Crystallography Open Database

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Searching year of publication is 2025

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1571675 CIFC22 H27 N5 O4 SP 1 21 19.189; 12.6757; 10.9694
90; 114.013; 90
1167.1Rehman, Zainab; Lubay, Jairah; Franks, W. Trent; Bartók, Albert P; Corlett, Emily K.; Nguyen, Bao; Scrivens, Garry; Samas, Brian M.; Frericks-Schmidt, Heather; Brown, Steven P.
Organic NMR crystallography: enabling progress for applications to pharmaceuticals and plant cell walls.
Faraday discussions, 2025, 255, 222-243
1571705 CIFC9 H15 N2 O3.5P 1 21 15.9813; 11.3702; 14.985
90; 93.681; 90
1017Ramalhete, Susana M.; Nartowski, Karol P.; Green, Hayley; Angulo, Jesús; Iuga, Dinu; Fábián, László; Lloyd, Gareth O.; Khimyak, Yaroslav Z.
Probing assembly/disassembly of ordered molecular hydrogels.
Faraday discussions, 2025, 255, 495-519
1572649 CIFLi12 Nb4 O16C 1 2/m 110.389; 11.9401; 5.201
90; 109.899; 90
606.6Ko, Sarah L.; Dorrell, Jordan A.; Morris, Andrew J.; Griffith, Kent J.
Metastable layered lithium-rich niobium and tantalum oxides <i>via</i> nearly instantaneous cation exchange.
Faraday discussions, 2025, 255, 429-450
1572650 CIFNa12 Nb4 O16C 1 2/m 111.1218; 13.00203; 5.75288
90; 109.49; 90
784.23Ko, Sarah L.; Dorrell, Jordan A.; Morris, Andrew J.; Griffith, Kent J.
Metastable layered lithium-rich niobium and tantalum oxides <i>via</i> nearly instantaneous cation exchange.
Faraday discussions, 2025, 255, 429-450
1572651 CIFNa12 Nb4 O16C 1 2/m 111.0923; 12.97113; 5.73501
90; 109.429; 90
778.16Ko, Sarah L.; Dorrell, Jordan A.; Morris, Andrew J.; Griffith, Kent J.
Metastable layered lithium-rich niobium and tantalum oxides <i>via</i> nearly instantaneous cation exchange.
Faraday discussions, 2025, 255, 429-450
1572652 CIFLi12 Nb4 O16C 1 2/m 110.362; 11.9047; 5.179
90; 109.83; 90
601Ko, Sarah L.; Dorrell, Jordan A.; Morris, Andrew J.; Griffith, Kent J.
Metastable layered lithium-rich niobium and tantalum oxides <i>via</i> nearly instantaneous cation exchange.
Faraday discussions, 2025, 255, 429-450
1572854 CIF
HKL
C32 H34 N4 O9 S3P -111.2834; 13.3905; 13.4806
113.251; 105.083; 98.375
1734.64Mulholland, Michael E.; Filiatrault, Heather L.; Maris, Thierry; Skene, W. G.
Structural study of an electroactive allyl ester thiophenoazomethine for PDMS blending
Journal of Molecular Structure, 2025, 1320, 139416-1-139416-8
1572930 CIFC60 H72 N3 O3 Pd3 Se3P -114.0778; 15.5286; 31.7803
79.873; 77.515; 64.584
6099.4Sarkar, Prasenjit; Manamel, Litty Thomas; Saha, Puranjay; Jana, Chinmay; Sarmah, Amrit; Mohanan, Kannan Udaya; Das, Bikas C.; Mukherjee, Chandan
A triradical-containing trinuclear Pd(II) complex: spin-polarized electronic transmission, analog resistive switching and neuromorphic advancements.
Materials horizons, 2025, 12, 246-257
1572973 CIFC20 H21 N O3P -19.2173; 9.4972; 9.5809
88.263; 82.367; 85.479
828.51Fu, Shijie; Jia, Hao; Meng, Xinmiao; Wang, Chengyuan; Li, Qian; Li, Lei; Yang, Jiaxiang; Niu, Helin
Fine-tuning the molecular conformation and packing structures of coumarin-based luminogens to achieve distinct piezochromic properties upon mechanical grinding and under hydrostatic pressures.
Materials horizons, 2025, 12, 293-302
1572974 CIFC20 H18 N2 O2P -16.633; 7.5002; 17.4918
79.488; 81.308; 64.528
769.83Fu, Shijie; Jia, Hao; Meng, Xinmiao; Wang, Chengyuan; Li, Qian; Li, Lei; Yang, Jiaxiang; Niu, Helin
Fine-tuning the molecular conformation and packing structures of coumarin-based luminogens to achieve distinct piezochromic properties upon mechanical grinding and under hydrostatic pressures.
Materials horizons, 2025, 12, 293-302
1572975 CIFC20 H18 N2 O2P 1 21/c 111.443; 13.277; 10.8931
90; 99.297; 90
1633.24Fu, Shijie; Jia, Hao; Meng, Xinmiao; Wang, Chengyuan; Li, Qian; Li, Lei; Yang, Jiaxiang; Niu, Helin
Fine-tuning the molecular conformation and packing structures of coumarin-based luminogens to achieve distinct piezochromic properties upon mechanical grinding and under hydrostatic pressures.
Materials horizons, 2025, 12, 293-302
1572976 CIFC20 H21 N O3P 1 21/n 16.4917; 19.911; 12.759
90; 90.73; 90
1649Fu, Shijie; Jia, Hao; Meng, Xinmiao; Wang, Chengyuan; Li, Qian; Li, Lei; Yang, Jiaxiang; Niu, Helin
Fine-tuning the molecular conformation and packing structures of coumarin-based luminogens to achieve distinct piezochromic properties upon mechanical grinding and under hydrostatic pressures.
Materials horizons, 2025, 12, 293-302
1573032 CIFC18 H20 O4P b c a4.8827; 10.6999; 29.5508
90; 90; 90
1543.86Pinson, Dana M.; Eckstrom, Francesca D.; Ostrom, Gregory S.; Randall McClain, K.; Baldwin, Lawrence C.; Harvey, Benjamin G.
[Ru]-Catalyzed olefin metathesis and ethenolysis for the synthesis and recycling of bio-based polycarbonates and polycyanurates
Polymer Chemistry, 2025, 16, 133-148
1573033 CIFC21 H22 O5C 1 2/c 115.9421; 8.679; 13.2926
90; 101.624; 90
1801.46Pinson, Dana M.; Eckstrom, Francesca D.; Ostrom, Gregory S.; Randall McClain, K.; Baldwin, Lawrence C.; Harvey, Benjamin G.
[Ru]-Catalyzed olefin metathesis and ethenolysis for the synthesis and recycling of bio-based polycarbonates and polycyanurates
Polymer Chemistry, 2025, 16, 133-148
1573034 CIFC33 H33 N3 O6P 1 21/n 113.0353; 11.7214; 20.182
90; 107.691; 90
2937.8Pinson, Dana M.; Eckstrom, Francesca D.; Ostrom, Gregory S.; Randall McClain, K.; Baldwin, Lawrence C.; Harvey, Benjamin G.
[Ru]-Catalyzed olefin metathesis and ethenolysis for the synthesis and recycling of bio-based polycarbonates and polycyanurates
Polymer Chemistry, 2025, 16, 133-148
1573045 CIFC66 H44 B Cl4 F20 N O P2P -113.37; 15.247; 16.3
87.59; 75.11; 79.81
3161You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573046 CIFC63 H48 B Cl2 F20 N O P2C 1 c 110.1018; 31.87; 18.321
90; 92.637; 90
5892.1You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573047 CIFC65 H42 B F20 N O P2P -113.124; 16.183; 17.493
110.67; 95.58; 113.696
3057You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573048 CIFC32.5 H34 Cl2 N O P2P -112.944; 13.582; 19.223
103.948; 103.841; 97.75
3117.5You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573049 CIFC71 H48 B Cl2 F20 N O P2P -114.195; 15.574; 16.591
82.59; 77.118; 64.527
3226You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573050 CIFC71 H58 B Cl4 F20 N O P2P -113.127; 16.617; 17.814
114.495; 98.862; 91.899
3473.5You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573051 CIFC48 H34 Al F36 N O5 P2P b c a20.836; 18.713; 29.74
90; 90; 90
11596You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573052 CIFC63 H40 B F20 N O2 P2P 1 21/c 111.884; 16.729; 31.882
90; 96.442; 90
6298You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573053 CIFC64 H42 B F20 N O2 P2C 1 2/c 150.046; 10.705; 27.527
90; 123.266; 90
12331You, Lijun; Roth, Daniel; Greb, Lutz
Structural constraint at a P-P bond: phosphinophosphination of alkenes, alkynes, and carbonyls by a concerted mechanism.
Chemical science, 2025, 16, 1716-1721
1573160 CIFC84 H100 Ga2 N4I 41 c d17.2516; 17.2516; 47.4743
90; 90; 90
14129.2Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573161 CIFC80 H78 F16 Ga2 N4P 1 21/c 119.4377; 19.6182; 19.7964
90; 100.679; 90
7418.3Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573162 CIFC82.88 H87 Fe1.97 Ga2 I0.06 N4 O7.88P -110.8571; 14.302; 25.6182
98.115; 96.616; 102.807
3795.66Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573163 CIFC78 H90 Cl4 Ga2 N4P 1 21/n 110.3023; 18.4534; 20.0384
90; 103.039; 90
3711.3Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573164 CIFC73 H86 Ga2 N4P -112.7988; 14.6243; 18.1282
80.487; 79.632; 85.811
3288.5Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573165 CIFC66 H78 Ga2 I4 N4P -110.5694; 12.1801; 13.6704
101.963; 98.911; 107.53
1596.52Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573166 CIFC88 H88 F12 Ga2 N6C 1 2/c 121.1589; 19.2641; 19.4975
90; 91.377; 90
7945Merschel, Arne; Heda, Shkelqim; Vishnevskiy, Yury V.; Neumann, Beate; Stammler, Hans-Georg; Ghadwal, Rajendra S.
Annulated carbocyclic gallylene and bis-gallylene with two-coordinated Ga(i) atoms.
Chemical science, 2025, 16, 2222-2230
1573171 CIFC144 H84 Cu16 F54 N12 P3 S25R 3 c :H24.815; 24.815; 66.157
90; 90; 120
35281Kumar, Shibaditya; Mishra, Saikat; Das, Aniruddha; Mahiya, Kuldeep; Laha, Sourav; Maji, Milan; Patra, Apurba K.
Analogous copper nanoclusters (Cu<sub>16/17</sub>) with two electron superatomic and mixed valence copper(II)/copper(I) and copper(I)/copper(0) characters.
Nanoscale, 2025, 17, 982-991
1573172 CIFC212 H172 Cl Cu16 F36 N12 O4 S25C 1 2/c 139.487; 20.216; 31.428
90; 113.044; 90
23086Kumar, Shibaditya; Mishra, Saikat; Das, Aniruddha; Mahiya, Kuldeep; Laha, Sourav; Maji, Milan; Patra, Apurba K.
Analogous copper nanoclusters (Cu<sub>16/17</sub>) with two electron superatomic and mixed valence copper(II)/copper(I) and copper(I)/copper(0) characters.
Nanoscale, 2025, 17, 982-991
1573173 CIFC163 H113 Cu17 F54 N13 O2 P3 S24R 3 c :H24.8645; 24.8645; 66.598
90; 90; 120
35658Kumar, Shibaditya; Mishra, Saikat; Das, Aniruddha; Mahiya, Kuldeep; Laha, Sourav; Maji, Milan; Patra, Apurba K.
Analogous copper nanoclusters (Cu<sub>16/17</sub>) with two electron superatomic and mixed valence copper(II)/copper(I) and copper(I)/copper(0) characters.
Nanoscale, 2025, 17, 982-991
1573192 CIF
Paper
C20 H12P 1 21/c 14.5384; 20.439; 13.531
90; 97.006; 90
1245.8Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573193 CIFC20 H12P 1 21/c 14.2338; 19.838; 12.9059
90; 95.613; 90
1078.8Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573194 CIFC20 H12P 1 21/c 13.5971; 21.658; 12.7908
90; 95.339; 90
992.2Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573195 CIFC20 H12P -13.4912; 12.687; 21.531
91.51; 90.434; 95.82
948.4Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573196 CIFC20 H12P -13.4134; 12.5674; 21.367
91.675; 90.433; 95.755
911.5Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573197 CIFC20 H12P -13.3501; 12.453; 21.244
91.709; 90.417; 95.599
881.6Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573198 CIFC20 H12P -13.2931; 12.347; 21.133
91.42; 90.439; 95.29
855.3Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573199 CIFC20 H12P -13.1883; 12.1605; 20.825
91.99; 90.297; 95.206
803.6Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573200 CIFC20 H12P -13.1077; 11.995; 20.571
91.56; 89.92; 95.171
763.4Zhou, Wenju; Aslandukov, Andrey; Minchenkova, Anastasiia; Hanfland, Michael; Dubrovinsky, Leonid; Dubrovinskaia, Natalia
Structural transformations and stability of benzo[a]pyrene under high pressure.
IUCrJ, 2025, 12
1573201 CIFC20 H14 O2P 1 21/c 17.1494; 10.9139; 17.7592
90; 102.584; 90
1352.42Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573202 CIFC20 H14 O2P 1 21/c 17.17156; 10.9455; 17.7694
90; 102.742; 90
1360.48Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573203 CIFC20 H14 O2P 1 21/c 17.1945; 10.9948; 17.7698
90; 102.926; 90
1370.01Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573204 CIFC20 H14 O2P 1 21/c 17.2211; 11.0779; 17.7769
90; 103.161; 90
1384.7Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573205 CIFC20 H14 O2P 1 21/c 17.2277; 11.248; 17.7562
90; 103.578; 90
1403.2Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573206 CIFC20 H14 O2P 1 21/c 17.2522; 11.4389; 17.705
90; 104.385; 90
1422.71Zwolenik, A.; Makal, A.
Tracking anharmonic oscillations in the structure of β-1,3-diacetylpyrene.
IUCrJ, 2025, 12
1573216 CIFC17 H24 Cu2 I3 N5 OP 1 21/c 110.8995; 16.7093; 13.8142
90; 108.662; 90
2383.61Chen, Jingwen; Zhou, Kang; Li, Jingbai; Xu, Guozhong; Hei, Xiuze; Li, Jing
Strongly photoluminescent and radioluminescent copper(i) iodide hybrid materials made of coordinated ionic chains.
Chemical science, 2025, 16, 1106-1114
1573217 CIFC18 H26 Cu2 I3 N5 OP 1 21/c 111.453; 17.025; 12.8883
90; 94.855; 90
2504Chen, Jingwen; Zhou, Kang; Li, Jingbai; Xu, Guozhong; Hei, Xiuze; Li, Jing
Strongly photoluminescent and radioluminescent copper(i) iodide hybrid materials made of coordinated ionic chains.
Chemical science, 2025, 16, 1106-1114
1573218 CIFC34 H47 Cu4 I6 N9 O2P -110.1107; 11.2297; 11.9172
73.93; 67.168; 71.862
1166.1Chen, Jingwen; Zhou, Kang; Li, Jingbai; Xu, Guozhong; Hei, Xiuze; Li, Jing
Strongly photoluminescent and radioluminescent copper(i) iodide hybrid materials made of coordinated ionic chains.
Chemical science, 2025, 16, 1106-1114
1573219 CIFC15 H19 Cu2 I3 N4 O2P 1 21/n 111.4886; 13.4361; 15.0603
90; 98.972; 90
2296.3Chen, Jingwen; Zhou, Kang; Li, Jingbai; Xu, Guozhong; Hei, Xiuze; Li, Jing
Strongly photoluminescent and radioluminescent copper(i) iodide hybrid materials made of coordinated ionic chains.
Chemical science, 2025, 16, 1106-1114
1573220 CIFC26 H58 B F4 N P2 PtP 1 21/n 18.585; 12.11; 29.773
90; 90.461; 90
3095.2Atterberry, Benjamin A.; Wimmer, Erik J.; Klostermann, Sina; Frey, Wolfgang; Kästner, Johannes; Estes, Deven P.; Rossini, Aaron J.
Structural characterization of surface immobilized platinum hydrides by sensitivity-enhanced <sup>195</sup>Pt solid state NMR spectroscopy and DFT calculations.
Chemical science, 2025, 16, 1271-1287
1573221 CIFC24 H57 B F4 O P2 PtP 1 21/c 111.5231; 16.5896; 16.5713
90; 106.8; 90
3032.63Atterberry, Benjamin A.; Wimmer, Erik J.; Klostermann, Sina; Frey, Wolfgang; Kästner, Johannes; Estes, Deven P.; Rossini, Aaron J.
Structural characterization of surface immobilized platinum hydrides by sensitivity-enhanced <sup>195</sup>Pt solid state NMR spectroscopy and DFT calculations.
Chemical science, 2025, 16, 1271-1287
1573222 CIFC26 H59 B Cl4 F4 P2 PtC 1 c 111.1587; 19.7667; 16.9439
90; 96.666; 90
3712.06Atterberry, Benjamin A.; Wimmer, Erik J.; Klostermann, Sina; Frey, Wolfgang; Kästner, Johannes; Estes, Deven P.; Rossini, Aaron J.
Structural characterization of surface immobilized platinum hydrides by sensitivity-enhanced <sup>195</sup>Pt solid state NMR spectroscopy and DFT calculations.
Chemical science, 2025, 16, 1271-1287
1573223 CIFC70 H92 Cl2 N6 O26 Zr6P n m a14.0277; 31.9593; 20.8847
90; 90; 90
9362.9Morey, Merissa N.; Montone, Christine M.; Dworzak, Michael R.; Yap, Glenn P. A.; Bloch, Eric D.
Tunable synthesis of heteroleptic zirconium-based porous coordination cages.
Chemical science, 2025, 16, 816-823
1573224 CIFC9 H5 As S2P 1 21/n 110.5045; 6.2032; 13.9819
90; 102.093; 90
890.86Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573225 CIFC17 H9 As S2C 1 2/c 113.4892; 8.5408; 23.219
90; 97.422; 90
2652.6Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573226 CIFC17 H9 As S2P 1 21/c 113.1348; 8.5422; 12.1986
90; 93.983; 90
1365.38Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573227 CIFC17 H9 P S2C 1 2/c 113.2423; 8.4253; 23.582
90; 97.092; 90
2610.9Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573228 CIFC34 H20 O3 P2 S4P -17.4187; 13.2453; 17.9755
77.315; 81.898; 76.885
1670.53Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573229 CIFC34 H16 As2 S4P -18.0954; 11.366; 15.4655
87.822; 85.309; 80.114
1396.77Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573230 CIFC17 H9 As S2P 1 21/c 114.5703; 3.9421; 23.8017
90; 99.317; 90
1349.08Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573231 CIFC15 H11 As O4 S2P 1 21/c 110.403; 14.0494; 10.7101
90; 99.246; 90
1545.01Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573232 CIFC9 H5 As S2P 1 n 16.1248; 11.3296; 12.9122
90; 95.535; 90
891.82Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573233 CIFC14 H5 As O5 S2 WP -17.312; 10.1653; 11.2954
92.355; 106.909; 100.48
785.92Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573234 CIFC23 H13 As S2I 1 2/a 116.1897; 7.1373; 31.4478
90; 90.732; 90
3633.5Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573235 CIFC23 H15 As O4 S2P n a 2117.8326; 7.736; 30.234
90; 90; 90
4170.9Sumida, Akifumi; Saeki, Akinori; Matsuo, Kyohei; Naka, Kensuke; Imoto, Hiroaki
Dithienoarsinines: stable and planar π-extended arsabenzenes.
Chemical science, 2025, 16, 1126-1135
1573239 CIFC40 H54 Ag6 F9 N5 O7 S3P b c a21.868; 22.557; 22.892
90; 90; 90
11292Nakatani, Riki; Sakai, Jin; Saha, Aishik; Kondo, Ayumu; Tomioka, Rina; Kawawaki, Tokuhisa; Das, Saikat; Negishi, Yuichi
Designed construction of two new atom-precise three-dimensional and two-dimensional Ag<sub>12</sub> cluster-assembled materials.
Nanoscale, 2025, 17, 813-822
1573240 CIFC18 H23 Ag2 F3 N O3.5 SR -3 :H24.5604; 24.5604; 21.6065
90; 90; 120
11287.2Nakatani, Riki; Sakai, Jin; Saha, Aishik; Kondo, Ayumu; Tomioka, Rina; Kawawaki, Tokuhisa; Das, Saikat; Negishi, Yuichi
Designed construction of two new atom-precise three-dimensional and two-dimensional Ag<sub>12</sub> cluster-assembled materials.
Nanoscale, 2025, 17, 813-822
1573241 CIFC72 H86 O9 P4 Ru2C 1 2/c 113.34263; 22.71892; 22.67074
90; 98.27; 90
6800.72Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573242 CIFC59 H69 O6 P2 RuP -113.32259; 13.34539; 17.15744
103.497; 94.3216; 118.437
2545.56Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573243 CIFC42 H34 O6 P2 RuP -4 21 c14.82724; 14.82724; 16.45463
90; 90; 90
3617.5Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573244 CIFC34 H38 P2 RuI 1 2/a 120.4141; 13.33648; 22.581
90; 104.798; 90
5943.81Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573245 CIFC41 H52 O6 P2 RuP 1 21/n 111.0204; 20.042; 18.3864
90; 97.977; 90
4021.72Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573246 CIFC61 H52 Cl2 F12 O9 P4 Ru2P 1 21/c 119.9752; 19.5957; 16.0602
90; 96.739; 90
6243Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573247 CIFC41 H36 O6 P2 RuP b c a17.3865; 18.59091; 22.10176
90; 90; 90
7143.97Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573248 CIFC338 H309 O41 P16 Ru8P -114.1251; 23.585; 23.8891
88.9659; 76.443; 76.138
7505.2Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573249 CIFC99 H114 O10 P4 Ru2P 1 21/n 113.8453; 24.5721; 29.3748
90; 101.926; 90
9777.8Saib, Asad; Goy, Roman; Medlock, Jonathan; Wüstenberg, Bettina; Kociok-Köhn, Gabriele; Lyall, Catherine L.; Lowe, John P.; Hintermair, Ulrich
Catalyst speciation and deactivation in the ruthenium-mediated transformation of ethynyl-β-ionol to α,β-unsaturated esters for vitamin A synthesis
Catalysis Science & Technology, 2025, 15, 355-375
1573253 CIFC27 H40 B2 Cu F8 N10 O2P 1 21/n 112.4491; 13.8403; 19.8972
90; 97.153; 90
3401.59Nowicka, Daria; Garbaczewski, Karol; Łuczak, Teresa; Forte, Giuseppe; Consiglio, Giuseppe; Kubicki, Maciej; Patroniak, Violetta; Gorczyński, Adam
Application of a simple copper(II) complex compound as an epinephrine selective voltammetric sensor in the presence of uric acid under aqueous conditions.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 1000-1012
1573257 CIFC32 H60 N Ni S8P 1 21/c 114.6673; 17.9434; 16.4154
90; 115.109; 90
3912Abhervé, Alexandre; Mroweh, Nabil; Cui, HengBo; Kato, Reizo; Vanthuyne, Nicolas; Alemany, Pere; Canadell, Enric; Avarvari, Narcis
Enantiomorphic single component conducting nickel(II) and platinum(II) bis(diethyl-dddt) crystalline complexes.
Nanoscale, 2025, 17, 1350-1361
1573258 CIFC16 H24 Ni S8P 41 21 214.6382; 14.6382; 20.8242
90; 90; 90
4462.15Abhervé, Alexandre; Mroweh, Nabil; Cui, HengBo; Kato, Reizo; Vanthuyne, Nicolas; Alemany, Pere; Canadell, Enric; Avarvari, Narcis
Enantiomorphic single component conducting nickel(II) and platinum(II) bis(diethyl-dddt) crystalline complexes.
Nanoscale, 2025, 17, 1350-1361
1573259 CIFC16 H24 Ni S8P 41 21 214.2738; 14.2738; 21.703
90; 90; 90
4421.8Abhervé, Alexandre; Mroweh, Nabil; Cui, HengBo; Kato, Reizo; Vanthuyne, Nicolas; Alemany, Pere; Canadell, Enric; Avarvari, Narcis
Enantiomorphic single component conducting nickel(II) and platinum(II) bis(diethyl-dddt) crystalline complexes.
Nanoscale, 2025, 17, 1350-1361
1573260 CIFC16 H24 Pt S8P 41 21 214.313; 14.313; 21.769
90; 90; 90
4459.6Abhervé, Alexandre; Mroweh, Nabil; Cui, HengBo; Kato, Reizo; Vanthuyne, Nicolas; Alemany, Pere; Canadell, Enric; Avarvari, Narcis
Enantiomorphic single component conducting nickel(II) and platinum(II) bis(diethyl-dddt) crystalline complexes.
Nanoscale, 2025, 17, 1350-1361
1573261 CIFC16 H24 Pt S8P 43 21 214.7208; 14.7208; 20.8598
90; 90; 90
4520.36Abhervé, Alexandre; Mroweh, Nabil; Cui, HengBo; Kato, Reizo; Vanthuyne, Nicolas; Alemany, Pere; Canadell, Enric; Avarvari, Narcis
Enantiomorphic single component conducting nickel(II) and platinum(II) bis(diethyl-dddt) crystalline complexes.
Nanoscale, 2025, 17, 1350-1361
1573269 CIFC166 H123C 1 2/c 143.6143; 10.572; 25.1335
90; 98.309; 90
11467.2Sanderson, Hugh J.; Helbig, Andreas; Kociok-Köhn, Gabriele; Helten, Holger; Hintermair, Ulrich
Reversible formation of tetraphenylpentalene, a room temperature stable antiaromatic hydrocarbon.
Chemical science, 2025, 16, 952-961
1573283 CIFC35 H21 N3 OP 1 21/n 115.5452; 4.78961; 32.495
90; 103.488; 90
2352.7Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr
π-Curved Blatter radicals: Blatter helicenes.
Chemical communications (Cambridge, England), 2025, 61, 496-499
1573284 CIFC27 H16 N3 OR -3 :H43.189; 43.189; 5.1711
90; 90; 120
8353.3Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr
π-Curved Blatter radicals: Blatter helicenes.
Chemical communications (Cambridge, England), 2025, 61, 496-499
1573285 CIFC35 H20 N3 OP 1 21/c 121.3059; 11.4684; 9.6844
90; 94.685; 90
2358.42Singh, Hemant K.; Bodzioch, Agnieszka; Pietrzak, Anna; Kaszyński, Piotr
π-Curved Blatter radicals: Blatter helicenes.
Chemical communications (Cambridge, England), 2025, 61, 496-499
1573300 CIFC30 H25 N O3P 19.9067; 11.5214; 11.6032
93.702; 109.012; 103.102
1205.68He, Yicheng; Yan, Biwei; Ma, Cheng; Ni, Shaofei; Guo, Wusheng
Ni-catalyzed asymmetric decarboxylation for the construction of carbocycles with contiguous quaternary carbon stereocenters.
Chemical science, 2025, 16, 834-839
1573301 CIFC30 H27 N O3P 21 21 217.51317; 15.2775; 21.463
90; 90; 90
2463.58He, Yicheng; Yan, Biwei; Ma, Cheng; Ni, Shaofei; Guo, Wusheng
Ni-catalyzed asymmetric decarboxylation for the construction of carbocycles with contiguous quaternary carbon stereocenters.
Chemical science, 2025, 16, 834-839
1573302 CIFC28 H21 N O2P 21 21 216.22984; 15.4298; 22.0803
90; 90; 90
2122.47He, Yicheng; Yan, Biwei; Ma, Cheng; Ni, Shaofei; Guo, Wusheng
Ni-catalyzed asymmetric decarboxylation for the construction of carbocycles with contiguous quaternary carbon stereocenters.
Chemical science, 2025, 16, 834-839
1573303 CIFC22 H24 Cu F12 N10 O8 S4P -110.3863; 13.163; 14.3802
90.6959; 101.511; 104.786
1858.52Nishiguchi, Taichi; Ohara, Yuki; Kadota, Kentaro; Zheng, Xin; Noro, Shin-Ichiro; Horike, Satoshi
Mechanically induced polyamorphism in a one-dimensional coordination polymer.
Chemical science, 2025, 16, 621-626
1573304 CIFC36 H39 Au3 N6P -15.92744; 13.7395; 20.7053
79.4971; 83.0769; 85.9397
1643.84Solea, Atena B.; Dermutas, Davide; Fadaei-Tirani, Farzaneh; Leanza, Luigi; Delle Piane, Massimo; Pavan, Giovanni M.; Severin, Kay
Nano onions based on an amphiphilic Au<sub>3</sub>(pyrazolate)<sub>3</sub> complex.
Nanoscale, 2025, 17, 1007-1012
1573306 CIFC36 H31 N2 O0.5P 21 21 221.6586; 12.8689; 9.8744
90; 90; 90
2752.22Wei, Xuyang; Li, Dong; Liu, Xitong; Zhang, Weifeng; Li, Hao; Yang, Shuai; Luo, Hao; Yu, Gui
Magnetoresistance effect of pyridine-capped <i>s</i>-indacene-based conjugated radicals.
Materials horizons, 2025, 12, 1524-1531
1573307 CIFC36 H30 N2P b c a15.9161; 17.8282; 18.1544
90; 90; 90
5151.4Wei, Xuyang; Li, Dong; Liu, Xitong; Zhang, Weifeng; Li, Hao; Yang, Shuai; Luo, Hao; Yu, Gui
Magnetoresistance effect of pyridine-capped <i>s</i>-indacene-based conjugated radicals.
Materials horizons, 2025, 12, 1524-1531
1573308 CIFC39 H55 Cl N2 O2 P2 RuP 1 21/c 110.6687; 15.5241; 22.9366
90; 92.854; 90
3794.1Donnelly, Laurie J.; Gelfand, Benjamin S.; Piers, Warren E.
Rapid and selective formic acid dehydrogenation catalysis by molecular ruthenium hydrides supported by rigid PCcarbeneP pincer ligands
Catalysis Science & Technology, 2025, 15, 100-106
1573309 CIFC14 H15 N3P -18.7161; 9.2511; 9.8844
63.309; 64.432; 72.772
637.16Mandal, Mrinal; Mardanya, Sukumar; Saha, Arijit; Singh, Manjeev; Ghosh, Swarnali; Chatterjee, Tanmay; Patra, Ramen; Bhunia, Surojit; Mandal, Saptarshi; Mukherjee, Soumen; Debnath, Rahul; Reddy, C. Malla; Das, Mousumi; Mandal, Prasun K.
Charge-transfer mediated J-aggregation in red emitting ultra-small-single-benzenic <i>meta</i>-fluorophore crystals.
Chemical science, 2025, 16, 901-909
1573310 CIFC12 H11 N3P 1 21/c 115.292; 10.45; 6.872
90; 97.614; 90
1088.5Mandal, Mrinal; Mardanya, Sukumar; Saha, Arijit; Singh, Manjeev; Ghosh, Swarnali; Chatterjee, Tanmay; Patra, Ramen; Bhunia, Surojit; Mandal, Saptarshi; Mukherjee, Soumen; Debnath, Rahul; Reddy, C. Malla; Das, Mousumi; Mandal, Prasun K.
Charge-transfer mediated J-aggregation in red emitting ultra-small-single-benzenic <i>meta</i>-fluorophore crystals.
Chemical science, 2025, 16, 901-909
1573311 CIFC29 H20 Cl NP 1 21/n 113.644; 9.9782; 15.7628
90; 91.274; 90
2145.5Chaturvedi, Anjali; Sharma, Vishal; Rawal, Ravindra K.; Singh, Manpreet; Singh, Virender
Sustainable protocol for Cu-catalysed A<sup>3</sup>-coupling under solvent-free conditions.
Organic & biomolecular chemistry, 2025, 23, 854-863
1573312 CIFC26 H32 O15P -17.3123; 8.6811; 22.3521
80.512; 83.401; 69.983
1312.31Mo, Shuyuan; Huang, Zhihong; Zeng, Hanxiao; Wang, Jianping; Zhang, Yonghui; Hu, Zhengxi
Penicichrysol A: an unprecedented polyketide produced by <i>Penicillium chrysogenum</i>.
Organic & biomolecular chemistry, 2025, 23, 608-613
1573313 CIFC18 H18 O8P 1 21/n 110.8884; 13.4388; 11.5204
90; 99.491; 90
1662.67Mo, Shuyuan; Huang, Zhihong; Zeng, Hanxiao; Wang, Jianping; Zhang, Yonghui; Hu, Zhengxi
Penicichrysol A: an unprecedented polyketide produced by <i>Penicillium chrysogenum</i>.
Organic & biomolecular chemistry, 2025, 23, 608-613
1573348 CIFO10 Si2 Zn4P n n 28.1695; 10.658; 5.0531
90; 90; 90
439.98Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573349 CIFH4 O10 Si2 Zn4I m m 28.35707; 10.714; 5.11006
90; 90; 90
457.54Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573350 CIFO10 Si2 Zn4P n n 28.1572; 10.64; 5.0499
90; 90; 90
438.29Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573351 CIFO10 Si2 Zn4P n n 28.0991; 10.54; 5.0319
90; 90; 90
429.5Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573352 CIFO10 Si2 Zn4P n n 28.1701; 10.6651; 5.0554
90; 90; 90
440.5Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573353 CIFO10 Si2 Zn4I m m 28.2334; 10.717; 5.0641
90; 90; 90
446.8Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573354 CIFO10 Si2 Zn4P n n 28.1412; 10.6227; 5.0448
90; 90; 90
436.28Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573355 CIFO10 Si2 Zn4P n n 28.1559; 10.636; 5.0475
90; 90; 90
437.85Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573356 CIFO10 Si2 Zn4P n n 28.1865; 10.67; 5.0479
90; 90; 90
440.9Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573357 CIFO10 Si2 Zn4I m m 28.2501; 10.694; 5.06794
90; 90; 90
447.13Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573358 CIFH4 O10 Si2 Zn4I m m 28.2846; 10.697; 5.0823
90; 90; 90
450.4Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573359 CIFH0 O10 Si2 Zn4P n n 28.0977; 10.5415; 5.0266
90; 90; 90
429.08Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573360 CIFH4 O10 Si2 Zn4P n n 28.2199; 10.6921; 5.0603
90; 90; 90
444.74Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573361 CIFH4 O10 Si2 Zn4P n n 28.1356; 10.6329; 5.0386
90; 90; 90
435.86Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573362 CIFH4 O10 Si2 Zn4P n n 28.0899; 10.5425; 5.0237
90; 90; 90
428.46Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573363 CIFH4 O10 Si2 Zn4I m m 28.31709; 10.706; 5.09489
90; 90; 90
453.66Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573364 CIFH4 O10 Si2 Zn4I m m 28.2502; 10.685; 5.0695
90; 90; 90
446.89Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573365 CIFH4 O10 Si2 Zn4P n n 28.2161; 10.673; 5.0579
90; 90; 90
443.53Gajda, Roman; Sławiński, Wojciech; Poręba, Tomasz; Parafiniuk, Jan; Mezouar, Mohamed; Dera, Przemysław; Woźniak, Krzysztof
Incommensurately modulated structure of Zn<sub>4</sub>Si<sub>2</sub>O<sub>7</sub>(OH)<sub>2</sub>·H<sub>2</sub>O at high pressure.
