Crystallography Open Database

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1557396 CIFC30 H26 B BrP 1 21/c 116.2062; 8.1904; 17.137
90; 91.218; 90
2274.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557397 CIFC36 H36 B BrP -18.4803; 9.1672; 19.9099
80.254; 85.195; 68.593
1419.82Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557398 CIFC22 H26 B Br O2P 1 21/n 16.4265; 15.8695; 20.617
90; 97.511; 90
2084.6Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557399 CIFC62 H78 B2 Br2P -19.4752; 9.8107; 15.1088
93.579; 100.145; 90.47
1379.57Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557400 CIFC22 H26 B Br O2P c a 2120.7096; 6.4384; 15.5735
90; 90; 90
2076.52Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557401 CIFC14 H10 B Br3P 1 21/n 113.2781; 5.936; 18.4485
90; 100.58; 90
1429.37Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557402 CIFC44 H42 B2 Br2 O2P c c n42.071; 29.3977; 6.6541
90; 90; 90
8229.7Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557403 CIFC28 H22 B Br OP 1 21/c 116.0697; 19.1015; 7.184
90; 99.697; 90
2173.7Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557404 CIFC100 H108 B4 Br4P -18.0182; 16.5443; 17.4491
64.933; 86.117; 77.027
2042.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557405 CIFC62 H56 B2 Br2P -19.836; 10.894; 14.514
82.02; 73.02; 71.06
1405.2Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557406 CIFC64 H68 B2 Br2P -113.45; 14.624; 15.214
91.36; 92.15; 116.43
2675.1Yuan, K.; Kahan, R. J.; Si, C.; Williams, A.; Kirschner, S.; Uzelac, M.; Zysman-Colman, E.; Ingleson, M. J.
The synthesis of brominated-boron-doped PAHs by alkyne 1,1-bromoboration: mechanistic and functionalisation studies
Chemical Science, 2020, 11, 3258-3267
1557428 CIFC33 H27 N2 O2 PP -110.6898; 11.775; 11.9913
71.708; 65.4407; 89.239
1291.4Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong
Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress
Chemical Science, 2020, 11, 3405-3417
1557429 CIFC33 H27 N2 O2 PP -19.1957; 10.841; 13.3381
100.85; 100.343; 93.057
1279.46Zhuang, Zeyan; Dai, Jun; Yu, Maoxing; Li, Jianqing; Shen, Pingchuan; Hu, Rong; Lou, Xiaoding; Zhao, Zujin; Tang, Ben Zhong
Type I photosensitizers based on phosphindole oxide for photodynamic therapy: apoptosis and autophagy induced by endoplasmic reticulum stress
Chemical Science, 2020, 11, 3405-3417
1557430 CIFC228 H104 B4 Cl4 F96 N12 O2 Pd2C 1 2/c 140.6116; 14.3027; 43.1791
90; 108.163; 90
23831.1Martí-Centelles, Vicente; Spicer, Rebecca L.; Lusby, Paul J.
Non-covalent allosteric regulation of capsule catalysis
Chemical Science, 2020, 11, 3236-3240
1557435 CIFC20 H19 B N2 O5P 1 21/c 19.8085; 8.9262; 21.7277
90; 99.222; 90
1877.73Williams, Alexander F.; White, Andrew J. P.; Spivey, Alan C.; Cordier, Christopher J.
