Synthesis and characterization of nitro fulleropyrrolidine derivatives

Hanneng Cailiao/Chinese Journal of Energetic Materials

Volumn 17, Issue 3, 2009, Pages 287-292

  Jin, Bo ^a   Peng, Ru Fang ^a,b   Tan, Bi Sheng ^a   Huang, Yi Min ^b   Shu, Yuan Jie ^b   Chu, Shi Jin ^a   Fu, Yi Bei ^b  

^a SOUTHWEST UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b RESEARCH CENTER OF LASER FUSION   (China)

Author keywords

Fullerene; HMX; Nitro fulleropyrrolidine; Organic chemistry; Sensitivity

Indexed keywords

EID: 68049109312     PISSN: 10069941     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (19)

1. 60: Buckminsterfullerene[J]. Nature, 1985, 318: 162-163.
2. 60: A new form carbon[J]. Nature, 1990, 347: 354-358.
3. Brabec C J, Padinger F, Hummelen J C, et al. Realization of large area flexible fullerene-conjugated polymer photocells: A route to plastic solar cells[J]. Synthetic Metals, 1999, 102: 861-864.
4. 60-fullerene monomalonate adducts selectively inactivate neuronal nitric oxide synthase by uncoupling the formation of reactive oxygen intermediates from nitric oxide production[J]. Biochemistry, 2001, 40: 37-45.
5. 60 and its ferro-complexes: Syntheses and magnetic properties[J]. Polymer, 2002, 43: 1563-1566.
6. Mashino T, Usui N, Okuda K, et al. Respiratory chain inhibition by fullerene derivatives: Hydrogen peroxide production caused by fullerene derivatives and a respiratory chain system[J]. Bioorganic and Medicinal Chemistry, 2003, 11: 1433-1438.
7. 60 end-capped polymers under microwave irradiation[J]. Journal of Applied Polymer Science, 2006, 99: 828-834.
8. LI Shu-fen, HE De-qiu, SHAN Wen-gang, et al. A study on comprehensive characteristics of RDX-CMDB propellants containing fullerene[J]. Journal of Propulsion Technology, 1997, 18(6): 79-83.
9. 60 soot in ammonium nitrate propellants[J]. Journal of Propulsion and Power, 2003, 19: 713-715.
10. JIN Bo, PENG Ru-fang, SHU Yuan-jie, et al. Study on the synthesis of new energetic fullerene derivative[J]. Chinese Journal High Pressure Physics, 2006, 20: 220-225.
11. JIN Bo, PENG Ru-fang, SHU Yuan-jie, et al. Study on the synthesis and properties of N-methyl-2-(3-nitrophenyl)fulleropyrrolidine[J]. Chinese Journal of Energetic Materials, 2007, 15: 196-198.
12. WANG Guan-wu, CHEN Xiao-ping, CHENG Xin. Unexpected reactions of [60]fullerene involving tertiary amines and insight into the reaction mechanisms[J]. Chemistry-A European Journal, 2006, 12: 7246-7253.
13. ZHANG Gai-hong, HUANG Shao-hua, GAN Liang-bing, et al. Preparation of azafullerene derivatives from fullerene-mixed peroxides and single crystal X-ray structures of azafulleroid and azafullerene[J]. Journal of the American Chemical Society, 2008, 130, 12614-12615.
14. Ikeda A, Sue T, Akiyama M, et al. Preparation of highly photosensitizing liposomes with fullerene-doped lipid bilayer using dispersion-controllable molecular exchange reactions[J]. Organic Letters, 2008, 10(18): 4077-4080.
15. Maria D L T, Andrea G P R, Augusto C T, et al. [60]Fullerene-flavonoid dyads[J]. Tetrahedron, 2004, 60(16): 3581-3592.
16. Alonso A M, Prato M. Synthesis of a soluble fullerene-rotaxane incorporating a furamide template[J]. Tetrahedron, 2006, 62(9): 2003-2007.
17. Gollapalli R D, Muhammad S R., D'Souza F. N-(2, 4-dinitrophenyl)-2-phenylfulleropyrrolidine: An electroactive organofullerene dyad[J]. Chemical Communications, 1999: 849-850.
18. Langa F, de la Cruz P, Espíldora E, et al. Fullerene chemistry under microwave irradiation[J]. Carbon, 2000, 38: 1641-1646.
19. 60-acceptor dyads[J]. European Journal of Organic Chemistry, 1999: 3433-3436.