88 H44 Cu N12P -113.329; 15.694; 21.415
78.765; 75.079; 68.029
3990Jangra, Reena; Bulbul, Amir Sohel; Sankar, Muniappan
π-Extended Cis- and Trans-Bis(Tetracyanobutadiene) Cu-Porphyrins with Unusual Multiredox Behavior
Chemical Communications, 2025
7135066 CIFC25 H31 N O2C 1 c 145.525; 7.0641; 6.6022
90; 94.133; 90
2117.7Xiao, Yao; Pan, Xue-Lan; Cao, Xiang-Jian; Qi, Xin; Qiu, Sheng-Qi; Yu, Zhen-Qiang
A room temperature nematic luminescent liquid crystal: a FRET donor for amplified circularly polarized luminescence.
Chemical communications (Cambridge, England), 2025, 61, 17922-17925
7135067 CIFC29 H29 N3 O4P 1 21/n 111.4876; 12.9087; 17.8682
90; 106.868; 90
2535.67Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135068 CIFC29 H29 N3 O4P 1 2/n 111.9144; 11.0129; 20.0815
90; 97.27; 90
2613.75Roper, Natalie J.; Hardy, George M.; Wootton, Jack M.; Waddell, Paul G.; Wilson, James; Armstrong, Roly J.
A multicomponent approach for the stereoselective synthesis of atropisomeric N-N peptide analogues.
Chemical communications (Cambridge, England), 2025, 61, 17388-17391
7135069 CIFC20 H25.69 Mn2 N8 O8.85P 1 21/c 113.7898; 12.1567; 17.2696
90; 103.019; 90
2820.6Howlett, Thomas; Wang, Ziqi; Tang, Wendy; Arora, Nyati; Shende, Prapti M.; Liu, Phillip; Kumari, Sneha; Joy, Monu; Wriedt, Mario; Smaldone, Ronald A.; Gassensmith, Jeremiah J.
From Spontaneous Ligand Evolution to High-Throughput Water-Based Synthesis: Scalable Access to CO2 Selective Mixed-Ligand Metal Organic Frameworks
Chemical Communications, 2025
7135070 CIFC68 H137.5 Al I Mo6 N Na3 O94.25P 1 21 114.6954; 34.3474; 25.064
90; 105.154; 90
12211.1Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135071 CIFC208 H400 Al2 I2 Mo12 N2 O223P 1 21/n 128.963; 17.363; 37.324
90; 109.111; 90
17735Liu, Chun-Yan; Mu, Yun-Jing; Chen, Wu-Ji; Liu, Cheng-Shuai; Lin, Chang-Gen; Song, Yu-Fei
Size-matched supramolecular assembly between an asymmetric Anderson-type polyoxometalate hybrid and α-/γ-cyclodextrins.
Chemical communications (Cambridge, England), 2025, 61, 17886-17889
7135072 CIFC30 H28P c c n16.2667; 16.4045; 18.0519
90; 90; 90
4817.1Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135073 CIFC30 H28P 1 2/n 113.061; 6.7745; 13.079
90; 91.233; 90
1157Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135074 CIFC30 H28P 1 21/c 121.3224; 5.817; 19.767
90; 109.562; 90
2310.2Gao, Feng; Xu, Yanning; Ding, Zeyang; Liu, Hanwen; Wang, Haoran; Alam, Parvej; Qiu, Zijie; Tang, Ben Zhong
Through-space conjugation engineering in methylated tetraphenylethene derivatives.
Chemical communications (Cambridge, England), 2025, 61, 18100-18103
7135075 CIFC42 H38 N2 O9P -15.9506; 11.9443; 13.0049
83.657; 78.757; 84.862
898.85Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135076 CIFC38 H30 N2 O8P -14.7799; 11.7694; 14.1229
94.792; 91.588; 93.494
789.83Hu, Longhao; Lin, Chaohui; Zeng, Dailin; Qin, Xianjiao; Lai, Xiao-Li; Gong, Lingshan; Ye, Yingxiang; AlShahrani, Thamraa; Ma, Shengqian
Solvent-induced conformational changes in color-tunable hydrogen-bonded organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 17882-17885
7135077 CIFC13 H9 SP 1 21/n 112.122; 5.585; 14.566
90; 107.22; 90
941.9Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135078 CIFC26 H8 F10 S2P 1 21/c 113.016; 4.9514; 17.4745
90; 102.038; 90
1101.42Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135079 CIFC26 H16 Br2 S2P 1 21/n 18.9039; 5.6737; 22.1636
90; 101.035; 90
1098.96Nag, Bedabara; Kumar, Akshai
Key role of oxygen and base in catalytic thioetherification: access to sulfur bridged poly-aromatic hydrocarbons.
