Crystallography Open Database

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1576078 CIFC10 H26 B6 OsP 1 21 17.1489; 13.4533; 8.2583
90; 108.226; 90		754.41Kar, Ketaki; Joshi, Gaurav; Jemmis, Eluvathingal D.; Ghosh, Sundargopal
All-boron analogue of planar benzene on an osmium template.
Chemical science, 2026, 17, 196-204
1576079 CIFC10 H24 B4 OsP 21 21 218.1325; 12.8806; 14.1056
90; 90; 90		1477.58Kar, Ketaki; Joshi, Gaurav; Jemmis, Eluvathingal D.; Ghosh, Sundargopal
All-boron analogue of planar benzene on an osmium template.
Chemical science, 2026, 17, 196-204
1576080 CIFC10 H27 B5 OsP n a 2113.9545; 8.2607; 13.1269
90; 90; 90		1513.19Kar, Ketaki; Joshi, Gaurav; Jemmis, Eluvathingal D.; Ghosh, Sundargopal
All-boron analogue of planar benzene on an osmium template.
Chemical science, 2026, 17, 196-204
1576135 CIFC Br3 N2 Pb0.84 Sn0.16P m -3 m5.9577; 5.9577; 5.9577
90; 90; 90		211.46Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576136 CIFC Br3 N2 Pb0.21 Sn0.79P m -3 m5.959; 5.959; 5.959
90; 90; 90		211.6Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576137 CIFC1.232 H6.159 Br3 N2 Pb0.22 Sn0.664P m -3 m6.0213; 6.0213; 6.0213
90; 90; 90		218.31Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576138 CIFC0.888 H0 Br3 N1.759 Sn0.944P m -3 m6.0226; 6.0226; 6.0226
90; 90; 90		218.45Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576139 CIFC1.121 H5.602 Br3 N2 Pb0.418 Sn0.522P m -3 m6.0075; 6.0075; 6.0075
90; 90; 90		216.81Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576140 CIFC1.356 H6.78 Br3 N2 Pb0.422 Sn0.4P m -3 m6.0315; 6.0315; 6.0315
90; 90; 90		219.42Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576141 CIFC Br3 N2 Pb0.5 Sn0.5P m -3 m5.9617; 5.9617; 5.9617
90; 90; 90		211.89Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576142 CIFC1.245 H6.225 Br3 N2 Pb0.693 Sn0.185P m -3 m6.0133; 6.0133; 6.0133
90; 90; 90		217.44Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576143 CIFC1.45 H7.254 Br3 N2 Pb0.607 Sn0.168P m -3 m6.0566; 6.0566; 6.0566
90; 90; 90		222.17Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576144 CIFC1.11 H5.552 Br3 N2 Pb0.753 Sn0.187P m -3 m6.0203; 6.0203; 6.0203
90; 90; 90		218.2Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576145 CIFC1.35 H6.75 Br3 N2 Pb0.648 Sn0.177P m -3 m6.0379; 6.0379; 6.0379
90; 90; 90		220.12Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576146 CIFC1.198 H5.979 Br3 N2 Sn0.902P m -3 m6.0324; 6.0324; 6.0324
90; 90; 90		219.52Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576147 CIFC1.275 H6.378 Br3 N2 Sn0.862P m -3 m6.0349; 6.0349; 6.0349
90; 90; 90		219.79Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576148 CIFC1.332 H6.65 Br3 N2 Sn0.835P m -3 m6.0371; 6.0371; 6.0371
90; 90; 90		220.03Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576149 CIFC1.38 H6.53 Br3 N2 Pb0.422 Sn0.425P m -3 m6.0413; 6.0413; 6.0413
90; 90; 90		220.491Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576150 CIFC1.093 H5.5 Br3 N2 Pb0.237 Sn0.716P m -3 m5.997; 5.997; 5.997
90; 90; 90		215.68Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576151 CIFC1.341 H6.684 Br3 N2 Pb0.22 Sn0.611P m -3 m6.0644; 6.0644; 6.0644
90; 90; 90		223.03Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576152 CIFC1.275 H6.378 Br3 N2 Pb0.225 Sn0.638P m -3 m6.0411; 6.0411; 6.0411
90; 90; 90		220.47Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576153 CIFC1.226 H5.966 Br3 N2 Pb0.429 Sn0.474P m -3 m6.0236; 6.0236; 6.0236
90; 90; 90		218.56Balvanz, Adam; Pournara, Anastasia; Reynolds, Robert P.; Meza, Patricia E.; Malliakas, Christos D.; Fletcher, Jared D.; Seshadri, Ram; Dravid, Vinayak P.; Kanatzidis, Mercouri G.
Tuning optical properties and local lone-pair off-centering in "hollow" FA<sub>1-<i>x</i></sub> {<i>en</i>} <sub><i>x</i></sub> Pb <sub><i>η</i>-<i>y</i></sub> Sn <sub><i>y</i></sub> Br<sub>3</sub> perovskites.
Chemical science, 2026, 17, 526-543
1576154 CIFC93 H142 N6 P6C 1 2/c 148.656; 15.8779; 48.7057
90; 93.165; 90		37570.4Meier, David C.; García-Romero, Álvaro; González-Pinardo, Daniel; Rees, Nicholas H.; Lovstedt, Alex; Fernández, Israel; Goicoechea, Jose M.
Exceptionally large "through-space" nuclear spin coupling in a 2,4,6-tri(phosphanyl)-1,3,5-triphosphabenzene.
Chemical science, 2026, 17, 544-554
1576155 CIFC54 H76 N4 P4P -113.5678; 13.7534; 15.5834
79.661; 86.029; 65.26		2598.1Meier, David C.; García-Romero, Álvaro; González-Pinardo, Daniel; Rees, Nicholas H.; Lovstedt, Alex; Fernández, Israel; Goicoechea, Jose M.
Exceptionally large "through-space" nuclear spin coupling in a 2,4,6-tri(phosphanyl)-1,3,5-triphosphabenzene.
Chemical science, 2026, 17, 544-554
1576156 CIFC87 H128 N6 P6P 1 21/c 112.8201; 21.8399; 30.291
90; 92.626; 90		8472.3Meier, David C.; García-Romero, Álvaro; González-Pinardo, Daniel; Rees, Nicholas H.; Lovstedt, Alex; Fernández, Israel; Goicoechea, Jose M.
Exceptionally large "through-space" nuclear spin coupling in a 2,4,6-tri(phosphanyl)-1,3,5-triphosphabenzene.