IUCrJ, 2025, 12
1573368 CIFC59 H82 Ga2 N4 O P2P 1 21/c 123.5423; 13.8181; 17.4303
90; 96.371; 90
5635.2Sharma, Mahendra K.; Wölper, Christoph; Siera, Hannah; Haberhauer, Gebhard; Schulz, Stephan
Synthesis and reactivity of a six-membered heterocyclic 1,3-diphosphaallene.
Chemical science, 2025, 16, 1189-1196
1573369 CIFC72 H108 Ga2 N6 O P2C 1 2/c 126.3977; 13.4903; 40.1349
90; 91.7723; 90
14285.7Sharma, Mahendra K.; Wölper, Christoph; Siera, Hannah; Haberhauer, Gebhard; Schulz, Stephan
Synthesis and reactivity of a six-membered heterocyclic 1,3-diphosphaallene.
Chemical science, 2025, 16, 1189-1196
1573370 CIFC69 H106 Ga2 N4 O P2 SiP 1 21/c 115.1894; 13.1269; 34.6139
90; 96.719; 90
6854.3Sharma, Mahendra K.; Wölper, Christoph; Siera, Hannah; Haberhauer, Gebhard; Schulz, Stephan
Synthesis and reactivity of a six-membered heterocyclic 1,3-diphosphaallene.
Chemical science, 2025, 16, 1189-1196
1573371 CIFC79 H111 Ga2 N6 O P2C 1 2/c 120.731; 18.24; 39.5206
90; 95.9543; 90
14863.4Sharma, Mahendra K.; Wölper, Christoph; Siera, Hannah; Haberhauer, Gebhard; Schulz, Stephan
Synthesis and reactivity of a six-membered heterocyclic 1,3-diphosphaallene.
Chemical science, 2025, 16, 1189-1196
1573374 CIFC15 H23 B O4P -19.1472; 9.2824; 9.3217
97.608; 94.602; 101.377
764.48Vyas, Het; Gangani, Ashvin J.; Mini, Aiswarya; Pathil, Melissa; Ruth, Austin; Sharma, Abhishek
Strain-release enables access to carbonyl conjugated allylic diborons and alkenyl boronates having multiple contiguous stereocenters in a one-pot process.
Chemical science, 2025, 16, 1205-1215
1573375 CIFC22 H28 B N O7P 1 21/c 117.4121; 10.4286; 13.1111
90; 109.67; 90
2241.84Vyas, Het; Gangani, Ashvin J.; Mini, Aiswarya; Pathil, Melissa; Ruth, Austin; Sharma, Abhishek
Strain-release enables access to carbonyl conjugated allylic diborons and alkenyl boronates having multiple contiguous stereocenters in a one-pot process.
Chemical science, 2025, 16, 1205-1215
1573376 CIFC9 H7 F6 N5P n a 2110.0705; 18.6804; 5.758
90; 90; 90
1083.2Michelini, Lorenzo; Slaney, Tanya; Virk, Seerat; Rafic, Estefanía; Qie, L. Charlie; Corejova, Klara; Lepage, Mathieu L.; Musolino, Stefania F.; Oliver, Allen G.; Etchenique, Roberto; Hong, W. David; DiLabio, Gino A.; Wulff, Jeremy E.
A diazirine's central carbon is sp<sup>2</sup>-hybridized, facilitating conjugation to dye molecules.
Chemical science, 2025, 16, 970-979
1573377 CIFC24 H56 Cd Cl4 N2C 1 2/c 132.768; 13.9365; 15.0048
90; 109.374; 90
6464.2Xu, Ou; Peng, Hui; Wei, Qilin; Kong, Linghang; Wang, Xiao; Zhang, Heng; Zhao, Jialong; Zou, Bingsuo
Large-scale preparation of Sb<sup>3+</sup>-activated hybrid metal halides with efficient tunable emission from visible to near-infrared regions for advanced photonic applications.
Materials horizons, 2025, 12, 1596-1608
1573378 CIFC24 H56 Br4 Cd N2C 1 2/c 133.373; 14.437; 14.999
90; 111.357; 90
6730Xu, Ou; Peng, Hui; Wei, Qilin; Kong, Linghang; Wang, Xiao; Zhang, Heng; Zhao, Jialong; Zou, Bingsuo
Large-scale preparation of Sb<sup>3+</sup>-activated hybrid metal halides with efficient tunable emission from visible to near-infrared regions for advanced photonic applications.
Materials horizons, 2025, 12, 1596-1608
1573381 CIFC22 H29 Al N O4P -17.0781; 11.3798; 12.8321
79.573; 86.427; 88.799
1014.5Ganta, Prasanna Kumar; Huang, Fei; Halima, Taoufik Ben; Kamaraj, Rajiv; Chu, Yu-Ting; Tseng, Hsi-Ching; Ding, Shangwu; Wu, Kuo-Hui; Chen, Hsuan-Ying
Evolution of aluminum aminophenolate complexes in the ring-opening polymerization of ε-caprolactone: electronic and amino-chelating effects.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 511-532
1573382 CIFC23 H31 Al Br2 N2 O3P 1 21/c 117.3914; 10.0911; 14.2716
90; 104.702; 90
2422.64Ganta, Prasanna Kumar; Huang, Fei; Halima, Taoufik Ben; Kamaraj, Rajiv; Chu, Yu-Ting; Tseng, Hsi-Ching; Ding, Shangwu; Wu, Kuo-Hui; Chen, Hsuan-Ying
Evolution of aluminum aminophenolate complexes in the ring-opening polymerization of ε-caprolactone: electronic and amino-chelating effects.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 511-532
1573383 CIFC18 H30 Al N O2P n a 2119.0286; 8.4573; 11.545
90; 90; 90
1857.94Ganta, Prasanna Kumar; Huang, Fei; Halima, Taoufik Ben; Kamaraj, Rajiv; Chu, Yu-Ting; Tseng, Hsi-Ching; Ding, Shangwu; Wu, Kuo-Hui; Chen, Hsuan-Ying
Evolution of aluminum aminophenolate complexes in the ring-opening polymerization of ε-caprolactone: electronic and amino-chelating effects.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 511-532
1573384 CIFC40 H56 Al Cl O3P b c a10.6759; 17.5313; 40.2687
90; 90; 90
7536.8Ganta, Prasanna Kumar; Huang, Fei; Halima, Taoufik Ben; Kamaraj, Rajiv; Chu, Yu-Ting; Tseng, Hsi-Ching; Ding, Shangwu; Wu, Kuo-Hui; Chen, Hsuan-Ying
Evolution of aluminum aminophenolate complexes in the ring-opening polymerization of ε-caprolactone: electronic and amino-chelating effects.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 511-532
1573385 CIFC39 H56 Al N O7P b c a14.5245; 19.871; 25.5065
90; 90; 90
7361.6Ganta, Prasanna Kumar; Huang, Fei; Halima, Taoufik Ben; Kamaraj, Rajiv; Chu, Yu-Ting; Tseng, Hsi-Ching; Ding, Shangwu; Wu, Kuo-Hui; Chen, Hsuan-Ying
Evolution of aluminum aminophenolate complexes in the ring-opening polymerization of ε-caprolactone: electronic and amino-chelating effects.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 511-532
1573388 CIFC74 H172 Ag16 Cl4 O24 P12 Pd S26P 1 21/n 118.2605; 21.6169; 18.9717
90; 96.372; 90
7442.5Ni, Yu-Rong; Pillay, Michael N.; Chiu, Tzu-Hao; Liang, Hao; Kahlal, Samia; Chen, Jie-Ying; Chen, Yuan-Jang; Saillard, Jean-Yves; Liu, C. W.
Sulfide-mediated growth of NIR luminescent Pd/Ag atomically precise nanoclusters.
Nanoscale, 2025, 17, 1990-1996
1573389 CIFC96 H216 Ag16 O24 P12 Pd S26P c c n26.454; 27.073; 23.35
90; 90; 90
16723Ni, Yu-Rong; Pillay, Michael N.; Chiu, Tzu-Hao; Liang, Hao; Kahlal, Samia; Chen, Jie-Ying; Chen, Yuan-Jang; Saillard, Jean-Yves; Liu, C. W.
Sulfide-mediated growth of NIR luminescent Pd/Ag atomically precise nanoclusters.
Nanoscale, 2025, 17, 1990-1996
1573390 CIFC96 H216 Ag14 O24 P12 Pd6 S25P -115.605; 18.06; 18.102
119.776; 93.951; 103.556
4200Ni, Yu-Rong; Pillay, Michael N.; Chiu, Tzu-Hao; Liang, Hao; Kahlal, Samia; Chen, Jie-Ying; Chen, Yuan-Jang; Saillard, Jean-Yves; Liu, C. W.
Sulfide-mediated growth of NIR luminescent Pd/Ag atomically precise nanoclusters.
Nanoscale, 2025, 17, 1990-1996
1573391 CIFC87 H81 B Cu F4 N4 O2.5 P2C 1 2/c 119.927; 21.694; 34.974
90; 104.466; 90
14640Wang, Xinwei; Li, Weijun; Li, Xiao; Hou, Chenlu; Wei, Sanyue; Lei, Wenxin; Chen, Xu-Lin
TADF-emitting copper(i) and silver(i) complexes featuring intra-ligand charge transfer based on a donor–acceptor–donor ligand
New Journal of Chemistry, 2025, 49, 755-760
1573392 CIFC85 H76 Ag B F4 N4 O2 P2P -119.2498; 25.6897; 31.4864
77.9013; 78.6755; 89.8003
14916.9Wang, Xinwei; Li, Weijun; Li, Xiao; Hou, Chenlu; Wei, Sanyue; Lei, Wenxin; Chen, Xu-Lin
TADF-emitting copper(i) and silver(i) complexes featuring intra-ligand charge transfer based on a donor–acceptor–donor ligand
New Journal of Chemistry, 2025, 49, 755-760
1573393 CIFC9 H7 N7 O5P 1 21/c 110.556; 5.7279; 21.606
90; 97.049; 90
1296.5Cai, Ziwu; Shi, Junhao; Yu, Qian; Jiang, Tianyu; Zhang, Wenquan
4-Amino-1,2,3-triazine 2-oxide: a promising structural unit for the design and synthesis of novel energetic materials with good thermal stability and low impact sensitivity
New Journal of Chemistry, 2025, 49, 302-310
1573394 CIFC7 H5 N7 O5P 21 21 215.8169; 10.8115; 15.0344
90; 90; 90
945.5Cai, Ziwu; Shi, Junhao; Yu, Qian; Jiang, Tianyu; Zhang, Wenquan
4-Amino-1,2,3-triazine 2-oxide: a promising structural unit for the design and synthesis of novel energetic materials with good thermal stability and low impact sensitivity
New Journal of Chemistry, 2025, 49, 302-310
1573395 CIFC14 H13 N OP b c a9.1158; 9.8374; 25.365
90; 90; 90
2274.6Qin, Chang-Qing; Liu, Xin-Ni; Gu, Man-Zhen; Xu, Yi-Bing; Chen, Guo-Shu; Liu, Yun-Lin
DBU-mediated synthesis of amides from carbodiimides and unstrained 1,3-diketones
New Journal of Chemistry, 2025, 49, 366-370
1573396 CIFC14 H13 N3 O2P b c a9.9581; 9.1704; 27.6575
90; 90; 90
2525.68Maessen, Stefan J. D.; Lekanne Deprez, Siebe; Vermeeren, Pascal; van den Bersselaar, Bart W. L.; Lutz, Martin; Heuts, Johan P. A.; Fonseca Guerra, Célia; Palmans, Anja R. A.
Structure-property relationships to direct the dynamic properties of acylsemicarbazide-based materials.
Polymer chemistry, 2025, 16, 290-300
1573397 CIFC15 H13 N3 O3P 1 21/c 19.7633; 27.5437; 10.4855
90; 98.644; 90
2787.7Maessen, Stefan J. D.; Lekanne Deprez, Siebe; Vermeeren, Pascal; van den Bersselaar, Bart W. L.; Lutz, Martin; Heuts, Johan P. A.; Fonseca Guerra, Célia; Palmans, Anja R. A.
Structure-property relationships to direct the dynamic properties of acylsemicarbazide-based materials.
Polymer chemistry, 2025, 16, 290-300
1573398 CIFC34 H28 N2 O6P b c a10.6143; 13.2575; 19.9774
90; 90; 90
2811.2Zhou, Huan; Zhang, Yuxuan; Zheng, Zhiye; Wan, Junhua; Zhang, Hui; Lin, Kunhua; Sessler, Jonathan L.; Wang, Hongyu
Internally diketopyrrolopyrrole-bridged bis-anthracene macrocycle: a multifunctional fluorescent platform.
Chemical science, 2025, 16, 910-919
1573399 CIFC80 H66 N16 O8P -111.1096; 11.2145; 15.2337
68.402; 79.501; 69.937
1654.2Zhou, Huan; Zhang, Yuxuan; Zheng, Zhiye; Wan, Junhua; Zhang, Hui; Lin, Kunhua; Sessler, Jonathan L.; Wang, Hongyu
Internally diketopyrrolopyrrole-bridged bis-anthracene macrocycle: a multifunctional fluorescent platform.
Chemical science, 2025, 16, 910-919
1573400 CIFC100 H92 Cl3 N16 O18P -114.3247; 17.1233; 23.0646
96.822; 98.846; 108.196
5226.07Wang, Shuhe; Sigl, Johannes; Allmendinger, Lars; Maurizot, Victor; Huc, Ivan
Design of an abiotic unimolecular three-helix bundle.
Chemical science, 2025, 16, 1136-1146
1573401 CIFC104.52 H93.44 Cl2 N19 O17.94P -113.1606; 17.3713; 24.34
95.661; 93.989; 105.354
5313.14Wang, Shuhe; Sigl, Johannes; Allmendinger, Lars; Maurizot, Victor; Huc, Ivan
Design of an abiotic unimolecular three-helix bundle.
Chemical science, 2025, 16, 1136-1146
1573402 CIFC17 H16 F N O2P 1 21 16.4767; 15.7755; 7.425
90; 100.19; 90
746.67Tian, Kui; Jin, Zhuan; Liu, Xin-Lian; He, Ling; Liu, Hong-Fu; Yu, Pin-Ke; Chang, Xin; Dong, Xiu-Qin; Wang, Chun-Jiang
Stereodivergent assembly of δ-valerolactones with an azaarene-containing quaternary stereocenter enabled by Cu/Ru relay catalysis.
Chemical science, 2025, 16, 1233-1240
1573403 CIFC16 H19 N3P 1 21 17.8385; 5.253; 16.8163
90; 103.167; 90
674.22Pilopp, Yannic; Beer, Henrik; Bresien, Jonas; Michalik, Dirk; Villinger, Alexander; Schulz, Axel
Designing a visible light-mediated double photoswitch: a combination of biradical and azobenzene structural motifs that can be switched independently.
Chemical science, 2025, 16, 876-888
1573404 CIFC65 H67 N5 P2P 1 21/c 110.8196; 21.236; 24.229
90; 102.703; 90
5430.7Pilopp, Yannic; Beer, Henrik; Bresien, Jonas; Michalik, Dirk; Villinger, Alexander; Schulz, Axel
Designing a visible light-mediated double photoswitch: a combination of biradical and azobenzene structural motifs that can be switched independently.
Chemical science, 2025, 16, 876-888
1573405 CIFC17 H17 N3P 1 21/c 17.2792; 9.3758; 20.838
90; 99.559; 90
1402.4Pilopp, Yannic; Beer, Henrik; Bresien, Jonas; Michalik, Dirk; Villinger, Alexander; Schulz, Axel
Designing a visible light-mediated double photoswitch: a combination of biradical and azobenzene structural motifs that can be switched independently.
Chemical science, 2025, 16, 876-888
1573406 CIFC65 H66 F N5 P2P 1 21/n 110.8647; 21.2993; 24.1947
90; 102.911; 90
5457.4Pilopp, Yannic; Beer, Henrik; Bresien, Jonas; Michalik, Dirk; Villinger, Alexander; Schulz, Axel
Designing a visible light-mediated double photoswitch: a combination of biradical and azobenzene structural motifs that can be switched independently.
Chemical science, 2025, 16, 876-888
1573407 CIFC17 H19 N3 OP 21 21 214.6237; 9.0404; 35.034
90; 90; 90
1464.4Pilopp, Yannic; Beer, Henrik; Bresien, Jonas; Michalik, Dirk; Villinger, Alexander; Schulz, Axel
Designing a visible light-mediated double photoswitch: a combination of biradical and azobenzene structural motifs that can be switched independently.
Chemical science, 2025, 16, 876-888
1573408 CIFC206 H123 Al8 F233 O24 Y2P 1 21/n 118.06498; 19.02813; 39.8336
90; 94.9425; 90
13641.6Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573409 CIFC74 H154 B12 Dy6P -115.6166; 16.3417; 21.7358
90.725; 110.278; 117.066
4536Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573410 CIFC62 H25 Al2 Dy F78 O8P 1 21/c 121.7517; 20.9203; 18.7796
90; 93.564; 90
8529.2Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573411 CIFC10 H23 B2 DyP 1 21/c 18.3735; 20.8167; 8.5037
90; 117.93; 90
1309.61Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573412 CIFC40 H92 B8 Y4P 1 21/c 116.9654; 21.7125; 14.5559
90; 90.735; 90
5361.39Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573413 CIFC60 H54 Al2 F57 O6 Si3 YP -116.6426; 16.7663; 18.4889
105.461; 104.692; 113.53
4163.3Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573414 CIFC206 H123 Al8 Dy2 F233 O24P 1 21/n 118.2139; 19.314; 40.1803
90; 94.849; 90
14084.2Corner, Sophie C.; Blackmore, William J. A.; Gransbury, Gemma K.; Mattioni, Andrea; Whitehead, George F. S.; Chilton, Nicholas F.; Mills, David P.
A fluorobenzene-bound dysprosium half-sandwich dication single-molecule magnet.
Chemical science, 2025, 16, 610-620
1573415 CIFC14 H16 N4 O4 WC 1 2/c 18.6484; 14.2399; 13.3208
90; 97.498; 90
1626.5Jankins, Tanner C.; Rubel, Camille Z.; Ho, Hang Chi; Martin-Montero, Raul; Engle, Keary M.
Tungsten-catalyzed stereodivergent isomerization of terminal olefins.
Chemical science, 2025, 16, 2307-2315
1573416 CIFC38 H46 N2 O12 W2P -18.9455; 10.6935; 12.0535
66.56; 71.07; 71.049
974.88Jankins, Tanner C.; Rubel, Camille Z.; Ho, Hang Chi; Martin-Montero, Raul; Engle, Keary M.
Tungsten-catalyzed stereodivergent isomerization of terminal olefins.
Chemical science, 2025, 16, 2307-2315
1573417 CIFC18 H20 Cl N O Pd SeP -19.2684; 13.6019; 14.1589
86.53; 85.322; 82.685
1762.29Singh, Sohan; Mahala, Suman; Bhuvanesh, Nattamai; Joshi, Hemant
Pd(ii) NCSe–pincer complexes for regioselective cross-dehydrogenative coupling of arylthiophenes with hetero(arenes)
Catalysis Science & Technology, 2025, 15, 523-536
1573418 CIFC24 H26 Cl N O Pd SeP 1 21/c 16.7272; 20.8455; 15.5747
90; 92.371; 90
2182.2Singh, Sohan; Mahala, Suman; Bhuvanesh, Nattamai; Joshi, Hemant
Pd(ii) NCSe–pincer complexes for regioselective cross-dehydrogenative coupling of arylthiophenes with hetero(arenes)
Catalysis Science & Technology, 2025, 15, 523-536
1573419 CIFC92 H94 Cl4 N5 O12P 114.924; 15.705; 17.535
89.652; 88.476; 78.232
4022.1Gao, Ke; Lee, Sang Hyuk; Zhao, Wenkai; Ahn, Jaeyong; Kim, Tae Woo; Li, Zhenping; Zhuo, Huagui; Wang, Zhiwei; Zheng, Xinglong; Yan, Yang; Chang, Gang; Ma, Wei; Zhang, Mingming; Long, Guankui; Oh, Joon Hak; Shang, Xiaobo
Reversal of chirality in solutions and aggregates of chiral tetrachlorinated diperylene diimides towards efficient circularly polarized light detection.
Materials horizons, 2025, 12, 1903-1912
1573430 CIFC51 H43 N3P 1 21/n 112.0996; 10.9016; 29.2496
90; 96.378; 90
3834.3Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573431 CIFC49 H39 B N2 O2P 1 21/c 113.211; 20.856; 15.732
90; 114.86; 90
3933Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573432 CIFC55 H43 B N2P -112.2357; 13.4613; 14.9649
78.284; 77.397; 76.902
2312.08Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573433 CIFC50 H41 B N2 O2P -114.4553; 15.13; 21.027
92.22; 94.235; 98.658
4528.2Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573434 CIFC49 H39 B N2 OP -111.919; 12.5825; 14.8081
104.186; 110.328; 96.071
1974Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573435 CIFC49 H39 B N2P -111.6677; 12.7694; 14.5328
103.399; 109.908; 94.935
1948Liu, Le; Song, Shuangji; Lee, Jiyeon; Rao, Yutao; Xu, Ling; Zhou, Mingbo; Yin, Bangshao; Oh, Juwon; Kim, Jiwon; Osuka, Atsuhiro; Song, Jianxin
Sub-<i>m</i>-benziporphyrin: a subcarbaporphyrinoid and its B<sup>III</sup> complex with an unprecedented planar tridentate 14π-aromatic network.
Chemical science, 2025, 16, 1155-1160
1573436 CIFC20 H27 Br Co N3 O5P 1 21/c 19.5864; 13.892; 17.545
90; 100.802; 90
2295.1Sahoo, Sangita; Pandey, Vipin K.; Barik, Jogendrananda; Rit, Arnab
Cobalt–NHC promoted selective functionalization of alkynes via auxiliary-ligand modulation
Catalysis Science & Technology, 2025, 15, 734-740
1573437 CIFC126 H170 Mo12 N26 O74P 1 21/n 123.4316; 20.2535; 24.6419
90; 104.086; 90
11342.7Yadav, Ankit K.; Gładysiak, Andrzej; Wolpert, Emma H.; Ganose, Alex M.; Samel-Garloff, Bronson; Koley, Dipankar; Jelfs, Kim E.; Stylianou, Kyriakos C.
Solvatomorphic diversity dictates the stability and solubility of metal-organic polyhedra.
Chemical science, 2025, 16, 2589-2599
1573438 CIFC108 H108 Mo12 N18 O72P 6/m20.6212; 20.6212; 15.9529
90; 90; 120
5874.87Yadav, Ankit K.; Gładysiak, Andrzej; Wolpert, Emma H.; Ganose, Alex M.; Samel-Garloff, Bronson; Koley, Dipankar; Jelfs, Kim E.; Stylianou, Kyriakos C.
Solvatomorphic diversity dictates the stability and solubility of metal-organic polyhedra.
Chemical science, 2025, 16, 2589-2599
1573439 CIFC120 H132 Mo12 N18 O72P -118.9295; 20.8274; 31.777
84.01; 86.075; 80.923
12286.5Yadav, Ankit K.; Gładysiak, Andrzej; Wolpert, Emma H.; Ganose, Alex M.; Samel-Garloff, Bronson; Koley, Dipankar; Jelfs, Kim E.; Stylianou, Kyriakos C.
Solvatomorphic diversity dictates the stability and solubility of metal-organic polyhedra.
Chemical science, 2025, 16, 2589-2599
1573440 CIFC144 H204 Mo12 N24 O72P 1 21/n 123.4926; 21.0361; 24.7119
90; 103.643; 90
11867.9Yadav, Ankit K.; Gładysiak, Andrzej; Wolpert, Emma H.; Ganose, Alex M.; Samel-Garloff, Bronson; Koley, Dipankar; Jelfs, Kim E.; Stylianou, Kyriakos C.
Solvatomorphic diversity dictates the stability and solubility of metal-organic polyhedra.
Chemical science, 2025, 16, 2589-2599
1573441 CIFC112 H122 Mo12 N20 O72C m c e37.4589; 29.3487; 20.1896
90; 90; 90
22195.8Yadav, Ankit K.; Gładysiak, Andrzej; Wolpert, Emma H.; Ganose, Alex M.; Samel-Garloff, Bronson; Koley, Dipankar; Jelfs, Kim E.; Stylianou, Kyriakos C.
Solvatomorphic diversity dictates the stability and solubility of metal-organic polyhedra.
Chemical science, 2025, 16, 2589-2599
1573442 CIFC54.83 H67.65 Cl1.65 N6 O2P -18.0413; 14.3206; 21.6156
78.691; 88.151; 87.222
2437.3Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573443 CIFC54 H66 N6 S2P -16.81179; 8.26449; 20.8251
92.8453; 96.3218; 95.0155
1158.7Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573444 CIFC54 H64 N8 O6C 1 2/c 147.3727; 10.9462; 9.5717
90; 90.519; 90
4963.2Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573445 CIFC32 H22 N6 S2P 1 21/c 16.73075; 13.0685; 14.6429
90; 91.099; 90
1287.76Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573446 CIFC32 H22 N6 O2C 1 2/c 123.4345; 7.9786; 13.6019
90; 105.599; 90
2449.54Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573447 CIFC54 H66 N6 S2P 1 21/c 126.3539; 5.7949; 16.2792
90; 106.857; 90
2379.3Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573448 CIFC46 H50 N6 O4P 1 21/n 112.653; 17.7756; 18.8818
90; 102.848; 90
4140.47Szymański, Bartosz; Sahoo, Smruti Ranjan; Vakuliuk, Olena; Valiev, Rashid; Ramazanov, Ruslan; Łaski, Piotr; Jarzembska, Katarzyna N.; Kamiński, Radosław; Teimouri, Mohammad B.; Baryshnikov, Glib; Gryko, Daniel T.
Shedding new light on quadrupolar 1,4-dihydropyrrolo[3,2-<i>b</i>]pyrroles: impact of electron-deficient scaffolds over emission.
Chemical science, 2025, 16, 2170-2179
1573449 CIFC60 H59 N24 O29.5 Zn9R -3 c :H15.31573; 15.31573; 56.9773
90; 90; 120
11574.7Tao, Ye; Dong, Qiubing; Wan, Jingmeng; Huang, Fu-Ping; Duan, Jingui; Zeng, Ming-Hua
Evolution from [Zn<sub>9</sub>] to a record-high [Zn<sub>54</sub>] subblock and engineering a hierarchical supramolecular framework for enhanced iodine uptake.
Chemical science, 2025, 16, 1730-1736
1573450 CIFC348 H288 I56.6 N156 O118.8 Zn54F d -3 :258.9792; 58.9792; 58.9792
90; 90; 90
205162Tao, Ye; Dong, Qiubing; Wan, Jingmeng; Huang, Fu-Ping; Duan, Jingui; Zeng, Ming-Hua
Evolution from [Zn<sub>9</sub>] to a record-high [Zn<sub>54</sub>] subblock and engineering a hierarchical supramolecular framework for enhanced iodine uptake.
Chemical science, 2025, 16, 1730-1736
1573451 CIFC523.2 H705.2 N195.61 O170 Zn54F d -3 :258.3017; 58.3017; 58.3017
90; 90; 90
198173Tao, Ye; Dong, Qiubing; Wan, Jingmeng; Huang, Fu-Ping; Duan, Jingui; Zeng, Ming-Hua
Evolution from [Zn<sub>9</sub>] to a record-high [Zn<sub>54</sub>] subblock and engineering a hierarchical supramolecular framework for enhanced iodine uptake.
Chemical science, 2025, 16, 1730-1736
1573452 CIFC18 H30 Co2 Mo8 N14 O34P b c a15.5814; 16.4046; 17.843
90; 90; 90
4560.8Xie, Tinghui; Wang, Xinfang; Cao, Tingting; Huang, Zuogang; Yu, Huaguang
A series of isostructural polyoxometalate-based metal-organic frameworks of 3,5-bis(1',2',4'-triazol-1'-yl)pyridine: synthesis, structures and electrocatalytic properties.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 903-907
1573453 CIFC18 H30 Mo8 N14 O34 Zn2P b c a15.5823; 16.4405; 17.8841
90; 90; 90
4581.6Xie, Tinghui; Wang, Xinfang; Cao, Tingting; Huang, Zuogang; Yu, Huaguang
A series of isostructural polyoxometalate-based metal-organic frameworks of 3,5-bis(1',2',4'-triazol-1'-yl)pyridine: synthesis, structures and electrocatalytic properties.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 903-907
1573454 CIFC18 H30 Mo8 N14 Ni2 O34P b c a15.7082; 16.2936; 17.7195
90; 90; 90
4535.2Xie, Tinghui; Wang, Xinfang; Cao, Tingting; Huang, Zuogang; Yu, Huaguang
A series of isostructural polyoxometalate-based metal-organic frameworks of 3,5-bis(1',2',4'-triazol-1'-yl)pyridine: synthesis, structures and electrocatalytic properties.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 903-907
1573455 CIFC34 H22 Br2 F2 N4 O2C 1 2/c 113.8725; 29.1188; 9.362
90; 127.298; 90
3008.4Qi, Liang-Wen; Twumasi, Emmanuella Bema; Li, Xiao-Wei; Li, Rui; Lu, Yixin
Reductive coupling of azonaphthalenes for the synthesis of BINAMs <i>via</i> a diboron-enabled [5,5]-sigmatropic rearrangement.
Chemical science, 2025, 16, 1441-1446
1573456 CIFC28 H19 N O SP 1 21/c 120.812; 7.486; 13.413
90; 105.313; 90
2015.5Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573457 CIFC25 N O SP 1 21/c 123.545; 7.4959; 24.005
90; 117.294; 90
3765Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573458 CIFC24 H17 N O SP 1 21/n 111.7018; 13.6726; 21.985
90; 91.133; 90
3516.8Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573459 CIFC25 H19 N O SP 1 21/n 18.381; 20.496; 11.336
90; 105.075; 90
1880.3Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573460 CIFC24 H19 N O SR -3 :H32.1279; 32.1279; 9.3505
90; 90; 120
8358.5Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573461 CIFC30 H21 N O SP 1 21 15.9514; 16.6; 22.163
90; 90.368; 90
2189.5Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573462 CIFC26 H19 N O SP 1 21/n 112.2581; 25.0852; 12.7705
90; 95.524; 90
3908.7Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573463 CIFC24 H17 N O2 SP 21 21 217.3105; 9.5818; 26.479
90; 90; 90
1854.8Sharangi, Sanhati; Chakraborty, Barsha; Jha, Raushan Kumar; Mandal, Swarnadeep; Koner, Apurba Lal; Kumar, Sangit
Regio- and diastereoselective synthesis of cyclobutylated phenothiazines <i>via</i> [2 + 2] photocycloaddition: demonstrating wavelength-gated cycloreversion inside live cells.
Chemical science, 2025, 16, 709-720
1573464 CIFC26 H25 F O6P -17.2891; 9.7884; 15.6447
88.064; 84.589; 80.174
1094.77Zhang, Kuan; Gao, Zhengyang; Xia, Yan; Li, Pengfei; Gao, Pin; Duan, Xin-Hua; Guo, Li-Na
Synthesis of fluorine-containing bicyclo[4.1.1]octenes <i>via</i> photocatalyzed defluorinative (4 + 3) annulation of bicyclo[1.1.0]butanes with <i>gem</i>-difluoroalkenes.
Chemical science, 2025, 16, 1411-1416
1573465 CIFC22 H19 F O2P n a 2111.4103; 16.6264; 9.2337
90; 90; 90
1751.75Zhang, Kuan; Gao, Zhengyang; Xia, Yan; Li, Pengfei; Gao, Pin; Duan, Xin-Hua; Guo, Li-Na
Synthesis of fluorine-containing bicyclo[4.1.1]octenes <i>via</i> photocatalyzed defluorinative (4 + 3) annulation of bicyclo[1.1.0]butanes with <i>gem</i>-difluoroalkenes.
Chemical science, 2025, 16, 1411-1416
1573466 CIFC27 H22 F3 Fe N O2 SP 21 21 219.5134; 9.874; 24.656
90; 90; 90
2316.1Parganiha, Devendra; Thorat, Raviraj Ananda; Dhumale, Ashwini Dilip; Upadhyay, Yagya Dutt; Jha, Raushan Kumar; Raju, Saravanan; Kumar, Sangit
Substrate NOBINAc ligand affinity for Pd<sup>II</sup>-catalyzed enantioselective C-H activation over reactive β-C-H bonds in ferrocenyl amines.
Chemical science, 2025, 16, 700-708
1573467 CIFC22 H20 F3 Fe N O2 SP -19.65; 10.5668; 11.6109
89.893; 69.144; 67.203
1007.15Parganiha, Devendra; Thorat, Raviraj Ananda; Dhumale, Ashwini Dilip; Upadhyay, Yagya Dutt; Jha, Raushan Kumar; Raju, Saravanan; Kumar, Sangit
Substrate NOBINAc ligand affinity for Pd<sup>II</sup>-catalyzed enantioselective C-H activation over reactive β-C-H bonds in ferrocenyl amines.
Chemical science, 2025, 16, 700-708
1573468 CIFC27 H22 F3 Fe N O2 SP 21 21 219.5665; 9.829; 25.415
90; 90; 90
2389.8Parganiha, Devendra; Thorat, Raviraj Ananda; Dhumale, Ashwini Dilip; Upadhyay, Yagya Dutt; Jha, Raushan Kumar; Raju, Saravanan; Kumar, Sangit
Substrate NOBINAc ligand affinity for Pd<sup>II</sup>-catalyzed enantioselective C-H activation over reactive β-C-H bonds in ferrocenyl amines.
Chemical science, 2025, 16, 700-708
1573469 CIFC24 H21 Ag2 Cl3 F12 N12 P2P -18.0608; 14.5789; 16.1846
72.495; 82.655; 74.413
1744.9Panda, Subhra Jyoti; Khator, Kanha Ram; Deswal, Priyanka; Nayak, Shashwat; Pandey, Durgesh; Patel, Suraj K.; Agrawalla, Suraj Kumar; Ghosh, Dibyajyoti; Senanayak, Satyaprasad P.; Purohit, Chandra Shekhar
Silver-purine MOFs for high-performance multi-terminal neuromorphic memory.
Materials horizons, 2025, 12, 2208-2222
1573470 CIFC6 H5 Ag Cl F6 N4 SbP 1 21/c 112.0279; 8.6719; 12.8186
90; 108.416; 90
1268.57Panda, Subhra Jyoti; Khator, Kanha Ram; Deswal, Priyanka; Nayak, Shashwat; Pandey, Durgesh; Patel, Suraj K.; Agrawalla, Suraj Kumar; Ghosh, Dibyajyoti; Senanayak, Satyaprasad P.; Purohit, Chandra Shekhar
Silver-purine MOFs for high-performance multi-terminal neuromorphic memory.
Materials horizons, 2025, 12, 2208-2222
1573471 CIFC6 H5 Ag Cl F6 N4 PP 1 21/c 111.9676; 8.4366; 12.5599
90; 108.484; 90
1202.7Panda, Subhra Jyoti; Khator, Kanha Ram; Deswal, Priyanka; Nayak, Shashwat; Pandey, Durgesh; Patel, Suraj K.; Agrawalla, Suraj Kumar; Ghosh, Dibyajyoti; Senanayak, Satyaprasad P.; Purohit, Chandra Shekhar
Silver-purine MOFs for high-performance multi-terminal neuromorphic memory.
