Crystallography Open Database

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7134184 CIFC13 H17 Cl N2 O4 SP 1 21/c 122.112; 5.91; 12.384
90; 103.404; 90
1574.3Fang, Yi-Jun; Wu, Xiao-Bao; Wang, Qi-Ming; Xie, Zu-Kui; Yao, Chuan-Zhi; Jiang, Hua-Jie; Yu, Jie
High-performance anionic stereogenic-at-cobalt(III) complex/halide salts/oxone catalytic system for enantioselective halocyclization of olefins.
Chemical communications (Cambridge, England), 2025, 61, 2814-2817
7134185 CIFC13 H17 Br N2 O4 SC 1 2 112.403; 5.914; 22.599
90; 104.87; 90
1602Fang, Yi-Jun; Wu, Xiao-Bao; Wang, Qi-Ming; Xie, Zu-Kui; Yao, Chuan-Zhi; Jiang, Hua-Jie; Yu, Jie
High-performance anionic stereogenic-at-cobalt(III) complex/halide salts/oxone catalytic system for enantioselective halocyclization of olefins.
Chemical communications (Cambridge, England), 2025, 61, 2814-2817
7134186 CIFC13 H17 Br N2 O4 SP 1 21 110.0954; 6.1839; 13.3904
90; 106.362; 90
802.09Fang, Yi-Jun; Wu, Xiao-Bao; Wang, Qi-Ming; Xie, Zu-Kui; Yao, Chuan-Zhi; Jiang, Hua-Jie; Yu, Jie
High-performance anionic stereogenic-at-cobalt(III) complex/halide salts/oxone catalytic system for enantioselective halocyclization of olefins.
Chemical communications (Cambridge, England), 2025, 61, 2814-2817
7134187 CIFC124 H186 Ag10 F12 N8 O8 P6 S4P -116.8356; 22.3238; 26.6877
70.721; 73.976; 71.123
8796.2Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Prathapa, Siriyara Jagannatha; Roy, Sudipta
Isolation of mixed valence charge-neutral Ag<sub>12</sub>, and dicationic Ag<sub>10</sub> nano-clusters stabilized by carbene-phosphaalkenides.
Chemical communications (Cambridge, England), 2025, 61, 1379-1382
7134188 CIFC120 H186 Ag12 Cl3 N6 P6R -3 :H32.5258; 32.5258; 16.6904
90; 90; 120
15291.6Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Prathapa, Siriyara Jagannatha; Roy, Sudipta
Isolation of mixed valence charge-neutral Ag<sub>12</sub>, and dicationic Ag<sub>10</sub> nano-clusters stabilized by carbene-phosphaalkenides.
Chemical communications (Cambridge, England), 2025, 61, 1379-1382
7134189 CIFC26 H31 N3 O3 SP 1 21/c 112.6627; 15.3055; 12.8279
90; 101.373; 90
2437.34Chaudhary, Dhananjay; Maurya, Chandra Shekhar; Unnikrishnan, Urmila; Kuram, Malleswara Rao
HFIP-mediated cascade aminomethylation and intramolecular cyclization of allenamides with <i>N</i>,<i>O</i>-acetals to access tetrahydro-β-carboline derivatives.
Chemical communications (Cambridge, England), 2025, 61, 2981-2984
7134190 CIFC17 H22 Cr F3 N2 O6 SP -19.0515; 11.5963; 15.9542
70.366; 89.852; 81.103
1556.08Shen, Zhi-Kai; Li, Zi-Jian; Zou, Zhigang; Yu, Zhen-Tao
Identification of the Cr(V)O intermediate in electrocatalytic water oxidation by a chromium(III)-aqua complex.
Chemical communications (Cambridge, England), 2025, 61, 3387-3390
7134191 CIFB45 K18 Na3 O90 Sr3 Y6R 3 2 :H12.974; 12.974; 15.367
90; 90; 120
2240.1Liu, Mengru; Kong, Xianghao; Li, Shuaifeng; Ye, Ning; Hu, Zhanggui; Wu, Yicheng; Li, Conggang
Designing rare earth borates as UV nonlinear optical crystals exhibiting strong second-harmonic generation responses.
Chemical communications (Cambridge, England), 2025, 61, 3155-3158
7134192 CIFB2.5 Ba0.17 Lu0.33 O5 Rb1.17R 3 2 :H13.5347; 13.5347; 15.719
90; 90; 120
2493.7Liu, Mengru; Kong, Xianghao; Li, Shuaifeng; Ye, Ning; Hu, Zhanggui; Wu, Yicheng; Li, Conggang
Designing rare earth borates as UV nonlinear optical crystals exhibiting strong second-harmonic generation responses.
Chemical communications (Cambridge, England), 2025, 61, 3155-3158
7134193 CIFC11 H9 Br N O2P -16.7614; 7.298; 11.361
82.509; 89.624; 84.148
552.9Wang, Jingjing; Qin, Yuran; Cui, Ke; Li, Xueqi; Cui, Mingyue; Cao, Sheng; Zhang, Linbo; Shen, Qin; Wang, Teng; Li, Feng
Solvent-controlled silver catalyzed radical transformation of α-imino-oxy acids with cyclic aldimines.
Chemical communications (Cambridge, England), 2025, 61, 3359-3362
7134194 CIFC12 H12 N2 O3 SP -17.7907; 9.2425; 9.679
106.943; 105.014; 96.858
629.44Wang, Jingjing; Qin, Yuran; Cui, Ke; Li, Xueqi; Cui, Mingyue; Cao, Sheng; Zhang, Linbo; Shen, Qin; Wang, Teng; Li, Feng
Solvent-controlled silver catalyzed radical transformation of α-imino-oxy acids with cyclic aldimines.
Chemical communications (Cambridge, England), 2025, 61, 3359-3362
7134195 CIFC18 H18 N2 O4 S2P -19.0198; 9.8165; 11.3146
89.792; 89.757; 63.581
897.19Pal, Kuntal; Dash, Om Prakash; Volla, Chandra M. R.
Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from <i>N</i>-sulfonyl-1,2,3-triazoles.
Chemical communications (Cambridge, England), 2025, 61, 3872-3875
7134196 CIFC23 H30 Cl N O2 SP -114.5277; 14.8392; 32.2982
98.541; 98.294; 90.455
6810.5Kang, Bangxiong; Li, Wei; Jiang, Huanfeng; Qi, Chaorong
Metal-free four-component coupling of cyclic diarylchloronium salts, tetrahydrothiophene, amines and carbon dioxide.
Chemical communications (Cambridge, England), 2025, 61, 3395-3398
7134197 CIFC59 H86 K N O3 Te2P 1 21/n 19.372; 18.509; 32.59
90; 96.362; 90
5618Gray, Novan A. G.; Britten, James F.; Emslie, David J. H.
Potassium-telluroether interactions: structural characterisation and computational analysis.
Chemical communications (Cambridge, England), 2025, 61, 3143-3146
7134198 CIFC47 H61 K N Te2P 1 21/c 124.534; 18.432; 10.716
90; 97.869; 90
4800Gray, Novan A. G.; Britten, James F.; Emslie, David J. H.
Potassium-telluroether interactions: structural characterisation and computational analysis.
Chemical communications (Cambridge, England), 2025, 61, 3143-3146
7134199 CIFC55 H78 K N O2 Se2P 1 21/c 19.342; 18.461; 29.14
90; 92.67; 90
5020Gray, Novan A. G.; Britten, James F.; Emslie, David J. H.
Potassium-telluroether interactions: structural characterisation and computational analysis.
Chemical communications (Cambridge, England), 2025, 61, 3143-3146
7134200 CIFC65 H100 K N O3 Se2P 1 21/c 19.312; 18.55; 35.565
90; 95.108; 90
6119Gray, Novan A. G.; Britten, James F.; Emslie, David J. H.
Potassium-telluroether interactions: structural characterisation and computational analysis.
Chemical communications (Cambridge, England), 2025, 61, 3143-3146
7134201 CIFC65 H41 Cl3P -111.8264; 21.1618; 21.7622
111.549; 102.509; 99.005
4775.4Sujilkumar, Suvarna; Hari, Avinash; Hariharan, Mahesh
Through-space conjugation driven luminescence enhancement in crystalline butterfly architectures.
Chemical communications (Cambridge, England), 2025, 61, 3331-3334
7134202 CIFC64 H40C 1 2/c 122.7452; 7.7582; 24.2788
90; 94.036; 90
4273.7Sujilkumar, Suvarna; Hari, Avinash; Hariharan, Mahesh
Through-space conjugation driven luminescence enhancement in crystalline butterfly architectures.
Chemical communications (Cambridge, England), 2025, 61, 3331-3334
7134203 CIFC44 H64 F6 N3 O PP 1 21/c 18.6738; 29.966; 17.4
90; 97.838; 90
4480.3Park, Hojeong; Niu, Guangle; Wong, Alex Y. H.; Yu, Eric Y.; Kwok, Ryan T. K.; Tang, Ben Zhong
Reaction-free mitochondrial membrane potential independent luminogens with aggregation-induced emission characteristics for live neuron imaging.
Chemical communications (Cambridge, England), 2025, 61, 3536-3539
7134204 CIFC26.25 H27.5 Bi Br2 Cl0.5 N2P 1 21/n 113.2163; 8.2052; 28.5094
90; 96.531; 90
3071.6Deuter, Katharina L.; Balaba, Daisy J. J.; Linseis, Michael; Winter, Rainer F.
Room-temperature near-infrared phosphorescence of a bismuthinidene N,C,N pincer complex.
Chemical communications (Cambridge, England), 2025, 61, 3548-3551
7134205 CIFC26 H27 Br N2P 21 21 218.5116; 10.8836; 24.405
90; 90; 90
2260.8Deuter, Katharina L.; Balaba, Daisy J. J.; Linseis, Michael; Winter, Rainer F.
Room-temperature near-infrared phosphorescence of a bismuthinidene N,C,N pincer complex.
Chemical communications (Cambridge, England), 2025, 61, 3548-3551
7134206 CIFC14 H11 F3 N2P 1 21/c 17.639; 21.17; 8.402
90; 99.33; 90
1341Singh, Shashank; Kundu, Arindam; Empel, Claire; Koenigs, René Michael; Singh, Ravi P.
A radical approach towards polarity-reversed <i>para</i>-substitution of electron-deficient arenes.
Chemical communications (Cambridge, England), 2025, 61, 3888-3891
7134207 CIFC19 H11 F3 N2P 1 21/c 113.1854; 8.7585; 14.5343
90; 101.895; 90
1642.4Singh, Shashank; Kundu, Arindam; Empel, Claire; Koenigs, René Michael; Singh, Ravi P.
A radical approach towards polarity-reversed <i>para</i>-substitution of electron-deficient arenes.
Chemical communications (Cambridge, England), 2025, 61, 3888-3891
7134208 CIFC50.41 H41.1 I6 N12 O2.51 Zn3C 1 2/c 134.3966; 14.9997; 31.701
90; 101.865; 90
16006.3Pearce, James E.; Hodgson, Jack; Folgueiras-Amador, Ana A; Fish, Johanna A.; Carroll, Robert C.; Coles, Simon J.; Parsons, Philip J.; Brown, Richard C. D.; Harrowven, David C.
The electrosynthesis of highly encumbered biaryls from aryl <i>o</i>-iodobenzyl ethers by a radical to polar crossover sequence.
Chemical communications (Cambridge, England), 2025, 61, 4042-4045
7134209 CIFC39.42 H28.84 I6 N12 O0.14 Zn3C 1 2/c 135.0015; 14.8912; 31.1462
90; 101.513; 90
15907.2Pearce, James E.; Hodgson, Jack; Folgueiras-Amador, Ana A; Fish, Johanna A.; Carroll, Robert C.; Coles, Simon J.; Parsons, Philip J.; Brown, Richard C. D.; Harrowven, David C.
The electrosynthesis of highly encumbered biaryls from aryl <i>o</i>-iodobenzyl ethers by a radical to polar crossover sequence.
Chemical communications (Cambridge, England), 2025, 61, 4042-4045
7134210 CIFC30 H51 B3 Te2 Ti3P -18.2544; 11.6397; 18.6492
91.086; 91.102; 102.584
1747.93Bairagi, Subhash; Chatterjee, Debipada; Giri, Soumen; Ghosh, Sundargopal
Hypoelectronic titanaboranes: icosahedral and tetracapped tetrahedral clusters comprising bridging hydrides.
Chemical communications (Cambridge, England), 2025, 61, 3696-3699
7134211 CIFC30 H53 B9 Cl2 Ti3P n a 2117.2436; 11.5096; 18.5384
90; 90; 90
3679.3Bairagi, Subhash; Chatterjee, Debipada; Giri, Soumen; Ghosh, Sundargopal
Hypoelectronic titanaboranes: icosahedral and tetracapped tetrahedral clusters comprising bridging hydrides.
Chemical communications (Cambridge, England), 2025, 61, 3696-3699
7134212 CIFC32 H49 B5 Se2 Ti2P b c a15.9297; 16.0271; 29.237
90; 90; 90
7464.4Bairagi, Subhash; Chatterjee, Debipada; Giri, Soumen; Ghosh, Sundargopal
Hypoelectronic titanaboranes: icosahedral and tetracapped tetrahedral clusters comprising bridging hydrides.
Chemical communications (Cambridge, England), 2025, 61, 3696-3699
7134213 CIFC79 H112 B2 Br2 Cl2 N2 P4 Pt2P -111.0758; 11.5452; 17.0605
74.577; 85.39; 82.42
2082.3Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134214 CIFC40 H69 B Br N P2 PtP -110.5156; 12.0709; 17.3124
84.53; 78.986; 68.327
2003.8Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134215 CIFC32 H65 B Br N P2 PtP -110.6332; 11.0382; 17.2246
91.194; 94.582; 113.932
1838.8Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134216 CIFC39 H65 B Br D6 N O2 P2 PtC 1 2/c 139.0652; 10.9573; 21.2389
90; 112.278; 90
8412.7Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134217 CIFC36 H67 Br P2 PtP 1 21/n 113.0812; 12.5821; 23.0932
90; 106.007; 90
3653.5Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134218 CIFC36 H66 P2 PtC 1 2/c 116.6373; 9.5591; 22.1962
90; 91.983; 90
3527.9Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134219 CIFC66 H97 B2 Br2 N2 P3 Pt2P 1 c 115.9051; 13.8819; 19.7934
90; 112.643; 90
4033.4Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134220 CIFC36 H69 B Br N P2 PtP 1 21/c 112.351; 16.632; 19.686
90; 101.65; 90
3960.6Ordyszewska, Anna; Czaplewski, Antoni; Wojnowski, Tomasz; Anusiewicz, Iwona; Chojnacki, Jarosław; Grubba, Rafał
Side-on phosphinoboryl platinum(II) complexes.
Chemical communications (Cambridge, England), 2025, 61, 3728-3731
7134221 CIFC28 H23 N O5P -111.9433; 12.3276; 20.132
75.06; 81.142; 75.914
2764.6Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134222 CIFC35 H31 Br O5P 31 2 111.5209; 11.5209; 40.4128
90; 90; 120
4645.39Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134223 CIFC25 H25 N O2P c a 2111.3577; 12.6655; 27.035
90; 90; 90
3889Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134224 CIFC34 H26 Br N O5P 21 21 2110.4122; 13.8828; 19.5704
90; 90; 90
2828.9Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134225 CIFC27 H27 N O3P -110.0943; 12.4294; 18.1764
85.359; 80.756; 85.323
2238.1Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134226 CIFC1.697 H1.515 N0.061 O0.242P -19.838; 11.101; 11.425
97.664; 97.936; 110.262
1137.1Huang, Xuelian; Yang, Gaosheng; Chai, Zhuo
Diastereoselective synthesis of benzazocines by Zn(OTf)<sub>2</sub>-catalyzed (4+4) cyclocondensation of multisubstituted donor-acceptor cyclopropanes with anthranils.
Chemical communications (Cambridge, England), 2025, 61, 3704-3707
7134227 CIFC17 H14 N2 O2C 1 2/c 129.648; 6.1467; 15.396
90; 101.548; 90
2748.9Tyagi, Kartikay; Dixit, Tejal; Venkatesh, V.
Visible light-induced photoisomerization of indole-oxindole constructs: molecular disassembly and ROS-mediated apoptosis.
Chemical communications (Cambridge, England), 2025, 61, 3892-3895
7134228 CIFC9.5 H7 N O0.5P 1 21 110.576; 4.7113; 14.303
90; 102.737; 90
695.1Tyagi, Kartikay; Dixit, Tejal; Venkatesh, V.
Visible light-induced photoisomerization of indole-oxindole constructs: molecular disassembly and ROS-mediated apoptosis.
Chemical communications (Cambridge, England), 2025, 61, 3892-3895
7134229 CIFC19 H14 N2 OP 1 21/n 117.846; 3.9434; 19.519
90; 97.487; 90
1361.9Tyagi, Kartikay; Dixit, Tejal; Venkatesh, V.
Visible light-induced photoisomerization of indole-oxindole constructs: molecular disassembly and ROS-mediated apoptosis.
Chemical communications (Cambridge, England), 2025, 61, 3892-3895
7134230 CIFC51 H43 Cl3 N6 O2P 1 21/n 119.8975; 7.5952; 28.4543
90; 95.405; 90
4281.1Tyagi, Kartikay; Dixit, Tejal; Venkatesh, V.
Visible light-induced photoisomerization of indole-oxindole constructs: molecular disassembly and ROS-mediated apoptosis.
Chemical communications (Cambridge, England), 2025, 61, 3892-3895
7134231 CIFC92 H60 N12 O20 S4P 1 21/c 138.655; 9.417; 22.232
90; 93.433; 90
8078Tyagi, Kartikay; Dixit, Tejal; Venkatesh, V.
Visible light-induced photoisomerization of indole-oxindole constructs: molecular disassembly and ROS-mediated apoptosis.
Chemical communications (Cambridge, England), 2025, 61, 3892-3895
7134232 CIFC28 H61 B11 Cu N3 P2P -110.6546; 12.1371; 16.1366
80.076; 84.718; 73.091
1964.7Zhang, Kang; Feng, Luting; Jin, Yujie; Liu, Jiyong; Duttwyler, Simon
A σ,π-type monocarborane copper acetylide for regioselective 1,4-disubstituted 1,2,3-triazoles.
Chemical communications (Cambridge, England), 2025, 61, 4026-4029
7134233 CIFC18 H38 B11 Cl N4P 1 21/c 111.4412; 20.7434; 11.2483
90; 90.394; 90
2669.49Zhang, Kang; Feng, Luting; Jin, Yujie; Liu, Jiyong; Duttwyler, Simon
A σ,π-type monocarborane copper acetylide for regioselective 1,4-disubstituted 1,2,3-triazoles.
Chemical communications (Cambridge, England), 2025, 61, 4026-4029
7134234 CIFC23 H23 N O5 SP -19.5157; 9.7021; 11.1463
98.202; 100.953; 94.096
994.82Griggs, Samuel D.; Piticari, Amalia-Sofia; Liver, Samuel; Arter, Chris; Sievers, Sonja; Marsden, Stephen P.; Nelson, Adam
Phenotype-directed discovery of diverse, biologically-relevant molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 3528-3531
7134235 CIFC25 H25 N O5P 1 21/c 113.806; 8.8682; 18.6122
90; 108.601; 90
2159.74Griggs, Samuel D.; Piticari, Amalia-Sofia; Liver, Samuel; Arter, Chris; Sievers, Sonja; Marsden, Stephen P.; Nelson, Adam
Phenotype-directed discovery of diverse, biologically-relevant molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 3528-3531
7134236 CIFC23 H23 N O5 SP -19.502; 10.1598; 12.2054
66.075; 69.398; 75.945
1001.24Griggs, Samuel D.; Piticari, Amalia-Sofia; Liver, Samuel; Arter, Chris; Sievers, Sonja; Marsden, Stephen P.; Nelson, Adam
Phenotype-directed discovery of diverse, biologically-relevant molecular scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 3528-3531
7134237 CIFC101 H152 Al2 B2 N2 P2P -110.6564; 10.7517; 20.7177
88.332; 80.801; 84.137
2330.74Wellnitz, Tim; Wüst, Leonie; Braunschweig, Holger; Hering-Junghans, Christian
A BNAlP-heterocycle.
Chemical communications (Cambridge, England), 2025, 61, 4014-4017
7134238 CIFC58 H80 Al B N PP -110.1884; 13.0766; 21.5233
73.285; 82.107; 75.427
2651.49Wellnitz, Tim; Wüst, Leonie; Braunschweig, Holger; Hering-Junghans, Christian
A BNAlP-heterocycle.
Chemical communications (Cambridge, England), 2025, 61, 4014-4017
7134239 CIFC66 H102 Al B N PP -112.62854; 16.37572; 16.40523
64.5271; 81.4188; 85.6856
3028.3Wellnitz, Tim; Wüst, Leonie; Braunschweig, Holger; Hering-Junghans, Christian
A BNAlP-heterocycle.
Chemical communications (Cambridge, England), 2025, 61, 4014-4017
7134240 CIFC36 H20 F4P 1 21/c 15.0076; 9.6663; 25.6388
90; 92.792; 90
1239.57Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134241 CIFC36 H20 Cl2 F2C 1 2/c 127.2651; 5.2855; 20.7563
90; 117.617; 90
2650.4Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134242 CIFC36 H20 Cl2 F2C 1 2/c 127.271; 5.2838; 20.6495
90; 117.193; 90
2646.6Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134243 CIFC36 H20 Br2 F2I 1 2/a 121.3528; 5.3799; 25.3593
90; 109.492; 90
2746.21Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134244 CIFC36 H20 F4C 1 2/c 127.762; 4.8707; 19.2419
90; 108.206; 90
2471.64Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134245 CIFC36 H20 Br2 F2P -18.7937; 11.0552; 14.1737
81.594; 80.336; 81.165
1331.95Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134246 CIFC36 H24P -19.2666; 10.944; 13.7572
72.986; 78.424; 66.751
1220Shu, Yilin; Huang, Jianmin; Yang, Junfang; Shangguan, Zhichun; Ma, Junlong; Li, Cheng; Zhang, Guanxin; Peng, Qian; Zhang, Xi-Sha; Fan, Qitang; Wang, Bing; Zhang, Deqing
Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation <i>via</i> annulation.
Chemical communications (Cambridge, England), 2025, 61, 3994-3997
7134247 CIFC98 H166 N16 O71 S8P -113.8167; 16.0738; 32.1757
102.88; 95.113; 95.376
6890.7Li, Shu-Hui; Cao, Li-Hui; Zhang, Wenmin; Bai, Xiang-Tian; Chen, Xu-Yong
Multi-hydrophilic groups synergistic assembly ionic HOFs with multiple-water clusters and superprotonic single-crystal conductivity.
Chemical communications (Cambridge, England), 2025, 61, 4034-4037
7134248 CIFC144 H258 N28 O112 S12P -115.89692; 24.3336; 31.3004
82.4312; 76.3819; 78.0115
11467.1Li, Shu-Hui; Cao, Li-Hui; Zhang, Wenmin; Bai, Xiang-Tian; Chen, Xu-Yong
Multi-hydrophilic groups synergistic assembly ionic HOFs with multiple-water clusters and superprotonic single-crystal conductivity.
