Crystallography Open Database

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7233377 CIFC17 H17 N3 SeP 1 21/c 112.5515; 5.93199; 21.5896
90; 101.138; 90
1577.18Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233378 CIFC16 H14 F N3 SeP -110.7344; 11.4734; 13.5667
92.85; 109.342; 97.713
1554.36Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233379 CIFC17 H14 F3 N3 SeP 1 21/c 15.7537; 23.2453; 12.4112
90; 90.937; 90
1659.73Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233380 CIFC16 H14 N4 O2 SeP 1 21/n 18.0441; 16.3997; 12.5446
90; 106.994; 90
1582.63Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233381 CIFC18 H17 N3 O2 SeP b c a12.6478; 10.1017; 26.833
90; 90; 90
3428.3Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233382 CIFC16 H14 Br N3 SeP 1 21/c 19.4439; 26.141; 12.8829
90; 91.719; 90
3179Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233383 CIFC16 H13 Br N4 O2 SeP -17.8948; 7.9369; 31.3002
83.404; 89.627; 60.612
1694.8Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233384 CIFC19 H19 N3 O2 SeP 1 21/c 14.8207; 36.9783; 10.4021
90; 95.86; 90
1844.6Jakubczyk, Michał; Mkrtchyan, Satenik; Madura, Izabela D.; Marek, Paulina H.; Iaroshenko, Viktor O.
Copper-catalyzed direct C–H arylselenation of 4-nitro-pyrazoles and other heterocycles with selenium powder and aryl iodides. Access to unsymmetrical heteroaryl selenides
RSC Advances, 2019, 9, 25368
7233385 CIFC14 H19 N2 O6 ZnC 1 2/c 117.23; 19.96; 9.432
90; 105.708; 90
3123He, Zimo; Zhao, Xi; Pan, Xinbo; Li, Yuanyuan; Wang, XiaoXiao; Xu, Haitao; Xu, Zhenliang
Ligand geometry controlling Zn-MOF partial structures for their catalytic performance in Knoevenagel condensation
RSC Advances, 2019, 9, 25170
7233386 CIFC23 H21 N5 O7 ZnP -18.585; 10.181; 14.86
104.46; 101.001; 102.349
1186.9He, Zimo; Zhao, Xi; Pan, Xinbo; Li, Yuanyuan; Wang, XiaoXiao; Xu, Haitao; Xu, Zhenliang
Ligand geometry controlling Zn-MOF partial structures for their catalytic performance in Knoevenagel condensation
RSC Advances, 2019, 9, 25170
7233387 CIFC22 H21 N5 O8 ZnP 1 21/c 114.74; 8.444; 19.15
90; 106.957; 90
2280He, Zimo; Zhao, Xi; Pan, Xinbo; Li, Yuanyuan; Wang, XiaoXiao; Xu, Haitao; Xu, Zhenliang
Ligand geometry controlling Zn-MOF partial structures for their catalytic performance in Knoevenagel condensation
RSC Advances, 2019, 9, 25170
7233388 CIFC33 H42 F12 N3 O9 P ZnP 1 21/n 112.4608; 16.0495; 22.7935
90; 99.656; 90
4493.9Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C‒ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233389 CIFC58 H76 F24 N6 O20 P2 Zn2P 1 21/n 115.7902; 11.3758; 23.2214
90; 105.424; 90
4020.9Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C‒ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233390 CIFC30 H37 F12 N2 O9 P ZnP 1 21/c 113.121; 12.1695; 25.591
90; 98.367; 90
4042.8Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C‒ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233391 CIFC36 H53 F12 N2 O9 P Si ZnP -111.3993; 13.6801; 16.1856
96.668; 94.471; 100.497
2452.3Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C‒ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233392 CIFC19 H36 N3 O5 PC 1 2/c 116.2198; 9.6226; 29.4018
90; 93.873; 90
4578.5Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C–ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233393 CIFC68 H78 F36 N6 O20 P2 Zn3P -115.4251; 17.7197; 19.8153
86.523; 70.362; 67.35
4692.9Audran, Gérard; Bagryanskaya, Elena; Bagryanskaya, Irina; Edeleva, Mariya; Joly, Jean-Patrick; Marque, Sylvain R. A.; Iurchenkova, Anna; Kaletina, Polina; Cherkasov, Sergey; Hai, Tung To; Tretyakov, Evgeny; Zhivetyeva, Svetlana
How intramolecular coordination bonding (ICB) controls the homolysis of the C‒ON bond in alkoxyamines
RSC Advances, 2019, 9, 25776
7233414 CIFC39 H39 N O4 Si2P -110.0776; 11.8793; 16.4275
95.541; 104.025; 112.585
1721.7Wu, Ya; Chen, Hua; Yang, Wenyu; Fan, Yu; Gao, Lu; Su, Zhishan; Hu, Changwei; Song, Zhenlei
Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon
RSC Advances, 2019, 9, 26209
7233415 CIFC32 H36 O Si2P 21 21 2110.5099; 14.8311; 18.254
90; 90; 90
2845.31Wu, Ya; Chen, Hua; Yang, Wenyu; Fan, Yu; Gao, Lu; Su, Zhishan; Hu, Changwei; Song, Zhenlei
Asymmetric retro-[1,4]-Brook rearrangement of 3-silyl allyloxysilanes via chirality transfer from silicon to carbon
RSC Advances, 2019, 9, 26209
7233419 CIFAl3 B4 Ca3 O15 YP 63/m10.38775; 10.38775; 5.69198
90; 90; 120
531.909Yue, Cheng; Zhu, Dachuan; Yan, Qun; Pu, Yong
A red-emitting Sr3La(1−x)Eux(AlO)3(BO3)4 phosphor with high thermal stability and color purity for near-UV-excited wLEDs
RSC Advances, 2019, 9, 26364

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