Chenhuai Deng , Yuanhao Lin , Xuehui Ge , Hongjie Yang , Linxi Hou , Longqiang Xiao
{"title":"Facile synthesis of carbon dioxide and UV light dual-responsive asymmetric tetrablock polymers","authors":"Chenhuai Deng , Yuanhao Lin , Xuehui Ge , Hongjie Yang , Linxi Hou , Longqiang Xiao","doi":"10.1016/j.reactfunctpolym.2024.106077","DOIUrl":null,"url":null,"abstract":"<div><div>This work reports the synthesis of CO<sub>2</sub>/ultraviolet (UV) light dual-responsive CABC-type asymmetric tetrablock polymers (CABC-ATP) based on organocatalyzed reversible complexation-mediated radical polymerization (RCMP) with methyl methacrylate (MMA), 2-Propenoic acid, 2-methyl-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester (CMMA), and 2-(dimethylamino)ethyl methacrylate (DMAEMA) as block monomers by three steps. The obtained CABC-ATP has controllable number average molecular weight (<em>M</em><sub>n</sub>) and narrow molecular weight distribution (<em>M</em><sub>w</sub>/<em>M</em><sub>n</sub> = 1.18–1.29). The hydrodynamic diameter and fluorescence intensity were measured using dynamic light scattering coupled with fluorescence assays. Notably, the vesicle volume increased from an initial measurement of 247.6 nm to 285.4 nm post-experiment. The initial fluorescence emission intensity recorded was 4971, which decreased to 1412 following the introduction of carbon dioxide for 20 min. Subsequently, the fluorescence intensity recovered to 5199 upon nitrogen exposure. The response behavior of CABC-ATP to UV light is due to the cross-linking of coumarin-based monomer, resulting in the change of fluorescence intensity at the macro level. Besides, the protonation of tertiary amine is promoted by the stimulation of CO<sub>2</sub>, generating of the change of vesicle volume at the micro level.</div></div>","PeriodicalId":20916,"journal":{"name":"Reactive & Functional Polymers","volume":"205 ","pages":"Article 106077"},"PeriodicalIF":4.5000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive & Functional Polymers","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381514824002529","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0
Abstract
This work reports the synthesis of CO2/ultraviolet (UV) light dual-responsive CABC-type asymmetric tetrablock polymers (CABC-ATP) based on organocatalyzed reversible complexation-mediated radical polymerization (RCMP) with methyl methacrylate (MMA), 2-Propenoic acid, 2-methyl-4-methyl-2-oxo-2H-1-benzopyran-7-yl ester (CMMA), and 2-(dimethylamino)ethyl methacrylate (DMAEMA) as block monomers by three steps. The obtained CABC-ATP has controllable number average molecular weight (Mn) and narrow molecular weight distribution (Mw/Mn = 1.18–1.29). The hydrodynamic diameter and fluorescence intensity were measured using dynamic light scattering coupled with fluorescence assays. Notably, the vesicle volume increased from an initial measurement of 247.6 nm to 285.4 nm post-experiment. The initial fluorescence emission intensity recorded was 4971, which decreased to 1412 following the introduction of carbon dioxide for 20 min. Subsequently, the fluorescence intensity recovered to 5199 upon nitrogen exposure. The response behavior of CABC-ATP to UV light is due to the cross-linking of coumarin-based monomer, resulting in the change of fluorescence intensity at the macro level. Besides, the protonation of tertiary amine is promoted by the stimulation of CO2, generating of the change of vesicle volume at the micro level.
期刊介绍:
Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers.
Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.