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Title: Ultraviolet photochemistry of Co{sup III}L(H{sub 2}O)SO{sub 3}{sup +} [L = Me{sub 6}[14]dieneN{sub 4}, [14]aneN{sub 4}] complexes. Quandaries about the linkage isomerization to O-bonded sulfite and the photogeneration of cobalt(I) in sequential biphotonic photolysis

Journal Article · · Inorganic Chemistry
DOI:https://doi.org/10.1021/ic9813213· OSTI ID:682138
; ;  [1]
  1. Univ. of Notre Dame, IN (United States)

The catalyzed and uncatalyzed oxidation of sulfite have been a matter of continued interest. Attention to these processes has a basic science motive as well as the need to resolve a number of long-recognized technical problems, i.e., gas desulfurization, pollution, and health problems. Two new macrocyclic complexes with S-bonded sulfite, Co(Me{sub 6}[14]diene N{sub 4})(H{sub 2}O)SO{sub 3}{sup +} and Co([14]ane N{sub 4})(H{sub 2}O)SO{sub 3}{sup +}, were prepared. The type of the So{sub 3}{sup 2{minus}} linkage in [Co(Me{sub 6}[14]diene N{sub 4})(H{sub 2}O)SO{sub 3}]ClO{sub 4} was established by means of the X-ray structure (crystal system, orthorhombic). In a study of the photochemical properties, transient spectra revealed the photoredox formation of Co(II) macrocycles and the photoisomerization to O-bonded sulfite. Precursors of these products were also observed and tentatively identified as an ion pair and an adduct of the SO{sub 3}{sup {sm_bullet}{minus}} radical and the unsaturated macrocycle Me{sub 6}[14]diene N{sub 4}. The photogeneration of SO{sub 3}{sup {sm_bullet}{minus}} was verified by means of the radical`s ESR spectrum. High power laser irradiations resulted in the secondary photolysis of the intermediates and the formation of Co(I) products. The mechanism of the primary and secondary photolysis is discussed.

Sponsoring Organization:
USDOE, Washington, DC (United States)
OSTI ID:
682138
Journal Information:
Inorganic Chemistry, Vol. 38, Issue 12; Other Information: PBD: 14 Jun 1999
Country of Publication:
United States
Language:
English

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