Chemical communications (Cambridge, England), 2025, 61, 4034-4037
7134249 CIFC31 H20 B F7 N6 SbC 1 2/c 117.0434; 15.2817; 23.1365
90; 101.53; 90
5904.3Zhou, Wen; McKearney, Declan; Okada, Yusuke; Kobayashi, Nagao; Leznoff, Daniel B.
Isolating the ring-redox states of boron sub-phthalocyanines.
Chemical communications (Cambridge, England), 2025, 61, 3832-3835
7134250 CIFC30 H18 B F N6P 1 21/m 110.8237; 14.3172; 16.0555
90; 108.756; 90
2355.9Zhou, Wen; McKearney, Declan; Okada, Yusuke; Kobayashi, Nagao; Leznoff, Daniel B.
Isolating the ring-redox states of boron sub-phthalocyanines.
Chemical communications (Cambridge, England), 2025, 61, 3832-3835
7134251 CIFC263 H255 Ag4 B8 F80 N48 O32 Sb12I 1 2/a 123.995; 15.571; 26.2282
90; 107.704; 90
9335.4Zhou, Wen; McKearney, Declan; Okada, Yusuke; Kobayashi, Nagao; Leznoff, Daniel B.
Isolating the ring-redox states of boron sub-phthalocyanines.
Chemical communications (Cambridge, England), 2025, 61, 3832-3835
7134252 CIFC527 H294 B18 K18 N108 O45P 327.0235; 27.0235; 21.5015
90; 90; 120
13598.2Zhou, Wen; McKearney, Declan; Okada, Yusuke; Kobayashi, Nagao; Leznoff, Daniel B.
Isolating the ring-redox states of boron sub-phthalocyanines.
Chemical communications (Cambridge, England), 2025, 61, 3832-3835
7134253 CIFC48 H44 Cu10 N16 O22I -4 c 223.1107; 23.1107; 18.0067
90; 90; 90
9617.5Xiong, Li; Tang, Wenlei; Xiong, Chaozhi; Du, Jiajun; Zhang, Zhiyuan; Qiu, Yuqing; Shao, Zhen-Wu; Zhou, Xuemei; Liu, Chong
Construction of robust Cu-MOFs from bifunctional pyridine-hydroxamate linkers for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 4030-4033
7134254 CIFC6 H4 Cu N2 O2P n a 2111.5203; 15.0467; 4.4357
90; 90; 90
768.9Xiong, Li; Tang, Wenlei; Xiong, Chaozhi; Du, Jiajun; Zhang, Zhiyuan; Qiu, Yuqing; Shao, Zhen-Wu; Zhou, Xuemei; Liu, Chong
Construction of robust Cu-MOFs from bifunctional pyridine-hydroxamate linkers for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 4030-4033
7134255 CIFC24 H16 Cu5 N8 O8I -4 c 223.9056; 23.9056; 14.4066
90; 90; 90
8233.1Xiong, Li; Tang, Wenlei; Xiong, Chaozhi; Du, Jiajun; Zhang, Zhiyuan; Qiu, Yuqing; Shao, Zhen-Wu; Zhou, Xuemei; Liu, Chong
Construction of robust Cu-MOFs from bifunctional pyridine-hydroxamate linkers for photocatalytic CO<sub>2</sub> reduction.
Chemical communications (Cambridge, England), 2025, 61, 4030-4033
7134256 CIFC56.5 H49 F3 O4 P2 S2P -110.0296; 12.2752; 22.7212
80.179; 80.228; 67.613
2531.69Zafar, Mohammad; Shamali, Donia; Barel, Nitsan; Danovich, David; Tulchinsky, Yuri
Bicyclic sulfonium pincer ligand with a thiatriptycenium backbone-synthesis and applications in π-acid catalysis.
Chemical communications (Cambridge, England), 2025, 61, 4559-4562
7134257 CIFC13 H14 O3P -18.402; 8.472; 9.245
109.344; 101.143; 100.258
588Bhattacharyya, Hemanga; Saha, Sharajit; Verma, Kshitiz; Punniyamurthy, Tharmalingam
Palladium-catalyzed substrate-switchable C-H alkenylation and alkylation of benzoic acids using MBH alcohols.
Chemical communications (Cambridge, England), 2025, 61, 4200-4203
7134258 CIFC2 H7 F14 N3 O2 Sb2P 1 n 16.5268; 8.42; 12.0682
90; 102.487; 90
647.53Nitzer, Alexander; Jessen, Christoph; Kornath, Andreas J.
Charge distribution and aromaticity in protonated urazole.
Chemical communications (Cambridge, England), 2025, 61, 4367-4370
7134259 CIFC2 H5 As2 F12 N3 O2P b c a9.4694; 11.68; 21.1896
90; 90; 90
2343.6Nitzer, Alexander; Jessen, Christoph; Kornath, Andreas J.
Charge distribution and aromaticity in protonated urazole.
Chemical communications (Cambridge, England), 2025, 61, 4367-4370
7134260 CIFC2 H5 F10 Ge2 N3 O2P 1 21/n 17.8994; 18.299; 8.1991
90; 114.751; 90
1076.3Nitzer, Alexander; Jessen, Christoph; Kornath, Andreas J.
Charge distribution and aromaticity in protonated urazole.
Chemical communications (Cambridge, England), 2025, 61, 4367-4370
7134261 CIFC2 H4 F6 N3 O2 SbP 1 21/c 110.5271; 8.3036; 10.5808
90; 118.384; 90
813.71Nitzer, Alexander; Jessen, Christoph; Kornath, Andreas J.
Charge distribution and aromaticity in protonated urazole.
Chemical communications (Cambridge, England), 2025, 61, 4367-4370
7134262 CIFC19 H15 N OP b c a16.4292; 7.6601; 22.9023
90; 90; 90
2882.24Wong, Karina S.; Ghanbari, Mohammad; Arndtsen, Bruce A.
Design of a modular, palladium-catalyzed carbonylative synthesis of pyrido[2,1-α]isoindoles <i>via</i> benzyne 1,3-dipolar cycloaddition.
Chemical communications (Cambridge, England), 2025, 61, 4192-4195
7134263 CIFC3.5 H5 Br Cu0.5 NP 1 21/m 16.7527; 8.6037; 9.204
90; 98.41; 90
528.99Yang, Chuanyao; Zheng, Jia; Xu, Chang; Xiao, Chong; Chang, Yuanyuan; Zhou, Lei; Gong, Xiangnan
Unveiling the photophysical mechanisms in low-dimensional Zn/Cu-based metal halides.
Chemical communications (Cambridge, England), 2025, 61, 4379-4382
7134264 CIFC6 H8 Br N2 Zn0.5C 1 2/c 17.0944; 12.2277; 18.1167
90; 92.812; 90
1569.7Yang, Chuanyao; Zheng, Jia; Xu, Chang; Xiao, Chong; Chang, Yuanyuan; Zhou, Lei; Gong, Xiangnan
Unveiling the photophysical mechanisms in low-dimensional Zn/Cu-based metal halides.
Chemical communications (Cambridge, England), 2025, 61, 4379-4382
7134265 CIFC36 H32 Cl2 O4P -112.1015; 12.1074; 12.1083
79.338; 64.387; 79.372
1561.17Lv, Jiaoyue; Lang, Yatao; Li, Chao-Jun; Zeng, Huiying
Visible-light-induced synthesis of bibenzofuranones <i>via</i> a cerium-mediated energy transfer process.
Chemical communications (Cambridge, England), 2025, 61, 4054-4057
7134266 CIFC32 H96 Ag4 Si16F d d d :226.7344; 33.5536; 43.8428
90; 90; 90
39328.5Ishii, Reon; Wada, Yoshimasa; Sunada, Yusuke
Silyl- and germyl-bridged neutral square-planar Ag<sub>4</sub> clusters with short Ag-Ag distances exhibiting red emission.
Chemical communications (Cambridge, England), 2025, 61, 4391-4394
7134267 CIFC32 H96 Ag4 Ge4 Si12F d d d :226.89331; 33.7727; 43.981
90; 90; 90
39946.2Ishii, Reon; Wada, Yoshimasa; Sunada, Yusuke
Silyl- and germyl-bridged neutral square-planar Ag<sub>4</sub> clusters with short Ag-Ag distances exhibiting red emission.
Chemical communications (Cambridge, England), 2025, 61, 4391-4394
7134268 CIFC29 H24 N2 O3 S2 SeP 1 21/c 18.5751; 15.3208; 20.3759
90; 90; 90
2676.9Shi, Tongtong; Tian, Miao; Sun, Zongfei; Zou, Ruixiao; Zhang, Zexuan; Xie, Na; Hao, Erjun; Xu, Xinming; Sun, Kai
Photochemical aerobic sulfonylation-cyclization-selenylation to indole-fused medium-sized N-heterocycles in 2-Me-THF.
Chemical communications (Cambridge, England), 2025, 61, 4066-4069
7134269 CIFC23 H17 N3 OP 21 21 219.6588; 13.5399; 14.1363
90; 90; 90
1848.73Valvi, Mangesh Biramya; Badhani, Gaurav; More, Karan Prakash; Adimurthy, Subbarayappa
Brønsted acid-mediated mono- and di-substitution of quinoxalines with indoles: a pathway to indolocarbazole-quinoxaline scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 4698-4701
7134270 CIFC24 H20 N4P -19.2942; 10.902; 11.0378
62.717; 71.571; 89.138
931.76Valvi, Mangesh Biramya; Badhani, Gaurav; More, Karan Prakash; Adimurthy, Subbarayappa
Brønsted acid-mediated mono- and di-substitution of quinoxalines with indoles: a pathway to indolocarbazole-quinoxaline scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 4698-4701
7134271 CIFC14 H10 Br F3P 1 21 17.78987; 5.88492; 13.8221
90; 101.509; 90
620.9Liu, Lidong; Guo, Yawen; Shi, Lin; Wang, Yihan; Lei, Xingyu; Jiao, Peng
Building trisubstituted ethylenes from terminal alkenes <i>via</i> debrominative ring-opening trifluoromethylations of geminal dibromocyclopropanes.
Chemical communications (Cambridge, England), 2025, 61, 5170-5173
7134272 CIFC16 H13 F3P b c a5.6746; 17.715; 25.651
90; 90; 90
2578.6Liu, Lidong; Guo, Yawen; Shi, Lin; Wang, Yihan; Lei, Xingyu; Jiao, Peng
Building trisubstituted ethylenes from terminal alkenes <i>via</i> debrominative ring-opening trifluoromethylations of geminal dibromocyclopropanes.
Chemical communications (Cambridge, England), 2025, 61, 5170-5173
7134273 CIFC5 H8 F3 N O2 SP 1 21/c 19.4692; 9.0363; 10.229
90; 108.996; 90
827.59Liu, Lidong; Guo, Yawen; Shi, Lin; Wang, Yihan; Lei, Xingyu; Jiao, Peng
Building trisubstituted ethylenes from terminal alkenes <i>via</i> debrominative ring-opening trifluoromethylations of geminal dibromocyclopropanes.
Chemical communications (Cambridge, England), 2025, 61, 5170-5173
7134274 CIFC58 H42P -17.7801; 12.75; 21.284
74.037; 80.782; 86.993
2003.6Maurya, Neha; Jana, Palash; Sharma, Himanshu; Bandyopadhyay, Subhajit; Das, Soumyajit
5,5'-Biindeno[2,1-<i>c</i>]fluorene: importance of C5-C5' linkage for an indeno[2,1-<i>c</i>]fluorene dimer exhibiting an open-shell ground state.
Chemical communications (Cambridge, England), 2025, 61, 4808-4811
7134275 CIFC76 H96 Cl N7 O28 S6P 1 2 115.2633; 16.5145; 17.4282
90; 90.1; 90
4393Ma, Yifan; Song, Zihang; Guo, Sidan; Han, Han; Cai, Kang
A sulfone-functionalized molecular triangle as a strong anion receptor driven by anion-π interactions.
Chemical communications (Cambridge, England), 2025, 61, 4531-4534
7134276 CIFC62 H66 Cl2 N6 O25 S6P 1 21 114.5385; 20.395; 17.647
90; 103.576; 90
5086.4Ma, Yifan; Song, Zihang; Guo, Sidan; Han, Han; Cai, Kang
A sulfone-functionalized molecular triangle as a strong anion receptor driven by anion-π interactions.
Chemical communications (Cambridge, England), 2025, 61, 4531-4534
7134277 CIFC58 H34 N4 O4C 1 2/c 119.711; 13.865; 19.089
90; 106.378; 90
5005Upadhyay, Manoj; Ray, Debdas
Regulation of aggregation-enhanced thermally activated delayed fluorescence in butterfly-shaped donor-acceptor conjugates.
Chemical communications (Cambridge, England), 2025, 61, 5015-5018
7134278 CIFC70 H38 N4 O4 S2C 1 c 122.499; 11.6; 21.856
90; 100.493; 90
5609Upadhyay, Manoj; Ray, Debdas
Regulation of aggregation-enhanced thermally activated delayed fluorescence in butterfly-shaped donor-acceptor conjugates.
Chemical communications (Cambridge, England), 2025, 61, 5015-5018
7134279 CIFC38 H30 N2 O2 P2P 1 21/c 115.3; 17.905; 12.534
90; 112.995; 90
3161Xu, Dong-Ping; Huang, Fei; Jin, Li-Zhen; Huang, Meng-Ya; Zhang, Wu
DBU-promoted cascade phosphorylation/cyclization for the synthesis of phosphorylated 3-aminoindoles.
Chemical communications (Cambridge, England), 2025, 61, 4816-4819
7134280 CIFC27 H25 N2 O2 PP -18.3695; 10.144; 14.956
72.992; 78.674; 80.115
1181.7Xu, Dong-Ping; Huang, Fei; Jin, Li-Zhen; Huang, Meng-Ya; Zhang, Wu
DBU-promoted cascade phosphorylation/cyclization for the synthesis of phosphorylated 3-aminoindoles.
Chemical communications (Cambridge, England), 2025, 61, 4816-4819
7134281 CIFC77 H73 Cu F3 Fe N8 O8 P2 SP -111.242; 18.8746; 20.485
89.5; 76.095; 81.258
4168.53Huber, Matthias; Kumar, Ajeet; Hauer, Jürgen; Thyrhaug, Erling; Hess, Corinna R.
Photoredox capacity expanded by the Cu site of CuFe-Mabiq
Chemical Communications, 2025, 61, 5731-5734
7134282 CIFC327 H450 Cl6 Cu24 N27 O77.25 S24P -122.2855; 22.2953; 40.7937
75.732; 84.188; 89.715
19538.4Wilson, Lucinda R. B.; Nichol, Gary S.; Dalgarno, Scott J.; Brechin, Euan K.
A [CuII24] truncated octahedron and its [CuII8] building block.
Chemical communications (Cambridge, England), 2025, 61, 4722-4725
7134283 CIFC96 H126 Br5 Cu8 N5 O18 S8P b c a23.499; 25.0057; 43.0467
90; 90; 90
25294.6Wilson, Lucinda R. B.; Nichol, Gary S.; Dalgarno, Scott J.; Brechin, Euan K.
A [CuII24] truncated octahedron and its [CuII8] building block.
Chemical communications (Cambridge, England), 2025, 61, 4722-4725
7134284 CIFC23 H19 B Cl4 F2 N2P b c n14.694; 16.305; 9.87
90; 90; 90
2364.7Lv, Fan; Guo, Xing; Zhu, Shuangshuang; Huang, Sen; Li, Li; Wang, Shaozhen; Jiao, Lijuan; Hao, Erhong
A cascade strategy for vinyl chloride-substituted BODIPYs with tunable photophysical properties.
Chemical communications (Cambridge, England), 2025, 61, 4975-4978
7134285 CIFC26 H25 B Cl4 F2 N2P b c n16.744; 17.965; 9.147
90; 90; 90
2751.47Lv, Fan; Guo, Xing; Zhu, Shuangshuang; Huang, Sen; Li, Li; Wang, Shaozhen; Jiao, Lijuan; Hao, Erhong
A cascade strategy for vinyl chloride-substituted BODIPYs with tunable photophysical properties.
Chemical communications (Cambridge, England), 2025, 61, 4975-4978
7134286 CIFC12 H13 Mn N2 O4C 1 2/c 113.0025; 14.8905; 14.8729
90; 92.647; 90
2876.5Mondal, Avijit; Phukan, Hirak Jyoti; Mohar, Kailash; Pal, Debjyoti; Sharma, Rahul; Purkayastha, Siddhartha; Guha, Ankur Kanti; Srimani, Dipankar
Designing a NNO-manganese complex overcoming steric constraints in (de)hydrogenative coupling.
Chemical communications (Cambridge, England), 2025, 61, 4796-4799
7134287 CIFC11 H12 Br Mn N2 O4P 1 21/n 17.963; 21.994; 8.314
90; 98.6; 90
1439.7Mondal, Avijit; Phukan, Hirak Jyoti; Mohar, Kailash; Pal, Debjyoti; Sharma, Rahul; Purkayastha, Siddhartha; Guha, Ankur Kanti; Srimani, Dipankar
Designing a NNO-manganese complex overcoming steric constraints in (de)hydrogenative coupling.
Chemical communications (Cambridge, England), 2025, 61, 4796-4799
7134288 CIFC12 H14 Br Mn N2 O4P -17.3733; 8.8785; 12.8155
79.837; 75.722; 71.616
767.09Mondal, Avijit; Phukan, Hirak Jyoti; Mohar, Kailash; Pal, Debjyoti; Sharma, Rahul; Purkayastha, Siddhartha; Guha, Ankur Kanti; Srimani, Dipankar
Designing a NNO-manganese complex overcoming steric constraints in (de)hydrogenative coupling.
Chemical communications (Cambridge, England), 2025, 61, 4796-4799
7134289 CIFC144 H124 Mn4 N28 O16P -19.1397; 19.8181; 26.775
88.264; 88.73; 78.204
4744.6Li, Zhi-Wei; Huang, Anlian; Wang, Zhenguo; Gao, Rui; Lan, Bang; Chen, Guosheng; Ouyang, Gangfeng
Solvent-mediated subcomponent self-assembly of covalent metallacycles for hierarchical porous materials synthesis.
Chemical communications (Cambridge, England), 2025, 61, 4836-4839
7134290 CIFC47.5 H61 B0.5 Cl0.5 Ge O S0.5P -114.7736; 15.137; 20.2706
99.678; 103.18; 100.588
4232.79Kern, Ralf H.; Schmiedel, Paul L.; Schubert, Hartmut; Wesemann, Lars
Heterocycles in reactions with boradigermaallyl.
Chemical communications (Cambridge, England), 2025, 61, 4844-4847
7134291 CIFC97 H118 B Cl Ge2 N2 OP 1 21/n 114.5539; 14.7287; 44.0318
90; 96.793; 90
9372.4Kern, Ralf H.; Schmiedel, Paul L.; Schubert, Hartmut; Wesemann, Lars
Heterocycles in reactions with boradigermaallyl.
Chemical communications (Cambridge, England), 2025, 61, 4844-4847
7134292 CIFC211 H260 B2 Cl2 Ge4 N8 O2P 1 2/c 122.2383; 13.1321; 31.4611
90; 93.324; 90
9172.3Kern, Ralf H.; Schmiedel, Paul L.; Schubert, Hartmut; Wesemann, Lars
Heterocycles in reactions with boradigermaallyl.
Chemical communications (Cambridge, England), 2025, 61, 4844-4847
7134293 CIFC96 H126 B Cl Ge2 O2P -118.673; 21.1109; 23.361
106.864; 90.263; 106.295
8421.8Kern, Ralf H.; Schmiedel, Paul L.; Schubert, Hartmut; Wesemann, Lars
Heterocycles in reactions with boradigermaallyl.
Chemical communications (Cambridge, England), 2025, 61, 4844-4847
7134294 CIFC44 H55 N7 Si2P 1 21/n 19.369; 18.222; 24.667
90; 99.08; 90
4158.4Pandey, Madhusudan K.; Hendi, Zohreh; Wang, Xiaobai; Muhammed, Shahila; Kumar, Arun; Singh, Mukesh K.; Herbst-Irmer, Regine; Stalke, Dietmar; Parameswaran, Pattiyil; Roesky, Herbert W.
Synthesis and characterization of triazole-functionalized mixed-valent Si(i)–Si(iii) and bis(germylene) compounds
Chemical Communications, 2025, 61, 5581-5584
7134295 CIFC44 H55 Ge2 N7P -110.199; 13.117; 17.906
106.21; 90.75; 110.7
2135Pandey, Madhusudan K.; Hendi, Zohreh; Wang, Xiaobai; Muhammed, Shahila; Kumar, Arun; Singh, Mukesh K.; Herbst-Irmer, Regine; Stalke, Dietmar; Parameswaran, Pattiyil; Roesky, Herbert W.
Synthesis and characterization of triazole-functionalized mixed-valent Si(i)–Si(iii) and bis(germylene) compounds
Chemical Communications, 2025, 61, 5581-5584
7134296 CIFC344 H422 Au40 O0.5 P2 S24P -119.7765; 22.8122; 41.4682
77.52; 89.86; 76.37
17728.5Li, Jialing; Wang, Zhewei; Ye, Jiansheng; Li, Qinzhen; Yang, Sha; Chai, Jinsong; Zhu, Manzhou
Diphosphine-induced morphological modification in Au nanoclusters and its implications for catalytic activity regulation.
Chemical communications (Cambridge, England), 2025, 61, 5146-5149
7134297 CIFC28 H26 Br N OP 21 21 2115.4584; 15.9977; 18.8777
90; 90; 90
4668.43Zhao, Yuting; Ji, Xin; Xiao, Yuanjing; Wu, Xingxing; Liu, Lu
Copper-catalyzed chemoselective C-H functionalization/dearomatization sequence: direct access to indole-based spirocyclic scaffolds.
Chemical communications (Cambridge, England), 2025, 61, 5162-5165
7134298 CIFC21 H20 Br N O2P 1 21/n 18.9741; 18.6365; 11.5094
90; 103.833; 90
1869.07Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Verma, Akhilesh K.
Gold/silver-catalyzed synthesis of functionalized indoles from <i>N</i>-allyl-2-alkynylanilines and α-diazo compounds <i>via</i> 1,3-allyl migration.
Chemical communications (Cambridge, England), 2025, 61, 5313-5316
7134299 CIFC21 H19 Br F N O2P 1 21/n 19.0327; 19.2302; 11.7338
90; 103.989; 90
1977.7Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Verma, Akhilesh K.
Gold/silver-catalyzed synthesis of functionalized indoles from <i>N</i>-allyl-2-alkynylanilines and α-diazo compounds <i>via</i> 1,3-allyl migration.
Chemical communications (Cambridge, England), 2025, 61, 5313-5316
7134300 CIFC25 H23 N O2P 1 21/c 111.4169; 8.2709; 20.4762
90; 91.528; 90
1932.84Thakur, Deepika; Meena, Shivam A.; Sharma, Manvi; Verma, Akhilesh K.
Gold/silver-catalyzed synthesis of functionalized indoles from <i>N</i>-allyl-2-alkynylanilines and α-diazo compounds <i>via</i> 1,3-allyl migration.
