Engineering modifiers bearing benzophenone with enhanced reactivity to construct surface microstructures?
Polymer Chemistry Pub Date: 2019-08-08 DOI: 10.1039/C9PY00764D
Abstract
Surface microstructures with desirable functions are a critical factor that influence the performance of microdevices. Modification of surfaces with polymer modifiers is a popular and effective way to develop surface microstructures. However, constructing a patterned surface with controllable thickness is still a challenge for common modification methods. In this work, we propose a novel strategy to increase the graft efficiency of a benzophenone (BP)-capped modifier via tuning the chain backbone, so that the coated molecules can be chemically preserved and the thickness of the functional layer is controllable. Modifiers with a single BP end-group were designed and synthesized by using polyether (BP-CO), alkyl (BP-C), and perfluoroalkyl (BP-CF) as the chain backbone, respectively. For the modified layer, a graft efficiency of 91% was obtained by using BP-CO, which is over ten times higher than that of BP-C and BP-CF, making the layer thickness up to micrometers. Two hydrophilic polymer modifiers (BPEG and BPS) with the main chain composed of polyether and polyolefin were also prepared. Compared to BPS, a modified layer based on BPEG showed obvious anti-platelet adhesion and constructed a patterned surface with controllable thickness easily. This simple and effective strategy could provide new insights into designing modifiers to build a functional surface microstructure.
Recommended Literature
- [1] Exchangeability of amino acid residues with similar physicochemical properties in coiled-coil interactions? Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng CaiChem. Commun., 2013,49, 11086-11088 10.1039/C3CC46560H
- [2] Evidence of rutile-to-anatase photo-induced electron transfer in mixed-phase TiO2 by solid-state NMR spectroscopy? Weili Dai,Guangjun Wu,Michael HungerChem. Commun., 2015,51, 13779-13782 10.1039/C5CC04971G
- [3] Emergence of cationic polyamine dendrimersomes: design, stimuli sensitivity and potential biomedical applications Partha Laskar,Christine DufèsNanoscale Adv., 2021,3, 6007-6026 10.1039/D1NA00536G
- [4] Evolution and characterization of a benzylguanine-binding RNA aptamer? J. Xu,T. J. Carrocci,A. A. HoskinsChem. Commun., 2016,52, 549-552 10.1039/C5CC07605F
- [5] Fate of nitrogen-15 in the subsequent growing season of greenhouse tomato plants (Lycopersicon esculentum Mill) as influenced by alternate partial root-zone irrigation Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue GaoRSC Adv., 2017,7, 34392-34400 10.1039/C7RA05271E
- [6] Evidence of pre-micellar aggregates in aqueous solution of amphiphilic PDMS–PEO block copolymer? Domenico Lombardo,Gianmarco Munaò,Pietro Calandra,Luigi Pasqua,Maria Teresa CaccamoPhys. Chem. Chem. Phys., 2019,21, 11983-11991 10.1039/C9CP02195G
- [7] Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China? Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing LiFood Funct., 2018,9, 4234-4245 10.1039/C8FO00787J
- [8] Excess electrons in lithium–ethylamine solutions—density, electrical conductivity and EPR studies Phys. Chem. Chem. Phys., 1999,1, 3561-3565 10.1039/A900683D
- [9] Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction? Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei SehJ. Mater. Chem. A, 2018,6, 21885-21890 10.1039/C8TA06567E
- [10] Dissociation of aryl sulfonyl phthalimide radical anions: relevance to the biological activity of arylsulfonyl amides? Abdelaziz Houmam,Emad M. HamedChem. Commun., 2012,48, 11328-11330 10.1039/C2CC36835H
Journal Name:Polymer Chemistry
research_products
-
CAS no.: 89640-58-4