Materials horizons, 2025, 12, 2208-2222
1573472 CIFC24 H21 Ag2 Cl3 F12 N12 Sb2P 1 21/c 116.2142; 17.5601; 13.5028
90; 106.381; 90
3688.5Panda, Subhra Jyoti; Khator, Kanha Ram; Deswal, Priyanka; Nayak, Shashwat; Pandey, Durgesh; Patel, Suraj K.; Agrawalla, Suraj Kumar; Ghosh, Dibyajyoti; Senanayak, Satyaprasad P.; Purohit, Chandra Shekhar
Silver-purine MOFs for high-performance multi-terminal neuromorphic memory.
Materials horizons, 2025, 12, 2208-2222
1573473 CIFC11 H11 Cl2 N3 O2 PdI 1 2/a 119.6202; 9.6407; 14.9332
90; 91.131; 90
2824.1Reusser, Esaïe; Aeschlimann, Michael; Albrecht, Martin
Enhancing activity and selectivity of palladium catalysts in ketone α-arylation by tailoring the imine chelate of pyridinium amidate (PYA) ligands.
Catalysis science & technology, 2025, 15, 867-877
1573474 CIFC19 H20 Cl2 N4 O PdP 1 21/n 111.62997; 14.78476; 11.92053
90; 105.047; 90
1979.42Reusser, Esaïe; Aeschlimann, Michael; Albrecht, Martin
Enhancing activity and selectivity of palladium catalysts in ketone α-arylation by tailoring the imine chelate of pyridinium amidate (PYA) ligands.
Catalysis science & technology, 2025, 15, 867-877
1573475 CIFC14 H18 Cl2 N4 O PdP 21 21 218.91557; 10.26115; 18.9836
90; 90; 90
1736.7Reusser, Esaïe; Aeschlimann, Michael; Albrecht, Martin
Enhancing activity and selectivity of palladium catalysts in ketone α-arylation by tailoring the imine chelate of pyridinium amidate (PYA) ligands.
Catalysis science & technology, 2025, 15, 867-877
1573476 CIFC12 H14 Cl2 N4 O PdP c c n10.9705; 23.0363; 14.0725
90; 90; 90
3556.4Reusser, Esaïe; Aeschlimann, Michael; Albrecht, Martin
Enhancing activity and selectivity of palladium catalysts in ketone α-arylation by tailoring the imine chelate of pyridinium amidate (PYA) ligands.
Catalysis science & technology, 2025, 15, 867-877
1573477 CIF
Paper
C16 H16 N2 O4I 1 2/a 116.6633; 4.7294; 19.6488
90; 110.091; 90
1454.24Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573478 CIFC16 H16 N2 O4I 1 2/a 116.6728; 4.7388; 19.668
90; 110.024; 90
1460.01Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573479 CIFC16 H16 N2 O4I 1 2/a 116.6842; 4.7293; 19.692
90; 110.036; 90
1459.75Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573480 CIFC16 H16 N2 O4I 1 2/a 116.6876; 4.7329; 19.6859
90; 110.002; 90
1461.02Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573481 CIFC16 H16 N2 O4I 1 2/a 116.6834; 4.7362; 19.6927
90; 109.981; 90
1462.37Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573482 CIFC16 H16 N2 O4I 1 2/a 116.6852; 4.7457; 19.6763
90; 109.949; 90
1464.54Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573483 CIFC16 H16 N2 O4I 1 2/a 116.6821; 4.7392; 19.6849
90; 109.948; 90
1462.91Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573484 CIFC16 H16 N2 O4I 1 2/a 116.6868; 4.7394; 19.6945
90; 109.936; 90
1464.21Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573485 CIFC16 H16 N2 O4I 1 2/a 116.6819; 4.7422; 19.6945
90; 109.915; 90
1464.84Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573486 CIFC16 H16 N2 O4I 1 2/a 116.6847; 4.7475; 19.6847
90; 109.844; 90
1466.65Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573487 CIFC16 H16 N2 O4I 1 2/a 116.6837; 4.75; 19.6845
90; 109.814; 90
1467.6Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573488 CIFC16 H16 N2 O4I 1 2/a 116.6837; 4.7513; 19.6812
90; 109.784; 90
1468.03Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573489 CIFC16 H16 N2 O4I 1 2/a 116.68; 4.7547; 19.6846
90; 109.773; 90
1469.11Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573490 CIFC16 H16 N2 O4I 1 2/a 116.6841; 4.7564; 19.6818
90; 109.74; 90
1470.09Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573491 CIFC16 H16 N2 O4I 1 2/a 116.6798; 4.7618; 19.6808
90; 109.657; 90
1472.07Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573492 CIFC16 H16 N2 O4I 1 2/a 116.684; 4.7634; 19.6972
90; 109.674; 90
1474.01Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573493 CIFC16 H16 N2 O4I 1 2/a 116.6906; 4.7903; 19.6824
90; 109.367; 90
1484.62Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573494 CIFC16 H16 N2 O4I 1 2/a 116.692; 4.8145; 19.6756
90; 109.059; 90
1494.53Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573495 CIFC16 H16 N2 O4I 1 2/a 116.6911; 4.8164; 19.6669
90; 109.032; 90
1494.62Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573496 CIFC16 H18 N2 O4I 1 2/a 116.6; 4.7781; 19.218
90; 110.32; 90
1429Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573497 CIFC16 H18 N2 O4I 1 2/a 116.56; 4.7226; 19.187
90; 110.99; 90
1401Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573498 CIFC16 H18 N2 O4I 1 2/a 116.6147; 4.8463; 19.3274
90; 109.551; 90
1466.51Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573499 CIFC16 H18 N2 O4I 1 2/a 116.6128; 4.8607; 19.3367
90; 109.37; 90
1473.05Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573500 CIFC16 H18 N2 O4I 1 2/a 116.55; 4.6266; 19.089
90; 111.96; 90
1356Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573501 CIFC16 H18 N2 O4I 1 2/a 116.6153; 4.8619; 19.34
90; 109.35; 90
1474.07Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573502 CIFC16 H18 N2 O4I 1 2/a 116.6155; 4.8646; 19.3384
90; 109.321; 90
1475.05Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573503 CIFC16 H18 N2 O4I 1 2/a 116.6252; 4.8647; 19.3379
90; 109.278; 90
1476.3Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573504 CIFC16 H18 N2 O4I 1 2/a 116.6176; 4.8671; 19.3394
90; 109.301; 90
1476.25Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573505 CIFC16 H18 N2 O4I 1 2/a 116.6174; 4.8695; 19.3375
90; 109.268; 90
1477.11Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573506 CIFC16 H18 N2 O4I 1 2/a 116.6187; 4.872; 19.3377
90; 109.242; 90
1478.23Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573507 CIFC16 H18 N2 O4I 1 2/a 116.6197; 4.8747; 19.3362
90; 109.217; 90
1479.25Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573508 CIFC16 H18 N2 O4I 1 2/a 116.6216; 4.877; 19.3388
90; 109.193; 90
1480.54Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573509 CIFC16 H18 N2 O4I 1 2/a 116.6256; 4.8792; 19.3393
90; 109.164; 90
1481.86Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573510 CIFC16 H18 N2 O4I 1 2/a 116.6268; 4.881; 19.3397
90; 109.141; 90
1482.75Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573511 CIFC16 H18 N2 O4I 1 2/a 116.6279; 4.8825; 19.3411
90; 109.105; 90
1483.73Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573512 CIFC16 H18 N2 O4I 1 2/a 116.53; 4.5612; 19.065
90; 112.63; 90
1326.8Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573513 CIFC16 H18 N2 O4I 1 2/a 116.6313; 4.8871; 19.3441
90; 109.05; 90
1486.16Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573514 CIFC16 H18 N2 O4I 1 2/a 116.6408; 4.8878; 19.3501
90; 109.048; 90
1487.7Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573515 CIFC16 H18 N2 O4I 1 2/a 116.48; 4.5205; 19.083
90; 113.24; 90
1306Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573516 CIFC16 H18 N2 O4I 1 2/a 116.6494; 4.9069; 19.3575
90; 108.812; 90
1497Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573517 CIFC16 H18 N2 O4I 1 2/a 116.469; 4.4857; 19.042
90; 113.63; 90
1288.8Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573518 CIFC16 H18 N2 O4I 1 2/a 116.462; 4.4828; 19.038
90; 113.66; 90
1286.8Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573519 CIFC16 H18 N2 O4I 1 2/a 116.446; 4.46879; 19.038
90; 113.81; 90
1280.1Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573520 CIFC16 H18 N2 O4I 1 2/a 116.33; 4.4824; 19.06
90; 113.4; 90
1280Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573521 CIFC16 H18 N2 O4I 1 2/a 116.6688; 4.9269; 19.3733
90; 108.522; 90
1508.63Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573522 CIFC16 H18 N2 O4I 1 2/a 116.661; 4.9284; 19.3767
90; 108.52; 90
1508.7Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573523 CIFC16 H18 N2 O4I 1 2/a 116.429; 4.4214; 19.02
90; 114.32; 90
1259Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573524 CIFC16 H18 N2 O4I 1 2/a 116.44; 4.4104; 18.97
90; 114; 90
1257Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573525 CIFC16 H18 N2 O4I 1 2/a 116.46; 4.3839; 18.94
90; 114.3; 90
1246Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573526 CIFC16 H18 N2 O4I 1 2/a 116.6711; 4.9272; 19.3744
90; 108.512; 90
1509.1Patyk-Kaźmierczak, Ewa; Szymańska, Kornelia; Kaźmierczak, Michał
Managing negative linear compressibility and thermal expansion through steric hindrance: a case study of 1,2-bis(4'-pyridyl)ethane cocrystals.
IUCrJ, 2025, 12
1573527 CIFC16 H21 Cl2 O2 P SP 1 21/n 16.6911; 21.7491; 12.1069
90; 103.068; 90
1716.23Bouzid, Moad; Poinsot, Didier; Mboyi, Clève D; Ochmann, Lukas; Domenichini, Bruno; Schreiner, Peter R.; Hierso, Jean-Cyrille
Sulfur functionalized diamondoid phosphines enable building nanocomposites interfacing sp<sup>3</sup>-carbon and gold nanolayers.
Nanoscale, 2025, 17, 4123-4131
1573528 CIFC14 H21 P SP 1 21/c 17.7405; 13.6302; 12.6387
90; 104.82; 90
1289.08Bouzid, Moad; Poinsot, Didier; Mboyi, Clève D; Ochmann, Lukas; Domenichini, Bruno; Schreiner, Peter R.; Hierso, Jean-Cyrille
Sulfur functionalized diamondoid phosphines enable building nanocomposites interfacing sp<sup>3</sup>-carbon and gold nanolayers.
Nanoscale, 2025, 17, 4123-4131
1573529 CIFAl2 Ca H6 O13 Si3C 1 c 16.5252; 18.9769; 9.7779
90; 108.857; 90
1145.79Tajiri, Hiroo; Kohara, Shinji; Kimura, Koji; Halubai, Sekhar; Morimoto, Haruto; Happo, Naohisa; Stellhorn, Jens R.; Onodera, Yohei; Qiao, Xvsheng; Urushihara, Daisuke; Hu, Peidong; Wakihara, Toru; Kinoshita, Toyohiko; Hayashi, Koichi
Diffractometer for element-specific analysis on local structures using a combination of X-ray fluorescence holography and anomalous X-ray scattering.
Journal of synchrotron radiation, 2025, 32, 125-132
1573535 CIF
Paper
C30 H41 La2 N10 O18.5P 1 21/c 111.117; 17.8366; 11.8094
90; 114.213; 90
2135.7Ndiaye-Gueye, Mbossé; Traoré, Bocar; Thiam, Ibrahima Elhadji; Diouf, Ousmane; Wenger, Emmanuel; Sall, Abdou Salam; Lecomte, Claude; Gaye, Mohamed
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 85-89
1573538 CIF
Paper
C9 H10 N4 O2P 1 21/c 13.7638; 9.286; 26.194
90; 93.786; 90
913.5Boutheina, Boualia; Zakaria, Bouhidel; Cherouana, Aouatef; El-Eulmi, Bendeif
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 80-84
1573541 CIFC22 H28 Na4 O10 P2P 1 21/c 112.6672; 6.1624; 18.016
90; 106.967; 90
1345.1Zhang, Yan; Apostol, Petru; Rambabu, Darsi; Guo, Xiaolong; Liu, Xuelian; Lin, Xiaodong; Xie, Haijiao; Chen, Xiaohua; Robeyns, Koen; Wang, Jiande; Wang, Junzhong; Vlad, Alexandru
Ionically conducting Li- and Na-phosphonates as organic electrode materials for rechargeable batteries.
Chemical science, 2025, 16, 1819-1825
1573542 CIFC86 H44 N2I 1 2/a 115.8224; 21.9763; 28.7119
90; 93.501; 90
9965Nakamura, Tomoya; Nagai, Takabumi; Miyake, Yuki; Yamada, Takumi; Miura, Makoto; Yoshida, Hiroyuki; Kanemitsu, Yoshihiko; Truong, Minh Anh; Murdey, Richard; Wakamiya, Atsushi
Single-isomer bis(pyrrolidino)fullerenes as electron-transporting materials for tin halide perovskite solar cells.
Chemical science, 2025, 16, 2265-2272
1573543 CIFC27 H20 F2 O3P -19.86943; 17.5275; 26.1199
95.7908; 99.8803; 106.339
4218.1Li, Na; Li, Chenghui; Zhou, Qianying; Zhang, Xin; Deng, Zhouming; Jiang, Zhong-Xing; Yang, Zhigang
General access to furan-substituted <i>gem</i>-difluoroalkenes enabled by PFTB-promoted cross-coupling of ene-yne-ketones and difluorocarbene.
Chemical science, 2025, 16, 1455-1464
1573544 CIFC11 H21 B O3 SP 1 21/c 113.0315; 6.515; 15.334
90; 98.689; 90
1286.9Kumar, Ashok; Gupta, Rohit; Subramaniyan, Vasudevan; Mani, Ganesan
DMSO-catalyzed CO2 reduction with 9-BBN: selective formation of either formoxy- or methoxyborane under mild conditions and C-methylenation of indoles
Catalysis Science & Technology, 2025, 15, 678-688
1573545 CIFC26 H21 B N4 OP 1 21/n 19.804; 16.35; 13.564
90; 108.989; 90
2056Watson, Alexander E. R.; Boyle, Paul D.; Ragogna, Paul J.; Gilroy, Joe B.
Ligand protonation leads to highly fluorescent boronium cations.
Chemical science, 2025, 16, 2258-2264
1573546 CIFC34 H32 B Cl3 N4 OP 21 21 219.673; 16.008; 20.119
90; 90; 90
3115Watson, Alexander E. R.; Boyle, Paul D.; Ragogna, Paul J.; Gilroy, Joe B.
Ligand protonation leads to highly fluorescent boronium cations.
Chemical science, 2025, 16, 2258-2264
1573547 CIFB2 Ba Ca Cs F O5P -4 21 m8.8668; 8.8668; 8.7669
90; 90; 90
689.25Chen, Fuqiang; Wu, Hongping; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng; Yu, Hongwei
Rational design of a series of non-centrosymmetric antiperovskite and double antiperovskite borate fluorides.
Chemical science, 2025, 16, 2015-2023
1573548 CIFB2 Ba Ca F O5 RbP -4 21 m8.7713; 8.7713; 4.3173
90; 90; 90
332.15Chen, Fuqiang; Wu, Hongping; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng; Yu, Hongwei
Rational design of a series of non-centrosymmetric antiperovskite and double antiperovskite borate fluorides.
Chemical science, 2025, 16, 2015-2023
1573549 CIFB2 Ba Ca F K O5P -4 21 m8.7276; 8.7276; 4.284
90; 90; 90
326.32Chen, Fuqiang; Wu, Hongping; Hu, Zhanggui; Wang, Jiyang; Wu, Yicheng; Yu, Hongwei
Rational design of a series of non-centrosymmetric antiperovskite and double antiperovskite borate fluorides.
Chemical science, 2025, 16, 2015-2023
1573550 CIFC38 H32 N4 O2P -17.2089; 9.3281; 11.0857
97.148; 92.22; 96.254
734.23Mandal, Debasish; Sarkar, Abani; Behera, Kanhu Charan; Ravikanth, Mangalampalli
pH-responsive supramolecular switch of a rationally designed dipyrroethene-based chromophore.
Chemical science, 2025, 16, 1772-1782
1573551 CIFC42 H34 F6 N4 O6C 1 2/c 113.3398; 12.3038; 25.4069
90; 97.608; 90
4133.3Mandal, Debasish; Sarkar, Abani; Behera, Kanhu Charan; Ravikanth, Mangalampalli
pH-responsive supramolecular switch of a rationally designed dipyrroethene-based chromophore.
Chemical science, 2025, 16, 1772-1782
1573552 CIFC19 H17 N3P -19.295; 9.499; 10.348
79.673; 65.183; 63.713
743.5Mandal, Debasish; Sarkar, Abani; Behera, Kanhu Charan; Ravikanth, Mangalampalli
pH-responsive supramolecular switch of a rationally designed dipyrroethene-based chromophore.
Chemical science, 2025, 16, 1772-1782
1573553 CIFC64 H92 N4 Tb2P n a 2130.8903; 10.27991; 18.11204
90; 90; 90
5751.47Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573554 CIFC10.09 H14.96 Cl0.17 Dy0.17 N0.7C 1 2/c 123.9612; 10.5893; 22.5423
90; 112.235; 90
5294.4Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573555 CIFC65 H94 I N4 YI 1 2/a 125.2282; 10.9625; 23.8393
90; 116.041; 90
5923.8Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573556 CIFC58 H86 Cl N4 TbC 1 2/c 123.9599; 10.5837; 22.4979
90; 112.183; 90
5282.8Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573557 CIFC67 H99 Dy2 N4P 1 21/c 110.8382; 38.9439; 15.0078
90; 105.063; 90
6116.87Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573558 CIFC67 H99 N4 Y2P 1 21/c 110.8398; 38.9679; 15.0051
90; 105.029; 90
6121.42Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573559 CIFC75 H120 N4 Tb2P -114.4004; 15.4059; 18.05
97.598; 103.094; 112.008
3510.01Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573560 CIFC65 H94 Gd I N4C 1 2/c 126.171; 11.0443; 23.94
90; 119.762; 90
6006.9Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573561 CIFC64 H92 Gd2 N4P b c a18.1193; 35.666; 36.498
90; 90; 90
23587Jin, Peng-Bo; Luo, Qian-Cheng; Gransbury, Gemma K.; Winpenny, Richard E. P.; Mills, David P.; Zheng, Yan-Zhen
Rare earth benzene tetraanion-bridged amidinate complexes.
Chemical science, 2025, 16, 1907-1924
1573562 CIFC27 H36 B N3 OP 1 21/c 112.67284; 9.17962; 22.43254
90; 96.7556; 90
2591.5Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573563 CIFC53 H74 B N5 P2P 1 21/c 112.8968; 19.8442; 40.8371
90; 96.999; 90
10373.4Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573564 CIFC45 H52.4 B2 K N3 O2I -422.7178; 22.7178; 15.9414
90; 90; 90
8227.3Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573565 CIFC33 H42 B N3P 1 21/n 19.7098; 16.9985; 17.7195
90; 93.843; 90
2918.06Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573566 CIFC60 H81 B3 N6 OC 1 2/c 122.2498; 13.5031; 37.4373
90; 99.081; 90
11106.7Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573567 CIFC27 H36 B N3 SI 1 2/a 116.90996; 9.55705; 33.35081
90; 94.9584; 90
5369.63Tang, Jianqin; Hu, Chenyang; Crumpton, Agamemnon E.; Griffin, Liam P.; Goicoechea, Jose M.; Aldridge, Simon
Metathesis chemistry of inorganic cumulenes driven by B-O bond formation.
Chemical science, 2025, 16, 2231-2237
1573570 CIFC31 H29 F2 O4 PP -19.6234; 10.4927; 14.0802
99.31; 98.054; 100.619
1357.67Huang, Mao-Gui; Fu, Yue-Liu-Ting; Li, Jia-Wei; Liu, Yue-Jin
Ruthenium-catalyzed three-component tandem remote C-H functionalization of naphthalenes: modular and concise synthesis of multifunctional naphthalenes.
Chemical science, 2025, 16, 1957-1965
1573571 CIFC42 H40 Br4 N12 Ni2 O6P 1 21/c 114.4927; 9.522; 24.7089
90; 137.895; 90
2286.3Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573572 CIFC40 H38 Br4 Cl4 N12 Ni2 O4P 1 21/c 113.4368; 9.1144; 20.483
90; 108.664; 90
2376.6Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573573 CIFC20.57 H18.49 N6.86 O2.39I 1 2/a 113.0278; 14.7154; 34.4476
90; 99.152; 90
6519.86Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573574 CIFC13.82 H12.36 Br0.73 N5.09 Ni0.36 O1.45P 1 21/c 117.1742; 13.6415; 17.8507
90; 103.715; 90
4062.85Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573575 CIFC17 H14 N6 O2P -16.6161; 11.0537; 11.1219
84.188; 74.575; 88.159
780.03Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573576 CIFC11.5 H12.5 N2.5 O2P 1 21/c 19.8012; 8.1826; 27.1202
90; 94.448; 90
2168.47Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573577 CIFC39 H52 N5 Ni O4.5C 1 2/c 133.3183; 9.9346; 21.7721
90; 91.007; 90
7205.54Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573578 CIFC37 H32 Br N5 Ni O3 PP 1 21/n 119.3695; 17.6564; 19.5992
90; 93.297; 90
6691.75Rodriguez-Lugo, Rafael E; Sander, Joan; Dietzmann, Simon; Rittner, Thomas; Rückel, Jannes; Landaeta, Vanessa R.; Park, Jiyong; Nuernberger, Patrick; Baik, Mu-Hyun; Wolf, Robert
Mechanistic insights into the visible-light-driven <i>O</i>-arylation of carboxylic acids catalyzed by xanthine-based nickel complexes.
Chemical science, 2025, 16, 2751-2762
1573579 CIF
Paper
C14 H13 N3 O4 S2P -111.2439; 11.2772; 13.4027
65.901; 87.254; 79.439
1524.37Jeziorna, Agata; Malinska, Maura; Sugden, Isaac; Paluch, Piotr; Dolot, Rafał; Dudek, Marta K.
SCXRD, CSP-NMRX and microED in the quest for three elusive polymorphs of meloxicam.
IUCrJ, 2025, 12
1573580 CIF
Paper
C21 H19 Cl O6P 1 21/c 116.752; 7.27831; 15.9369
90; 100.013; 90
1913.53Pham, Phuong-Truc T.; Bader, Mamoun M.
4-Chlorocurcumin
IUCrData, 2025, 10, x241243
1573581 CIF
Paper
C9 H10 Cl N O6P 1 21/c 15.6911; 7.9862; 24.9303
90; 91.008; 90
1132.91Sadikhova, Nurlana D.; Muradova, Farida M.; Guliyeva, Narmina A.; Hasanov, Khudayar I.; Javadzade, Tahir A.; Zangrando, Ennio; Belay, Alebel N.
Pyridin-1-ium carboxyformate–2-chloroacetic acid (1/1)
IUCrData, 2025, 10, x241242
1573582 CIFC41 H40 Cl2 N2 O Ru S2P b c a8.31031; 20.0084; 44.3627
90; 90; 90
7376.45Matveeva, Maria; Trzaskowski, Bartosz; Kajetanowicz, Anna
Modifications of substituents on the chelating oxygen atom in stereoretentive Hoveyda–Grubbs-type complexes and their influence on catalytic properties
Catalysis Science & Technology, 2025, 15, 783-793
1573583 CIFC49 H69 Mg N4 P SiP -110.9738; 12.7041; 18.1148
85.417; 85.746; 80.856
2480.5Nath, Priyanku; Sagar, Shweta; Ray, Aranya; Karmakar, Himadri; Sarkar, Alok; Chandrasekhar, Vadapalli; Panda, Tarun K.
Crafting tailored, well-defined block copolymers of cyclic esters with an organomagnesium initiator.
Chemical communications (Cambridge, England), 2025, 61, 2341-2344
1573584 CIFC24 O13 Zn4F m -3 m25.415; 25.415; 25.415
90; 90; 90
16416.1Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573585 CIFC24 O13 Zn4P m -3 m12.8235; 12.8235; 12.8235
90; 90; 90
2108.7Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573586 CIFC96 O64 Zn16F m -3 m25.6171; 25.6171; 25.6171
90; 90; 90
16810.9Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573587 CIFC96 O64 Zn16F m -3 m25.6455; 25.6455; 25.6455
90; 90; 90
16866.8Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573588 CIFC96 O64 Zn16F m -3 m25.6396; 25.6396; 25.6396
90; 90; 90
16855.2Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573589 CIFC96 O64 Zn16F m -3 m25.6309; 25.6309; 25.6309
90; 90; 90
16838Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573590 CIFC14 N O5 ZnC 1 2/c 113.6279; 16.9199; 19.7799
90; 91.635; 90
4559Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573591 CIFC96 O64 Zn16F m -3 m25.6731; 25.6731; 25.6731
90; 90; 90
16921.3Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573592 CIFC96 O64 Zn16F m -3 m25.6846; 25.6846; 25.6846
90; 90; 90
16944.1Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573593 CIFC96 O64 Zn16F m -3 m25.6483; 25.6483; 25.6483
90; 90; 90
16872.4Kim, Hyunyong; Cohen, Seth M.
Metal-organic frameworks generated from oligomeric ligands with functionalized tethers.
Chemical science, 2025, 16, 2344-2350
1573594 CIFC29 H17 N3 O3P 1 21/c 17.2038; 11.3027; 26.8583
90; 92.223; 90
2185.2Sneddon, Dorian S.; Kevorkian, Paul V.; Hoye, Thomas R.
Rapid (≤25 °C) cycloisomerization of anhydride-tethered triynes to benzynes - origin of a remarkable anhydride linker-induced rate enhancement.
Chemical science, 2025, 16, 2898-2906
1573595 CIFC47 H41 N5 O5P 1 21/n 113.0754; 19.067; 15.68
90; 104.258; 90
3788.7Bae, Sungryul; Jeong, Younjae; Lee, Dongwhan
Mutually antagonistic molecular clips: symmetry-breaking non-covalent bonds at the chiral-nonchiral interface.
Chemical science, 2025, 16, 3459-3469
1573596 CIFC56 H42 N6 O5P -18.418; 12.809; 40.083
91.42; 92.29; 106.79
4131.5Bae, Sungryul; Jeong, Younjae; Lee, Dongwhan
Mutually antagonistic molecular clips: symmetry-breaking non-covalent bonds at the chiral-nonchiral interface.
Chemical science, 2025, 16, 3459-3469
1573597 CIFC44 H36 N4 O3P b c a15.283; 14.723; 30.471
90; 90; 90
6856Bae, Sungryul; Jeong, Younjae; Lee, Dongwhan
Mutually antagonistic molecular clips: symmetry-breaking non-covalent bonds at the chiral-nonchiral interface.
Chemical science, 2025, 16, 3459-3469
1573598 CIFC84 H69 N9 O8P 21 21 2114.434; 15.041; 30.493
90; 90; 90
6620Bae, Sungryul; Jeong, Younjae; Lee, Dongwhan
Mutually antagonistic molecular clips: symmetry-breaking non-covalent bonds at the chiral-nonchiral interface.
Chemical science, 2025, 16, 3459-3469
1573599 CIFC13 H16 I N O2P -15.4287; 8.9764; 13.4695
96.706; 95.087; 90.122
649.26Shiels, Oisin J.; Brydon, Samuel C.; Poad, Berwyck L. J.; Marshall, David L.; Houston, Sevan D.; Xing, Hui; Bernhardt, Paul V.; Savage, G. Paul; Williams, Craig M.; Harman, David G.; Kirk, Benjamin B.; da Silva, Gabriel; Blanksby, Stephen J.; Trevitt, Adam J.
Electrostatically tuning radical addition and atom abstraction reactions with distonic radical ions.
Chemical science, 2025, 16, 2861-2878
1573600 CIFC26 H44 N2 O4P -16.5625; 13.4728; 14.2734
75.183; 78.29; 80.854
1186.97Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573601 CIFC33 H48 N3 O9P -111.4038; 12.7819; 13.6007
88.897; 70.005; 65.733
1681.25Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573602 CIFC20 H22 N4 O8 S2P 1 21/n 110.4623; 5.916; 20.1437
90; 104.968; 90
1204.49Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573603 CIFC23 H40 N2 O6 SP -15.8262; 9.25; 24.521
79.998; 88.376; 80.227
1282.5Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573604 CIFC28 H44 N2 O6P c a 2121.69; 6.077; 22.48
90; 90; 90
2963Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573605 CIFC22 H39 N O4P -16.657; 13.21; 13.286
106.992; 91.051; 96.242
1109.2Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573606 CIFC32 H46 N4 O4P -16.4847; 7.741; 16.693
91.501; 98.704; 108.733
781.9Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573607 CIFC26 H34 N4 O4P 1 21/n 19.788; 6.098; 21.09
90; 96.993; 90
1249.4Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573608 CIFC29 H50 N2 O4P 1 21/c 120.775; 6.448; 21.727
90; 97.79; 90
2884Roy, Nabanita; Ghosh, Subhajit; Dutta, Abhishek; Dastidar, Parthasarathi
Designing anti-bacterial supramolecular gels from primary ammonium dicarboxylate (PAD) salts for self-delivery applications.
Faraday discussions, 2025, 260, 283-309
1573609 CIFC28 H58.58 Br5.42 Ce2 Mn O14.58P 21 21 2115.244; 15.3069; 21.3108
90; 90; 90
4972.63Liu, Huanyu; Yu, Gang; Huo, Peihao; Guo, Ruoyao; Li, Yujia; Qi, Hao; Zheng, Jiayin; Jin, Tong; Zhao, Zifeng; Bian, Zuqiang; Liu, Zhiwei
Structural relaxation chirality transfer enhanced circularly polarized luminescence in heteronuclear Ce<sup>III</sup>-Mn<sup>II</sup> complexes.
Materials horizons, 2025, 12, 2650-2655
1573610 CIFC28 H58.39 Br5.61 La2 Mn O14.39P 21 21 2115.5414; 15.5635; 21.415
90; 90; 90
5179.8Liu, Huanyu; Yu, Gang; Huo, Peihao; Guo, Ruoyao; Li, Yujia; Qi, Hao; Zheng, Jiayin; Jin, Tong; Zhao, Zifeng; Bian, Zuqiang; Liu, Zhiwei
Structural relaxation chirality transfer enhanced circularly polarized luminescence in heteronuclear Ce<sup>III</sup>-Mn<sup>II</sup> complexes.
Materials horizons, 2025, 12, 2650-2655
1573611 CIFC28 H58.52 Br5.48 Ce2 Mn O14.52P 21 21 2115.3088; 15.3451; 21.3976
90; 90; 90
5026.62Liu, Huanyu; Yu, Gang; Huo, Peihao; Guo, Ruoyao; Li, Yujia; Qi, Hao; Zheng, Jiayin; Jin, Tong; Zhao, Zifeng; Bian, Zuqiang; Liu, Zhiwei
Structural relaxation chirality transfer enhanced circularly polarized luminescence in heteronuclear Ce<sup>III</sup>-Mn<sup>II</sup> complexes.
Materials horizons, 2025, 12, 2650-2655
1573612 CIFC16 H36 Br5 Ce O8 ZnP 41 21 210.2108; 10.2108; 58.9846
90; 90; 90
6149.8Liu, Huanyu; Yu, Gang; Huo, Peihao; Guo, Ruoyao; Li, Yujia; Qi, Hao; Zheng, Jiayin; Jin, Tong; Zhao, Zifeng; Bian, Zuqiang; Liu, Zhiwei
Structural relaxation chirality transfer enhanced circularly polarized luminescence in heteronuclear Ce<sup>III</sup>-Mn<sup>II</sup> complexes.
Materials horizons, 2025, 12, 2650-2655
1573613 CIF
Paper
C20 H16 B Cl F4 N2 RuP 1 21/c 18.4191; 23.1476; 9.9079
90; 94.709; 90
1924.35Varadhan, Manikandan; Passi, Ibanpynhunlang; Chinnathangavel, Thangaraja; Rajendiran, Venugopal
(η6-Benzene)chlorido[2-(pyridin-2-yl)quinoline-κ2 N,N′]ruthenium(II) tetrafluoridoborate
IUCrData, 2025, 10, x241240
1573614 CIF
Paper
C32 H24 O5P 43 21 29.5725; 9.5725; 27.576
90; 90; 90
2526.86Ndima, Lubabalo; Hosten, Eric Cyriel; Betz, Richard
Tetraphenylglycolide tetrahydrofuran monosolvate
IUCrData, 2025, 10, x241241
1573615 CIF
Paper
C10 H18 N2 S2 SnP b c m9.6669; 11.944; 36.0164
90; 90; 90
4158.5Kamrowski, Anne; Reuter, Hans
Di-tert-butyldiisothiocyanatotin(IV)
IUCrData, 2025, 10, x241244
1573616 CIFC2 H5 Cu I NP 62 2 217.5937; 17.5937; 7.3368
90; 90; 120
1966.76Panda, Sankalpa N.; Pradhan, Prabhanjan; Nath, Satyapriya; Mohapatra, Jeebanjyoti; Patra, Biplab K.; Biswal, Bishnu P.
Inducing piezoelectric behavior in a copper iodide cubane cluster-based metal-organic framework <i>via</i> linker engineering.
Chemical communications (Cambridge, England), 2025, 61, 2536-2539
1573617 CIFC29 H22 OC 1 2/c 126.9512; 9.4305; 17.329
90; 111.921; 90
4086Wang, Shiyin; Liu, Haichao; Zhao, Shuaiqiang; Wu, Qiaolin; Yang, Zhiqiang; Yang, Daojie; Lv, Yingbo; Su, Qing; Zhang, Shi-Tong; Yang, Bing
A comparative investigation on excimer fluorescence toward its bright future.
Chemical science, 2025, 16, 3275-3284
1573618 CIFC43 H30 OP -19.1255; 17.9972; 18.3091
90.153; 90.817; 94.909
2995.6Wang, Shiyin; Liu, Haichao; Zhao, Shuaiqiang; Wu, Qiaolin; Yang, Zhiqiang; Yang, Daojie; Lv, Yingbo; Su, Qing; Zhang, Shi-Tong; Yang, Bing
A comparative investigation on excimer fluorescence toward its bright future.
Chemical science, 2025, 16, 3275-3284
1573619 CIFC61 H38 Cl3 N8 O6 ZnP -19.431; 16.704; 19.162
64.511; 81.957; 85.757
2697.8Bulbul, Amir Sohel; Mogilipuri, Jhansi; Soma, Venugopal Rao; Sankar, Muniappan
<i>Meso</i>-β, β-β' trifused porphyrins: synthesis, spectral, electrochemical and DFT studies and their femtosecond third-order nonlinear optical properties.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3679-3694
1573620 CIFC54 H67 Cu K N6 O9P -19.0901; 13.3962; 22.3177
77.196; 86.431; 82.887
2628.01Das, Soumadip; Roy, Aritra; Chakrabarti, Navonil; Mukhopadhyay, Narottam; Sarkar, Aniruddha; Sen Gupta, Sayam
Self-sensitized Cu(ii)-complex catalyzed solar driven CO<sub>2</sub> reduction.