Chemical communications (Cambridge, England), 2025, 61, 5313-5316
7134301 CIFC46 H36 O4P 21 21 219.6229; 15.1406; 22.4142
90; 90; 90
3265.67Yano, Riko; Ito, Suguru
Multi-color luminescent crystals derived from dynamic diastereomers of a perylene-substituted binaphthol derivative.
Chemical communications (Cambridge, England), 2025, 61, 5305-5308
7134302 CIFC42 H28 O2P 17.8625; 10.7582; 18.321
76.6; 89.561; 72.009
1430.38Yano, Riko; Ito, Suguru
Multi-color luminescent crystals derived from dynamic diastereomers of a perylene-substituted binaphthol derivative.
Chemical communications (Cambridge, England), 2025, 61, 5305-5308
7134303 CIFC91 H64 O4P 1 21 17.6602; 25.9534; 15.6096
90; 95.261; 90
3090.24Yano, Riko; Ito, Suguru
Multi-color luminescent crystals derived from dynamic diastereomers of a perylene-substituted binaphthol derivative.
Chemical communications (Cambridge, England), 2025, 61, 5305-5308
7134304 CIFC11 H8 Br F2 N OC 1 2/c 123.396; 6.177; 16.234
90; 111.845; 90
2177.6Cao, Tian-Zheng; Nie, Cai-Jian; Li, Jing; Liu, Ming-Dong; Wang, Zi-Tong; Kong, Yi-Fei; Wang, Xin; Sun, Yuan-Yuan; Li, Jin-Heng; Zhu, Yan-Ping
Photocatalytically switchable chemoselective difluoramidation of olefins for the synthesis of diversified difluoro-γ-lactams.
Chemical communications (Cambridge, England), 2025, 61, 5150-5153
7134305 CIFC16 H16 O4 SP 1 21 15.7878; 33.2044; 30.9443
90; 89.996; 90
5946.89Wei, Jun; Yi, Zhi-Yuan; Jin, Zhuan; Liu, Yi; Wang, Zuo-Fei; Dong, Xiu-Qin; Wang, Chun-Jiang
Synthesis of chiral β-hydroxy allylic sulfides via iridium-catalyzed asymmetric cascade allylation/acyl transfer rearrangement
Chemical Communications, 2025, 61, 5609-5612
7134306 CIFC24 H13 F3 OP c a 2114.865; 12.8982; 9.3217
90; 90; 90
1787.3Zhang, Xu; Ni, Tongtong; Chang, Mengfan; Li, Wenguang; Xu, Xuefeng
Palladium-catalyzed oxidative cycloaddition of 1-indanones and internal aryl alkynes toward benzo[<i>c</i>]fluorenone derivatives.
Chemical communications (Cambridge, England), 2025, 61, 5186-5189
7134307 CIFC26 H37 Br N2 Ru SiP 1 21/c 113.9782; 12.5557; 16.6745
90; 110.614; 90
2739.1Ramachandran, Arya; Bauri, Somnath; Rit, Arnab
Alkene-promoted NHC ligand substitution in orthometalated Ru-NHC complexes <i>via</i> σ-bond metathesis: a mechanistic insight.
Chemical communications (Cambridge, England), 2025, 61, 5011-5014
7134308 CIFC15 H15 N O2 SP n a 2118.433; 14.974; 4.8692
90; 90; 90
1344Nan, Jiang; Yang, Shuai; Huang, Guanjie; Fan, Liangxin
Radical-mediated chemo-divergent recyclization of 1,2,3,4-benzothiatriazine-1,1-dioxides: alkyl migration and dearomatization.
Chemical communications (Cambridge, England), 2025, 61, 5503-5506
7134309 CIFC13 H11 N O3 SP n m a15.049; 6.8887; 11.412
90; 90; 90
1183.1Nan, Jiang; Yang, Shuai; Huang, Guanjie; Fan, Liangxin
Radical-mediated chemo-divergent recyclization of 1,2,3,4-benzothiatriazine-1,1-dioxides: alkyl migration and dearomatization.
Chemical communications (Cambridge, England), 2025, 61, 5503-5506
7134310 CIFC66 H78 N4 O4 S4P -19.3937; 12.665; 14.285
107.715; 102.575; 96.844
1548.3Nan, Jiang; Yang, Shuai; Huang, Guanjie; Fan, Liangxin
Radical-mediated chemo-divergent recyclization of 1,2,3,4-benzothiatriazine-1,1-dioxides: alkyl migration and dearomatization.
Chemical communications (Cambridge, England), 2025, 61, 5503-5506
7134311 CIFC48 H16 Br8P -117.889; 18.24; 20.214
90.963; 115.553; 101.147
5800.8Misselwitz, Erik; Spengler, Jonas; Rominger, Frank; Kivala, Milan
Octacyano-substituted tridecacyclene: a non-benzenoid cyanocarbon with low-lying LUMO and multistage redox properties
Chemical Communications, 2025, 61, 5754-5757
7134312 CIFC62 H42 Cl2 F10P -110.584; 13.468; 19.022
76.198; 85.461; 77.856
2573.1Jiang, Zhongyao; Liu, Chenglin; Wu, Mingxia; Xu, Erhao; Wu, Xin-Xing
Palladium-catalyzed intermolecular formal [3+2] cyclization/C-H alkylation of polyfluoroarenes.
Chemical communications (Cambridge, England), 2025, 61, 5365-5368
7134313 CIFC27 H24 N P SeI 1 a 19.8139; 17.3013; 26.7081
90; 98.701; 90
4482.7Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134314 CIFC29 H28 N O P SeP 1 21/n 110.9052; 17.7869; 12.694
90; 98.305; 90
2436.43Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134315 CIFC31 H20 F12 N P SeP 21 21 216.8359; 12.3127; 35.205
90; 90; 90
2963.1Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134316 CIFC27 H24 N O P SeP b c a17.428; 9.6355; 26.6337
90; 90; 90
4472.5Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134317 CIFC27 H24 N P Se2C 1 2/c 116.0502; 10.1153; 29.8261
90; 103.173; 90
4714.9Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134318 CIFC33 H27 Cl2 N2 P SeP 1 21/n 116.6851; 9.8964; 18.0914
90; 105.983; 90
2871.82Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134319 CIFC27 H24 Au Cl N P SeP b c a17.2293; 14.1326; 19.9231
90; 90; 90
4851.2Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134320 CIFC41 H39 Cl2 N2 O3 P Pd S SeP 1 21/n 112.1825; 15.409; 21.4921
90; 105.099; 90
3895.2Masuda, Ryosuke; Yano, Tamaki; Kusama, Hiroyuki
Selenoamides with two reactive sites: synthesis, structures, and dual reactivity of (selenocarbamoyl)phosphines.
Chemical communications (Cambridge, England), 2025, 61, 4955-4958
7134321 CIFC40 H36.5 N6 O10.25R -3 :H30.6005; 30.6005; 19.9577
90; 90; 120
16184.5Li, Bing-Sha; Cao, Li-Hui; Chen, Xu-Yong; Tian, Yu
Encryption application of a fast stimulus-responsive hydrogen-bonded organic framework based on FRET.
Chemical communications (Cambridge, England), 2025, 61, 5345-5348
7134322 CIFC24 H12 Br4P 1 c 17.9052; 12.3181; 22.0431
90; 90.006; 90
2146.49Sujilkumar, Suvarna; Kalyani, Agaja; Hariharan, Mahesh
Room-temperature phosphorescence in crystalline bifurcating halogen⋯halogen synthon containing chromophore.
Chemical communications (Cambridge, England), 2025, 61, 5463-5466
7134323 CIFC28 H24 F6 Si2P 1 21/c 18.6747; 15.1646; 10.2043
90; 103.579; 90
1304.84Feng, Jianbin; Samedov, Kerim; Lu, Yanfei; Chen, Dongcheng; Cai, Yuanjing
1,5-Disila-<i>s</i>-indacene-based emitters: a molecular design towards efficient blue OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 5491-5494
7134324 CIFC42 H30 F12 Si2P -16.2534; 11.9611; 12.8145
94.062; 91.359; 103.177
930.13Feng, Jianbin; Samedov, Kerim; Lu, Yanfei; Chen, Dongcheng; Cai, Yuanjing
1,5-Disila-<i>s</i>-indacene-based emitters: a molecular design towards efficient blue OLEDs.
Chemical communications (Cambridge, England), 2025, 61, 5491-5494
7134325 CIFC28 H16 F2 N4 O2P 1 21/c 18.9992; 11.0091; 29.001
90; 91.719; 90
2871.9Zhang, Chuan-Bao; Xu, Jiying; Wang, Xiao-Qing; Deng, Yi-Hang; Dou, Pei-Hao; Xu, Wen-Li; Han, Qiu-Xia; Zhao, Lili; Fu, Ji-Ya
Synthesis of highly substituted 2-hydroxybenzophenones through skeletal clipping of 3-benzofuranones
Chemical Communications, 2025, 61, 5645-5648
7134326 CIFC28 H22 N2 O3P c a 2116.1597; 10.6689; 13.0214
90; 90; 90
2245Zhang, Chuan-Bao; Xu, Jiying; Wang, Xiao-Qing; Deng, Yi-Hang; Dou, Pei-Hao; Xu, Wen-Li; Han, Qiu-Xia; Zhao, Lili; Fu, Ji-Ya
Synthesis of highly substituted 2-hydroxybenzophenones through skeletal clipping of 3-benzofuranones
Chemical Communications, 2025, 61, 5645-5648
7134327 CIFC120 H117.84 Br0.16 N10P -18.9922; 10.9314; 28.0249
81.537; 84.208; 88.326
2710.58Su, Jie; Wei, Jian; Ye, Kaishun; Li, Feiyang; Wang, Mengzhu; Li, Qiuxia; Yuan, Aihua; Zhao, Qiang; Shi, Chao
Tuning charge transfer properties in symmetric and asymmetric pyrrolo[3,2-<i>b</i>]pyrrole derivatives with hybridized local and charge-transfer characteristics.
Chemical communications (Cambridge, England), 2025, 61, 5475-5478
7134328 CIFC17 H11 Cl N2 OP 1 21/c 120.4063; 4.2344; 15.0153
90; 91.449; 90
1297.03Jangir, Tarun; Nipate, Dhananjay S.; Rangan, Krishnan; Kumar, Anil
Ru(ii)-catalyzed oxidative (4+3) C–H/C–H annulation of 2-aryl-4H-pyrido[1,2-a]pyrimidin-4-ones with allyl alcohol
Chemical Communications, 2025, 61, 5762-5765
7134329 CIFC23 H14 F6 Se2P b c a13.7002; 21.455; 27.9931
90; 90; 90
8228.2Watanabe, Yoshiyuki; Kim, Sunnam; Kosumi, Daisuke; Kitagawa, Daichi; Kobatake, Seiya; Fukaminato, Tsuyoshi
Synthesis and photochromism of a turn-on fluorescent diarylethene having benzo[b]selenophene groups as the aryl units
Chemical Communications, 2025, 61, 6304-6307
7134330 CIFC23 H20 Se2P 21 21 219.0615; 11.8873; 17.2354
90; 90; 90
1856.54Watanabe, Yoshiyuki; Kim, Sunnam; Kosumi, Daisuke; Kitagawa, Daichi; Kobatake, Seiya; Fukaminato, Tsuyoshi
Synthesis and photochromism of a turn-on fluorescent diarylethene having benzo[b]selenophene groups as the aryl units
Chemical Communications, 2025, 61, 6304-6307
7134331 CIFC19 H12 F3 N O2P 1 21 17.4749; 9.2492; 11.6066
90; 94.679; 90
799.77Pandidurai, Solai; Chinababu, Maddala; Sekar, Govindasamy
Domino 1,3-dipolar cycloaddition/ring-opening/ring-cleavage: synthesis of trisubstituted pyrrole and chiral dihydropyrrole-3-carbaldehydes
Chemical Communications, 2025, 61, 5806-5809
7134332 CIFC21 H21 N5 O7 Se ZnP -110.0822; 10.1131; 11.3662
95.063; 92.398; 98.918
1138.63Aliyeva, Vusala A.; André, Vânia; Martins, Luísa M. D. R. S.; Gurbanov, Atash V.; Gomila, Rosa M.; Frontera, Antonio; Cruz, Tiago F. C.; Mahmudov, Kamran T.
Chalcogen bonded metal–organic frameworks: insights from X-ray analysis and theoretical calculations
Chemical Communications, 2025, 61, 5962-5965
7134333 CIFC46 H50 Cd2 N10 O14 Se2P -111.593; 15.1366; 16.7568
67.251; 89.644; 68.013
2481.26Aliyeva, Vusala A.; André, Vânia; Martins, Luísa M. D. R. S.; Gurbanov, Atash V.; Gomila, Rosa M.; Frontera, Antonio; Cruz, Tiago F. C.; Mahmudov, Kamran T.
Chalcogen bonded metal–organic frameworks: insights from X-ray analysis and theoretical calculations
Chemical Communications, 2025, 61, 5962-5965
7134334 CIFC16 H18 O3 SP 1 21/c 123.9875; 6.6512; 9.5172
90; 99.885; 90
1495.9Biswas, Ashish; Pradhan, Priyanka; Wakpanjar, Sumit Ashok; Kancharla, Pavan K.
Direct organocatalytic esterification of carboxylic acids and alcohols by redox neutral sulfur(iv) catalysis via intramolecularly interrupted Pummerrer intermediates
Chemical Communications, 2025, 61, 5746-5749
7134335 CIFC70 H9 N O2 S2P 1 21/c 112.8911; 14.7; 20.0129
90; 105.966; 90
3646.14Zhang, Qian-Wen; Liu, Yuanyuan; Yin, Zheng-Chun; Qiu, Wen-Jie; Huang, Xinmin; Li, Jian-Feng; Wang, Guan-Wu
Synthesis of [60]fullerene-fused dihydroindolizines via copper-catalyzed dearomative N-heteroannulation
Chemical Communications, 2025, 61, 5653-5656
7134336 CIFC32 H25 Fe O P TeP 1 21/n 17.6985; 19.2903; 17.9591
90; 92.031; 90
2665.37Burt, Liam K.; Kirk, Ryan M.; Hill, Anthony F.
Alkynyltellurolato ligands including a solvatochromic rhenium(i) complex
Chemical Communications, 2025, 61, 6150-6153
7134337 CIFC18 H17 N2 O3 Re Si TeP 17.096; 7.1524; 11.2227
80.861; 73.077; 72.852
519.04Burt, Liam K.; Kirk, Ryan M.; Hill, Anthony F.
Alkynyltellurolato ligands including a solvatochromic rhenium(i) complex
Chemical Communications, 2025, 61, 6150-6153
7134338 CIFC64 H58 Cl6 N10 P2 Ru2P -114.3295; 15.7024; 20.0157
105.317; 97.2517; 107.059
4050Cui, Tianhua; Gong, Huihua; Ji, Li; Kong, Yuxuan; Yang, Siheng; Xue, Weichao; Zheng, Xueli; Fu, Haiyan; Cheng, Chong; Li, Shuang; Chen, Hua; Li, Ruixiang; Xu, Jiaqi
CO2-mediated hydrogen storage and release cycles realized by a bimetallic ruthenium complex in pure water
Chemical Communications, 2025, 61, 5946-5949
7134339 CIFC35 H36 Cl2 N5 P RuP 21 21 2110.7554; 16.9347; 18.5184
90; 90; 90
3372.9Cui, Tianhua; Gong, Huihua; Ji, Li; Kong, Yuxuan; Yang, Siheng; Xue, Weichao; Zheng, Xueli; Fu, Haiyan; Cheng, Chong; Li, Shuang; Chen, Hua; Li, Ruixiang; Xu, Jiaqi
CO2-mediated hydrogen storage and release cycles realized by a bimetallic ruthenium complex in pure water
Chemical Communications, 2025, 61, 5946-5949
7134340 CIFC25 H18 O2 SP -19.4203; 10.4873; 11.2604
111.406; 97.093; 111.432
920.79Hemamalini, Vijayakumar; Senthil, Maheswaran; Shankar, Bhaskaran; Ramesh, Subburethinam
Serendipitous pathway to naphtho[2,1-b]furan and its thioether enabled by triflic acid and thiol-mediated reaction
Chemical Communications, 2025, 61, 6356-6359
7134341 CIFC19 H14 OP 1 21/c 126.0468; 6.2973; 8.0249
90; 93.462; 90
1313.88Hemamalini, Vijayakumar; Senthil, Maheswaran; Shankar, Bhaskaran; Ramesh, Subburethinam
Serendipitous pathway to naphtho[2,1-b]furan and its thioether enabled by triflic acid and thiol-mediated reaction
Chemical Communications, 2025, 61, 6356-6359
7134342 CIFC15 H12 Br N SP 1 21/c 17.968; 5.187; 33.21
90; 94.005; 90
1369.2Sun, Guangping; Li, Menghang; Li, Jiaji; Feng, Jin; Yan, Zhenhao; Sun, Yiwen; Pu, Liangtao; Zhu, Jinli; Tang, Yanfeng; Yao, Yong
Enhanced emission in a supramolecular artificial light-harvesting system for a photocatalytic thiol–ene reaction
Chemical Communications, 2025, 61, 6360-6363
7134343 CIFC43 H39 Co N2 O10P 1 21/c 117.7931; 14.996; 16.0649
90; 113.13; 90
3941.95Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Wang, Yutong; Fan, Weidong; Sun, Daofeng
Solvent-etching-induced in situ crystal structure transformation in hydrogen-bonded organic frameworks
Chemical Communications, 2025, 61, 6166-6169
7134344 CIFC43 H39 Co N2 O10P -111.4687; 13.007; 14.1101
74.105; 88.003; 71.393
1915.37Wang, Xiaokang; Liu, Hongyan; Sun, Meng; Gao, Fei; Feng, Xueying; Xu, Mingming; Wang, Yutong; Fan, Weidong; Sun, Daofeng
Solvent-etching-induced in situ crystal structure transformation in hydrogen-bonded organic frameworks
Chemical Communications, 2025, 61, 6166-6169
7134345 CIFC16 H12 N2 O3P 1 21/c 110.7772; 12.8183; 8.8804
90; 92.39; 90
1225.72Sk, Asikul; Banerji, Biswadip
Access to pyrido-pyrimidinone and imidazopyridine via Fe(iii)-mediated denitrogenative annulation of tetrazolopyridine with β-keto ester
Chemical Communications, 2025, 61, 6312-6315
7134346 CIFC14 H10 N2 O2P 1 2/c 117.4261; 6.7139; 19.0884
90; 103.337; 90
2173.06Sk, Asikul; Banerji, Biswadip
Access to pyrido-pyrimidinone and imidazopyridine via Fe(iii)-mediated denitrogenative annulation of tetrazolopyridine with β-keto ester
Chemical Communications, 2025, 61, 6312-6315
7134347 CIFC42 H46 Br3 Cu O P2C 1 c 110.1684; 23.201; 17.4735
90; 105.108; 90
3979.8Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134348 CIFC21 H22 Cu I2 PP 1 21/n 111.6293; 12.4221; 15.4045
90; 94.582; 90
2218.23Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134349 CIFC21 H22 Cu I2 PP 1 21/n 111.6304; 12.4197; 15.4062
90; 94.555; 90
2218.34Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134350 CIFC21 H22 Cu I2 PP 1 21/n 111.6568; 12.3997; 15.3791
90; 94.502; 90
2216Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134351 CIFC21 H22 Cu I2 PP 1 21/n 111.6416; 12.4211; 15.4172
90; 94.557; 90
2222.3Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134352 CIFC42 H45.25 Cu I3 O0.62 P2C 1 c 110.1359; 23.6427; 17.8625
90; 102.533; 90
4178.57Yang, Lin; Li, Yani; Liu, Xia; Li, Bohan; Xu, Yan
Halogen and solvent effects induced structural transformation and isostructural luminescence regulation in copper-based hybrid halides
Chemical Communications, 2025, 61, 6619-6622
7134353 CIFC82 H161 N13 Nb2 O72 P8 S2 V14P 1 21/n 118.4212; 25.9376; 29.3062
90; 92.117; 90
13993Fang, Renbo; Zhang, Di; Dong, Jing; Feng, Yeqin; Liu, Chengpeng; Yao, Liaoyuan; Chi, Yingnan; Hu, Changwen
An open hollow polyoxovanadate cage based on {Nb(V5)} pentagons with size-selective encapsulation properties
Chemical Communications, 2025, 61, 6182-6185
7134354 CIFC72 H135 Cs4 N11 Nb2 O72 P8 S4 V14P n m a26.0643; 31.9841; 16.5506
90; 90; 90
13797.3Fang, Renbo; Zhang, Di; Dong, Jing; Feng, Yeqin; Liu, Chengpeng; Yao, Liaoyuan; Chi, Yingnan; Hu, Changwen
An open hollow polyoxovanadate cage based on {Nb(V5)} pentagons with size-selective encapsulation properties
Chemical Communications, 2025, 61, 6182-6185
7134355 CIFC80 H142 N12 Nb2 O69 P8 S2 V14P 1 21/n 118.1749; 25.9752; 29.0297
90; 90.119; 90
13704.8Fang, Renbo; Zhang, Di; Dong, Jing; Feng, Yeqin; Liu, Chengpeng; Yao, Liaoyuan; Chi, Yingnan; Hu, Changwen
An open hollow polyoxovanadate cage based on {Nb(V5)} pentagons with size-selective encapsulation properties
Chemical Communications, 2025, 61, 6182-6185
7134356 CIFC80 H152 N11 Nb2 O70 P8 S2 V14P 1 21/n 118.0624; 25.9485; 29.2392
90; 90.278; 90
13704Fang, Renbo; Zhang, Di; Dong, Jing; Feng, Yeqin; Liu, Chengpeng; Yao, Liaoyuan; Chi, Yingnan; Hu, Changwen
An open hollow polyoxovanadate cage based on {Nb(V5)} pentagons with size-selective encapsulation properties
Chemical Communications, 2025, 61, 6182-6185
7134357 CIFC17 H24 Cl3 N2 O2P 1 21/c 112.68805; 14.41773; 10.39362
90; 102.513; 90
1856.17Sowiński, Mateusz P.; Mocanu, Elena M.; Ruskin-Dodd, Hannah; McKay, Aidan P.; Cordes, David B.; Lovett, Janet E.; Haugland-Grange, Marius
Sigmatropic rearrangement enables access to a highly stable spirocyclic nitroxide for protein spin labelling
Chemical Communications, 2025, 61, 6755-6758
7134358 CIFC39 H46 Cl2 F6 Ge O8 P2 S2P -111.237; 13.727; 15.396
86.231; 72.039; 80.057
2225Kumari, Akanksha; Peddi, Balakrishna; Yildiz, Cem. B.; Majumdar, Moumita
An intramolecular phosphine-oxide stabilized germanium(iv) di-cation with enhanced Lewis acidity and catalytic applications
Chemical Communications, 2025, 61, 6506-6509
7134359 CIFC37 H45 F3 Ge O5 P2 SP -110.664; 11.806; 14.963
94.403; 96.594; 98.318
1843.3Kumari, Akanksha; Peddi, Balakrishna; Yildiz, Cem. B.; Majumdar, Moumita
An intramolecular phosphine-oxide stabilized germanium(iv) di-cation with enhanced Lewis acidity and catalytic applications
Chemical Communications, 2025, 61, 6506-6509
7134360 CIFC89 H114 Cl6 F24 Ge2 N4 O4 P4 Sb4C 1 2/c 142.865; 16.681; 14.76
90; 95.368; 90
10508Kumari, Akanksha; Peddi, Balakrishna; Yildiz, Cem. B.; Majumdar, Moumita
An intramolecular phosphine-oxide stabilized germanium(iv) di-cation with enhanced Lewis acidity and catalytic applications
Chemical Communications, 2025, 61, 6506-6509
7134361 CIFC45 H60 F4 Ge O7 P2 SP -112.3052; 12.8654; 15.2505
73.204; 72.985; 81.658
2205.3Kumari, Akanksha; Peddi, Balakrishna; Yildiz, Cem. B.; Majumdar, Moumita
An intramolecular phosphine-oxide stabilized germanium(iv) di-cation with enhanced Lewis acidity and catalytic applications
Chemical Communications, 2025, 61, 6506-6509
7134362 CIFC24 H31 Br3 N6 O2P -17.1766; 11.8425; 16.5364
84.628; 87.323; 81.602
1383.46Raza, Asif; Nikkhah, Sousa Javan; Croitor, Lilia; Attallah, Ahmed Gamal; Hirschmann, Eric; Vandichel, Matthias; Mukherjee, Soumya
An ionic ultramicroporous polymer with engineered nanopores enables enhanced acetylene/carbon dioxide separation
Chemical Communications, 2025, 61, 6466-6469
7134363 CIFC16 H24 N12 O8 S2P 1 21/n 112.3149; 7.8964; 12.79
90; 112.156; 90
1151.9Chen, Xu-Yong; Fei, Guiqiang; Bai, Xiang-Tian; Qi, Simeng; Cao, Xiao-Jie; Gao, Yi-Da; Luo, Xin; Cao, Li-Hui
Anthraquinone substituents modulate ionic hydrogen-bonded organic frameworks to achieve high ionic conductivity for alkali metal ions
Chemical Communications, 2025, 61, 6538-6541
7134364 CIFC16 H24 N12 O8 S2P b c a6.8832; 14.6525; 23.2897
90; 90; 90
2348.91Chen, Xu-Yong; Fei, Guiqiang; Bai, Xiang-Tian; Qi, Simeng; Cao, Xiao-Jie; Gao, Yi-Da; Luo, Xin; Cao, Li-Hui
Anthraquinone substituents modulate ionic hydrogen-bonded organic frameworks to achieve high ionic conductivity for alkali metal ions
Chemical Communications, 2025, 61, 6538-6541
7134365 CIFC30 H34 N2 O2P 1 21/n 111.5525; 7.9187; 28.056
90; 96.854; 90
2548.2Senapati, Siddhartha Kumar; Das, Animesh
Reductive alkylation of azoarenes to N-alkylated hydrazines enabled by hexafluoroisopropanol
Chemical Communications, 2025, 61, 8596-8599
7134366 CIFC28 H30 N2 O8P 1 21 110.0574; 30.2497; 9.2025
90; 106.742; 90
2681Qian, Xue-Wei; Lin, Hong; Hu, Tianjiao; Yang, Xiaodi; Sun, Xing-Wen
Synthesis of enantioenriched spirocyclic oxindoles catalyzed by bifunctional thiourea
Chemical Communications, 2025, 61, 6348-6351
7134367 CIFC31 H26 N2 O6P 1 21/n 16.0191; 21.3231; 20.4562
90; 90.459; 90
2625.38Wang, Jiali; Luan, Runze; Liu, Tianming; Liu, Siqing; Du, Yu; Su, Weiping
Native group-directed double Heck arylation of internal alkenes via selective β-H elimination
Chemical Communications, 2025, 61, 6526-6529
7134368 CIFC44 H70 N2 P2P -19.5127; 11.3592; 11.7695
113.315; 102.042; 107.947
1028.5Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Ungur, Liviu; Schwarz, Björn; Roy, Sudipta
Isolation and oxygen activation of electron-rich CoII4O metallic clusters having a 3-fold symmetry
Chemical Communications, 2025, 61, 6897-6900
7134369 CIFC54 H86 Cl2 Co2 N2 O6 P2P -19.2221; 11.5488; 14.3412
110.948; 96.154; 94.802
1405.9Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Ungur, Liviu; Schwarz, Björn; Roy, Sudipta
Isolation and oxygen activation of electron-rich CoII4O metallic clusters having a 3-fold symmetry
Chemical Communications, 2025, 61, 6897-6900
7134370 CIFC44 H70 Cl2 Co2 N2 O4 P2P 1 21/n 110.1686; 12.4842; 18.9809
90; 96.897; 90
2392.13Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Ungur, Liviu; Schwarz, Björn; Roy, Sudipta
Isolation and oxygen activation of electron-rich CoII4O metallic clusters having a 3-fold symmetry
Chemical Communications, 2025, 61, 6897-6900
7134371 CIFC46 H70 N2 P2P 1 21/n 112.005; 10.958; 16.343
90; 91.104; 90
2149.5Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Ungur, Liviu; Schwarz, Björn; Roy, Sudipta
Isolation and oxygen activation of electron-rich CoII4O metallic clusters having a 3-fold symmetry
Chemical Communications, 2025, 61, 6897-6900
7134372 CIFC66 H105 Cl3 Co4 N3 O P3R 3 c :H23.4395; 23.4395; 21.026
90; 90; 120
10004.2Francis, Maria; Patra, Asutosh; Salam, Farsana Abdul; Ungur, Liviu; Schwarz, Björn; Roy, Sudipta
Isolation and oxygen activation of electron-rich CoII4O metallic clusters having a 3-fold symmetry
Chemical Communications, 2025, 61, 6897-6900
7134373 CIFC264 H192 Au3 Cl27 N48 Pd12C m c 2130.46; 23.068; 28.45
90; 90; 90
19990Cao, Feng-Lin; Zhang, Ze-Sheng; Dong, Meng-Lin; Ning, Ye; Zhang, Wen-Hua; Mao, Yiming; Young, David J.