Chemical communications (Cambridge, England), 2025, 61, 18120-18123
7135080 CIFC28 H24 N2 O6P -19.9897; 11.2443; 12.144
108.063; 102.688; 90.502
1260.85Tang, Shou-Yang; Sang, Qian-Qian; Chen, Ze-Le; Cai, Bao-Gui; Xuan, Jun
Visible-light-promoted synthesis of imidazo[1,5-<i>a</i>]indole-3-ones <i>via</i> cascade carbene N-H insertion and oxidative cyclization.
Chemical communications (Cambridge, England), 2025, 61, 17870-17873
7135081 CIFC2.21 H2.34 N0.28 O0.62P 1 21/c 121.4354; 9.9487; 15.1153
90; 104.054; 90
3126.92Biswas, Sourabh; Srinivasu, Vinjamuri; Mallick, Manasi; Chandu, Palasetty; Sureshkumar, Devarajulu
Photoredox-driven tandem ring-opening and vinylation: a route to distal alkenyl ketones from cyclopropenes.
Chemical communications (Cambridge, England), 2025, 61, 18388-18391
7135082 CIFC16 H11 F3 O6P -19.1458; 9.3792; 10.2964
86.62; 77.558; 63.535
771.41Ni, Tongtong; Xu, Xuefeng; Li, Wenguang; Li, Shiyuan; Sheng, Heyun; Zhang, Xu
Nickel-catalyzed [4+2] cycloadditions of β-ketoesters and alkynes.
Chemical communications (Cambridge, England), 2025, 61, 17645-17648
7135083 CIFC22 H23 N O2P 21 21 218.541; 12.2915; 17.0269
90; 90; 90
1787.51Manna, Sabyasachi; Sreedhara, Rahul Halanuru; Punesh, Thanay Umesh; Prabhu, Kandikere Ramaiah
Use of tailored boronic acids both as a radical donor and acceptor in a visible light-mediated di-functionalization of maleimides: rapid access to fused benzo[<i>e</i>]isoindole-1,3-diones.
Chemical communications (Cambridge, England), 2025, 61, 17669-17672
7135084 CIFC8 H24 Cl6 Mo N2 NaP 1 21/n 19.0726; 6.8264; 15.7029
90; 90.066; 90
972.53Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135085 CIFC8 H24 Ag Cl6 Mo N2P 63/m m c9.054; 9.054; 6.7638
90; 90; 120
480.18Binwal, Devesh Chandra; Vishnoi, Pratap
One-dimensional magnetic halide double perovskites [N(CH<sub>3</sub>)<sub>4</sub>]<sub>2</sub>M<sup>I</sup>MoCl<sub>6</sub> (M<sup>I</sup> = Na, Ag) with large A-site cations.
Chemical communications (Cambridge, England), 2025, 61, 18352-18355
7135086 CIFC71 H133 Fe K N7 O11 Si4P 1 21/c 118.115; 19.364; 25.348
90; 106.419; 90
8528.9Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135087 CIFC39 H83 Fe K N5 O6 Si4P -112.6097; 13.1708; 17.6115
110.391; 93.952; 93.322
2724.6Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135088 CIFC44 H96 Fe K N5 O6 Si4P -112.6019; 13.1359; 17.7179
110.508; 93.368; 93.329
2732.63Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135089 CIFC72 H152 F4 Fe2 K2 N8 O12 S4 Si8P -111.8028; 15.389; 29.1949
103.183; 92.864; 99.764
5066.5Gonzalez, Andres; Casnati, Alessandra; Willingshofer, Moritz; Radovic, Aleksa; Cutsail, 3rd, George E; Demeshko, Serhiy; Meyer, Franc; Werncke, C. Gunnar
The flexible behaviour of a trigonal arylimido iron complex.
Chemical communications (Cambridge, England), 2025, 61, 18440-18443
7135090 CIFC28.6 H22.9 Cl Cu N6.3C 1 2/c 123.24; 30.2; 7.495
90; 97.687; 90
5213.1David, A. John; Seethapathy, Logeshwari; Kumar, S. Vijay; Das, Rajorshi; Das, Anjan
Photocatalytic carboxylation of aryl halides/alkenes with a copper(I) complex bypassing the demand for dual catalysts.
