Crystallography Open Database

Result: there are 1914 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'Chemical Science' volume of publication is 16

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 20 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
1573776 CIFC22 H20 B10P -111.4881; 13.9932; 14.0464
80.467; 79.395; 71.939		2095.8Wang, Zhen; Yu, Jiahui; Zhang, Jie; Zhang, Dengsong; Qiu, Zaozao; Xie, Zuowei
Palladium-catalyzed intramolecular aerobic oxidative cross-coupling of BH/CH between <i>o</i>-carborane and arenes.
Chemical science, 2025, 16, 3705-3712
1573777 CIFC28 H28 B10 OP 1 21/c 115.0683; 18.877; 18.5211
90; 90.849; 90		5267.6Wang, Zhen; Yu, Jiahui; Zhang, Jie; Zhang, Dengsong; Qiu, Zaozao; Xie, Zuowei
Palladium-catalyzed intramolecular aerobic oxidative cross-coupling of BH/CH between <i>o</i>-carborane and arenes.
Chemical science, 2025, 16, 3705-3712
1573779 CIFC64 H60 O2C 1 2/c 115.8746; 19.1113; 17.1888
90; 97.354; 90		5171.9Xu, Xiang; Ma, Hao-Ran; Cui, Jian-Fang; Peng, Xiao-Shui; Wong, Henry N. C.
Regioselective late-stage functionalization of tetraphenylenes: rapid construction of double helical architectures and potential hole transport materials.
Chemical science, 2025, 16, 4342-4351
1573780 CIFC17 H18 N2 O2 SP -16.0084; 9.2515; 15.0308
102.542; 99.903; 102.191		776.13Erchinger, Johannes E.; Lenz, Madina; Mukherjee, Poulami; Li, Yan-Bo; Suresh, Adhya; Daniliuc, Constantin G.; Gutierrez, Osvaldo; Glorius, Frank
Mechanistic insights into the regiodivergent insertion of bicyclo[1.1.0]butanes towards carbocycle-tethered N-heteroarenes.
Chemical science, 2025, 16, 4006-4013
1573781 CIFC17 H18 N2 O2 SP 1 21/c 15.7579; 16.2633; 16.7223
90; 95.874; 90		1557.7Erchinger, Johannes E.; Lenz, Madina; Mukherjee, Poulami; Li, Yan-Bo; Suresh, Adhya; Daniliuc, Constantin G.; Gutierrez, Osvaldo; Glorius, Frank
Mechanistic insights into the regiodivergent insertion of bicyclo[1.1.0]butanes towards carbocycle-tethered N-heteroarenes.
Chemical science, 2025, 16, 4006-4013
1573782 CIFC17 H15 N3 O S2P b c a10.758; 7.7718; 38.4713
90; 90; 90		3216.5Erchinger, Johannes E.; Lenz, Madina; Mukherjee, Poulami; Li, Yan-Bo; Suresh, Adhya; Daniliuc, Constantin G.; Gutierrez, Osvaldo; Glorius, Frank
Mechanistic insights into the regiodivergent insertion of bicyclo[1.1.0]butanes towards carbocycle-tethered N-heteroarenes.
Chemical science, 2025, 16, 4006-4013
1573783 CIFC27 H41 Cl2 N2 P SiP 1 21/n 18.9802; 15.5193; 21.2731
90; 100.955; 90		2910.7Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573784 CIFC54 H80 B2 N4 P2 Si2P 1 21/n 19.951; 24.2287; 11.914
90; 114.187; 90		2620.29Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573785 CIFC27 H40 Cl N2 P SiP n a 2115.8487; 10.8456; 16.0281
90; 90; 90		2755.05Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573786 CIFC61 H88 B2 Cl2.03 I1.97 N4 P2 Si2P -110.922; 12.04; 13.307
105.263; 106.255; 95.783		1591.7Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573787 CIFC27 H40 B Cl I3 N2 P SiP 1 21/n 19.1943; 20.6319; 17.5682
90; 98.264; 90		3298Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573788 CIFC31 H48 B Cl3 N2 O P SiP 21 21 2111.1528; 22.0855; 27.2759
90; 90; 90		6718.5Phang, Si Jia Isabel; Zhang, Zheng-Feng; Wu, Chi-Shiun; Wong, Zhen Xuan; Su, Ming-Der; So, Cheuk-Wai
A silicon analogue of a fused bicyclic borirene derivative.
Chemical science, 2025, 16, 4512-4518
1573801 CIFC24 H20P 21 21 218.421; 13.116; 15.113
90; 90; 90		1669.2Martinez-Fernandez, L; Wu, Peicong; Bao, Lin-Tao; Wang, Xueli; Zhang, Rui-Hua; Wang, Wei; Yang, Hai-Bo; Chen, Jinquan; Improta, R.
On the nature of the triplet electronic states of naphthalene dimers.
