We present the complete off-shell structure of conformal supergravity in ten dimensions. It is based on 128 + 128 degrees of freedom and its formulation requires differential constraints. We study how these constraints are resolved in four and five dimensions. Covariant conditions are given that restrict conformal supergravity to its on-shell Poincar6 counterpart. In ten dimensions the relationship between the two theories has new and unusual aspects, which we explore in a variety of ways. We rewrite on-shell Poincar6 supergravity in a superconformally invariant form, from which we deduce that its off-shell version must contain at least a scalar (chiral) multiplet. We analyze some aspects of the non-linear structure of the field representation based on the conformal fields combined with one scalar multiplet.
The mechanism and the reactive species involved in the oxidation of alkenes, and alcohols with H 2 O 2 , catalysed by an in situ prepared mixture of a Mn II salt, pyridine-2-carboxylic acid and a ketone is elucidated using substrate competition experiments, kinetic isotope effect (KIE) measurements, and atom tracking with 18 O labelling. The data indicate that a single reactive species engages in the oxidation of both alkenes and alcohols. The primary KIE in the oxidation of benzyl alcohols is ca. 3.5 and shows the reactive species to be selective despite a zero order dependence on substrate concentration, and the high turnover frequencies (up to 30 s À 1 ) observed. Selective 18 O labelling identifies the origin of the oxygen atoms transferred to the substrate during oxidation, and is consistent with a highly reactive, e. g., [Mn V (O)(OH)] or [Mn V (O) 2 ], species rather than an alkylperoxy or hydroperoxy species.
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