SET-LRP from Programmed Difunctional Initiators Encoded with Double Single-Cleavage and Double Dual-Cleavage Groups

被引:15
|
作者
Moreno, Adrian [1 ]
Ronda, Juan C. [1 ]
Cadiz, Virginia [1 ]
Galia, Marina [1 ]
Lligadas, Gerard [1 ,2 ]
Percec, Virgil [2 ]
机构
[1] Univ Rovira & Virgili, Dept Analyt Chem & Organ Chem, Lab Sustainable Polymers, E-43007 Tarragona, Spain
[2] Univ Penn, Dept Chem, Roy & Diana Vagelos Labs, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
LIVING RADICAL POLYMERIZATION; CLICK CHEMISTRY; BIPHASIC MIXTURES; ELECTRON TRANSFER; POLYMERS; WATER; MACROMONOMERS; DISULFIDE; SOLVENT; STIMULI;
D O I
10.1021/acs.biomac.9b00892
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of stimuli-cleavable difunctional initiators containing a discrete single-type cleavable junction represents a general strategy to prepare mid-chain-degradable vinylic polymers. Here, we present a series of alpha-haloester-type programmed initiators encoding multiple single-type and dual-type cleavable junctions. Multiple single-cleavage groups increase the cleavage rate, whereas double-dual sites provide access to multiple mechanisms for cleavage. Single-electron transfer living radical polymerization was employed to generate well-defined mid-chain-cleavable poly(methyl acrylate)s designed with low-pH, low-pH/reduction, or low-pH/UV light cleavable linkages. Kinetic studies demonstrated that the polymerizations are living when using various catalytic Cu(0) sources (wire and powder), ligands (Me-6-TREN and TREN), and solvent sources (homogeneous and "programmed" biphasic). Moreover, structural analyses by NMR and matrix-assisted laser desorption/ionization-time-of-flight confirmed the near-perfect chain-end functionality of these stimuli-cleavable polymers derived from programmed initiators. A rigorous gel permeation chromatography study demonstrated that the combination of multiple acetal, disulfide, or 2-nitroresorcinol-derived acetal junctions offer attractive possibilities in terms of selective cleavage and orthogonal degradation.
引用
收藏
页码:3200 / 3210
页数:11
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