Chemical science, 2025, 16, 4469-4479
1573802 CIFC24 H20P 1 21/c 18.4113; 11.9596; 8.1538
90; 105.735; 90		789.5Martinez-Fernandez, L; Wu, Peicong; Bao, Lin-Tao; Wang, Xueli; Zhang, Rui-Hua; Wang, Wei; Yang, Hai-Bo; Chen, Jinquan; Improta, R.
On the nature of the triplet electronic states of naphthalene dimers.
Chemical science, 2025, 16, 4469-4479
1573803 CIFC24 H20P 1 21 18.4807; 8.4592; 11.4471
90; 96.815; 90		815.41Martinez-Fernandez, L; Wu, Peicong; Bao, Lin-Tao; Wang, Xueli; Zhang, Rui-Hua; Wang, Wei; Yang, Hai-Bo; Chen, Jinquan; Improta, R.
On the nature of the triplet electronic states of naphthalene dimers.
Chemical science, 2025, 16, 4469-4479
1573804 CIFC24 H20P 43 21 28.9248; 8.9248; 20.831
90; 90; 90		1659.23Martinez-Fernandez, L; Wu, Peicong; Bao, Lin-Tao; Wang, Xueli; Zhang, Rui-Hua; Wang, Wei; Yang, Hai-Bo; Chen, Jinquan; Improta, R.
On the nature of the triplet electronic states of naphthalene dimers.
Chemical science, 2025, 16, 4469-4479
1573805 CIFC30 H20 Br N3 O3P 1 21/c 115.7313; 13.606; 24.1199
90; 108.505; 90		4895.7Luo, Wenjun; Zheng, Xinghua; Lin, Hehua; Fu, Li; Long, Lipeng; Yu, Daohong; Chen, Zhengwang; Yang, Min; Wang, Zhong-Xia
Discovery of intermolecular cascade annulation for dihydrobenzo[<i>b</i>][1,8]naphthyridine-ylidene-pyrrolidinetriones.
Chemical science, 2025, 16, 4119-4126
1573806 CIFC69.07 H62 Cl6 O4 P2 S2P 1 21/n 113.3952; 7.8096; 30.55
90; 95.775; 90		3179.7Dadgaryeganeh, Reza; LeBlanc, Jesse; Pradhan, Ekadashi; Miao, Dandan; Hussein, Amaar; Hunter, Howard N.; Zeng, Tao; Romero-Nieto, Carlos; Baumgartner, Thomas
From flat to twisted - multifunctional phosphacyclic nanocarbons based on Vat Orange 3.
Chemical science, 2025, 16, 3680-3692
1573807 CIFC72 H76 Cl6 O4 P2P -18.2286; 11.7231; 17.5716
92.692; 93.084; 108.449		1601.93Dadgaryeganeh, Reza; LeBlanc, Jesse; Pradhan, Ekadashi; Miao, Dandan; Hussein, Amaar; Hunter, Howard N.; Zeng, Tao; Romero-Nieto, Carlos; Baumgartner, Thomas
From flat to twisted - multifunctional phosphacyclic nanocarbons based on Vat Orange 3.
Chemical science, 2025, 16, 3680-3692
1573808 CIFC70 H80.01 O7 P2C 1 2/c 122.2953; 32.7948; 8.1542
90; 101.91; 90		5833.8Dadgaryeganeh, Reza; LeBlanc, Jesse; Pradhan, Ekadashi; Miao, Dandan; Hussein, Amaar; Hunter, Howard N.; Zeng, Tao; Romero-Nieto, Carlos; Baumgartner, Thomas
From flat to twisted - multifunctional phosphacyclic nanocarbons based on Vat Orange 3.
Chemical science, 2025, 16, 3680-3692
1573809 CIFC35 H37 O2 PP c c n18.8221; 34.2599; 8.6524
90; 90; 90		5579.4Dadgaryeganeh, Reza; LeBlanc, Jesse; Pradhan, Ekadashi; Miao, Dandan; Hussein, Amaar; Hunter, Howard N.; Zeng, Tao; Romero-Nieto, Carlos; Baumgartner, Thomas
From flat to twisted - multifunctional phosphacyclic nanocarbons based on Vat Orange 3.
Chemical science, 2025, 16, 3680-3692
1573810 CIFC70 H71.53 O4 P2C 1 2/c 158.8812; 8.3047; 34.7288
90; 97.344; 90		16842.7Dadgaryeganeh, Reza; LeBlanc, Jesse; Pradhan, Ekadashi; Miao, Dandan; Hussein, Amaar; Hunter, Howard N.; Zeng, Tao; Romero-Nieto, Carlos; Baumgartner, Thomas
From flat to twisted - multifunctional phosphacyclic nanocarbons based on Vat Orange 3.
