Crystallography Open Database

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7135333 CIFC32 H47 B21 Cu PP 1 21/c 112.6977; 13.7024; 23.9248
90; 103.948; 90
4039.9Thornton, Ragene; French, Kirk; Shuford, Kevin; Martin, Caleb Daniel
Reactivity of Gold and Copper Acetylide with a Secondary Borane
Chemical Communications, 2026
7135332 CIFC32 H47 Au B21 PP 1 21/c 115.4148; 16.6168; 15.9182
90; 97.988; 90
4037.8Thornton, Ragene; French, Kirk; Shuford, Kevin; Martin, Caleb Daniel
Reactivity of Gold and Copper Acetylide with a Secondary Borane
Chemical Communications, 2026
7135331 CIFC15 H8 O2 S2P 1 21/n 16.8001; 14.5918; 12.0415
90; 94.287; 90
1191.48Ueda, Masafumi; Uehara, Asuka; Usui, Kazuteru; Hasegawa, Masashi
A Folded Mechanochromic Organic Fluorophore Based on Thianthrene-Fused Coumarin
Chemical Communications, 2026
7135330 CIFC15 H8 O2 S2I 1 2/a 113.5461; 3.8602; 46.3601
90; 95.505; 90
2413.02Ueda, Masafumi; Uehara, Asuka; Usui, Kazuteru; Hasegawa, Masashi
A Folded Mechanochromic Organic Fluorophore Based on Thianthrene-Fused Coumarin
Chemical Communications, 2026
7135329 CIFC108 H155 Cs2 O12 P7 Pd6P n a 2130.981; 14.8646; 25.5815
90; 90; 90
11780.8Krämer, Felix; Kennedy, Alan; Fernandez, Israel; Mulvey, Robert E.
A Palladium Inverse Crown: Synthesis and Characterisation
Chemical Communications, 2026
7135328 CIFC23 H15 NP 1 21/c 118.3518; 5.289; 17.3164
90; 109.188; 90
1587.4Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135327 CIFC23 H13 F2 NC 1 2/c 117.2254; 7.4849; 26.994
90; 107.221; 90
3324.32Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135326 CIFC24 H14 F3 NP 1 21/c 14.6753; 36.904; 10.6315
90; 100.522; 90
1803.49Wang, Zhengcheng; Gao, Lin; Yu, Qi; Wang, Guo-Ming
Substituent-modulated organic single crystals with rapid natural light photomechanical response
Chemical Communications, 2026
7135325 CIFC28 H22 Fe O2P 21 21 218.2412; 11.3911; 21.879
90; 90; 90
2053.9Parganiha, Devendra; Upadhyay, Yagya Dutt; Khevariya, Sumit; Patil, Pruthviraj Amar; Jaiswal, Svastik; Dhasmana, Yogesh; Kumar, Sangit
Native Carboxylate-Assisted Enantioselective C-H Annulations with Allenes and 1,3-Dienes on Ferrocene
Chemical Communications, 2026
7135324 CIFC22 H13 B F N3 OP -17.5432; 8.0975; 14.2914
95.85; 95.816; 103.652
836.72Figliola, Carlotta; Chériaux, Camille; Oppé, Nicolas; Estaque, Lilian; Retailleau, Pascal; Vanthuyne, Nicolas; Pieters, Gregory; Jacquemin, Denis; Ulrich, Gilles
Design of Heavy-Atom Free Dipyridomethene Boron Complexes for Singlet Oxygen Emission with Induced Chirality
Chemical Communications, 2026
7135323 CIFC19 H14 B F2 N3 OP 1 21/c 111.1316; 18.2559; 8.0791
90; 99.445; 90
1619.56Figliola, Carlotta; Chériaux, Camille; Oppé, Nicolas; Estaque, Lilian; Retailleau, Pascal; Vanthuyne, Nicolas; Pieters, Gregory; Jacquemin, Denis; Ulrich, Gilles
Design of Heavy-Atom Free Dipyridomethene Boron Complexes for Singlet Oxygen Emission with Induced Chirality
Chemical Communications, 2026
7135322 CIFC43 H63 Cl Fe N7 O4P 19.0356; 13.1688; 17.9549
88.5; 81.057; 88.78
2109.4Dey Biswas, Doyel; Das, Soumadip; Pal, Debraj; Sen Gupta, Sayam
Enantioselective C-H Bond Oxidation using Bio-Inspired Chiral Fe-TAML Catalyst
Chemical Communications, 2026
7135321 CIFC43 H63 Cl Fe N7 O4P 19.0318; 13.1643; 17.9475
88.547; 81.094; 88.722
2107.14Dey Biswas, Doyel; Das, Soumadip; Pal, Debraj; Sen Gupta, Sayam
Enantioselective C-H Bond Oxidation using Bio-Inspired Chiral Fe-TAML Catalyst
Chemical Communications, 2026
7135320 CIFC4 H4 Cl2 Fe N2C m m m12.015; 7.2065; 3.5729
90; 90; 90
309.36Lassoued, Mohamed Saber; Huang, Xue-Qi; Hussain, Abid; Zheng, Yan-Zhen
A Stable Narrow-Bandgap 2D Iron–Pyrazine Framework Exhibiting High Photoconductivity and Spin–Charge Coupling
Chemical Communications, 2026
7135319 CIFC36 H33 B F15 O PR 3 :H17.232; 17.232; 9.882
90; 90; 120
2541.2NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135318 CIFC39 H20 B F15 O SbP -113.4947; 15.3391; 19.1866
76.297; 81.376; 68.207
3574.3NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135317 CIFC33.5 H15 B F15 O SbP 1 21/n 110.1599; 15.9561; 19.0317
90; 99.943; 90
3038.9NGUYEN, THIEN; González-Ortiz, Francisca; Camaret, Ethan; PARK, GYEONGJIN
From Oxygen Atom Transfer by Stibine Oxide to Hydroxoantimony Formation via Lewis Acid Capture
Chemical Communications, 2026
7135316 CIFC40 H28 N6 SP 1 21/c 125.61; 7.253; 17.715
90; 106.797; 90
3150Nakamura, Ryo; Sawamura, Yuta; Nakada, Kazushi; Mizoguchi, Ryusuke; Ishii, Ayumi; Yamashita, Tomohiro; Yokota, Hiroko; Richards, Gary James; Hori, Akiko
Red-fluorescence under UV and green-SHG under NIR dual-mode emission in yellow crystal of 1,2,5-thiadiazole derivative
Chemical Communications, 2026
7135315 CIFC16 H10 N4 SC 1 c 111.947; 17.077; 7.029