A high-entropy coordination cage featuring an Au-porphyrin metalloligand for the photodynamic therapy of liver cancer
Chemical Communications, 2025, 61, 6663-6666
7134374 CIFC29 H27 B F3 N O3P 1 21/n 113.9881; 13.1835; 14.3886
90; 104.046; 90
2574.1Zhang, Tingting; Gui, Jinhai; Mo, Yu; Pu, Yuchuan; Zhao, Hongping; Liu, Yong; He, Chengyu
Cu-catalyzed borylative cyclization of N-(o-alkynylaryl)imines
Chemical Communications, 2025, 61, 6799-6802
7134375 CIFC55 H38 Cl2 N4 O2 S2P 1 21/n 18.8159; 14.0135; 18.159
90; 99.121; 90
2215Belmonte-Vázquez, José L; Cortes-Muñoz, Juan L; Romo-Pérez, Adriana; Rodríguez-Molina, Braulio; Jiménez-Sánchez, Arturo
ESIPT-driven imaging: a thiazole probe for lipid droplets and plasma membranes.
Chemical communications (Cambridge, England), 2025, 61, 5023-5026
7134376 CIFC176 H180 Ag5 Cu5 F24 P6 S12P 114.1667; 15.8384; 18.0867
90.711; 97.321; 110.931
3752.2Nong, Yan; Dai, Juefei; Yang, Chao; Su, Haifeng; Feng, Chengcheng; Shi, Chuanhua; Zhang, Zhixun; Yu, Xianyong; Zhang, Xueji; Yang, Huayan
Highly stable bidentate thiol-protected Ag5Cu4 nanoclusters: a stable catalyst for enhanced Knoevenagel condensation
Chemical Communications, 2025, 61, 6933-6936
7134377 CIFC176 H180 Ag5 Cu5 F24 P6 S12P 114.1112; 15.576; 21.554
96.62; 104.668; 111.928
4133.7Nong, Yan; Dai, Juefei; Yang, Chao; Su, Haifeng; Feng, Chengcheng; Shi, Chuanhua; Zhang, Zhixun; Yu, Xianyong; Zhang, Xueji; Yang, Huayan
Highly stable bidentate thiol-protected Ag5Cu4 nanoclusters: a stable catalyst for enhanced Knoevenagel condensation
Chemical Communications, 2025, 61, 6933-6936
7134378 CIFC90 H592 Mo154 N10 Na6 O712C 1 2 136.4929; 42.8827; 31.3674
90; 108.525; 90
46543.8Guo, Haiyang; He, Donglin; Long, De-Liang; Cronin, Leroy
Robotic exploration of amino-acid functionalised molybdenum blue polyoxometalate nanoclusters
Chemical Communications, 2025, 61, 7121-7124
7134379 CIFC81 H687 Mo154 N9 Na4 O762P 21 21 246.7285; 44.1396; 47.1586
90; 90; 90
97268.3Guo, Haiyang; He, Donglin; Long, De-Liang; Cronin, Leroy
Robotic exploration of amino-acid functionalised molybdenum blue polyoxometalate nanoclusters
Chemical Communications, 2025, 61, 7121-7124
7134380 CIFC126 H1332 Mo308 N14 Na12 O1519P -130.4172; 34.0113; 46.8336
93.901; 94.711; 95.166
47951.8Guo, Haiyang; He, Donglin; Long, De-Liang; Cronin, Leroy
Robotic exploration of amino-acid functionalised molybdenum blue polyoxometalate nanoclusters
Chemical Communications, 2025, 61, 7121-7124
7134381 CIFC54 H595 Mo154 N6 Na11 O730A e a 230.3874; 56.1686; 50.1012
90; 90; 90
85513.6Guo, Haiyang; He, Donglin; Long, De-Liang; Cronin, Leroy
Robotic exploration of amino-acid functionalised molybdenum blue polyoxometalate nanoclusters
Chemical Communications, 2025, 61, 7121-7124
7134382 CIFC23 H18 SiP 1 21/n 16.1767; 12.3479; 23.1083
90; 96.222; 90
1752.07Mu, Delong; Zhu, Xinrui; Chen, Jiean
Facile synthesis of 1-silaacenaphthenes by transition metal-catalyzed intramolecular C(sp3)–H silylation
Chemical Communications, 2025, 61, 7073-7076
7134383 CIFC27 H26 N O3 PP 1 21/c 110.0643; 8.1662; 28.399
90; 99.579; 90
2301.5Ghosh, Palash; Das, Pralay; Mainkar, Prathama S.; Madhavachary, Rudrakshula; Chandrasekhar, Srivari
Harnessing phosphorus-centered radicals for the synthesis of cyclopenta[b]indole and pyrrolo[1,2-a]indole frameworks
Chemical Communications, 2025, 61, 7807-7810
7134384 CIFC2 H7 N5 O2F d d 210.8075; 27.3498; 7.4467
90; 90; 90
2201.1Yadav, Abhishek Kumar; Ghule, Vikas D.; Dharavath, Srinivas
Revisiting the sensitive nature of H-FOX: interplay of nitro and hydrazine functionalities to construct an insensitive energetic material
Chemical Communications, 2025, 61, 6901-6904
7134385 CIFC36 H38 Cl2 N O5 PP 1 21 112.6352; 6.4448; 20.921
90; 106.627; 90
1632.4Mondal, Anirban; Dašková, Vanda; Chen, Xiaobing; Thiel, Niklas O.; Alachouzos, Georgios; Feringa, Ben L.
Diastereoselective C(sp3)–H acetoxylation of phosphoramidites
Chemical Communications, 2025, 61, 6510-6513
7134386 CIFC16 H18 O2P 21 21 216.3279; 8.1376; 25.4842
90; 90; 90
1312.28Pomikło, Dominika; Romaniuk, Krzysztof; Sieroń, Lesław; Albrecht, Anna
Electroorganocatalytic asymmetric Diels–Alder cycloaddition of hydroquinones with α,β-unsaturated aldehydes
Chemical Communications, 2025, 61, 6655-6658
7134387 CIFC24 H26 N2 OP 21 21 217.1976; 23.2687; 24.5001
90; 90; 90
4103.2Wu, Shuaijie; Xu, Shiji; He, Yanru; Sun, Jing; Jiang, Wei; Yan, Chao-Guo; Hu, Weiming; Wang, Lei
Palladium-catalysed alleneamination of γ,δ-unsaturated hydrazones with propargylic acetates: access to tetrahydropyridazines bearing allenes
Chemical Communications, 2025, 61, 6647-6650
7134388 CIFC7 H5 As Mo O2 P2P b c a10.8696; 7.5409; 24.336
90; 90; 90
1994.74Zimmermann, Lisa; Land, Michael A.; Riesinger, Christoph; Macdonald, Charles L. B.; Scheer, Manfred
Synthesis of heteropnictogen ligands via PI transfer
Chemical Communications, 2025, 61, 6973-6976
7134389 CIFC7 H5 Mo O2 P2.42 Sb0.58P 1 21/n 16.1295; 11.3835; 14.6754
90; 96.459; 90
1017.48Zimmermann, Lisa; Land, Michael A.; Riesinger, Christoph; Macdonald, Charles L. B.; Scheer, Manfred
Synthesis of heteropnictogen ligands via PI transfer
Chemical Communications, 2025, 61, 6973-6976
7134390 CIFC67 H37 As2 B F24 Mo5 O10 P2P 1 21/c 118.8305; 20.6156; 20.0687
90; 113.556; 90
7141.5Zimmermann, Lisa; Land, Michael A.; Riesinger, Christoph; Macdonald, Charles L. B.; Scheer, Manfred
Synthesis of heteropnictogen ligands via PI transfer
Chemical Communications, 2025, 61, 6973-6976
7134391 CIFC67 H37 B F24 Mo5 O10 P2 Sb2P 1 21/c 118.9232; 20.718; 20.1171
90; 113.323; 90
7242.47Zimmermann, Lisa; Land, Michael A.; Riesinger, Christoph; Macdonald, Charles L. B.; Scheer, Manfred
Synthesis of heteropnictogen ligands via PI transfer
Chemical Communications, 2025, 61, 6973-6976
7134392 CIFC25 H28 Cl N S2P 1 21 16.422; 9.473; 21.111
90; 95.15; 90
1279.12Zhou, Jie; Chen, Zhizheng; Nie, Mengna; Li, Wenhao; Tong, Wen-Yan; Wei, Haonan; Yan, Hang; Gao, Qianwen; Qu, Shuanglin; Wang, Xi
Nickel-catalyzed enantioselective reductive iminodisulfuration of alkene-tethered oxime esters with dithiosulfonate
Chemical Communications, 2025, 61, 7329-7332
7134393 CIFC25 H34 I NP 1 21/c 117.4227; 9.8519; 13.1335
90; 97.198; 90
2236.56Kolařík, Václav; Hromádková, Aneta; Knirsch, Adam; Prucková, Zdeňka; Janovský, Petr; Rouchal, Michal; Ward, Jas S.; Rissanen, Kari; Vícha, Robert
Metal cations switch geometry of β-cyclodextrin complexes
Chemical Communications, 2025, 61, 7077-7080
7134394 CIFC21 H26 Cl N OP c c n42.2883; 9.4126; 9.1436
90; 90; 90
3639.54Kolařík, Václav; Hromádková, Aneta; Knirsch, Adam; Prucková, Zdeňka; Janovský, Petr; Rouchal, Michal; Ward, Jas S.; Rissanen, Kari; Vícha, Robert
Metal cations switch geometry of β-cyclodextrin complexes
Chemical Communications, 2025, 61, 7077-7080
7134395 CIFC24 H32 I N OP b c a12.498; 11.2458; 31.4625
90; 90; 90
4422.05Kolařík, Václav; Hromádková, Aneta; Knirsch, Adam; Prucková, Zdeňka; Janovský, Petr; Rouchal, Michal; Ward, Jas S.; Rissanen, Kari; Vícha, Robert
Metal cations switch geometry of β-cyclodextrin complexes
Chemical Communications, 2025, 61, 7077-7080
7134396 CIFC17 H15 Br OC 1 2/c 123.556; 5.9633; 21.912
90; 108.089; 90
2925.9Mondal, Subhashis; Pramanik, Shyamal; Maity, Soumitra
Thiocyanate: a visible-light-driven traceless auxiliary for stereoselective cyclopropyl ketone construction
Chemical Communications, 2025, 61, 7999-8002
7134397 CIFC25 H23 N O2P 1 21/c 110.5319; 6.0342; 30.383
90; 93.08; 90
1928.1Chai, Yi-Xin; Yang, Yu-Fan; Zhang, Feng-Yu; Zhao, Ji-Yan; Wang, Ya-Ting; Chen, Yanmei; Sun, Yuan-Yuan; Li, Jin-Heng; Zhu, Yan-Ping
Palladium/norbornene cooperative catalysis triple functionalization: carbamoylation/double-annulation of (hetero)aryl iodides
Chemical Communications, 2025, 61, 7133-7136
7134398 CIFC12 H9 Cl F2 I N OP b c a8.6441; 11.7421; 24.791
90; 90; 90
2516.3Sharma, Ruchi; Sihag, Naveen; Gupta, Poorvi; Manna, Kuntal; Yadav, M. Ramu
Photoinduced Ni-catalyzed carbohalogenation of monofluoro, gem-difluoro, and trifluoromethyl tethered alkenes
Chemical Communications, 2025, 61, 7273-7276
7134399 CIFC10.9 H8.8 F3 I0.94 N OP 1 21/n 18.28658; 12.189; 12.0734
90; 94.993; 90
1214.85Sharma, Ruchi; Sihag, Naveen; Gupta, Poorvi; Manna, Kuntal; Yadav, M. Ramu
Photoinduced Ni-catalyzed carbohalogenation of monofluoro, gem-difluoro, and trifluoromethyl tethered alkenes
Chemical Communications, 2025, 61, 7273-7276
7134400 CIFC11 H11 F I N OP 1 21/c 113.1305; 11.7122; 16.4642
90; 112.747; 90
2335.05Sharma, Ruchi; Sihag, Naveen; Gupta, Poorvi; Manna, Kuntal; Yadav, M. Ramu
Photoinduced Ni-catalyzed carbohalogenation of monofluoro, gem-difluoro, and trifluoromethyl tethered alkenes
Chemical Communications, 2025, 61, 7273-7276
7134401 CIFC16 H13 N OP -15.6306; 10.8781; 11.2166
116.604; 95.399; 96.893
601.32Liu, Yu-Chao; Cao, Dun-Xu; Ban, Qi-Yang; Ma, Wen-Jie; Xiao, Bin
Catalytic acceptorless dehydrogenation of alcohols using cobalt(i) pincer complexes supported by a P–GeH–P ligand
Chemical Communications, 2025, 61, 6917-6920
7134402 CIFC38 H28 Cl Co Ge O2 P2P -110.7973; 11.7778; 14.3651
89.199; 83.702; 87.712
1814.23Liu, Yu-Chao; Cao, Dun-Xu; Ban, Qi-Yang; Ma, Wen-Jie; Xiao, Bin
Catalytic acceptorless dehydrogenation of alcohols using cobalt(i) pincer complexes supported by a P–GeH–P ligand
Chemical Communications, 2025, 61, 6917-6920
7134403 CIFC39 H31 Co Ge O2 P2P 1 21/c 110.2474; 13.9407; 23.4568
90; 99.028; 90
3309.4Liu, Yu-Chao; Cao, Dun-Xu; Ban, Qi-Yang; Ma, Wen-Jie; Xiao, Bin
Catalytic acceptorless dehydrogenation of alcohols using cobalt(i) pincer complexes supported by a P–GeH–P ligand
Chemical Communications, 2025, 61, 6917-6920
7134404 CIFC38 H29 Co Ge O2 P2P 1 21 110.4565; 14.8378; 10.8171
90; 93.354; 90
1675.41Liu, Yu-Chao; Cao, Dun-Xu; Ban, Qi-Yang; Ma, Wen-Jie; Xiao, Bin
Catalytic acceptorless dehydrogenation of alcohols using cobalt(i) pincer complexes supported by a P–GeH–P ligand
Chemical Communications, 2025, 61, 6917-6920
7134405 CIFC36 H30 Ge P2P -111.028; 12.8596; 12.8744
95.058; 113.143; 108.781
1540.38Liu, Yu-Chao; Cao, Dun-Xu; Ban, Qi-Yang; Ma, Wen-Jie; Xiao, Bin
Catalytic acceptorless dehydrogenation of alcohols using cobalt(i) pincer complexes supported by a P–GeH–P ligand
Chemical Communications, 2025, 61, 6917-6920
7134406 CIFC168 H136 Cl16 Co4 N32P 1 21/n 117.7001; 29.4982; 34.4252
90; 90.631; 90
17973Lu, Ke; Chen, Yu-Xiao; Hu, Jie-Sheng; Liu, Zhi-Kun; Shi, Xin-Li; Yu, Meng; Starikova, Alyona A.; Tao, Jun
Spin-state modulation by host–guest chemistry with cucurbiturils
Chemical Communications, 2025, 61, 7137-7140
7134407 CIFC42 H29 Cd2 N3 O9P -19.5832; 12.5689; 16.4854
68.806; 87.073; 80.317
1824.9Povarov, Svyatoslav A.; Iukhnevich, Ekaterina D.; Alekseevskiy, Pavel V.; Pavlov, Dmitry I.; Potapov, Andrei S.; Yushina, Irina D.; Milichko, Valentin A.; Kulakova, Alena N.
Co-ligand tuning of MOF structural anisotropy for giant optical birefringence
Chemical Communications, 2025, 61, 8047-8050
7134408 CIFC43 H30 Cd2 N2 O9P -19.5713; 12.6619; 16.6423
68.088; 86.824; 80.224
1843.9Povarov, Svyatoslav A.; Iukhnevich, Ekaterina D.; Alekseevskiy, Pavel V.; Pavlov, Dmitry I.; Potapov, Andrei S.; Yushina, Irina D.; Milichko, Valentin A.; Kulakova, Alena N.
Co-ligand tuning of MOF structural anisotropy for giant optical birefringence
Chemical Communications, 2025, 61, 8047-8050
7134409 CIFC60 H50 Cd2 N6 O11P -18.8208; 9.4521; 33.3336
82.639; 89.466; 71.506
2612.5Povarov, Svyatoslav A.; Iukhnevich, Ekaterina D.; Alekseevskiy, Pavel V.; Pavlov, Dmitry I.; Potapov, Andrei S.; Yushina, Irina D.; Milichko, Valentin A.; Kulakova, Alena N.
