posted on 2018-10-10, 00:00authored byO. Guselnikova, A. Olshtrem, Y. Kalachyova, I. Panov, P. Postnikov, V. Svorcik, O. Lyutakov
Utilization
of plasmonics as a driving tool for chemical transformation
triggering enables to achieve unprecedented results regarding photochemical
conversion efficiency and chemical selectivity regulation. In this
study, the bimetallic surface plasmon-polariton-supported grating
is proposed as an effective background for plasmon-induced hydrogenation
of alkynyl groups of absolute chemoselectivity. The periodical bimetallic
structure consists of spatially modulated gold layers, covered with
the nanometer-thick platinum layer. The alkyne bonds are covalently
attached to the surface of the catalytic system through covalent grafting
of the bimetallic surface with 4-ethynylbenzenediazonium tosylate,
with triple bonds separated from the platinum layer by the benzene
rings. The proposed bimetallic structure enables selective hydrogenation
of alkyne bonds to alkenyl or alkyl moieties using cyclohexene as
a hydrogen source. The selectivity of hydrogenation can be controlled
by changing the structure parameters, for example, the thickness of
the upper platinum layer.