90; 111.18; 90
1337.2Nakamura, Ryo; Sawamura, Yuta; Nakada, Kazushi; Mizoguchi, Ryusuke; Ishii, Ayumi; Yamashita, Tomohiro; Yokota, Hiroko; Richards, Gary James; Hori, Akiko
Red-fluorescence under UV and green-SHG under NIR dual-mode emission in yellow crystal of 1,2,5-thiadiazole derivative
Chemical Communications, 2026
7135314 CIFC108 H35 Co N5C 1 2/c 125.189; 22.7748; 24.3234
90; 96.945; 90
13851Wang, Tao; Song, Yupeng; Wang, Chong; Wang, Hongyi; Zhang, Youpeng; Jiang, Ying; Dong, Tianyang; Wu, Bo; Wang, Chun-Ru
Fullerene–Porphyrin Nanosheet as an Efficient Catalyst Enables Solar-Light-Driven Ammonia Synthesis
Chemical Communications, 2026
7135313 CIFC4.09 H3.74 N0.17 O0.61 P0.09C 1 2 119.0074; 11.0694; 18.0225
90; 110.883; 90
3542.9Devi, Manju; Jain, Gyanshree; Gupta, Navya; Ansari, Najmuddin; Singh, Ravi Prakash
Atroposelective Synthesis of Barbiturate Substituted Chiral Styrenes
Chemical Communications, 2026
7135312 CIFC31 H24 Br N2 O4P 1 21 19.214; 14.22; 11.153
90; 111.181; 90
1362.6Devi, Manju; Jain, Gyanshree; Gupta, Navya; Ansari, Najmuddin; Singh, Ravi Prakash
Atroposelective Synthesis of Barbiturate Substituted Chiral Styrenes
Chemical Communications, 2026
7135311 CIFC44 H28 F18 N6 P2 RuP -19.0051; 11.4959; 22.2845
86.46; 80.555; 74.909
2196.74Mandal, Arif Ali; Kumar, Saurav; Singh, Srijan; Mandal, Apurba; Banerjee, Samya; Dhar, Prodyut
Novel Ru(II)-Photo-antibiotics for Development of Infection-Resistant Mask Coatings
Chemical Communications, 2026
7135310 CIFC27 H25 Cs N2P 1 21/c 114.4348; 12.0323; 26.6844
90; 100.598; 90
4555.59Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135309 CIFC46 H69 Cs2 Li N4 Si4P c a 2125.3737; 12.0154; 17.5574
90; 90; 90
5352.82Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135308 CIFC27 H25 N2 RbP 1 21/c 114.3566; 11.8396; 26.4983
90; 101.79; 90
4409.06Burnett, Stuart; Kennedy, Alan; Mansell, Stephen M.; Weetman, Catherine Ellen
Fluorenyl-Tethered N-Heterocyclic Carbene Complexes of the Heavy Alkali Metals
Chemical Communications, 2026
7135307 CIFC75.73 H107.19 La S2C 1 2/c 121.1388; 18.2563; 36.118
90; 91.482; 90
13933.9Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135306 CIFC75.53 H106.59 La S2C 1 2/c 121.0895; 18.2926; 36.1914
90; 92.017; 90
13953.3Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135305 CIFC75.63 H106.89 La S2C 1 2/c 121.1136; 18.2758; 36.158
90; 91.79; 90
13945.4Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135304 CIFC75.87 H107.61 La S2C 1 2/c 121.1776; 18.2359; 36.0813
90; 91.179; 90
13931.4Stennett, Cary R.; Luevano, Makayla R.; Ziller, Joseph W.; Evans, William J.
<i>In crystallo</i> homolytic cleavage of a terminal lanthanum(III)-methyl bond by Cu Kα X-radiation forms a La(II) complex.
Chemical communications (Cambridge, England), 2025
7135303 CIFC35 H24 I N OC 1 2/c 125.9967; 13.28; 17.7015
90; 93.282; 90
6101.2Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135302 CIFC38 H29 I N2 O2P 1 21 114.085; 7.2681; 15.308
90; 97.143; 90
1554.9Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135301 CIFC36 H23 F3 I N OP 1 21/n 16.9559; 28.73; 14.9096
90; 96.72; 90
2959.1Jagota, Shivankar; Rana, Samim Sohel; Barman, Chhotan; Choudhury, Joyanta
Annulated oxazolium salts as anion-π + interaction-enabled solid-state room-temperature phosphorescent materials
Chemical Communications, 2026
7135300 CIFC27 H20 O5 SP 1 21/c 114.2771; 37.754; 17.4551
90; 107.017; 90
8996.7Yang, Zhi-Yuan; Li, Xue-Song; Zhang, Ming-Li; You, Zi-Xin; Liang, Yong-Min; Zhou, Ming-Dong
Lewis Acid Catalysed Cyclization of Pyridinium 1,4-Zwitterionic Thiolates with Propargyl Alcohols and Fluorescence Applications
Chemical Communications, 2026
7135299 CIFC32 H29.34 N O4.17 SP 1 21/n 110.2097; 12.1202; 21.9452
90; 100.603; 90
2669.21Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135298 CIFC27 H29 N O5P 1 21/c 17.6653; 32.012; 9.0652
90; 99.477; 90
2194.07Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135297 CIFC26.25 H21.25 Cl0.75 N SP -19.4521; 14.7452; 14.7989
101.038; 95.116; 97.429
1993.62Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135296 CIFC27 H27 Cl3 N2 O6P -17.4109; 9.9848; 18.796
96.494; 99.614; 104.201
1312.01Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135295 CIFC33 H30 Cl3 N O5P -110.1653; 11.261; 13.4588
76.983; 77.769; 87.169
1466.98Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135294 CIFC31 H36 Cl3 N O4P -17.3825; 10.0528; 20.4633
100.577; 90.989; 99.932
1468.62Shoji, Taku; Ariga, Yukino; Ito, Daichi; Ito, Fuyuki; Hamasaki, Atom; Mori, Shigeki; Okujima, Tetsuo; Sekiguchi, Ryuta; Ito, Shunji
Azulenes exhibiting solid-state fluorescence: synthesis and photophysics of 2-aryl-6-pyrrolidinylazulenes.