Chemical science, 2025, 16, 3680-3692
1573816 CIFC109 H108 Cl2 N8 Pd6 Si2P -116.1964; 18.6192; 18.8234
83.984; 80.702; 73.139		5351Mitomo, Taiga; Wada, Yoshimasa; Suda, Tetsuro; Tamura, Atsushi; Yagi, Shunsuke; Kikkawa, Soichi; Yamazoe, Seiji; Sunada, Yusuke
A coordination polymer with a silylene-supported Pd<sub>6</sub> core as an efficient heterogeneous hydrogenation catalyst.
Chemical science, 2025, 16, 4450-4455
1573833 CIFC18 H33 F6 N2 O6 PP 1 21/n 111.9665; 10.5773; 19.8113
90; 100.165; 90		2468.2Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573834 CIFC12 H18 F6 N4 PP 1 21/c 17.8459; 9.828; 10.5087
90; 92.439; 90		809.6Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573835 CIFC18 H33 F6 N2 O6 PP 1 21/n 112.022; 10.629; 19.921
90; 100.318; 90		2504.4Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573836 CIFC18 H33 F6 N2 O6 PP 1 21/n 111.994; 10.463; 19.815
90; 100.89; 90		2441.9Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573837 CIFC18 H33 F6 N2 O6 PP 1 21/n 112.137; 10.6827; 20.015
90; 100.751; 90		2549.5Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573838 CIFC18 H33 F6 N2 O6 PP 1 21/n 111.985; 10.522; 19.813
90; 100.634; 90		2455.6Zhu, Ming; Huang, Pei-Zhi; Li, Lin-Mei; Yang, Yi-Xuan; Pan, Lei; Wang, Zhi-Jie; Ni, Hao-Fei; Zhang, Feng-Wen; Teri, Gele; Zhang, Zhi-Xu; Liu, Zunqi; Fu, Da-Wei; Zhang, Yi
Thermal-responsive luminescence/dielectric responses with reversibly shifted light emissions.
Chemical science, 2025, 16, 4101-4108
1573839 CIFC27 H9 O18 Th2F d -3 m :213.6682; 13.6682; 13.6682
90; 90; 90		2553.49Gaidimas, Madeleine A.; Smoljan, Courtney S.; Ye, Zi-Ming; Stern, Charlotte L.; Malliakas, Christos D.; Kirlikovali, Kent O.; Farha, Omar K.
Thorium metal-organic framework crystallization for efficient recovery from rare earth element mixtures.
Chemical science, 2025, 16, 3895-3903
1573840 CIFC10 H6 O4F d d 214.617; 30.092; 3.6052
90; 90; 90		1585.8Dunning, Samuel G.; Hari, Anirudh; Zhu, Li; Chen, Bo; Cody, George D.; Romi, Sebastiano; Zhang, Dongzhou; Strobel, Timothy A.
Double-core nanothread formation from α-furil <i>via</i> a pressure-induced planarization pathway.
Chemical science, 2025, 16, 4144-4151
1573841 CIFC10 H6 O4P 1 21/n 114.586; 7.0535; 3.4512
90; 93.132; 90		354.54Dunning, Samuel G.; Hari, Anirudh; Zhu, Li; Chen, Bo; Cody, George D.; Romi, Sebastiano; Zhang, Dongzhou; Strobel, Timothy A.
Double-core nanothread formation from α-furil <i>via</i> a pressure-induced planarization pathway.
Chemical science, 2025, 16, 4144-4151
1573842 CIFC10 H6 O4P 1 21/n 13.313; 6.957; 14.228
90; 94.48; 90		326.9Dunning, Samuel G.; Hari, Anirudh; Zhu, Li; Chen, Bo; Cody, George D.; Romi, Sebastiano; Zhang, Dongzhou; Strobel, Timothy A.
Double-core nanothread formation from α-furil <i>via</i> a pressure-induced planarization pathway.
Chemical science, 2025, 16, 4144-4151
1573843 CIFHg3 N2 O16 Te4P n m a9.2209; 8.3046; 19.3943
90; 90; 90		1485.14Tang, Ru-Ling; Lv, Yi-Lei; Ma, Liang; Miao, Bing-Wei; Liu, Wenlong; Guo, Sheng-Ping
"All-four-in-one": a novel mercury tellurite-nitrate Hg<sub>3</sub>(TeO<sub>3</sub>)(Te<sub>3</sub>O<sub>7</sub>)(NO<sub>3</sub>)<sub>2</sub> exhibiting exceptional optical anisotropy.
Chemical science, 2025, 16, 4749-4754
1573844 CIFC18 H20 O7P 1 21 17.2202; 13.9741; 9.0021
90; 111.683; 90		844.01Paciorek, Jan; Steinborn, Christian; Gordiy, Igor; Plangger, Immanuel; Schmutzler, Dirk; Barber, David M.; Wurst, Klaus; Riniker, Sereina; Magauer, Thomas
Asymmetric total synthesis of glauconic and glaucanic acid.
