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Two-Photon-Triggered NO Release via a Ruthenium–Nitrosyl Complex with a Star-Shaped Architecture
Author(s) -
Margarita Romero Ávila,
Andrés Felipe León Rojas,
Pascal G. Lacroix,
Isabelle Malfant,
Norberto Farfán,
Rana Mhanna,
Rosa Santillán,
Gabriel RamosOrtíz,
JeanPierre Malval
Publication year - 2020
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.0c01953
Subject(s) - delocalized electron , ruthenium , absorption (acoustics) , terpyridine , photochemistry , materials science , coupling (piping) , photon , star (game theory) , two photon absorption , chemistry , optics , physics , composite material , catalysis , organic chemistry , metal , laser , astrophysics , metallurgy
We report herein a molecular engineering strategy based on the design of a multipolar ruthenium-nitrosyl (Ru-NO) complex with a three-branched architecture. The three Ru-NO units are introduced at the periphery of a highly π-delocalized truxene core bearing three terpyridine ligands. The two-photon absorption capabilities of the complex were investigated by the Z-scan technique. The strong electronic coupling among the individual arms gives rise to a very strong two-photon absorption response (δ 800 nm ∼ 1600 GM), which corresponds to a 16-fold enhancement of the capability of a single-arm reference, thereby promoting an efficient light-driven NO release process in aqueous media.

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