Chemical communications (Cambridge, England), 2025, 61, 17677-17680
7135091 CIFC17 H16 N2 OP 1 21/n 18.8248; 13.1914; 11.6734
90; 102.126; 90
1328.6Liu, Xiang; Wu, Wen-Rong; Ma, Shaohong; Chen, Juan; Meng, Yuan-Jie; Yang, Zi-Feng; Zhang, Shang-Shi; Feng, Pengju
Base-promoted [3+2] annulation of <i>N</i>-aminoisoquinolinium derivatives with cyclic iodonium ylide/2,2-difluorovinyl tosylate.
Chemical communications (Cambridge, England), 2025, 61, 17673-17676
7135092 CIFC16 H17 N3 SP 1 21/c 17.8135; 27.8711; 13.276
90; 90.854; 90
2890.8Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135093 CIFC39 H22 B Cl2 F10 N3 SP -112.0186; 12.5059; 13.7414
95.301; 106.618; 113.936
1756.94Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135094 CIFC27 H13 B F10 N2 O SP -19.6678; 10.2025; 13.9028
104.522; 95.869; 111.606
1205.04Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135095 CIFC28 H16 B F10 N3 SP -19.8457; 10.564; 13.7846
105.553; 90.551; 113.918
1251.18Murali, Anna Chandrasekar; Raj, Ankit; Veerapathiran, Sabari; Senanayak, Satyaprasad P.; Venkatasubbaiah, Krishnan; Chandrasekhar, Vadapalli
Highly emissive boron-α-thioimidinates: substituent control of photophysics and charge transport properties.
Chemical communications (Cambridge, England), 2025, 61, 18396-18399
7135096 CIFC17 H19 F6 O P SiP -18.9992; 10.1647; 11.3907
99.1849; 91.1844; 112.8
944.31Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135097 CIFC18 H21 F6 O P SiP -110.0771; 10.5675; 11.3486
92.695; 109.345; 114.43
1014.09Kopp, Richard O.; Rigo, Massimo; Groth, Lucie J.; Coles, Nathan T.; Neale, Samuel E.; Frank, Samantha; Ernst, Moritz J.; Weber, Manuela; Müller, Christian
Dynamic activation of alcohols by an electrophilic phosphinine.
Chemical communications (Cambridge, England), 2025, 61, 18625-18628
7135098 CIFC44 H88 Cl4 Cu4 Si4P -17.4937; 13.8967; 27.206
100.646; 91.838; 91.599
2781.3Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135099 CIFC88 H168 Cu8 Si8P 21 21 2114.9963; 22.5357; 30.877
90; 90; 90
10434.9Gupta, Arvind Kumar; Fayet, Océane Y O; Tian, Lei; Berger, Raphael J. F.; Lomoth, Reiner; Orthaber, Andreas
Base-mediated alkynyl-cubane to Cu<sub>8</sub>-alkynide cluster transformation.
Chemical communications (Cambridge, England), 2025, 61, 18673-18676
7135100 CIFC34 H20 F4 N2 SC 1 2/c 129.3094; 14.7807; 6.9665
90; 98.9151; 90
2981.5Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135101 CIFC22 H16 N2 SP 1 21/c 19.5987; 15.087; 11.7651
90; 101.039; 90
1672.25Gnanasekaran, Premkumar; Chen, Chia-Yu; Chu, Ting-Hung; Lin, Po-Heng; Chang, Yuan Jay
Eco-friendly synthesis of highly emissive benzothiadiazole-based fluorophores <i>via</i> a solvent-free hand-grinding Horner-Wadsworth-Emmons reaction in ≤1 minute.
Chemical communications (Cambridge, England), 2025, 61, 18148-18151
7135102 CIFC13 H9 B F2 N2 SP 1 21/c 112.1127; 9.1231; 11.7692
90; 113.578; 90
1191.98Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135103 CIFC15 H13 B F2 N2 SP 1 21/c 16.9891; 13.5514; 14.4026
90; 95.392; 90
1358.06Tian, Liang; Cao, Yiman; Chen, Can; Ni, Zhigang; Fan, Cong; Mack, John; Dai, Peidi; Lu, Hua; Gai, Lizhi
Small is different: <i>N</i>,<i>N</i>-chelated organoboron complexes with seven-membered rings.