Co-ligand tuning of MOF structural anisotropy for giant optical birefringence
Chemical Communications, 2025, 61, 8047-8050
7134410 CIFCs Ga5 Mg S9P 18.9771; 9.6445; 9.7174
95.806; 115.504; 93.64
750.06Huang, Yi-Bing; Liu, Bin-Wen; Guo, Guo-Cong
CsMgGa5S9: a diamond-like network made of mixed tetrahedral units for excellent nonlinear optical properties
Chemical Communications, 2025, 61, 7608-7611
7134411 CIFC27 H17 O12 Os3P 1 21/n 112.3904; 14.3475; 16.448
90; 96.858; 90
2903.1Liang, Xin; Gulyas, Balasz; Palanivel, Mathangi; Leong, Weng Kee
A triosmium carbonyl cluster that inhibits α-synuclein aggregation and disassembles preformed aggregates
Chemical Communications, 2025, 61, 7446-7449
7134412 CIFC23 H16 O SP 1 21/n 112.7462; 9.1384; 15.0589
90; 95.183; 90
1746.9Yan, Kelu; Sun, Yuhang; Wen, Jiangwei; Li, Qiuyun; Yu, Xinming; Shang, Wenxu; Wang, Xiu
Synthesis of 1H-isothiochromenes by regioselective C–C and C–S bond formation of enaminothiones with alkynes under rhodium catalysis
Chemical Communications, 2025, 61, 7482-7485
7134413 CIFC26 H26 I N O4P b c a15.9209; 13.7113; 22.3081
90; 90; 90
4869.77He, Jingrui; Zhou, Xinrui; Mei, Haibo; Makarem, Ata; Javahershenas, Ramin; Soloshonok, Vadim A.; Han, Jianlin
Electrochemical reaction of indole-tethered alkynes enabling stereoselective synthesis of iodovinyl spiroindolenine-cyclopentanes
Chemical Communications, 2025, 61, 7454-7457
7134414 CIFC22 H21 N O2C 1 2/c 124.3399; 12.3406; 14.444
90; 120.693; 90
3730.8Lu, Jin-Bo; Wang, Yi-Fan; Xu, Xue-Ting; Wang, Bing-Xia; Liang, Ren-Xiao; Jia, Yi-Xia
Dearomative 1,6-enyne cycloisomerization of alkyne-tethered benzofurans and indoles via a 6-endo-dig cyclization
Chemical Communications, 2025, 61, 7616-7619
7134415 CIFC28 H30 N2 O2P 1 21/n 112.3912; 11.2049; 16.6414
90; 91.031; 90
2310.2Lu, Jin-Bo; Wang, Yi-Fan; Xu, Xue-Ting; Wang, Bing-Xia; Liang, Ren-Xiao; Jia, Yi-Xia
Dearomative 1,6-enyne cycloisomerization of alkyne-tethered benzofurans and indoles via a 6-endo-dig cyclization
Chemical Communications, 2025, 61, 7616-7619
7134416 CIFC24 H15 N O2P 1 21/n 19.3265; 16.1716; 11.842
90; 92.342; 90
1784.6Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Karjee, Pallab; Punniyamurthy, Tharmalingam
Rh-catalyzed [3+3]-annulation of quinolines with cyclopropenones: access to functionalized 2-quinolones
Chemical Communications, 2025, 61, 7875-7878
7134417 CIFC24 H17 N OP b c a6.918; 16.8553; 29.099
90; 90; 90
3393.1Debnath, Bijoy; Mandal, Santu; Saha, Sharajit; Karjee, Pallab; Punniyamurthy, Tharmalingam
Rh-catalyzed [3+3]-annulation of quinolines with cyclopropenones: access to functionalized 2-quinolones
Chemical Communications, 2025, 61, 7875-7878
7134418 CIFC56 H64 Br8 N4 Pb2P -111.6289; 11.6771; 22.39
97.483; 90.784; 90.022
3014.2Liu, Qingxiang; Wu, Xinan; Coffey, Aidan H.; Yang, Hanjun; Park, Jee Yung; Hu, Qixuan; Ma, Ke; Zhu, Chenhui; Zhao, Yong Sheng; Dou, Letian; Wang, Kang
Spacer cation enabled dimension control for efficient and wavelength-tunable blue perovskite light-emitting diodes
Chemical Communications, 2025, 61, 7644-7647
7134419 CIFC96 H72 Cd2 N4 O8P -19.4671; 13.1364; 15.9602
75.787; 89.627; 75.979
1863.8Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134420 CIFC48 H34 Cd Cl2 N2 O4P -110.0275; 13.3466; 15.3424
82.544; 79.682; 86.948
2002.1Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134421 CIFC48 H34 Br2 Cd N2 O4P -19.9999; 13.5052; 15.3052
81.589; 80.261; 86.058
2013.2Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134422 CIFC96 H72 Cd2 N4 O8P -19.4813; 12.7868; 16.4751
108.737; 90.68; 101.439
1847.8Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134423 CIFC48 H34 Cd Cl2 N2 O4P -19.9972; 13.3335; 15.2941
82.257; 83.648; 87.075
2006.3Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134424 CIFC96 H68 Br4 Cd2 N4 O8P -111.1738; 11.5824; 15.6194
105; 97.655; 93.633
1925Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134425 CIFC48 H34 Br2 Cd N2 O4P -19.9893; 13.4359; 15.3143
81.433; 84.652; 86.378
2021.1Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134426 CIFC96 H68 Cd2 Cl4 N4 O8P -111.1501; 11.4178; 15.5836
104.359; 97.79; 93.708
1894.22Kurakula, Uma; Naaz, Sanobar; Roy, Sourav; Khan, Samim; Puthan Peedikakkal, Abdul Malik; Medishetty, Raghavender; Mir, Mohammad Hedayetullah
Light-driven structural transformations in isotypical Cd(ii) complexes: stereoselectivity and photosalient motion
Chemical Communications, 2025, 61, 7494-7497
7134427 CIFC2 H12 I4 N6 PbP -19.1051; 12.466; 14.0938
67.82; 85.226; 87.169
1475.9Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134428 CIFC2 H12 I4 N6 PbP 1 21/n 112.742; 26.914; 9.2472
90; 88.992; 90
3170.7Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134429 CIFC H6 Cs I4 N3 PbP n n m18.217; 12.3881; 11.9171
90; 90; 90
2689.4Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134430 CIFC H6 Cs I4 N3 PbP n n m17.69; 11.8898; 11.531
90; 90; 90
2425Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134431 CIFC H6 Cs I4 N3 PbP n n m17.738; 11.9435; 11.5372
90; 90; 90
2444Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134432 CIFC H6 Cs I4 N3 PbP n n m17.29; 11.9193; 11.5884
90; 90; 90
2388Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134433 CIFC2 H12 I4 N6 PbP 1 21/n 112.673; 26.7036; 9.163
90; 88.468; 90
3099.8Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134434 CIFC H6 Cs I4 N3 PbP n n m18.5595; 12.7464; 12.2365
90; 90; 90
2894.75Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134435 CIFC2 H12 I4 N6 PbP 1 21/n 112.843; 27.036; 9.2962
90; 90.783; 90
3227.6Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134436 CIFC H6 Cs I4 N3 PbP n n m18.043; 12.2374; 11.7887
90; 90; 90
2602.9Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134437 CIFC H6 Cs I4 N3 PbP n n m17.914; 12.0823; 11.6499
90; 90; 90
2521.5Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134438 CIFC H6 Cs I4 N3 PbI m m a12.2916; 6.39616; 18.5282
90; 90; 90
1456.67Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134439 CIFC H6 Cs I4 N3 PbP n n m17.6; 11.8686; 11.4888
90; 90; 90
2400Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134440 CIFC H6 Cs I4 N3 PbP n n m17.475; 11.8768; 11.5309
90; 90; 90
2393Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134441 CIFC H6 Cs I4 N3 PbP n n m18.409; 12.5357; 12.0511
90; 90; 90
2781Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134442 CIFC H6 Cs I4 N3 PbI m m a12.28699; 6.38954; 18.5355
90; 90; 90
1455.19Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134443 CIFC H6 Cs I4 N3 PbP n n m17.82; 12.0233; 11.6046
90; 90; 90
2486.3Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134444 CIFC H6 Cs I4 N3 PbP n n m17.799; 11.9757; 11.5555
90; 90; 90
2463.1Drushliak, Viktoriia; Szafrański, Marek
Effect of pressure and temperature on the structure and optical properties of two-dimensional lead iodide perovskites
Chemical Communications, 2025, 61, 8019-8022
7134445 CIFC25 H29 N O3P -18.6101; 9.4347; 15.4023
98.502; 101.701; 112.023
1100.7Takeda, Norihiko; Fujita, Sora; Murakami, Kaho; Honda, Chihiro; Tomoda, Hina; Yasui, Motohiro; Yamada, Takahiro; Ueda, Masafumi
Zinc(ii)-catalysed cyclocondensation of oxime ethers triggered by polarity inversion: construction of fused pyrroles
Chemical Communications, 2025, 61, 7995-7998
7134446 CIFC24 H22 Br N OP 1 21 18.5551; 6.0134; 19.1446
90; 94.893; 90
981.31Takeda, Norihiko; Fujita, Sora; Murakami, Kaho; Honda, Chihiro; Tomoda, Hina; Yasui, Motohiro; Yamada, Takahiro; Ueda, Masafumi
Zinc(ii)-catalysed cyclocondensation of oxime ethers triggered by polarity inversion: construction of fused pyrroles
Chemical Communications, 2025, 61, 7995-7998
7134447 CIFC36 H22 N2 O2P c a 2134.2132; 7.3693; 40.2679
90; 90; 90
10152.6Liu, Xiang-Ru; Yin, Yihao; Xiao, Xian-Xian; Zheng, Lin; Lu, Yan-Na; Chen, Jun-Shuai; Gu, Jin-Hui; Lu, Yunjie; Xie, Jia-Sen; Gu, Mingwei; Xu, Zhi-Guang; Ge, Jin
Bistricyclic aromatic enes with fast conformational transition for ultrathin piezochromic films
Chemical Communications, 2025, 61, 7506-7509
7134448 CIFC168 H200 B6 F24 N32 O38 Pd3 S14P 1 21/c 116.149; 26.246; 30.52
90; 93.016; 90
12918Dakua, Trilochan; Mishra, Srabani Srotoswini; Kumar, Ashish; Krishnaswamy, Shobhana; Chand, Dillip Kumar
Multi-cavity discrete coordination cages encapsulating up to four units of pyrazine-N,N′-dioxide: molecular soybeans
Chemical Communications, 2025, 61, 8007-8010
7134449 CIFC27 H30 N6P c a 2114.35; 13.941; 23.623
90; 90; 90
4725.9Divya,; Panday, Ravi Rajan; Ali, Shahjad; Ali, Md Ehesan; Kalla, Sarita; Pandey, Rakesh K.; Jangir, Ritambhara
An electron rich triazine-based covalent organic framework as an aqueous electrolyte symmetric supercapacitor
Chemical Communications, 2025, 61, 7831-7834
7134450 CIFC77 H96 B F12 N3 O Sb2P -115.2096; 16.6088; 17.4936
63.221; 81.517; 89.492
3893.7Yang, Peiyuan; Chen, Yizhou; Kuroda, Takuma; Morishita, Haruto; Fukumoto, Hiroki; Morita, Masato; Masada, Koichiro; Sasamori, Takahiro; Kubo, Kazuya; Marumoto, Kazuhiro; Inoue, Ryo; Kato, Shin-ichiro; Agou, Tomohiro
Dicationic dibenzo[1,4]azaborine with an open-shell electronic structure
Chemical Communications, 2025, 61, 7847-7850
7134451 CIFC56 H28 B F20 Fe2 P S2C 1 2/c 116.27; 16.235; 38.13
90; 98.979; 90
9948Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134452 CIFC63 H36 B F20 Fe2 P Se2P -110.8629; 15.1456; 17.3801
71.852; 75.728; 87.113
2632.3Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134453 CIFC57 H28 B Cl2 F20 Fe2 P Se2P 1 21/n 116.326; 9.99; 32.781
90; 98.502; 90
5288Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134454 CIFC56 H28 B F20 Fe2 P Se2C 1 2/c 116.24; 16.332; 38.51
90; 98.942; 90
10090Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134455 CIFC64 H36 B F20 Fe4 P Se2P -113.4185; 13.8756; 15.8321
100.509; 95.382; 92.036
2881.4Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134456 CIFC57 H30 B Cl2 F20 Fe2 P Te2P -110.3907; 15.4524; 18.1339
104.965; 103.652; 92.341
2717.3Stoian, Corina; Schmidt, Nils; Kuczmera, Thomas J.; Puylaert, Pim; Lork, Enno; Nachtsheim, Boris J.; Hupf, Emanuel; Beckmann, Jens
Oxidative addition of diaryldichalcogenides to the diferrocenylphosphenium ion: synthesis, structure and organocatalytic activity
Chemical Communications, 2025, 61, 8256-8259
7134457 CIFC93 H82 Cl2 O12P -113.0383; 15.157; 20.5626
82.547; 78.926; 81.93
3926.3Lagerna, Oleksandra; Shivanyuk, Alexander; Kienko, Tetyana; Shishkina, Svitlana V.; Lukin, Oleg; Fetyukhin, Volodymyr
Acyl migrations sensitive to supramolecular encapsulation
Chemical Communications, 2025, 61, 8500-8503
7134458 CIFC198 H180 F0 N48 P0 Pd6P 63/m m c25.0141; 25.0141; 60.039
90; 90; 120
32534Hu, Yu-Hang; Yin, Fan; Hong, Shun-Xing; Zhou, Li-Peng; Tang, Ke-Han; Zhong, Ying-Mei; Li, Chen-Chen; Cai, Li-Xuan; Sun, Qing-Fu
Coordination-assembly of a redox-active Pd6L3 cage for aerobic C(sp3)–H bond photooxidation of aromatic cyclic ethers
Chemical Communications, 2025, 61, 7819-7822
7134459 CIFC52 H22 Eu2 F36 N6 O12 S2C 1 2/c 115.0598; 22.67; 19.377
90; 92.999; 90
6606.4Fréroux, Yoann; Kiraev, Salauat; Galangau, Olivier; Phan, Tuan-Anh; Roisnel, Thierry; Maury, Olivier; Rigaut, Stéphane; Norel, Lucie
Photomodulation of dinuclear europium(iii) complex luminescence using thermally reversible photochromism of diarylethene
Chemical Communications, 2025, 61, 8051-8054
7134460 CIFC52 H22 F36 N6 O12 S2 Yb2P 1 21/n 112.4171; 32.1311; 18.2736
90; 105.03; 90
7041.3Fréroux, Yoann; Kiraev, Salauat; Galangau, Olivier; Phan, Tuan-Anh; Roisnel, Thierry; Maury, Olivier; Rigaut, Stéphane; Norel, Lucie
Photomodulation of dinuclear europium(iii) complex luminescence using thermally reversible photochromism of diarylethene
Chemical Communications, 2025, 61, 8051-8054
7134461 CIFC144 H188.41 Na6 O41 S12 Si6P -120.808; 22.891; 23.911
94.956; 106.576; 108.561
10149Diack, Youssoupha; Mallet-Ladeira, Sonia; Lesage, Denis; Guerra, João V. S.; Bourissou, Didier; Szalóki, György
Confinement-supported aurophilic interaction
Chemical Communications, 2025, 61, 8003-8006
7134462 CIFC148 H195 Au6 N2 O24 P12 Si6C 1 2/c 137.0345; 25.8098; 23.2625
90; 94.174; 90
22176.6Diack, Youssoupha; Mallet-Ladeira, Sonia; Lesage, Denis; Guerra, João V. S.; Bourissou, Didier; Szalóki, György
Confinement-supported aurophilic interaction
Chemical Communications, 2025, 61, 8003-8006
7134463 CIFC154.76 H219 Au2 Na4 O38 P3.96 Si6P -117.1106; 22.0464; 26.2211
89.918; 89.321; 70.05
9297.1Diack, Youssoupha; Mallet-Ladeira, Sonia; Lesage, Denis; Guerra, João V. S.; Bourissou, Didier; Szalóki, György
Confinement-supported aurophilic interaction
Chemical Communications, 2025, 61, 8003-8006
7134464 CIFC30 H60 Ca N P2 Si2P 1 21/c 112.4016; 14.4612; 20.6761
90; 94.648; 90
3695.9Messori, Alessandro; Potocnik, Marcel; Belazregue, Sara; Collins, Richard; Krämer, Tobias; Chadwick, F. Mark
PCP and POCOP complexes of calcium
Chemical Communications, 2025, 61, 7827-7830
7134465 CIFC36 H62 Ca O4 P4P n a 2117.9482; 17.8327; 12.6949
90; 90; 90
4063.19Messori, Alessandro; Potocnik, Marcel; Belazregue, Sara; Collins, Richard; Krämer, Tobias; Chadwick, F. Mark
PCP and POCOP complexes of calcium
Chemical Communications, 2025, 61, 7827-7830
7134466 CIFC44 H78 Ca O4 P4C 1 2/c 123.5873; 11.5583; 20.9001
90; 119.236; 90
4972.1Messori, Alessandro; Potocnik, Marcel; Belazregue, Sara; Collins, Richard; Krämer, Tobias; Chadwick, F. Mark
PCP and POCOP complexes of calcium
Chemical Communications, 2025, 61, 7827-7830
7134467 CIFC28 H46 O2 P2 SiP 1 21/c 111.4317; 19.1095; 14.6851
90; 106.607; 90
3074.21Messori, Alessandro; Potocnik, Marcel; Belazregue, Sara; Collins, Richard; Krämer, Tobias; Chadwick, F. Mark
PCP and POCOP complexes of calcium
Chemical Communications, 2025, 61, 7827-7830
7134468 CIFC28 H57 Ca N O2 P2 Si2P b c a14.8629; 19.3315; 25.3975
90; 90; 90
7297.26Messori, Alessandro; Potocnik, Marcel; Belazregue, Sara; Collins, Richard; Krämer, Tobias; Chadwick, F. Mark
PCP and POCOP complexes of calcium
Chemical Communications, 2025, 61, 7827-7830
7134469 CIFC23 H37 B N O2 PP -17.7665; 11.5656; 13.5181
80.546; 88.085; 87.299
1196.02Zheng, Tianyu; Jiang, Hao; Ma, Jiawei; Chen, Haochi; Shi, Zhuangzhi; Liang, Yong
Dispersion-controlled C6-selective C–H borylation of indoles
Chemical Communications, 2025, 61, 8208-8211
7134470 CIFC37 H53 B N O2 PP 1 21/n 113.0888; 12.8677; 20.7793
90; 108.194; 90
3324.7Zheng, Tianyu; Jiang, Hao; Ma, Jiawei; Chen, Haochi; Shi, Zhuangzhi; Liang, Yong
Dispersion-controlled C6-selective C–H borylation of indoles
Chemical Communications, 2025, 61, 8208-8211
7134471 CIFC35 H54.6 Br0.38 Cl0.62 Ga NC 1 2/c 132.7341; 23.0166; 9.2046
90; 92.844; 90
6926.5Jiang, Yuqi; Pan, Guo; Zhou, Ren; Huang, Ruihao; Ran, Dongmei; Xu, Daqian; Su, Yuanting
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Chemical Communications, 2025, 61, 8192-8195
7134472 CIFC64 H96 Ga2 N2P -19.926; 12.299; 14.106
107.74; 103.724; 102.71
1511.7Jiang, Yuqi; Pan, Guo; Zhou, Ren; Huang, Ruihao; Ran, Dongmei; Xu, Daqian; Su, Yuanting
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Chemical Communications, 2025, 61, 8192-8195
7134473 CIFC43 H66 Ga N O2P -19.0948; 12.5381; 18.2742
81.321; 80.234; 73.737
1959.65Jiang, Yuqi; Pan, Guo; Zhou, Ren; Huang, Ruihao; Ran, Dongmei; Xu, Daqian; Su, Yuanting
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Chemical Communications, 2025, 61, 8192-8195
7134474 CIFC70 H100 Cl2 Ga2 N2I 41/a :218.6669; 18.6669; 39.267
90; 90; 90
13682.7Jiang, Yuqi; Pan, Guo; Zhou, Ren; Huang, Ruihao; Ran, Dongmei; Xu, Daqian; Su, Yuanting
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Chemical Communications, 2025, 61, 8192-8195
7134475 CIFC24 H15 F N2 O5P -18.651; 10.0429; 13.0902
106.123; 95.593; 112.022
986.56Bouda, Maria; Hana, Grace E.; Xhili, Dea; Sripada, Archita; Bertke, Jeffery A.; Wolf, Christian
Organocatalytic atroposelective fluorooxindole addition to coumarin Michael acceptors
Chemical Communications, 2025, 61, 7883-7886
7134476 CIFC18 H10 Br F N2 O5P -18.0949; 8.6881; 12.6768
74.929; 84.954; 73.257
824.31Bouda, Maria; Hana, Grace E.; Xhili, Dea; Sripada, Archita; Bertke, Jeffery A.; Wolf, Christian
Organocatalytic atroposelective fluorooxindole addition to coumarin Michael acceptors
Chemical Communications, 2025, 61, 7883-7886
7134477 CIFC18 H10 Cl F N2 O5P 1 21 19.761; 10.0249; 17.7207
90; 104.683; 90
1677.4Bouda, Maria; Hana, Grace E.; Xhili, Dea; Sripada, Archita; Bertke, Jeffery A.; Wolf, Christian
Organocatalytic atroposelective fluorooxindole addition to coumarin Michael acceptors
Chemical Communications, 2025, 61, 7883-7886
7134478 CIFB Cs H2 O3P 1 21/n 17.5268; 6.9794; 7.8192
90; 113.612; 90
376.37Fan, Jinbin; Zhang, Luyong; Chen, Zilong; Li, Huimin; Yang, Zhihua; Yang, Yun; Zhang, Fangfang; Pan, Shilie
CsBO(OH)2: a new hydroxyborate with the rare [BO(OH)2] group and a deep ultraviolet cutoff edge
Chemical Communications, 2025, 61, 8196-8199
7134479 CIFC16 H16 O2P 1 21 18.6971; 5.873; 12.5155
90; 94.239; 90
637.52Othman, Karwan Abdulmajed; Xiang, Yimin; Wang, Yue; Huang, Nianyu; Wang, Nengzhong; Li, Linxuan; Yao, Hui
Stereoselective synthesis of C-glycosides from glycals and organotrifluoroborate salts
Chemical Communications, 2025, 61, 7867-7870
7134480 CIFC15 H14 O2P 1 21 110.87836; 4.91995; 21.8073
90; 91.9801; 90
1166.45Othman, Karwan Abdulmajed; Xiang, Yimin; Wang, Yue; Huang, Nianyu; Wang, Nengzhong; Li, Linxuan; Yao, Hui
Stereoselective synthesis of C-glycosides from glycals and organotrifluoroborate salts
Chemical Communications, 2025, 61, 7867-7870
7134481 CIFC14 H21 O5.5P 21 21 214.8369; 14.8689; 37.6287
90; 90; 90
2706.23Othman, Karwan Abdulmajed; Xiang, Yimin; Wang, Yue; Huang, Nianyu; Wang, Nengzhong; Li, Linxuan; Yao, Hui
Stereoselective synthesis of C-glycosides from glycals and organotrifluoroborate salts
Chemical Communications, 2025, 61, 7867-7870
7134482 CIFC56 H56 O8 Si4P 4/n :224.8118; 24.8118; 5.1576
90; 90; 90
3175.15Iwamoto, Takahiro; Amano, Sota; Maeda, Kousuke; Shibama, Natsuki; Sekiguchi, Wakana; Kazama, Yuki; Nakamura, Yasuyuki; Sugamata, Koh; Imoto, Hiroaki; Naka, Kensuke; Ishii, Youichi
Exclusive macrocyclization through multiple Si–O bond formations from diol and dichlorosilane
Chemical Communications, 2025, 61, 8180-8183
7134483 CIFC16 H20 O4 Si2P 1 21/c 113.3626; 10.537; 12.8771
90; 112.376; 90
1676.6Iwamoto, Takahiro; Amano, Sota; Maeda, Kousuke; Shibama, Natsuki; Sekiguchi, Wakana; Kazama, Yuki; Nakamura, Yasuyuki; Sugamata, Koh; Imoto, Hiroaki; Naka, Kensuke; Ishii, Youichi
Exclusive macrocyclization through multiple Si–O bond formations from diol and dichlorosilane
Chemical Communications, 2025, 61, 8180-8183
7134484 CIFC35 H28 N2 O5 SP -19.0966; 12.2949; 14.6504
104.644; 102.93; 111.566
1379.99Xu, Fuxing; Xiong, Zongli; Qin, Wenling; Yao, Weijun; Wang, Zhen
Asymmetric synthesis of quinolinone-based polycyclic indoles through [1,3]-rearrangement/cyclization reaction
Chemical Communications, 2025, 61, 8403-8406
7134485 CIFC42 H36 N2 O5 S2P 1 21/c 110.7401; 18.2838; 18.5074
90; 92.761; 90
3630.08Xu, Fuxing; Xiong, Zongli; Qin, Wenling; Yao, Weijun; Wang, Zhen
Asymmetric synthesis of quinolinone-based polycyclic indoles through [1,3]-rearrangement/cyclization reaction
Chemical Communications, 2025, 61, 8403-8406
7134486 CIFC24 H12 Cu2 F4 N2 O4I 1 2/a 119.1711; 14.3457; 16.0551
90; 94.317; 90
4403Li, Yifei; Wang, Fenglei; Xiang, Shengchang; Fan, Xi; Zhang, Zhangjing
Restructuring of mortise-and-tenon frameworks at the molecular level
Chemical Communications, 2025, 61, 8343-8346
7134487 CIFC24 H16 Cu2 F2 N2 O4P 1 21/n 111.632; 7.8201; 23.9312
90; 92.22; 90
2175.23Li, Yifei; Wang, Fenglei; Xiang, Shengchang; Fan, Xi; Zhang, Zhangjing
Restructuring of mortise-and-tenon frameworks at the molecular level
Chemical Communications, 2025, 61, 8343-8346
7134488 CIFC36 H25 Fe3 O34 S6P 6319.6053; 19.6053; 17.9744
90; 90; 120
5983.2Xue, Chaozhuang; Peng, Hui; Hou, Jinle; Qu, Konggang
Pore space partition on a sulfonate-rich metal–organic framework for purification of methane from natural gas
Chemical Communications, 2025, 61, 8244-8247
7134489 CIFC58 H30 Fe3 N9 O31 S6P 6319.2686; 19.2686; 18.143
90; 90; 120
5833.6Xue, Chaozhuang; Peng, Hui; Hou, Jinle; Qu, Konggang
Pore space partition on a sulfonate-rich metal–organic framework for purification of methane from natural gas
Chemical Communications, 2025, 61, 8244-8247
7134490 CIFC168 H120 Fe4 N48 O12P -4 3 n26.4918; 26.4918; 26.4918
90; 90; 90
18592.4Hao, Yang; Yang, Yang; Yang, Fengyu; Shi, Youpeng; Jing, Xu; Duan, Chunying
An Ir(ppy)3 encapsulated metal–organic tetrahedral cage for photocatalytic dehydrogenation cross-couplings
Chemical Communications, 2025, 61, 8576-8579
7134491 CIFC158.54 H132.81 F36 Fe3 N46.27 O36 S12P -116.7218; 17.6792; 34.026
96.548; 100.632; 100.345
9612.3Hao, Yang; Yang, Yang; Yang, Fengyu; Shi, Youpeng; Jing, Xu; Duan, Chunying
An Ir(ppy)3 encapsulated metal–organic tetrahedral cage for photocatalytic dehydrogenation cross-couplings
Chemical Communications, 2025, 61, 8576-8579
7134492 CIFC11 H13 O3 PP 1 21 110.5361; 8.4344; 12.6771
90; 98.8044; 90
1113.28Souza, Edson Leonardo Scarpa de; Ahrens, Sebastian; Spannenberg, Anke; Neumann, Helfried; Junge, Kathrin; Correia, Carlos Roque Duarte; Jackstell, Ralf; Beller, Matthias
Development of highly efficient and selective palladium catalysts for telomerization of 1,3-butadiene with alcohols
Chemical Communications, 2025, 61, 9083-9086
7134493 CIFC68 H52 Co3 N8 O20C 1 2/c 121.925; 15.3495; 23.0003
90; 101.183; 90
7593.5Zhang, Dan; Zhang, Mengrui; Jing, Xu; Duan, Chunying
Carbazole-functionalized MOFs for efficient selective photocatalytic oxidation of thioethers to sulfoxides
Chemical Communications, 2025, 61, 8260-8263
7134494 CIFC74 H66 Mn3 N10 O22C 1 2/c 121.3652; 15.6738; 22.9732
90; 98.797; 90
7602.6Zhang, Dan; Zhang, Mengrui; Jing, Xu; Duan, Chunying
Carbazole-functionalized MOFs for efficient selective photocatalytic oxidation of thioethers to sulfoxides
Chemical Communications, 2025, 61, 8260-8263
7134495 CIFC1.57 H1.41 O0.39P 1 21/n 113.1701; 6.1476; 22.2657
90; 104.251; 90
1747.26Bhadra, Sayan; Bandyopadhyay, Manas; Pathak, Swastik; Escorihuela, Jorge; Bera, Mrinal K.