Chemical communications (Cambridge, England), 2025, 61, 19481-19484
7135293 CIFC7 H14 B9 Cl2 NC 1 2/c 120.226; 7.0287; 19.947
90; 96.446; 90
2817.8Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135292 CIFC7 H15 B9 Cl NC 1 2/c 120.3463; 6.4323; 20.4209
90; 103.65; 90
2597.1Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135291 CIFC14 H20 B9 N O2P -16.5542; 10.0432; 14.4842
79.901; 79.8; 74.684
896.7Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135290 CIFC13 H19 B9 N2 O2P 1 21/n 19.3624; 15.562; 12.4785
90; 106.649; 90
1741.9Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135289 CIFC9 H18 B9 N O2P -17.035; 9.707; 11.99
97.167; 102.787; 102.826
765.4Li, Xinrui; Zhou, Ningning; Tu, Deshuang; Lu, Chang-sheng; Yan, Hong
Metal-free regioselective B–O coupling in carboranes for constructing aggregation-induced emission luminogens
Chemical Communications, 2026
7135288 CIFC37 H42 Fe O2 PbP 21 21 218.3897; 18.0566; 21.6854
90; 90; 90
3285.1Cao, Phuong Anh; Phung, Alice C.; Schwirzke, Ella L.; Fettinger, James C.; Rusmore, Theo A. H.; Mears, Kristian L.; Vasko, Petra; Power, Philip P.
Ammonia reactivity with ferriotetrylenes: a structural snapshot of a highly dynamic process.
Chemical communications (Cambridge, England), 2025, 61, 19092-19095
7135287 CIFC37 H45 Fe N O2 SnP 21 21 2110.7163; 14.799; 21.254
90; 90; 90
3370.7Cao, Phuong Anh; Phung, Alice C.; Schwirzke, Ella L.; Fettinger, James C.; Rusmore, Theo A. H.; Mears, Kristian L.; Vasko, Petra; Power, Philip P.
Ammonia reactivity with ferriotetrylenes: a structural snapshot of a highly dynamic process.
Chemical communications (Cambridge, England), 2025, 61, 19092-19095
7135286 CIFC40 H59 Cl2 N2 P RuP 1 21/n 112.2189; 18.2929; 17.8873
90; 103.89; 90
3881.24Pontavatchai, Apicha; Schwedtmann, Kevin; Royla, Philipp; Schwedtmann, Kai; Khamnaen, Tossapol; Schwarzenbolz, Uwe; Henle, Thomas; Somsook, Ekasith; Weigand, Jan J.
Chain-length-dependent reactivity of alkenyl phosphates in ruthenium-catalyzed cross-metathesis
Chemical Communications, 2026
7135285 CIFC34 H36 N4 O6P -19.0582; 11.4917; 16.1874
102.344; 104.774; 102.029
1528.74Luan, Yu-Yong; Li, Jin-Ye; Liu, Xue-Yuan; Liang, Yong-Min
Ru-Catalyzed C-H Annulation: Accessing Quinazolinone-BCP Hybrids from Stable Precursors
Chemical Communications, 2026
7135284 CIFC6 N1.5 O11.917 P0.333 W3 Zr0.5R -3 m :H22.6915; 22.6915; 39.2399
90; 90; 120
17497.9Liang, Zhijie; Yao, Yiqing; Ding, Yuyang; Wang, Haifeng; Li, Huafeng; Feng, Gang
Stable Zr-based polyoxometalate as a green catalyst for selective oxidation of aniline
Chemical Communications, 2026
7135283 CIFC18 H21 NP 1 21/c 18.355; 16.065; 11.289
90; 108.475; 90
1437.2Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135282 CIFC24 H21 NP 1 21/n 18.1945; 21.1; 11.376
90; 107.258; 90
1878.4Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135281 CIFC16 H17 N OP 21 21 215.5367; 7.7309; 29.9149
90; 90; 90
1280.47Pal, Anit; Borah, Asish; Das, Animesh
Chromium-catalyzed reductive alkylation of N heteroarenes using alkyl formates as transfer hydroalkylation reagents
Chemical Communications, 2025
7135280 CIFC17 H18 O3P -18.4589; 9.2758; 9.7016
93.006; 108.39; 93.186
719.26Samantaray, Swati; Saha, Sharajit; Punniyamurthy, Tharmalingam
Rh-catalyzed chemodivergent [4+1]-annulation/allylation of sulfoxonium ylides with α-methylene-β-lactones: access to α-indanonyl/α-benzyl acrylates
Chemical Communications, 2026
7135279 CIFC26 H32 O4 SP 1 21/c 121.4284; 10.2324; 11.5649
90; 105.207; 90
2447Samantaray, Swati; Saha, Sharajit; Punniyamurthy, Tharmalingam
Rh-catalyzed chemodivergent [4+1]-annulation/allylation of sulfoxonium ylides with α-methylene-β-lactones: access to α-indanonyl/α-benzyl acrylates
Chemical Communications, 2026
7135278 CIFC236 H317 F30 N20 O89.5 Pd5 S10P 1 21/a 133.1133; 45.6826; 41.2995
90; 92.8019; 90
62399Sakata, Yoko; Nakamura, Ryosuke; Saito, Takuho; Ogoshi, Tomoki; Tashiro, Shohei; Akine, Shigehisa
Size-selective formation of metallonanobelts <i>via</i> tethering-template-directed self-assembly.
