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

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