Chemical communications (Cambridge, England), 2025, 61, 18641-18644
7135104 CIFC105 H102 Cl6 N18 Se3P 3119.6339; 19.6339; 26.1675
90; 90; 120
8735.9Liu, Chao; Du, Ziwei; Ding, Xu; Wang, Zhixuan; Cao, Lili; Zhou, Ziwen; Chen, Jia; Zhang, Ning
Precise Heteroatoms Engineering for Iodine Capture Promotion in Porous Organic Cages
Chemical Communications, 2025
7135105 CIFC27 H26 N O2 SeP 1 21 15.4585; 20.644; 21.236
90; 93.871; 90
2387.5Reddy, Chada Raji; Vinaya, Puthiya Purayil; Ajaykumar, Uprety; Nagendraprasad, Thallamapuram
Electrophilic aryl migration of <i>N</i>-benzyl propiolamides to functionalized-acrylamides.
Chemical communications (Cambridge, England), 2025, 61, 18669-18672
7135106 CIFC34 H52 B2 F2 O10 S2P -18.7369; 10.5221; 11.1567
69.401; 88.06; 71.327
905.93Wang, Shuting; Tang, Shuai; Han, Xiao-Le; Zhang, Hua
Regioselective postmodification of aryl sulfonyl fluorides <i>via</i> iridium(I)-catalysed C-H borylation.
Chemical communications (Cambridge, England), 2025, 61, 18830-18833
7135107 CIFC52 H52 Ag2 F6 N12 O8 S4P 18.38282; 13.97902; 14.3924
115.939; 100.085; 95.7768
1462.99Sawant, Diksha U.; Halat, Peter; McKay, Alasdair I.; Izgorodina, Ekaterina I.; Turner, David R.
Dependence of an anion template on amino acid binding in DMSO/H<sub>2</sub>O by a chiral Ag/urea-based tweezer.
Chemical communications (Cambridge, England), 2025, 61, 18846-18849
7135108 CIFC23 H25 Cl N2 O2P 21 21 2110.5633; 10.5879; 18.4454
90; 90; 90
2062.99Liu, Shiqi; Ma, Yao-Rui; Leitch, David; Arseniyadis, Stellios; Jean, Alexandre; Clark, Paul; Keenan, Thomas; Huang, Jingjun; Hasija, Avantika; Huang, Pei-Qiang
Palladium-Catalysed Asymmetric Allylic Alkylation of Hydantoins using Bench-Stable Chiral Palladium Precatalysts
Chemical Communications, 2025
7135109 CIFC29 H20 N2 O3 S2 Se2P 1 21/c 15.7891; 14.1638; 32.308
90; 94.605; 90
2640.6Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135110 CIFC14 H4 Cl2 N2 Se2P -17.8604; 8.7632; 11.4837
93.4629; 106.53; 112.541
687.45Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135111 CIFC36 H34 N2 O4 S2P 1 21/n 15.9391; 23.454; 23.02
90; 93.477; 90
3200.7Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135112 CIFC28 H18 N2 O4 S2P 1 21/c 111.6031; 16.6534; 12.2098
90; 96.077; 90
2346.1Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135113 CIFC28 H18 N2 O2 S4P 1 n 16.1558; 16.8897; 12.1311
90; 103.961; 90
1224Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135114 CIFC36 H34 N2 O2 S2 Se2P -15.6312; 17.0766; 17.206
86.595; 81.468; 87.677
1632.5Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135115 CIFC31.5 H26 N2 O2 S2 Se2P -16.2952; 11.3991; 20.6848
104.048; 91.718; 99.82
1414.88Schmiedtchen, Marco; Thulaseedharan Nair Sailaja, Sidharth; Lorberg, Rick Y.; Wölper, Christoph; Galstyan, Anzhela; Voskuhl, Jens
Tuneable phosphorescence and singlet oxygen production of bridged ethers <i>via</i> chalcogen variation and photocyclisation.
Chemical communications (Cambridge, England), 2025, 61, 18810-18813
7135116 CIFC32 H27 F O2 SC 1 2/c 135.9609; 12.6981; 11.4122
90; 91.584; 90
5209.2Yu, Tianxin; Shi, Tingchang; Zhang, Zhilei; Xu, Hai-Bing; He, Zikai; Jiang, Lang; Gu, Xinggui; Wang, Erjing
Boosting aggregation-induced emission of hydroxylated tetraphenylthiophene via biogenic amine entangling
Chemical Communications, 2025
7135117 CIFC31 H29 I O3P 1 21/c 120.985; 10.746; 12.2193
90; 102.749; 90
2687.57Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-Catalyzed Stereoselective Desymmetrization of Prochiral Cyclopentane-1,3-diones via Alkoxyallylation
Chemical Communications, 2025
7135118 CIFC25 H28 O3P 1 21 18.4261; 11.7773; 11.2319
90; 107.842; 90
1061.01Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-Catalyzed Stereoselective Desymmetrization of Prochiral Cyclopentane-1,3-diones via Alkoxyallylation
Chemical Communications, 2025
7135119 CIFC25 H18 N2 O4P -18.1541; 8.182; 15.3186
103.249; 101.047; 92.876
971.63Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135120 CIFC47 H32 N4 O2P 1 21/c 114.78458; 16.90271; 14.64273
90; 108.139; 90
3477.36Liu, Luyao; Xiao, Chenfa; Li, Yin; Wan, Jiaxing; Tang, Ben Zhong; Wang, Zhiming
An ultra-simple construction strategy for uncommon 3,4-diaryl-modified maleimide luminophores and their unique aggregation-induced asymmetric effect (AIAE) on conformation.
