Transcending the Trade-off in Refractive Index and Abbe Number for Highly Refractive Polymers: Synergistic Effect of Polarizable Skeletons and Robust Hydrogen Bonds

IF 4.7 Q1 POLYMER SCIENCE
Seigo Watanabe, Teru Takayama and Kenichi Oyaizu*, 
{"title":"Transcending the Trade-off in Refractive Index and Abbe Number for Highly Refractive Polymers: Synergistic Effect of Polarizable Skeletons and Robust Hydrogen Bonds","authors":"Seigo Watanabe,&nbsp;Teru Takayama and Kenichi Oyaizu*,&nbsp;","doi":"10.1021/acspolymersau.2c00030","DOIUrl":null,"url":null,"abstract":"<p >High-refractive-index polymers (HRIPs) are attractive materials for the development of optical devices with high performances. However, because practical components and structures for HRIPs are limited from the viewpoint of synthetic techniques, it has proved difficult using traditional strategies to enhance the refractive index (RI) of HRIPs to more than a certain degree (over 1.8) while maintaining their visible transparency. Here, we found that poly(phenylene sulfide) (<b>PPS</b>) derivatives featuring both methylthio and hydroxy groups can simultaneously exhibit balanced properties of an ultrahigh RI of <i>n</i><sub>D</sub> = 1.85 and Abbe number of ν<sub>D</sub> = 20 owing to the synergistic effect of high molar refraction and dense intermolecular hydrogen bonds (H-bonds). This brand new strategy is anticipated to contribute to the development of HRIPs displaying ultrahigh RI with adequate Abbe numbers beyond the empirical <i>n</i><sub>D</sub>–ν<sub>D</sub> threshold, which has not been achieved to date.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"2 6","pages":"458–466"},"PeriodicalIF":4.7000,"publicationDate":"2022-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/86/12/lg2c00030.PMC9955235.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.2c00030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 1

Abstract

High-refractive-index polymers (HRIPs) are attractive materials for the development of optical devices with high performances. However, because practical components and structures for HRIPs are limited from the viewpoint of synthetic techniques, it has proved difficult using traditional strategies to enhance the refractive index (RI) of HRIPs to more than a certain degree (over 1.8) while maintaining their visible transparency. Here, we found that poly(phenylene sulfide) (PPS) derivatives featuring both methylthio and hydroxy groups can simultaneously exhibit balanced properties of an ultrahigh RI of nD = 1.85 and Abbe number of νD = 20 owing to the synergistic effect of high molar refraction and dense intermolecular hydrogen bonds (H-bonds). This brand new strategy is anticipated to contribute to the development of HRIPs displaying ultrahigh RI with adequate Abbe numbers beyond the empirical nD–νD threshold, which has not been achieved to date.

Abstract Image

超越高折射聚合物折射率和阿贝数的权衡:可极化骨架和坚固氢键的协同效应
高折射率聚合物(HRIPs)是开发高性能光学器件的重要材料。然而,从合成技术的角度来看,由于hrip的实际组件和结构有限,使用传统的策略很难将hrip的折射率(RI)提高到一定程度以上(大于1.8),同时保持其可见光透明度。本研究发现,由于高的摩尔折射和密集的分子间氢键(h -键)的协同作用,具有甲基硫基和羟基的聚苯硫醚(PPS)衍生物可以同时表现出nD = 1.85的超高RI和νD = 20的阿贝数的平衡性质。这种全新的策略预计将有助于开发具有超高RI的hrip,其阿贝数超过经验nD -νD阈值,这是迄今为止尚未实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
2.50
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信