Chemical science, 2025, 16, 4159-4166
1573846 CIFC57 H68 Br Cu N4P -112.3872; 15.6834; 16.433
90.934; 111.881; 110.488		2735.3Zhou, Jiajing; Zhang, Zhiqiang; Cao, Yan; Xie, Weilong
Multiligand-enabled, copper-catalyzed Hiyama coupling of arylsilanes with unactivated secondary alkyl halides: reaction development and mechanistic insights.
Chemical science, 2025, 16, 5109-5117
1573847 CIFC23 H21 B3 N2 O3P b c a6.81856; 18.79523; 32.85532
90; 90; 90		4210.62Procter, Richard J.; Alamillo-Ferrer, Carla; Shabbir, Usman; Britton, Phyllida; Bučar, Dejan-Krešimir; Dumon, Alexandre S.; Rzepa, Henry S.; Burés, Jordi; Whiting, Andrew; Sheppard, Tom D.
Borate-catalysed direct amidation reactions of coordinating substrates.
Chemical science, 2025, 16, 4718-4724
1573849 CIFC10 H11 N3 O3 SP b c n7.2257; 13.4248; 24.382
90; 90; 90		2365.1Lu, Jiachen; Ok, Kang Min
Synergistic engineering of ultraviolet metal-free crystals with exceptional birefringence <i>via</i> pyridine-derived dimers.
Chemical science, 2025, 16, 4703-4709
1573850 CIFC15 H15 N3 O5 SP 1 21/c 117.5972; 7.0455; 12.8268
90; 90.881; 90		1590.09Lu, Jiachen; Ok, Kang Min
Synergistic engineering of ultraviolet metal-free crystals with exceptional birefringence <i>via</i> pyridine-derived dimers.
Chemical science, 2025, 16, 4703-4709
1573851 CIFC122 H170 Mg4 N8 P8P 1 21/c 126.4049; 18.7396; 27.4993
90; 118.57; 90		11950.2Thum, Stefan; Townrow, Oliver P. E.; Langer, Jens; Harder, Sjoerd
Tuning the selectivity of P<sub>4</sub> reduction at alkaline-earth metal centres.
Chemical science, 2025, 16, 4528-4536
1573852 CIFC74 H114 Mg2 N4 P4P n m a26.1211; 21.8425; 12.8482
90; 90; 90		7330.5Thum, Stefan; Townrow, Oliver P. E.; Langer, Jens; Harder, Sjoerd
Tuning the selectivity of P<sub>4</sub> reduction at alkaline-earth metal centres.
Chemical science, 2025, 16, 4528-4536
1573853 CIFC90 H154 Ca2 N4 O4 P4P 1 21/c 113.4588; 23.0603; 15.7858
90; 111.861; 90		4547.04Thum, Stefan; Townrow, Oliver P. E.; Langer, Jens; Harder, Sjoerd
Tuning the selectivity of P<sub>4</sub> reduction at alkaline-earth metal centres.
Chemical science, 2025, 16, 4528-4536
1573854 CIFC97 H146 B2 Ca2 N4P -112.7375; 16.5295; 21.8122
106.025; 90.612; 98.438		4359.87Thum, Stefan; Townrow, Oliver P. E.; Langer, Jens; Harder, Sjoerd
Tuning the selectivity of P<sub>4</sub> reduction at alkaline-earth metal centres.
Chemical science, 2025, 16, 4528-4536
1573855 CIFC131 H211 Ca3 N6 O4 P7P -120.4699; 20.4809; 21.4594
70.084; 81.755; 64.564		7638.6Thum, Stefan; Townrow, Oliver P. E.; Langer, Jens; Harder, Sjoerd
Tuning the selectivity of P<sub>4</sub> reduction at alkaline-earth metal centres.
Chemical science, 2025, 16, 4528-4536
1573868 CIFC25 H10 Cl10 NP -18.305; 8.8068; 19.111
97.232; 96.934; 95.16		1368.7Gao, Shengxiang; Wu, Chunxiao; Zhang, Ming; Li, Feng
Stable luminescent diphenylamine biphenylmethyl radicals with α-type D<sub>0</sub> → D<sub>1</sub> transition and antiferromagnetic properties.
Chemical science, 2025, 16, 4668-4675
1573869 CIFC25 H14 Cl6 NP 1 21/c 116.4717; 8.3566; 17.0028
90; 103.423; 90		2276.5Gao, Shengxiang; Wu, Chunxiao; Zhang, Ming; Li, Feng
Stable luminescent diphenylamine biphenylmethyl radicals with α-type D<sub>0</sub> → D<sub>1</sub> transition and antiferromagnetic properties.
Chemical science, 2025, 16, 4668-4675
1573870 CIFC7 H2.4 O6.2 VI m m a16.342; 6.8717; 10.284
90; 90; 90		1154.9Smoljan, Courtney S.; Formalik, Filip; Barsoum, Michael L.; Fahy, Kira M.; Gaidimas, Madeleine A.; Son, Florencia A.; Xie, Haomiao; Idrees, Karam B.; Farha, Omar K.; Snurr, Randall Q.