Chemical science, 2025, 16, 3114-3123
1573621 CIFC44 H48 Cl Cu N7 O3P -19.6787; 10.7885; 20.4415
96.743; 90.805; 99.865
2087.09Das, Soumadip; Roy, Aritra; Chakrabarti, Navonil; Mukhopadhyay, Narottam; Sarkar, Aniruddha; Sen Gupta, Sayam
Self-sensitized Cu(ii)-complex catalyzed solar driven CO<sub>2</sub> reduction.
Chemical science, 2025, 16, 3114-3123
1573622 CIFC98 H118 F6 N6 O2 S4C 1 2/c 125.2111; 22.7564; 33.5239
90; 108.292; 90
18261.3Wang, Yan-Bo; Tsai, Chia-Lin; Xue, Yung-Jing; Jiang, Bing-Huang; Lu, Han-Cheng; Hong, Jun-Cheng; Huang, Yu-Chi; Huang, Kuo-Hsiu; Chien, Su-Ying; Chen, Chih-Ping; Cheng, Yen-Ju
Fluorinated and methylated <i>ortho</i>-benzodipyrrole-based acceptors suppressing charge recombination and minimizing energy loss in organic photovoltaics.
Chemical science, 2025, 16, 3259-3274
1573623 CIFC100 H124 F4 N6 O2 S4P -121.223; 21.3687; 32.1128
91.951; 91.3666; 103.586
14140.1Wang, Yan-Bo; Tsai, Chia-Lin; Xue, Yung-Jing; Jiang, Bing-Huang; Lu, Han-Cheng; Hong, Jun-Cheng; Huang, Yu-Chi; Huang, Kuo-Hsiu; Chien, Su-Ying; Chen, Chih-Ping; Cheng, Yen-Ju
Fluorinated and methylated <i>ortho</i>-benzodipyrrole-based acceptors suppressing charge recombination and minimizing energy loss in organic photovoltaics.
Chemical science, 2025, 16, 3259-3274
1573624 CIFC15 H22 Au O PP b 21 a17.021; 9.85683; 16.7157
90; 90; 90
2804.44Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573625 CIFC15 H22 Au O PP b c a16.5751; 9.7432; 16.0297
90; 90; 90
2588.71Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573626 CIFC15 H22 Au O PP b c a16.8809; 9.84471; 16.2781
90; 90; 90
2705.22Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573627 CIFC15 H22 Au O PP b c a16.758; 9.8015; 16.1729
90; 90; 90
2656.5Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573628 CIFC15 H22 Au O PP b 21 a17.0148; 9.8534; 16.7117
90; 90; 90
2801.8Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573629 CIFC15 H22 Au O PP b 21 a17.0137; 9.85586; 16.7032
90; 90; 90
2800.87Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573630 CIFC15 H22 Au O PP b 21 a16.9319; 9.83974; 16.6583
90; 90; 90
2775.36Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573631 CIFC15 H22 Au O PP b 21 a16.9299; 9.84107; 16.663
90; 90; 90
2776.19Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573632 CIFC15 H22 Au O PP b 21 a16.9414; 9.8439; 16.6593
90; 90; 90
2778.26Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573633 CIFC15 H22 Au O PP b c a16.3373; 11.3081; 17.9484
90; 90; 90
3315.9Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573634 CIFC15 H22 Au O PP b 21 a17.0066; 9.85656; 16.7104
90; 90; 90
2801.11Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573635 CIFC15 H22 Au O PP b 21 a16.9382; 9.83503; 16.6637
90; 90; 90
2776Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573636 CIFC15 H22 Au O PP b 21 a16.9414; 9.8439; 16.6593
90; 90; 90
2778.26Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573637 CIFC15 H22 Au O PP b 21 a17.014; 9.85573; 16.71022
90; 90; 90
2802.06Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573638 CIFC15 H22 Au O PP b c a16.7535; 9.80417; 16.1656
90; 90; 90
2655.27Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573639 CIFC15 H22 Au O PP b c a16.883; 9.85238; 16.2916
90; 90; 90
2709.91Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573640 CIFC15 H22 Au O PP b c a16.7442; 9.80349; 16.1545
90; 90; 90
2651.79Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573641 CIFC15 H22 Au O PP b c a16.7395; 9.79915; 16.1723
90; 90; 90
2652.79Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573642 CIFC15 H22 Au O PP b c a16.8614; 9.8359; 16.3043
90; 90; 90
2704Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573643 CIFC15 H22 Au O PP b c a16.7395; 9.79915; 16.1723
90; 90; 90
2652.79Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573644 CIFC15 H22 Au O PP b c a16.5856; 9.7494; 16.0285
90; 90; 90
2591.8Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573645 CIFC15 H22 Au O PP b c a16.5789; 9.75229; 16.0089
90; 90; 90
2588.35Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573646 CIFC15 H22 Au O PP b c a16.883; 9.85238; 16.2916
90; 90; 90
2709.91Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573647 CIFC15 H22 Au O PP b c a16.5856; 9.7494; 16.0285
90; 90; 90
2591.8Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573648 CIFC15 H22 Au O PP b 21 a16.786; 9.8051; 16.5696
90; 90; 90
2727.2Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573649 CIFC15 H22 Au O PP b 21 a17.17; 9.9744; 17.6072
90; 90; 90
3015.4Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573650 CIFC15 H22 Au O PP b 21 a17.2929; 9.9154; 16.8744
90; 90; 90
2893.39Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573651 CIFC15 H22 Au O PP b 21 a17.1407; 9.8864; 16.8388
90; 90; 90
2853.5Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573652 CIFC15 H22 Au O PP b 21 a16.9003; 9.837; 16.6364
90; 90; 90
2765.8Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573653 CIFC15 H22 Au O PP b 21 a17.3429; 9.9201; 16.9287
90; 90; 90
2912.47Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573654 CIFC15 H22 Au O PP b c a16.0628; 11.0945; 17.707
90; 90; 90
3155.5Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573655 CIFC15 H22 Au O PP 1 1 a16.7021; 9.883; 16.8029
90; 90; 93.865
2767.29Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573656 CIFC15 H22 Au O PP b 21 a17.6564; 9.9742; 17.1118
90; 90; 90
3013.5Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573657 CIFC15 H22 Au O PP b c a16.527; 11.2886; 17.901
90; 90; 90
3340Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573658 CIFC15 H22 Au O PP b c a16.178; 11.1922; 17.8018
90; 90; 90
3223.3Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573659 CIFC15 H22 Au O PP b 21 a16.9596; 9.881; 16.6423
90; 90; 90
2788.9Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573660 CIFC15 H22 Au O PP b c a16.168; 10.9575; 17.526
90; 90; 90
3104.9Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573661 CIFC15 H22 Au O PP b 21 a17.0578; 9.8693; 16.7532
90; 90; 90
2820.38Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573662 CIFC15 H22 Au O PP b c a16.9137; 9.8518; 16.3267
90; 90; 90
2720.5Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573663 CIFC15 H22 Au O PP b c a16.7686; 9.8173; 16.1828
90; 90; 90
2664.1Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573664 CIFC15 H22 Au O PP b 21 a17.5579; 9.9652; 17.0487
90; 90; 90
2983Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573665 CIFC15 H22 Au O PP b 21 a17.0308; 9.858; 16.7203
90; 90; 90
2807.2Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573666 CIFC15 H22 Au O PP b c a16.215; 11.0942; 17.732
90; 90; 90
3189.9Dziewiątkowska, Róża; Krzeszczakowska, Joanna; Głodek, Marta; Łomzik, Michał; Plażuk, Damian; Makal, Anna
Pressure-induced phase transitions in a new luminescent gold(I)-arylacetylide.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3362-3374
1573667 CIFC10 H19 B10 N OP 1 21/c 18.7742; 22.4893; 7.9927
90; 103.148; 90
1535.8Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573668 CIFC9 H17 B10 N OP 1 21/n 110.2765; 21.3974; 13.8904
90; 108.8; 90
2891.4Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573669 CIFC19 H31 B10 N2 O2 SP -110.2795; 15.2051; 17.1951
90.72; 100.394; 105.753
2538.8Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573670 CIFC20 H26 B10 N PP -115.1375; 16.6265; 16.7014
79.222; 67.177; 63.665
3471.7Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573671 CIFC10 H19 B10 N SeP 1 21/n 16.7117; 17.891; 13.374
90; 92.059; 90
1604.9Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573672 CIFC10 H19 B10 N SP 21 21 2110.231; 11.712; 13.304
90; 90; 90
1594.2Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573673 CIFC10 H20 B9 N SP 1 21/c 19.9493; 11.5647; 13.7718
90; 93.242; 90
1582.06Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573674 CIFC10 H21 B10 N SP b c a11.1107; 11.3129; 26.083
90; 90; 90
3278.5Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573675 CIFC18 H32 B20 N2 S2P b c a12.0591; 10.8146; 45.473
90; 90; 90
5930.3Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573676 CIFC10 H20 B9 N O SP -17.0558; 10.3528; 11.3035
69.599; 87.608; 88.14
773.08Crujeiras, Pablo; Vázquez-Carballo, Irene; Sousa-Pedrares, Antonio
Application of the aza-Wittig reaction for the synthesis of carboranyl Schiff bases, benzothiazoles and benzoselenazolines.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 2819-2832
1573677 CIFC11 H15 B F2 I N O6C 1 2/c 151.208; 7.1184; 31.56
90; 126.597; 90
9236.1Wu, Hengbo; Luo, Ruitong; Peng, Jingjing; Han, Zijian; Zhang, Renjie; Xu, Zhijian; Zhu, Weiliang; Liu, Hong; Li, Chunpu
B(MIDA)-directed site-selective intermolecular halofluoroalkylation of alkenes: synthesis of diversely functionalized building blocks.
Chemical science, 2025, 16, 2710-2717
1573678 CIFCu10 S13 Te4I -4 3 m10.2609; 10.2609; 10.2609
90; 90; 90
1080.33Zhang, Bo; Zhou, Sheng-Hua; Li, Bing-Xuan; Wu, Xin-Tao; Lin, Hua; Zhu, Qi-Long
Exploring new horizons in mid-to-far infrared nonlinear optical crystals: the significant potential of trigonal pyramidal [TeS<sub>3</sub>]<sup>2-</sup> functional units.
Chemical science, 2025, 16, 3218-3227
1573679 CIF
Paper
C19.5 H21.5 N4.5 O1.5P -19.1009; 11.0914; 18.5952
81.381; 83.221; 86.838
1841.52El Moutaouakil Ala Allah, Abderrazzak; M. Kariuki, Benson; Guerrab, Walid; Alsubari, Abdulsalam; A. Said, Musa; Mague, Joel T.; Ramli, Youssef
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 109-113
1573680 CIF
Paper
C2 H7 Ce O8 SP -16.8424; 6.9984; 8.7888
110.448; 90.099; 107.307
373.851Ruser, Niklas; Näther, Christian; Stock, Norbert
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 104-108
1573681 CIF
Paper
C18 H15 I3 SP 1 21/n 112.8971; 11.9414; 13.0718
90; 92.374; 90
2011.45Artis, Rylan; Callaway, Waylan; Heyward, Elizabeth; Reyes, Naomi; Roberts, Gavin; Van Ostenbridge, Kaitlyn; Padgett, Clifford W.; Lynch, Will E.
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 114-119
1573682 CIF
Paper
C18 H15 Cl O4 SP 1 21 19.1289; 19.1565; 9.3314
90; 90.611; 90
1631.76Artis, Rylan; Callaway, Waylan; Heyward, Elizabeth; Reyes, Naomi; Roberts, Gavin; Van Ostenbridge, Kaitlyn; Padgett, Clifford W.; Lynch, Will E.
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 114-119
1573683 CIF
Paper
C18 H15 F6 P SP 1 21/n 18.4524; 18.1483; 11.4344
90; 98.251; 90
1735.84Artis, Rylan; Callaway, Waylan; Heyward, Elizabeth; Reyes, Naomi; Roberts, Gavin; Van Ostenbridge, Kaitlyn; Padgett, Clifford W.; Lynch, Will E.
Acta Crystallographica, Section E: Crystallographic Communications, 2025, 81, 114-119
1573684 CIF
Paper
C13 H18 O9P 1 21 18.1174; 9.5597; 10.258
90; 109.734; 90
749.27Culver, Shawn; Rhoad, Jonathan S.
IUCrData, 2025, 10, x250016
1573685 CIF
Paper
C13 H15.5 N3 O3.25 SP -112.47742; 15.1037; 15.7031
75.3037; 72.5571; 71.7565
2639.28Uran, Erik; Cotman, Andrej Emanuel; Lozinšek, Matic
IUCrData, 2025, 10, x241249
1573686 CIFC126 H160 K O6C m c 2126.623; 12.2818; 36.081
90; 90; 90
11797.7Zhu, Yikun; Borstelmann, Jan; Neiss, Christian; Wei, Zheng; Görling, Andreas; Kivala, Milan; Petrukhina, Marina A.
Stepwise reduction of an asymmetric π-expanded pyracylene towards the crystalline radical trianion.
Chemical science, 2025, 16, 3211-3217
1573687 CIFC186 H270 N6 O25.5 Rb3P -114.192; 23.883; 28.136
88.137; 80.21; 77.124
9161Zhu, Yikun; Borstelmann, Jan; Neiss, Christian; Wei, Zheng; Görling, Andreas; Kivala, Milan; Petrukhina, Marina A.
Stepwise reduction of an asymmetric π-expanded pyracylene towards the crystalline radical trianion.
Chemical science, 2025, 16, 3211-3217
1573688 CIFC136 H170 O14.5 Rb2I 41/a :227.4995; 27.4995; 70.8136
90; 90; 90
53550.8Zhu, Yikun; Borstelmann, Jan; Neiss, Christian; Wei, Zheng; Görling, Andreas; Kivala, Milan; Petrukhina, Marina A.
Stepwise reduction of an asymmetric π-expanded pyracylene towards the crystalline radical trianion.
Chemical science, 2025, 16, 3211-3217
1573689 CIFC30 H29 B N2 O3P 1 21/n 111.04999; 23.491; 22.4123
90; 100.772; 90
5715.2Qin, Hao-Ni; Jiang, Hao-Wen; Zhao, Yi; Qurban, Saira; Wang, Ke-Chun; Xu, Peng-Fei
Photocatalytic [3 + 2]-annulation <i>via</i> sodium tetraarylborate: a fundamental approach for synthesizing 1,4,2-diazaborole analogs.
Chemical science, 2025, 16, 2837-2842
1573690 CIFC21 H34 I N O5 SiP 21 21 218.9672; 14.2728; 19.4271
90; 90; 90
2486.42Seo, Seung Mo; Kim, Dongwook; Kim, Taewan; Han, Sunkyu
Total synthesis of (-)-flueggenine A and (-)-15'-<i>epi</i>-flueggenine D.
Chemical science, 2025, 16, 1216-1221
1573691 CIFC24 H26 N2 O4P 1 21 111.95; 6.4623; 13.674
90; 103.465; 90
1026.9Seo, Seung Mo; Kim, Dongwook; Kim, Taewan; Han, Sunkyu
Total synthesis of (-)-flueggenine A and (-)-15'-<i>epi</i>-flueggenine D.
Chemical science, 2025, 16, 1216-1221
1573692 CIFC24 H45 N O5 Si2P 1 21 16.8112; 9.0531; 23.2935
90; 95.8682; 90
1428.81Seo, Seung Mo; Kim, Dongwook; Kim, Taewan; Han, Sunkyu
Total synthesis of (-)-flueggenine A and (-)-15'-<i>epi</i>-flueggenine D.
Chemical science, 2025, 16, 1216-1221
1573693 CIFC23 H35 I N O5 SiP 21 21 28.5047; 46.069; 6.8117
90; 90; 90
2668.8Seo, Seung Mo; Kim, Dongwook; Kim, Taewan; Han, Sunkyu
Total synthesis of (-)-flueggenine A and (-)-15'-<i>epi</i>-flueggenine D.
Chemical science, 2025, 16, 1216-1221
1573694 CIFC36 H50 N2 O12P 1 21 117.7153; 5.8663; 18.0482
90; 99.613; 90
1849.3Seo, Seung Mo; Kim, Dongwook; Kim, Taewan; Han, Sunkyu
Total synthesis of (-)-flueggenine A and (-)-15'-<i>epi</i>-flueggenine D.
Chemical science, 2025, 16, 1216-1221
1573695 CIFC7 H9 Br2 N7 O ZnI -4 3 m16.77164; 16.77164; 16.77164
90; 90; 90
4717.66Liang, Zi-Jun; Dong, Fang-Di; Ye, Le; Zheng, Kai; Hu, Ding-Yi; Feng, Xi; Su, Wen-Yu; Wang, Zhi-Shuo; Zhou, Mu-Yang; Fang, Zi-Luo; Zhou, Dong-Dong; Zhang, Jie-Peng; Chen, Xiao-Ming
Introducing halogen-bonded gates into zeolitic frameworks for efficient benzene/cyclohexene/cyclohexane separation.
Chemical science, 2025, 16, 3307-3312
1573696 CIFC10.96 H8.96 Br2 N6 ZnI -4 3 m16.7719; 16.7719; 16.7719
90; 90; 90
4717.88Liang, Zi-Jun; Dong, Fang-Di; Ye, Le; Zheng, Kai; Hu, Ding-Yi; Feng, Xi; Su, Wen-Yu; Wang, Zhi-Shuo; Zhou, Mu-Yang; Fang, Zi-Luo; Zhou, Dong-Dong; Zhang, Jie-Peng; Chen, Xiao-Ming
Introducing halogen-bonded gates into zeolitic frameworks for efficient benzene/cyclohexene/cyclohexane separation.
Chemical science, 2025, 16, 3307-3312
1573697 CIFO7 S Te TiP 1 21 14.9516; 7.6029; 7.1865
90; 105.062; 90
261.25Li, Zhenhua; Liang, Zhengli; Wan, Jiahao; Liu, Lehui; Wu, Chunxiang; Wang, Ping; Jiang, Xingxing; Lin, Zheshuai; Liu, Hongming
Different p-block elements induce C<sub>3</sub>[111] octahedral distortion in titanium to generate an intense nonlinear effect.
Chemical science, 2025, 16, 3329-3335
1573698 CIFC51 H66 Mg N2 PP -110.5976; 19.2049; 23.4676
76.93; 89.321; 78.848
4562.1Zhang, Rongping; Cai, Yanping; Xu, Xin
Synthesis and characterization of heterotrimetallic Mg-Ni-Mg complexes with amidinato ligands.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3437-3443
1573699 CIFC120 H140 Mg2 N4 Ni P2P 1 2/c 118.2558; 15.2714; 18.9886
90; 104.001; 90
5136.6Zhang, Rongping; Cai, Yanping; Xu, Xin
Synthesis and characterization of heterotrimetallic Mg-Ni-Mg complexes with amidinato ligands.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3437-3443
1573700 CIFC50 H88 Mg2 N4 Ni P2P -19.0128; 10.6971; 15.9172
107.928; 93.399; 105.329
1391.49Zhang, Rongping; Cai, Yanping; Xu, Xin
Synthesis and characterization of heterotrimetallic Mg-Ni-Mg complexes with amidinato ligands.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3437-3443
1573701 CIFC58 H104 Mg2 N4 Ni O2 P2C 1 2/c 119.0876; 11.5755; 28.1191
90; 95.476; 90
6184.5Zhang, Rongping; Cai, Yanping; Xu, Xin
Synthesis and characterization of heterotrimetallic Mg-Ni-Mg complexes with amidinato ligands.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3437-3443
1573702 CIFC96 H113 Mg2 N4 Ni O2 P2P -115.0759; 18.5965; 20.2198
110.227; 101.922; 108.78
4702.6Zhang, Rongping; Cai, Yanping; Xu, Xin
Synthesis and characterization of heterotrimetallic Mg-Ni-Mg complexes with amidinato ligands.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 3437-3443
1573703 CIFC72 H54 F3 N5 O4 S2P -111.823; 13.6657; 23.0648
100.582; 94.663; 108.17
3442.01Liu, Junxiang; Wang, Kangmin; Wan, Liqiu; Yang, Xianhui; Li, Bijin
Ruthenium-catalyzed C-H bond activation and annulation of phenothiazine-3-carbaldehydes: facile access to dual-emission materials.
Chemical science, 2025, 16, 3107-3113
1573704 CIFC21 H20 F3 N ZrP 1 21/n 18.1766; 15.5546; 14.6671
90; 99.429; 90
1840.21Bonfante, Sara; Tanner, Theo F. N.; Lorber, Christian; Lynam, Jason M.; Simonneau, Antoine; Slattery, John M.
Zirconium-mediated carbon-fluorine bond functionalisation through cyclohexyne "umpolung".
Chemical science, 2025, 16, 3552-3559
1573705 CIFC5 H8 O S2P -18.2387; 8.2964; 10.4688
93.346; 92.138; 109.112
673.76Liu, Long-Hai; Wang, Si-Qi; Fan, Hua-Zhong; Cao, Qing; Cai, Zhongzheng; Zhu, Jian-Bo
Chemically recyclable poly(thioether-thioester)s via ring-opening polymerization of seven-membered thiolactones
Polymer Chemistry, 2025, 16, 972-978
1573706 CIFC15 H15 N3 O SP 1 21/n 19.889; 23.89; 12.335
90; 98.52; 90
2882Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573707 CIFC14 H13 N3 SP -15.9879; 10.235; 11.312
66.744; 82.452; 86.562
631.4Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573708 CIFC14 H11 Cl2 N3 SP -17.866; 8.231; 11.963
92.336; 96.812; 111.933
710.4Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573709 CIFC14 H14 N4 O SP 21 21 216.643; 7.435; 28.49
90; 90; 90
1407Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573710 CIFC12 H11 N3 S2P -15.689; 10.012; 11.393
71.163; 82.543; 87.953
609Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573711 CIFC12 H11 N3 O SP -15.823; 9.744; 11.011
70.013; 83.399; 88.167
583.2Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573712 CIFC14 H8 F5 N3 SC 1 2/c 128.98; 6.951; 14.974
90; 110.329; 90
2828.5Sentürk, Bengi; Butschke, Burkhard; Eisenreich, Fabian
Thiosemicarbazones as versatile photoswitches with light-controllable supramolecular activity.
Chemical science, 2025, 16, 3130-3140
1573713 CIFC27 H19 F3 O2 SiP -18.589; 9.902; 14.679
106.882; 94.204; 111.756
1086.3Matsuo, Tomotoki; Sano, Masaki; Sumida, Yuto; Ohmiya, Hirohisa
Organic photoredox-catalyzed unimolecular PCET of benzylic alcohols.
Chemical science, 2025, 16, 3150-3156
1573714 CIFC24 H42 N12 O58 Si W12P -110.8473; 12.4152; 13.176
99.7051; 91.9863; 103.746
1693.76Greijer, Björn; Nefedova, Alexandra; Agback, Tatiana; Agback, Peter; Kisand, Vambola; Rausalu, Kai; Vanetsev, Alexander; Seisenbaeva, Gulaim A.; Ivask, Angela; Kessler, Vadim G.
Molecular mechanisms behind the anti corona virus activity of small metal oxide nanoparticles.
Nanoscale, 2025, 17, 3728-3738
1573715 CIFC24 H42 N6 O56 S3 Si W12P 1 21/c 132.191; 14.8183; 15.3532
90; 91.018; 90
7322.6Greijer, Björn; Nefedova, Alexandra; Agback, Tatiana; Agback, Peter; Kisand, Vambola; Rausalu, Kai; Vanetsev, Alexander; Seisenbaeva, Gulaim A.; Ivask, Angela; Kessler, Vadim G.
Molecular mechanisms behind the anti corona virus activity of small metal oxide nanoparticles.
Nanoscale, 2025, 17, 3728-3738
1573716 CIFC10 H11 Br O SeP 1 21/n 17.767; 10.906; 12.122
90; 90.8; 90
1026.7Telo, João P; Veiros, Luis F.; André, Vânia; da Silva, João Ferreira; Justino, Gonçalo C; Antunes, Alexandra M. M.
Monoterpenoid selenophenes derived from (-)-carvone with GPx-like activity.
Organic & biomolecular chemistry, 2025, 23, 2153-2161
1573717 CIFC10 H12 O SeP 1 21/n 17.3; 10.358; 12.964
90; 91.02; 90
980.1Telo, João P; Veiros, Luis F.; André, Vânia; da Silva, João Ferreira; Justino, Gonçalo C; Antunes, Alexandra M. M.
Monoterpenoid selenophenes derived from (-)-carvone with GPx-like activity.
Organic & biomolecular chemistry, 2025, 23, 2153-2161
1573718 CIFC20 H22 O2 Se2P -110.0831; 10.4303; 10.7237
71.641; 70.303; 63.501
932Telo, João P; Veiros, Luis F.; André, Vânia; da Silva, João Ferreira; Justino, Gonçalo C; Antunes, Alexandra M. M.
Monoterpenoid selenophenes derived from (-)-carvone with GPx-like activity.
Organic & biomolecular chemistry, 2025, 23, 2153-2161
1573719 CIFNi2 O7 P2P 1 21/c 1 (2*a+c,b,c)13.146361; 8.262589; 8.977835
90; 104.96; 90
942.147Patil, Satyajeet S.; Patil, Akhilesh P.; Redekar, Rahul S.; Pawar, Shweta M.; Tarwal, Nilesh L.; Patil, Pramod S.
Study of 2D layered nickel pyrophosphate using 3D Bode mapping and stability forecasting for supercapacitors
Colloids and Surfaces A: Physicochemical and Engineering, 2025, 707, 135829
1573721 CIFC58 H52 Co F24 N6 O P4 Re2P n n a22.3235; 15.8553; 17.5716
90; 90; 90
6219.39Csucker, Joshua; Grundmann, Nora Sophie; Blacque, Olivier; Spingler, Bernhard; Alberto, Roger
The role of [Re(η6-arene)2]+ substituents in electro- and photocatalytic water reduction with [Co(terpy)2]3+ catalysts
Catalysis Science & Technology, 2025, 15, 1627-1633
1573722 CIFC46 H38 Co F18 N10 P3C 1 2/c 114.7621; 16.5626; 20.9736
90; 101.077; 90
5032.48Csucker, Joshua; Grundmann, Nora Sophie; Blacque, Olivier; Spingler, Bernhard; Alberto, Roger
The role of [Re(η6-arene)2]+ substituents in electro- and photocatalytic water reduction with [Co(terpy)2]3+ catalysts
Catalysis Science & Technology, 2025, 15, 1627-1633
1573723 CIFC54 H44 Co F30 N8 P5 Re2P 1 21/n 112.1888; 21.4924; 24.0881
90; 104.142; 90
6119Csucker, Joshua; Grundmann, Nora Sophie; Blacque, Olivier; Spingler, Bernhard; Alberto, Roger
The role of [Re(η6-arene)2]+ substituents in electro- and photocatalytic water reduction with [Co(terpy)2]3+ catalysts
Catalysis Science & Technology, 2025, 15, 1627-1633
1573724 CIFC54 H44 Co F24 N8 P4 Re2P 1 21/c 19.24728; 27.2919; 24.3585
90; 95.1273; 90
6122.9Csucker, Joshua; Grundmann, Nora Sophie; Blacque, Olivier; Spingler, Bernhard; Alberto, Roger
The role of [Re(η6-arene)2]+ substituents in electro- and photocatalytic water reduction with [Co(terpy)2]3+ catalysts
Catalysis Science & Technology, 2025, 15, 1627-1633
1573725 CIFC29 H17 NP 1 21/n 110.4701; 8.8984; 19.622
90; 99.531; 90
1802.89Maekawa, Takehisa; Itami, Kenichiro
Rapid access to functionalized nanographenes through a palladium-catalyzed multi-annulation sequence.
Chemical science, 2025, 16, 3092-3098
1573726 CIFC16 H13 N3 O3P 1 21/n 18.029; 12.7021; 13.0187
90; 93.446; 90
1325.31Korica, Milenko; Komar, Mario; Molnar, Maja; Nemec, Vinko; Cinčić, Dominik; Balić, Tomislav
Structural and thermal properties of 3-substituted quinazolinone Schiff base conjugates
New Journal of Chemistry, 2025, 49, 3067-3077
1573727 CIFC16 H13 N3 OP 1 21/c 111.4544; 15.8163; 7.4627
90; 103.569; 90
1314.25Korica, Milenko; Komar, Mario; Molnar, Maja; Nemec, Vinko; Cinčić, Dominik; Balić, Tomislav
Structural and thermal properties of 3-substituted quinazolinone Schiff base conjugates
New Journal of Chemistry, 2025, 49, 3067-3077
1573728 CIFC16 H13 N3 O3P 1 21/n 13.9386; 29.5669; 11.7999
90; 96.592; 90
1365.04Korica, Milenko; Komar, Mario; Molnar, Maja; Nemec, Vinko; Cinčić, Dominik; Balić, Tomislav
Structural and thermal properties of 3-substituted quinazolinone Schiff base conjugates
New Journal of Chemistry, 2025, 49, 3067-3077
1573729 CIFC16 H12 Cl N3 OP -17.9879; 13.1032; 14.7678
71.525; 76.046; 81.964
1419.4Korica, Milenko; Komar, Mario; Molnar, Maja; Nemec, Vinko; Cinčić, Dominik; Balić, Tomislav
Structural and thermal properties of 3-substituted quinazolinone Schiff base conjugates
New Journal of Chemistry, 2025, 49, 3067-3077
1573730 CIFC17 H17 N3 O4P 1 21/n 18.7501; 8.951; 21.2255
90; 97.446; 90
1648.4Korica, Milenko; Komar, Mario; Molnar, Maja; Nemec, Vinko; Cinčić, Dominik; Balić, Tomislav
Structural and thermal properties of 3-substituted quinazolinone Schiff base conjugates
New Journal of Chemistry, 2025, 49, 3067-3077
1573731 CIFC24 H56 Br4 N2 ZnI 1 2/a 115.0869; 14.2481; 31.3091
90; 96.596; 90
6685.6Yang, Yongqi; Ke, Bao; Yang, Chengzhi; Xue, Yang; Huang, Kaihuang; Lu, Xintong; Zou, Bingsuo
Multifunctional applications enabled by tunable multi-emission and ultra-broadband VIS-NIR luminescence <i>via</i> energy transfer in Sn<sup>2+</sup>/Mn<sup>2+</sup>-doped lead-free Zn-based metal halides.
Materials horizons, 2025, 12, 2564-2576
1573732 CIFC79 H80 B5 F24 N5 O2 SnP -115.245; 17.2704; 17.6243
92.495; 102.397; 112.807
4136.1Niu, Dechuang; Kostenko, Arseni; Kelly, John A.; Sarkar, Debotra; Xu, Huihui; Inoue, Shigeyoshi
CO<sub>2</sub> hydrosilylation catalyzed by an N-heterocyclic carbene (NHC)-stabilized stannyliumylidene.
Chemical science, 2025, 16, 4014-4022
1573733 CIFC70.01 H61 B F24 N4 SnP -113.4232; 17.0569; 18.5469
102.535; 101.839; 109.969
3711.1Niu, Dechuang; Kostenko, Arseni; Kelly, John A.; Sarkar, Debotra; Xu, Huihui; Inoue, Shigeyoshi
CO<sub>2</sub> hydrosilylation catalyzed by an N-heterocyclic carbene (NHC)-stabilized stannyliumylidene.
Chemical science, 2025, 16, 4014-4022
1573734 CIFC72 H61 B F24 N4 O4 SnP -110.4739; 16.089; 23.3384
109.831; 92.107; 102.86
3579.7Niu, Dechuang; Kostenko, Arseni; Kelly, John A.; Sarkar, Debotra; Xu, Huihui; Inoue, Shigeyoshi
CO<sub>2</sub> hydrosilylation catalyzed by an N-heterocyclic carbene (NHC)-stabilized stannyliumylidene.
Chemical science, 2025, 16, 4014-4022
1573735 CIFC70 H86 Cl2 Cu6 F9 N7 O7 S4P n m a36.1356; 16.4719; 28.0985
90; 90; 90
16724.8Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573736 CIFC124 H178.5 Cu6 N18.5 O10.5 S4P a -330.937; 30.937; 30.937
90; 90; 90
29609.7Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573737 CIFC82 H99 Cu7 F9 N15 O15 S4C 1 2/c 140.186; 17.9336; 43.303
90; 108.171; 90
29651Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573738 CIFC3.21 H3.97 Cl0.49 Cu0.48 F0.57 N0.19 O0.38 S0.29P -113.4577; 13.9427; 13.9994
82.041; 82.058; 75.543
2504.4Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573739 CIFC42.5 H48 Cl5 Cu6 F3 N4 O2 S8I m m a24.6205; 17.0084; 22.4482
90; 90; 90
9400.3Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573740 CIFC27 H37 Cl2 Cu5 F6 N4 O4 S3P 1 21/c 113.9234; 11.9576; 23.9446
90; 91.901; 90
3984.4Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573741 CIFC2.8 H3.28 Cl0.16 Cu0.4 F0.48 N0.16 O0.32 S0.4P 1 21/c 120.5359; 15.906; 18.1932
90; 102.802; 90
5795Das, Saikat; Sakai, Jin; Nakatani, Riki; Kondo, Ayumu; Tomioka, Rina; Das, Subhabrata; Takahashi, Shuntaro; Kawawaki, Tokuhisa; Biswas, Sourav; Negishi, Yuichi
Tunable structural rearrangement in Cu cluster assemblies through linker and solvent alterations.
Chemical science, 2025, 16, 2600-2608
1573742 CIFC50 H42 B2 N2 O2C 1 2/c 117.9182; 19.9055; 13.5411
90; 127.513; 90
3831Xue, Zhuixing; Xiao, Zhengqi; Zou, Yang; Chen, Zhanxiang; Liu, Jiahui; Huang, Zhongyan; Yang, Chuluo
A mesityl-functionalized double-boron-nitrogen-oxygen-embedded multi-resonance framework achieves anti-quenching narrowband deep-blue electroluminescence with EQE over 30% and CIE <sub><i>y</i></sub> of 0.046.
Chemical science, 2025, 16, 3655-3661
1573743 CIFC68 H62 B2 N2 O2P -116.4777; 19.3715; 19.7104
82.656; 89.376; 77.021
6079.5Xue, Zhuixing; Xiao, Zhengqi; Zou, Yang; Chen, Zhanxiang; Liu, Jiahui; Huang, Zhongyan; Yang, Chuluo
A mesityl-functionalized double-boron-nitrogen-oxygen-embedded multi-resonance framework achieves anti-quenching narrowband deep-blue electroluminescence with EQE over 30% and CIE <sub><i>y</i></sub> of 0.046.
