Abstract
The first tetraaza macrocycle supported zirconium imido complex [Zr(tmtaa)(NC6H3Pri2-2,6(py)] and the new titanium imido base-free analogues [Ti(tmtaa)(NAr)](Ar = Ph or C6H4Me-4) react with isocyanates to give N,N′-bound ureate complexes; these can undergo exchange reactions with excess aryl isocyanate via reversible insertion into the Ti-N(ureate) bond; the X-ray structure of [Zr(tmtaa)-{(NC2H3Pri2-2,6)(CO)(NBut)}] is described {H2tmtaa = tetramethyldibenzotetraaza[14]annulene).
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