meta-Selective C‒H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester
Chemical Science, 2020, 11, 3301-3306
1557437 CIFC172 H168 Ca F21 N24 O30 Rh6 S7P 6323.302; 23.302; 21.347
90; 90; 120
10038Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557438 CIFC333 H250 F35 K2 N99 O100 Rh12 S7P -122.5096; 25.221; 39.36
72.977; 89.886; 76.76
20747Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557439 CIFC170 H185 F24 N24 O34.5 Rh6 S8 SrP 6322.673; 22.673; 20.482
90; 90; 120
9118Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557440 CIFC173 H189 F24 N24 O37.5 Rh6 S8 SrP 6322.564; 22.564; 20.375
90; 90; 120
8984Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557441 CIFC190 H252 Ba2 F30 N24 O60 Rh6 S14C 1 2/c 172.911; 20.9282; 33.246
90; 106.419; 90
48661Dang, Li-Long; Gao, Xiang; Lin, Yue-Jian; Jin, Guo-Xin
s-Block metal ions induce structural transformations between figure-eight and double trefoil knots
Chemical Science, 2020, 11, 1226-1232
1557442 CIFC16 H20 N2 Ni O2P 1 21/n 114.557; 10.2366; 8.2137
90; 141.27; 90
765.8Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557443 CIFC20 H28 N2 Ni O6P 1 21/n 18.3939; 14.9329; 8.7611
90; 108.791; 90
1039.63Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557444 CIFC31 H35 F6 N5 Ni O2 PI 1 2/a 122.4997; 8.4913; 17.7726
90; 111.646; 90
3156Fisher, Katherine J.; Feuer, Margalit L.; Lant, Hannah M. C.; Mercado, Brandon Q.; Crabtree, Robert H.; Brudvig, Gary W.
Concerted proton-electron transfer oxidation of phenols and hydrocarbons by a high-valent nickel complex.
Chemical science, 2020, 11, 1683-1690
1557445 CIFC14 H8 S2P -15.8903; 7.8065; 11.6922
90.458; 101.223; 93.037
526.52Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557446 CIFC20 H14 S4P 1 21/c 17.45474; 16.2651; 6.76866
90; 90.98; 90
820.59Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557447 CIFC16 H12 S4P 1 21/c 17.6311; 17.4783; 5.2771
90; 91.18; 90
703.7Wang, Chengyuan; Hashizume, Daisuke; Nakano, Masahiro; Ogaki, Takuya; Takenaka, Hiroyuki; Kawabata, Kohsuke; Takimiya, Kazuo
“Disrupt and induce” intermolecular interactions to rationally design organic semiconductor crystals: from herringbone to rubrene-like pitched π-stacking
Chemical Science, 2020, 11, 1573-1580
1557448 CIFC26 H26P 1 21 19.423; 10.032; 11.391
90; 104.61; 90
1042Lei, Guangyue; Zhang, Hanwen; Chen, Bin; Xu, Meichen; Zhang, Guozhu
Copper-catalyzed enantioselective arylalkynylation of alkenes.
Chemical science, 2020, 11, 1623-1628
1557449 CIFC55 H72 Cl F3 N3 O3 P SP -111.0592; 12.9006; 18.7834
98.063; 91.131; 103.315
2578.25Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557450 CIFC59 H80 Cl15 Ga3 N3 PP 1 21/c 119.16275; 13.46701; 28.2924
90; 94.584; 90
7277.92Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557451 CIFC57 H76 N3 PP 1 21/c 118.56527; 11.96597; 22.85445
90; 101.614; 90
4973.19Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557452 CIFC54 H72 Cl8 Ga2 N3 PP b c a24.13916; 18.9021; 26.08922
90; 90; 90
11904Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557453 CIFC54 H72 Cl4 Ga N3 PP 1 21/c 111.5123; 12.8811; 37.2397
90; 97.724; 90
5472.21Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557454 CIFC54 H72 N3 PP 1 21/n 112.5627; 15.9337; 23.6169
90; 93.554; 90
4718.31Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557455 CIFC115 H154 Cl10 Ga2 N6 P2C 1 2/c 140.7612; 12.3237; 23.4798
90; 101.398; 90
11562Sharma, Mahendra K.; Blomeyer, Sebastian; Glodde, Timo; Neumann, Beate; Stammler, Hans-Georg; Hinz, Alexander; van Gastel, Maurice; Ghadwal, Rajendra S.