Chemical science, 2026, 17, 544-554
1576157 CIFC24 H27 Cl3 Ir N3 OP n a 2116.5538; 8.328; 36.149
90; 90; 90		4983.5Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576158 CIFC21 H25 Cl2 Co N3 OP 21 21 218.5814; 11.8073; 21.467
90; 90; 90		2175.1Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576159 CIFC25 H33 Cl Co N3 SP 21 21 2110.7384; 12.7561; 18.1854
90; 90; 90		2491.04Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576160 CIFC25 H33 Cl2 Co N3 SP 1 21 115.7078; 9.7905; 18.7603
90; 114.343; 90		2628.6Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576161 CIFC30 H36 Cl5 Co N3 OP 1 21 114.2795; 10.5999; 21.1288
90; 93.703; 90		3191.4Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576162 CIFC22 H28 Co N3 OP 1 21 111.1019; 8.0219; 12.0462
90; 103.955; 90		1041.15Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576163 CIFC32 H41 Co N4P 21 21 2110.8009; 11.5483; 47.229
90; 90; 90		5891Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576164 CIFC30 H38 Co N3 OP 21 21 219.2773; 14.4865; 20.6304
90; 90; 90		2772.64Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576165 CIFC29 H35 Cl Co N3 OP 112.19; 12.9109; 16.9559
95.359; 91.044; 92.146		2654.4Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576166 CIFC31 H38 Cl2 Co N4P 21 21 2115.7505; 18.8119; 20.1927
90; 90; 90		5983Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576167 CIFC15 H15 N O3 SP 1 21 18.0536; 5.2646; 16.5289
90; 94.986; 90		698.16Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576168 CIFC46 H70 Cl4 Co2 N6 O4P 1 21 113.5345; 10.737; 17.4919
90; 100.729; 90		2497.5Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576169 CIFC39 H57 Cl3 F6 Fe2 N2 O14 S2 Si4P 1 21/c 117.3643; 21.3942; 15.459
90; 93.77; 90		5730.52Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576170 CIFC26 H36 Co N3 OP 1 21 19.3878; 11.3926; 12.0509
90; 102.847; 90		1256.6Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576171 CIFC20 H30 Co N3 OC 1 2 124.2715; 6.0591; 13.7733
90; 108.095; 90		1925.37Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576172 CIFC35 H40 Cl Co N4P 1 21 110.3786; 12.1026; 12.7904
90; 106.534; 90		1540.15Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576173 CIFC25 H33 Cl2 Co N3 OP 1 21 116.9108; 9.8083; 15.5403
90; 97.61; 90		2554.9Zheng, Chenggong; Liu, Jiyong; Wang, Yongtao; Li, Haoran; Wang, Yuwen; Lu, Zhan
The structural parameter of spin states of <i>C</i> <sub>1</sub>-symmetric four-coordinate cobalt complexes: <i>D</i> <sub>4</sub>.
Chemical science, 2026, 17, 492-499
1576185 CIFC111 H112 B2 N4 P2 S2P -111.4849; 14.1923; 16.0109
66.987; 69.582; 75.458		2231.1Hong, Xian-Fang; Wei, Yi; Xing, Hao-Ran; Wang, Yu; Xi, Jia-Qi; Wu, Chen-Yang; Yuan, Li; Li, Cheng-Hui; Zheng, You-Xuan
Phenphosphine-X(O, S, Se) locking multi-resonance thermally activated delayed fluorescence materials.
Chemical science, 2026, 17, 274-282
1576186 CIFC59 H60 B N2 O PP -110.7415; 13.639; 16.481
92.727; 97.742; 99.273		2355.3Hong, Xian-Fang; Wei, Yi; Xing, Hao-Ran; Wang, Yu; Xi, Jia-Qi; Wu, Chen-Yang; Yuan, Li; Li, Cheng-Hui; Zheng, You-Xuan
Phenphosphine-X(O, S, Se) locking multi-resonance thermally activated delayed fluorescence materials.
Chemical science, 2026, 17, 274-282
1576187 CIFC212 H216 B4 Cl8 N8 P4 Se4P -111.912; 19.904; 21.598
105.673; 93.452; 106.204		4683.4Hong, Xian-Fang; Wei, Yi; Xing, Hao-Ran; Wang, Yu; Xi, Jia-Qi; Wu, Chen-Yang; Yuan, Li; Li, Cheng-Hui; Zheng, You-Xuan
Phenphosphine-X(O, S, Se) locking multi-resonance thermally activated delayed fluorescence materials.
Chemical science, 2026, 17, 274-282
1576192 CIFC50 H34 N4 O8 P2P 21 21 2114.0473; 15.0466; 19.4211
90; 90; 90		4104.9Liu, Wenqi; Ling, Zhijie; Liu, Yang-Zi; Deng, Wei-Ping
Catalytic asymmetric construction of remote P or other heteroatom (Si/S) stereogenic axially chiral scaffolds.
Chemical science, 2026, 17, 240-246
1576193 CIFC39 H30 Cl N2 O2 P2C 1 2 116.097; 8.807; 25.224
90; 109.127; 90		3378.5Liu, Wenqi; Ling, Zhijie; Liu, Yang-Zi; Deng, Wei-Ping
Catalytic asymmetric construction of remote P or other heteroatom (Si/S) stereogenic axially chiral scaffolds.
Chemical science, 2026, 17, 240-246
1576195 CIFC19 H13 Br N2 O3 SeP b c a11.205; 8.3911; 37.457
90; 90; 90		3521.8Zhou, Wei; Wang, Yan; Zhang, Shuning; Zhang, Chengwei; Pang, Jiacheng; Hou, Shaoneng; Li, Jie; Yao, Ying; Su, An; Ma, Peixiang; Xu, Hongtao; Hou, Wei
Highly selective and AI-predictable Se-N exchange chemistry between benzoselenazolones and boronic acids for programmable, parallel, and DNA-encoded library synthesis.
Chemical science, 2026, 17, 225-239
1576196 CIFC28 H25 N3 O4 PdP -17.3114; 10.4814; 16.3409
105.447; 92.784; 97.477		1192.22Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576197 CIFC44 H32 N6 O4 ZnI 41/a :221.5097; 21.5097; 15.9157
90; 90; 90		7363.7Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576198 CIFC48 H44 N6 O6 Pd S2C 1 2/c 138.9049; 5.6739; 24.1051
90; 126.913; 90		4254.4Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576199 CIFC28 H25 N3 O4 PdP 1 21/n 17.0141; 17.2303; 20.2314
90; 97.876; 90		2422Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576200 CIFC46 H36 N6 O4 ZnI 41/a :221.7492; 21.7492; 15.5858
90; 90; 90		7372.5Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576201 CIFC69 H54 Co N9 O6P a -323.5997; 23.5997; 23.5997
90; 90; 90		13143.8Schomberg-Sanchez, Isaac S; Robinson, William C.; Sanderson, Makayla E.; Mosquera, Martín A; Lemon, Christopher M.
Hangman dipyrrin complexes.
Chemical science, 2026, 17, 602-616
1576202 CIFC47 H72 Cs F N O8 PP 1 21/n 19.9121; 23.2605; 21.4065
90; 93.563; 90		4926Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576203 CIFC43 H52 N O2 PP -112.0403; 12.4082; 14.2936
102.973; 98.828; 106.389		1941.96Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576204 CIFC72 H90 N2 O4 P2P 1 21/c 112.6836; 44.721; 11.8935
90; 98.973; 90		6663.7Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576205 CIFC52 H83 K N O8 PP -19.2969; 15.9116; 18.7341
79.756; 79.904; 79.803		2654.3Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576206 CIFC56 H89 K N O10 PP 1 21/c 114.5374; 21.5756; 19.1473
90; 96.87; 90		5962.5Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576207 CIFC41.25 H51.75 F0.75 N O2 PP 1 21/n 110.5896; 15.6048; 22.7972
90; 90.184; 90		3767.2Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576208 CIFC78 H95 F N2 O4 P2P -114.5273; 16.7003; 17.1757
118.647; 101.045; 96.322		3489.12Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576209 CIFC86 H128 Li4 N4 O7 P2P 1 21/c 112.2271; 19.3733; 19.2094
90; 96.632; 90		4519.9Escoudé, Emile; Pedrón, Manuel; Bourqui, Lilian; Gontard, Geoffrey; Vitale, Maxime R.; Ciofini, Ilaria; Lakhdar, Sami; Grimaud, Laurence
Photochemical activation of pincer-ligated phosphoranides: mechanistic insight for reduction of aryl halides.
Chemical science, 2026, 17, 579-584
1576226 CIFC16 H14 F4 N O2 PC 1 2/c 117.9924; 11.0902; 15.8252
90; 100.242; 90		3107.43Pan, Ailin; Rotella, Madeline E.; Meng, Yamiao; Tian, Xun; Duan, Shengzu; Jiang, Yonggang; Deng, Guogang; Limburg, Bart; Zhang, Hongbin; Kozlowski, Marisa C.; Walsh, Patrick J.; Yang, Xiaodong
1,2-Hydrogen atom transfer of aminyl radicals under photoredox catalysis for the synthesis of α-amino phosphine oxides.