Chemical communications (Cambridge, England), 2025, 61, 18380-18383
7135121 CIFC13 H10 N4 O7P -17.4442; 9.0095; 10.8263
88.03; 76.686; 87.558
705.721Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135122 CIFC6 H6 N2 OP 1 21/c 115.999; 8.007; 9.943
90; 105.312; 90
1228.5Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135123 CIFC19 H16 N6 O8P -18.1848; 10.8341; 12.2177
71.159; 81.7; 89.974
1013.38Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135124 CIFC14 H11 N3 O8P 1 21/n 18.4196; 13.3701; 13.4639
90; 101.402; 90
1485.7Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135125 CIFC31 H23 N7 O14C 1 2/c 117.8367; 12.2586; 13.8777
90; 90.554; 90
3034.26Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135126 CIFC19 H19 N5 O4P -17.9234; 8.7843; 13.3922
92.797; 101.022; 95.147
909.16Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135127 CIFC20 H17 N5 O9P -17.2524; 8.8044; 16.4118
93.805; 91.218; 94.787
1041.61Scheepers, Matthew C.; Haynes, Delia A.
Design and synthesis of ternary multi-component crystals by sublimation.
Chemical communications (Cambridge, England), 2025
7135128 CIFC46 H45 Cl2 Fe2 N O6 S4P 21 21 2110.6274; 13.5606; 31.507
90; 90; 90
4540.6Li, Shiguang; Wang, Jiang; Lv, Ya; Chi, Yonggui Robin; Gan, Xiuhai; Wu, Xingxing
N-Heterocyclic Carbene-Catalyzed Asymmetric Synthesis of Bis-Ferrocene Derivatives bearing Two Stereogenic Planes
Chemical Communications, 2025
7135129 CIFC22 H18 F N O3P 1 21/n 111.0201; 7.3436; 21.6386
90; 94.376; 90
1746.05Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135130 CIFC11 H9 F0.5 N0.5 O1.5P 1 21/n 17.3449; 9.4651; 25.5608
90; 93.017; 90
1774.53Lin, Wei; Luo, Zhenli; Zhu, Huixuan; Hu, Jinhui; Xiong, Zhuang; Wu, Jia-Qiang
Rh(III)-catalyzed C-H activation/β-F elimination/Michael addition: diastereoselective access to dihydroisoquinolinones featuring β-amino α-fluorocarbonyl motif.
Chemical communications (Cambridge, England), 2025, 61, 18709-18712
7135131 CIFF K1.999 Na0.501 O4 P Sc0.5P -3 m 111.2963; 11.2963; 7.1996
90; 90; 120
795.63Zhao, Huijian; Li, Conggang; Ye, Ning; Hu, Zhanggui
Tailoring UV waveplate materials <i>via</i> rational assembly of functional motifs in scandium fluoride phosphate.
Chemical communications (Cambridge, England), 2025, 61, 17145-17148
7135132 CIFC25 H19 N O5P 1 21/c 19.51124; 15.99027; 12.44468
90; 101.867; 90
1852.23Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135133 CIFC20 H16 O5P 1 21/c 110.2969; 9.8246; 14.8656
90; 93.018; 90
1501.76Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135134 CIFC20.5 H16.98 Cl O6C 1 2/c 120.9727; 8.1208; 20.9626
90; 100.685; 90
3508.34Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135135 CIFC19 H14 O5P 1 21/c 18.3627; 10.9839; 16.0035
90; 97.525; 90
1457.34Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135136 CIFC20 H18 O3P -17.8446; 8.6853; 11.0599
77.008; 83.439; 81.312
723.3Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135137 CIFC16 H11 N O3 SP 1 21/c 110.3033; 16.8149; 7.3464
90; 92.449; 90
1271.59Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135138 CIFC22 H21 I O6P -19.0209; 9.603; 13.967
73.695; 71.448; 66.6
1036.01Harrowven, David; Powderly, Marian; Lindup, Toby; Jackman, Edward Henry; Light, Mark E.; Legros, Julien; Chataigner, Isabelle
Photocyclisations of o-Iodobenzyl-Indanones and Tetralones infer the Intermediacy of Triplet Aryl Cations.