Isolation of singlet carbene derived 2-phospha-1,3-butadienes and their sequential one-electron oxidation to radical cations and dications
Chemical Science, 2020, 11, 1975-1984
1557456 CIFC46 H88 Ag2 Li4 N6 O2P -18.3861; 11.5994; 14.05
86.881; 79.282; 83.876
1334.35Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557457 CIFC36 H72 Ag2 Li2 N4C 1 2/c 122.1326; 8.3936; 22.8868
90; 109.561; 90
4006.34Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557458 CIFC42 H56 Ag Li N2 O3P 1 21/n 112.4986; 14.8962; 21.7554
90; 93.742; 90
4041.82Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557459 CIFC56 H84 Ag2 Li2 N4 O2P 1 21/c 113.3743; 18.2477; 22.9463
90; 103.316; 90
5449.49Tezuka, Noriyuki; Hirano, Keiichi; Peel, Andrew J.; Wheatley, Andrew E. H.; Miyamoto, Kazunori; Uchiyama, Masanobu
Lipshutz-type bis(amido)argentates for directed ortho argentation
Chemical Science, 2020, 11, 1855-1861
1557502 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.7583; 20.7341; 12.2345
90; 101.16; 90
2677.47Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557503 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.866; 21.1945; 12.2707
90; 101.413; 90
2770.1Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557504 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.874; 20.9284; 12.2372
90; 101.859; 90
2725.4Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557505 CIFC42 H56 Cl6 Fe2 N2 O12P 1 21/n 110.9375; 21.278; 12.2835
90; 100.818; 90
2807.9Chen, Jian; Sekine, Yoshihiro; Okazawa, Atsushi; Sato, Hiroyasu; Kosaka, Wataru; Miyasaka, Hitoshi
Chameleonic layered metal‒organic frameworks with variable charge-ordered states triggered by temperature and guest molecules
Chemical Science, 2020, 11, 3610-3618
1557506 CIFC140 H104 Cu4 N8 O20P -114.987; 16.858; 17.478
116.53; 107.31; 93.21
3679Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557507 CIFC218 H138 Cu8 N6 O48P -113.914; 20.891; 21.446
71.94; 87.87; 81.2
5857Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557508 CIFC116 H84 Cu4 N4 O24P 1 21/c 114.0177; 28.7314; 17.0738
90; 110.611; 90
6436.3Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557509 CIFC53 H31 Cu2 N O12I 1 2/m 125.8186; 22.6806; 27.2079
90; 109.69; 90
15000.9Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557510 CIFC106 H60 Cu4 O24C 1 2/m 119.687; 28.163; 10.475
90; 97.91; 90
5753Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557511 CIFC108 H72 Cu4 O24 S4C 1 2/c 114.151; 32.563; 26.766
90; 102.26; 90
12052Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557512 CIFC168 H124 Cu4 N12 O20P 1 21/n 120.979; 21.168; 23.76
90; 108.37; 90
10014Bloch, Witold M.; Babarao, Ravichandar; Schneider, Matthew L.