Chemical communications (Cambridge, England), 2025
7135277 CIFC54 H78 B2 N14 O4 Ti2P -114.5243; 15.2715; 20.314
102.862; 110.431; 101.972
3910.78Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135276 CIFC38 H60 B2 I2 N14 O2 Ti2P 1 21/n 110.9341; 15.8235; 32.5097
90; 95.991; 90
5593.97Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135275 CIFC30 H48 B N7 O2 Si TiP -111.3501; 11.8716; 13.3789
85.07; 72.758; 80.766
1697.99Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135274 CIFC29 H43 B Cl N6 O TiP 1 21/n 18.7343; 21.1361; 16.4149
90; 91.354; 90
3029.49Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135273 CIFC58 H86 B2 N14 O2 Ti2P 1 21/n 115.2132; 17.9147; 26.801
90; 91.589; 90
7301.5Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135272 CIFC62 H94 B2 N14 O4 Ti2P 1 21/n 122.5766; 14.9516; 23.4386
90; 105.686; 90
7617.19Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135271 CIFC31 H47 B Cl N6 O2 TiP 1 21/n 110.8294; 15.1747; 20.4317
90; 94.178; 90
3348.68Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135270 CIFC27 H39 B Cl N6 O2 TiP 1 21/n 110.5793; 15.3351; 18.0389
90; 94.362; 90
2918.06Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135269 CIFC29 H49 B N7 O Si2 TiP -111.9183; 12.1325; 14.2731
79.695; 71.091; 65.428
1773.34Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135268 CIFC46 H78 B2 N14 O4 Ti2P 43 21 214.9943; 14.9943; 29.2
90; 90; 90
6565.01Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135267 CIFC114 H75 N3 O6C 1 2/c 121.5241; 26.661; 42.4881
90; 100.448; 90
23977.7Liu, Chenrui; Peng, Lingya; Chen, Yumeng; An, Jingyi; Li, Zhaoxin; Huang, Wenshuang; Cui, Ganglong; Hu, Shaowei
Catalytic Dinitrogen Silylation by Tris(pyrazolyl)borate-Supported Titanium Complexes
Chemical Communications, 2025
7135266 CIFC4 H1.5 Cu0.12 F0.75 N Si0.12I 4/m m m15.391; 15.391; 8.068
90; 90; 90
1911.17Huang, Yun-Tao; Song, Zi-Meng; Zhao, Xin-Ye; Li, Bei-Bei; Di, Zhengyi; Li, Cheng-Peng
A stable amino-functionalized fluorinated metal-organic framework for efficient separation of propyne/propylene
Chemical Communications, 2025
7135265 CIFC3.4 H3.4 N0.2 O0.2 S0.2P -17.929; 9.6466; 10.3599
76.164; 68.361; 71.046
690.17Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135264 CIFC17 H16 Br N O SP 1 21/c 18.0318; 19.4472; 10.3438
90; 101.538; 90
1583.01Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135263 CIFC17 H16 Br N O SeP 1 21/c 17.9325; 19.3831; 10.3168
90; 100.504; 90
1559.7Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135262 CIFC23 H19 Br2 N O Se2P 1 21/n 18.4802; 8.4836; 30.641
90; 90.366; 90
2204.3Kar, Malobika; Sharma, Nagendra K.
Ag(I)-Mediated Mono-selective C(sp2)─H Chalcogenation of α-Aminotropones and Their Peptides at Room Temperature
Chemical Communications, 2025
7135261 CIFC40.3 H83.7 Al Ca N5 O Si4P 1 21/n 111.049; 19.6928; 23.4848
90; 98.614; 90
5052.32Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135260 CIFC33 H68 Al Mg N5 Si4P b c a12.85853; 20.3422; 32.09584
90; 90; 90
8395.33Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135259 CIFC54 H96 Al2 Ca N8 Si4P 1 21/c 111.6207; 25.9517; 21.1162
90; 100.348; 90
6264.58Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135258 CIFC33 H66 Al Ca N5 Si4P c a 2112.6499; 15.8975; 20.806
90; 90; 90
4184.1Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135257 CIFC33 H68 Al Mg N5 Si4P 1 21/c 19.9558; 17.0612; 24.8384
90; 100.093; 90
4153.71Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135256 CIFC21 H32 Al N3P 1 21/n 110.931; 9.974; 19.421
90; 91.464; 90
2116.7Mandal, Chhotan; Kundu, Abhishek; Panda, Sourav; Mukherjee, Debabrata
Intriguing Metal-Ligand Interplays Leading to Diverse Al-H-M (M = Mg, Ca) Heterobimetallic Hydrides on a Picolyl-Based 3N Ligand
Chemical Communications, 2025
7135255 CIFC41.5 H73 Al Fe N2 O P2 SiP 1 21/c 117.6664; 11.4726; 22.7577
90; 95.962; 90
4587.57Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135254 CIFC51 H82 Al Fe N3 O P2 SiP 1 21/c 114.59351; 10.0249; 35.96271
90; 94.4545; 90
5245.4Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135253 CIFC41.5 H73 Al Fe N2 O P2 SiP 1 21/c 117.6664; 11.4726; 22.7577
90; 95.962; 90
4587.57Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135252 CIFC33 H62 Al Fe N2 O P3P 1 21/n 115.2649; 14.4485; 17.2914
90; 91.259; 90
3812.78Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135251 CIFC37 H59 Al Fe N4 O P2P 1 21 112.7184; 17.9691; 17.6796
90; 90.455; 90
4040.34Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135250 CIFC43.25 H74 Al Fe N4 P2 SiP -111.9256; 12.237; 18.8626
85.197; 81.93; 61.139
2386.51Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135249 CIFC35 H57 Al Fe N2 P2 SiP -110.8871; 11.7522; 16.8494
75.091; 80.271; 71.666
1968.4Crimmin, Mark Richard; Stadler, Benedek
A Heterometallic σ-Silane Adduct from Cooperative Reactivity of an Iron–Aluminium Complex
Chemical Communications, 2025
7135248 CIFC126.1 H154.9 Cl6.9 Cu14 O37.2 P8 Si16P -114.2336; 16.6267; 18.4779
94.817; 94.588; 94.845
4325.19Arteev, Ivan S.; Khrustalev, Victor N.; Shul'pina, Lidia S.; Rodionov, Alexey N.; Shubina, Elena S.; Ragimov, Karim; Wang, Zhi; Bilyachenko, Alexey N.