Chemical science, 2025, 16, 3655-3661
1573744 CIFC312 H372 N36 O42 S24 Ti12P -120.926; 20.984; 21.932
64.82; 76.693; 77.002
8393Meng, Ru-Xin; Zhao, Lan-Cheng; Luo, Li-Pan; Tian, Yi-Qi; Shao, Yong-Liang; Tang, Qing; Wang, Likai; Yan, Jun; Liu, Chao
Atomic-level engineering of single Ag1+ site distribution on titanium–oxo cluster surfaces to boost CO2 electroreduction
Chemical Science, 2025, 16, 6845-6852
1573745 CIFC82 H90.68 Ag2 N O11 S8 Ti2I 1 2/m 116.0181; 18.7809; 30.2892
90; 92.8776; 90
9100.5Meng, Ru-Xin; Zhao, Lan-Cheng; Luo, Li-Pan; Tian, Yi-Qi; Shao, Yong-Liang; Tang, Qing; Wang, Likai; Yan, Jun; Liu, Chao
Atomic-level engineering of single Ag1+ site distribution on titanium–oxo cluster surfaces to boost CO2 electroreduction
Chemical Science, 2025, 16, 6845-6852
1573746 CIFC265.64 H306.46 Ag4.51 N12.82 O42.76 S24 Ti12P 1 21/n 121.329; 34.611; 23.413
90; 116.73; 90
15437Meng, Ru-Xin; Zhao, Lan-Cheng; Luo, Li-Pan; Tian, Yi-Qi; Shao, Yong-Liang; Tang, Qing; Wang, Likai; Yan, Jun; Liu, Chao
Atomic-level engineering of single Ag1+ site distribution on titanium–oxo cluster surfaces to boost CO2 electroreduction
Chemical Science, 2025, 16, 6845-6852
1573747 CIFC200 H221.72 Na O36 S20 Ti8P 1 21/c 133.1669; 21.7916; 35.921
90; 91.759; 90
25950Meng, Ru-Xin; Zhao, Lan-Cheng; Luo, Li-Pan; Tian, Yi-Qi; Shao, Yong-Liang; Tang, Qing; Wang, Likai; Yan, Jun; Liu, Chao
Atomic-level engineering of single Ag1+ site distribution on titanium–oxo cluster surfaces to boost CO2 electroreduction
Chemical Science, 2025, 16, 6845-6852
1573748 CIFC2.95 H5.9 In0.1 N0.29 O0.38P -111.919; 12.4961; 13.0349
61.504; 89.234; 89.801
1706.07Riu, Martin-Louis Y; Shan, Jing-Ran; Houk, K. N.; Nava, Matthew
Metal-ligand cooperativity enables zero-valent metal transfer.
Chemical science, 2025, 16, 3888-3894
1573749 CIFC31 H62 Al N3 O4P -111.7623; 12.4407; 12.9344
118.532; 91.442; 90.128
1662.09Riu, Martin-Louis Y; Shan, Jing-Ran; Houk, K. N.; Nava, Matthew
Metal-ligand cooperativity enables zero-valent metal transfer.
Chemical science, 2025, 16, 3888-3894
1573750 CIFC31 H62 Ga N3 O4P -111.7627; 12.4302; 12.9451
118.425; 91.211; 90.139
1664.01Riu, Martin-Louis Y; Shan, Jing-Ran; Houk, K. N.; Nava, Matthew
Metal-ligand cooperativity enables zero-valent metal transfer.
Chemical science, 2025, 16, 3888-3894
1573751 CIFC18 H36 In2 N2 O2C m c e12.4969; 9.4605; 18.0744
90; 90; 90
2136.9Riu, Martin-Louis Y; Shan, Jing-Ran; Houk, K. N.; Nava, Matthew
Metal-ligand cooperativity enables zero-valent metal transfer.
Chemical science, 2025, 16, 3888-3894
1573752 CIFC27 H56 Ga N3 O3P 1 21/n 112.0657; 12.8632; 19.2485
90; 94.979; 90
2976.2Riu, Martin-Louis Y; Shan, Jing-Ran; Houk, K. N.; Nava, Matthew
Metal-ligand cooperativity enables zero-valent metal transfer.
Chemical science, 2025, 16, 3888-3894
1573753 CIFC3 H5 Ag O2 SP 1 21/c 113.61196; 6.63372; 5.94002
90; 99.6952; 90
528.711Zhang, Shengrui; Yu, Zhongqi; Demessence, Aude; Guillou, Nathalie; Xu, Shujue; Liu, Han; Fu, Yuru; Zhang, Jingpei; Li, Minjie
Self-assembly processes of 2D Au(I)-S(CH<sub>2</sub>)<sub>2</sub>COOH lamellae.
Nanoscale, 2025, 17, 5270-5279
1573754 CIFC20 H13 N O2 SP -17.8169; 8.3525; 12.4587
81.958; 82.535; 78.805
785.68Patra, Debabrata; Mondal, Mohabul Alam; Saha, Amit
Disulfide-mediated ruthenium-catalyzed direct C-H thiolation in benzoxazinone systems: selective synthesis of <i>ortho</i>-thiolated 2-arylbenzoxazinones.
Organic & biomolecular chemistry, 2025, 23, 2229-2234
1573755 CIFC27 H31 N O2P 1 21/n 112.5383; 9.5231; 18.69
90; 97.104; 90
2214.52Meng, Huan; Jia, Jun-Song; Yang, Peng-Fei; Li, Yu-Long; Yu, Qiong; Shu, Wei
Ni-catalyzed regioselective and site-divergent reductive arylalkylations of allylic amines.
Chemical science, 2025, 16, 4442-4449
1573756 CIFC27 H28 N2 OC 1 c 113.8063; 17.9373; 9.9554
90; 113.319; 90
2264.04Meng, Huan; Jia, Jun-Song; Yang, Peng-Fei; Li, Yu-Long; Yu, Qiong; Shu, Wei
Ni-catalyzed regioselective and site-divergent reductive arylalkylations of allylic amines.
Chemical science, 2025, 16, 4442-4449
1573757 CIFC3 H10 I3 N O PbP 21 21 214.5931; 11.6051; 22.0202
90; 90; 90
1173.75Li, Hongxu; Cao, Rui; Tao, Min; Jiang, Jiawei; Xiao, Yin
Chiral perovskites with a unique 1D chain structure: impact of chiral ligand geometry on local inversion asymmetry and chiral-induced spin selectivity.
Chemical science, 2025, 16, 4057-4065
1573758 CIFC3 H10 I3 N O PbP 21 21 214.5899; 11.5987; 22.0076
90; 90; 90
1171.62Li, Hongxu; Cao, Rui; Tao, Min; Jiang, Jiawei; Xiao, Yin
Chiral perovskites with a unique 1D chain structure: impact of chiral ligand geometry on local inversion asymmetry and chiral-induced spin selectivity.
Chemical science, 2025, 16, 4057-4065
1573759 CIFC21 H22 N2 O3 SP 1 21/c 19.0752; 20.3258; 11.2289
90; 111.107; 90
1932.33Lai, Ze-Min; Xie, Ying; Huang, Le-Le; Guo, Jing; Lu, Gui
Catalytic enantioselective synthesis of α-C chiral sulfones enabled by merging photoactive electron donor-acceptor complexes with nickel catalysis.
Chemical science, 2025, 16, 4352-4359
1573760 CIFC24 H25 I N2 OP -18.6576; 11.4823; 11.8769
70.882; 79.329; 82.137
1092.57Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573761 CIFC28 H28 N2 O2P 1 21/c 18.3156; 15.8552; 17.6204
90; 101.442; 90
2277Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573762 CIFC30 H30 N2 OP 1 21/c 111.85289; 23.3855; 8.96547
90; 104.164; 90
2409.55Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573763 CIFC29 H36 N2 OP 1 21 18.7877; 13.2804; 10.4903
90; 93.628; 90
1221.81Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573764 CIFC25 H28 N2 OP -19.0247; 13.2322; 18.6064
100.728; 100.909; 105.883
2030.78Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573765 CIFC30 H30 N2 OP -19.0232; 10.8445; 12.5529
95.795; 99.084; 96.98
1194.85Wootton, Jack M.; Roper, Natalie J.; Morris, Catrin E.; Maguire, Victoria E.; Duff, Lee C.; Waddell, Paul G.; Whitwood, Adrian C.; Gammons, Richard J.; Miah, Afjal H.; Lynam, Jason M.; Armstrong, Roly J.; Unsworth, William P.
Stereoselective synthesis of atropisomeric amides enabled by intramolecular acyl transfer.
Chemical science, 2025, 16, 3938-3945
1573766 CIFC20 H24 B10 OP -110.5221; 12.1599; 18.0206
73.817; 78.768; 78.192
2144.08Wang, 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
1573767 CIFC26 H24 B10P -110.8412; 19.4475; 23.3896
75.392; 80.868; 87.318
4711.3Wang, 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
1573768 CIFC14 H18 B10P 1 21/c 19.9506; 13.287; 12.6971
90; 101.393; 90
1645.65Wang, 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
1573769 CIFC13 H18 B10 OP 1 21/n 17.1385; 22.1234; 10.2306
90; 95.391; 90
1608.6Wang, 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
1573770 CIFC14 H18 B10P 1 21/c 111.0634; 14.0548; 20.6273
90; 92.773; 90
3203.66Wang, 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
1573771 CIFC19 H20 B10C 1 2/c 124.0114; 8.3879; 19.3844
90; 99.3; 90
3852.8Wang, 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
1573772 CIFC18 H28 B10 SiP 1 21/n 110.7343; 15.469; 13.0999
90; 94.563; 90
2168.33Wang, 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
1573773 CIFC21 H24 B10P b c a17.6926; 7.5803; 31.0434
90; 90; 90
4163.39Wang, 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
1573774 CIFC26 H28 B10 OP 21 21 2110.1324; 15.565; 16.148
90; 90; 90
2546.71Wang, 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
1573775 CIFC22 H20 B10P 1 21 17.4914; 17.9215; 16.097
90; 90.673; 90
2160.99Wang, 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
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
1573778 CIFC14 H34 N2 O10P -18.0865; 11.5014; 12.6813
63.784; 86.101; 85.115
1053.66Chandran, Aruna; Dominique, Nathaniel; Kaur, Gurkiran; Clark, Vincent; Nalaoh, Phattananawee; Aloisio, Mark D.; Ekowo, Lilian Chinenye; Jensen , Isabel M; Crudden, Cathleen; Arroyo-Currás, Netzahualcóyotl; Jenkins, David; Camden, Jon
Forming N-Heterocyclic Carbene Monolayers: Not All Deposition Methods are the Same
Nanoscale, 2025
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
1573789 CIFC124 H149 Au6 N20 P4 Pd3 S10P -116.7465; 17.5624; 26.3391
99.096; 90.215; 91.009
7647.8Fu, Ziwei; Li, Chen; Tian, Ye; Alam, Fakhari; Hu, Daqiao; Shen, Honglei; Kang, Xi; Zhu, Manzhou
Heteroatom number-dependent cluster frameworks in structurally comparable Pd-Au nanoclusters.
Nanoscale, 2025, 17, 4494-4501
1573790 CIFC254 H309.49 Au12 N40 P8 Pd5 S20P 1 21/n 117.13; 53.449; 17.415
90; 90.68; 90
15944Fu, Ziwei; Li, Chen; Tian, Ye; Alam, Fakhari; Hu, Daqiao; Shen, Honglei; Kang, Xi; Zhu, Manzhou
Heteroatom number-dependent cluster frameworks in structurally comparable Pd-Au nanoclusters.
Nanoscale, 2025, 17, 4494-4501
1573791 CIFC30 H25 N O2 SiP 1 21/n 18; 21.9129; 14.2074
90; 105.405; 90
2401.12Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin
Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence.
Chemical communications (Cambridge, England), 2025, 61, 4662-4665
1573792 CIFC54 H36 B Cl2 F4 N OP n a 2115.799; 10.5487; 24.3174
90; 90; 90
4052.7Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin
Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence.
Chemical communications (Cambridge, England), 2025, 61, 4662-4665
1573793 CIFC29 H23 N O SiP 1 21/c 17.7962; 22.1366; 13.7791
90; 105.129; 90
2295.6Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin
Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence.
Chemical communications (Cambridge, England), 2025, 61, 4662-4665
1573794 CIFC80 H55.93 B2 Br0.07 N2 O0P 1 21/c 125.5585; 9.9428; 24.0807
90; 91.408; 90
6117.6Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin
Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence.
Chemical communications (Cambridge, England), 2025, 61, 4662-4665
1573795 CIFC44.66667 H33 N O2 PtP -112.7645; 18.0822; 22.7774
89.964; 81.068; 85.594
5177.8Cadart, Timothée; Feriancová, Lucia; Henke, Petr; Gyepes, Robert; Císařová, Ivana; Kalíková, Květa; Kotora, Martin
Synthesis of highly fluorescent helical quinolizinium salts by a Rh-catalyzed cyclotrimerization/C-H activation sequence.
Chemical communications (Cambridge, England), 2025, 61, 4662-4665
1573796 CIFC21 H21 N O2P b c a9.3805; 17.9125; 20.6371
90; 90; 90
3467.61Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min
One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones.
Chemical communications (Cambridge, England), 2025, 61, 3720-3723
1573797 CIFC18 H16 Cl N O2P 1 21 19.7449; 12.6197; 12.8104
90; 91.761; 90
1574.65Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min
One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones.
Chemical communications (Cambridge, England), 2025, 61, 3720-3723
1573798 CIFC21 H19 F2 N O2I 1 a 19.7705; 13.1781; 14.487
90; 103.85; 90
1811.07Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min
One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones.
Chemical communications (Cambridge, England), 2025, 61, 3720-3723
1573799 CIFC18 H16 F N O2P 1 21/n 18.35635; 20.16774; 9.47069
90; 111.53; 90
1484.72Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min
One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones.
Chemical communications (Cambridge, England), 2025, 61, 3720-3723
1573800 CIFC21 H19 Br2 N O2I 1 2/a 116.9874; 9.81932; 24.6758
90; 109.044; 90
3890.77Hu, Yue-Hong; Chen, Yu-Ting; He, Zhi-Juan; Gan, Zhang-Yan; Zhang, Ling-Hui; Xi, Wen-Jie; Li, Baosheng; Zhang, Fu-Min
One-pot Nazarov cyclization/oxidative 1,2-carbon rearrangement/Ritter reaction to access 5-quaternary-4-amidocyclopent-2-enones and 2-quaternary-3-amidoindanones.
Chemical communications (Cambridge, England), 2025, 61, 3720-3723
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
1573811 CIFC39 H29 In N2 O6 S6P 1 n 110.9278; 9.492; 19.0268
90; 97.401; 90
1957.14Pratap, Rajesh; Sahani, Raj Kumar; Maddeshiya, Tarkeshwar; Tripathi, Himanshu Shekhar; Pandey, Mrituanjay D.; Bhattacharya, Subrato
Synthesis and characterization of In(III) <i>S</i>-thiobenzoylthioglycolate complexes and their catalytic applications in CO<sub>2</sub> fixation and multicomponent synthetic reactions.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 4518-4529
1573812 CIFC14 H14 In N2 Na O5 S2P 1 21/c 115.735; 7.9458; 14.7384
90; 110.678; 90
1723.99Pratap, Rajesh; Sahani, Raj Kumar; Maddeshiya, Tarkeshwar; Tripathi, Himanshu Shekhar; Pandey, Mrituanjay D.; Bhattacharya, Subrato
Synthesis and characterization of In(III) <i>S</i>-thiobenzoylthioglycolate complexes and their catalytic applications in CO<sub>2</sub> fixation and multicomponent synthetic reactions.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 4518-4529
1573813 CIFC37 H29 In N2 O6 S6P c a 2128.2437; 17.5038; 14.8073
90; 90; 90
7320.3Pratap, Rajesh; Sahani, Raj Kumar; Maddeshiya, Tarkeshwar; Tripathi, Himanshu Shekhar; Pandey, Mrituanjay D.; Bhattacharya, Subrato
Synthesis and characterization of In(III) <i>S</i>-thiobenzoylthioglycolate complexes and their catalytic applications in CO<sub>2</sub> fixation and multicomponent synthetic reactions.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 4518-4529
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
1573817 CIFC130 H100 Cl4 Cu4 F12 N8 P6 Pt2P 1 21/n 114.4294; 24.0473; 18.0186
90; 92.752; 90
6245Hu, Xue-Ning; Zhong, Xu-Hang; Zhong, Rui-Ru; Zhang, Lin-Mei; Hao, De-Bo; Xu, Qian; Wei, Hui-Zhi; Zhou, Rui; Wei, Jianyu; Liu, Kuan-Guan; Yuan, Shang-Fu; Li, Dong-Sheng; Wu, Tao
Significantly enhanced NIR emission of solid-state clusters based on Cu<sub>4</sub>Pt<sub>2</sub> triggered with volatile organic compounds.
Nanoscale, 2025, 17, 5829-5837
1573821 CIFC15 H14 O3 S2P -16.196; 10.6217; 11.347
82.619; 74.785; 73.76
690.62Cheng, Shihao; Ni, Xiao; Cui, Guanyou; Dong, Chenhu; Ma, Yujie; Li, Jinlong; Bao, Xiaofeng; Zhao, Yu
Diastereoselective thia-[3 + 2] cyclization of acetylpyranuloses and β-oxodithioesters.
Organic & biomolecular chemistry, 2025, 23, 2362-2364
1573822 CIFC36 H36 N2C 1 2/c 128.4509; 9.183; 11.7236
90; 115.082; 90
2774.1Zhang, Wentao; Wang, Luyao; Zhou, Yufeng; Chen, Zhifang; Xiong, Heng-Ying; Zhang, Guangwu
Synthesis of the 3,3'-bipyrrole scaffold from diyne.
Organic & biomolecular chemistry, 2025, 23, 2463-2466
1573823 CIFC36 H36 N2C 1 c 126.6157; 9.4617; 11.378
90; 98.543; 90
2833.5Zhang, Wentao; Wang, Luyao; Zhou, Yufeng; Chen, Zhifang; Xiong, Heng-Ying; Zhang, Guangwu
Synthesis of the 3,3'-bipyrrole scaffold from diyne.
Organic & biomolecular chemistry, 2025, 23, 2463-2466
1573824 CIFC46 H36 N2P 1 21/n 116.6526; 5.8534; 18.1057
90; 109.461; 90
1664.01Zhang, Wentao; Wang, Luyao; Zhou, Yufeng; Chen, Zhifang; Xiong, Heng-Ying; Zhang, Guangwu
Synthesis of the 3,3'-bipyrrole scaffold from diyne.
Organic & biomolecular chemistry, 2025, 23, 2463-2466
1573825 CIFC38 H32 N2 O2C 1 2/c 126.2762; 10.1154; 12.3299
90; 116.268; 90
2938.8Zhang, Wentao; Wang, Luyao; Zhou, Yufeng; Chen, Zhifang; Xiong, Heng-Ying; Zhang, Guangwu
Synthesis of the 3,3'-bipyrrole scaffold from diyne.
Organic & biomolecular chemistry, 2025, 23, 2463-2466
1573826 CIFC32 H47 Br3 N2 Ni2 O3P -19.1461; 9.5974; 20.7405
97.081; 102.662; 92.41
1758.26Lu, Yuan; Ji, Gang; Yu, Shuyang; Ning, Xiaoshan; Sun, Xiu-Li; Gao, Yanshan; Wang, Xiaoyan; Tang, Yong
Binuclear Ni catalyzed ethylene copolymerization with short chain alkenol monomers
Polymer Chemistry, 2025, 16, 1146-1154
1573827 CIFC39 H61 Br3 N2 Ni2 O3P 1 21/c 114.9658; 19.0661; 16.9642
90; 98.546; 90
4786.8Lu, Yuan; Ji, Gang; Yu, Shuyang; Ning, Xiaoshan; Sun, Xiu-Li; Gao, Yanshan; Wang, Xiaoyan; Tang, Yong
Binuclear Ni catalyzed ethylene copolymerization with short chain alkenol monomers
Polymer Chemistry, 2025, 16, 1146-1154
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
1573856 CIFC17 H17 N O2P -19.639; 9.806; 14.785
89.903; 89.916; 81.105
1380.7Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573857 CIFC13 H9 N O2P 1 21/c 118.691; 3.898; 26.717
90; 90.349; 90
1946.5Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573858 CIFC14 H11 N O2C 1 2/c 17.0702; 18.754; 16.522
90; 96.935; 90
2174.7Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573859 CIFC12 H7 N O2P 1 21/n 111.0018; 5.4073; 15.6669
90; 108.949; 90
881.52Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573860 CIFC15 H13 N O2P 1 21/c 19.3455; 6.8284; 19.0394
90; 97.03; 90
1205.86Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573861 CIFC18 H19 N O2P 1 21/n 18.2305; 16.3481; 11.3549
90; 103.244; 90
1487.2Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573862 CIFC16 H15 N O2P 21 21 214.7154; 12.531; 22.215
90; 90; 90
1312.7Meher, Niranjan; Khatun, Mst Nasima; Parui, Retwik; Iyer, Parameswar Krishnan
Non-conjugated alkyl chain engineering to tune condensed state photophysical and supramolecular assembly properties.
Nanoscale, 2025, 17, 6685-6694
1573863 CIFC42 H28 Fe N6 S2P c c n14.2537; 14.2713; 17.4543
90; 90; 90
3550.53Valverde-Muñoz, Francisco Javier; Torres Ramírez, Ricardo Guillermo; Trzop, Elzbieta; Bataille, Thierry; Daro, Nathalie; Denux, Dominique; Guionneau, Philippe; Cailleau, Hervé; Chastanet, Guillaume; Le Guennic, Boris; Collet, Eric
Stabilizing low symmetry-based functions of materials at room temperature through isosymmetric electronic bistability.
Materials horizons, 2025, 12, 1463-1472
1573864 CIFC42 H28 Fe N6 S2P 1 21/c 115.6569; 14.5792; 16.8595
90; 93.153; 90
3842.6Valverde-Muñoz, Francisco Javier; Torres Ramírez, Ricardo Guillermo; Trzop, Elzbieta; Bataille, Thierry; Daro, Nathalie; Denux, Dominique; Guionneau, Philippe; Cailleau, Hervé; Chastanet, Guillaume; Le Guennic, Boris; Collet, Eric
Stabilizing low symmetry-based functions of materials at room temperature through isosymmetric electronic bistability.
Materials horizons, 2025, 12, 1463-1472
1573865 CIF
Paper
C16 H31.2 Ni5 O20.6I 41/a :223.3025; 23.3025; 11.2648
90; 90; 90
6116.9Pfeiffer, Maximilian; Stöger, Berthold; Weil, Matthias
Poly[[bis(μ4-acetato-κ4 O:O:O′:O′)tetrakis(μ3-acetato-κ3 O:O:O′)bis(μ2-acetato-κ2 O:O′)bis(μ3-hydroxido)pentanickel(II)] 2.60-hydrate]
IUCrData, 2025, 10, x250082
1573866 CIF
Paper
C18 H28 Br N3P 1 c 114.9741; 6.3842; 10.0741
90; 90.435; 90
963.03Albert, Daniel R.; Gau, Michael; Rajaseelan, Edward
4-(4-tert-Butylbenzyl)-1-neopentyl-1,2,4-triazolium bromide
IUCrData, 2025, 10, x250092
1573867 CIFCo O4 WP 14.686; 5.703; 4.969
90; 90; 90
132.79Siddhi V Patil, Amitkumar R Patil, Tukaram D Dongale, Santosh S Sutar, Keshav Y Rajpure,
Capacitance-induced non-zero crossing hysteresis in CoWO4 thin-film resistive memory
Colloids and Surfaces A: Physicochemical and Engineering Aspects', 2025, 711, 136348
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
1573871 CIFC30 H20 N2C 1 2/c 127.885; 5.6072; 27.8067
90; 111.567; 90
4043.37Du, Jiajun; Chen, Jinling; Ouyang, Beilin; Sun, Anxin; Tian, Congcong; Zhuang, Rongshan; Chen, Chen; Liu, Shuo; Chen, Qianwen; Li, Ziyi; Wu, Xiling; Cai, Jingyu; Zhao, Yuyang; Li, Ran; Xue, Teng; Cen, Tiantian; Zhao, Kaibo; Chen, Chun-Chao
Face-on oriented self-assembled molecules with enhanced π–π stacking for highly efficient inverted perovskite solar cells on rough FTO substrates
Energy & Environmental Science, 2025, 18, 3196-3210
1573872 CIFC18 H13 NP 1 21 16.4624; 7.3908; 13.2977
90; 101.493; 90
622.39Du, Jiajun; Chen, Jinling; Ouyang, Beilin; Sun, Anxin; Tian, Congcong; Zhuang, Rongshan; Chen, Chen; Liu, Shuo; Chen, Qianwen; Li, Ziyi; Wu, Xiling; Cai, Jingyu; Zhao, Yuyang; Li, Ran; Xue, Teng; Cen, Tiantian; Zhao, Kaibo; Chen, Chun-Chao
Face-on oriented self-assembled molecules with enhanced π–π stacking for highly efficient inverted perovskite solar cells on rough FTO substrates
Energy & Environmental Science, 2025, 18, 3196-3210
1573873 CIFC10 H16 N2 O3 SP 21 21 215.17; 10.11; 20.71
90; 90; 90
1082.5Vlahakis, Niko; Clauss, Arden; Rodriguez, Jose A.
Accounting for electron-beam-induced warping of molecular nanocrystals in MicroED structure determination.
IUCrJ, 2025, 12
1573874 CIFC12 H24 Cu2 N4 O12P 1 21 15.51; 8.24; 9.72
90; 90.33; 90
441.3Vlahakis, Niko; Clauss, Arden; Rodriguez, Jose A.
Accounting for electron-beam-induced warping of molecular nanocrystals in MicroED structure determination.
IUCrJ, 2025, 12
1573875 CIFC20 H40 N4 O8 S4 Zn2P 1 21 19.07; 4.91; 14.97
90; 106.94; 90
637.7Vlahakis, Niko; Clauss, Arden; Rodriguez, Jose A.
Accounting for electron-beam-induced warping of molecular nanocrystals in MicroED structure determination.
IUCrJ, 2025, 12
1573876 CIFC12 H16 N6 O4 ZnP 43 21 27.09; 7.09; 29.07
90; 90; 90
1461.3Vlahakis, Niko; Clauss, Arden; Rodriguez, Jose A.
Accounting for electron-beam-induced warping of molecular nanocrystals in MicroED structure determination.
IUCrJ, 2025, 12
1573877 CIFC44 H28 Co N4P -19.6; 13.145; 13.28
79.53; 71.78; 69.39
1485.1Vlahakis, Niko; Clauss, Arden; Rodriguez, Jose A.
Accounting for electron-beam-induced warping of molecular nanocrystals in MicroED structure determination.
IUCrJ, 2025, 12
1573878 CIFC20 H18 Br4 N2 O2P 1 2/n 115.9413; 9.245; 16.0151
90; 110.54; 90
2210.2Jeba Silviya, S. Benita; Ruphina Maragatham, S. Michlin; Andrews, S. G. Jebastin; Bhuvanesh, Nattamai S. P.; Jebaraj, J. Winfred; Balakrishnan, Chithiraivel
A robust PET-based chiral Schiff base molecular probe for recognition of Hg<sup>2+</sup> and Pb<sup>2+</sup> and its application in live cell imaging.
Analytical methods : advancing methods and applications, 2025, 17, 2342-2354
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
1573892 CIFC15 H16 N2 SP b c n11.6219; 13.9013; 8.4102
90; 90; 90
1358.75Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573893 CIFC17 H22 N2 O5 S4I 1 2/a 18.7466; 11.0403; 22.1225
90; 93.972; 90
2131.13Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573894 CIFC15 H10 F6 N2 SP 1 21/c 114.27; 7.5957; 14.4949
90; 102.715; 90
1532.58Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573895 CIFC15 H10 N4 SF d d 224.301; 13.2694; 8.6371
90; 90; 90
2785.12Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573896 CIFC17 H18 N4 O5 SP -16.9039; 10.665; 12.8313
69.245; 89.785; 83.28
876.66Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573897 CIFC17 H20 N2 SP b c a10.778; 9.3346; 30.4546
90; 90; 90
3063.99Yu, Yongjiang; Chen, Wang; Hu, Rongrong; Tang, Ben Zhong
The base-free multicomponent polymerization of elemental sulfur, difluoromethylene phosphobetaine and amines toward electron-deficient aromatic polythioureas
Polymer Chemistry, 2025, 16, 1509-1518
1573898 CIFC17 H25 Br N2 O11P 1 21 112.8648; 4.7385; 18.137
90; 104.231; 90
1071.7Yamashita, Kotoyo; Ito, Akitaka; Ishida, Masashi; Shintani, Yuki; Ikeda, Masato; Hadano, Shingo; Izumi, Masayuki; Ochi, Rika
Stereoisomerism-dependent gelation and crystal structures of glycosylated <i>N</i>-methylbromomaleimide-based supramolecular hydrogels.
Soft matter, 2025, 21, 2124-2132
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
1573922 CIFC41 H52 Fe4 N3 O13 PP 1 21/c 117.157; 10.6828; 25.135
90; 97.4945; 90
4567.5Pattanayak, Santanu; Siegel, Rachel E.; Liu, Yiming; Fettinger, James C.; Berben, Louise A.
Amine groups alter product selectivity and rate of catalytic hydride transfer reactions
Chemical Science, 2025
1573923 CIFC74 H62 Fe4 N4 O10 P4P -112.2009; 16.4108; 17.708
82.274; 76.135; 84.742
3404.5Pattanayak, Santanu; Siegel, Rachel E.; Liu, Yiming; Fettinger, James C.; Berben, Louise A.
Amine groups alter product selectivity and rate of catalytic hydride transfer reactions
Chemical Science, 2025
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
1573925 CIF
Paper
C50 H62 N4 Ni O6P -15.5532; 12.0594; 17.023
86.599; 83.723; 82.426
1122.11Khan, Sultana Shakila; Howlader, Md. Belayet Hossain; Sheikh, Md. Chanmiya; Miyatake, Ryuta; Zangrando, Ennio
Bis{4-(allyloxy)-N′-[4-(octyloxy)benzylidene]benzohydrazidato}nickel(II)
IUCrData, 2025, 10, x250120
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
1573943 CIFC68 H50 Ag2 Au2 P2P 1 21/n 111.3993; 21.628; 21.962
90; 93.759; 90
5402.95Shehzad, Aamir; Yi, Qiuhao; Cui, Chaonan; Luo, Zhixun
Electrocatalytic nitrogen reduction to ammonia by graphene-supported Au<sub>4</sub>Cu<sub>2</sub> and Au<sub>2</sub>Ag<sub>2</sub> nanoclusters.
Nanoscale, 2025, 17, 7453-7459
1573944 CIFC26.33333 H20.66667 Au Cl0.66667 PP 1 21/n 113.1746; 12.7141; 39.686
90; 94.67; 90
6625.5Shehzad, Aamir; Yi, Qiuhao; Cui, Chaonan; Luo, Zhixun
Electrocatalytic nitrogen reduction to ammonia by graphene-supported Au<sub>4</sub>Cu<sub>2</sub> and Au<sub>2</sub>Ag<sub>2</sub> nanoclusters.
Nanoscale, 2025, 17, 7453-7459
1573945 CIFC84 H60 Au4 Cu2 P2P -112.6398; 16.7456; 18.52
88.962; 76.498; 69.963
3572.7Shehzad, Aamir; Yi, Qiuhao; Cui, Chaonan; Luo, Zhixun
Electrocatalytic nitrogen reduction to ammonia by graphene-supported Au<sub>4</sub>Cu<sub>2</sub> and Au<sub>2</sub>Ag<sub>2</sub> nanoclusters.
Nanoscale, 2025, 17, 7453-7459
1573946 CIFC33 H39 Cl6 N6 SbP 1 21 19.736; 26.6108; 14.4804
90; 91.792; 90
3749.8Jiang, Chunyan; Yan, Jing; Qiu, Jianrong; Wu, Mingmei; Xu, Beibei
Regulating intermolecular interactions for stable multifunctional organic-inorganic metal halide hybrid glasses.
Materials horizons, 2025, 12, 3515-3524
1573947 CIFC44 H52 Cl10 N8 Sb2I -417.5697; 17.5697; 8.7813
90; 90; 90
2710.7Jiang, Chunyan; Yan, Jing; Qiu, Jianrong; Wu, Mingmei; Xu, Beibei
Regulating intermolecular interactions for stable multifunctional organic-inorganic metal halide hybrid glasses.
Materials horizons, 2025, 12, 3515-3524
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
1573951 CIFC43 H51 Cr F9 I4 N11 O10 S3P 1 21/n 111.8195; 22.8812; 22.7016
90; 100.664; 90
6033.5Ye, 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
1573953 CIFC41 H26 N4 OP -110.327; 11.0712; 13.0992
93.047; 92.234; 102.161
1460.1Chu, Lizhi; Ma, Chenglin; Zhang, Li; Zhou, Yannan; Song, Jingru; Sun, Qikun; Zhang, Shi-Tong; Yang, Wenjun; Xue, Shanfeng
Multifunctional oxadiazole-based ultraviolet-emitting materials used as hosts for multicolor phosphorescence.
Chemical science, 2025, 16, 5252-5259
1573954 CIFC41 H26 N4 OP 1 21/n 15.505; 19.8183; 27.3727
90; 95.443; 90
2972.89Chu, Lizhi; Ma, Chenglin; Zhang, Li; Zhou, Yannan; Song, Jingru; Sun, Qikun; Zhang, Shi-Tong; Yang, Wenjun; Xue, Shanfeng
Multifunctional oxadiazole-based ultraviolet-emitting materials used as hosts for multicolor phosphorescence.
Chemical science, 2025, 16, 5252-5259
1573955 CIFC32 H21 N3 OC 1 2/c 153.653; 9.11; 11.0235
90; 95.524; 90
5363Chu, Lizhi; Ma, Chenglin; Zhang, Li; Zhou, Yannan; Song, Jingru; Sun, Qikun; Zhang, Shi-Tong; Yang, Wenjun; Xue, Shanfeng
Multifunctional oxadiazole-based ultraviolet-emitting materials used as hosts for multicolor phosphorescence.
Chemical science, 2025, 16, 5252-5259
1573956 CIFC16 H18 F4 I4 N8 PbP n m a12.9388; 30.291; 6.6444
90; 90; 90
2604.1Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573957 CIFC16 H18 F4 I4 N8 PbP n m a12.8444; 29.723; 6.5815
90; 90; 90
2512.6Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573958 CIFC16 H18 F4 I4 N8 PbP n m a12.4841; 27.931; 6.2972
90; 90; 90
2195.8Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573959 CIFC16 H18 F4 I4 N8 PbP n m a12.5017; 27.526; 6.2872
90; 90; 90
2163.6Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573960 CIFC16 H18 F4 I4 N8 PbP n m a12.6989; 28.912; 6.47
90; 90; 90
2375.5Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573961 CIFC16 H18 F4 I4 N8 PbP n m a12.5029; 27.709; 6.2997
90; 90; 90
2182.5Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573962 CIFC16 H18 F4 I4 N8 PbP n m a12.699; 28.928; 6.4727
90; 90; 90
2377.8Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573963 CIFC16 H18 F4 I4 N8 PbP n m a12.9028; 30.077; 6.6218
90; 90; 90
2569.8Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573964 CIFC16 H18 F4 I4 N8 PbP n m a12.5704; 28.337; 6.3725
90; 90; 90
2269.9Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573965 CIFC16 H18 F4 I4 N8 PbP n m a12.5155; 28.112; 6.3307
90; 90; 90
2227.37Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573966 CIFC16 H18 F4 I4 N8 PbP n m a12.6346; 28.617; 6.4221
90; 90; 90
2322Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573967 CIFC16 H18 F4 I4 N8 PbP n m a12.7582; 29.234; 6.5183
90; 90; 90
2431.2Maufort, Arthur; Van Landeghem, Melissa; Deutsch, Maxime; Banks, Peter; La Magna, Paola; Van Hecke, Kristof; Cerdá, Jesús; Lutsen, Laurence; Vanderzande, Dirk; Quarti, Claudio; Beljonne, David; Pillet, Sébastien; Vandewal, Koen; Van Gompel, Wouter T. M.