Electrochemical oxidation of propargyl alcohol: rapid access to an unprecedented dioxo-orthoester under mild conditions
Chemical Communications, 2025, 61, 7879-7882
7134496 CIFC11 H16 O0.5 Si0.5P 1 21 19.5045; 10.0122; 11.2032
90; 112.142; 90
987.48Kato, Ritsuki; Sakaue, Takaya; Tawatari, Tsukasa; Takasu, Kiyosei; Takikawa, Hiroshi
Arylative double bond transposition of allylic alcohols via silicon-tethered intramolecular benzyne–ene reactions
Chemical Communications, 2025, 61, 8347-8350
7134497 CIFC23 H30 O SiP 1 21/c 17.62484; 37.0647; 7.72583
90; 108.96; 90
2064.96Kato, Ritsuki; Sakaue, Takaya; Tawatari, Tsukasa; Takasu, Kiyosei; Takikawa, Hiroshi
Arylative double bond transposition of allylic alcohols via silicon-tethered intramolecular benzyne–ene reactions
Chemical Communications, 2025, 61, 8347-8350
7134498 CIFC16 H21 N OC 1 2/m 119.461; 7.0742; 10.8476
90; 103.577; 90
1451.7Gowda, Punith S.; Sharada, Duddu S.; Satyanarayana, Gedu
A TBADT-enabled photo-induced radical cyclization pathway: concise access to functionalized oxindoles
Chemical Communications, 2025, 61, 8391-8394
7134499 CIFC10 H8 I N OP 1 21/c 19.9735; 11.629; 8.9604
90; 98.377; 90
1028.2Gowda, Punith S.; Sharada, Duddu S.; Satyanarayana, Gedu
A TBADT-enabled photo-induced radical cyclization pathway: concise access to functionalized oxindoles
Chemical Communications, 2025, 61, 8391-8394
7134500 CIFC13 H15 N O3P 1 21/c 15.1369; 9.3444; 25.1733
90; 92.3; 90
1207.38Gowda, Punith S.; Sharada, Duddu S.; Satyanarayana, Gedu
A TBADT-enabled photo-induced radical cyclization pathway: concise access to functionalized oxindoles
Chemical Communications, 2025, 61, 8391-8394
7134501 CIFC28 H24 Cl N OP 21 21 2110.2452; 14.4399; 14.5364
90; 90; 90
2150.51Wang, Lishu; Wang, Han; Nie, Xukun; Li, Jun; Tang, Yurong; Cai, Yunfei
Stereoselective construction of 5-6-5 aza-tricyclic scaffolds via catalytic asymmetric aza-Piancatelli/Diels–Alder reactions
Chemical Communications, 2025, 61, 8395-8398
7134502 CIFC48 H36 Cl Fe N4P -111.5966; 12.6443; 14.8717
68.725; 70.726; 67.345
1828.74Rathi, Shivani; Ahmad, Ikrar; Sankar, Muniappan
Unveiling the potential of tailored β-substituted iron-porphyrins for highly efficient oxygen reduction reactions (ORR)
Chemical Communications, 2025, 61, 8512-8515
7134503 CIFC24 H29 N O2 SiP 21 21 216.5493; 10.4222; 33.5349
90; 90; 90
2289.03Li, Xin; Liu, Nai-Xuan; Sun, Jian-Ting; Nie, Xiao-Di; Si, Chang-Mei; Wei, Bang-Guo
An [(IPr)AuCl]-catalyzed formal [4+2] process of N-Ar N,O-acetals with arylacetylenes for the construction of pyrrolo[1,2-a]quinolines
Chemical Communications, 2025, 61, 8411-8414
7134504 CIFC18 H14 Cl N OP 1 21/c 19.888; 11.0027; 13.3415
90; 101.844; 90
1420.58Li, Xin; Liu, Nai-Xuan; Sun, Jian-Ting; Nie, Xiao-Di; Si, Chang-Mei; Wei, Bang-Guo
An [(IPr)AuCl]-catalyzed formal [4+2] process of N-Ar N,O-acetals with arylacetylenes for the construction of pyrrolo[1,2-a]quinolines
Chemical Communications, 2025, 61, 8411-8414
7134505 CIFC15 H11 F3 N2P 1 21/n 111.7069; 7.8689; 14.4296
90; 105.523; 90
1280.77Liang, Miaomiao; Xu, Yuanshuang; Yang, Xueying; Zhang, Xinying; Fan, Xuesen
Synthesis of 2-CF3-indoles or 2-CF3-indolin-3-ones via anaerobic or aerobic reactions of N-phenylpyridin-2-amines with TFISYs
Chemical Communications, 2025, 61, 8735-8738
7134506 CIFC20 H14 F3 N3 OP b c a17.0044; 10.7501; 18.938
90; 90; 90
3461.85Liang, Miaomiao; Xu, Yuanshuang; Yang, Xueying; Zhang, Xinying; Fan, Xuesen
Synthesis of 2-CF3-indoles or 2-CF3-indolin-3-ones via anaerobic or aerobic reactions of N-phenylpyridin-2-amines with TFISYs
Chemical Communications, 2025, 61, 8735-8738
7134507 CIFC31 H20 Fe2 O6 P2 S2P -112.259; 15.825; 16.51
86.072; 71.586; 89.707
3031.3Munshi, Sandip; Ravel-Massol, Raphaël; Garcia-Serres, Ricardo; Suaud, Nicolas; Maurice, Rémi; Saffon-Merceron, Nathalie; Mézailles, Nicolas; Fustier-Boutignon, Marie
Freed from iron: easy release of a stable ketene from the reaction of CO with di-iron bis-μ2-alkylidenes
Chemical Communications, 2025, 61, 8687-8690
7134508 CIFC26 H20 O P2 S2C 1 2/c 124.929; 9.3898; 21.714
90; 112.245; 90
4704.5Munshi, Sandip; Ravel-Massol, Raphaël; Garcia-Serres, Ricardo; Suaud, Nicolas; Maurice, Rémi; Saffon-Merceron, Nathalie; Mézailles, Nicolas; Fustier-Boutignon, Marie
Freed from iron: easy release of a stable ketene from the reaction of CO with di-iron bis-μ2-alkylidenes
Chemical Communications, 2025, 61, 8687-8690
7134509 CIFC34 H28 Bi Cl4 N2 PP -19.3023; 12.9358; 14.6401
104.068; 102.057; 90.055
1668.7Zhang, Bo-Lun; Song, Wen-Tao; Zhang, Jian-Jun; Chen, Jun; Miao, Lei; Shi, Wen-Jing; Wang, Rui-Hong; Cai, Mengmeng; Ni, Jun; Zhao, Zongbin
Awakening of high-energy phosphorescence by enhanced weak interactions for ratiometric detection of trichloromethane vapor
Chemical Communications, 2025, 61, 8560-8563
7134510 CIFC35 H30 Bi Cl7 N2 O0.5 PP -18.948; 13.456; 17.067
71.085; 76.978; 83.504
1892.2Zhang, Bo-Lun; Song, Wen-Tao; Zhang, Jian-Jun; Chen, Jun; Miao, Lei; Shi, Wen-Jing; Wang, Rui-Hong; Cai, Mengmeng; Ni, Jun; Zhao, Zongbin
Awakening of high-energy phosphorescence by enhanced weak interactions for ratiometric detection of trichloromethane vapor
Chemical Communications, 2025, 61, 8560-8563
7134511 CIFC234 H232 Cu6 N30 O16 P12 Re4P -117.7996; 19.284; 21.9051
111.005; 99.5; 110.975
6171.8Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134512 CIFC242.2 H224.8 Cu6 N31.6 O14.6 P12 Re4P -117.8452; 19.7115; 21.973
111.983; 99.066; 110.968
6301.9Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134513 CIFC58.45 H44.9 Cl0.9 N7 P2 ReP 1 21/c 18.7303; 54.337; 21.586
90; 92.476; 90
10230.4Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134514 CIFC59 H49 N6 O3 P2 ReP 1 c 18.336; 14.4518; 21.376
90; 91.822; 90
2573.9Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134515 CIFC44 H34 N5 P2 ReP 1 21/c 117.768; 9.5496; 27.529
90; 102.419; 90
4561.7Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134516 CIFC62 H54 N6 O4 P2 ReP 1 21 113.4644; 17.279; 13.82
90; 119.085; 90
2809.8Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134517 CIFC243 H230 Cu6 N32 O17 P12 Re4P -117.501; 18.19; 22.25
71.562; 72.401; 62.918
5876.7Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134518 CIFC228.22 H176 Cu6 N33.29 O0.36 P12 Re4P -117.8262; 19.473; 21.915
111.371; 99.586; 110.633
6238.7Liberka, Michal; Gas, Piotr; Chorazy, Szymon
Decanuclear {CuI6ReV4} clusters utilizing cyanido and nitrido molecular bridges as efficient ligand-modulated luminophores
Chemical Communications, 2025, 61, 8580-8583
7134519 CIFC24 H25 N4 SbP 1 21/c 112.2927; 7.5486; 23.983
90; 103.267; 90
2166.1Zhang, Lingjie; Huang, Minghao; Zhou, Jiliang
A dicationic distibine stabilized by intramolecular π–π interaction and second-sphere coordination
Chemical Communications, 2025, 61, 8592-8595
7134520 CIFC57 H53 Co2 N9 O7 Sb2P -112.196; 15.812; 16.798
73.724; 70.084; 76.072
2885.5Zhang, Lingjie; Huang, Minghao; Zhou, Jiliang
A dicationic distibine stabilized by intramolecular π–π interaction and second-sphere coordination
Chemical Communications, 2025, 61, 8592-8595
7134521 CIFC34.5 H37 F6 N4 P SbC 1 2/c 119.8847; 14.7666; 23.377
90; 96.49; 90
6820.2Zhang, Lingjie; Huang, Minghao; Zhou, Jiliang
A dicationic distibine stabilized by intramolecular π–π interaction and second-sphere coordination
Chemical Communications, 2025, 61, 8592-8595
7134522 CIFC22 H28 N2 O5 SP -110.0397; 10.2947; 11.3136
84.709; 76.197; 89.722
1130.54Zhang, Li-Hua; Xie, Yang; Xuan, Jun
Dearomatizative aminoetherification and diamination of indoles enabled by photochemical nitrene transfer reactions
Chemical Communications, 2025, 61, 8528-8531
7134523 CIFC15 H19 N OP 1 21/c 18.7665; 18.8687; 8.1487
90; 102.511; 90
1315.89Ghosh, Arijit; Pawar, Amit B.
Harnessing sulfilimine as an oxidizing directing group in Cp*Co(iii)-catalyzed [4+2] annulation with alkynes and 1,3-diynes
Chemical Communications, 2025, 61, 8240-8243
7134524 CIFC31 H31 N OP 1 21/c 110.5297; 13.4796; 18.0553
90; 92.422; 90
2560.41Ghosh, Arijit; Pawar, Amit B.
Harnessing sulfilimine as an oxidizing directing group in Cp*Co(iii)-catalyzed [4+2] annulation with alkynes and 1,3-diynes
Chemical Communications, 2025, 61, 8240-8243
7134525 CIFC15 H10 F5 I N2 O5 S2P 1 21/c 113.9965; 9.6084; 15.2172
90; 90.161; 90
2046.46Yuan, Zong-Rui; Sun, Meng-Qi; Chen, Wei-Chen; Zhang, Zhi-Qi; Ma, Jun-An; Zhang, Fa-Guang
Transition metal/photocatalyst-free skeletal editing of indene with iodonium difluorodiazo reagent to access 2-(difluoromethyl)naphthalene
Chemical Communications, 2025, 61, 8667-8670
7134526 CIFC26 H29 F2 N O2P b c a8.0436; 64.4922; 8.4579
90; 90; 90
4387.53Yuan, Zong-Rui; Sun, Meng-Qi; Chen, Wei-Chen; Zhang, Zhi-Qi; Ma, Jun-An; Zhang, Fa-Guang
Transition metal/photocatalyst-free skeletal editing of indene with iodonium difluorodiazo reagent to access 2-(difluoromethyl)naphthalene
Chemical Communications, 2025, 61, 8667-8670
7134527 CIFC54 H52 I2 N4 O3 S4P -110.702; 11.213; 12.216
107.31; 104.509; 102.423
1286.6Guan, Li; Li, Jun; Zhou, Yanyan; Li, Anyang; Yin, Lili; Guan, Wenhui; Fu, Yile
Construction of polymethine chain-modified pentamethylene cyanine dyes for G-quadruplex imaging in live cells
Chemical Communications, 2025, 61, 8719-8722
7134528 CIFC30.5 H28 Cl2 N2C 1 2/c 121.8221; 10.4425; 23.4492
90; 95.989; 90
5314.4Dunscomb, Rachel J.; Frye, Connor W.; Murray, Xavier; Tonks, Ian A.
