Chen Li, Khan Masood A., Richter-Addo George B., Young Victor G., Powell Douglas R.
X-ray Structural Laboratory, Department of Chemistry, University of Wisconsin, 1101 University Avenue, Madison, Wisconsin 53706.
Inorg Chem. 1998 Sep 7;37(18):4689-4696. doi: 10.1021/ic980463u.
The reactions of (por)Os(CO) (por = TPP, TTP, OEP, TMP) with nitrosoarenes (ArNO; Ar = Ph, o-tol) in refluxing toluene generate the (por)Os(ArNO)(2) complexes in 45-76% yields (TTP = 5,10,15,20-tetra-p-tolylporphyrinato dianion, TPP = 5,10,15,20-tetraphenylporphyrinato dianion, OEP = 2,3,7,8,12,13,17,18-octaethylporphyrinato dianion, TMP = 5,10,15,20-tetramesitylporphyrinato dianion). The nu(NO) of the coordinated PhNO groups in the (por)Os(PhNO)(2) complexes occur in the 1295-1276 cm(-)(1) range, and decrease slightly in the order TPP (1295 cm(-)(1)) > TTP (1291 cm(-)(1)) > OEP (1286 cm(-)(1)) > TMP (1276 cm(-)(1)). The reaction of (TTP)Os(CO) with 1 equiv of PhNO in CH(2)Cl(2) at room temperature generates a 1:3 mixture of (TTP)Os(CO)(PhNO) and (TTP)Os(PhNO)(2) in ca. 40% isolated yield. The nu(CO) of (TTP)Os(CO)(PhNO) is at 1972 cm(-)(1) (KBr), which is 56 cm(-)(1) higher in energy than that of the precursor (TTP)Os(CO). When this mixture and excess PhNO are dissolved in toluene and the solution is heated to reflux, quantitative conversion to the (TTP)Os(PhNO)(2) product occurs. IR monitoring of the reactions of (por)Os(CO) with 1 equiv of PhNO in CH(2)Cl(2) reveal similar formations of the respective (por)Os(CO)(PhNO) intermediates for the TTP (1968 cm(-)(1); Deltanu(CO) = +74 cm(-)(1)), TMP (1966 cm(-)(1); Deltanu(CO) = +63 cm(-)(1)), and OEP (1958 cm(-)(1); Deltanu(CO) = +72 cm(-)(1)) analogues. Five of these (por)Os(ArNO)-containing complexes have been fully characterized by spectroscopic methods and by single-crystal X-ray crystallography. All the nitrosoarene ligands in these complexes are attached to the formally Os(II) centers via an eta(1)-N binding mode.