Structural rigidity, thermochromism and piezochromism of layered hybrid perovskites containing an interdigitated organic bilayer.
Chemical science, 2025, 16, 5662-5675
1573968 CIFC15 H12 N2P 1 21/c 15.5513; 9.0805; 22.6176
90; 93.832; 90
1137.57Shaydullin, Ruslan R.; Galushko, Alexey S.; Ilyushenkova, Valentina V.; Vlasova, Yulia S.; Ananikov, Valentine P.
Are activation barriers of 50-70 kcal mol<sup>-1</sup> accessible for transformations in organic synthesis in solution?
Chemical science, 2025, 16, 5289-5298
1573969 CIFC123 H94 B2 Cl6 N6 ZnC 1 2/c 127.5951; 13.4831; 29.7605
90; 114.537; 90
10073Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573970 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.51; 13.52; 30.45
90; 113.67; 90
10373Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573971 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.79; 13.68; 30.56
90; 113.4; 90
10662Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573972 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.31; 13.37; 30.17
90; 114.31; 90
10039Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573973 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.71; 13.64; 30.55
90; 113.46; 90
10592Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573974 CIFC133 H118 B2 Cl2 Co N6 O2C 1 2/c 127.429; 13.479; 29.817
90; 114.3; 90
10047Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573975 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.35; 13.4; 30.24
90; 114.19; 90
10110Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573976 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.38; 13.44; 30.33
90; 113.99; 90
10197Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573977 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.44; 13.47; 30.39
90; 113.83; 90
10275Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573978 CIFC132 H116 B2 Fe N6 O2C 1 2/c 127.64; 13.59; 30.52
90; 113.51; 90
10513Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573979 CIFC129 H109 B2 Mn N6 O1.5P -117.0314; 17.0463; 21.0901
80.916; 69.604; 60.143
4976.4Janetzki, Jett T.; Brown, Dominic S.; Daumann, Florian; Ismail, I. Haseena; Gable, Robert W.; Hay, Moya A.; Mulder, Roger J.; Starikova, Alyona A.; Weber, Birgit; Giansiracusa, Marcus J.; Boskovic, Colette
Thermal- and light-induced valence tautomerism with a concerted spin transition in an iron tris(diimine) complex.
Chemical science, 2025, 16, 5857-5871
1573980 CIFC40 H29 N O2P 21 21 217.7089; 24.161; 30.34
90; 90; 90
5650.97Sun, Haodong; Xiao, Yuxin; He, Yunfei; Wei, Xiaoyu; Zou, Jindou; Luo, Yuanda; Wu, Yazhang; Zhao, Jiaxin; Au, Vonika Ka-Man; Yu, Tao
3D printable organic room-temperature phosphorescent materials and printed real-time sensing and display devices.
Chemical science, 2025, 16, 5299-5309
1573981 CIFC33 H23 Cl2 N O2P 1 21/c 112.8697; 26.1356; 7.9805
90; 107.143; 90
2565.04Sun, Haodong; Xiao, Yuxin; He, Yunfei; Wei, Xiaoyu; Zou, Jindou; Luo, Yuanda; Wu, Yazhang; Zhao, Jiaxin; Au, Vonika Ka-Man; Yu, Tao
3D printable organic room-temperature phosphorescent materials and printed real-time sensing and display devices.
Chemical science, 2025, 16, 5299-5309
1573982 CIFC44 H29 N O2P 1 21/c 115.739; 16.068; 13.9254
90; 107.433; 90
3359.9Sun, Haodong; Xiao, Yuxin; He, Yunfei; Wei, Xiaoyu; Zou, Jindou; Luo, Yuanda; Wu, Yazhang; Zhao, Jiaxin; Au, Vonika Ka-Man; Yu, Tao
3D printable organic room-temperature phosphorescent materials and printed real-time sensing and display devices.
Chemical science, 2025, 16, 5299-5309
1573983 CIFC20 H24 Br N O2P 1 21 110.495; 15.3001; 11.7177
90; 97.033; 90
1867.4Masukawa, Kazuki; Kojima, Amu; Sato, Takuma; Terada, Masahiro; Nakamura, Itaru
Cu-catalyzed [1,3]-asymmetric methoxy rearrangement of N-methoxyanilines: mechanistic insight
Catalysis Science & Technology, 2025, 15, 2138-2142
1573984 CIF
Paper
Ni0.92 Ti V0.08P m -3 m2.9895; 2.9895; 2.9895
90; 90; 90
26.717Liu, Huizi; Fan, Changzeng; Wen, Bin; Zhang, Lifeng
Titanium vanadium nickel, TiV0.08Ni0.92
IUCrData, 2025, 10, x250147
1573985 CIFC12 H33 B11 N2 O2P n m a10.0719; 10.9585; 18.5142
90; 90; 90
2043.47Sun, Wanqi; Jin, Yujie; Wang, Yongtao; Wen, Zeyu; Sun, Jizeng; Yao, Jia; Duttwyler, Simon; Li, Haoran
Oxidation-induced nucleophilic substitution at the electron-rich B(12) vertex in [CB<sub>11</sub>H<sub>12</sub>]<sup>-</sup> under catalyst-free conditions.
Chemical science, 2025, 16, 5942-5947
1573986 CIFC24 H55 B11 N2 O7P -110.4232; 11.4832; 14.7581
93.391; 94.642; 91.388
1756.8Sun, Wanqi; Jin, Yujie; Wang, Yongtao; Wen, Zeyu; Sun, Jizeng; Yao, Jia; Duttwyler, Simon; Li, Haoran
Oxidation-induced nucleophilic substitution at the electron-rich B(12) vertex in [CB<sub>11</sub>H<sub>12</sub>]<sup>-</sup> under catalyst-free conditions.
Chemical science, 2025, 16, 5942-5947
1573987 CIFC21 H53 B11 Cl6 N2 O2P 1 21/c 123.2378; 9.4437; 17.9211
90; 109.429; 90
3708.8Sun, Wanqi; Jin, Yujie; Wang, Yongtao; Wen, Zeyu; Sun, Jizeng; Yao, Jia; Duttwyler, Simon; Li, Haoran
Oxidation-induced nucleophilic substitution at the electron-rich B(12) vertex in [CB<sub>11</sub>H<sub>12</sub>]<sup>-</sup> under catalyst-free conditions.
Chemical science, 2025, 16, 5942-5947
1573988 CIFC21 H54 B11 N3 O2P 1 21/c 113.1967; 22.4636; 20.8837
90; 92.836; 90
6183.3Sun, Wanqi; Jin, Yujie; Wang, Yongtao; Wen, Zeyu; Sun, Jizeng; Yao, Jia; Duttwyler, Simon; Li, Haoran
Oxidation-induced nucleophilic substitution at the electron-rich B(12) vertex in [CB<sub>11</sub>H<sub>12</sub>]<sup>-</sup> under catalyst-free conditions.
Chemical science, 2025, 16, 5942-5947
1573989 CIFC18 H15 Br Fe O2P 17.613; 8.5829; 12.8193
80.36; 73.628; 82.082
788.68Hang, Nan-Nan; Tong, En-Guang; Qi, Ting; Sun, Chao; Ming, Jialin
Asymmetric synthesis of metallocenes with planar and central chirality by rhodium-catalyzed desymmetrization reactions.
Chemical science, 2025, 16, 5880-5886
1573990 CIFC10 H17 N2 O4 Re S2P 1 21/c 17.79663; 10.5671; 18.0745
90; 101.425; 90
1459.61Melis, Diana R.; Segers, Charlotte; Wellens, Jasmien; Van de Voorde, Michiel; Blacque, Olivier; Ooms, Maarten; Gasser, Gilles; Opsomer, Tomas
Cysteine-selective [<sup>188</sup>Re]Re(v) radiolabelling of a Nanobody® for targeted radionuclide therapy using a "chelate-then-click" approach.
Chemical science, 2025, 16, 6089-6098
1573991 CIFC8 H13 N2 O4 Re S2F d d 227.8226; 20.249; 8.86174
90; 90; 90
4992.53Melis, Diana R.; Segers, Charlotte; Wellens, Jasmien; Van de Voorde, Michiel; Blacque, Olivier; Ooms, Maarten; Gasser, Gilles; Opsomer, Tomas
Cysteine-selective [<sup>188</sup>Re]Re(v) radiolabelling of a Nanobody® for targeted radionuclide therapy using a "chelate-then-click" approach.
Chemical science, 2025, 16, 6089-6098
1573992 CIFC42 H42 Co F3 N2 P4P 1 21/c 111.0941; 22.838; 15.192
90; 93.182; 90
3843.2Fitzsimmons, Matthew C.; Seith, Maria C.; Moore, Curtis E.; Thomas, Christine M.
Efficient and selective hydroboration of alkenes catalyzed by an air-stable (PP<sup>CF3</sup>P)CoI<sub>2</sub> precatalyst.
Chemical science, 2025, 16, 5717-5725
1573993 CIFC41.5 H37 Cl5 Co F3 I2 N2 P3P -112.5715; 13.3397; 15.6881
87.496; 73.663; 62.081
2218.77Fitzsimmons, Matthew C.; Seith, Maria C.; Moore, Curtis E.; Thomas, Christine M.
Efficient and selective hydroboration of alkenes catalyzed by an air-stable (PP<sup>CF3</sup>P)CoI<sub>2</sub> precatalyst.
Chemical science, 2025, 16, 5717-5725
1573994 CIFC55 H57 Co F3 N2 O2 P3P c a 2124.0754; 12.3634; 34.026
90; 90; 90
10128Fitzsimmons, Matthew C.; Seith, Maria C.; Moore, Curtis E.; Thomas, Christine M.
Efficient and selective hydroboration of alkenes catalyzed by an air-stable (PP<sup>CF3</sup>P)CoI<sub>2</sub> precatalyst.
Chemical science, 2025, 16, 5717-5725
1573995 CIFC23 H18 N2 O3 SP 1 21/c 111.0055; 12.1682; 14.8532
90; 104.525; 90
1925.52Gu, Jun; Zhang, Li-Hong; Zhuang, Hong-Feng; He, Ying
Atroposelective [4+1] annulation for the synthesis of isotopic isoindolinones bearing both central and axial chirality.
Chemical science, 2025, 16, 5735-5744
1573996 CIFC23 H20 N2 O3 SP 21 21 218.843; 12.33; 18.0497
90; 90; 90
1968.03Gu, Jun; Zhang, Li-Hong; Zhuang, Hong-Feng; He, Ying
Atroposelective [4+1] annulation for the synthesis of isotopic isoindolinones bearing both central and axial chirality.
Chemical science, 2025, 16, 5735-5744
1573997 CIFC23 H18 N2 O3 SP 1 21 18.3879; 12.8676; 9.7824
90; 111.619; 90
981.56Gu, Jun; Zhang, Li-Hong; Zhuang, Hong-Feng; He, Ying
Atroposelective [4+1] annulation for the synthesis of isotopic isoindolinones bearing both central and axial chirality.
Chemical science, 2025, 16, 5735-5744
1573998 CIFC23 H18 N2 O3 SP 1 21 18.3907; 12.8791; 9.7624
90; 111.393; 90
982.28Gu, Jun; Zhang, Li-Hong; Zhuang, Hong-Feng; He, Ying
Atroposelective [4+1] annulation for the synthesis of isotopic isoindolinones bearing both central and axial chirality.
Chemical science, 2025, 16, 5735-5744
1573999 CIFC10 H15.5 Ag2 F3 N O3.25 SP n -3 :220.9199; 20.9199; 20.9199
90; 90; 90
9155.4Chandrashekar, Priyanka; Karmakar, Arun; Aparna, Ravari Kandy; Singh, Laddi; Mondal, Pradip Kumar; Kundu, Subrata; Bhattacharyya, Kalishankar; Mandal, Sukhendu
Linker driven site-specific catalysis in atomically precise silver cluster assemblies.
Chemical science, 2025, 16, 5726-5734
1574000 CIFC45 H58 Ag6 F9 N4 O7 S3C 1 2/c 125.337; 24.666; 19.661
90; 109.96; 90
11549Chandrashekar, Priyanka; Karmakar, Arun; Aparna, Ravari Kandy; Singh, Laddi; Mondal, Pradip Kumar; Kundu, Subrata; Bhattacharyya, Kalishankar; Mandal, Sukhendu
Linker driven site-specific catalysis in atomically precise silver cluster assemblies.
Chemical science, 2025, 16, 5726-5734
1574001 CIFC42 H52 Ag6 F9 N7 O7 S3C 1 2/c 126.994; 14.021; 29.259
90; 92.57; 90
11063Chandrashekar, Priyanka; Karmakar, Arun; Aparna, Ravari Kandy; Singh, Laddi; Mondal, Pradip Kumar; Kundu, Subrata; Bhattacharyya, Kalishankar; Mandal, Sukhendu
Linker driven site-specific catalysis in atomically precise silver cluster assemblies.
Chemical science, 2025, 16, 5726-5734
1574002 CIFC39 H45 Ag6 F9 N3 O6 S3P n n m22.946; 27.85; 18.982
90; 90; 90
12130Chandrashekar, Priyanka; Karmakar, Arun; Aparna, Ravari Kandy; Singh, Laddi; Mondal, Pradip Kumar; Kundu, Subrata; Bhattacharyya, Kalishankar; Mandal, Sukhendu
Linker driven site-specific catalysis in atomically precise silver cluster assemblies.
Chemical science, 2025, 16, 5726-5734
1574003 CIFC4 H8 N3 O4 PP 21 21 214.4906; 8.7661; 19.496
90; 90; 90
767.46Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574004 CIFC5 H9 N3 O3 SP 1 21/c 15.1632; 10.2883; 15.253
90; 93.922; 90
808.4Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574005 CIFC12 H16 N6 O4P 1 21/c 15.3958; 19.471; 6.9453
90; 104.63; 90
706.03Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574006 CIFC4 H8 N4 O3 SC 1 2/c 123.329; 8.9732; 7.4927
90; 101.254; 90
1538.3Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574007 CIFC4 H6 B F4 N3P 1 21/n 14.9961; 20.906; 7.0582
90; 102.398; 90
720.03Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574008 CIFC4 H11 B2 N3 O6P 1 21/c 110.2656; 3.7235; 13.2934
90; 107.188; 90
485.43Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574009 CIFC9 H11 F3 N6 O3 SP -18.658; 8.791; 9.477
71.944; 81.828; 83.043
676.6Arif, Muhammad; Liu, Xu; Jia, Hangwei; Yang, Zhihua; Hou, Xueling; Pan, Shilie
Optimizing optical anisotropy in low-dimensional structures <i>via</i> intralayer hydrogen bonding modulation and anionic substitution.
Materials horizons, 2025, 12, 3538-3545
1574010 CIFC30 H42 B N OP 1 21/c 19.1568; 11.115; 26.1678
90; 95.763; 90
2649.84Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574011 CIFC33 H50 B N O SeP n a 2114.2386; 14.0447; 15.3868
90; 90; 90
3077Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574012 CIFC32 H51 B N PP -19.6984; 11.0467; 14.5864
96.819; 105.427; 92.382
1491.38Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574013 CIFC45 H74 B Li2 N O4 SeP -110.7762; 16.8779; 24.5726
81.439; 86.226; 88.794
4409.59Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574014 CIFC58 H84 B2 N2 Te2P -110.1565; 10.3469; 14.2245
69.78; 80.935; 81.899
1379.14Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574015 CIFC64 H88 B2 F7.79 N2 P0.96 Te2P -112.7992; 16.2783; 17.3761
106.637; 94.029; 96.39
3427.31Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574016 CIFC29 H42 B N SP 1 21/c 118.006; 8.4637; 17.399
90; 93.337; 90
2647.07Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574017 CIFC74 H116 B2 Li2 N2 O4 S2P -110.5609; 13.0367; 14.8835
82.383; 79.577; 68.461
1869.7Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574018 CIFC70 H108 B2 Li4 N2 O3 S2P 1 21 110.6514; 21.0348; 16.8392
90; 106.025; 90
3626.22Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574019 CIFC45 H74 B Li2 N O4 TeP -110.7784; 16.9121; 24.8131
82.133; 86.65; 88.61
4472.24Michel, Maximilian; Endres, Lukas; Fantuzzi, Felipe; Krummenacher, Ivo; Braunschweig, Holger
Harnessing transient CAAC-stabilized mesitylborylenes for chalcogen activation.
Chemical science, 2025, 16, 5632-5639
1574020 CIFBi2 Br3 Cs3 I5.22P -3 m 18.2207; 8.2207; 10.104
90; 90; 120
591.35Singh, Kuntal; Hossain, Mozakkar; Nayak, Pabitra Kumar; Karmakar, Sougata; Tripathi, Akash; Sarkar, Prakash; Rudra, Pratyasha; Ali, A. V. Muhammed; Grandhi, G. Krishnamurthy; Vivo, Paola; Mondal, Swastik; Adarsh, K. V.; Ghosh, Dibyajyoti; Rao, K. D. M.
Benign mid-gap halide vacancy states in 2D-bismuth-based halide perovskite microcrystals for enhanced broadband photodetectors.
Materials horizons, 2025, 12, 3865-3877
1574021 CIF
Paper
C29 H44 N2 O2P 1 21/c 18.8766; 17.645; 17.2008
90; 91.5518; 90
2693.13Zmeškalová, Eliška; Stara, František; Havlůjová, Tereza; Šoóš, Miroslav
Surface analysis of cannabigerol cocrystals: linking crystal structure to enhanced properties.
IUCrJ, 2025, 12
1574022 CIF
Paper
C25 H42 N2 O2P 1 21/n 18.7047; 26.7487; 11.0627
90; 111.236; 90
2400.92Zmeškalová, Eliška; Stara, František; Havlůjová, Tereza; Šoóš, Miroslav
Surface analysis of cannabigerol cocrystals: linking crystal structure to enhanced properties.
IUCrJ, 2025, 12
1574023 CIF
Paper
C21 H32 O2P 21 21 214.5073; 11.4901; 36.7494
90; 90; 90
1903.23Zmeškalová, Eliška; Stara, František; Havlůjová, Tereza; Šoóš, Miroslav
Surface analysis of cannabigerol cocrystals: linking crystal structure to enhanced properties.
IUCrJ, 2025, 12
1574024 CIFC18 H18 B N3P 1 21/n 113.9391; 11.2303; 20.3661
90; 104.938; 90
3080.4Parui, Retwik; Roy, Hirakjyoti; Meher, Niranjan; Ghosh, Siddhartha Sankar; Iyer, Parameswar Krishnan
Mechanistic investigation on cellular internalization triggering structure-induced conformational modulation of boron-nitrogen luminogens.
Chemical science, 2025, 16, 6023-6034
1574025 CIFC16 H12 B Cl N2P 1 21 14.7299; 10.3015; 13.5889
90; 96.628; 90
657.69Parui, Retwik; Roy, Hirakjyoti; Meher, Niranjan; Ghosh, Siddhartha Sankar; Iyer, Parameswar Krishnan
Mechanistic investigation on cellular internalization triggering structure-induced conformational modulation of boron-nitrogen luminogens.
Chemical science, 2025, 16, 6023-6034
1574026 CIFC16 H12 B F N2I -422.7941; 22.7941; 5.0803
90; 90; 90
2639.6Parui, Retwik; Roy, Hirakjyoti; Meher, Niranjan; Ghosh, Siddhartha Sankar; Iyer, Parameswar Krishnan
Mechanistic investigation on cellular internalization triggering structure-induced conformational modulation of boron-nitrogen luminogens.
Chemical science, 2025, 16, 6023-6034
1574027 CIFC16 H12 B Br N2P 1 21/n 112.963; 6.412; 16.767
90; 92.356; 90
1392.5Parui, Retwik; Roy, Hirakjyoti; Meher, Niranjan; Ghosh, Siddhartha Sankar; Iyer, Parameswar Krishnan
Mechanistic investigation on cellular internalization triggering structure-induced conformational modulation of boron-nitrogen luminogens.
Chemical science, 2025, 16, 6023-6034
1574028 CIFC17 H12 B N3P 1 21/n 18.2259; 26.151; 19.2586
90; 95.282; 90
4125.2Parui, Retwik; Roy, Hirakjyoti; Meher, Niranjan; Ghosh, Siddhartha Sankar; Iyer, Parameswar Krishnan
Mechanistic investigation on cellular internalization triggering structure-induced conformational modulation of boron-nitrogen luminogens.
Chemical science, 2025, 16, 6023-6034
1574029 CIFC168 H168 Au36 S24C 1 2/c 164.631; 22.2308; 32.333
90; 106.89; 90
44452Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574030 CIFC168 H168 Au36 O24 S24I -425.2346; 25.2346; 17.8151
90; 90; 90
11344.4Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574031 CIFC192 H216 Au36 S24P 1 21/n 119.579; 30.2707; 37.2286
90; 94.218; 90
22004.5Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574032 CIFC240 H168 Au36 S24P 1 21 120.1507; 61.3884; 20.3138
90; 92.729; 90
25100.1Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574033 CIFC168 H168 Au36 S24P -118.9703; 19.2923; 28.0221
82.1999; 75.0794; 88.529
9817.6Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574034 CIFC192 H216 Au36 S24P 1 21 119.4037; 32.0462; 19.7066
90; 90.054; 90
12253.9Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574035 CIFC144 H96 Au36 Cl24 S24P -119.0323; 19.229; 30.6431
81.994; 87.439; 66.468
10180.9Lin, Yan-Yan; Nan, Zi-Ang; Lei, Zhen; Wang, Quan-Ming
Efficient synthesis of Au<sub>36</sub>(SR)<sub>24</sub> nanoclusters <i>via</i> the cluster-from-cluster approach.
Nanoscale, 2025, 17, 8724-8730
1574036 CIF
Paper
C14 H14 O4P 1 21/c 115.37; 5.4488; 16.339
90; 117.426; 90
1214.6Abou, Akoun; Bazié, Hypolite; Akonan, Ludovic; Djandé, Abdoulaye; Francotte, Pierre
2-Oxo-2H-chromen-7-yl 3-methylbutanoate
IUCrData, 2025, 10, x250161
1574037 CIF
Paper
C27 H36 O5P -110.3372; 11.3286; 12.4559
105.428; 114.185; 97.344
1235.3Suresh Babu, N.; Anbu Chudar Azhagan, S.; Loganathan, B.; Sughanya, V.; Ayyappan, J.
2,2′-[(4-Butoxyphenyl)methylene]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one)
IUCrData, 2025, 10, x250180
1574038 CIF
Paper
C12 H19 Br N2 O2 SeP -18.4924; 9.3927; 9.7799
71.379; 86.439; 74.119
710.78Schollmeyer, Dieter; Detert, Heiner
3-(2-Ethoxy-2-oxoethyl)-4,5,6,7,8,9-hexahydrocycloocta[d][1,2,3]selenadiazol-3-ium bromide
IUCrData, 2025, 10, x250143
1574039 CIFC20 H17 Cl N2 O3P 15.872; 7.735; 20.137
98.57; 97.62; 91.31
895.6Tian, Jiabao; Ling, Jiahao; Wang, Yanan; Zhou, Lei
Blue light-induced diazo cross-coupling: synthesis of allyldiazo compounds through reshuffling of functionalities.
Chemical science, 2025, 16, 5701-5706
1574040 CIFC20 H17 Cl N2 O3P c a 217.6916; 5.838; 40.645
90; 90; 90
1825.11Tian, Jiabao; Ling, Jiahao; Wang, Yanan; Zhou, Lei
Blue light-induced diazo cross-coupling: synthesis of allyldiazo compounds through reshuffling of functionalities.
Chemical science, 2025, 16, 5701-5706
1574041 CIFC21 H19 Cl N2 O3C 1 c 120.171; 9.765; 39.079
90; 99.308; 90
7596Tian, Jiabao; Ling, Jiahao; Wang, Yanan; Zhou, Lei
Blue light-induced diazo cross-coupling: synthesis of allyldiazo compounds through reshuffling of functionalities.
Chemical science, 2025, 16, 5701-5706
1574042 CIFC18 H22 N O PP 21 21 219.9528; 10.6897; 16.8353
90; 90; 90
1791.15Zhang, Jialiang; Guo, Jiajia; Xu, Ruhui; Zheng, Di; Lian, Kai; Zhang, Zhaoxia; Cao, Shanshan; Jiang, Zhiyong
Asymmetric copper-catalyzed hydrophosphinylation of ethynylazaarenes to access <i>P</i>-chiral 2-azaaryl-ethylphosphine oxides.
Chemical science, 2025, 16, 5957-5966
1574043 CIFC31 H48 O4P 21 21 217.5983; 14.6061; 25.287
90; 90; 90
2806.39Dethe, Dattatraya H.; Siddiqui, Salman A.; Singha, Chirantan
Biomimetic syntheses of kadcoccitane H and kadcotrione C methyl ester.
Chemical science, 2025, 16, 6099-6103
1574044 CIFC9.82 H5.45 Ce0.36 O2.18P 1 21/c 112.1955; 27.6141; 7.7042
90; 93.382; 90
2590Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574045 CIFC27 H15.8 La O6.4P 1 21/c 112.1008; 27.7464; 7.8237
90; 93.673; 90
2621.44Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574046 CIFC36 H37 Dy N3 O9.5P 1 21 18.0212; 26.89; 16.3817
90; 92.297; 90
3530.5Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574047 CIFC35.26 H34.26 La N2.75 O8.75P 1 21/c 116.7495; 26.5927; 8.4965
90; 95.014; 90
3769.98Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574048 CIFC33.3 H29.7 La N2.1 O8.1P 1 21/c 115.0013; 27.7449; 16.1774
90; 97.287; 90
6678.8Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574049 CIFC31.5 H27.5 N1.5 O8.5 PrP 1 21/c 115.0438; 28.0476; 16.0831
90; 97.259; 90
6731.8Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574050 CIFC32.55 H27.95 Ce N1.85 O7.85P 1 21/c 115.0927; 27.9263; 16.165
90; 97.249; 90
6758.8Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574051 CIFC28.32 H21.49 La N0.44 O8.15P 1 21/n 115.4232; 20.5544; 32.285
90; 94.546; 90
10202.6Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574052 CIFC28.5 H19 Ce N0.5 O6.75P 1 21/n 115.3286; 20.5857; 32.2184
90; 94.423; 90
10136.2Gómez-Muñoz, Iván; Hu, Ziqi; Vitórica-Yrezábal, Iñigo J; Coronado, Eugenio; Mínguez Espallargas, Guillermo
Implementing magnetic properties on demand with a dynamic lanthanoid-organic framework.
Chemical science, 2025, 16, 2879-2885
1574053 CIFC30 H27 N O2P 1 21 18.6278; 12.3083; 10.9519
90; 95.711; 90
1157.25He, Ze-Liang; Li, Li; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Palladium-catalysed asymmetric cascade transformations of 4-alken-2-ynyl carbonates to construct complex frameworks.
Chemical science, 2025, 16, 3124-3129
1574054 CIFC29 H28 N2 O4 SP -17.4687; 12.636; 14.057
86.841; 76.742; 75.308
1249He, Ze-Liang; Li, Li; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Palladium-catalysed asymmetric cascade transformations of 4-alken-2-ynyl carbonates to construct complex frameworks.
Chemical science, 2025, 16, 3124-3129
1574055 CIFC28 H20 F3 N O2P -19.9196; 9.9973; 11.8824
91.791; 104.104; 102.384
1111.91He, Ze-Liang; Li, Li; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Palladium-catalysed asymmetric cascade transformations of 4-alken-2-ynyl carbonates to construct complex frameworks.
Chemical science, 2025, 16, 3124-3129
1574056 CIFC36 H32 N2 O3 SP 43 21 212.4257; 12.4257; 42.988
90; 90; 90
6637.3He, Ze-Liang; Li, Li; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Palladium-catalysed asymmetric cascade transformations of 4-alken-2-ynyl carbonates to construct complex frameworks.
Chemical science, 2025, 16, 3124-3129
1574057 CIFC43 H34 N2 O4C 1 2/c 121.731; 9.151; 34.748
90; 107.204; 90
6601He, Ze-Liang; Li, Li; Chen, Zhi-Chao; Du, Wei; Chen, Ying-Chun
Palladium-catalysed asymmetric cascade transformations of 4-alken-2-ynyl carbonates to construct complex frameworks.
Chemical science, 2025, 16, 3124-3129
1574058 CIFC33 H34 Cr O4 P2P c a 2120.1424; 10.949; 13.4777
90; 90; 90
2972.36Zhao, Xing; Xie, Haojie; Zuo, Jing; Wang, Jihe; Zhao, Mei-Xin; Zhang, Jun
PCCP ligands with a semi-rigid backbone for chromium-catalyzed selective ethylene tri-/tetramerization
Catalysis Science & Technology, 2025, 15, 2713-2721
1574059 CIFC33 H28 Cr O4 P2P 1 21 111.6589; 9.9032; 14.3096
90; 112.88; 90
1522.2Zhao, Xing; Xie, Haojie; Zuo, Jing; Wang, Jihe; Zhao, Mei-Xin; Zhang, Jun
PCCP ligands with a semi-rigid backbone for chromium-catalyzed selective ethylene tri-/tetramerization
Catalysis Science & Technology, 2025, 15, 2713-2721
1574060 CIFC14 H17 O7 PP 16.35385; 7.76034; 16.0686
92.9757; 90.6187; 101.846
774.2Platt, Ffion M.; Wang, Yihong; Cordes, David B.; McKay, Aidan P.; Slawin, Alexandra M. Z.; Panchal, Heena; Smith, Andrew D.
Isothiourea-catalysed enantioselective synthesis of phosphonate-functionalised β-lactones
Chemical Science, 2025, 16, 6828-6836
1574061 CIFC16 H17 O5 PP 21 21 216.279; 8.1645; 30.231
90; 90; 90
1549.79Platt, Ffion M.; Wang, Yihong; Cordes, David B.; McKay, Aidan P.; Slawin, Alexandra M. Z.; Panchal, Heena; Smith, Andrew D.
Isothiourea-catalysed enantioselective synthesis of phosphonate-functionalised β-lactones
Chemical Science, 2025, 16, 6828-6836
1574062 CIFC19 H17 O5 P SP 1 21 110.3633; 7.8457; 12.019
90; 110.666; 90
914.35Platt, Ffion M.; Wang, Yihong; Cordes, David B.; McKay, Aidan P.; Slawin, Alexandra M. Z.; Panchal, Heena; Smith, Andrew D.
Isothiourea-catalysed enantioselective synthesis of phosphonate-functionalised β-lactones
Chemical Science, 2025, 16, 6828-6836
1574063 CIFC84 H69 Cs4 O3P -112.3931; 13.0388; 22.218
75.614; 85.704; 77.205
3390.55Shen, Yongbing; Cui, Mengxing; Zhang, Haitao; Guo, Hanjie; Nakamura, Jumpei G.; Embs, Jan Peter; Zhao, Jinkui; Yamashita, Masahiro; Fu, Zhendong
Signatures of the quantum spin liquid state in triangular-based zig-zag polyaromatic hydrocarbon radicals
Chemical Science, 2025, 16, 6345-6354
1574064 CIFC12 H18 Cd2 Cl5 N O2P 1 21/c 17.5573; 15.3477; 16.6274
90; 94.566; 90
1922.4Zhang, Ke; Qi, Zhikai; Zhang, Nan; Zhao, Xingxing; Fan, Yanli; Sun, Long; Zhou, Guojun; Li, Shi-Li; Zhang, Xian-Ming
Efficient energy transfer from organic triplet states to Mn<sup>2+</sup> dopants for dynamic tunable multicolor afterglow in 1D hybrid cadmium chloride.
Chemical science, 2025, 16, 6104-6113
1574065 CIF
Paper
C19 H17 Cl2 F6 N2 P RuP 1 21/c 115.4238; 16.1528; 18.2354
90; 111.508; 90
4226.8Gichumbi, Joel; Friedrich, Holger B.; Zamisa, Sizwe J.
Chlorido{2-[(4-chlorophenyl)iminomethyl]pyridine-κ2 N,N′}(η6-toluene)ruthenium(II) hexafluoridophosphate
IUCrData, 2025, 10, x250103
1574066 CIFMn O3 SrP m -3 m3.806; 3.806; 3.806
90; 90; 90
55.132Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574067 CIFO3 Sr TiP m -3 m3.9059; 3.9059; 3.9059
90; 90; 90
59.589Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574068 CIFMn0.1 O3 Sr Ti0.9P m -3 m3.8959; 3.8959; 3.8959
90; 90; 90
59.132Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574069 CIFMn0.2 O3 Sr Ti0.8P m -3 m3.8874; 3.8874; 3.8874
90; 90; 90
58.746Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574070 CIFMn0.3 O3 Sr Ti0.7P m -3 m3.876; 3.876; 3.876
90; 90; 90
58.231Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574071 CIFMn0.5 O3 Sr Ti0.5P m -3 m3.8602; 3.8602; 3.8602
90; 90; 90
57.521Lebeda, Miroslav; Drahokoupil, Jan; Kamba, Stanislav; Svoboda, Šimon; Smola, Vojtěch; Dabrowski, Bogdan; Vlčák, Petr
Lattice parameters and bulk modulus of SrTi1-xMnxO3 perovskites: A comparison of exchange-correlation functionals with experimental validation
Computational Condensed Matter, 2025, 43, e01030
1574072 CIFC44.22 H41 Cl1.78 F2 N2 PdC 1 c 121.5561; 9.39102; 19.5924
90; 106.024; 90
3812.06Wang, Yan; Dai, Shengyu
Exploring the o-aryl halogen effects of α-diimine Pd(ii) catalysts on ethylene (co)polymerization
Catalysis Science & Technology, 2025, 15, 2822-2828
1574073 CIFC32 H56 B10 Ga I2 N4 Si2C m c m23.2436; 18.9817; 13.9956
90; 90; 90
6174.9Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574074 CIFC32 H56 Al2 B10 I3 N4 Si2P -112.2257; 13.2295; 17.0355
109.939; 102.833; 100.765
2419.65Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574075 CIFC46 H72 Al B10 I2 N4 Si2P -114.6482; 14.829; 18.4781
105.669; 106.625; 100.731
3548.9Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574076 CIFC48 H96 Al B10 I2 K N4 O4 Si2P 1 21/n 114.7194; 30.6034; 15.2868
90; 94.863; 90
6861.4Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574077 CIFC32 H56 Al2 B10 I6 N4 Si2P 1 21/n 114.4094; 17.2943; 23.7145
90; 92.257; 90
5905.1Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574078 CIFC58 H100 Al B10 K N4 O2 Si2P 1 21/c 121.7751; 15.1015; 24.8744
90; 109.723; 90
7699.8Saddington, Artemis; Yao, Shenglai; Lorent, Christian; Driess, Matthias
Redox non-innocent bis-silylene aluminium complexes with a carborane backbone
Chemical Science, 2025, 16, 6383-6391
1574079 CIFC26 H18 N2 Pt SP -111.2341; 13.2688; 17.1255
67.622; 89.72; 65.448
2111.14Tong, Ka-Ming; Toigo, Jessica; Wolf, Michael O.
Deep-blue phosphorescence from platinum(ii) bis(acetylide) complexes with sulfur-bridged dipyridyl ligands.