On/off porosity switching and post-assembly modifications of Cu4L4 metal‒organic polyhedra
Chemical Science, 2020, 11, 3664-3671
1557513 CIFC16 H21 N2 O0.1 PP n m a8.613; 17.7; 9.511
90; 90; 90
1450Zhang, Jingjing; Yang, Jin-Dong; Cheng, Jin-Pei
Diazaphosphinanes as hydride, hydrogen atom, proton or electron donors under transition-metal-free conditions: thermodynamics, kinetics, and synthetic applications
Chemical Science, 2020, 11, 3672-3679
1557531 CIFC21 Al F36 N O10 WP 4/n :213.699; 13.699; 9.5293
90; 90; 90
1788.29Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557532 CIFC30 Al2 F55 Mo O12P a -317.285; 17.285; 17.285
90; 90; 90
5164.3Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557533 CIFC22 Al F36 Mo O10P 4/n :213.759; 13.759; 9.5821
90; 90; 90
1813.99Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557534 CIFC30 Al2 F55 O12 WP a -317.3168; 17.3168; 17.3168
90; 90; 90
5192.82Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557535 CIFC21 Al F36 Mo N O10P 4/n :213.7152; 13.7152; 9.5418
90; 90; 90
1794.88Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557536 CIFC36 Al2 F73 O12 WP -111.5888; 11.5986; 12.7755
82.965; 67.136; 87.863
1570.27Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557537 CIFC32 Al2 Cl3 F55 O14 W2P -111.3269; 12.2795; 23.4349
76.883; 86.161; 66.485
2909.8Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557538 CIFC46 Al2 F72 I3 Mo3 O22P 1 21/n 113.9703; 28.8124; 20.6169
90; 90.443; 90
8298.4Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557539 CIFC30 Al2 F55 I O12 WP -110.5119; 12.5617; 21.1226
85.595; 76.545; 78.485
2656.7Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557540 CIFC68 Al4 F128 O26 W2P -115.848; 17.229; 22.395
94.072; 102.24; 101.653
5811.1Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557541 CIFC22 Al F36 I O10 WP 1 21/c 116.438; 28.3511; 17.5878
90; 110.764; 90
7664.2Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557542 CIFC96 Al6 F165 I6 Mo6 O42P -113.385; 21.4285; 31.305
85.822; 81.782; 83.84
8820.3Bohnenberger, Jan; Schmitt, Manuel; Feuerstein, Wolfram; Krummenacher, Ivo; Butschke, Burkhard; Czajka, Jakub; Malinowski, Przemysław J.; Breher, Frank; Krossing, Ingo
Completing the triad: synthesis and full characterization of homoleptic and heteroleptic carbonyl and nitrosyl complexes of the group VI metals
Chemical Science, 2020, 11, 3592-3603
1557543 CIFC57 H88 N2 OP 1 21/n 116.2198; 10.77; 28.9971
90; 96.1; 90
5036.7Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557544 CIFC71 H94 Mg2 N8P 1 21/c 112.8246; 21.5786; 24.2161
90; 103.493; 90
6516.52Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557545 CIFC49 H60 Mg2 N6P 1 21/c 112.4858; 12.0704; 31.1338
90; 92.762; 90
4686.68Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557546 CIFC137.5 H189.63 I0.04 Mg2 N4 O0.13P 1 21/n 118.2067; 26.3297; 25.8355
90; 105.806; 90
11916.7Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557547 CIFC117 H144 Mg4 N12 O4P -115.1058; 19.0783; 20.0582
85.762; 88.909; 66.998
5306.17Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557548 CIFC70 H86 Mg2 N8C 1 2/c 118.7699; 15.7829; 22.8274
90; 109.172; 90
6387.4Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557549 CIFC57 H76 Mg2 N6P 1 21/c 118.7194; 11.3129; 26.0645
90; 103.791; 90
5360.57Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557550 CIFC57 H87 I Mg N2 OP -110.437; 14.8235; 18.7188
84.547; 75.886; 71.426
2661.85Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557551 CIFC151 H208 Mg4 N12 O6P -117.919; 19.6004; 20.9467
79.292; 75.685; 86.86
7004Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557552 CIFC134 H184 Mg4 N12 O12P 1 21/c 115.48; 15.114; 27.505
90; 103.08; 90
6268Yuvaraj, K.; Douair, Iskander; Jones, Dafydd D. L.; Maron, Laurent; Jones, Cameron
Sterically controlled reductive oligomerisations of CO by activated magnesium(i) compounds: deltate vs. ethenediolate formation
Chemical Science, 2020, 11, 3516-3522
1557570 CIFC20 H18 N2 O5P -18.27; 9.1848; 12.4194
71.619; 82.065; 79.191
876.19Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557571 CIFC44 H44 N4 O11P 21 21 2110.9162; 11.3807; 31.809
90; 90; 90
3951.8Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557572 CIFC8 H8 O5P 1 21 19.2321; 18.768; 18.876
90; 93.72; 90
3263.7Yelgaonkar, Shweta P.; Swenson, Dale C.; MacGillivray, Leonard R.