Chemical Communications, 2025
7135139 CIFC56 H119 Au Cl N Sb2 Si9P 1 21/n 118.0962; 23.3405; 18.1023
90; 100.648; 90
7514.29Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa Maria; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au─Sb bimetallic linkage
Chemical Communications, 2025
7135140 CIFC106 H224 Au2 Cl2 N2 O Sb4 Si18P 1 21/n 112.5283; 36.1287; 17.215
90; 109.18; 90
7359.5Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa Maria; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au─Sb bimetallic linkage
Chemical Communications, 2025
7135141 CIFC40.5 H30 Cl6 Ir N5 S2P 1 21/c 113.353; 15.201; 20.751
90; 91.064; 90
4211.3Fernández-Moreira, Vanesa; Morales-Pioz, Eva; Redrado, Marta; Benedí Visiedo, Andrea; de Aquino, Araceli; García-Orduña, Pilar; Royo-Cañas, María; Godino, Javier; Marzo, Isabel; Rodriguez, Laura; Gimeno, M. Concepción
Cyclometallated Iridium(III) Complexes: Ligand-Driven Selectivity for Chemotherapy and Photodynamic Therapy
Chemical Communications, 2025
7135142 CIFC27 H19 BP -111.7047; 11.9303; 13.8652
98.8114; 95.4596; 94.8484
1894.93Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135143 CIFC26 H16 B FP 1 21/c 13.8479; 25.12; 18.2066
90; 92.161; 90
1758.6Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135144 CIFC46 H28 B2C 1 2/c 159.4616; 9.983; 21.9645
90; 105.428; 90
12568.4Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135145 CIFC48 H38 B2P 1 21/n 127.7844; 3.9198; 32.0442
90; 103.451; 90
3394.2Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135146 CIFC38 H26 B NP 1 21/c 19.2605; 31.4635; 10.1892
90; 116.391; 90
2659.39Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135147 CIFC29 H23 BP 1 21/c 111.4924; 4.8929; 36.2021
90; 97.4308; 90
2018.59Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135148 CIFC24 H21 BP -17.4166; 12.7823; 19.1202
79.8121; 89.9142; 85.4566
1778.29Chang, Ke-Wei; Lai, Ting-Yi; Chin, To-Jen; Anitha, Mandala; Liu, Yi-Hung; Ishiwari, Fumitaka; Saeki, Akinori; Farrell, Jeffrey M.
Facile π-extension of boron-doped polycyclic aromatic hydrocarbons by frustrated Lewis pair alkynylation.
Chemical communications (Cambridge, England), 2025
7135149 CIFC32 H26 N2 OP -18.8121; 10.1918; 13.9891
99.49; 97.145; 103.344
1188.33Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds
Chemical Communications, 2025
7135150 CIFC32 H26 N2 OP 21 21 2111.6092; 12.2172; 16.4574
90; 90; 90
2334.2Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds
Chemical Communications, 2025
7135151 CIFC59 H56 Cl6 N8 O3P -115.1639; 18.904; 20.266
89.732; 74.207; 89.827
5590Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular Engineering of Porous Organic Cages for Iodine Capture and Fluorescence Detection
Chemical Communications, 2025
7135152 CIFC73 H64 Cl12 N6 O3P -110.502; 17.367; 38.68
93.004; 90.221; 92.104
7040.2Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular Engineering of Porous Organic Cages for Iodine Capture and Fluorescence Detection
Chemical Communications, 2025
7135153 CIFC43 H40 F10 N4 O9 ZnP 1 21 110.981; 14.833; 13.238
90; 90.05; 90
2156.2Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P.; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically Interlocked Porphyrinoids: Self-Assembly of Metal-Stabilised Catenaphyrins
Chemical Communications, 2025
7135154 CIFC76 H64 N12 O8 Zn2P 31 2 123.123; 23.123; 16.184
90; 90; 120
7494Sarwa, Aleksandra; Matviyishyn, Maksym; Perdek, Jędrzej P.; Trzaskowski, Bartosz; Kulesza, Dagmara; Zych, Eugeniusz; Szyszko, Bartosz
Mechanically Interlocked Porphyrinoids: Self-Assembly of Metal-Stabilised Catenaphyrins
Chemical Communications, 2025
7135155 CIFC46 H59 Br Cl2 N2 PdP 1 21/c 113.0408; 15.0939; 21.6308
90; 95.267; 90
4239.75Tzouras, Nikolaos V.; Fleischer, Ruben; Satta, Pierpaolo; Manna, Sourav; Doppiu, Angelino; Goossen, Lukas J.