Chemical science, 2026, 17, 412-420
1576233 CIFC55 H12 Ag B2 F36 NP -111.4773; 15.0019; 17.379
111.95; 96.586; 109.074		2525.49Berg, Willi R.; Moshtaha, Amina L.; Sievers, Robin; Reimann, Marc; Streit, Tim-Niclas; Rupf, Susanne M.; Kaupp, Martin; Malischewski, Moritz
A facile route to 'naked' Ag<sup>+</sup> ions enabling the coordination of the weak Lewis base Ni(CO)<sub>4</sub>.
Chemical science, 2026, 17, 406-411
1576234 CIFC43.7 H6.2 Ag B2 Cl6.2 F30 N Ni0.9 O3.6P 1 21/c 113.288; 28.0807; 13.7219
90; 91.614; 90		5118.1Berg, Willi R.; Moshtaha, Amina L.; Sievers, Robin; Reimann, Marc; Streit, Tim-Niclas; Rupf, Susanne M.; Kaupp, Martin; Malischewski, Moritz
A facile route to 'naked' Ag<sup>+</sup> ions enabling the coordination of the weak Lewis base Ni(CO)<sub>4</sub>.
Chemical science, 2026, 17, 406-411
1576434 CIFC8 H9 N O6 ZnP 1 21/c 19.5078; 6.4427; 14.9087
90; 95.172; 90		909.53Zhang, Tongtong; Wang, Xiangyu; Wright, Jack D.; Whitehead, George F. S.; Tidey, Jeremiah P.; Wong, Lu Shin; Riddell, Imogen A.
Enhanced stability and reusability of recombinant silicatein upon biomimetic metal-organic framework crystallization.
Chemical science, 2026, 17, 3141-3147
1576438 CIFC10.5 H12.5 S0.5 Si0.5P -18.3908; 8.8613; 13.4687
97.962; 99.148; 90.96		978.4Isogai, Ryosuke; Yasui, Kosuke; Fukazawa, Aiko
Modular synthesis of benzothiophene-fused pentalenes reveals substituent-dependent antiaromaticity.
Chemical science, 2026, 17, 3005-3011
1576469 CIFC64 H72 N4 O18 S4P 1 21/c 121.9582; 15.4314; 20.0065
90; 109.032; 90		6408.5Alarcon-Miranda, Carlos; Middleton, Isis A.; Rusli, Olivia; Caceres-Herrera, Nicolas; Bhadbhade, Mohan; Rijs, Nicole J.; Thordarson, Pall; Kogan, Marcelo J.; Saitz, Claudio
<i>N</i>-Arylsulfonamidocalix[4]arenes with narrow pH-responsive binding near neutral pH.
Chemical science, 2026, 17, 3293-3299
1576470 CIFC68.75 H67 F12 N4 Na5 O24.75 S8I 1 2/c 120.84; 19.926; 22.459
90; 99.284; 90		9204Alarcon-Miranda, Carlos; Middleton, Isis A.; Rusli, Olivia; Caceres-Herrera, Nicolas; Bhadbhade, Mohan; Rijs, Nicole J.; Thordarson, Pall; Kogan, Marcelo J.; Saitz, Claudio
<i>N</i>-Arylsulfonamidocalix[4]arenes with narrow pH-responsive binding near neutral pH.
Chemical science, 2026, 17, 3293-3299
1576471 CIFC28.5 H29 B3 Cl N2 Os P Se2P -111.117; 15.9224; 17.8651
78.036; 81.905; 84.906		3056.97Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576472 CIFC48 H47 B2 N Os P2 Se2P 1 21/n 111.0801; 11.7542; 34.23
90; 90.696; 90		4457.7Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576473 CIFC28 H23 Cl N2 Os P Se2P 1 21/n 112.1253; 18.0329; 12.381
90; 91.515; 90		2706.2Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576474 CIFC10 H21 B7 N2 Os Se2P 1 21/c 112.7281; 9.4036; 15.1331
90; 101.48; 90		1775.04Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576475 CIFC46 H38 N2 Os P2 Se2P 1 21/c 119.9615; 17.6882; 11.2486
90; 95.367; 90		3954.3Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576476 CIFC41 H34 Cl2 N Os P2 SeP 1 21/n 19.5636; 15.361; 25.2268
90; 100.93; 90		3638.8Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576477 CIFC28 H33 B4 N2 Os P Se2P n a 2115.3411; 9.6807; 20.0705
90; 90; 90		2980.72Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576478 CIFC51 H39 B2 F12 N2 Os P Se3P 1 21/n 110.8616; 30.8022; 14.9297
90; 97.324; 90		4954.1Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576479 CIFC69.5 H49 B F12 N2 Os P2 S4P -120.9226; 24.4708; 24.7349
73.662; 84.215; 87.098		12087.5Assanar, Faneesha; Gayen, Sourav; Patel, Deepak Kumar; Pradeep, Thalappil; Ghosh, Sundargopal
Cooperative borane activation by tuning hemilability of different Os-κ<sup>2</sup>-<i>N</i>,<i>Se</i>-chelated complexes.
Chemical science, 2026, 17, 3129-3140
1576480 CIFC11 H10 F N O3 SP 21 21 215.8549; 10.5165; 18.8417
90; 90; 90		1160.14Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576481 CIFC11 H11 F I N O3 SP -17.3211; 8.0126; 11.5027
81.753; 75.228; 78.644		636.584Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576482 CIFC10 H8 F N O3 SP 1 21 17.4669; 7.9789; 9.334
90; 109.895; 90		522.91Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576483 CIFC5 H7 F I N O3 SC 1 2/c 114.3378; 5.8654; 21.9011
90; 105.905; 90		1771.31Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576484 CIFC20 H18 F2 I2 N2 O6 S2P -17.6473; 7.7662; 10.9617
74.713; 77.55; 77.289		603.94Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576485 CIFC22 H24 F N O7 SP 1 21/c 110.9165; 16.1273; 12.2969
90; 91.946; 90		2163.67Yamamoto, Daiki; Yamasaki, Shun; Hashimoto, Takuya
Se-catalyzed enantioselective lactamization enabled by a <i>N</i>-fluorosulfonyl group: total synthesis of diaporisoindole A.
Chemical science, 2026, 17, 3313-3319
1576495 CIFC19 H20 O SP 1 21 19.1143; 7.2877; 12.1106
90; 98.273; 90		796.04Yuwen, Liyan; Tang, Jiazhong; Qi, Yayu; Zou, Tianyi; Zhang, Shaotong; Zhang, Ya-Qian; Zhang, Qing-Wei
Diastereoselective synthesis of cyclopropyl sulfoxides <i>via</i> hydrosulfenation.
Chemical science, 2026, 17, 3171-3177
1576496 CIFC19 H25 F O3 SP 21 21 2110.1006; 10.2657; 17.658
90; 90; 90		1830.95Yuwen, Liyan; Tang, Jiazhong; Qi, Yayu; Zou, Tianyi; Zhang, Shaotong; Zhang, Ya-Qian; Zhang, Qing-Wei
Diastereoselective synthesis of cyclopropyl sulfoxides <i>via</i> hydrosulfenation.
Chemical science, 2026, 17, 3171-3177
1576497 CIFC19 H25 F O3 SP 21 21 216.9914; 8.3848; 30.4141
90; 90; 90		1782.92Yuwen, Liyan; Tang, Jiazhong; Qi, Yayu; Zou, Tianyi; Zhang, Shaotong; Zhang, Ya-Qian; Zhang, Qing-Wei
Diastereoselective synthesis of cyclopropyl sulfoxides <i>via</i> hydrosulfenation.