High-nuclearity Cu<sub>14</sub> ionic complex featuring 1,3-bis(diphenylphosphino)propane and methylsilsesquioxane ligands: highly efficient catalysis of mild peroxidative alkane fuctionalizations.
Chemical communications (Cambridge, England), 2025
7135247 CIFC68 H87 N5 Te ZnP -112.3684; 12.4059; 21.7277
91.49; 90.601; 111.293
3104.57Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135246 CIFC102 H124 N10 O2 Zn2P -111.9496; 13.6798; 15.5151
113.349; 103.698; 94.74
2217.57Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135245 CIFC96 H118 N10 Se2 Zn2P 1 21/n 115.7525; 14.9627; 19.4718
90; 112.101; 90
4252.3Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135244 CIFC63 H83 N5 Se ZnP -113.6388; 14.3737; 15.113
99.88; 92.266; 96.26
2896.27Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135243 CIFC48 H59 N5 Te ZnP 1 21/n 117.2703; 27.8793; 18.1885
90; 92.174; 90
8751.2Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135242 CIFC96 H122 N10 O2 Zn2P -112.0595; 12.8394; 15.0633
106.138; 108.774; 91.802
2102.42Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135241 CIFC62 H81 N5 S ZnP -113.5911; 14.3769; 15.09
100.512; 92.232; 96.334
2876.1Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135240 CIFC42 H55 N5 S6 ZnP 1 21/c 116.7048; 14.9584; 17.0574
90; 92.938; 90
4256.7Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135239 CIFC102 H124 N10 S2 Zn2P -110.9369; 13.6261; 16.2574
98.636; 93.497; 109.826
2236.97Rajput, Sagrika; PADHAN, SMRUTIRANI; M T, Nithya; Mukhopadhyay, Sayantan; Nembenna, Sharanappa
Nickel-Catalyzed Dehydrogenative Zn–Zn Coupling to a Zn(I) Dimer and Its Reactivity
Chemical Communications, 2025
7135238 CIFC22 H20 N O2P 1 21/c 18.7902; 31.2988; 7.0352
90; 110.298; 90
1815.35Ghosh, Abhipsa; Panda, Asutosh; Mahulkar, Pranav Shridhar; Ravikumar, Ponneri C.
Cobalt(III)-catalysed annulation of indoles with phenylethynyl ether for the synthesis of the ABC ring system of ergot alkaloids.
Chemical communications (Cambridge, England), 2025
7135237 CIFC460 H476 N40 O45P -117.8141; 20.6055; 28.5357
98.149; 104.186; 104.628
9591.7Huang, Jiaming; Martínez-Belmonte, Marta; Ballester, Pablo
Reducing rotatable bonds in one substrate accelerates a bimolecular Diels-Alder reaction in a bis-calix[4]pyrrole cage.
Chemical communications (Cambridge, England), 2025
7135236 CIFC62 H42 N4 O2 P2P b c a14.0167; 23.1649; 32.3543
90; 90; 90
10505.3Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135235 CIFC40 H32 N4 O3P 1 2/c 112.1304; 10.3755; 25.2295
90; 102.918; 90
3094.99Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135234 CIFC42 H32 N4 O4P -110.268; 11.7261; 14.837
104.156; 106.691; 100.305
1598.4Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135233 CIFC39 H26 Cl2 N4 OP 1 21/n 111.101; 10.5875; 26.8424
90; 96.405; 90
3135.14Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135232 CIFC42 H32 N4 O4P 1 21/c 114.0567; 12.8429; 19.1088
90; 111.022; 90
3220.1Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135231 CIFC42 H32 N4 O4P 1 21/n 112.5542; 14.0614; 18.8278
90; 96.095; 90
3304.9Zhang, Yin-Fu; Zhang, Shuqi; Zhao, Yan; Xu, Jiying; Wang, Xiao-Qing; Han, Qiu-Xia; Zhang, Chuan-Bao; Zhao, Lili; Fu, Ji-Ya
Divergent synthesis of polycyclic (aza)fluorenes <i>via</i> condition-controlled tandem reaction of <i>ortho</i>-hydroxyphenyl-substituted indene-dienes.
Chemical communications (Cambridge, England), 2025
7135230 CIFC12 H10 Cl N O2P 1 21/n 114.959; 5.3671; 15.422
90; 108.397; 90
1174.9Parthasarathy, Thiyagaraj; Bhowmik, Aritra; Bhattacharya, Biswajit; Mishra, Manish Kumar; Ghosh, Soumyajit
Reversible Twisting-Induced Crystalline–Polycrystalline Transformation in Cyanoacrylate Crystals
Chemical Communications, 2025
7135229 CIFC12 H10 Cl N O2P 1 21/n 114.959; 5.3671; 15.422
90; 108.397; 90
1174.9Parthasarathy, Thiyagaraj; Bhowmik, Aritra; Bhattacharya, Biswajit; Mishra, Manish Kumar; Ghosh, Soumyajit
Reversible Twisting-Induced Crystalline–Polycrystalline Transformation in Cyanoacrylate Crystals
Chemical Communications, 2025
7135228 CIFC23 H21 N O4 SP 1 21/n 19.927; 15.272; 13.8
90; 100.295; 90
2058.5Li, Wenkai; Fu, Liling; Xu, Yongqiang; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Atroposelective synthesis of isoquinolinone bearing two distinct C−N axes via cobalt-catalyzed enantioselective C−H activation/annulation
Chemical Communications, 2025
7135227 CIFC39 H31 Cl4 N3 O3 SP 1 21 112.1261; 9.8525; 15.413
90; 92.231; 90
1840Li, Wenkai; Fu, Liling; Xu, Yongqiang; Zhou, Yuhan; Qu, Jingping; Wang, Baomin
Atroposelective synthesis of isoquinolinone bearing two distinct C−N axes via cobalt-catalyzed enantioselective C−H activation/annulation
Chemical Communications, 2025
7135226 CIFC76 H40 Al3 F81 O14P -115.8741; 15.9964; 22.6
84.126; 82.511; 63.971
5106.2Benny, Annabel; Vijayan, Devika; Thayalan, Rajeshkumar; Maron, Laurent; Venugopal, Ajay
An aldehyde-stabilised alkoxyaluminium dication.
