Journal of Chemical Crystallography

, Volume 26, Issue 5, pp 355–360

Structures of 355-1355-1355-1tricarbonyl: structural evidence for the near-electroneutrality of the dialkylacetal substituent

  • Thomas M. Gilbert
  • Cary B. Bauer
  • Robin D. Rogers
Article

DOI: 10.1007/BF01677100

Cite this article as:
Gilbert, T.M., Bauer, C.B. & Rogers, R.D. J Chem Crystallogr (1996) 26: 355. doi:10.1007/BF01677100

Abstract

The structures of the (benzene dialkylacetal)tricarbonyl chromium complexes [η6-C6H5-CH(OR)2]Cr(CO)6 (R=Me,1; Et,2), are reported. The compounds were examined as part of a study of the conformations of the tripodal tricarbonylchromium group. For [η6-C6H5-CH(OMe)2]Cr(CO)3,1, monoclinic,P21/c (# 14),a=15.235(1) Å,b=6.5304(5) Å,c=12.702 Å, β=103.197(1)o,Z=4. For [η6-C6H5-CH(OEt)2]Cr(CO)3,2, monoclinic,P21/c (# 14),a=9.859(3) Å,b=10.547(3) Å,c=15.138(3) Å, β=108.42(2)o,Z=4. The data show that the molecules adopt the expected “three-legged piano stool” structure. The carbonyl ligands in1 adopt an eclipsed arrangement with respect to the arene ring and its substituent, while those in2 are staggered. These conformations are consistent with the notion that the acetal substituent behaves largely as an electroneutral group, or at most as a weak electronic acceptor.

Key Words

Chromium carbonyl arene acetal crystal structure conformation 

Copyright information

© Plenum Publishing Corporation 1996

Authors and Affiliations

  • Thomas M. Gilbert
    • 1
  • Cary B. Bauer
    • 1
  • Robin D. Rogers
    • 1
  1. 1.Department of ChemistryNorthern Illinois UniversityDeKalb

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