Chemical science, 2026, 17, 3171-3177
1576498 CIFC36 H40 O4 S2P 1 21 15.918; 8.0256; 16.8884
90; 98.632; 90		793.04Yuwen, Liyan; Tang, Jiazhong; Qi, Yayu; Zou, Tianyi; Zhang, Shaotong; Zhang, Ya-Qian; Zhang, Qing-Wei
Diastereoselective synthesis of cyclopropyl sulfoxides <i>via</i> hydrosulfenation.
Chemical science, 2026, 17, 3171-3177
1576499 CIFC22 H26 O SP 6517.922; 17.922; 11.4729
90; 90; 120		3191.37Yuwen, Liyan; Tang, Jiazhong; Qi, Yayu; Zou, Tianyi; Zhang, Shaotong; Zhang, Ya-Qian; Zhang, Qing-Wei
Diastereoselective synthesis of cyclopropyl sulfoxides <i>via</i> hydrosulfenation.
Chemical science, 2026, 17, 3171-3177
1576508 CIFC27 H26 N2 O2 SP 21 21 2110.2979; 11.7884; 19.1733
90; 90; 90		2327.56Xiao, Teng-Fei; Jian, Ke-Rui; Gu, Yu-Cheng; Xu, Guo-Qiang; Xu, Peng-Fei
Asymmetric vicinal C(sp<sup>3</sup>)-H difunctionalization of saturated cyclic amines <i>via</i> synergistic photoredox, copper and chiral phosphoric acid catalysis.
Chemical science, 2026, 17, 3240-3247
1576519 CIFC39 H44 N2 ZnP -112.5737; 15.727; 16.9192
82.334; 83.447; 77.717		3227.2Iwamoto, Hidemitsu; Sunada, Yusuke; Wada, Yoshimasa
Zincafluorene complex with an empty C-Zn π orbital that captures visible light.
Chemical science, 2026, 17, 3023-3030
1576520 CIFC49 H59 N ZnP b c a16.0503; 18.7163; 26.6927
90; 90; 90		8018.5Iwamoto, Hidemitsu; Sunada, Yusuke; Wada, Yoshimasa
Zincafluorene complex with an empty C-Zn π orbital that captures visible light.
Chemical science, 2026, 17, 3023-3030
1576521 CIFC37 H48 N O ZnP 1 21/n 113.8577; 16.6434; 14.0019
90; 92.432; 90		3226.48Iwamoto, Hidemitsu; Sunada, Yusuke; Wada, Yoshimasa
Zincafluorene complex with an empty C-Zn π orbital that captures visible light.
Chemical science, 2026, 17, 3023-3030
1576522 CIFC39 H46 N2 ZnP -112.6466; 15.9905; 17.0143
83.503; 84.141; 78.022		3333.24Iwamoto, Hidemitsu; Sunada, Yusuke; Wada, Yoshimasa
Zincafluorene complex with an empty C-Zn π orbital that captures visible light.
Chemical science, 2026, 17, 3023-3030
1576528 CIFC20 H25 N3 O4P 21 21 219.14295; 10.25505; 20.8149
90; 90; 90		1951.63Hughes, Owen R.; Tufail, Afzaal; Hutton, Esme; Nabarro, Joe; Howarth, Rachel; Yates, Nicholas D.; Whitwood, Adrian C.; Robson, Craig N.; Signoret, Nathalie; Fascione, Martin A.; Spicer, Christopher D.; Unsworth, William P.
N-terminal protein-macrocycles enabled by conjugate addition/ring expansion cascade reactions.
Chemical science, 2026, 17, 3320-3328
1576531 CIFC92 H188 Dy Mo12 O56 P5C 1 c 124.6687; 19.2311; 29.3029
90; 113.233; 90		12774.2Lowe, Ethan; Rouzières, Mathieu; Dugmore, Sarah K.; Kelly, Christopher; Wilson, Claire; Canaj, Angelos B.; Clérac, Rodolphe; Murrie, Mark
Highly reducible polyoxometalate-Dy(iii) SMM hybrid materials with exceptional charge stability.
Chemical science, 2026, 17, 3248-3258
1576532 CIFC72 H142 Dy Mo12 O49 P5C 1 c 124.5974; 19.2115; 29.5224
90; 113.102; 90		12832.1Lowe, Ethan; Rouzières, Mathieu; Dugmore, Sarah K.; Kelly, Christopher; Wilson, Claire; Canaj, Angelos B.; Clérac, Rodolphe; Murrie, Mark
Highly reducible polyoxometalate-Dy(iii) SMM hybrid materials with exceptional charge stability.
Chemical science, 2026, 17, 3248-3258
1576584 CIFC44 H58 B30 Cl2C 1 2/c 17.245; 31.353; 23.751
90; 91.88; 90		5392.2Yuhara, Kazuhiro; Takemori, Sota; Yanagihara, Takumi; Ohtani, Shunsuke; Ogoshi, Tomoki; Tanaka, Kazuo
Guest-induced emission enhancement in the permanent porous conjugated carboracycle crystal.
Chemical science, 2026, 17, 3691-3699
1576585 CIFC44 H58 B30 Br2C 1 2/c 17.2884; 31.271; 23.733
90; 92.054; 90		5406Yuhara, Kazuhiro; Takemori, Sota; Yanagihara, Takumi; Ohtani, Shunsuke; Ogoshi, Tomoki; Tanaka, Kazuo
Guest-induced emission enhancement in the permanent porous conjugated carboracycle crystal.
Chemical science, 2026, 17, 3691-3699
1576586 CIFC86 H102 Al2 F72 Ga2 O9 P4P -117.168; 17.984; 22.621
69.09; 67.933; 63.812		5653Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576587 CIFC90 H102 Al2 F72 Ga2 O9 P4P 21 21 2115.677; 23.421; 31.572
90; 90; 90		11592Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576588 CIFC86 H99 Al2 F72 Ga2 N O8 P4P 1 21 113.55; 27.099; 15.504
90; 91.2; 90		5692Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576589 CIFC90 H103 Al2 F72 Ga2 N O8 P4C 1 c 118.26; 29.497; 22.081
90; 96.514; 90		11816Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576590 CIFC96 H107 Al2 F72 Ga2 N O8 P4P -115.468; 18.034; 22.835
81.311; 72.12; 86.298		5991Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576591 CIFC278 H297 Al7 F244 Ga6 O26 P12P -118.462; 27.562; 37.435
86.961; 88.862; 75.387		18406Barthélemy, Antoine; Kub, Nico Gino; Regnat, Celine; Scherer, Harald; Krossing, Ingo
Why is a dicationic digallene so reactive towards activation of strong covalent bonds? Scope and mechanistic investigations.
Chemical science, 2026, 17, 4004-4020
1576597 CIFC19 H18 N2 O3P -19.5496; 10.108; 17.362
90.483; 97.956; 100.119		1633Liu, Yang; Xie, Zi-Yi; Kloene, Lennard; Xu, Cong-Lun; Tai, Jian-Peng; Zhu, Yu; Cai, Bao-Gui; Pan, Chongqing; Koenigs, Rene M.; Xuan, Jun
Visible light-induced 1,2-alkoxy shift of α-diazoacetates for Wolff rearrangements - access to oxyketenes.
Chemical science, 2026, 17, 3587-3592
1576598 CIFC23 H21 N O2P -18.505; 9.0705; 13.1678
84.919; 71.48; 75.36		931.91Liu, Yang; Xie, Zi-Yi; Kloene, Lennard; Xu, Cong-Lun; Tai, Jian-Peng; Zhu, Yu; Cai, Bao-Gui; Pan, Chongqing; Koenigs, Rene M.; Xuan, Jun
Visible light-induced 1,2-alkoxy shift of α-diazoacetates for Wolff rearrangements - access to oxyketenes.