Chemical science, 2025, 16, 5948-5956
1574080 CIFC28 H22 N2 Pt SP 1 21/n 110.8444; 11.2925; 18.702
90; 96.706; 90
2274.6Tong, Ka-Ming; Toigo, Jessica; Wolf, Michael O.
Deep-blue phosphorescence from platinum(ii) bis(acetylide) complexes with sulfur-bridged dipyridyl ligands.
Chemical science, 2025, 16, 5948-5956
1574081 CIFC26 H18 N2 O Pt SP -17.9676; 11.994; 12.5963
117.424; 97.964; 90.392
1054.74Tong, Ka-Ming; Toigo, Jessica; Wolf, Michael O.
Deep-blue phosphorescence from platinum(ii) bis(acetylide) complexes with sulfur-bridged dipyridyl ligands.
Chemical science, 2025, 16, 5948-5956
1574082 CIFC30 H26 Cl2 N2 O2 Pt SP 1 21/c 110.5828; 26.522; 9.987
90; 99.343; 90
2765.9Tong, Ka-Ming; Toigo, Jessica; Wolf, Michael O.
Deep-blue phosphorescence from platinum(ii) bis(acetylide) complexes with sulfur-bridged dipyridyl ligands.
Chemical science, 2025, 16, 5948-5956
1574083 CIFC28 H22 N2 O Pt SP -19.2869; 12.7332; 21.2615
89.275; 82.262; 71.515
2361.6Tong, Ka-Ming; Toigo, Jessica; Wolf, Michael O.
Deep-blue phosphorescence from platinum(ii) bis(acetylide) complexes with sulfur-bridged dipyridyl ligands.
Chemical science, 2025, 16, 5948-5956
1574084 CIFC12 H16 I2 N4 O SmP 1 21/m 18.94497; 7.9358; 12.43051
90; 93.4456; 90
880.79Viborg, Anton; Dunstan, Maja A.; Yutronkie, Nathan J.; Chanda, Amit; Trier, Felix; Pryds, Nini; Wilhelm, Fabrice; Rogalev, Andrei; Pinkowicz, Dawid; Pedersen, Kasper S.
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Chemical Science, 2025, 16, 6879-6885
1574085 CIFC12 H16 I2 N4 O SmP 1 21/m 19.0249; 8.0968; 12.6429
90; 94.567; 90
920.92Viborg, Anton; Dunstan, Maja A.; Yutronkie, Nathan J.; Chanda, Amit; Trier, Felix; Pryds, Nini; Wilhelm, Fabrice; Rogalev, Andrei; Pinkowicz, Dawid; Pedersen, Kasper S.
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Chemical Science, 2025, 16, 6879-6885
1574086 CIFC12 H16 I2 N4 O SrP 1 21/m 19.0739; 8.2039; 12.7161
90; 94.74; 90
943.366Viborg, Anton; Dunstan, Maja A.; Yutronkie, Nathan J.; Chanda, Amit; Trier, Felix; Pryds, Nini; Wilhelm, Fabrice; Rogalev, Andrei; Pinkowicz, Dawid; Pedersen, Kasper S.
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Chemical Science, 2025, 16, 6879-6885
1574087 CIFC12 H16 Ca I2 N4 OP 1 21/m 18.9739; 7.9879; 12.6087
90; 94.22; 90
901.37Viborg, Anton; Dunstan, Maja A.; Yutronkie, Nathan J.; Chanda, Amit; Trier, Felix; Pryds, Nini; Wilhelm, Fabrice; Rogalev, Andrei; Pinkowicz, Dawid; Pedersen, Kasper S.
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Chemical Science, 2025, 16, 6879-6885
1574088 CIFC12 H16 I2 N4 O SmP 1 21/m 19.07712; 8.15614; 12.7219
90; 94.6744; 90
938.72Viborg, Anton; Dunstan, Maja A.; Yutronkie, Nathan J.; Chanda, Amit; Trier, Felix; Pryds, Nini; Wilhelm, Fabrice; Rogalev, Andrei; Pinkowicz, Dawid; Pedersen, Kasper S.
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Chemical Science, 2025, 16, 6879-6885
1574089 CIFC39 H42 I2 N6 O4P -114.2539; 17.2346; 17.3593
106.528; 102.26; 90.213
3985.7Martínez-Vivas, Sebastián; Poyatos, Macarena; Peris, Eduardo
Fluoride-induced redox-switchable behaviour of a palladium(ii)/(iv) couple
Chemical Science, 2025, 16, 6257-6264
1574090 CIFC40 H42 Br3 Cl2 N6 O4 PdP 1 21/c 111.0685; 27.3218; 14.8974
90; 110.129; 90
4230Martínez-Vivas, Sebastián; Poyatos, Macarena; Peris, Eduardo
Fluoride-induced redox-switchable behaviour of a palladium(ii)/(iv) couple
Chemical Science, 2025, 16, 6257-6264
1574091 CIFC76 H55 B Cl F26 N7 O4 PdP -113.7465; 13.7475; 21.0944
72.438; 78.222; 81.747
3706.2Martínez-Vivas, Sebastián; Poyatos, Macarena; Peris, Eduardo
Fluoride-induced redox-switchable behaviour of a palladium(ii)/(iv) couple
Chemical Science, 2025, 16, 6257-6264
1574092 CIFC138 H96 N12 Pd3P -124.626; 24.7677; 25.97
69.586; 75.581; 63.458
13198.3Yu, Hao; Guo, Ziteng; Tang, Jie; Han, Ningxu; Shi, Junjuan; Li, Meng; Zhang, Houyu; Wang, Ming
Configurational control of low-symmetry heteroleptic metal-organic cages with asymmetric ligands.
Chemical science, 2025, 16, 6114-6120
1574093 CIFC282 H204 N24 Pd6P -3 1 c26.235; 26.235; 46.357
90; 90; 120
27632Yu, Hao; Guo, Ziteng; Tang, Jie; Han, Ningxu; Shi, Junjuan; Li, Meng; Zhang, Houyu; Wang, Ming
Configurational control of low-symmetry heteroleptic metal-organic cages with asymmetric ligands.
Chemical science, 2025, 16, 6114-6120
1574094 CIFC176 H128 N16 Pd4I m -3 m43.65; 43.65; 43.65
90; 90; 90
83167Yu, Hao; Guo, Ziteng; Tang, Jie; Han, Ningxu; Shi, Junjuan; Li, Meng; Zhang, Houyu; Wang, Ming
Configurational control of low-symmetry heteroleptic metal-organic cages with asymmetric ligands.
Chemical science, 2025, 16, 6114-6120
1574095 CIFC99 H107 Cl7 N8 O4 S4P -110.5853; 21.091; 23.544
69.159; 81.645; 89.253
4856Duan, Tainan; Wang, Jia; Zuo, Xiaochan; Zhong, Yanyi; Long, Yuhong; Wang, Peiran; Tu, Kaihuai; Zhong, Cheng; Zhang, Jiangbin; Rakitin, Oleg A.; Yao, Zhaoyang; Wan, Xiangjian; Zhao, Yan; Kan, Bin; Chen, Yongsheng
“Head surgery” of polycyclic o-quinones with cyanated aromatic rings towards high electron mobility acceptors enables 19.6% efficiency in additive-free binary organic solar cells
Energy & Environmental Science, 2025, 18, 3773-3783
1574096 CIFC90 H94 Cl4 N8 O2 S5C 1 2/c 129.131; 22.225; 14.008
90; 111.957; 90
8411Duan, Tainan; Wang, Jia; Zuo, Xiaochan; Zhong, Yanyi; Long, Yuhong; Wang, Peiran; Tu, Kaihuai; Zhong, Cheng; Zhang, Jiangbin; Rakitin, Oleg A.; Yao, Zhaoyang; Wan, Xiangjian; Zhao, Yan; Kan, Bin; Chen, Yongsheng
“Head surgery” of polycyclic o-quinones with cyanated aromatic rings towards high electron mobility acceptors enables 19.6% efficiency in additive-free binary organic solar cells
Energy & Environmental Science, 2025, 18, 3773-3783
1574097 CIFC14 H17 N OP 1 21 18.046; 18.2634; 8.5597
90; 108.345; 90
1193.9Sun, Hao; Yu, Cheng-Long; Zheng, Yu-Qing; Shu, Peng-Fei; Dong, Zhan; Xia, Yu-Chen; Liu, Wen-Bo
Pd-catalyzed enantioselective access to hydrocarbazolones containing contiguous quaternary and tertiary stereocenters
Chemical Science, 2025, 16, 6425-6433
1574098 CIFC23 H24.5 N O1.75P 1 21 18.9633; 18.6929; 11.3785
90; 90.154; 90
1906.46Sun, Hao; Yu, Cheng-Long; Zheng, Yu-Qing; Shu, Peng-Fei; Dong, Zhan; Xia, Yu-Chen; Liu, Wen-Bo
Pd-catalyzed enantioselective access to hydrocarbazolones containing contiguous quaternary and tertiary stereocenters
Chemical Science, 2025, 16, 6425-6433
1574099 CIFC112 H276 Mo12 N40 O138 Pd4 SiP 6355.438; 55.438; 34.467
90; 90; 120
91738Cai, Li-Xuan; Hu, Yu-Hang; Zhou, Li-Peng; Cheng, Pei-Ming; Guo, Xiao-Qing; Chan, Yi-Tsu; Sun, Qing-Fu
Polyoxometalate condensation and transformation mediated by adaptive coordination-assembled molecular flasks
Chemical Science, 2025, 16, 7956-7962
1574100 CIFC112 H319 N40 O151.5 Pd4 W10I 41/a :257.774; 57.774; 36.483
90; 90; 90
121774Cai, Li-Xuan; Hu, Yu-Hang; Zhou, Li-Peng; Cheng, Pei-Ming; Guo, Xiao-Qing; Chan, Yi-Tsu; Sun, Qing-Fu
Polyoxometalate condensation and transformation mediated by adaptive coordination-assembled molecular flasks
Chemical Science, 2025, 16, 7956-7962
1574101 CIFC112 H228 N40 O114 Pd4 Si W12P 1 21/n 133.1786; 35.0845; 58.0136
90; 89.8996; 90
67530.9Cai, Li-Xuan; Hu, Yu-Hang; Zhou, Li-Peng; Cheng, Pei-Ming; Guo, Xiao-Qing; Chan, Yi-Tsu; Sun, Qing-Fu
Polyoxometalate condensation and transformation mediated by adaptive coordination-assembled molecular flasks
Chemical Science, 2025, 16, 7956-7962
1574102 CIFC33 H45 B Cl3 N2 P SiP -19.0296; 9.2046; 23.1133
89.022; 79.051; 63.4122
1681.56Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574103 CIFC36 H54 B N2 P Si2P 1 21/c 111.8487; 10.1385; 30.475
90; 94.814; 90
3648Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574104 CIFC66 H90 B2 K2 N4 P2 Si2P -18.9473; 12.225; 15.6398
87.641; 89.746; 71.362
1619.5Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574105 CIFC43 H59 B F3 N2 O3 P S SiP 1 21/n 116.6108; 10.1947; 25.8173
90; 90.071; 90
4372Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574106 CIFC47 H61 B Ir N2 P SiP -115.2155; 15.695; 18.597
90.735; 105.707; 98.278
4224.5Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574107 CIFC81 H111 B2 Cu2 N4 P3 Si2P 1 21/c 115.9089; 12.3323; 40.245
90; 100.86; 90
7754.4Phang, Si Jia Isabel; Zhang, Zheng-Feng; Su, Ming-Der; So, Cheuk-Wai
An N-phosphinoamidinato borasilenide: a vinyl-analogous anion containing a base-stabilised BSi double bond
Chemical Science, 2025, 16, 6763-6769
1574108 CIFC52 H34 B N O2P b c a9.7393; 24.5507; 30.8103
90; 90; 90
7366.9Li, Quanwei; Zhao, Haisong; Zhao, Jinyang; Cao, Zhongxu; Yu, Chao; Yan, Shouke; Ren, Zhongjie
Enhancing electroluminescence performance of ultra-deep-blue through-space charge transfer emitters with CIEy ≈ 0.05 via methyl-modification
Chemical Science, 2025, 16, 6434-6442
1574109 CIFC54 H38 B N O2P b c a8.8277; 27.8654; 31.786
90; 90; 90
7819Li, Quanwei; Zhao, Haisong; Zhao, Jinyang; Cao, Zhongxu; Yu, Chao; Yan, Shouke; Ren, Zhongjie
Enhancing electroluminescence performance of ultra-deep-blue through-space charge transfer emitters with CIEy ≈ 0.05 via methyl-modification
Chemical Science, 2025, 16, 6434-6442
1574110 CIFC53 H36 B N O2P 1 21/n 116.7197; 8.873; 26.3102
90; 101.453; 90
3825.5Li, Quanwei; Zhao, Haisong; Zhao, Jinyang; Cao, Zhongxu; Yu, Chao; Yan, Shouke; Ren, Zhongjie
Enhancing electroluminescence performance of ultra-deep-blue through-space charge transfer emitters with CIEy ≈ 0.05 via methyl-modification
Chemical Science, 2025, 16, 6434-6442
1574111 CIFC241 H183 Ag7.17 Cl2 Cu39.83 F36 O24 P6 Se18C 1 c 121.2386; 36.7068; 38.4701
90; 98.345; 90
29673.8Sun, Jing; Liu, Jiahe; Su, Hai-Feng; Li, Simin; Tang, Xiongkai; Xie, Zhenlang; Xu, Zhen; Jiang, Wenya; Wei, Jianyu; Gong, Xuekun; He, Ayisha; Wang, Song; Jiang, De-en; Zheng, Nanfeng; Shen, Hui
Eight-electron copper-hydride nanoclusters: synthesis, structure, alloying chemistry and photoluminescence
Chemical Science, 2025, 16, 6392-6401
1574112 CIFC207 H156 Cl6 Cu47 F36 O24 P5 Se15P 63/m21.8398; 21.8398; 33.3259
90; 90; 120
13766.1Sun, Jing; Liu, Jiahe; Su, Hai-Feng; Li, Simin; Tang, Xiongkai; Xie, Zhenlang; Xu, Zhen; Jiang, Wenya; Wei, Jianyu; Gong, Xuekun; He, Ayisha; Wang, Song; Jiang, De-en; Zheng, Nanfeng; Shen, Hui
Eight-electron copper-hydride nanoclusters: synthesis, structure, alloying chemistry and photoluminescence
Chemical Science, 2025, 16, 6392-6401
1574113 CIFC38 H32 Cl4 Cu I O P2P 1 21/c 113.5563; 20.737; 14.8064
90; 116.901; 90
3711.92Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574114 CIFC40 H34 Cu I N2 O P2P 1 21/n 113.3463; 20.206; 14.7519
90; 116.536; 90
3559.1Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574115 CIFC72 H56 Cu2 I2 O2 P4P 1 21/c 113.4634; 18.73432; 23.9159
90; 147.569; 90
3235Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574116 CIFC73.6 H56 Cu2 I2 O5.12 P4P 1 21/n 113.3073; 19.2892; 14.7456
90; 116.688; 90
3381.77Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574117 CIFC36 H28 Cu I O P2P 1 21/c 113.5886; 18.8697; 14.651
90; 117.565; 90
3330.27Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574118 CIFC72.8 H56 Cu2 I2 O3.6 P4P 1 21/c 113.4567; 19.338; 14.8468
90; 116.934; 90
3444.44Zhang, Hong-Jin; Chen, Zong-Ren; Xu, Ji-Tong; Ye, Jia-Wen; Chen, Ling; Chen, Xiao-Ming
CO2-enhanced TADF of an ultra-stable Cu(i) cluster via guest–host π–π interaction
Chemical Science, 2025, 16, 6872-6878
1574119 CIFC16 H17 Cl N4 OI 1 2/a 17.506; 11.5648; 34.8112
90; 90.678; 90
3021.59Zhu, Shiyang; Zhang, Hairuo; Sun, Boyang; Bai, Ziqian; He, Gang; Chen, Gong; Wang, Hao
Nitrene-mediated aminative N–N–N coupling: facile access to triazene 1-oxides
Chemical Science, 2025, 16, 6458-6467
1574120 CIFC24 H14 F2 O4 SP 1 21/c 111.281; 12.9645; 14.2569
90; 111.52; 90
1939.75Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574121 CIFC31 H28 Cl O8 S0.25P 1 21/n 116.8686; 9.1625; 17.9678
90; 107.609; 90
2646.95Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574122 CIFC16 H10 Cl2 N2P 1 21/c 115.4787; 13.8797; 6.2389
90; 100.168; 90
1319.31Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574123 CIFC43 H36 Cl O8 S0.25P 1 21/c 110.5314; 13.6665; 25.0346
90; 92.809; 90
3598.83Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574124 CIFC25 H18 O5 SP 1 21/c 112.6189; 12.2607; 14.3744
90; 112.227; 90
2058.7Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574125 CIFC8 H7 NI 1 2/a 17.4555; 5.7258; 26.8292
90; 92.871; 90
1143.87Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574126 CIFC18 H10 F6 N2C 1 2/c 110.7515; 9.9866; 14.1041
90; 95.72; 90
1506.8Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574127 CIFC9.41 H6.12 O2.12 S1.41P 1 21/n 116.4453; 11.4878; 20.1149
90; 91.894; 90
3798Chang, Meng-Yang; Hsueh, Nai-Chen
One-pot synthesis of diaroyl benzothiepine-1,1-dioxides.
Organic & biomolecular chemistry, 2025, 23, 3572-3582
1574128 CIFC17 H31 Cl2 N Si TiP -16.6617; 17.3131; 28.1245
93.203; 92.284; 95.465
3220.61Kawatsu, Minaho; Fujioka, Taiga; Losio, Simona; Tritto, Incoronata; Nomura, Kotohiro
(Trialkylsilyl-cyclopentadienyl)titanium(iv) dichloride complexes containing ketimide ligands, Cp′TiCl2(NCtBu2) (Cp′ = Me3SiC5H4, Et3SiC5H4), as efficient catalysts for ethylene copolymerisation with norbornene and tetracyclododecene
Catalysis Science & Technology, 2025, 15, 2757-2765
1574129 CIFC20 H37 Cl2 N Si TiP 21 21 2112.2674; 13.776; 14.0063
90; 90; 90
2367Kawatsu, Minaho; Fujioka, Taiga; Losio, Simona; Tritto, Incoronata; Nomura, Kotohiro
(Trialkylsilyl-cyclopentadienyl)titanium(iv) dichloride complexes containing ketimide ligands, Cp′TiCl2(NCtBu2) (Cp′ = Me3SiC5H4, Et3SiC5H4), as efficient catalysts for ethylene copolymerisation with norbornene and tetracyclododecene
Catalysis Science & Technology, 2025, 15, 2757-2765
1574130 CIFC99.5 H88 N2 O4 Si4 TbP -117.3266; 23.1849; 24.3639
93.487; 110.59; 109.064
8487.2Xue, Tianjiao; Yang, Qing-Song; Li, Lei; Chang, Xiao-Yong; Ding, You-Song; Zheng, Zhiping
Supramolecular assemblies of tetravalent terbium complex units: syntheses, structure, and materials properties
Chemical Science, 2025, 16, 6805-6811
1574131 CIFC104 H112 N2 O12 Si4 TbC 1 2/c 122.7842; 18.3307; 23.9399
90; 111.875; 90
9278.6Xue, Tianjiao; Yang, Qing-Song; Li, Lei; Chang, Xiao-Yong; Ding, You-Song; Zheng, Zhiping
Supramolecular assemblies of tetravalent terbium complex units: syntheses, structure, and materials properties
Chemical Science, 2025, 16, 6805-6811
1574132 CIFC105 H92 N2 O4 Si4 TbP -117.784; 21.25; 25.315
109.025; 101.84; 90.039
8828.2Xue, Tianjiao; Yang, Qing-Song; Li, Lei; Chang, Xiao-Yong; Ding, You-Song; Zheng, Zhiping
Supramolecular assemblies of tetravalent terbium complex units: syntheses, structure, and materials properties
Chemical Science, 2025, 16, 6805-6811
1574133 CIFC208 H224 N4 O18 Si8 Tb2F d d d :232.278; 34.1126; 39.4068
90; 90; 90
43390Xue, Tianjiao; Yang, Qing-Song; Li, Lei; Chang, Xiao-Yong; Ding, You-Song; Zheng, Zhiping
Supramolecular assemblies of tetravalent terbium complex units: syntheses, structure, and materials properties
Chemical Science, 2025, 16, 6805-6811
1574134 CIFC210 H188 N4 O8 Si8 Tb2P -117.8325; 21.184; 25.671
109.037; 101.48; 90.122
8960.2Xue, Tianjiao; Yang, Qing-Song; Li, Lei; Chang, Xiao-Yong; Ding, You-Song; Zheng, Zhiping
Supramolecular assemblies of tetravalent terbium complex units: syntheses, structure, and materials properties
Chemical Science, 2025, 16, 6805-6811
1574135 CIFC21 H12 I N SeP 4110.9435; 10.9435; 14.7482
90; 90; 90
1766.25Li, Yuanyuan; Tao, Chenyu; Duan, Longhui; Gu, Zhenhua
Observation of the solvent enantio-isotope effect in asymmetric ring-opening of cyclic diaryliodoniums with selenocyanate
Chemical Science, 2025, 16, 6488-6494
1574136 CIFC22 H21 I N2 O SeP 19.3735; 11.1993; 11.3482
63.903; 80.905; 86.542
1056.34Li, Yuanyuan; Tao, Chenyu; Duan, Longhui; Gu, Zhenhua
Observation of the solvent enantio-isotope effect in asymmetric ring-opening of cyclic diaryliodoniums with selenocyanate
Chemical Science, 2025, 16, 6488-6494
1574137 CIFC272 H264 Cl45 N3 O6P -121.8575; 27.0119; 27.2218
78.849; 76.57; 80.26
15206.9Chen, Yan; Chen, Xingyu; Li, Lin; Chen, Xiangping; Xia, Jianlong; Zhang, Lei
A triply linked propellane-nanoring hybrid serving as a good host
Chemical Science, 2025, 16, 6822-6827
1574138 CIFC82 H88 Cl12C 1 2/c 116.4184; 29.5605; 16.8961
90; 101.849; 90
8025.56Chen, Yan; Chen, Xingyu; Li, Lin; Chen, Xiangping; Xia, Jianlong; Zhang, Lei
A triply linked propellane-nanoring hybrid serving as a good host
Chemical Science, 2025, 16, 6822-6827
1574139 CIFC528 H353 N3 O6P -122.4394; 25.032; 34.7003
84.936; 79.688; 67.852
17756.8Chen, Yan; Chen, Xingyu; Li, Lin; Chen, Xiangping; Xia, Jianlong; Zhang, Lei
A triply linked propellane-nanoring hybrid serving as a good host
Chemical Science, 2025, 16, 6822-6827
1574140 CIFC14 H8 Cl F3 O5 SP -16.6746; 8.0822; 13.784
95.756; 99.723; 97.231
721.43Krammer, Leo; Darnhofer, Barbara; Kljajic, Marko; Liesinger, Laura; Schittmayer, Matthias; Neshchadin, Dmytro; Gescheidt, Georg; Kollau, Alexander; Mayer, Bernd; Fischer, Roland C.; Wallner, Silvia; Macheroux, Peter; Birner-Gruenberger, Ruth; Breinbauer, Rolf
A general approach for activity-based protein profiling of oxidoreductases with redox-differentiated diarylhalonium warheads
Chemical Science, 2025, 16, 6240-6256
1574141 CIFC14 H8 F3 I O5 SP -17.0091; 10.6673; 11.7572
63.23; 75.79; 85.689
760.2Krammer, Leo; Darnhofer, Barbara; Kljajic, Marko; Liesinger, Laura; Schittmayer, Matthias; Neshchadin, Dmytro; Gescheidt, Georg; Kollau, Alexander; Mayer, Bernd; Fischer, Roland C.; Wallner, Silvia; Macheroux, Peter; Birner-Gruenberger, Ruth; Breinbauer, Rolf
A general approach for activity-based protein profiling of oxidoreductases with redox-differentiated diarylhalonium warheads
Chemical Science, 2025, 16, 6240-6256
1574142 CIFC14 H8 Br F3 O5 SP 1 21/n 16.4902; 18.8943; 12.3367
90; 95.462; 90
1505.95Krammer, Leo; Darnhofer, Barbara; Kljajic, Marko; Liesinger, Laura; Schittmayer, Matthias; Neshchadin, Dmytro; Gescheidt, Georg; Kollau, Alexander; Mayer, Bernd; Fischer, Roland C.; Wallner, Silvia; Macheroux, Peter; Birner-Gruenberger, Ruth; Breinbauer, Rolf
A general approach for activity-based protein profiling of oxidoreductases with redox-differentiated diarylhalonium warheads
Chemical Science, 2025, 16, 6240-6256
1574143 CIFC28 H44 Cl N3 O6P 1 21/n 116.3631; 10.4157; 17.9697
90; 105.921; 90
2945.15Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574144 CIFC28 H40 Br N3 O4P 1 21/c 15.8177; 12.2664; 38.8851
90; 93.872; 90
2768.6Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574145 CIFC28 H41 N5 O10P 1 21/n 18.733; 10.044; 34.856
90; 94.022; 90
3049.8Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574146 CIFC30 H48 N3 O9 PP -18.9527; 11.559; 16.499
100.869; 100.793; 97.455
1622.8Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574147 CIFC28 H46 Cl N3 O7P 1 21 19.2405; 12.572; 13.1588
90; 96.847; 90
1517.78Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574148 CIFC28 H47 N3 O15 S2P 1 21/c 111.8559; 34.775; 8.4372
90; 90.259; 90
3478.5Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574149 CIFC56 H84 Cl N6 O13 PP -112.5749; 14.8653; 16.1941
82.653; 80.4795; 76.8419
2894.2Kanagavel, Manimurugan; Sparjan Samuvel, Rajan Marystella; Ramalingam, Vaikundamoorthy; Nechipadappu, Sunil Kumar
Structural landscape of new salts of the antihistamine drug bilastine: implications in physicochemical properties and anticancer activity against skin cancer
CrystEngComm, 2025, 27, 2317-2332
1574150 CIFC57 H77 K N O6 PP -113.0425; 14.2978; 15.5953
95.495; 99.469; 108.484
2686.4Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574151 CIFC57 H77 N Na O8 PP -110.4814; 20.0122; 26.3567
91.519; 99.269; 99.707
5370Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574152 CIFC57.01 H77.01 K N O6 P S2P 1 21/n 112.4061; 40.667; 22.5868
90; 91.183; 90
11393Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574153 CIFC55 H73 N Na O7 PP -112.76; 12.763; 16.898
92.4; 107.37; 91.81
2621.3Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574154 CIFC86 H122 N2 Na2 O12 P2P -114.5215; 18.3696; 20.0346
82.909; 83.658; 77.776
5163.6Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574155 CIFC44.5 H61 N Na O5 PP -114.468; 17.705; 18.868
70.73; 77.25; 75.49
4366.2Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574156 CIFC57 H77 K N O7 PP 1 21/c 110.4542; 20.5804; 25.3528
90; 92.771; 90
5448.3Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574157 CIFC57 H77 K N O8 PP -110.4129; 14.6924; 19.2865
98.68; 90.422; 110.288
2730.22Nasrullah, Ayu Afiqah; Zander, Edgar; Dankert, Fabian; Petrov, Andrey; Surkau, Jonas; Baráth, Eszter; Hering-Junghans, Christian
Coordination isomerism in dioxophosphorane cyanides
Chemical Science, 2025, 16, 6909-6917
1574158 CIFC12 H12 Br F2 N O SP 19.5072; 11.2492; 13.1335
92.018; 92.253; 106.884
1341.42Baldon, Simone; Paut, Julien; Anselmi, Elsa; Dagousset, Guillaume; Tuccio, Béatrice; Pelosi, Giorgio; Cuadros, Sara; Magnier, Emmanuel; Dell’Amico, Luca
Radical photochemical difluorosulfoximination of alkenes and propellanes
Chemical Science, 2025, 16, 6957-6964
1574159 CIF
Paper
C8 H8 N2 SP 21 21 214.438; 10.5115; 17.3105
90; 90; 90
807.54Lange, Erik de; Hosten, Eric Cyriel; Betz, Richard
2-Methyl-4-thiocyanatoaniline
IUCrData, 2025, 10, x250216
1574160 CIFC55 H79 As Ga N4 PP 1 21/c 121.3086; 13.9591; 20.6685
90; 118.573; 90
5399.07Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574161 CIFC68 H93 As Ga N5 O PP 1 21/n 112.2864; 25.6905; 20.8532
90; 92.473; 90
6576.05Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574162 CIFC62 H93 As Ga N4 O2 PP 1 21/c 113.3562; 24.7151; 18.592
90; 91.831; 90
6134.08Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574163 CIFC129.5 H200 As2 Ga2 N8 P2 S4P -118.1433; 18.6339; 20.1323
77.529; 85.25; 79.331
6524.4Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574164 CIFC74 H107 As Ga N6 PP 21 21 2113.4475; 20.8956; 24.4457
90; 90; 90
6869.08Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574165 CIFC68 H107 Ga N4 P2 S2P 1 21 115.3228; 14.2179; 15.4652
90; 92.946; 90
3364.77Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574166 CIFC62 H91 As Ga N7 PP -112.6878; 22.5101; 22.5732
75.984; 77.148; 87.776
6097.57Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574167 CIFC86 H109 As Ga N4 O PP 1 21/c 121.6461; 16.5972; 22.5185
90; 106.036; 90
7775.3Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574168 CIFC57 H79 As Ga N4 O4 PP n a 2116.3651; 18.4812; 18.6521
90; 90; 90
5641.27Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574169 CIFC63 H87 As Ga N4 O P SP n a 2126.5128; 13.4752; 33.7623
90; 90; 90
12062.1Szych, Lilian S.; Bresien, Jonas; Fischer, Lukas; Ernst, Moritz J.; Goicoechea, Jose M.
Reactivity of an arsanyl-phosphagallene: decarbonylation of CO2 and COS to form phosphaketenes
Chemical Science, 2025, 16, 7397-7410
1574170 CIFC176 H80 In8 O64F m m 224.3316; 30.387; 18.6976
90; 90; 90
13824.3Li, Jiantang; Song, Zitong; Zhou, Xia; Wang, Xue; Feng, Meng; Wang, Dongmei; Chen, Banglin
Reticular chemistry guided function customization: a case study of constructing low-polarity channels for efficient C3H6/C2H4 separation
Chemical Science, 2025, 16, 7411-7417
1574171 CIFC29 H31 I N PP 1 21/c 111.1724; 14.0119; 17.0939
90; 99.724; 90
2637.5Wei, Jun-Hua; Xiao, Yao; Luo, Jian-Bin; He, Zi-Lin; Chen, Jing-Hua; Peng, Qing-Peng; Kuang, Dai-Bin
Anion–π interaction guided switchable TADF and low-temperature phosphorescence in phosphonium salts for multiplexed anti-counterfeiting
Chemical Science, 2025, 16, 7239-7248
1574172 CIFC29 H31 B F4 N PP 1 21/n 19.6378; 8.2283; 32.674
90; 94.38; 90
2583.6Wei, Jun-Hua; Xiao, Yao; Luo, Jian-Bin; He, Zi-Lin; Chen, Jing-Hua; Peng, Qing-Peng; Kuang, Dai-Bin
Anion–π interaction guided switchable TADF and low-temperature phosphorescence in phosphonium salts for multiplexed anti-counterfeiting
Chemical Science, 2025, 16, 7239-7248
1574173 CIFC30 H31 F3 N O3 P SP 21 21 219.2871; 13.5822; 21.8141
90; 90; 90
2751.61Wei, Jun-Hua; Xiao, Yao; Luo, Jian-Bin; He, Zi-Lin; Chen, Jing-Hua; Peng, Qing-Peng; Kuang, Dai-Bin
Anion–π interaction guided switchable TADF and low-temperature phosphorescence in phosphonium salts for multiplexed anti-counterfeiting
Chemical Science, 2025, 16, 7239-7248
1574174 CIFC22 H24 B10P 1 21/n 111.896; 12.504; 14.801
90; 99.23; 90
2173.1Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574175 CIFC22 H22 B10 Br2C 1 2/c 130.14; 10.366; 17.799
90; 123.658; 90
4628.7Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574176 CIFC26 H26 B10 SP -19.459; 11.316; 12.775
109.65; 100.826; 99.41
1226.3Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574177 CIFC22 H23 B10 BrC 1 2/c 130.08; 10.105; 17.857
90; 124.97; 90
4448Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574178 CIFC22 H24 B10P 1 21/n 111.912; 12.511; 14.825
90; 99.261; 90
2180.6Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574179 CIFC22 H24 B10P 1 21/n 111.91; 12.514; 14.838
90; 99.142; 90
2183.4Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574180 CIFC30 H28 B10 S2P 1 21/c 111.075; 19.436; 13.485
90; 97.585; 90
2877.3Yuhara, Kazuhiro; Tanaka, Kazuo
Solid-state temperature-dependent luminescence of C,C′-diaryl-o-carboranes based on restriction of excited-state structural relaxation
Chemical Science, 2025, 16, 6495-6506
1574181 CIFC26.25 H23.5 Br Cl0.5 N O2 PP 110.6028; 14.0739; 18.2273
79.307; 73.787; 73.152
2483.4Luo, Shihui; Yuan, Xinzhu; Cheng, Jiangtao; Yang, Zhiping; Huang, Zhongxing; Wang, Jun (Joelle)
Enantioselective Zn-catalyzed hydrophosphinylation of nitrones: an efficient approach for constructing chiral α-hydroxyamino-phosphine oxides
Chemical Science, 2025, 16, 7051-7056
1574182 CIFC66 H46 B2 N2 O2R -3 :H41.575; 41.575; 17.6054
90; 90; 120
26354Wang, Xiaowei; Hua, Tao; Li, Nengquan; Chen, Guohao; Chen, Zhanxiang; Miao, Jingsheng; Cao, Xiaosong; Yang, Chuluo
Narrowband multi-resonance pure-red emitters via enhanced molecular orbital delocalization for high-performance organic light-emitting diodes
Chemical Science, 2025, 16, 7495-7502
1574183 CIFC28 H34 Br K0.89 N2 Na0.11 O10P -17.2681; 10.3927; 19.5823
89.272; 87.184; 87.05
1475.3Zaleskaya-Hernik, Marta; Salam, Rayhanus; González, Mario J.; Wilczek, Marcin; Dobrzycki, Łukasz; Busschaert, Nathalie; Romański, Jan
Squaramide-based ion pair receptors can facilitate transmembrane transport of KCl and zwitterions including highly polar amino acids
Chemical Science, 2025, 16, 6982-6990
1574184 CIFC49 H69 Hf N3 O7P -110.4131; 14.6873; 16.6466
114.844; 102.121; 98.221
2180.8Zhao, Tiankun; Zhang, Qi; Zhao, Jialiu; Mei, Dongyu; Ma, Jing; Correia, Isabel; Yang, Zhongduo; Kim, Sa-Hyun; Huhn, Thomas
Synthesis and X-ray structure analysis of cytotoxic 2-picolylamino-type Hf<sup>IV</sup>-bis-chelated complexes.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 6674-6683
1574185 CIFC43 H52 Cl Hf N3 O6P 1 21/n 114.8827; 21.1323; 16.3445
90; 113.719; 90
4706.2Zhao, Tiankun; Zhang, Qi; Zhao, Jialiu; Mei, Dongyu; Ma, Jing; Correia, Isabel; Yang, Zhongduo; Kim, Sa-Hyun; Huhn, Thomas
Synthesis and X-ray structure analysis of cytotoxic 2-picolylamino-type Hf<sup>IV</sup>-bis-chelated complexes.