Exceeding flexpectations: a combined experimental and computational investigation of structural flexibility in 3-dimensional linker-based metal-organic frameworks.
Chemical science, 2025, 16, 4831-4841
1573879 CIFC48 H68 N2 Ni S4P -18.8358; 9.0954; 14.2686
94.49; 97.731; 97.231		1121.94Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573880 CIFC11 H12 Cl2 N2 S2P n m a14.5441; 6.8348; 13.3132
90; 90; 90		1323.41Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573881 CIFC64 H88 N4 Ni O2 S4P 1 21/n 110.3602; 22.0224; 13.6369
90; 91.721; 90		3109.94Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573882 CIFC39 H63 N5 Ni S2P 1 21/c 114.4786; 13.8664; 19.8298
90; 94.856; 90		3966.86Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573883 CIFC14 H18 N2 S2P 1 21/n 111.8352; 8.4874; 15.0477
90; 107.19; 90		1444.02Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573884 CIFC44 H66 N6 Ni O S2P 21 21 2112.6464; 14.4357; 24.9817
90; 90; 90		4560.65Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573885 CIFC62 H66 N4 Ni S4P 1 21/c 116.3996; 12.5018; 14.1711
90; 101.833; 90		2843.68Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573886 CIFC52 H74 N6 Ni S2P -112.2463; 13.0402; 18.3208
84.384; 76.105; 64.184		2556.58Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573887 CIFC116 H176 N24 Ni4 O S8R -3 :H41.9148; 41.9148; 19.7374
90; 90; 120		30030Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573888 CIFC68 H96 K N4 Ni O3 S4P 21 21 2112.2516; 19.8503; 27.2496
90; 90; 90		6627.05Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573889 CIFC54 H86 K N2 Ni O3 S4P 1 21/n 111.042; 30.096; 34.2823
90; 96.44; 90		11320.8Luff, Martin S.; Filipovic, Tin M.; Corsei, Celine S.; Oppel, Kai; Krummenacher, Ivo; Bertermann, Rüdiger; Finze, Maik; Braunschweig, Holger; Radius, Udo
Azolium-2-dithiocarboxylates as redox active ligands in nickel chemistry.
Chemical science, 2025, 16, 5142-5154
1573890 CIFC136 H150 Al8 Dy2 N16 Na2 O67P 4 n c17.1664; 17.1664; 15.3325
90; 90; 90		4518.3Yan, Han; Calado, Claudia M. S.; Wang, Hao; Murugesu, Muralee; Sun, Wen-Bin
A novel Ln<sup>3+</sup>/Al<sup>3+</sup> metallacrown multifunctional material for latent fingerprint detection, luminescent thermometers and luminescent sensors.
Chemical science, 2025, 16, 4821-4830
1573891 CIFC38 H26 F8 N2 O2P -19.4208; 9.893; 9.9488
87.466; 62.402; 89.609		820.83Górski, Krzysztof; Shelton, Steve; Lingagouder, Jaijanarthanan; Data, Przemyslaw; Jacquemin, Denis; Gryko, Daniel T.
1,4-Dihydropyrrolo[3,2-<i>b</i>]pyrrole modified with dibenzoxazepine: a highly efficient core for charge-transfer-based OLED emitters.
Chemical science, 2025, 16, 5223-5233
1573902 CIFC56 H72 Au2 N4P -19.3309; 12.6622; 14.2997
72.396; 72.255; 82.124		1531.89Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573903 CIFC32.5 H42 Au N4 SP 1 21/n 110.7024; 27.593; 12.0247
90; 92.657; 90		3547.2Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573904 CIFC72 H108 Au2 N4 O4P 1 21/n 112.7986; 15.2227; 18.1384
90; 101.827; 90		3458.9Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573905 CIFC32 H45 Au N2 SiP -19.0241; 12.0583; 15.9337
80.824; 89.441; 78.132		1674.58Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573906 CIFC48 H55 Au N2 O4P 1 21/n 118.4242; 13.8027; 18.9461
90; 109.094; 90		4553Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573907 CIFC150 H178 Au4 N8 O4P -113.4415; 29.354; 36.128
93.781; 94.261; 100.703		13922Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573908 CIFC38 H51 Au N2 O4 SiP 1 21/n 112.7366; 15.5654; 19.9574
90; 92.718; 90		3952.1Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573909 CIFC62 H78 Au2 N4 O4P c c a36.539; 12.2149; 29.581
90; 90; 90		13202.6Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573910 CIFC84 H108 Au3 F3 N6 O3 SP 1 21/n 116.3416; 20.8456; 30.6473
90; 100.38; 90		10269.2Cayuela-Castillo, Juan; Fernández-de-Córdova, Francisco J; See, Matthew S.; Fernández, Israel; Ríos, Pablo
Stepwise alkyne insertion in Au(i) acetylides: influence of the nuclearity.