Chemical science, 2026, 17, 3587-3592
1576599 CIFC10.01 H12.01 F2 Li N5 O4 S2P 21 21 212.8522; 12.8465; 5.2547
90; 90; 90		867.58Nishiguchi, Taichi; Kageyama, Kotoha; Kurihara, Takuya; Shimanaka, Nanae; Tokuda, Shun; Tsuda, Shuto; Ma, Nattapol; Horike, Satoshi
Soft crystalline properties of 2D frameworks constructed from lithium ions and dinitriles.
Chemical science, 2026, 17, 3669-3674
1576600 CIFC26 H24 F6 Li N5 O4 S2P -421.3025; 21.3025; 6.4513
90; 90; 90		2927.58Nishiguchi, Taichi; Kageyama, Kotoha; Kurihara, Takuya; Shimanaka, Nanae; Tokuda, Shun; Tsuda, Shuto; Ma, Nattapol; Horike, Satoshi
Soft crystalline properties of 2D frameworks constructed from lithium ions and dinitriles.
Chemical science, 2026, 17, 3669-3674
1576601 CIFC9 H10 F2 Li N5 O4 S2P b c m5.1756; 15.2002; 20.2029
90; 90; 90		1589.4Nishiguchi, Taichi; Kageyama, Kotoha; Kurihara, Takuya; Shimanaka, Nanae; Tokuda, Shun; Tsuda, Shuto; Ma, Nattapol; Horike, Satoshi
Soft crystalline properties of 2D frameworks constructed from lithium ions and dinitriles.
Chemical science, 2026, 17, 3669-3674
1576602 CIFC17 H12 N2 O SC 1 2/c 113.6403; 7.84; 25.3454
90; 94.102; 90		2703.49Chen-Wu, Jialei; Benitez-Martin, Carlos; González-Delgado, José A; de Jong, Flip; Fron, Eduard; Steurs, Gert; Martínez-Martínez, Antonio J; Nájera, Francisco; Grøtli, Morten; Hofkens, Johan; Andréasson, Joakim; Pischel, Uwe
Heteroaryl iminothioindoxyl (HA-ITI) photoswitches <i>via</i> regioselective aza-Wittig synthesis: unifying red-shifted absorption, large <i>E</i>/<i>Z</i> band separation, and tunable thermal recovery.
Chemical science, 2026, 17, 3658-3668
1576603 CIFC15 H9 N3 O SI 1 2/a 119.736; 4.8714; 26.2576
90; 101.07; 90		2477.49Chen-Wu, Jialei; Benitez-Martin, Carlos; González-Delgado, José A; de Jong, Flip; Fron, Eduard; Steurs, Gert; Martínez-Martínez, Antonio J; Nájera, Francisco; Grøtli, Morten; Hofkens, Johan; Andréasson, Joakim; Pischel, Uwe
Heteroaryl iminothioindoxyl (HA-ITI) photoswitches <i>via</i> regioselective aza-Wittig synthesis: unifying red-shifted absorption, large <i>E</i>/<i>Z</i> band separation, and tunable thermal recovery.
Chemical science, 2026, 17, 3658-3668
1576604 CIFC16 H11 N3 O SP -17.6266; 7.9225; 24.4377
81.144; 82.116; 64.126		1308.64Chen-Wu, Jialei; Benitez-Martin, Carlos; González-Delgado, José A; de Jong, Flip; Fron, Eduard; Steurs, Gert; Martínez-Martínez, Antonio J; Nájera, Francisco; Grøtli, Morten; Hofkens, Johan; Andréasson, Joakim; Pischel, Uwe
Heteroaryl iminothioindoxyl (HA-ITI) photoswitches <i>via</i> regioselective aza-Wittig synthesis: unifying red-shifted absorption, large <i>E</i>/<i>Z</i> band separation, and tunable thermal recovery.
Chemical science, 2026, 17, 3658-3668
1576654 CIFC17 H18 Au Cl N2 O3 SP 21 21 214.8602; 14.2036; 25.7174
90; 90; 90		1775.33Ochs, Jasmine; Metzler-Nolte, Nils
Identification of Au-hydrides as key intermediates in the reduction of Au(iii) prodrugs to active Au(i) species under protic conditions.
Chemical science, 2026, 17, 4183-4190
1576655 CIFC32 H42 Au2 Cl4 N4 O6 S2P 1 21 117.2761; 6.7454; 18.9344
90; 115.37; 90		1993.71Ochs, Jasmine; Metzler-Nolte, Nils
Identification of Au-hydrides as key intermediates in the reduction of Au(iii) prodrugs to active Au(i) species under protic conditions.
Chemical science, 2026, 17, 4183-4190
1576656 CIFC52 H44 Eu2 N14 O18P 19.5245; 12.652; 12.721
75.746; 68.755; 77.174		1369.73Li, Ru-Yan; Tang, Meng-Juan; Li, Yun-Lan; Yang, Fan; Zou, Hua-Hong; Wang, Hai-Ling; Zhu, Zhong-Hong
Improving the conjugation of organic ligands enhances the antenna effect and promotes the luminescence and optical imaging of chiral mononuclear Eu(iii) complexes.
Chemical science, 2026, 17, 4157-4167
1576657 CIFC52 H44 Eu2 N14 O18P 19.5275; 12.6485; 12.7241
75.718; 68.74; 77.16		1369.8Li, Ru-Yan; Tang, Meng-Juan; Li, Yun-Lan; Yang, Fan; Zou, Hua-Hong; Wang, Hai-Ling; Zhu, Zhong-Hong
Improving the conjugation of organic ligands enhances the antenna effect and promotes the luminescence and optical imaging of chiral mononuclear Eu(iii) complexes.
Chemical science, 2026, 17, 4157-4167
1576658 CIFC35 H43 Mn N6 O5P b a n :227.554; 28.71; 17.7286
90; 90; 90		14024.7De, Puja; Adabala, Snehith; Samanta, Soumya; Mukhopadhyay, Kuntal; Ghosh, Soumya; Sen Gupta, Sayam
Unprecedented HAT rate acceleration in water by a non-heme manganese oxo complex.
Chemical science, 2026, 17, 4042-4049
1576659 CIFC3.55 H5.2 Cl0.08 Mn0.08 N0.58 O0.33P b c a13.9931; 16.3697; 37.9318
90; 90; 90		8688.77De, Puja; Adabala, Snehith; Samanta, Soumya; Mukhopadhyay, Kuntal; Ghosh, Soumya; Sen Gupta, Sayam
Unprecedented HAT rate acceleration in water by a non-heme manganese oxo complex.
Chemical science, 2026, 17, 4042-4049
1576660 CIFC34 H30P 1 21/c 116.485; 6.2347; 12.105
90; 99.627; 90		1226.6Shi, Xiaomei; Chen, Xinyu; Huang, Yu; Liu, Zuyuan; Zhao, Bo; Yan, Lingpeng; Zhang, Teng-Shuo; Fu, Hongbing; Wang, Long
Efficient singlet fission in rubicene null aggregates.
Chemical science, 2026, 17, 4168-4173
1576661 CIFC26 H23 N3 O2P b c a15.0386; 14.8556; 18.6742
90; 90; 90		4172Nakata, Kanami; Matsuoka, Wataru; Ito, Hideto; Itami, Kenichiro
<i>L</i>-region-selective annulative π-extension through dearomative activation of polycyclic aromatic hydrocarbons.
Chemical science, 2026, 17, 3998-4003
1576662 CIFC25 H21 N3 O2P 1 21/c 114.901; 10.1314; 13.5202
90; 104.524; 90		1975.9Nakata, Kanami; Matsuoka, Wataru; Ito, Hideto; Itami, Kenichiro
<i>L</i>-region-selective annulative π-extension through dearomative activation of polycyclic aromatic hydrocarbons.