Mild cross-coupling of tertiary alkoxides with aryl chlorides enabled by a shelf-stable methylnaphthyl palladium NHC complex
Chemical Communications, 2025
7135156 CIFC20 H17 Br N4 O3P 1 21/c 120.707; 6.5276; 13.766
90; 95.222; 90
1853Shivpuje, Umesh; Ahmad, Manzoor; Roy, Naveen Joseph; Talukdar, Pinaki
Ligand-responsive ON-OFF anion transport using copper-caged acylhydrazone transporters
Chemical Communications, 2025
7135157 CIFC64 H84 O4 S4I 41/a :228.37523; 28.37523; 14.57079
90; 90; 90
11731.7Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135158 CIFC52 H72 O4 S4P -110.7957; 11.4363; 12.1971
68.795; 86.611; 62.936
1240.07Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135159 CIFC52 H72 O4 S4P c c n13.5017; 24.9584; 14.6029
90; 90; 90
4920.9Losus, Renny Maria; Bleus, Sem; Bon, Volodymyr; Kaskel, Stefan; Dehaen, Wim; Dobrzańska, Liliana
Adaptive crystals of homothiacalix[4]arene capable of molecular recognition, with preferential uptake of benzene over cyclohexane.
Chemical communications (Cambridge, England), 2025
7135160 CIFC257 H205 Co4 N11 O45P -122.5652; 22.5982; 30.2731
77.825; 85.366; 65.661
13748.6Ma, Li-Li; Liu, Shengjin; Yang, Feinian; Cao, Jian; Ding, Longyi; Li, Yang; Yuan, Guozan
Integration of perylene diimide into a two-dimensional cobalt-organic framework for enhanced photocatalysis
Chemical Communications, 2025
7135161 CIFC29 H27 N3 O4 S2I 1 2/a 121.6291; 8.6367; 30.4166
90; 94.806; 90
5661.97Yadav, Anup Kumar; Kumar, Vipin; Singh, Saurabh; Samai, Subhasis; Singh, Maya Shankar
Synthesis of pyrrolo[3,4-c]pyridines via metal-free cross-coupling/cyclization cascades of β-ketothioamides with 2aroylmalononitrile at room temperature
Chemical Communications, 2025
7135162 CIFC20 H20 N2 OP c a 2112.718; 6.6198; 20.0762
90; 90; 90
1690.2Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135163 CIFC23 H26 N2 OP 1 21/n 114.5518; 7.7103; 18.9048
90; 110.142; 90
1991.4Hu, Qianqian; Hu, Cangzhu; Tang, Tian; Wu, Qing; Hu, Weiming; Dai, Qiang; Wang, Lei
Palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes: access to imidazolidinones bearing alkynes and allenes.
Chemical communications (Cambridge, England), 2025, 61, 17898-17901
7135164 CIFC316 H654 N34 O236 P16 V52C 1 2/c 139.393; 29.71; 48.245
90; 103.779; 90
54839Han, Shicheng; Liu, Fangcheng; Fu, Gang; Guo, Ji; Lin, Jiaheng; Wu, Hongyu; Mu, Chengyi; Fang, Xikui
Diphosphonate Functionalization of a Polyoxometalate-Organic Cage Enhances Proton Conductivity
Chemical Communications, 2025
7135165 CIFC H N OP -19.7302; 10.877; 11.3278
108.364; 92.134; 90.464
1136.79Saikia, Anil Kumar; Arandhara, Pallav Jyoti; Chutia, Archana
Leveraging cascade annulation of 2-alkynylcyclopropanes with substituted azides to access fused N-heterocyclic scaffolds
Chemical Communications, 2025
7135166 CIFB8 F12 K4 Na8 O24 Y8P 41 21 26.674; 6.674; 19.991
90; 90; 90
890.4Zhao, Huijian; Liu, Mengru; Nan, Weina; Yang, Ning; Li, Conggang; Ye, Ning; Hu, Zhanggui
KNa<sub>2</sub>Y<sub>2</sub>B<sub>2</sub>O<sub>6</sub>F<sub>3</sub>: a beryllium free deep-UV nonlinear optical crystal with well-balanced properties.
