期刊文献+

N-亚硝基吲哚系列化合物及其自由基负离子在乙腈介质中N—NO键断裂能的测定 被引量:4

Determination of N—NO Bond Dissociation Energies of N-Nitrosoindoles and Their Radical Anions in Acetonitrile
下载PDF
导出
摘要 利用滴定量热技术并结合适当的热力学循环测定了乙腈溶液中7个取代的N-亚硝基吲哚化合物中N—NO键的异裂能和均裂能,能量范围分别为206.1~246.2 kJ/mol和119.1~124.6 kJ/mol.表明N-亚硝基吲哚均裂释放NO自由基(NO.)比异裂释放NO正离子(NO^+)要容易得多,通过热力学循环得到的相应自由基负离子中N—NO键的异裂能和均裂能的能量范围分别为25.5~34.4和5.0~40.5 kJ/mol,表明所研究化合物的自由基负离子在室温下很不稳定. The heterolytic and homolytic N—NO bond dissociation energies of seven N-nitrosoindole derivatives were evaluated by using titration calorimetry and relative thermodynamic cycles. The energetic scales of the heterolytic and homolytic N—NO bond dissociation energies of N-nitrosoindoles cover the ranges from 206. 1 to 246.2 kJ/mol and from 119.1 to 124. 6 kJ/mol, respectively, which indicates that N-nitrosoindoles are much easier to release a NO radical(NO^+) rather than a NO cation(NO^+). The estimation of the hetero- lytic and homolytic (N—NO) ^- + bond dissociation energies of the N-nitrosoindoles radical anions gives the energetic ranges from 25.5 to 33.4 k J/tool and from 5.0 to 40.5 k J/tool for the (N-NO) ^- + bond homolysis and heterolysis, respectively, which means that N-nitrosoindole radical anions are unstable at room temperature.
机构地区 南开大学化学系
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2007年第12期2295-2298,共4页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:20272027)资助
关键词 N-亚硝基吲哚 N-亚硝基吲哚自由基负离子 N—NO键能 滴定量热 N-Nitrosoindoles Radical anions of N-nitrosoindoles N—NO bond energy Titration calorimetry
  • 相关文献

参考文献18

  • 1Wang P. G., Xian M., Tang X., et al.. Chem. Rev.[J], 2002, 102:1091 -1134
  • 2Zhang Y. Y., Xu A. M., Nomen M., et al.. J. Biol. Chem.[J], 1996, 271:14271-14279
  • 3Lucas L. T. , Gatehouse D. , Jones G. D. D. , et al.. Chem. Res. [J], 2001, 14:158-164
  • 4Kitsch M. , Fuchs A. , Groot H.. J. Bio. Chem. [J], 2003, 278:11931-11936
  • 5Sonnenschein K. , Groot H. , Kirsch M.. J. Biol. Chem. [ J], 2004, 279:45433-45440
  • 6Blanchard F. B. , Servy C. , Ducroeq C.. Free Radical Res. [J] , 2001,35(6) : 857-866
  • 7Cheng J. P., Xian M., Wang K., et al.. J. Am. Chem. Soc. [J], 1998, 120:10266-10267
  • 8Cheng J. P. , Wang K. , Yin Z. , et al.. Tetrahedron Lett. [J] , 1998, 39:7925-7928
  • 9Xian M. , Zhu X., Lu J., et al.. Org. Lett.[J], 2000, 2:265-268
  • 10Zhu X. Q. , He J. , Xian M. , et al.. J. Org. Chem. [J], 2000, 65:6729-6735

二级参考文献7

共引文献3

同被引文献56

  • 1Li X. , Deng H. , Zhu X. Q. , Wang X. , Liang H. , Cheng J. P.. J. Org. Chem. [J], 2009, 74:4472-4478.
  • 2Duan X. M. , Song G. L. , LiZ. H. , Wang X. L. , Chen G. H. , Fan K.. J. Chem. Phys[J], 2004, 121:7086-7095.
  • 3WangX. J., HuL. H., WongL. H., ChenG. H.. Mol. Simul. [J], 2004, 30: 9-15.
  • 4WangX. J., WongL. H., HuL. H., ChanC. Y., SuZ. M., ChenG. H.. J. Phys. Chem. A[J],2004, 108:8514-8525.
  • 5Duan X. M., Li Z. H., Song G. L., Wang W. N., Chen G. H., Fan K. N.. Chem. Phys. Lett. [J], 2005, 410:125-130.
  • 6Balabin R. M. , Lomakina E. I. , Safieva R. Z.. Fuel[J] , 2011,90:2007-2015.
  • 7Eros D. , Keri G. , Kovesdi I. , Szantai-Kis C. , Meszaros G. , Orfi L.. Mini. Rev. Med. Chem. [J], 2004, 4:167-177.
  • 8Hu L. H. , Wang X. J. , Wong L. H. , Chen G. H.. J. Chem. Phys. [J] , 2003, 119:11501-11507.
  • 9GaoT., SunS. L., ShiL. L., LiH., LiH. Z., Su Z . M., LuY. H.. J. Chem. Phys.[J], 2009, 130:184104-184107.
  • 10Frisch M. J. , Trucks G. W. , Schlegel H. B. , Scuseria G. E. , Robb M. A. , Cheeseman J. R. , Montgomery J. A. Jr. , Vreven T. , Kudin K. N. , Burant J. C. , Millam J. M. , Iyengar S. S. , Tomasi J. , Barone V. , Mennucci B. , Cossi M. , Scalmani G. , Rega N. ,Petersson G. A. , Nakatsuji H. , Hada M. , Ehara M. , Toyota K. , Fukuda R. , Hasegawa J. , Ishida M. , Nakajima T. , Honda Y. , Kitao O. , Nakai H. , Klene M. , Li X. , Knox J. E. , Hratchian H. P. , Cross J. B. , Adamo C. , Jaramillo J. , Gomperts R. , Stratmann R. E. , Yazyev O. , Austin A. J. , Cammi R. , Pomelli C. , Ochterski J. W. , Ayala P. Y. , Morokunaa K. , Voth G. A. , Salvador P. , Dannenberg J. J. , Zakrzewski V. G. , Dapprich S. , Daniels A. D. , Strain M. C. , Farkas O. Malick D. K. , Rabuck A. D. , Raghavachari K. , Foresman J. B. , Ortiz J. V. , Cui Q. , Baboul A. G. , Clifford S. , Cioslowski J. , Stefanov B. B. , Liu G. , Liashenko, A. , Piskorz P. , Komaromi I. , Martin R. L. , Fox D. J. , Keith T. , Al-Lahain M. A. , Pertg C. Y. , Nanayakkara A. , Challacornhe M. , Gill P. M. W., Johnson B., Chen W., Wong M. W., Gonzalez C., Pople J. A.. Gaussian 03, Revision C. 02[ CP], Pittsburgh PA: Gaussian Inc. , 2003.

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部