1,2-Dihydropyrimidine synthesis via titanium-mediated multicomponent coupling of alkynes, nitriles, and aldehydes
Chemical Communications, 2025, 61, 8695-8698
7134529 CIFC19 H19 N O4 SeP 21 21 225.6226; 19.4121; 7.0602
90; 90; 90
3511.66Cao, Ren-Fei; Wei, Zheng-Wei; Li, Shu-Kun; Ding, Tong-Mei; Ke, Hua; Chen, Zhi-Min
Organocatalytic asymmetric electrophilic tandem selenylation semipinacol rearrangement of 1-(1-arylvinyl)cyclobutanols
Chemical Communications, 2025, 61, 8532-8535
7134530 CIFC18 H18 F N O3 SeP 1 21 17.23267; 28.5347; 8.41764
90; 103.353; 90
1690.29Cao, Ren-Fei; Wei, Zheng-Wei; Li, Shu-Kun; Ding, Tong-Mei; Ke, Hua; Chen, Zhi-Min
Organocatalytic asymmetric electrophilic tandem selenylation semipinacol rearrangement of 1-(1-arylvinyl)cyclobutanols
Chemical Communications, 2025, 61, 8532-8535
7134531 CIFC7 H16 Br5 N2 SbP 21 21 218.7842; 12.4619; 13.8984
90; 90; 90
1521.43Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134532 CIFC14 Br10 N4 Sb2P n m a14.1887; 8.8334; 12.4471
90; 90; 90
1560.1Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134533 CIFC7 H16 I5 N2 SbP n a 2114.8591; 13.0389; 9.1663
90; 90; 90
1775.94Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134534 CIFC14 Cl10 N4 Sb2P n m a13.9507; 8.5795; 11.995
90; 90; 90
1435.68Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134535 CIFC14 I10 N4 Sb2P n m a14.8988; 9.196; 13.1209
90; 90; 90
1797.69Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134536 CIFC7 H15 Cl5 N2 SbP 21 21 218.5619; 11.9096; 13.6606
90; 90; 90
1392.96Wei, Ying; Zhou, Jie; Zhou, Lin; Wei, Zhenhong
Three antimony-based organic–inorganic hybrid perovskites (1,4-3.2.2-H2dabcn)SbX5 (X = Cl, Br, I) show progressively decreasing phase transition temperatures and bandgaps
Chemical Communications, 2025, 61, 8600-8603
7134537 CIFC2.43 H1.57 N0.35 O0.61C 1 2/c 119.1986; 7.3351; 16.724
90; 95.816; 90
2343Sau, Subham; Das, Krishna Mohan; Thakur, Arunabha
Visible-light triggered Cu-catalyzed C–H bond activation to afford isocoumarin and isoquinolinone scaffolds at room temperature
Chemical Communications, 2025, 61, 8851-8854
7134538 CIFC21 H17 N5 O4 SP -17.5805; 8.7953; 15.9373
94.493; 102.417; 97.971
1021.26Sau, Subham; Das, Krishna Mohan; Thakur, Arunabha
Visible-light triggered Cu-catalyzed C–H bond activation to afford isocoumarin and isoquinolinone scaffolds at room temperature
Chemical Communications, 2025, 61, 8851-8854
7134539 CIFC50 H84 Br8 Dy6 N14 O28P 1 21/n 111.907; 17.303; 20.936
90; 97.553; 90
4276Yang, Qianqian; Wu, Jianfeng; Zhao, Chen; Ying, Xu; Zhu, Dong-Mei; Guo, Xuefeng; Liu, Dan; Zhang, Yi-Quan; Tang, Jinkui
Coupling Dy3 toroics in macrocycles
Chemical Communications, 2025, 61, 8751-8754
7134540 CIFC28 H77.19 Mo4 N4 O64.59 P8 V4C 1 2/m 117.3825; 14.0926; 16.5564
90; 107.986; 90
3857.54Morla, Kalyankumar S.; Thakre, Dewendra; Mourya, Adarsh K.; Singh, Piyush; Karnamkkott, Harsha S.; Ahamed, Subuhan; Sahoo, Subham; Bhattacharya, Ishita; Banerjee, Siddhartha; Sarma, Debajit; Mondal, Kartik Chandra; Ghosh, Sujit Kumar; Wankhade, Atul V.; Banerjee, Abhishek
A mixed metallic and mixed valence MoV4VIV2VIII2 complex as an electron transfer photo-catalyst for the hydrogen evolution reaction
Chemical Communications, 2025, 61, 8919-8922
7134541 CIFC14 H46 Mo4 N2 O42 P4 VP 1 21 112.4325; 10.9812; 17.2749
90; 99.879; 90
2323.46Morla, Kalyankumar S.; Thakre, Dewendra; Mourya, Adarsh K.; Singh, Piyush; Karnamkkott, Harsha S.; Ahamed, Subuhan; Sahoo, Subham; Bhattacharya, Ishita; Banerjee, Siddhartha; Sarma, Debajit; Mondal, Kartik Chandra; Ghosh, Sujit Kumar; Wankhade, Atul V.; Banerjee, Abhishek
A mixed metallic and mixed valence MoV4VIV2VIII2 complex as an electron transfer photo-catalyst for the hydrogen evolution reaction
Chemical Communications, 2025, 61, 8919-8922
7134542 CIFC272 H256 N16 O40 S8C 1 c 15.6866; 20.2872; 48.7011
90; 93.313; 90
5609.02Maitra, Chandrima; Chuang, Ting-Yi; Yang, Tzuhsiung; Liu, Rai-Shung
Gold-catalyzed bicyclic annulations between 4-hydroxy-1,5-diynamides and nitrones for the synthesis of cyclopentene-fused isoxazole carboxamides
Chemical Communications, 2025, 61, 8931-8934
7134543 CIFC38 H38 N2 O5 SP -19.1231; 10.6595; 19.4826
76.205; 81.449; 76.849
1782.77Maitra, Chandrima; Chuang, Ting-Yi; Yang, Tzuhsiung; Liu, Rai-Shung
Gold-catalyzed bicyclic annulations between 4-hydroxy-1,5-diynamides and nitrones for the synthesis of cyclopentene-fused isoxazole carboxamides
Chemical Communications, 2025, 61, 8931-8934
7134544 CIFC33 H29 Cl N2 O4 SP -113.713; 14.0218; 18.249
110.301; 109.587; 94.916
3018.42Maitra, Chandrima; Chuang, Ting-Yi; Yang, Tzuhsiung; Liu, Rai-Shung
Gold-catalyzed bicyclic annulations between 4-hydroxy-1,5-diynamides and nitrones for the synthesis of cyclopentene-fused isoxazole carboxamides
Chemical Communications, 2025, 61, 8931-8934
7134545 CIFC26 H21 N5 Ni2 O10P b c a10.0638; 20.4928; 29.083
90; 90; 90
5997.9Das, Chhatan; Naskar, Pappu; Banerjee, Anjan; Laha, Sourav; Mukherjee, Moumita; Datta, Ayan; Mahata, Partha
Unlocking enhanced hydrogen evolution with a bimetal–organic framework: a synergistic approach
Chemical Communications, 2025, 61, 9107-9110
7134546 CIFC22 H34 B Br N4 O2P -18.5419; 12.0415; 13.374
68.584; 76.132; 76.223
1225.92Sharma, Raju; Kenguva, Gowtham; Dandela, Rambabu; Daw, Prosenjit
Boron appended Ru-NHC catalyzed selective deoxygenative hydrogenation of tertiary amides and desulfurization of thioamides
Chemical Communications, 2025, 61, 9460-9463
7134547 CIFC32 H47 B Cl F6 N4 O2 P RuP 1 21/c 118.2664; 13.851; 14.4079
90; 90.422; 90
3645.2Sharma, Raju; Kenguva, Gowtham; Dandela, Rambabu; Daw, Prosenjit
Boron appended Ru-NHC catalyzed selective deoxygenative hydrogenation of tertiary amides and desulfurization of thioamides
Chemical Communications, 2025, 61, 9460-9463
7134548 CIFC55 H85 B10 Cl0 Cu N6 Si3P -113.9122; 14.0705; 19.039
105.727; 99.055; 103.428
3391.3Shan, Changkai; Dai, Chenshu; Yao, Shenglai; Zhu, Jun; Driess, Matthias
Unprecedented bis(silylene)-supported silylone–metal complexes with Si0→ CuI, Si0→ NiI, and Si0→ NiII dative bonds
Chemical Communications, 2025, 61, 8875-8878
7134549 CIFC24 H29 Cu N2 OP -18.6854; 9.9657; 13.5329
70.233; 83.025; 79.949
1082.95Shan, Changkai; Dai, Chenshu; Yao, Shenglai; Zhu, Jun; Driess, Matthias
Unprecedented bis(silylene)-supported silylone–metal complexes with Si0→ CuI, Si0→ NiI, and Si0→ NiII dative bonds
Chemical Communications, 2025, 61, 8875-8878
7134550 CIFC75 H113 B10 N6 Ni Si3C 1 2/c 120.2917; 15.5689; 25.7309
90; 106.87; 90
7779.1Shan, Changkai; Dai, Chenshu; Yao, Shenglai; Zhu, Jun; Driess, Matthias
Unprecedented bis(silylene)-supported silylone–metal complexes with Si0→ CuI, Si0→ NiI, and Si0→ NiII dative bonds
Chemical Communications, 2025, 61, 8875-8878
7134551 CIFC65 H67 B10 F24 N4 Ni O Si3P -116.2051; 18.1741; 19.452
102.73; 97.912; 104.587
5293.5Shan, Changkai; Dai, Chenshu; Yao, Shenglai; Zhu, Jun; Driess, Matthias
Unprecedented bis(silylene)-supported silylone–metal complexes with Si0→ CuI, Si0→ NiI, and Si0→ NiII dative bonds
Chemical Communications, 2025, 61, 8875-8878
7134552 CIFC35 H27 Br O4P 1 21/n 117.213; 7.777; 25.463
90; 105.237; 90
3288.8Barman, Jyotish; Pan, Subhas Chandra
Highly regio- and diastereoselective (3+3)-cycloannulation of carbonyl ylides and 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis
Chemical Communications, 2025, 61, 9119-9122
7134553 CIFC17 H14 O4C 1 c 117.442; 7.489; 12.142
90; 117.13; 90
1411.5Roy, Sajal; Saha, Sharajit; Bhattacharyya, Hemanga; Punniyamurthy, Tharmalingam
Cascade C–H functionalization/annulation of 2-aryl-1,3-dicarbonyls with Morita–Baylis–Hillman adducts: access to α-iso-/benzochromenyl acrylates
Chemical Communications, 2025, 61, 9095-9098
7134554 CIFC64 H88 B4 N12 Ru4P 1 21/c 113.185; 25.185; 21.033
90; 98.321; 90
6911Koshino, Haruka; Goo, Zi Lang; Sugimoto, Kunihisa; Mochida, Tomoyuki
Solvent-free photochemical formation of cubane-type Ru complexes from organometallic ionic liquids with cyanoborate anions
Chemical Communications, 2025, 61, 9258-9261
7134555 CIFC64 H88 B4 N12 Ru4I -414.005; 14.005; 19.628
90; 90; 90
3849.8Koshino, Haruka; Goo, Zi Lang; Sugimoto, Kunihisa; Mochida, Tomoyuki
Solvent-free photochemical formation of cubane-type Ru complexes from organometallic ionic liquids with cyanoborate anions
Chemical Communications, 2025, 61, 9258-9261
7134556 CIFC64 H88 B4 N12 Ru4I a -3 d34.657; 34.657; 34.657
90; 90; 90
41627Koshino, Haruka; Goo, Zi Lang; Sugimoto, Kunihisa; Mochida, Tomoyuki
Solvent-free photochemical formation of cubane-type Ru complexes from organometallic ionic liquids with cyanoborate anions
Chemical Communications, 2025, 61, 9258-9261
7134557 CIFC31 H29 N O2P 1 21/c 120.5218; 10.6991; 10.4618
90; 90.148; 90
2297Dutta, Arnab; Dzieszkowski, Krzysztof; Kijewska, Monika; Siczek, Miłosz; Orzeł, Łukasz; Pawlicki, Miłosz
A switchable red-emitting fluorophore involving a 7.6.6 defect
Chemical Communications, 2025, 61, 9424-9427
7134558 CIFC62.3 H56.6 Cl0.6 N2 O4P -112.788; 14.331; 14.493
99.07; 98.6; 91.04
2591Dutta, Arnab; Dzieszkowski, Krzysztof; Kijewska, Monika; Siczek, Miłosz; Orzeł, Łukasz; Pawlicki, Miłosz
A switchable red-emitting fluorophore involving a 7.6.6 defect
Chemical Communications, 2025, 61, 9424-9427
7134559 CIFC24 H20 Br2 Ni P2 SP 1 21/n 18.6617; 14.1619; 19.4168
90; 92.73; 90
2379.08Flecken, Franziska; Grell, Toni; Hanf, Schirin
Short-bite PSP-type ligands: coordination chemistry and ligand rearrangement reactions
Chemical Communications, 2025, 61, 9262-9265
7134560 CIFC74 H64 Cl4 Ni3 P6 S4P 1 21/n 112.1053; 13.2856; 22.4508
90; 96.619; 90
3586.6Flecken, Franziska; Grell, Toni; Hanf, Schirin
Short-bite PSP-type ligands: coordination chemistry and ligand rearrangement reactions
Chemical Communications, 2025, 61, 9262-9265
7134561 CIFC24 H20 I2 Ni P2 SI 1 2 111.983; 7.826; 14.014
90; 108.88; 90
1243.5Flecken, Franziska; Grell, Toni; Hanf, Schirin
Short-bite PSP-type ligands: coordination chemistry and ligand rearrangement reactions
Chemical Communications, 2025, 61, 9262-9265
7134562 CIFC48 H40 Ni2 P4 S5P -113.784; 16.4338; 21.9103
93.043; 96.228; 110.795
4590Flecken, Franziska; Grell, Toni; Hanf, Schirin
Short-bite PSP-type ligands: coordination chemistry and ligand rearrangement reactions
Chemical Communications, 2025, 61, 9262-9265
7134563 CIFC23 H20 N2 O4 S3P -18.5103; 11.3848; 13.169
67.846; 83.629; 75.229
1142.51Yuan, Qingbing; Wu, Caiqiong; Bao, Yonghu; Huang, Zengming; Wang, Hua; Wei, Yun; Wang, Shaowu
Copper-catalyzed three-component radical aminoazolation of vinylarenes with N-fluorobenzenesulfonimide and trimethylsilylazole derivatives
Chemical Communications, 2025, 61, 9238-9241
7134564 CIFC16 H25 N O4 SP 1 21/c 111.7519; 17.4233; 8.7618
90; 106.248; 90
1722.4Zhou, Zhi-Hua; Wang, Ben; Tan, Jie; Chen, Wei-Yi; Tian, Jie-Sheng
Oxidative N-functionalization of primary sulfonamides with aliphatic aldehydes: a green synthesis of α-sulfonamido acetals
Chemical Communications, 2025, 61, 9226-9229
7134565 CIFC131 H53 N4 Ni S2 Ti3C 1 2/m 126.6365; 17.0732; 17.8293
90; 108.18; 90
7703.5He, Zhiwen; Cao, Zhengkai; Yao, Yang-Rong; Chen, Ning
Ti3C3@C2v(9)-C82: a double-butterfly tri-metal carbide cluster inside a fullerene cage
Chemical Communications, 2025, 61, 9432-9435
7134566 CIFC24 H18 Br N O4 SP n a 2119.4774; 19.8681; 5.66262
90; 90; 90
2191.31Jia, Xiaoni; Kan, Yuanmeng; Li, Wenguang; Kong, Weiguang; Gao, Wenchao; Chen, Ming; Ye, Long-Wu; Li, Ting
Gold-catalyzed ligand-controlled annulation for the construction of indoles and furoindoles
Chemical Communications, 2025, 61, 9294-9297
7134567 CIFC24 H19 N O4 SP -18.5808; 9.8636; 12.7357
69.355; 80.379; 85.929
994.43Jia, Xiaoni; Kan, Yuanmeng; Li, Wenguang; Kong, Weiguang; Gao, Wenchao; Chen, Ming; Ye, Long-Wu; Li, Ting
Gold-catalyzed ligand-controlled annulation for the construction of indoles and furoindoles
Chemical Communications, 2025, 61, 9294-9297
7134568 CIFC254 H351 Cl5 Fe20 N12 O65 S20 V8I 426.9722; 26.9722; 22.8711
90; 90; 90
16638.7Li, Qiqi; Zou, Yuhan; Mao, Dongao; Tian, Hongrui; Hang, Xinxin; Bi, Yanfeng
Thiacalixarene-supported M20V8 (M = Fe, Co, Ni) square pyramid nanocages for visible light photothermal catalysis
Chemical Communications, 2025, 61, 9266-9269
7134569 CIFC262 H375 Cl5 N12 Ni20 O69 S20 V8I 426.771; 26.771; 23.0428
90; 90; 90
16514Li, Qiqi; Zou, Yuhan; Mao, Dongao; Tian, Hongrui; Hang, Xinxin; Bi, Yanfeng
Thiacalixarene-supported M20V8 (M = Fe, Co, Ni) square pyramid nanocages for visible light photothermal catalysis
Chemical Communications, 2025, 61, 9266-9269
7134570 CIFC260 H369 Cl5 Co20 N12 O68 S20 V8I 426.857; 26.857; 23.006
90; 90; 90
16594Li, Qiqi; Zou, Yuhan; Mao, Dongao; Tian, Hongrui; Hang, Xinxin; Bi, Yanfeng
Thiacalixarene-supported M20V8 (M = Fe, Co, Ni) square pyramid nanocages for visible light photothermal catalysis
Chemical Communications, 2025, 61, 9266-9269
7134571 CIFC22 H27 N O4P 21 21 217.9888; 9.7763; 26.1295
90; 90; 90
2040.74Smith, Lydia G.; Di Leva, Dalila; Shaw, Lloyd A.; Hughes, Eric; Kenwright, Alan M.; Beeby, Andrew; Wilson, Mark R.; Mahon, Clare S.
An unexpected chlorination of an organic sunscreen
Chemical Communications, 2025, 61, 9314-9317
7134572 CIFC24 H30.788 Cl0.212 N O4I 1 2/a 115.8699; 7.9825; 33.9739
90; 96.083; 90
4279.6Smith, Lydia G.; Di Leva, Dalila; Shaw, Lloyd A.; Hughes, Eric; Kenwright, Alan M.; Beeby, Andrew; Wilson, Mark R.; Mahon, Clare S.
An unexpected chlorination of an organic sunscreen
Chemical Communications, 2025, 61, 9314-9317
7134573 CIFC17 H14 F O3 P SP 21 21 217.7392; 13.4287; 15.1509
90; 90; 90
1574.6Paul, Tripti; Basak, Shubhajit; Nanjegowda, Maniya V.; Punniyamurthy, Tharmalingam
Cascade heteroarylation/annulation of arylphosphonic acid monoesters with benzothiophenes: access to benzothieno-fused oxaphosphacycles
Chemical Communications, 2025, 61, 9480-9483
7134574 CIFC5 H6 N O8 UP 1 21/n 16.109; 16.627; 8.964
90; 92.301; 90
909.8Gu, Qinyan; Lei, Ji; Deng, Wenjie; Zhang, Heyao; Zhang, Zhi-Hui; Lu, Huangjie; Hu, Baowei; Xie, Jian
A uranyl-based luminescent dosimeter for ultralow-dose tracking of UV and X-ray radiation
Chemical Communications, 2025, 61, 9322-9325
7134575 CIFC5 H5 N O8 UP 1 21/n 16.1; 16.6677; 8.9638
90; 92.771; 90
910.31Gu, Qinyan; Lei, Ji; Deng, Wenjie; Zhang, Heyao; Zhang, Zhi-Hui; Lu, Huangjie; Hu, Baowei; Xie, Jian
A uranyl-based luminescent dosimeter for ultralow-dose tracking of UV and X-ray radiation
Chemical Communications, 2025, 61, 9322-9325
7134576 CIFC5 H7 N7P b c a6.906; 12.145; 15.993
90; 90; 90
1341.39Nehe, Sagar; Yadav, Abhishek Kumar; Ghule, Vikas D.; Dharavath, Srinivas
Trinitromethyl- and nitramino-substituted triazolo-pyridazines: synthesis and energetic performance
Chemical Communications, 2025, 61, 9047-9050
7134577 CIFC6 H2 Cl N7 O6P -19.172; 9.4996; 13.2063
104.376; 97.79; 102.786
1064.67Nehe, Sagar; Yadav, Abhishek Kumar; Ghule, Vikas D.; Dharavath, Srinivas
Trinitromethyl- and nitramino-substituted triazolo-pyridazines: synthesis and energetic performance
Chemical Communications, 2025, 61, 9047-9050
7134578 CIFC26 H21 Cl6 N O4P n a 2124.004; 7.0053; 31.8407
90; 90; 90
5354.18Tanioka, Masaru; Kitamura, Fumino; Oyama, Masaya; Chen, Shiyu; Ohishi, Yuki; Yamada, Tsuyoshi; Matsuya, Yuji
Design strategy for tautomerization-based small panchromatic molecules
Chemical Communications, 2025, 61, 9298-9301
7134579 CIFC32 H30 F6 N2 O7P 1 c 110.3718; 56.7017; 16.5454
90; 105.472; 90
9377.71Tanioka, Masaru; Kitamura, Fumino; Oyama, Masaya; Chen, Shiyu; Ohishi, Yuki; Yamada, Tsuyoshi; Matsuya, Yuji
Design strategy for tautomerization-based small panchromatic molecules
Chemical Communications, 2025, 61, 9298-9301
7134580 CIFC44 H31 Cl2 O PP -18.9149; 12.5272; 15.9069
104.806; 90.682; 96.21
1705.95Higashino, Tomohiro; Minobe, Riku; Machino, Tomoya; Imahori, Hiroshi
Unexpected cyclization of β-(hydroxymethyl)phosphole into 1-phospha-1,6a-dihydrophosphapentalene: a fused 1,3-butadiene-based luminophore
Chemical Communications, 2025, 61, 9420-9423
7134581 CIFC35 H25 O PP 1 21/c 18.798; 15.004; 19.105
90; 94.067; 90
2515.6Higashino, Tomohiro; Minobe, Riku; Machino, Tomoya; Imahori, Hiroshi
Unexpected cyclization of β-(hydroxymethyl)phosphole into 1-phospha-1,6a-dihydrophosphapentalene: a fused 1,3-butadiene-based luminophore
Chemical Communications, 2025, 61, 9420-9423
7134582 CIFC43 H29 O PP 1 21/c 19.9397; 18.8675; 15.917
90; 94.485; 90
2975.9Higashino, Tomohiro; Minobe, Riku; Machino, Tomoya; Imahori, Hiroshi
Unexpected cyclization of β-(hydroxymethyl)phosphole into 1-phospha-1,6a-dihydrophosphapentalene: a fused 1,3-butadiene-based luminophore
Chemical Communications, 2025, 61, 9420-9423
7134583 CIFC40 H60 K Li N4 O P2P -112.0377; 12.2718; 14.9623
90.125; 107.078; 100.987
2070.12Crabbe, Michelle H.; O’Meara, Danielle; Kennedy, Alan R.; Weetman, Catherine E.; Mulvey, Robert E.
[(TMEDA)Li(μ-PPh2)2K(TMEDA)(THF)]: a heterobimetallic molecular lithium–potassium phosphide complex
Chemical Communications, 2025, 61, 9436-9439
7134584 CIFC49 H51.88 Br0.56 Cd N9 O12.44F d d d :29.679; 36.891; 54.555
90; 90; 90
19480Tanabe, Tappei; Qu, Liyuan; Ueno, Kenta; Takaishi, Shinya; Yamashita, Masahiro; Hijikata, Yuh; Matsuda, Ryotaro; Sakamoto, Ryota; Iguchi, Hiroaki
Uncommon quadruple stacking topology in a honeycomb-sheet MOF compatible with through-space conduction
Chemical Communications, 2025, 61, 9500-9503
7134585 CIFC21 H21 N O4P 1 21 16.22346; 22.0539; 13.8854
90; 101.653; 90
1866.51Sui, Kaixia; Jiang, Shiliang; Leng, Yuting; Wu, Yusheng; Wu, Yangjie
Photoredox catalyzed three-component tandem cyclization of 1,5-dienes with α-keto acids and water to access pyrrolidinones
Chemical Communications, 2025, 61, 9456-9459
7134586 CIFC44 H42 F6 Ir N3 O P2P -110.7418; 13.3809; 15.7147
103.603; 109.915; 91.657
2049.36Fayafrou, Oussama; Zanzi, Juliette; Duhayon, Carine; Sortais, Jean-Baptiste; Baslé, Olivier; Canac, Yves
Cyclometallated phosphonium ylide-based iridium(iii) photocatalysts
Chemical Communications, 2025, 61, 9932-9935
7134587 CIFC42 H26 F16 Ir N3 P2P 1 21/n 113.2187; 15.435; 20.4572
90; 108.506; 90
3958.07Fayafrou, Oussama; Zanzi, Juliette; Duhayon, Carine; Sortais, Jean-Baptiste; Baslé, Olivier; Canac, Yves
Cyclometallated phosphonium ylide-based iridium(iii) photocatalysts
Chemical Communications, 2025, 61, 9932-9935
7134588 CIFC25 H21 N O2 SP 21 21 215.1889; 17.9266; 21.5874
90; 90; 90
2008.05Huang, Xiang; Yang, Jin-Ming
Lewis acid-catalyzed intramolecular cyclization of 7-alkynylcycloheptatrienes with carbonyls: access to 3,4-disubstituted 2,5-dihydropyrroles
Chemical Communications, 2025, 61, 9686-9689
7134589 CIFC25 H23 N O3 SP 1 21/c 113.6274; 13.9439; 22.4596
90; 99.933; 90
4203.8Huang, Xiang; Yang, Jin-Ming
Lewis acid-catalyzed intramolecular cyclization of 7-alkynylcycloheptatrienes with carbonyls: access to 3,4-disubstituted 2,5-dihydropyrroles
Chemical Communications, 2025, 61, 9686-9689
7134590 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7459; 13.1934; 17.3101
90; 93.237; 90
4274.34Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134591 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7418; 13.2211; 17.2876
90; 93.051; 90
4277.57Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134592 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7443; 13.2668; 17.2602
90; 92.809; 90
4287.06Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134593 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7466; 13.2327; 17.2816
90; 92.997; 90
4281.15Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134594 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7437; 13.2961; 17.2393
90; 92.596; 90
4291.94Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134595 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7412; 13.2846; 17.2461
90; 92.697; 90
4288.99Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134596 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7459; 13.308; 17.2328
90; 92.512; 90
4294.9Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134597 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7558; 13.323; 17.2355
90; 92.421; 90
4303Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134598 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.758; 13.3886; 17.1946
90; 91.757; 90
4316.3Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134599 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7584; 13.3728; 17.1991
90; 91.925; 90
4312Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134600 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7462; 13.2001; 17.3014
90; 93.184; 90
4274.65Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134601 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7603; 13.4307; 17.1661
90; 91.022; 90
4324.55Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134602 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7454; 13.2104; 17.2938
90; 93.134; 90
4276.13Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134603 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.745; 13.2533; 17.2693
90; 92.876; 90
4284.86Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134604 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.741; 13.2729; 17.2493
90; 92.731; 90
4285.85Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134605 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7457; 13.2436; 17.2756
90; 92.917; 90
4283.29Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134606 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7559; 13.3309; 17.2217
90; 92.314; 90
4302.48Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134607 CIFC7 H15 B10 NP n a 2114.5733; 11.9319; 7.2118
90; 90; 90
1254.04Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134608 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7566; 13.3398; 17.211
90; 92.214; 90
4303.14Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134609 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7581; 13.3559; 17.208
90; 92.085; 90
4308.29Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134610 CIFC12 H18 B10 N2P 1 21/c 115.7644; 10.3772; 9.8017
90; 96.299; 90
1593.78Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134611 CIFC12 H18 B10 N2P 1 21/c 17.9697; 10.5301; 9.6227
90; 106.128; 90
775.77Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134612 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7575; 13.4154; 17.1735
90; 91.283; 90
4320.45Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134613 CIFC17 H20 B5 N2 O5 ZnC 1 2/c 118.7567; 13.4002; 17.1866
90; 91.538; 90
4318.18Windsor, Hunter J.; Carraro, Thomas J. C.; Walwyn, Robert J.; Rendina, Louis M.; Kepert, Cameron J.