Chemical science, 2026, 17, 3998-4003
1576663 CIFC25.04 H20.04 I N3 O2P 1 21/c 115.3604; 9.5211; 15.3873
90; 107.325; 90		2148.3Nakata, Kanami; Matsuoka, Wataru; Ito, Hideto; Itami, Kenichiro
<i>L</i>-region-selective annulative π-extension through dearomative activation of polycyclic aromatic hydrocarbons.
Chemical science, 2026, 17, 3998-4003
1576664 CIFC17 H10C 1 2/c 126.78; 3.886; 19.6341
90; 102.831; 90		1992.2Nakata, Kanami; Matsuoka, Wataru; Ito, Hideto; Itami, Kenichiro
<i>L</i>-region-selective annulative π-extension through dearomative activation of polycyclic aromatic hydrocarbons.
Chemical science, 2026, 17, 3998-4003
1576665 CIFC50 H42 O10P b c a13.5872; 14.1035; 25.9503
90; 90; 90		4972.8Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576666 CIFC60 H58 O8P b c a14.9347; 14.1589; 25.2455
90; 90; 90		5338.4Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576667 CIFC98 H74 O16P b c a13.444; 14.142; 25.861
90; 90; 90		4916.8Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576668 CIFC52 H46 O8P b c a13.4088; 14.1154; 25.8758
90; 90; 90		4897.5Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576669 CIFC50 H34 O8P b c a13.4893; 14.0799; 25.9348
90; 90; 90		4925.7Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576670 CIFC51 H34 O8P b c a13.4346; 14.1142; 25.8466
90; 90; 90		4901Cai, Youlie; Li, Jing-Hong; Xiao, Xiaoyan; Wei, Runzhi; Lin, Rui-Biao; Chen, Banglin; Gao, Junkuo
Spatial pinning of globally inert pores in a superhydrophobic hydrogen-bonded organic framework for inverse ethane/ethylene separation.
Chemical science, 2026, 17, 4256-4267
1576671 CIFC98 H88 Cl I2 N52 O24 S2P 1 21/n 118.355; 27.2455; 34.3754
90; 99.767; 90		16941.7Nie, Haigen; Tan, Jiao; Luo, Yi; Ni, Xin-Long
A cucurbit[8]uril-triggered ionic photosensitizer in solution and solid states: selective control of <sup>1</sup>O<sub>2</sub> and O<sub>2</sub>˙<sup>-</sup> generation.
Chemical science, 2026, 17, 4137-4144
1576672 CIFC100 H92 Cl I2 N52 O26 S2P 1 21/n 118.2818; 27.2752; 34.8195
90; 101.584; 90		17008.7Nie, Haigen; Tan, Jiao; Luo, Yi; Ni, Xin-Long
A cucurbit[8]uril-triggered ionic photosensitizer in solution and solid states: selective control of <sup>1</sup>O<sub>2</sub> and O<sub>2</sub>˙<sup>-</sup> generation.
Chemical science, 2026, 17, 4137-4144
1576683 CIFC13 H22 Cl2 N2 RuP -18.0151; 10.3158; 10.4456
69.794; 68.844; 78.767		753.45Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576684 CIFC12 H17 Cl2 N RuP 1 21/c 119.55034; 11.01135; 12.79041
90; 99.3053; 90		2717.23Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576685 CIFC17 H26 N2 O3 RuP 1 21/c 18.13073; 11.29004; 19.3239
90; 101.849; 90		1736.06Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576686 CIFC15 H24 Cl4 N2 RuP -18.8497; 10.6779; 11.6417
69.313; 75.853; 76.141		983.62Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576687 CIFC16 H26 Cl2 N2 RuP b c a11.43884; 15.3631; 19.58592
90; 90; 90		3441.95Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576688 CIFC20 H35 Cl2 N3 RuP 1 21/n 110.69797; 9.17128; 22.3384
90; 92.6898; 90		2189.3Righetti, Gianluca; Koidan, Georgyi; Filimonchuk, Sergiy L.; Shishkina, Svitlana; Kostyuk, Aleksandr; Albrecht, Martin
Ligand flexibility as a concept to unlock catalytic activity: acyclic carbenes for base-free transfer ruthenium hydrogenation catalysis.
Chemical science, 2026, 17, 4325-4331
1576699 CIFC33 H30 I N5 O8 SP 21 21 217.346; 26.0025; 34.85
90; 90; 90		6656.9Zhong, Yangyang; Zeng, Jie; Li, Mingwei; Liang, Yuli; Guan, Shuman; Zhao, Kehan; Mu, Jiayi; Tang, Pei; Wang, Huijing; Chen, Fener
Stereodivergent access to α- and β-azanucleosides <i>via</i> catalyst-free, achiral modulator-controlled iodocyclization: a concise synthesis of forodesine.
Chemical science, 2026, 17, 4126-4136
1576700 CIFC28 H33 Cl2 N O Ru SeP -19.7647; 10.092; 15.3151
107.239; 98.9646; 105.768		1340.54Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576701 CIFC22 H21 I2 N3 PtP -18.3972; 11.7055; 12.11
93.48; 98.668; 104.169		1135.01Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576702 CIFC9 H10 I2 N2 Pt SP 61 2 29.2044; 9.2044; 29.2718
90; 90; 120		2147.69Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576703 CIFC9 H9 Au I N OP n a 216.92293; 28.2837; 16.3408
90; 90; 90		3199.63Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576704 CIFC32 H34 Cl4 N2 RuP 1 21/n 115.0757; 12.3164; 18.0889
90; 114.216; 90		3063.2Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576705 CIFC9 H9 Au Br N SC 1 2/c 116.4314; 9.4384; 13.8055
90; 94.094; 90		2135.58Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576706 CIFC9 H10 I2 N2 O PtP 1 21/c 18.8706; 15.328; 19.83
90; 90.089; 90		2696.3Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576707 CIFC11 H14 Au I N2C 1 2/c 110.6281; 16.7383; 7.17
90; 93.494; 90		1273.15Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576708 CIFC28 H33 Cl2 N O Ru SP -19.75755; 10.13025; 15.2002
107.338; 98.0674; 106.18		1335.9Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576709 CIFC10 H13 I2 N3 PtP 65 2 29.25931; 9.25931; 30.8237
90; 90; 120		2288.61Romano-deGea, Jan; Sinenko, Irina L.; Pânzar, Peter M F; Neves Vieira, Adriana; Frederiksen, Lindsey E. K.; Glinkina, Kseniya; Fadaei-Tirani, Farzaneh; Scopelliti, Rosario; Kuttler, Fabien; Lau, Kelvin; Dyson, Paul J.
Unconventional chalcogen-containing azolylidene metal complexes as potential anticancer therapeutics.
Chemical science, 2026, 17, 4296-4306
1576710 CIFC54 H67 Cl2 N3 Si2P 1 21/n 110.5011; 36.2781; 13.3571
90; 91.845; 90		5085.9Lončarić, Doroteja; Kaletová, Eva; Varga, Katarina Majerová; Hurtado, Carina Santos; Mašát, Milan; Císařová, Ivana; Kaleta, Jiří
Cucurbit[7]uril as a universal anchor for photoswitchable monolayers on gold.
Chemical science, 2026, 17, 3991-3997
1576711 CIFC37 H35 Cl3 N4 OP -112.2842; 16.8227; 34.6745
77.137; 82.673; 74.771		6722.3Lončarić, Doroteja; Kaletová, Eva; Varga, Katarina Majerová; Hurtado, Carina Santos; Mašát, Milan; Císařová, Ivana; Kaleta, Jiří
Cucurbit[7]uril as a universal anchor for photoswitchable monolayers on gold.