Chemical communications (Cambridge, England), 2025, 61, 16074-16077
7135225 CIFC8 H10 Cl2 N SbP 1 21/c 19.0035; 7.6161; 16.2664
90; 97.081; 90
1106.9Benny, Annabel; Vijayan, Devika; Thayalan, Rajeshkumar; Maron, Laurent; Venugopal, Ajay
An aldehyde-stabilised alkoxyaluminium dication.
Chemical communications (Cambridge, England), 2025, 61, 16074-16077
7135224 CIFC64 H46 N14 NiR -3 :H18.651; 18.651; 23.358
90; 90; 120
7037Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135223 CIFC66 H48 N12 Ni O8 Re2R -3 :H18.7166; 18.7166; 23.4717
90; 90; 120
7120.8Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135222 CIFC66 H48 N12 NiR -3 :H18.959; 18.959; 20.322
90; 90; 120
6326Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135221 CIFC33 H24 N6 Ni O3R -3 :H18.4326; 18.4326; 19.6463
90; 90; 120
5780.8Sheng, Daopeng; Zhai, Fuwan; Li, Baoyu; Guo, Chenglong; Hou, Minglei; Jin, Yusheng; Zhang, Yugang; Zhang, Mingxing; Shen, Nannan; Diwu, Juan; Li, Jie; Wang, Shuao
Correlation between coordination environments and sorption selectivity to <sup>99</sup>TcO<sub>4</sub><sup>-</sup> in two-dimensional metal-organic frameworks.
Chemical communications (Cambridge, England), 2025, 61, 16082-16085
7135220 CIFC30 H44 N5P -111.9464; 14.9849; 17.3068
67.949; 89.902; 84.01
2853.52Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135219 CIFC44 H72 N5P -111.0521; 13.746; 15.6376
69.62; 76.6492; 89.3974
2160.43Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135218 CIFC31 H41 N6P 1 21/n 113.9813; 15.2468; 15.1459
90; 112.159; 90
2990.2Shu, Ruifeng; Naota, Takeshi; Shiomi, Daisuke; Suzuki, Shuichi
Multistage control of near-infrared and magnetic properties <i>via</i> π-dimer modulation in TCNQ radical anion salts.
Chemical communications (Cambridge, England), 2025, 61, 17021-17024
7135217 CIFC27 H21 F N2P 1 21/c 113.68938; 17.62391; 8.08
90; 92.3948; 90
1947.68Liu, Xingwang; Xiao, Shunli; Huang, Hao; Bai, Lele; Lai, Wenze; Wu, Gaorong
Ru(II)-catalyzed stereoselective C(7)-H α-fluoroalkenylation of indolines.
Chemical communications (Cambridge, England), 2025, 61, 18850-18853
7135216 CIFC18 H22 O5P 1 21/c 18.1345; 10.4932; 20.272
90; 95.961; 90
1721Luo, Xue-Ling; Lv, Yu; Luo, Di-Jing; Qin, Lu-Lu; Li, Shu-Hui; Ye, Zhi-Peng; Xie, Zhen-Zhen; Xia, Peng-Ju
Photoinduced [3+2] cycloaddition <i>via</i> HFIP-promoted <i>in situ</i> formation of isobutylene from the Boc group.
Chemical communications (Cambridge, England), 2025, 61, 18180-18183
7135215 CIFC58 H84 Bi Fe O4 P WP 1 21/c 116.3885; 15.0042; 29.725
90; 92.94; 90
7299.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135214 CIFC34 H31 B Bi Fe PP 1 21/c 19.1589; 16.358; 19.491
90; 96.875; 90
2899.2Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135213 CIFC34 H31 B Bi Fe PP 1 21/n 18.8411; 29.7793; 11.1614
90; 101.634; 90
2878.22Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135212 CIFC34 H18 F10 Fe P SbP 1 21/n 19.0076; 15.7671; 20.942
90; 94.116; 90
2966.59Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135211 CIFC34 H18 F10 Fe P SbP -111.2557; 11.3367; 13.0357
101.126; 96.212; 110.747
1497.76Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135210 CIFC24 H17 F6 Fe SbP 1 21/c 111.2444; 20.5216; 9.9176
90; 103.895; 90
2221.55Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135209 CIFC24 H23 Fe SbP 1 21/n 113.5485; 8.7852; 17.4796
90; 106.904; 90
1990.64Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135208 CIFC38 H28 Bi Fe O4 P WP 1 21/n 19.7245; 15.1827; 22.7398
90; 101.645; 90
3288.3Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135207 CIFC36 H28 Bi Fe O2 P W0.5P -19.1002; 10.1731; 16.7783
98.928; 97.552; 92.666
1517.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135206 CIFC34 H31 B Fe P SbP -18.9845; 16.3617; 20.0366
82.755; 82.306; 86.952
2893.6Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135205 CIFC22 H9 F10 Fe SbP 1 21/n 17.3495; 19.1515; 14.5035
90; 99.657; 90
2012.5Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135204 CIFC34 H28 Bi2 FeP 1 21/n 114.2965; 12.9935; 15.2543
90; 91.357; 90
2832.9Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135203 CIFC22 H19 Bi FeP -18.2785; 9.4737; 12.7844
97.188; 101.459; 110.864
896.98Rezazgui, David; Schulz, Jiří; Štěpnička, Petr
Practical synthesis of ferrocenyldiarylstibines and bismuthines.