Chemical science, 2025, 16, 4684-4694
1573911 CIFC15 H13 Cl2 N3 O2 SP 1 21/c 115.203; 14.457; 7.3056
90; 95.595; 90		1598Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573912 CIFC11 H13 N O2 SP 1 21/n 19.744; 8.942; 12.444
90; 99.429; 90		1069.6Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573913 CIFC19 H21 B N2 O4 SP 1 21/c 110.87; 7.36; 24.2055
90; 102.98; 90		1887Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573914 CIFC24 H26 O4 SP 21 21 216.1887; 15.3738; 21.416
90; 90; 90		2037.6Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573915 CIFC14 H12 O5 SP -18.5144; 11.3398; 13.7819
91.78; 101.702; 90.986		1302Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573916 CIFC16 H20 N6 O2 S2P 1 21/c 17.0417; 21.4946; 12.9761
90; 104.119; 90		1904.71Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573917 CIFC18 H20 N2 O4 SP 1 21/c 111.72; 13.2505; 11.8575
90; 111.107; 90		1717.9Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573918 CIFC23 H20 Cl N3 O3 SP b c a16.5203; 11.144; 23.4626
90; 90; 90		4319.52Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573919 CIFC17 H17 Cl N O3 SP 1 21/c 111.096; 10.649; 14.752
90; 107.211; 90		1665.1Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573920 CIFC47 H46 N3 O10 S2P -19.952; 12.022; 18.755
78.612; 77.456; 84.925		2144.8Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573921 CIFC17 H18 N3 O2 S2P 1 21/n 113.3042; 15.8775; 16.5955
90; 110.243; 90		3289.1Datta, Paramita; Maji, Subir; Biswas, Prativa; Jain, Divya; Dey, Partha Protim; Mandal, Swadhin K.
An organophotocatalytic redox-neutral strategy for late-stage drug functionalization with SO<sub>2</sub> gas.
Chemical science, 2025, 16, 5064-5075
1573924 CIFC270 H210 N30 O18 Zn3P 63/m26.4305; 26.4305; 28.419
90; 90; 120		17192.9Xu, Ziwei; Ying, Xinwen; Li, Yi; Dong, Xiaoyan; Liu, Jiyong; Wang, Shuping; Little, Marc A.; Zhang, Dahao; Xie, Yongshu; Zhang, Zibin; Yu, Ling; Huang, Feihe; Li, Shijun
Template-directed self-assembly of porphyrin nanorings through an imine condensation reaction.
Chemical science, 2025, 16, 5166-5173
1573927 CIFC20 H21 F2 N O3P 1 21/c 110.45569; 18.57018; 10.44754
90; 115.809; 90		1826.19Fu, Hong; Wang, Zuo-Shuai; Li, Si-Jia; Zhu, Lin-Yuan; Wang, Xiao-Jian; Wang, Hong-Chen; Han, Bing
Photocatalytic 1,3-difluoroalkylcarboxylation of alkenes by triple kinetic-controlled radical self-ordering.
Chemical science, 2025, 16, 5849-5856
1573928 CIFC22 H23 F2 N O3P -19.938; 10.9753; 11.084
108.444; 102.977; 113.996		956.77Fu, Hong; Wang, Zuo-Shuai; Li, Si-Jia; Zhu, Lin-Yuan; Wang, Xiao-Jian; Wang, Hong-Chen; Han, Bing
Photocatalytic 1,3-difluoroalkylcarboxylation of alkenes by triple kinetic-controlled radical self-ordering.
Chemical science, 2025, 16, 5849-5856
1573929 CIFC47 H70 F3 Gd N6 O20 SP 1 21/c 116.8352; 17.2648; 18.6772
90; 94.3; 90		5413.37Bodman, Samantha E.; Stachelek, Patrycja; Rehman, Umatur; Plasser, Felix; Pal, Robert; Butler, Stephen J.
A switch-on luminescent europium(iii) probe for selective and time-resolved detection of adenosine diphosphate (ADP).
Chemical science, 2025, 16, 5602-5612
1573930 CIFC22 H19 Cl OP b c a11.8872; 10.1609; 28.5346
90; 90; 90		3446.5Wang, Yue; Miao, Junhao; Dong, Honglin; Zhang, Dongliang; Chen, Bei; Guan, Meihui; Zhang, Ge; Zhang, Qian
A photo- and cobalt-catalyzed highly selective and divergent hydrofunctionalization of 1,3-dienes with phenols.
Chemical science, 2025, 16, 5640-5650
1573931 CIFC69 H37.5 Au B F20 N4.5P 1 21/c 129.74; 16.255; 24.079
90; 98.901; 90		11500Haketa, Yohei; Nakajima, Ryoya; Maruyama, Yuto; Tanaka, Hiroki; Choi, Wookjin; Seki, Shu; Sato, Shunsuke; Baba, Hitomi; Ishii, Yoshiki; Watanabe, Go; Bulgarevich, Kirill; Takimiya, Kazuo; Deguchi, Kenzo; Ohki, Shinobu; Hashi, Kenjiro; Nakanishi, Takashi; Ishibashi, Yukihide; Asahi, Tsuyoshi; Ohta, Kazuchika; Maeda, Hiromitsu
Electrically conductive charge-segregated pseudo-polymorphs comprising highly planar expanded π-electronic cations.
