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  1. ; ; ; (, Chemical Communications)
    Structure, spectroscopic data and reactivity of the first isolated technetium(-1) compound, stabilized by a sterically encumbered isocyanide, are provided. 
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  2. ; ; ; ; ; (, Organometallics)
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  3. ; ; ; ; ; ; ; (, Organometallics)
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  4. ; ; ; ; ; ; (, Chemical Communications)
    The mixed isocyanide/carbonyl complexes cis - and trans -[Re(CO) 3 Br(CNAr Dipp2 ) 2 ] (Ar Dipp2 = 2,6-(2,6-(i-Pr) 2 C 6 H 3 ) 2 C 6 H 3 ) can be synthesized from reactions of [Re(CO) 5 Br] and CNAr Dipp2 depending on the conditions applied. Reduction of the neutral Re( i ) species gives the monoanionic complex [Re(CO) 3 (CNAr Dipp2 ) 2 ] − or the neutral [Re(CO) 3 (CNAr Dipp2 ) 2 ], which contain rhenium in the formal oxidation states “−1” and “0”, respectively. 
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  5. ; ; ; ; ; ; ; ; (, Angewandte Chemie International Edition)
    Abstract The first consistent series of mononuclear 17‐electron complexes of three Group 7 elements has been isolated in crystalline form and studied by X‐ray diffraction and spectroscopic methods. The paramagnetic compounds have a composition of [M0(CO)(CNp‐F‐ArDArF2)4] (M=Mn, Tc, Re; ArDArF2=2,6‐(3,5‐(CF3)2C6H3)2C6H2F) and are stabilized by four sterically encumbering isocyanides, which prevent the metalloradicals from dimerization. They have a square pyramidal structure with the carbonyl ligands as apexes. The frozen‐solution EPR spectra of the rhenium and technetium compounds are clearly anisotropic with large99Tc and185,187Re hyperfine interactions for one component. High‐field EPR (Q band and W band) has been applied for the elucidation of the EPR parameters of the manganese(0) complex. 
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