Chemical communications (Cambridge, England), 2025, 61, 18705-18708
7135202 CIFC17 H28 Au F3 N PP 1 21/c 115.643; 8.8608; 15.3181
90; 111.893; 90
1970.1Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135201 CIFC18 H29 Au F3 P SP 1 21/n 18.2996; 25.654; 10.1969
90; 105.659; 90
2090.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135200 CIFC25 H40 Au B F3 PP -18.6619; 9.6434; 17.4721
79.094; 85.397; 67.85
1327.3Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135199 CIFC19 H47 Au B10 F2 N4 P2P 21 21 2110.2254; 16.748; 18.788
90; 90; 90
3217.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135198 CIFC31 H24 Au F3 P2P b c a15.0808; 18.4456; 19.4861
90; 90; 90
5420.5Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135197 CIFC19 H46 Au B10 F3 N4 P2P 110.1568; 11.9327; 13.4874
98.078; 92.088; 91.572
1616.48Vesseur, David; Li, Shuo; Mallet-Ladeira, Sonia; Bourissou, Didier
Ligand exchange of tris(2,4-di-<i>tert</i>-butylphenyl) phosphite: a practical and efficient route to organo gold(I) complexes.
Chemical communications (Cambridge, England), 2025, 61, 18717-18720
7135196 CIFC47 H65 B2 N2 S2P -113.8574; 18.3602; 20.3029
64.529; 80.521; 79.824
4567.2Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135195 CIFC46 H60 B2 N2 SP -110.0786; 15.1951; 15.3131
75.107; 70.973; 75.478
2106.45Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135194 CIFC46 H60 B2 N2 SP 1 21/c 114.2244; 26.2529; 11.4501
90; 92.246; 90
4272.55Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135193 CIFC29.03 H42.41 B N2 SP -4 21 c23.7578; 23.7578; 10.4931
90; 90; 90
5922.65Chorbacher, Johannes; Hellinger, Anna; Klopf, Jonas; Friedrich, Alexandra; Helten, Holger
Thienyl flanked bis(aminoborane)s as inorganic-organic hybrid AIEgens.
Chemical communications (Cambridge, England), 2025, 61, 17149-17152
7135192 CIFC48 H73 N3 S4P 1 21/c 114.444; 17.6533; 18.4027
90; 96.711; 90
4660.2Lim, Gayeong; Cha, Jaegeum; Kim, Youngsuk
Reversible cyclodimerization of cyclic (alkyl)(amino)carbene-carbon disulfide adduct.
Chemical communications (Cambridge, England), 2025, 61, 18384-18387
7135191 CIFC10 Fe I3R -3 m :H8.5305; 8.5305; 17.0548
90; 90; 120
1074.8Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135190 CIFC9.99 Fe I3 PbP 63/m m c10.9271; 10.9271; 8.1291
90; 90; 120
840.59Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135189 CIFC10 H10 Fe I3 PbC 1 2/c 119.1013; 18.1903; 13.8623
90; 92.82; 90
4810.74Xu, Zhe-Kun; Wang, Zhong-Xia
A low-dimensional ferrocenium lead-iodide perovskite ferroelastic with a narrow band gap.
Chemical communications (Cambridge, England), 2025, 61, 15810-15813
7135188 CIFC41 H35 Cl4 O2 P2 ReP 1 21/n 112.6366; 10.614; 28.7173
90; 95.677; 90
3832.8Li, Lei; Fu, Bingjie; Zhao, Yue; Sun, Yue; Li, Yang; Jiang, Wenfeng; Bai, Wei
Synthesis and characterization of rhena-phenalenyl complexes.
Chemical communications (Cambridge, England), 2025, 61, 15858-15861
7135187 CIFC60 H65 Cl2 O5 P3 Re2P 1 21/n 112.2713; 15.3656; 30.0068
90; 97.177; 90
5613.6Li, Lei; Fu, Bingjie; Zhao, Yue; Sun, Yue; Li, Yang; Jiang, Wenfeng; Bai, Wei
Synthesis and characterization of rhena-phenalenyl complexes.
Chemical communications (Cambridge, England), 2025, 61, 15858-15861
7135186 CIFC23 H23 Cl2 N O4P b c a14.2188; 10.3324; 29.7421
90; 90; 90
4369.5Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135185 CIFC22 H21 Cl2 N O3P 1 21/n 15.9876; 29.771; 11.4497
90; 97.157; 90
2025.1Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
7135184 CIFC17 H17 N O4P -16.6452; 9.1816; 12.2867
81.324; 80.372; 85.557
729.59Nemichand, ?; Waghmode, Amol G.; Awchar, Vilas M.; Baskaran, Sundarababu
Oxidative cyclization of active methylene amides: efficient synthesis of functionalized 3-azabicyclo[<i>n</i>.1.0]alkanes.
Chemical communications (Cambridge, England), 2025
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
7135152 CIFC73 H64 Cl12 N6 O3P -110.502; 17.367; 38.68
93.004; 90.221; 92.104
7040.2Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular engineering of porous organic cages for iodine capture and fluorescence detection.
Chemical communications (Cambridge, England), 2025, 61, 19124-19127
7135151 CIFC59 H56 Cl6 N8 O3P -115.1639; 18.904; 20.266
89.732; 74.207; 89.827
5590Liu, Shuangbin; Xiang, Yuanke; Chen, Xinqi; Gao, Haofeng; Yang, Xiaoran; Li, Jinmei; Fan, Jianxian; Liu, Ziyuan; He, Tianwei; Qiu, Li
Molecular engineering of porous organic cages for iodine capture and fluorescence detection.