Chemical science, 2026, 17, 3991-3997
1576716 CIFC82 H71 Cu3 P6P 1 21/n 113.8301; 23.24282; 23.96377
90; 101.808; 90		7540.16Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576717 CIFC88 H54 Cu2 F20 O4 P4 Zn2P -112.6129; 13.151; 14.4377
82.473; 66.962; 64.233		1982.48Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576718 CIFC92 H60 Cu2 F20 P4 Zn2P 1 21/n 113.9446; 18.9372; 15.5207
90; 99.426; 90		4043.24Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576719 CIFC86 H54 Cu2 F20 P4 Zn2I 1 2/a 116.7872; 15.1283; 32.1498
90; 90.653; 90		8164.29Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576720 CIFC83 H74 Cu3 O4 P6P 1 21/c 110.8464; 41.8005; 17.7632
90; 94.963; 90		8023.4Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576721 CIFC118 H107 Cu5 P8P 1 n 115.8877; 14.8052; 44.2531
90; 97.051; 90		10330.5Cowie, Bradley E.; Phanopoulos, Andreas; Shaffer, Milo S. P.; Williams, Charlotte K.
Structural and reactivity investigations using organo-copper(i) and zinc(ii) complexes with hydrogen and carbon dioxide.
Chemical science, 2026, 17, 564-578
1576722 CIFC34 H40 F18 N2 O2 WP -110.5049; 13.561; 13.6443
87.086; 87.639; 81.043		1916.4Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576723 CIFC23 H23 F18 N O2 WC 1 2 120.517; 11.7363; 11.8494
90; 96.648; 90		2834.1Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576724 CIFC40 H52 F9 N3 O WP -111.223; 12.684; 16.267
77.46; 76.31; 70.79		2100Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576725 CIFC28 H44 N2 WP 1 21/n 113.3829; 18.8032; 22.2737
90; 106.681; 90		5369.1Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576726 CIFC24 H25 F18 N O2 WP b c a10.284; 18.2199; 30.9881
90; 90; 90		5806.3Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576727 CIFC58 H73 F9 N5 O1.5 W2P n a 2120.8163; 13.796; 39.1164
90; 90; 90		11233.5Maji, Milan; Zeng, Landley; Schrock, Richard R.; Conley, Matthew P.; Carta, Veronica
Formation of tungsten ethylidene complexes from diethyl complexes through a proton-catalyzed rearrangement of ethylene.
Chemical science, 2026, 17, 421-429
1576728 CIFC34 H22 Cl N OP 1 21/n 19.314; 24.125; 11.578
90; 92.692; 90		2598.7Kunhiraman, Anusree A.; Patra, Koushik; Kumar Choutipalli, Venkata Surya; Godara, Manjeet; Shuford, Kevin L.; Baidya, Mahiuddin
Unlocking radical reactivity of cyclic diaryl λ<sup>3</sup>-chloranes through NHC-catalyzed three-component coupling.
Chemical science, 2026, 17, 4277-4284
1576729 CIFC28 H20 Br Cl OP -19.8017; 10.1659; 11.4676
81.365; 84.82; 86.723		1124Kunhiraman, Anusree A.; Patra, Koushik; Kumar Choutipalli, Venkata Surya; Godara, Manjeet; Shuford, Kevin L.; Baidya, Mahiuddin
Unlocking radical reactivity of cyclic diaryl λ<sup>3</sup>-chloranes through NHC-catalyzed three-component coupling.
Chemical science, 2026, 17, 4277-4284
1576730 CIFC22 H24 N O7 PP 21 21 217.06; 11.8513; 26.174
90; 90; 90		2189.98Clarkson, Aidan J.; Alley, Kimberly A.; Werley, Bryn K.; Robins, Jacob G.; Liu, Shubin; Johnson, Jeffrey S.
Catalytic asymmetric P<sup>(III)</sup>-additions to salicylaldehydes enable divergent stereoselective dearomatizations of phenols.
Chemical science, 2026, 17, 2837-2846
1576731 CIFC24 H29 Br N O9 PP 1 21/c 19.0691; 26.0181; 11.561
90; 111.924; 90		2530.7Clarkson, Aidan J.; Alley, Kimberly A.; Werley, Bryn K.; Robins, Jacob G.; Liu, Shubin; Johnson, Jeffrey S.
Catalytic asymmetric P<sup>(III)</sup>-additions to salicylaldehydes enable divergent stereoselective dearomatizations of phenols.
Chemical science, 2026, 17, 2837-2846
1576732 CIFC38 H26 Br4 Cl2 Cu N2 O6P 1 21 110.8594; 8.1479; 21.4301
90; 90.222; 90		1896.15Clarkson, Aidan J.; Alley, Kimberly A.; Werley, Bryn K.; Robins, Jacob G.; Liu, Shubin; Johnson, Jeffrey S.
Catalytic asymmetric P<sup>(III)</sup>-additions to salicylaldehydes enable divergent stereoselective dearomatizations of phenols.
Chemical science, 2026, 17, 2837-2846
1576733 CIFC28 H25 F3 O2 SP 1 21 111.8702; 6.4382; 15.7216
90; 100.479; 90		1181.45Wei, Zheng-Wei; Cai, Qing-Yun; Yang, Li-Miao; Huo, Yu-Xuan; Li, Ze-Long; Gong, Xue-Qing; Chen, Zhi-Min
Chiral Lewis base/Lewis acid/Brønsted acid cooperative catalysis enabled regio- and enantioselective electrophilic sulfenylation/semipinacol rearrangement of allenols.
Chemical science, 2026, 17, 2802-2810
1576734 CIFC19 H15 F3 O2 SP 21 21 218.6591; 12.8618; 15.7626
90; 90; 90		1755.51Wei, Zheng-Wei; Cai, Qing-Yun; Yang, Li-Miao; Huo, Yu-Xuan; Li, Ze-Long; Gong, Xue-Qing; Chen, Zhi-Min
Chiral Lewis base/Lewis acid/Brønsted acid cooperative catalysis enabled regio- and enantioselective electrophilic sulfenylation/semipinacol rearrangement of allenols.
Chemical science, 2026, 17, 2802-2810
1576735 CIFC20 H16 Br F3 O SP 21 21 217.01707; 9.66742; 27.4191
90; 90; 90		1860.03Wei, Zheng-Wei; Cai, Qing-Yun; Yang, Li-Miao; Huo, Yu-Xuan; Li, Ze-Long; Gong, Xue-Qing; Chen, Zhi-Min
Chiral Lewis base/Lewis acid/Brønsted acid cooperative catalysis enabled regio- and enantioselective electrophilic sulfenylation/semipinacol rearrangement of allenols.
Chemical science, 2026, 17, 2802-2810
1576736 CIFC20 H16 Br F3 N0 O SP b c a17.8548; 8.0071; 25.9391
90; 90; 90		3708.4Wei, Zheng-Wei; Cai, Qing-Yun; Yang, Li-Miao; Huo, Yu-Xuan; Li, Ze-Long; Gong, Xue-Qing; Chen, Zhi-Min
Chiral Lewis base/Lewis acid/Brønsted acid cooperative catalysis enabled regio- and enantioselective electrophilic sulfenylation/semipinacol rearrangement of allenols.
Chemical science, 2026, 17, 2802-2810
1576737 CIFC50 H43 N3 O2P 21 21 216.3463; 16.7092; 36.0686
90; 90; 90		3824.77Wang, Dongmei; Chen, Xiao; Lin, Yuting; Wu, Lulu; Zhao, Zhichen; Xu, Xu; Yang, Shilong; Zhang, Jianyu; Wang, Wen-Jin; Zhao, Zheng; Wang, Shifa; Tang, Ben Zhong; Cai, Xu-Min
From nature-inspired electron acceptors to BioAIE materials with polarity- and polymorphism-dependence for anti-counterfeiting.
