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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 651-654 
    ISSN: 1434-1948
    Keywords: Manganese ; Coordination modes ; 1-Hydronaphthalene complexes ; Trimethylphosphite addition ; Photochemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tricarbonyl(2-4,4a,8a-η-1-hydronaphthalene)manganese (1) reacts readily with trimethyl phosphite to afford tricarbonyl(2-4-η-1-hydronaphthalene)(trimethyl phosphite)manganese (2), by a simultaneous η5-η3-hapticity change. Upon UV irradiation, one carbonyl ligand is preferentially cleaved from 2 to yield dicarbonyl(2-4,4a,8a-η-1-hydronaphthalene)(trimethyl phosphite)manganese (3), with a η5-coordinated 1-hydronaphthalene ligand. In a similar fashion 3 also reacts with trimethyl phosphite and forms dicarbonyl(2-4-η-1-hydronaphthalene)bis(trimethyl phosphite)manganese (4), which loses carbon monoxide upon UV irradiation to afford carbonyl(2-4,4a,8a-η-1-hydronaphthalene)bis(trimethyl phosphite)manganese (5). All compounds were characterized by IR and NMR spectroscopy. The η5-1-hydronaphthalene complexes 1, 3 and 5 show hindered 1,4-H shifts of 1-Hendo. Considerable energy barriers were also found for the rotation of the 1-hydronaphthalene ligand in 2-5.
    Type of Medium: Electronic Resource
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