Supramolecular chemistry under mechanochemical conditions: a small molecule template generated and integrated into a molecular-to-supramolecular and back-to-molecular cascade reaction
Chemical Science, 2020, 11, 3569-3573
1557580 CIFC15 H12 N4 O3 SP 21 21 216.4901; 13.5853; 17.2054
90; 90; 90
1517Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557581 CIFC25 H21 Cl N2 O3P 21 21 216.2023; 15.1707; 23.3424
90; 90; 90
2196.36Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557582 CIFC18 H14 Br2 N4 O3P 1 21 17.6364; 11.6851; 11.5473
90; 104.259; 90
998.65Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557583 CIFC19 H15 F N4 O3P 21 21 2110.3148; 11.9114; 14.6673
90; 90; 90
1802.08Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557584 CIFC25 H21 Cl N2 O3P 21 21 216.6447; 14.3101; 22.5008
90; 90; 90
2139.5Ding, Pei-Gang; Zhou, Feng; Wang, Xin; Zhao, Qiu-Hua; Yu, Jin-Sheng; Zhou, Jian
H-bond donor-directed switching of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins
Chemical Science, 2020, 11, 3852-3861
1557585 CIFC37 H61 Eu N8 O15F d d d :218.1194; 20.3557; 43.9834
90; 90; 90
16222.5Hewitt, Sarah H.; Macey, Georgina; Mailhot, Romain; Elsegood, Mark R. J.; Duarte, Fernanda; Kenwright, Alan M.; Butler, Stephen J.
Tuning the anion binding properties of lanthanide receptors to discriminate nucleoside phosphates in a sensing array
Chemical Science, 2020, 11, 3619-3628
1557586 CIFC22 H18 Br Cl0 N O2P 21 21 215.8675; 12.4208; 24.4967
90; 90; 90
1785.3Shen, Bin; He, Qianwen; Dong, Shunxi; Liu, Xiaohua; Feng, Xiaoming
A chiral cobalt(ii) complex catalyzed enantioselective aza-Piancatelli rearrangement/Diels‒Alder cascade reaction
Chemical Science, 2020, 11, 3862-3867
1557587 CIFC11 H10 Br N OP -16.732; 7.228; 12.0162
80.831; 86.517; 62.902
513.81Ikeda, Hideaki; Nishi, Kohei; Tsurugi, Hayato; Mashima, Kazushi
Chromium-catalyzed cyclopropanation of alkenes with bromoform in the presence of 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-dihydropyrazine
Chemical Science, 2020, 11, 3604-3609
1557598 CIFC18 H18 F3 N O4P 21 21 2110.186; 11.3558; 15.5296
90; 90; 90
1796.31Zhang, Shuyue; Greenhalgh, Mark D.; Slawin, Alexandra M. Z.; Smith, Andrew D.