Chemical science, 2025, 16, 4998-5006
1573932 CIFC46 H20 Au N9P b c a7.2275; 29.8407; 30.6964
90; 90; 90		6620.4Haketa, Yohei; Nakajima, Ryoya; Maruyama, Yuto; Tanaka, Hiroki; Choi, Wookjin; Seki, Shu; Sato, Shunsuke; Baba, Hitomi; Ishii, Yoshiki; Watanabe, Go; Bulgarevich, Kirill; Takimiya, Kazuo; Deguchi, Kenzo; Ohki, Shinobu; Hashi, Kenjiro; Nakanishi, Takashi; Ishibashi, Yukihide; Asahi, Tsuyoshi; Ohta, Kazuchika; Maeda, Hiromitsu
Electrically conductive charge-segregated pseudo-polymorphs comprising highly planar expanded π-electronic cations.
Chemical science, 2025, 16, 4998-5006
1573933 CIFC60 H20 Au B F20 N4P n n a7.6381; 27.9614; 28.9791
90; 90; 90		6189.1Haketa, Yohei; Nakajima, Ryoya; Maruyama, Yuto; Tanaka, Hiroki; Choi, Wookjin; Seki, Shu; Sato, Shunsuke; Baba, Hitomi; Ishii, Yoshiki; Watanabe, Go; Bulgarevich, Kirill; Takimiya, Kazuo; Deguchi, Kenzo; Ohki, Shinobu; Hashi, Kenjiro; Nakanishi, Takashi; Ishibashi, Yukihide; Asahi, Tsuyoshi; Ohta, Kazuchika; Maeda, Hiromitsu
Electrically conductive charge-segregated pseudo-polymorphs comprising highly planar expanded π-electronic cations.
Chemical science, 2025, 16, 4998-5006
1573934 CIFC80 H54 Au B F24 N6C 1 2/c 135.803; 21.342; 20.798
90; 116.122; 90		14269Haketa, Yohei; Nakajima, Ryoya; Maruyama, Yuto; Tanaka, Hiroki; Choi, Wookjin; Seki, Shu; Sato, Shunsuke; Baba, Hitomi; Ishii, Yoshiki; Watanabe, Go; Bulgarevich, Kirill; Takimiya, Kazuo; Deguchi, Kenzo; Ohki, Shinobu; Hashi, Kenjiro; Nakanishi, Takashi; Ishibashi, Yukihide; Asahi, Tsuyoshi; Ohta, Kazuchika; Maeda, Hiromitsu
Electrically conductive charge-segregated pseudo-polymorphs comprising highly planar expanded π-electronic cations.
Chemical science, 2025, 16, 4998-5006
1573935 CIFC70.67 H36 Au B Cl4 F24 N4C 1 2/c 125.853; 37.935; 20.488
90; 90.017; 90		20093Haketa, Yohei; Nakajima, Ryoya; Maruyama, Yuto; Tanaka, Hiroki; Choi, Wookjin; Seki, Shu; Sato, Shunsuke; Baba, Hitomi; Ishii, Yoshiki; Watanabe, Go; Bulgarevich, Kirill; Takimiya, Kazuo; Deguchi, Kenzo; Ohki, Shinobu; Hashi, Kenjiro; Nakanishi, Takashi; Ishibashi, Yukihide; Asahi, Tsuyoshi; Ohta, Kazuchika; Maeda, Hiromitsu
Electrically conductive charge-segregated pseudo-polymorphs comprising highly planar expanded π-electronic cations.
Chemical science, 2025, 16, 4998-5006
1573936 CIFC48 H40 O12 P4 Te2P -19.41547; 10.53235; 23.2502
93.7232; 99.2727; 91.1692		2269.61Xue, Miaomiao; Ye, Guigui; Zhang, Lei; Dong, Qiang; Lee, Chun-Sing; Li, Zhen; Zhang, Qichun
Preparation, single-crystal structure and room-temperature phosphorescence of a covalent organic polymer containing Te-O-P bonds.
Chemical science, 2025, 16, 5260-5265
1573937 CIFC38 H38 N2 O2P 1 21/n 113.536; 5.5532; 21.084
90; 92.725; 90		1583.1Zhao, Zhenxiang; Wang, Senhao; Shi, Xiaomei; Fu, Hongbing; Wang, Long
Multiple effects of aromatic substituents on excited-state properties and singlet fission process in azaquinodimethane systems.
