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Experimental and Theoretical Studies on Pyrolysis of O-Acetyl Derivatives of beta-phenylcinnamaldehyde and Benzaldehyde Oximes

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
[ReBr3(py)3]0.42[ReBr2(NO)(py)3]0.58 (1), trans-[ReBr4(OPPh3)2] (2), [ReBr(NO)(dppe)2]Br (3) and orthorhombic polymorph of mer-cis- [Re(NO)Br3(OPPh3)2] (4) complexes have been synthesized by reactions of monoclinic polymorph of mer-cis-[Re(NO)Br3(OPPh3)2] with pyridine, bis(diphenylophosphino) ethane, 2,2_-bipyridine, 1,10-phenanthroline. The NO group in 1 and 4 is coordinated in a linear way. Due to nitrosyl/bromine compositional disorder, the shortening of Re-NO distance [1.68(5) A] and the elongation of N-O bond length [1.38(10) A] are observed in1. The N-O bond length in 4 is extremely short [0.94(1) A], which results probably from steric interactions of two mutually cis OPPh3 molecules and a large discrepancy of Re-O-P angle values.
Rocznik
Strony
577--590
Opis fizyczny
Bibliogr. 27 poz., rys.
Twórcy
autor
  • Department of Inorganic and Radiation Chemistry, Institute of Chemistry,University of Silesia, 9th Szkolna St., 40-006 Katowice, Poland
autor
  • Department of Inorganic and Radiation Chemistry, Institute of Chemistry,University of Silesia, 9th Szkolna St., 40-006 Katowice, Poland
autor
  • Department of Inorganic and Radiation Chemistry, Institute of Chemistry,University of Silesia, 9th Szkolna St., 40-006 Katowice, Poland
Bibliografia
  • 1. Bunce R.A., Tetrahedron, 51, 13103 (1995).
  • 2. Padwa A., ECSOC-3, 1999, www.unibas.ch/mdpi/ecsoc-3/a0019.html.
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  • 4. Troszkiewicz C. and Glinka J., Roczn. Chem., 36, 1387 (1962); CA, 61, 1828e (1963).
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  • 6. Suwiński J. and Mohamed M.A.A., Polish J. Chem., 75, 965 (2001).
  • 7. Goszczyński S., Zesz. Nauk. Politech. ŚI. Chem., 25, 1 (1964), {in Polish, a long abstract in English see C. A. 63,4253 (1965)}.
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  • 11. Brady O.L. and Sharawy H.A.M., J. Chem. Soc., 4082 (1953).
  • 12. Woodward R.B. and Hoffmann R., ”Conservation of Orbital Symmetry”-, Academic Press, NY, 1970.
  • 13. Hauser C.R. and Hoffenberg D.S., J. Org. Chem., 20, 1491 (1955).
  • 14. Mitsuyuki M., Tomohito S., Masatomo N., Shigekazu K. and McCullough K.J., J. Org. Chem., 57 (8), 2285 (1992).
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  • 16. Smith P.A.S. and Hein G.E., J. Am. Chem. Soc., 82, 5731 (1960).
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  • 19. Rault V., Bull. Soc. Chim. Fr., 3315 (1968).
  • 20. Kubota T. et al., Bull. Chem. Soc. Jpn., 36, 1552 (1963).
  • 21. Hauser C.R. and Sullivan C.T., J. Am. Chem. Soc., 55, 4611 (1933).
  • 22. Brady O.L. and Goldstein A., J. Chem. Soc., 1923 (1926).
  • 23. Grammaticakis P., Bull. Soc. Chim. Fr., 8, 101 (1941).
  • 24. Crawford R.J. and Woo C., Canad. J. Chem., 43, 3178 (1965).
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  • 27. Winmopac 2.0 User Manual, Fujitsu Limited, Tokyo, Japan, (1997-1998).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0023-0118
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