Chemical communications (Cambridge, England), 2025, 61, 17878-17881
7135167 CIFC78 H100 Cl2 Cu2 N6 P2 Si2P b c a13.856; 18.909; 33.767
90; 90; 90
8847Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135168 CIFC48 H61 Cu N3 P SiP 1 21/c 111.1435; 21.864; 18.789
90; 104.38; 90
4434.4Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135169 CIFC42 H65 Cu N3 P SiP 1 21 110.0396; 19.1146; 11.968
90; 114.685; 90
2086.8Kaulage, Sandeep; Shah, Brij; Sharma, Himanshu; Panday, Rishukumar; Vanka, Kumar; Khan, Shabana
Silylene-Copper(I) Catalysis: Regioselective Protoboration of Terminal Alkynes
Chemical Communications, 2025
7135170 CIFC19 H13 N O2P 1 21/c 127.591; 8.5988; 12.4
90; 100.846; 90
2889.3Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135171 CIFC19 H13 N O2P 1 21/c 127.509; 8.6819; 12.636
90; 101.062; 90
2961.8Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135172 CIFC21 H19 N O3P 1 21/c 18.52527; 26.3892; 15.8287
90; 100.735; 90
3498.74Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135173 CIFC22 H21 N O3P 1 21/c 18.50169; 27.8458; 8.1178
90; 103.313; 90
1870.13Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135174 CIFC20 H17 N O3P 1 21/n 18.1669; 26.4699; 15.7893
90; 104.465; 90
3305.1Wang, Deliang; Wu, Hongzhuo; Lin, Songwang; Wang, Kangfan; Wang, Dong; Xiong, Yu; Tang, Ben Zhong
Manipulating RTP properties of the same organic molecule by polymorphic engineering.
Chemical communications (Cambridge, England), 2025
7135175 CIFC102 H63.43 Mn4 N10 O26.71P b c a22.7346; 13.7881; 26.2173
90; 90; 90
8218.3Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135176 CIFC75.7 H62.42 Mn4 N7 O30.91C 1 2/c 124.6796; 13.604; 21.497
90; 91.574; 90
7214.7Liu, Jiang; Xu, Sha-Sha; Liang, Jia-Zheng; Yao, Su-Juan; Li, Ning; Shi, Jing-Wen; Lan, Yaqian
Microenvironment Regulation of Active Sites for Efficient Photocatalytic Reduction of Nitrobenzene
Chemical Communications, 2025
7135177 CIFC23 H21 N O2 SP 21 21 216.4453; 14.9945; 20.1091
90; 90; 90
1943.42Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135178 CIFC18 H18 I N3 O2 SP 1 21/c 17.6989; 13.6394; 17.7709
90; 98.755; 90
1844.35Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135179 CIFC22 H19 N O3 SP c a 2115.1706; 11.7513; 21.1278
90; 90; 90
3766.5Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Nandy, Abhijit; Arora, Kirti; Banerjee, Shibdas; Verma, Akhilesh K.
Vinyl benzotriazole to indole: an iodine-mediated denitrogenative transannulation approach for the synthesis of indoles.
Chemical communications (Cambridge, England), 2025
7135180 CIFC26 H19 Br2 N O SP -18.2318; 10.8621; 13.1254
78.435; 79.26; 79.268
1116.05Chen, Jiahong; Huang, Yuanyuan; Wang, Nan; Wang, Mengke; Huang, Weichun; Wu, Xin-Xing; Xu, Xiao-Ping; Zi, You
Regioselective Functionalization of Sulfenamides: S-Arylation with Cyclic Diaryl λ3 -Bromanes and λ3 -Chloranes
Chemical Communications, 2025
7135181 CIFC40 H60 Mo2 O4 UC 1 2/c 116.2375; 13.6368; 17.8447
90; 95.875; 90
3930.55Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135182 CIFC40 H60 Cl Mo2 O4 UP n m a18.2457; 16.2988; 13.5222
90; 90; 90
4021.27Valerio, Leyla R.; Patra, Kamaless; Shiels, Dominic; Brennessel, William W.; Matson, Ellen M.
Synthesis and characterization of a low-valent uranium complex supported by a redox-active molybdenum oxide metalloligand.
Chemical communications (Cambridge, England), 2025
7135183 CIFC26 H30 N2 O6 S2P b c a10.405; 10.958; 23.3754
90; 90; 90
2665.2Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025

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