Crystallography Open Database

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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

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