Dalton transactions (Cambridge, England : 2003), 2025, 54, 6674-6683
1574186 CIFC80 H60 N6 O13C 1 2 120.1153; 24.4281; 15.72562
90; 89.9918; 90
7727.23Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574187 CIFC55 H38 Cl4 N4 O8R 3 2 :H24.6956; 24.6956; 25.1324
90; 90; 120
13274.1Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574188 CIFC193 H141 Cl21 N12 O24R 3 2 :H24.0509; 24.0509; 25.9832
90; 90; 120
13016.3Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574189 CIFC55 H38 Cl4 N4 O8R 3 2 :H24.712; 24.712; 25.1045
90; 90; 120
13276.9Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574190 CIFC57 H40 Cl2 N4 O8R 3 :H24.6536; 24.6536; 25.2258
90; 90; 120
13278.1Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574191 CIFC180 H120 N12 O24R 3 2 :H24.0472; 24.0472; 25.966
90; 90; 120
13003.6Cui, Jialin; Wang, Hui; Liu, Hui; Yu, Hailong; Wang, Wei; Wang, Yu; Zhao, Yingjie
Single-crystal chiral two-dimensional supramolecular organic frameworks for tunable circularly polarized luminescence
Chemical Science, 2025, 16, 7513-7522
1574192 CIFC84 H80 Cl6 O4 S2I 1 2/a 125.5478; 20.7666; 31.3909
90; 110.188; 90
15631Zhang, Ruiying; Chen, Xinyu; Zhu, Lingyun; Huang, Yanxia; Zhai, Zi'ang; Wang, Qiang; Wang, Lingding; Wang, Taosong; Wang, Wei-Zhen; Ye, Ke-Yin; Li, Yuanming
Thiophene-backbone arcuate graphene nanoribbons: shotgun synthesis and length dependent properties
Chemical Science, 2025, 16, 7366-7373
1574193 CIFC82 H78 S2P 1 21/c 110.3995; 16.4712; 40.5773
90; 91.448; 90
6948.36Zhang, Ruiying; Chen, Xinyu; Zhu, Lingyun; Huang, Yanxia; Zhai, Zi'ang; Wang, Qiang; Wang, Lingding; Wang, Taosong; Wang, Wei-Zhen; Ye, Ke-Yin; Li, Yuanming
Thiophene-backbone arcuate graphene nanoribbons: shotgun synthesis and length dependent properties
Chemical Science, 2025, 16, 7366-7373
1574194 CIF
Paper
C18 H18 Fe N10 OP b c n32.5164; 8.8531; 13.5952
90; 90; 90
3913.7Setifi, Fatima; Setifi, Zouaoui; Reuter, Hans; Al-Douh, Mohammad Hadi; Addala, Abderezak
Bis(azido-κN)bis(quinolin-8-amine-κ2 N,N′)iron(II) monohydrate
IUCrData, 2025, 10, x250235
1574195 CIFC40.5 H61 Mo O3 P2 SP -111.6654; 19.2138; 19.8632
93.254; 103.495; 105.235
4143.8Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574196 CIFC35 H55 I Mo N P2 SP -110.0985; 12.043; 16.428
76.957; 82.444; 73.782
1863.9Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574197 CIFC41 H65.5 Mo N O2 P2 SP c c a31.877; 14.204; 18.861
90; 90; 90
8540Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574198 CIFC41 H63 Cl I Mo N P2 SP 1 21/c 118.017; 13.531; 18.041
90; 97.035; 90
4365.1Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574199 CIFC38 H63.5 Mo N5 O0.75 P2 SP c c a31.9495; 14.14073; 18.9898
90; 90; 90
8579.39Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574200 CIFC37 H60 Cl3 Mo O0.5 P2 SC 1 2/c 137.379; 11.6548; 37.069
90; 90.266; 90
16149Mandal, Souvik; Zhou, Xiaoguang; Bruch, Quinton J.; Allen, Rachel N.; Giordano, Laurence W.; Walker, Nicholas J. I.; Emge, Thomas J.; Hasanayn, Faraj; Miller, Alexander J. M.; Malakar, Santanu; Goldman, Alan S.
Dinitrogen reduction to ammonia with a pincer-Mo complex: new insights into the mechanism of nitride-to-ammonia conversion
Chemical Science, 2025, 16, 7347-7365
1574201 CIFC17 H14 F3 N3 O2 SP -14.9533; 16.174; 32.778
101.872; 93.3; 97.149
2540.5Zhou, Zhengzheng; Joshi, Vikram Chandrashekhar; Guo, Yiwang; Xiang, Tianyi; Wang, Zijian; Sun, Changquan Calvin
How elastically flexible can molecular crystals be? - a new record.
Chemical science, 2025, 16, 5797-5802
1574202 CIFC183 H177 Ag14 O21 P7 Pt S6P -119.411; 20.798; 27.8
81.778; 75.137; 83.738
10705Liu, Tingting; Li, Yuansheng; Zuo, Yang; Ma, Along; Wang, Yifei; Zhang, Shuo; Ma, Xiaoshuang; Yin, Zhengmao; Yang, Junxian; Wang, Shuxin
Impact of free valence electron contraction on the optical and electrocatalytic properties of nanoclusters: based on M<sub>1</sub>Ag<sub>14</sub> (M = Pt/Pd) series nanoclusters.
Nanoscale, 2025, 17, 10886-10891
1574203 CIFC32 H32 F3 O4 P SP c a 2117.014; 9.10342; 18.838
90; 90; 90
2917.73Curran, Dara T.; Szydło, Marcin; Müller-Bunz, Helge; Nikitin, Kirill; Byrne, Peter A.
Direct synthesis of ethers from alcohols & aldehydes enabled by an oxocarbenium ion interception strategy
Chemical Science, 2025, 16, 6991-7003
1574204 CIFC29 H25 Cl3 F3 O4 P SP 1 21/n 19.49648; 16.7085; 18.7984
90; 95.9804; 90
2966.55Curran, Dara T.; Szydło, Marcin; Müller-Bunz, Helge; Nikitin, Kirill; Byrne, Peter A.
Direct synthesis of ethers from alcohols & aldehydes enabled by an oxocarbenium ion interception strategy
Chemical Science, 2025, 16, 6991-7003
1574205 CIFC32 H32 N10 O12 Zn2C 1 2/c 19.7701; 13.8333; 25.5578
90; 95.956; 90
3435.56Koirala, Shailendra; Gaspar, Miguel A.; Wijesundara, Yalini H.; Li, Dong-Hao; Gadhvi, Jashkaran G.; Ehrman, Ryanne N.; Cornelius, Samuel A.; Mariasoosai, Charles; Nguyen, Thien-Quang N.; Trashi, Orikeda; Trashi, Ikeda; Kumari, Sneha; Hagge, Laurel M.; Howlett, Thomas S.; Torabifard, Hedieh; Smith, Bradley D.; De Nisco, Nicole J.; Gassensmith, Jeremiah J.
Fluorescent molecular probe for in vivo and in vitro targeting and imaging of an intracellular bacterial infection
Chemical Science, 2025, 16, 7902-7911
1574206 CIFC38 H37 F6 N9 O11 Zn2P -110.165; 10.5732; 20.3723
100.082; 101.234; 94.294
2100.92Koirala, Shailendra; Gaspar, Miguel A.; Wijesundara, Yalini H.; Li, Dong-Hao; Gadhvi, Jashkaran G.; Ehrman, Ryanne N.; Cornelius, Samuel A.; Mariasoosai, Charles; Nguyen, Thien-Quang N.; Trashi, Orikeda; Trashi, Ikeda; Kumari, Sneha; Hagge, Laurel M.; Howlett, Thomas S.; Torabifard, Hedieh; Smith, Bradley D.; De Nisco, Nicole J.; Gassensmith, Jeremiah J.
Fluorescent molecular probe for in vivo and in vitro targeting and imaging of an intracellular bacterial infection
Chemical Science, 2025, 16, 7902-7911
1574207 CIFC36 H64 Cr O2 Si5P 1 21/m 112.061; 15.143; 12.602
90; 97.363; 90
2282.6Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574208 CIFC36 H64 O2 Si5 WP -111.5444; 12.8236; 15.6549
75.7391; 73.0022; 83.412
2145.74Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574209 CIFC56 H86 Mo N2 O4 Si5P 1 21/c 114.6764; 15.6767; 26.4415
90; 93.7959; 90
6070.25Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574210 CIFC63 H94 N2 O4 Si5 WP 1 21/c 113.441; 14.406; 34.6694
90; 99.326; 90
6624.34Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574211 CIFC44 H84 Mo N4 O2 Si7P 1 21/n 112.1671; 42.6785; 12.6572
90; 118.635; 90
5768.7Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574212 CIFC45 H75 Mo N O2 Si5P 1 21/n 113.2535; 22.9327; 16.6254
90; 98.153; 90
5002Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574213 CIFC36 H64 Mo O2 Si5P -111.5351; 12.8114; 15.6333
75.707; 73.035; 83.321
2138.9Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574214 CIFC40 H72 Mo O3 Si5P b c a17.438; 16.527; 33.683
90; 90; 90
9707Tomer, Kanishk; Schnakenburg, Gregor; Das, Ujjal; Filippou, Alexander C.
Metal–silicon triple bonds: reactivity of the silylidyne complexes [Cp*(CO)2M≡Si–Tbb] (M = Cr – W)
Chemical Science, 2025, 16, 7773-7793
1574215 CIFC112 H112 B4 F16 N20 O8 Pd PtP 1 21/m 19.683; 23.8429; 28.0717
90; 99.385; 90
6394.19Gearing, Hayden B.; Cziferszky, Monika; Söhnel, Tilo; Wright, L. James; Crowley, James D.; Hartinger, Christian G.
Pd(μ-L)4Pt vs. Pd(μ-L)4RuCl2: chlorido ancillary ligands as defining factors in the host–guest interactions of M(μ-L)4M′ heterodimetallic supramolecular architectures
Chemical Science, 2025, 16, 7294-7301
1574216 CIFC118 H134 Cl2 N16 O13 Pd Ru S9P 4/n c c :218.039; 18.039; 41.9278
90; 90; 90
13643.5Gearing, Hayden B.; Cziferszky, Monika; Söhnel, Tilo; Wright, L. James; Crowley, James D.; Hartinger, Christian G.
Pd(μ-L)4Pt vs. Pd(μ-L)4RuCl2: chlorido ancillary ligands as defining factors in the host–guest interactions of M(μ-L)4M′ heterodimetallic supramolecular architectures
Chemical Science, 2025, 16, 7294-7301
1574217 CIFC128 H128 B2 F8 N22 O16 Pd Pt S2P -115.47952; 19.9749; 21.2142
79.4685; 84.6071; 73.5233
6177.96Gearing, Hayden B.; Cziferszky, Monika; Söhnel, Tilo; Wright, L. James; Crowley, James D.; Hartinger, Christian G.
Pd(μ-L)4Pt vs. Pd(μ-L)4RuCl2: chlorido ancillary ligands as defining factors in the host–guest interactions of M(μ-L)4M′ heterodimetallic supramolecular architectures
Chemical Science, 2025, 16, 7294-7301
1574218 CIFC66 H54 N2 O2P 1 n 117.9514; 7.1173; 18.5132
90; 97.763; 90
2343.7Chen, Xu-Lang; Yu, Si-Qian; Zheng, Zi-You; Cheng, Zhao-Yi; Chen, An-Na; Liang, Jia-Qi; Sun, Xin; Zheng, Chunyang; Huang, Xiaohuan; Gong, Han-Yuan
Adaptive nitrogen-containing buckybowl: a versatile receptor for curved and planar aromatic molecules
Chemical Science, 2025, 16, 7537-7543
1574219 CIFC24 H30 N2 O4P 21 21 218.4366; 11.2441; 22.9481
90; 90; 90
2176.9Maity, Anirban; Balanna, Kuruva; Daniliuc, Constantin G.; Studer, Armido
Diastereoselective 1,3-nitrooxygenation of bicyclo[1.1.0]butanes
Chemical Science, 2025, 16, 7264-7269
1574220 CIFC4 N0.5 O10 Si5P 1 21/c 19.3494; 11.9607; 11.0756
90; 93.013; 90
1236.8Kemp, Kingsley Christian; Altundal, Ömer F.; Jo, Donghui; Huang, Weidong; Wang, Qiang; Deng, Feng; Sastre, German; Hong, Suk Bong
The role of structural defects in the fluoride-mediated synthesis of aluminosilicate zeolites
Chemical Science, 2025, 16, 7579-7589
1574221 CIFC4 N0.5 O10 Si5C 1 2/c 120.8038; 11.76087; 10.96997
90; 118.744; 90
2353.29Kemp, Kingsley Christian; Altundal, Ömer F.; Jo, Donghui; Huang, Weidong; Wang, Qiang; Deng, Feng; Sastre, German; Hong, Suk Bong
The role of structural defects in the fluoride-mediated synthesis of aluminosilicate zeolites
Chemical Science, 2025, 16, 7579-7589
1574222 CIFC24 H26 N4 PtP c a 2126.4912; 11.0501; 22.145
90; 90; 90
6482.5Dang, Vinh Q.; Jiang, Chenggang; Teets, Thomas S.
Enhanced blue phosphorescence in platinum acetylide complexes via a secondary heavy metal and anion-controlled aggregation
Chemical Science, 2025, 16, 7302-7310
1574223 CIFC50 H56 Ag2 Cl4 F12 N8 P2 Pt2P 1 21/n 111.611; 13.011; 21.235
90; 101.158; 90
3147Dang, Vinh Q.; Jiang, Chenggang; Teets, Thomas S.
Enhanced blue phosphorescence in platinum acetylide complexes via a secondary heavy metal and anion-controlled aggregation
Chemical Science, 2025, 16, 7302-7310
1574224 CIFC36 H38 N4 PtP -111.975; 15.698; 19.951
79.386; 84.09; 71.728
3496.3Dang, Vinh Q.; Jiang, Chenggang; Teets, Thomas S.
Enhanced blue phosphorescence in platinum acetylide complexes via a secondary heavy metal and anion-controlled aggregation
Chemical Science, 2025, 16, 7302-7310
1574225 CIFC53 H64 Cl2 Cu2 F12 N8 O P2 Pt2P -110.1312; 13.882; 25.808
89.634; 78.885; 75.512
3445Dang, Vinh Q.; Jiang, Chenggang; Teets, Thomas S.
Enhanced blue phosphorescence in platinum acetylide complexes via a secondary heavy metal and anion-controlled aggregation
Chemical Science, 2025, 16, 7302-7310
1574226 CIFC74 H60 B2 F8 Fe N28 O12P -111.012; 13.113; 14.893
80.8; 82.41; 67.88
1960.6Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574227 CIFC74 H60 B2 F8 Fe N28 O12P -110.747; 13.208; 14.68
93.24; 99.84; 113.19
1869.5Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574228 CIFC11 H8 N4 O2P -14.283; 9.818; 12.062
84.15; 81.63; 79.92
492.5Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574229 CIFC74 H60 B2 F8 Fe N28 O12P -110.755; 13.221; 14.686
93.25; 99.83; 113.15
1874.1Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574230 CIFC74 H60 B2 F8 Fe N28 O12P -110.816; 13.308; 14.753
93.25; 99.7; 112.47
1917.1Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574231 CIFC74 H60 B2 F8 Fe N28 O12P -110.71; 12.918; 14.735
81.53; 82.54; 68.41
1868.6Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574232 CIFC22 H16 N8 O4P -16.597; 12.473; 12.691
101.07; 99.32; 97.21
998Kaźmierczak, Marcin; Weselski, Marek; Siczek, Miłosz; Wolny, Juliusz A.; Schünemann, Volker; Bronisz, Robert
[2 + 2] Photocyclization converts thermally induced spin crossover effect into “hidden hysteresis” one
Chemical Science, 2025, 16, 7884-7893
1574233 CIF
Paper
C11 H16 N2 O2 SeP 1 21/n 17.4231; 13.2052; 12.2802
90; 99.725; 90
1186.45Schollmeyer, Dieter; Detert, Heiner
rac-4H,5H,6H,7H,8H,9H,10H,11H-Cyclodeca[d][1,2,3]selenadiazole-8-carboxylic acid
IUCrData, 2025, 10, x250242
1574234 CIFC16 H14 N4 OP 21 21 217.0728; 12.2024; 16.3422
90; 90; 90
1410.42R., Nandini; Kempegowda, Byresh B.; Srinivasa, Sudhanva M.; Kshirsagar, Umesh A.; Malecki, Jan Grzegorz; Patil, Siddappa A.; Shaikh, Shoyebmohamad F.; Mane, Manoj V.; Dateer, Ramesh B.
Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study
Catalysis Science & Technology, 2025, 15, 2878-2887
1574235 CIFC15 H11 Cl N4 OP 21 21 217.0038; 12.3433; 16.3586
90; 90; 90
1414.2R., Nandini; Kempegowda, Byresh B.; Srinivasa, Sudhanva M.; Kshirsagar, Umesh A.; Malecki, Jan Grzegorz; Patil, Siddappa A.; Shaikh, Shoyebmohamad F.; Mane, Manoj V.; Dateer, Ramesh B.
Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study
Catalysis Science & Technology, 2025, 15, 2878-2887
1574236 CIFC22 H18 N4 O2P -18.7311; 9.24; 12.135
98.305; 97.293; 105.502
919.31R., Nandini; Kempegowda, Byresh B.; Srinivasa, Sudhanva M.; Kshirsagar, Umesh A.; Malecki, Jan Grzegorz; Patil, Siddappa A.; Shaikh, Shoyebmohamad F.; Mane, Manoj V.; Dateer, Ramesh B.
Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study
Catalysis Science & Technology, 2025, 15, 2878-2887
1574237 CIFC21 H15 F N4 OP -17.6099; 9.9948; 12.3384
101.58; 91.165; 107.833
871.8R., Nandini; Kempegowda, Byresh B.; Srinivasa, Sudhanva M.; Kshirsagar, Umesh A.; Malecki, Jan Grzegorz; Patil, Siddappa A.; Shaikh, Shoyebmohamad F.; Mane, Manoj V.; Dateer, Ramesh B.
Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study
Catalysis Science & Technology, 2025, 15, 2878-2887
1574238 CIFC22 H18 N4 OP -17.5949; 9.8677; 12.6331
80.581; 89.927; 73.743
895.67R., Nandini; Kempegowda, Byresh B.; Srinivasa, Sudhanva M.; Kshirsagar, Umesh A.; Malecki, Jan Grzegorz; Patil, Siddappa A.; Shaikh, Shoyebmohamad F.; Mane, Manoj V.; Dateer, Ramesh B.
Sustainable copper nanocomposite for multicomponent synthesis of triazolo quinolines and triazolyl benzamide derivatives and their bioactivity study
Catalysis Science & Technology, 2025, 15, 2878-2887
1574239 CIFC12 H12 Fe0.67 N8 Zn1.33I 41 c d23.4527; 23.4527; 12.5316
90; 90; 90
6892.7León-Alcaide, Luis; Castillo-Blas, Celia; Martin-Diaconescu, Vlad; da Silva, Ivan; Keen, David A.; Bennett, Thomas D.; Mínguez Espallargas, Guillermo
Solvent-free approach for the synthesis of heterometallic Fe–Zn-ZIF glass via a melt-quenched process
Chemical Science, 2025, 16, 7946-7955
1574240 CIFC24 H26 Fe N16 Zn2P 1 21/c 110.3884; 13.2702; 10.4428
90; 92.554; 90
1438.17León-Alcaide, Luis; Castillo-Blas, Celia; Martin-Diaconescu, Vlad; da Silva, Ivan; Keen, David A.; Bennett, Thomas D.; Mínguez Espallargas, Guillermo
Solvent-free approach for the synthesis of heterometallic Fe–Zn-ZIF glass via a melt-quenched process
Chemical Science, 2025, 16, 7946-7955
1574241 CIFC28 H29 N3 O3P n a 2117.517; 14.5182; 9.5517
90; 90; 90
2429.1Patra, Koushik; Deb, Samiran; Kumar Choutipalli, Venkata Surya; Mulani, Sana; Mallik, Sumitava; Subramanian, Venkatesan; Baidya, Mahiuddin
Transforming 2D azolium salts to 3D caged tertiary amines via stereoselective dearomative cascade annulation
Chemical Science, 2025, 16, 7551-7559
1574242 CIFC23 H26 Br2 Cl2 N4 PdC 1 2/c 114.4693; 9.1908; 19.4408
90; 99.968; 90
2546.3Lodge, Rhys W.; Cull, William J.; Weilhard, Andreas; Argent, Stephen P.; Alves Fernandes, Jesum; Khlobystov, Andrei N.
A nanoscale chemical oscillator: reversible formation of palladium nanoparticles in ionic liquid.
Nanoscale, 2025, 17, 10105-10116
1574243 CIFC H N OP 1 21/c 18.5019; 31.998; 9.5689
90; 109.195; 90
2458.4Banik, Dipanjan; Banerjee, Shilpita; Halder, Satyajit; Ganguly, Rajdeep; Karak, Anirban; Ghosh, Pintu; Jana, Kuladip; Mahapatra, Ajit Kumar
A dual-responsive ratiometric fluorescent probe for the detection of hypochlorite and hydrazine in environmental samples, live cells, and plant tissues.
Analytical methods : advancing methods and applications, 2025, 17, 3290-3304
1574244 CIFC20 H14 B F3 N2P 1 21/c 124.4631; 9.3458; 15.1792
90; 106.165; 90
3333.17Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574245 CIFC33 H40 B Li N2 O2P 21 21 2111.2851; 15.51; 17.2399
90; 90; 90
3017.53Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574246 CIFC23 H23 B N2P 1 21/c 110.5979; 15.3284; 11.9288
90; 104.056; 90
1879.8Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574247 CIFC19 H15 B N2P 1 21/n 111.2275; 9.6336; 13.9575
90; 101.194; 90
1480.94Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574248 CIFC35 H51 B F N3P 1 21/n 19.8105; 16.1727; 20.3437
90; 97.146; 90
3202.71Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574249 CIFC22 H21 B N2P 1 21/c 113.3766; 12.6462; 11.1821
90; 110.669; 90
1769.85Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574250 CIFC20 H17 B N2 OP -16.5265; 9.4226; 14.2267
106.057; 93.734; 100.512
820.44Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574251 CIFC16 H19 B N2 O SiP -18.8219; 9.3512; 10.407
84.139; 68.542; 74.66
770.54Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574252 CIFC14 H13 B N2P c a 2123.6005; 6.8997; 14.1673
90; 90; 90
2306.95Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574253 CIFC13 H11 B N2 OP 1 21/c 112.4734; 10.9242; 15.9763
90; 90.072; 90
2176.96Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574254 CIFC41 H56 B N3C 1 2/c 112.2633; 17.3966; 16.986
90; 105.539; 90
3491.33Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574255 CIFC36 H50 B N4 OP 1 c 117.0832; 10.345; 18.6658
90; 91.804; 90
3297.09Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574256 CIFC36 H51 B N4P -19.5035; 18.6014; 19.0874
87.741; 87.477; 78.256
3298.8Wüst, Leonie; Chorbacher, Johannes; Wellnitz, Tim; Nees, Samuel; Helten, Holger; Braunschweig, Holger
Synthetic access to organyl-substituted 1,2,3-benzodiazaborines with turn-on fluorescence activity
Chemical Science, 2025, 16, 7284-7293
1574257 CIFC12 H10 F3 N3 O2P n a 2113.4921; 17.9826; 5.1708
90; 90; 90
1254.56Ji, Tingting; Yang, Xuesong; Chen, Quanliang; Zhang, Hongyu
Decimeter-length elastic organic crystals capable of mechanical post-processing and optical waveguide modulation at 77 K
Chemical Science, 2025, 16, 8099-8107
1574258 CIFC11 H8 F3 N3 OP 1 21/n 19.6318; 6.3855; 17.9069
90; 93.53; 90
1099.25Ji, Tingting; Yang, Xuesong; Chen, Quanliang; Zhang, Hongyu
Decimeter-length elastic organic crystals capable of mechanical post-processing and optical waveguide modulation at 77 K
Chemical Science, 2025, 16, 8099-8107
1574259 CIFC12 H10 F3 N3 O2P n a 2113.3841; 17.8129; 5.0896
90; 90; 90
1213.41Ji, Tingting; Yang, Xuesong; Chen, Quanliang; Zhang, Hongyu
Decimeter-length elastic organic crystals capable of mechanical post-processing and optical waveguide modulation at 77 K
Chemical Science, 2025, 16, 8099-8107
1574260 CIFC11 H8 F3 N3 OP 1 21/n 19.7492; 6.1659; 18.7972
90; 91.957; 90
1129.29Ji, Tingting; Yang, Xuesong; Chen, Quanliang; Zhang, Hongyu
Decimeter-length elastic organic crystals capable of mechanical post-processing and optical waveguide modulation at 77 K
Chemical Science, 2025, 16, 8099-8107
1574261 CIFC97 H132 B Cl Ge2 O2P -113.3309; 17.1204; 20.0227
78.851; 72.034; 84.771
4262.5Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574262 CIFC100 H127 B Cl Ge2 O3P -114.1976; 14.5282; 22.8599
87.845; 74.458; 75.249
4390.7Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574263 CIFC106 H140 B Cl Ge2 O2P 1 21/n 119.5707; 18.9384; 26.3009
90; 107.021; 90
9321.1Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574264 CIFC95 H116 B Cl Ge2 OP -113.5962; 16.671; 20.1773
81.8234; 87.251; 84.0915
4500.3Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574265 CIFC95 H118 B Cl Ge2 OP -113.7734; 16.6004; 20.096
83.116; 85.997; 84.814
4534.9Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574266 CIFC114.5 H150 B Cl Ge2 O2P 1 2/c 125.9105; 14.4062; 28.4018
90; 109.755; 90
9977.7Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574267 CIFC103 H136 B Cl Ge2 O3P -114.4877; 18.0318; 18.9385
77.231; 89.503; 73.895
4628.4Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574268 CIFC99 H118 B Cl Ge2 OP -115.9892; 19.2578; 20.5718
102.631; 112.298; 106.577
5221.48Kern, Ralf H.; Hiller, Noemi; Eichele, Klaus; Schubert, Hartmut; Tönshoff, Christina; Bettinger, Holger F.; Wesemann, Lars
Boradigermaallyl: inhibition of CH bond activation by borane CO adduct formation followed by CO insertion
Chemical Science, 2025, 16, 7759-7765
1574269 CIFC11 H15 F O2P -16.56; 14.795; 17.736
100.253; 98.746; 100.247
1636.6Trevisan, Lucia; Bond, Andrew D.; Hunter, Christopher A.
Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups
Chemical Science, 2025, 16, 7418-7423
1574270 CIFC11 H15 N O4P c c n13.7547; 19.2286; 8.4326
90; 90; 90
2230.28Trevisan, Lucia; Bond, Andrew D.; Hunter, Christopher A.
Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups
Chemical Science, 2025, 16, 7418-7423
1574271 CIFC34 H31 B2 N3 O2P 1 21 19.582; 43.689; 15.6237
90; 90.164; 90
6540.5Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574272 CIFC36 H17 B2 F18 N3 O2P 1 21/n 115.472; 16.178; 15.892
90; 109.432; 90
3751.3Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574273 CIFC30 H22 B2 Cl N3 O2P -110.3708; 11.0431; 11.9274
86.785; 74.699; 74.116
1267.07Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574274 CIFC32 H27 B2 N3 O2P -19.6663; 10.0753; 14.4164
92.413; 101.539; 93.307
1371.29Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574275 CIFC54 H40 B4 N6 O4P -115.483; 16.607; 18.455
63.503; 76.5; 65.205
3849Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574276 CIFC30 H23 B2 N3 O2P -19.9773; 10.9806; 13.4862
74.857; 79.474; 63.421
1271.77Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574277 CIFC38 H27 B2 N3 O2 SC 1 2/c 129.2198; 9.7169; 23.8263
90; 104.397; 90
6552.5Yu, Changjiang; Cheng, Chao; Liu, Zhangzhan; Ni, Zhigang; Zhao, Zujin; Lu, Hua; Hao, Erhong; Jiao, Lijuan
A novel boron-stereogenic fluorophore with dual-state circular polarization luminescence via a self-dispersing strategy
Chemical Science, 2025, 16, 7971-7980
1574278 CIF
Paper
C38 H34 Ag N O4 P2C 1 2/c 122.6427; 15.6971; 20.1469
90; 106.08; 90
6880.55Malan, Frederick P.; Potgieter, Kariska; Meijboom, Reinout
Bis[(2-methoxyphenyl)diphenylphosphane-κP](nitrito-κ2 O,O′)silver(I)
IUCrData, 2025, 10, x250193
1574279 CIF
Paper
C24 H28 N4 O8P 1 21/c 119.1096; 13.69762; 18.5399
90; 96.4031; 90
4822.66Palacios Rodríguez, José Carlos; Mendoza, Angel; Sosa Rivadeneyra, Martha; Bernès, Sylvain
2-[3-(1H-Benzimidazol-2-yl)propyl]-1H-benzimidazol-3-ium 3,4,5-trihydroxybenzoate trihydrate
IUCrData, 2025, 10, x250256
1574280 CIFC97 H86 Cl2 N38 O46P 21 21 2116.666; 21.729; 34.167
90; 90; 90
12373Liu, Jia; Han, Xiujie; Wen, Xin; Yu, Hao; Li, Bao; Wang, Ming; Liu, Minghua; Wu, Guanglu
Chiral ring-in-ring complexes with torsion-induced circularly polarized luminescence
Chemical Science, 2025, 16, 7858-7863
1574281 CIFC168 H144 Au12 Cl24 F12 Ir P14R -3 :H18.8392; 18.8392; 46.1573
90; 90; 120
14187.2Mutoh, Katsuya; Yahagi, Teppei; Takano, Shinjiro; Kawakita, Sonomi; Iwasa, Takeshi; Taketsugu, Tetsuya; Tsukuda, Tatsuya; Nakashima, Takuya
A nearly perfect icosahedral Ir@Au12 superatom with superior photoluminescence obtained by ligand engineering
Chemical Science, 2025, 16, 8240-8246
1574282 CIFC12 H8 Fe I2 O5 Pb3C m c e18.3688; 10.6562; 21.9752
90; 90; 90
4301.5Yin, Jinlin; He, Yani; Sun, Chen; Jiang, Yilin; Fei, Honghan
Coordination-driven assembly of a ferrocene-functionalized lead iodide framework with enhanced stability and charge transfer for photocatalytic CO2-to-CH3OH conversion
Chemical Science, 2025, 16, 8327-8337
1574283 CIFC70 H68 Br2 N6 O4 Si2P 1 21 17.1097; 31.4596; 14.5274
90; 97.891; 90
3218.55Cao, Qiuhui; Yang, Yuntian; Mei, Yiwen; Ji, Minghui; Wang, Fei; Feng, Xiaoming; Cao, Weidi
Catalytic asymmetric construction of 1,5-remote Si- and C-stereocenters via desymmetrizing ene reaction of bis(methallyl)silanes
Chemical Science, 2025, 16, 8454-8459
1574284 CIFC72 H106 F12 N6 Ni O15 S4P 1 21 114.5272; 18.2708; 16.2
90; 111.107; 90
4011.4Cao, Qiuhui; Yang, Yuntian; Mei, Yiwen; Ji, Minghui; Wang, Fei; Feng, Xiaoming; Cao, Weidi
Catalytic asymmetric construction of 1,5-remote Si- and C-stereocenters via desymmetrizing ene reaction of bis(methallyl)silanes
Chemical Science, 2025, 16, 8454-8459
1574286 CIFC33 H36 B2 Cl2 N2P 1 21/n 110.9726; 22.2877; 11.9968
90; 103.335; 90
2854.76Zuo, Jingyao; Lalancette, Roger A.; Prokopchuk, Demyan E.; Jäkle, Frieder
Regioselective access to B–N Lewis pair-functionalized anthracenes: mechanistic studies and optoelectronic properties
Chemical Science, 2025, 16, 8114-8124
1574287 CIFC33 H36 B2 Cl2 N2C 1 2/c 125.6047; 7.5629; 15.1153
90; 103.019; 90
2851.78Zuo, Jingyao; Lalancette, Roger A.; Prokopchuk, Demyan E.; Jäkle, Frieder
Regioselective access to B–N Lewis pair-functionalized anthracenes: mechanistic studies and optoelectronic properties
Chemical Science, 2025, 16, 8114-8124
1574288 CIFC20 H15 F6 I N2 O4P -18.3251; 8.8817; 14.9449
73.42; 86.607; 82.977
1050.81Otsuki, Shinya; Kanemoto, Kazuya; Martos, Daniel Carter; Kwon, Eunsang; Wencel-Delord, Joanna; Yoshikai, Naohiko
Diazomethyl-λ3-iodane meets aryne: dipolar cycloaddition and C-to-N iodane shift leading to indazolyl-λ3-iodanes
Chemical Science, 2025, 16, 8053-8059
1574289 CIFC72 H74 B2 N4P 1 21/n 120.2478; 12.0654; 24.41
90; 106.52; 90
5717.1Petrykowski, Wojciech D.; Vanthuyne, Nicolas; Naim, Carmelo; Bertocchi, Francesco; Poronik, Yevgen M.; Ciesielski, Arkadiusz; Cyrański, Michał K.; Terenziani, Francesca; Jacquemin, Denis; Gryko, Daniel T.
Double helicene possessing B–N dative bonds built on 1,4-dihydropyrrolo[3,2-b]pyrrole core
Chemical Science, 2025, 16, 8338-8345
1574290 CIFC76 H74 B2 N4 S2P 1 21/n 114.8961; 23.8496; 17.9551
90; 105.52; 90
6146.2Petrykowski, Wojciech D.; Vanthuyne, Nicolas; Naim, Carmelo; Bertocchi, Francesco; Poronik, Yevgen M.; Ciesielski, Arkadiusz; Cyrański, Michał K.; Terenziani, Francesca; Jacquemin, Denis; Gryko, Daniel T.
Double helicene possessing B–N dative bonds built on 1,4-dihydropyrrolo[3,2-b]pyrrole core
Chemical Science, 2025, 16, 8338-8345
1574291 CIFC30 H22 O2 SP 1 21/n 19.9735; 6.9462; 31.359
90; 97.373; 90
2154.5Knyazev, Daniil A.; George, Malini; Werz, Daniel B.
(3 + 2)-Cycloaddition of bicyclobutanes and thioketones: access to 2-thiabicyclo[2.1.1]hexanes without the use of catalysts or light
Chemical Science, 2025, 16, 8588-8593
1574292 CIFC32 H28 O SP 1 21/n 111.698; 12.037; 17.473
90; 102.844; 90
2398.8Knyazev, Daniil A.; George, Malini; Werz, Daniel B.
(3 + 2)-Cycloaddition of bicyclobutanes and thioketones: access to 2-thiabicyclo[2.1.1]hexanes without the use of catalysts or light
Chemical Science, 2025, 16, 8588-8593

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