Chemical science, 2025, 16, 5565-5572
1573938 CIFC34 H34 N2 O2 S2P -111.0327; 12.2831; 24.7672
77.396; 89.959; 64.379		2936.6Zhao, Zhenxiang; Wang, Senhao; Shi, Xiaomei; Fu, Hongbing; Wang, Long
Multiple effects of aromatic substituents on excited-state properties and singlet fission process in azaquinodimethane systems.
Chemical science, 2025, 16, 5565-5572
1573939 CIFC30 H24 N2 OC 1 2/c 139.3453; 6.1691; 22.6081
90; 116.888; 90		4894.3Liao, Huijuan; Dong, Jianyang; Zhou, Xuechen; Jiang, Qin; Lv, Zishan; Lei, Fang; Xue, Dong
Silver-mediated formal [4π + 2<i>σ</i>] cycloaddition reactions of bicyclobutanes with nitrile imines: access to 2,3-diazobicyclo[3.1.1]heptenes.
Chemical science, 2025, 16, 4654-4660
1573940 CIFC54 H60.7 Cu F6 N4.4 O6.55 PP -111.8395; 14.4553; 15.7362
70.349; 82.732; 88.868		2515.2Saeednia, Borna; Sragow, Aria M.; Lin, Yannan; Sheehan, Colton J.; Metlay, Amy S.; Gau, Michael R.; Dye, Samantha A.; O'Konski, Sarah P; Mallouk, Thomas E.; Dmochowski, Ivan J.
Unusually air-stable copper(i) complexes showing high selectivity for carbon monoxide.
Chemical science, 2025, 16, 5058-5063
1573941 CIFC62 H69.5 Cu F6 N7.5 O12.5 S2P 21 21 2115.4717; 18.0548; 22.9196
90; 90; 90		6402.3Saeednia, Borna; Sragow, Aria M.; Lin, Yannan; Sheehan, Colton J.; Metlay, Amy S.; Gau, Michael R.; Dye, Samantha A.; O'Konski, Sarah P; Mallouk, Thomas E.; Dmochowski, Ivan J.
Unusually air-stable copper(i) complexes showing high selectivity for carbon monoxide.
Chemical science, 2025, 16, 5058-5063
1573942 CIFC56 H61 Cu F3 N8 O9 SP 1 21/c 118.0509; 16.2265; 20.4026
90; 115.111; 90		5411.2Saeednia, Borna; Sragow, Aria M.; Lin, Yannan; Sheehan, Colton J.; Metlay, Amy S.; Gau, Michael R.; Dye, Samantha A.; O'Konski, Sarah P; Mallouk, Thomas E.; Dmochowski, Ivan J.
Unusually air-stable copper(i) complexes showing high selectivity for carbon monoxide.
Chemical science, 2025, 16, 5058-5063
1573948 CIFC10 H16 Ca N2 O10 S2P -16.986; 11.274; 11.59
67.534; 89.112; 88.67		843.3Xu, Longyun; Li, Conggang; Li, Shuaifeng; Zhao, Huijian; Kong, Xianghao; Qu, Zaixin; Feng, Wenjie; Xu, Kaidong; Ye, Ning; Hu, Zhanggui
Hydrogen bonding regulation-oriented design of pyridine sulfonate as a promising UV birefringent crystal characterized by enhanced structural anisotropy.
Chemical science, 2025, 16, 5186-5193
1573949 CIFC41 H48 Cr F9 N12 O9 S3P 1 21/c 121.2505; 11.5885; 20.6086
90; 92.21; 90		5071.3Ye, Yating; Poncet, Maxime; Yaltseva, Polina; Salcedo-Abraira, Pablo; Rodríguez-Diéguez, Antonio; Martín, Javier Heredia; Cuevas-Contreras, Laura; Cruz, Carlos M.; Doistau, Benjamin; Piguet, Claude; Wenger, Oliver S.; Herrera, Juan Manuel; Jiménez, Juan-Ramón
Modulating the spin-flip rates and emission energies through ligand design in chromium(iii) molecular rubies.
Chemical science, 2025, 16, 5205-5213
1573950 CIFC45 H54 Cr F9 N10 O19 S3P n a 2124.8078; 21.0257; 11.4987
90; 90; 90		5997.7Ye, Yating; Poncet, Maxime; Yaltseva, Polina; Salcedo-Abraira, Pablo; Rodríguez-Diéguez, Antonio; Martín, Javier Heredia; Cuevas-Contreras, Laura; Cruz, Carlos M.; Doistau, Benjamin; Piguet, Claude; Wenger, Oliver S.; Herrera, Juan Manuel; Jiménez, Juan-Ramón
Modulating the spin-flip rates and emission energies through ligand design in chromium(iii) molecular rubies.
Chemical science, 2025, 16, 5205-5213

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 20 | Next 100 Blue right arrow | Last Blue right arrow Blue right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!
Top of the page
All data in the COD and the database itself are dedicated to the public domain and licensed under the CC0 License . Users of the data should acknowledge the original authors of the structural data.