Chemical science, 2026, 17, 2847-2857
1576738 CIFC50 H43 N3 O2P 21 21 216.3435; 16.7303; 36.0895
90; 90; 90		3830.13Wang, Dongmei; Chen, Xiao; Lin, Yuting; Wu, Lulu; Zhao, Zhichen; Xu, Xu; Yang, Shilong; Zhang, Jianyu; Wang, Wen-Jin; Zhao, Zheng; Wang, Shifa; Tang, Ben Zhong; Cai, Xu-Min
From nature-inspired electron acceptors to BioAIE materials with polarity- and polymorphism-dependence for anti-counterfeiting.
Chemical science, 2026, 17, 2847-2857
1576739 CIFC39 H48 Cu F6 N6 PP 1 21/n 111.0022; 15.0039; 23.1511
90; 93.337; 90		3815.2Back, Nick; Guthrie, Emylie; Zhu, Chengxu; de Visser, Sam P.; Tahsini, Laleh
Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.
Chemical science, 2026, 17, 2087-2101
1576740 CIFC82 H82 Cu2 N12P -18.3559; 11.2732; 19.0233
90.952; 94.577; 95.28		1778.14Back, Nick; Guthrie, Emylie; Zhu, Chengxu; de Visser, Sam P.; Tahsini, Laleh
Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.
Chemical science, 2026, 17, 2087-2101
1576741 CIFC31 H33 Cu F6 N5 PP -18.9525; 12.2544; 14.4861
78.93; 83.833; 83.018		1542.32Back, Nick; Guthrie, Emylie; Zhu, Chengxu; de Visser, Sam P.; Tahsini, Laleh
Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.
Chemical science, 2026, 17, 2087-2101
1576742 CIFC31 H32 Cu N5P -19.1454; 11.536; 14.1953
69.605; 74.381; 80.865		1348.4Back, Nick; Guthrie, Emylie; Zhu, Chengxu; de Visser, Sam P.; Tahsini, Laleh
Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.
Chemical science, 2026, 17, 2087-2101
1576743 CIFC19 H24 Cu N5P 3110.6182; 10.6182; 43.2847
90; 90; 120		4226.36Back, Nick; Guthrie, Emylie; Zhu, Chengxu; de Visser, Sam P.; Tahsini, Laleh
Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.
Chemical science, 2026, 17, 2087-2101
1576744 CIFC16 H10P 1 21/n 16.6124; 6.0702; 14.6218
90; 101.223; 90		575.68Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576745 CIFC18 H14P -17.9679; 9.1231; 9.592
94.674; 108.09; 98.755		648.9Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576746 CIFC24 H14P 1 21/c 118.027; 6.0037; 7.4853
90; 100.955; 90		795.36Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576747 CIFC18 H8 F6 O2P -15.7176; 8.1893; 16.8245
102.49; 90.921; 91.588		768.64Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576748 CIFC18 H14C 1 2/c 128.1055; 6.0041; 8.0558
90; 91.627; 90		1358.85Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576749 CIFC16 H8 F2P 1 21/n 13.8729; 5.8479; 25.1558
90; 91.054; 90		569.64Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576750 CIFC10 H20 Cl4 Cu F4 N2C m c m23.9619; 7.9649; 9.2096
90; 90; 90		1757.69Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576751 CIFC16 H8 Cl2P 1 21/n 13.9499; 24.878; 6.5419
90; 92.301; 90		642.3Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576752 CIFC18 H8 F6P -17.7; 12.7133; 12.8164
67.196; 86.035; 78.018		1131.27Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576753 CIFC16 H8 F2P 1 21/n 13.9352; 5.8927; 25.1923
90; 91.318; 90		584.03Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576754 CIFC18 H14P 1 21/c 115.4811; 17.3094; 7.75492
90; 92.902; 90		2075.41Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576755 CIFC18 H8 F6 O2P -14.4784; 5.3235; 16.34
86.417; 86.14; 88.66		387.8Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576756 CIFC24 H26P 1 21/c 112.5044; 9.9663; 15.9532
90; 93.953; 90		1983.4Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576757 CIFC18 H8 F6 O2P -16.9786; 15.6479; 15.8333
106.824; 91.106; 90.882		1654.29Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576758 CIFC24 H14P 1 21/c 118.0232; 6.0194; 7.5591
90; 101.211; 90		804.43Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576759 CIFC10 H20 Cl4 Cu F4 N2C m c 2123.8905; 7.8128; 9.2079
90; 90; 90		1718.67Qi, Jun-Chao; Chen, Xiao-Gang; Wang, Zhen-Yu; Tang, Yuan-Yuan; Song, Xian-Jiang; Qin, Yan; Lv, Hui-Peng; Xiong, Ren-Gen; Liao, Wei-Qiang
Organic-inorganic perovskite ferroelectric catalytic selective alkyne coupling under ultrasound sonication.
Chemical science, 2026, 17, 1792-1800
1576766 CIFC11 H20 Cl Cu N2C 1 2/c 110.8524; 11.6698; 11.0084
90; 107.253; 90		1331.43Yan, Connly; Chang, Tieyan; Chen, Yu-Sheng; Paterson, Alexander L.; McElheny, Dan; Mankad, Neal P.
Hidden in plain sight: commonly used copper N-heterocyclic carbene catalysts gain stabilization from anagostic Cu⋯H-C interactions.
Chemical science, 2026, 17, 4734-4743
1576767 CIFC24 H24 O3P -19.8677; 10.1558; 10.8302
112.405; 101.117; 92.787		975.62Liu, Shuili; Liu, Xingji; Gu, Xiu; Dong, Shicheng; Huang, Nan; Shi, Lei; Jiang, Jun
Pyrene-based conjugated porous polymers as photocatalysts for oxidative cycloaddition of phenols.
Chemical science, 2026, 17, 4669-4677
1576768 CIFC21 H16 S2P b c a10.759; 15.6784; 20.0594
90; 90; 90		3383.7He, Zhanhui; Yang, Li; Zhou, Menghang; Zhong, Yue; Liu, Zheng; Zhang, Ziao; Xia, Feiyang; Deng, Xuezhe; Yan, Shuang; Xu, Cheng; Zhang, Cheng; Yin, Guodong
Rh(iii)-catalyzed heteroannular-selective heteroarylation of biaryls: facile access to heteroacenes with sulfur-embedded 5-7 ring topology.
Chemical science, 2026, 17, 4594-4600
1576769 CIFC20 H12 O2 S2P b c a7.8957; 16.3997; 24.1206
90; 90; 90		3123.3He, Zhanhui; Yang, Li; Zhou, Menghang; Zhong, Yue; Liu, Zheng; Zhang, Ziao; Xia, Feiyang; Deng, Xuezhe; Yan, Shuang; Xu, Cheng; Zhang, Cheng; Yin, Guodong
Rh(iii)-catalyzed heteroannular-selective heteroarylation of biaryls: facile access to heteroacenes with sulfur-embedded 5-7 ring topology.
Chemical science, 2026, 17, 4594-4600
1576770 CIFC20 H12 SP 21 21 215.2323; 8.9668; 29.1269
90; 90; 90		1366.55He, Zhanhui; Yang, Li; Zhou, Menghang; Zhong, Yue; Liu, Zheng; Zhang, Ziao; Xia, Feiyang; Deng, Xuezhe; Yan, Shuang; Xu, Cheng; Zhang, Cheng; Yin, Guodong
Rh(iii)-catalyzed heteroannular-selective heteroarylation of biaryls: facile access to heteroacenes with sulfur-embedded 5-7 ring topology.
Chemical science, 2026, 17, 4594-4600

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