Controlled dealkylation by BBr3: efficient synthesis of para-alkoxy-phenols
摘要:
Controlled dealkylation of dialkyl-aryl-ethers by substoichiometric BBr3 has been developed as a general tool for the differentiation of the oxygen functions in hydroquinone derivatives. The reaction proceeds smoothly at rt either on linear or branched alkyl-ethers and provides the corresponding p-alkoxy-phenols RO-Ar-OH in high yields. With respect to the conventional alkylation path of Ar(OH)(2), this process represents a tunable and convenient route to key intermediates for conjugated materials with differentiated side chains. (C) 2012 Elsevier Ltd. All rights reserved.
Amphiphilic polymers functionalized with glucose or a derivative thereof
申请人:Synchimia S.r.l.
公开号:EP2620461A1
公开(公告)日:2013-07-31
Amphiphilic polymers functionalized with glucose or derivatives thereof are described, in particular poly(p-phenylene ethynylene) substituted by a molecule of glucose or a derivative thereof. Said polymers find advantageous use in the field of fluorescence-quenching optical sensors or in the field of OLEDs (Organic Light Emitting Diodes).
Synthesis of double-conjugated-segment molecules and their application as ultra-broad two-photon-absorption optical limiters
作者:Junxiang Zhang、Yiping Cui、Mingliang Wang、Juzheng Liu
DOI:10.1039/b208190c
日期:2002.10.18
A series of novel double-conjugated-segment molecules, in which two conjugated segments are separated by an ether chain, were synthesized; these compounds provide a very broad two-photon absorption spectral range, which satisfies an urgent need in the optical limiting area.
Controlled dealkylation of dialkyl-aryl-ethers by substoichiometric BBr3 has been developed as a general tool for the differentiation of the oxygen functions in hydroquinone derivatives. The reaction proceeds smoothly at rt either on linear or branched alkyl-ethers and provides the corresponding p-alkoxy-phenols RO-Ar-OH in high yields. With respect to the conventional alkylation path of Ar(OH)(2), this process represents a tunable and convenient route to key intermediates for conjugated materials with differentiated side chains. (C) 2012 Elsevier Ltd. All rights reserved.