Chemical communications (Cambridge, England), 2025, 61, 19124-19127
7135150 CIFC32 H26 N2 OP 21 21 2111.6092; 12.2172; 16.4574
90; 90; 90
2334.2Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 19281-19284
7135149 CIFC32 H26 N2 OP -18.8121; 10.1918; 13.9891
99.49; 97.145; 103.344
1188.33Ma, Qiyuan; Qin, Hao; He, Xulong; Zheng, Zexi; Ding, Yawen; Yuan, Yu; Zhang, Shuwei; Jia, Xiaodong
Design, synthesis and structural investigation of a novel class of aggregation-induced emission (AIE) molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 19281-19284
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
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
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
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
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
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
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
7135141 CIFC40.5 H30 Cl6 Ir N5 S2P 1 21/c 113.353; 15.201; 20.751
90; 91.064; 90
4211.3Morales-Pioz, Eva; Redrado, Marta; Benedi, Andrea; de Aquino, Araceli; García-Orduña, Pilar; Royo-Cañas, María; Godino, Javier; Marzo, I.; Rodríguez, Laura; Gimeno, M Concepción; Fernández-Moreira, Vanesa
Cyclometallated iridium(III) complexes: ligand-driven selectivity for chemotherapy and photodynamic therapy.
Chemical communications (Cambridge, England), 2025, 61, 19237-19240
7135140 CIFC106 H224 Au2 Cl2 N2 O Sb4 Si18P 1 21/n 112.5283; 36.1287; 17.215
90; 109.18; 90
7359.5Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa M.; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au-Sb bimetallic linkage.
Chemical communications (Cambridge, England), 2025, 61, 19309-19312
7135139 CIFC56 H119 Au Cl N Sb2 Si9P 1 21/n 118.0962; 23.3405; 18.1023
90; 100.648; 90
7514.29Palui, Prasenjit; Bollenbeck, Matthias; Langellotti, Vincenzo; Schnakenburg, Gregor; Gomila, Rosa M.; Frontera, Antonio; Bismuto, Alessandro
Synthesis and reactivity of a small distibacycle featuring an Au-Sb bimetallic linkage.
Chemical communications (Cambridge, England), 2025, 61, 19309-19312
7135138 CIFC22 H21 I O6P -19.0209; 9.603; 13.967
73.695; 71.448; 66.6
1036.01Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135137 CIFC16 H11 N O3 SP 1 21/c 110.3033; 16.8149; 7.3464
90; 92.449; 90
1271.59Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135136 CIFC20 H18 O3P -17.8446; 8.6853; 11.0599
77.008; 83.439; 81.312
723.3Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135135 CIFC19 H14 O5P 1 21/c 18.3627; 10.9839; 16.0035
90; 97.525; 90
1457.34Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135134 CIFC20.5 H16.98 Cl O6C 1 2/c 120.9727; 8.1208; 20.9626
90; 100.685; 90
3508.34Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135133 CIFC20 H16 O5P 1 21/c 110.2969; 9.8246; 14.8656
90; 93.018; 90
1501.76Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
7135132 CIFC25 H19 N O5P 1 21/c 19.51124; 15.99027; 12.44468
90; 101.867; 90
1852.23Powderly, Marian E.; Lindup, Toby; Jackman, Edward H.; Light, Mark E.; Legros, Julien; Chataigner, Isabelle; Harrowven, David C.
Photocyclisations of <i>o</i>-iodobenzyl-indanones and tetralones infer the intermediacy of triplet aryl cations.
Chemical communications (Cambridge, England), 2025, 61, 19229-19232
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
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
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
7135128 CIFC46 H45 Cl2 Fe2 N O6 S4P 21 21 2110.6274; 13.5606; 31.507
90; 90; 90
4540.6Li, Shiguang; Wang, Jiang; Lv, Ya; Chi, Yonggui Robin; Gan, Xiuhai; Wu, Xingxing
N-Heterocyclic carbene-catalyzed asymmetric synthesis of bis-ferrocene derivatives bearing two stereogenic planes.
Chemical communications (Cambridge, England), 2025, 61, 19036-19039
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
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
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
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
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
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
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
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
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
7135118 CIFC25 H28 O3P 1 21 18.4261; 11.7773; 11.2319
90; 107.842; 90
1061.01Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-catalyzed stereoselective desymmetrization of prochiral cyclopentane-1,3-diones <i>via</i> alkoxyallylation.
Chemical communications (Cambridge, England), 2025, 61, 19108-19111
7135117 CIFC31 H29 I O3P 1 21/c 120.985; 10.746; 12.2193
90; 102.749; 90
2687.57Maurya, Sundaram; Patil, Vaibhav B.; Raghu Ramudu, G.; Amrutkar, Virendra S.; Mendapara, Yash G.; Nanubolu, Jagadeesh Babu; Chegondi, Rambabu
CuH-catalyzed stereoselective desymmetrization of prochiral cyclopentane-1,3-diones <i>via</i> alkoxyallylation.
Chemical communications (Cambridge, England), 2025, 61, 19108-19111
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
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
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
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
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
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
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
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
7135108 CIFC23 H25 Cl N2 O2P 21 21 2110.5633; 10.5879; 18.4454
90; 90; 90
2062.99Clark, Paul; Keenan, Thomas; Liu, Shiqi; Huang, Jingjun; Ma, Yao-Rui; Hasija, Avantika; Huang, Pei-Qiang; Jean, Alexandre; Leitch, David C.; Arseniyadis, Stellios
Palladium-catalysed asymmetric allylic alkylation of hydantoins using bench-stable chiral palladium precatalysts.
Chemical communications (Cambridge, England), 2025, 61, 19064-19067
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
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
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
7135104 CIFC105 H102 Cl6 N18 Se3P 3119.6339; 19.6339; 26.1675
90; 90; 120
8735.9Liu, Chao; Du, Ziwei; Ding, Xu; Wang, Zhixuan; Cao, Lili; Zhou, Ziwen; Chen, Jia; Zhang, Ning
Precise heteroatom engineering for iodine capture promotion in porous organic cages.
Chemical communications (Cambridge, England), 2025, 61, 19076-19079
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

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