A new carborane scaffold for assembling metal–organic frameworks
Chemical Communications, 2025, 61, 9634-9637
7134614 CIFC10 H18 Br NP 1 21/n 111.3591; 6.3615; 14.7799
90; 103.823; 90
1037.08Xu, Wei-Jian; Alikin, Denis; Fang, Zi-Luo; Romanyuk, Konstantin; Verissimo, Luis; Zelenovskii, Pavel; Zhang, Wei-Xiong; Kholkin, Andrei; Rocha, João
Unlocking ferroelectricity in a metal-free adamantane derivative via targeted symmetry reduction
Chemical Communications, 2025, 61, 9286-9289
7134615 CIFC10 H18 Br NP 1 21 17.7656; 6.4026; 10.1581
90; 102.526; 90
493.04Xu, Wei-Jian; Alikin, Denis; Fang, Zi-Luo; Romanyuk, Konstantin; Verissimo, Luis; Zelenovskii, Pavel; Zhang, Wei-Xiong; Kholkin, Andrei; Rocha, João
Unlocking ferroelectricity in a metal-free adamantane derivative via targeted symmetry reduction
Chemical Communications, 2025, 61, 9286-9289
7134616 CIFC10 H18 Br NP 1 21/m 17.8338; 6.447; 10.1896
90; 102.173; 90
503.05Xu, Wei-Jian; Alikin, Denis; Fang, Zi-Luo; Romanyuk, Konstantin; Verissimo, Luis; Zelenovskii, Pavel; Zhang, Wei-Xiong; Kholkin, Andrei; Rocha, João
Unlocking ferroelectricity in a metal-free adamantane derivative via targeted symmetry reduction
Chemical Communications, 2025, 61, 9286-9289
7134617 CIFC46 H35 N4C 1 2/c 134.526; 6.0518; 34.924
90; 91.885; 90
7293Upadhyay, Manoj; Deka, Raktim; Ray, Debdas
Charge transfer alteration and white light emission in photochromic triphenylamine-norbornadiene-triazine switch
Chemical Communications, 2025, 61, 9674-9677
7134618 CIFC28 H28 O2 S2P b c a7.8306; 30.1726; 30.2525
90; 90; 90
7147.74Shiokawa, Takumi; Fukazawa, Aiko
Rethinking aromaticity of reduced thienoquinoids: insights from an S-Pechmann dye dianion
Chemical Communications, 2025, 61, 10095-10098
7134619 CIFC28 H30 S2P 1 21/c 113.285; 6.0285; 15.0211
90; 105.958; 90
1156.66Shiokawa, Takumi; Fukazawa, Aiko
Rethinking aromaticity of reduced thienoquinoids: insights from an S-Pechmann dye dianion
Chemical Communications, 2025, 61, 10095-10098
7134620 CIFC68 H108 K2 N4 O15 S2P -111.408; 12.0912; 14.9019
73.723; 69.097; 70.197
1776.7Shiokawa, Takumi; Fukazawa, Aiko
Rethinking aromaticity of reduced thienoquinoids: insights from an S-Pechmann dye dianion
Chemical Communications, 2025, 61, 10095-10098
7134621 CIFC50 H34 Cl4 N4C m c 2129.934; 15.0767; 8.7946
90; 90; 90
3969.06Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134622 CIFC56 H40 N4C m c 2129.6967; 15.1954; 8.9495
90; 90; 90
4038.49Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134623 CIFC56 H40 N4P n a 2115.903; 28.781; 8.8898
90; 90; 90
4068.9Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134624 CIFC55 H38 N4C m c 2130.1235; 14.8515; 8.8086
90; 90; 90
3940.78Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134625 CIFC66 H48 N4P 1 21/c 129.0124; 9.1087; 19.0026
90; 107.111; 90
4799.45Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134626 CIFC56 H40 N4P 1 21 115.4109; 8.6328; 16.4219
90; 111.528; 90
2032.34Chen, Jin-Fa; Wang, Yuxuan; Shi, Bingbing; Yao, Hong; Wei, Tai-Bao; Lin, Qi
A V-shaped small molecule-based crystalline nonporous supramolecular organic framework for capturing benzene-based contaminants
Chemical Communications, 2025, 61, 9912-9915
7134627 CIFC56 H64 O12P 1 21/n 110.0684; 17.5734; 26.7319
90; 96.356; 90
4700.8Gharpure, Santosh J.; Gupta, Krishna S.; Yadav, Rakhi
Lewis acid-promoted cascade reactions of cyclopropenes: a unified approach to stereoselective synthesis of cyclic ethers and oxaspirolactones
Chemical Communications, 2025, 61, 9705-9708
7134628 CIFC10 H15 N11 O5P -16.616; 9.4274; 12.6888
81.897; 87.036; 79.394
769.86Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134629 CIFC21 H39 N23 O8P 1 21/n 113.9342; 14.6464; 16.6514
90; 98.281; 90
3362.88Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134630 CIFC8 H10 N10 O7P 1 21/c 15.1692; 19.0438; 13.7975
90; 96.071; 90
1350.63Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134631 CIFC5 H10 Cl2 N10 O8P -18.2784; 9.1672; 9.3028
92.785; 90.887; 103.678
684.89Jiang, Xiu’e; Fan, Mingren; Wang, Ruihui; Wang, Yi; Zhang, Qinghua
Facile synthesis of bicyclic heat-resistant energetic materials via a C–N coupling strategy
Chemical Communications, 2025, 61, 9924-9927
7134632 CIFC81 H119 I S2 UP -113.4289; 14.022; 21.405
85.41; 73.355; 80.472
3806.1Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134633 CIFC72 H98 K S2 UP 1 21/n 114.272; 19.9414; 24.2485
90; 98.185; 90
6830.9Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134634 CIFC72 H98 S2 UP -19.864; 17.52; 20.169
87.762; 84.587; 85.962
3460Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134635 CIFC92 H124 N2 O2 S2 UC 1 2/c 130.491; 18.735; 18.433
90; 113.138; 90
9683Queen, Joshua D.; Ma, Eric; Rajabi, Ahmadreza; Ziller, Joseph W.; Furche, Filipp; Evans, William J.
Four-electron oxidation and one-electron reduction of the bis(terphenylthiolate) U(II) complex, U(SAr<sup>iPr6</sup>)<sub>2</sub> [Ar<sup>iPr6</sup> = C<sub>6</sub>H<sub>3</sub>-2,6-(C<sub>6</sub>H<sub>2</sub>-2,4,6-<sup>i</sup>Pr<sub>3</sub>)<sub>2</sub>].
Chemical communications (Cambridge, England), 2025, 61, 10319-10322
7134636 CIFC26 H25 Cl2 Cu N3 O6P -19.1916; 11.5805; 13.772
70.993; 85.658; 72.744
1323.3Dutta, Lesa; Das, Avijit; Hasan, Babar; Paria, Sayantan; Mondal, Dhrubajyoti
Comparing electrocatalytic and chemical oxygen reduction reaction by a molecular copper complex
Chemical Communications, 2025, 61, 10158-10161
7134637 CIFC52 H51 Cl6 Cu2 N6 O22C 1 c 112.8921; 16.3316; 29.441
90; 96.406; 90
6160.1Dutta, Lesa; Das, Avijit; Hasan, Babar; Paria, Sayantan; Mondal, Dhrubajyoti
Comparing electrocatalytic and chemical oxygen reduction reaction by a molecular copper complex
Chemical Communications, 2025, 61, 10158-10161
7134638 CIFC25 H23 N O SeP -19.2189; 10.9073; 11.3585
97.835; 101.293; 106.079
1053.97MohanaKrishna, Silari; Prasad, Vadla Shiva; Ranga Rao, Vadithya; Ravi, Dharavath; Kumar, Chelukalapally Anil; Adiyala, Praveen Reddy
Stereoselective synthesis of chalcogen-tethered <i>γ</i>-lactams <i>via</i> 5-<i>exo-dig</i> cyclisation under visible-light irradiation.
Chemical communications (Cambridge, England), 2025, 61, 10363-10366
7134639 CIFC36 H55 Al N2P 1 21/n 110.4055; 25.6624; 12.8303
90; 103.621; 90
3329.7Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134640 CIFC30 H43 Al N2A e m 215.6163; 22.5091; 7.737
90; 90; 90
2719.6Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134641 CIFC28 H39 Al N2P 21 21 2116.5787; 20.7155; 29.815
90; 90; 90
10239.5Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134642 CIFC50 H54 O4 P2P 1 21 15.7275; 20.7047; 17.3578
90; 91.347; 90
2057.8Chen, Yiwen; Pang, Ziyuan; Li, Gege; Yang, Xiaobo; Yan, Wenliang; Li, Qifeng; Dong, Xuan; Ma, Xiaoli; Yang, Zhi
Alkylaluminium-catalyzed regioselective hydrophosphinylation of α,β-unsaturated ketones into γ-ketophosphine oxides
Chemical Communications, 2025, 61, 9666-9669
7134643 CIFC15 H13 N O2 SC 1 2/c 113.5806; 13.6; 14.5161
90; 101.264; 90
2629.4Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134644 CIFC21 H19 N O5P 1 21/c 118.065; 7.471; 13.402
90; 97.245; 90
1794.34Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134645 CIFC21 H17 N O3 SP -19.7767; 13.9453; 14.5788
103.754; 99.474; 108.72
1764.7Reddy, Chada Raji; Enagandhula, Damodar; Ramaraju, Andhavaram; Shivakrishna, Avula; Adepu, Raju
Divergent [3+2] annulations of oxime acetates with thioaurones/aurones leading to benzothiazino-/benzoyl-pyrroles
Chemical Communications, 2025, 61, 10162-10165
7134646 CIFC82 H78 Fe2 N2 P6P 1 21/c 122.7264; 15.2574; 21.1376
90; 108.97; 90
6931.3Smythe, Nathan C.; Mondal, Joydeb; Duque, Juan G.; Feller, Russell K.; Flores, Marco; Gordon, John C.; Henson, Neil J.; Paz-Pasternak, Moshe; Rein, Francisca N.; Scott, Brian L.; Taylor, R. Dean; Trovitch, Ryan J.
Historical account of dinitrogen-bridged diiron complex synthesis using a commercial tripodal ligand
Chemical Communications, 2025, 61, 9908-9911
7134647 CIFC9 H19 B11 Cl11 F6 N O4 S2 Si2P -115.9754; 16.3642; 17.2574
71.799; 72.239; 62.887
3743.54Daum, Joshua H.; Bhuvanesh, Nattamai; Ozerov, Oleg V.
Structure and reactivity of a triflimide-bridged bis(trimethylsilyl) cation.
Chemical communications (Cambridge, England), 2025, 61, 10816-10818
7134648 CIFC29 H39 Mo N3 O3 P2C 1 c 112.2585; 21.027; 11.8947
90; 102.628; 90
2991.8Benedict, Rory J.; Heiden, Zachariah M.; Stephens, David N.; Arulsamy, Navamoney; Mock, Michael T.
Catalytic NH<sub>3</sub> oxidation to N<sub>2</sub> by hydrogen atom abstraction using a low-valent molybdenum complex.
Chemical communications (Cambridge, England), 2025, 61, 10315-10318
7134649 CIFC33 H44 F Mo N3 O3 P2P 1 21/c 114.868; 13.21; 18.026
90; 108.924; 90
3349.1Benedict, Rory J.; Heiden, Zachariah M.; Stephens, David N.; Arulsamy, Navamoney; Mock, Michael T.
Catalytic NH<sub>3</sub> oxidation to N<sub>2</sub> by hydrogen atom abstraction using a low-valent molybdenum complex.
Chemical communications (Cambridge, England), 2025, 61, 10315-10318
7134650 CIFC30 H21 N OP 1 21/c 19.762; 19.29; 13.15
90; 110.326; 90
2322.1Ghosh, Suman; Rooj, Arnab; Deb, Shreya; Ganesh, Venkataraman
Cu<sup>(I)</sup>/Pd<sup>(0)</sup> cooperative catalysis enabled regioselective C(sp<sup>2</sup>)-carboboration of 1,3-diynes.
Chemical communications (Cambridge, England), 2025, 61, 10323-10326
7134651 CIFC20 H20 Cl In N2 O4P 1 21/c 113.5529; 7.6912; 19.3672
90; 106.088; 90
1939.74Baumeyer, Oliver; Wu, Andrew; Pandya, Aastha; Nelson, Peter; Hillesheim, Patrick C.; Zeller, Matthias; Carignan, Gia M.; Li, Jing; Ki, Daniel W.
Aggregation-induced emission-active indium complex as fluorescent turn-off chemosensor for perfluoroalkyl substances
Chemical Communications, 2025, 61, 10170-10173
7134652 CIFC28 H34 I2 N2 O2C 1 2/c 131.5672; 4.6473; 18.6492
90; 101.217; 90
2683.62Skonieczny, Kamil; Kielesiński, Łukasz; Grzybowski, Marek; Gryko, Daniel T.
Polysubstitution of dipyrrolonaphthyridinediones as a potent strategy towards strongly emitting fluorophores
Chemical Communications, 2025, 61, 10178-10181
7134653 CIFC28 H34 Br2 N2 O2P -14.5767; 9.1416; 16.102
74.174; 89.89; 76.786
629.67Skonieczny, Kamil; Kielesiński, Łukasz; Grzybowski, Marek; Gryko, Daniel T.
Polysubstitution of dipyrrolonaphthyridinediones as a potent strategy towards strongly emitting fluorophores
Chemical Communications, 2025, 61, 10178-10181
7134654 CIFC16 H20 Li N2 O2C 1 2/c 128.5128; 11.9757; 20.7828
90; 118.145; 90
6257.4Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134655 CIFC16 H20 Li N2 O2C 1 2/c 114.939; 5.9609; 18.837
90; 101.844; 90
1641.7Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134656 CIFC12 H12 N2 Na OC 1 2/c 120.749; 9.4724; 11.9937
90; 101.2; 90
2312.4Suo, Meng-Ting; Fleege, Jouke A.; Yutronkie, Nathan J.; Nadurata, Vincent L.; Chernyshov, Dmitry; Rouzières, Mathieu; Mailman, Aaron; Clérac, Rodolphe; Dechambenoit, Pierre
Syntheses and characterisation of terephthalonitrile radical salts
Chemical Communications, 2025, 61, 9972-9975
7134657 CIFC12 H32 Ag5 I7 N2P 3212.1737; 12.1737; 19.4498
90; 90; 120
2496.3Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134658 CIFC12 H32 Ag5 I7 N2P 3212.0472; 12.0472; 19.178
90; 90; 120
2410.5Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134659 CIFC12 H32 Ag5 I7 N2P 3112.0456; 12.0456; 19.1296
90; 90; 120
2403.8Liu, Tong; Zheng, Yong-Shen; Liang, Xiao-Wen; Yao, Zhao-Quan; Zhao, Jiong-Peng; Liu, Fu-Chen
One-dimensional silver iodide homo-helical chains induced by achiral ammonium featuring second-order optical nonlinearity.
Chemical communications (Cambridge, England), 2025, 61, 10327-10330
7134660 CIFC31 H17 Br Cl2 O2C 1 2 143.9803; 8.1757; 14.3605
90; 105.417; 90
4977.8Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134661 CIFC35 H36 N O7P 4316.7397; 16.7397; 10.5216
90; 90; 90
2948.34Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134662 CIFC32 H31 N O7P 1 21/c 18.2745; 33.3961; 10.3175
90; 104.258; 90
2763.27Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134663 CIFC32 H29 N O7P -110.3074; 10.562; 12.7619
102.425; 99.324; 101.043
1301.4Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134664 CIFC32 H29 Cl2 N O6P 1 21 17.0286; 19.9167; 10.5748
90; 103.574; 90
1438.98Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134665 CIFC33 H29 Cl2 N O4P 17.2896; 9.999; 10.356
90.903; 104.271; 97.532
724.321Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134666 CIFC32 H29 F O5P 1 21/c 110.7735; 28.0445; 8.8667
90; 104.427; 90
2594.48Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134667 CIFC62 H58 N2 O16P 1 21/n 122.0372; 9.6693; 26.7286
90; 110.983; 90
5317.76Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134668 CIFC32 H29 N O7P 21 21 2110.51673; 11.3459; 22.2044
90; 90; 90
2649.47Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134669 CIFC31 H28 Br2 O5P 1 21/c 114.4532; 14.9913; 12.6854
90; 101.185; 90
2696.37Xu, Ke; Zhao, Jiayi; Lin, Kejun; Zhu, Tingshun
Carbene-organocatalyzed enantioselective [5+5] annulation of dienols and dienals towards tetrahydroisochromen-1-ones.
Chemical communications (Cambridge, England), 2025, 61, 10602-10605
7134670 CIFC35 H25 N O4P -18.6029; 12.5447; 12.7442
75.647; 81.569; 89.219
1317.67Yu, Rongjing; Xia, Ting; Shen, Ruwei; Zhu, Shugao
Diastereoselective synthesis of succinimide-fused polycycles <i>via</i> intermolecular interception of indanone-allene intermediates with maleimides.
Chemical communications (Cambridge, England), 2025, 61, 10335-10338
7134671 CIFC45 H32 N2 O6P 1 21/c 112.264; 25.385; 13.1328
90; 93.156; 90
4082.3Yu, Rongjing; Xia, Ting; Shen, Ruwei; Zhu, Shugao
Diastereoselective synthesis of succinimide-fused polycycles <i>via</i> intermolecular interception of indanone-allene intermediates with maleimides.
Chemical communications (Cambridge, England), 2025, 61, 10335-10338
7134672 CIFC100 H107 Si4P 1 21 112.922; 20.382; 16.403
90; 92.435; 90
4316.3Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134673 CIFC216 H253.84 N8 Si8P 1 21/n 115.836; 14.482; 21.301
90; 91.927; 90
4882Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134674 CIFC105.49 H114.49 Cl2.7 O4.26 Si4P 112.6006; 14.1684; 15.1207
71.243; 73.484; 75.284
2411Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134675 CIFC111.05 H112.8 Cl11.07 O4 Si4P -110.9872; 13.9513; 18.9119
72.067; 86.454; 81.331
2726.2Krøll, Peter Lundgård; Strandfelt, Asger; Jokumsen, Maria Harbo; Nielsen, Mogens Brøndsted
Donor/acceptor-substituted radiaannulene segments of 6,6,12-graphyne
Chemical Communications, 2025, 61, 9416-9419
7134676 CIFC8 H5 Cl4 FP 1 21/n 19.8894; 6.0908; 16.5497
90; 96.434; 90
990.58Miele, Margherita; Castiglione, Davide; Prado-Roller, Alexander; Castoldi, Laura; Pace, Vittorio
Geminal homologative fluorination of carbonyl derivatives <i>en route</i> to 1-fluoro-2-haloethyl skeletons.
Chemical communications (Cambridge, England), 2025, 61, 10792-10795
7134677 CIFC14 H36 Cl4 Cu N2P -17.1278; 7.5; 20.0179
96.906; 91.564; 90.184
1061.94Kusumoto, Sotaro; Nagasawa, Sakura; Suzuki, Ryo; Tachibana, Masaru; Tsuji, Yuta; Zenno, Hikaru; Nakashima, Yuto; Hayami, Shinya; Kim, Yang; Koide, Yoshihiro
Ferromagnetic and plastically deformable organic-inorganic hybrid crystal: (C<sub>7</sub>H<sub>9</sub>NH<sub>3</sub>)<sub>2</sub>CuCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10303-10306
7134678 CIFC12 H32 Cl6 N2 SnP n m a12.3494; 7.306; 26.6362
90; 90; 90
2403.24Kusumoto, Sotaro; Nagasawa, Sakura; Suzuki, Ryo; Tachibana, Masaru; Tsuji, Yuta; Zenno, Hikaru; Nakashima, Yuto; Hayami, Shinya; Kim, Yang; Koide, Yoshihiro
Ferromagnetic and plastically deformable organic-inorganic hybrid crystal: (C<sub>7</sub>H<sub>9</sub>NH<sub>3</sub>)<sub>2</sub>CuCl<sub>4</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10303-10306
7134679 CIFC28 H23 N O3P 1 21/c 113.893; 20.91; 7.841
90; 100.45; 90
2240Hu, Kai; Wu, Haijian; Sun, Manman; Zhang, Jing; Wang, Zhiming; Yang, Jianguo; Zhu, Gangguo; Huang, Guo-Bo
HFIP-promoted synthesis of bicyclo[2.1.1]-hexanes through formal [2π+2σ] cycloaddition of bicyclo[1.1.0]butanes with α-cyano chalcones.
Chemical communications (Cambridge, England), 2025, 61, 10375-10378
7134680 CIFC37 H64 O8 SiP 21 21 217.3169; 13.642; 38.8677
90; 90; 90
3879.7Sennari, Goh; Watanabe, Akito; Ōno, Takanori; Oshita, Jun; Noguchi, Yoshihiko; Hirose, Tomoyasu; Sunazuka, Toshiaki
Macrocyclic skeletal modification approach to the anti-trypanosomal macrolides, actinoallolides.
Chemical communications (Cambridge, England), 2025, 61, 10367-10370
7134681 CIFC49 H74 Cu N12 O10P 1 21 17.0448; 24.6484; 15.2708
90; 94.92; 90
2641.9Kieninger, Christoph; Wurst, Klaus; Leitner, Daniel; Peters, Luis P.; Dinu, Dennis F.; Wiedemair, Markus; Zaretzke, Marc-Kevin; Bröring, Martin; Hohloch, Stephan; Liedl, Klaus R.; Kräutler, Bernhard
Encasing the paramagnetic copper(II)-ion by the ring-contracted corrin ligand of vitamin B<sub>12</sub>.
Chemical communications (Cambridge, England), 2025, 61, 10606-10609
7134682 CIFC14 H14 Cl N5 Pt SP 1 21/n 111.3054; 8.7072; 15.9931
90; 101.726; 90
1541.48Sheernaly, Nandan; Steinbrueck, Axel; Ochs, Jasmine; Peeters, Frank; Fiedler, Ronja; Narberhaus, Franz; Heinen-Weiler, Jacqueline; Metzler-Nolte, Nils
Design and application of a non-toxic platinum derivative of the metal chelator Dp44mT for use as a long-term stable lysosome tracker
Chemical Communications, 2025, 61, 9964-9967
7134683 CIFC25 H42 O3 SiP 21 21 219.6772; 10.2693; 24.1618
90; 90; 90
2401.15Chen, Louxi; Zhang, Chao-Han; Liu, Junyang; Li, Chuang-Chuang
Asymmetric synthesis of venezuelaene's core with a <i>trans</i>-fused [5-5] ring system.
Chemical communications (Cambridge, England), 2025, 61, 10823-10826

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