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Fullerene‐Promoted Singlet‐Oxygen Photochemical Oxygenations in Glass‐Polymer Microstructured Reactors
Author(s) -
Carofiglio Tommaso,
Donnola Paola,
Maggini Michele,
Rossetto Massimiliano,
Rossi Emiliano
Publication year - 2008
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200800459
Subject(s) - singlet oxygen , chemistry , reagent , photochemistry , covalent bond , polymer , photodegradation , fullerene , peroxide , oxygen , chemical engineering , organic chemistry , catalysis , photocatalysis , engineering
Abstract In this paper we report the fabrication of thiolene‐based microstructured reactors (MRs) that have been specifically designed to include solid‐supported reagents within the microchannels network. We propose a convenient solution to realize reversible press‐fit, leak‐proof interconnects that greatly simplify the MR coupling to the external environment such as capillary tubing, sample reservoirs and pumps. The MRs have been used to carry out the oxidation of α‐terpinene and methionine using [60]fullerene, covalently linked to Tentagel ® and silica gel matrices, as a singlet oxygen sensitizer. High conversions have been observed for both substrates although, in the case of α‐terpinene, a partial photodegradation of the endo ‐peroxide product was detected. Interestingly, in the case of methionine, a quantitative conversion to the corresponding sulfoxides was achieved in about 40 seconds, using low‐power, white LED illumination. The reaction time is considerably shorter when compared to the batch procedure that requires, for the same process, about one hour illumination and the use of a 300‐W tungsten halogen lamp.

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