Tandem sequential catalytic enantioselective synthesis of highly-functionalised tetrahydroindolizine derivatives
Chemical Science, 2020, 11, 3885-3892
1557603 CIFC21 H18 N2 O2 SC 1 2/c 117.4822; 9.78677; 20.9912
90; 103.576; 90
3491.13Li, Guofeng; Zhao, Man; Xie, Junqiu; Yao, Ying; Mou, Lingyun; Zhang, Xiaowei; Guo, Xiaomin; Sun, Wangsheng; Wang, Zheng; Xu, Jiecheng; Xue, Jianzhong; Hu, Tao; Zhang, Ming; Li, Min; Hong, Liang
Efficient synthesis of cyclic amidine-based fluorophores via 6π-electrocyclic ring closure
Chemical Science, 2020, 11, 3586-3591
1557604 CIFC20 H44 Cl2 N2 O2 P2 UP 1 21/c 112.7105; 28.115; 8.1727
90; 105.391; 90
2815.8Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557605 CIFC18 H40 Cl2 N2 O2 P2 UP 1 21/c 114.48; 14.59; 12.5668
90; 102.29; 90
2594.1Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557606 CIFC40 H88 Cl4 N4 O4 P4 Pd2 U2P c c n16.3226; 22.813; 14.7718
90; 90; 90
5500.5Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557607 CIFC44 H96 Cl4 N4 O6 P4 Pt3 U2C 1 2/c 112.663; 21.4809; 23.0838
90; 99.354; 90
6195.6Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557608 CIFC22 H48 Cl2 N2 Ni O3 P2 UP 1 21/n 111.3508; 12.914; 20.597
90; 95.165; 90
3006.9Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557609 CIFC44 H96 Cl4 N4 Ni2 O5 P4 U2P 1 21/n 114.5223; 15.8953; 27.339
90; 103.728; 90
6130.6Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557610 CIFC40 H63 Cl2 N2 O3 P3 Pd UP -112.208; 12.209; 17.048
108.557; 90.701; 108.839
2261Feng, Genfeng; McCabe, Karl N.; Wang, Shuao; Maron, Laurent; Zhu, Congqing
Construction of heterometallic clusters with multiple uranium‒metal bonds by using dianionic nitrogen‒phosphorus ligands
Chemical Science, 2020, 11, 7585-7592
1557613 CIFC22 H28 O5 SP -17.3975; 10.7485; 13.1441
92.571; 96.25; 97.449
1028.29Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557614 CIFC15 H22 O3P 1 21/n 17.6688; 22.4305; 15.4747
90; 101.329; 90
2610.02Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro–Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557615 CIFC12 H20 O2P 1 21/c 17.1285; 11.9273; 13.4833
90; 104.629; 90
1109.24Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557616 CIFC15 H20 O3P -17.2165; 8.3504; 11.317
82.649; 76.258; 68.964
617.61Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557617 CIFC23 H28 N2 O3 SP 1 21/c 110.3539; 19.9619; 11.8443
90; 113.384; 90
2246.95Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557618 CIFC22 H30 N2 O4 SP 1 21/n 19.961; 17.5295; 13.2899
90; 101.667; 90
2272.62Zhang, Ye; Zheng, Tian-Lu; Cheng, Fu; Dai, Kun-Long; Zhang, Kun; Ma, Ai-Jun; Zhang, Fu-Min; Zhang, Xiao-Ming; Wang, Shao-Hua; Tu, Yong-Qiang
Facile access to diverse all-carbon quaternary center containing spirobicycles by exploring a tandem Castro‒Stephens coupling/acyloxy shift/cyclization/semipinacol rearrangement sequence
Chemical Science, 2020, 11, 3878-3884
1557625 CIFC48 H55 Au F6 N4 O11 S2P 21 21 219.1199; 23.4191; 23.6083
90; 90; 90
5042.3Reid, Jolene P.; Hu, Mingyou; Ito, Susumu; Huang, Banruo; Hong, Cynthia M.; Xiang, Hengye; Sigman, Matthew S.; Toste, F. Dean
Strategies for remote enantiocontrol in chiral gold(iii) complexes applied to catalytic enantioselective γ,δ-Diels‒Alder reactions
Chemical Science, 2020, 11, 6450-6456
1557626 CIFC21 H9 N3 O6 TiP a -320.9953; 20.9953; 20.9953
90; 90; 90
9254.8Cao, Jing; Ma, Wenjie; Lyu, Kangjie; Zhuang, Lin; Cong, Hengjiang; Deng, Hexiang
Twist and sliding dynamics between interpenetrated frames in Ti-MOF revealing high proton conductivity
Chemical Science, 2020, 11, 3978-3985

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