{"title":"Synthesis and Optical Properties of Near-Infrared (NIR) Absorbing Azo Dyes","authors":"S. Patil, Amol S. Chaudhary","doi":"10.19080/ctftte.2019.04.555649","DOIUrl":null,"url":null,"abstract":"This chapter provides a general overview and information on near-infrared (NIR) absorbing azo dyes. In this work, we have developed an efficient and simple protocol for the synthesis of novel A- π -D- π -A NIR azo dyes. The near-infrared absorbing azo dyes were synthesized by using 2-hydroxy-1,4 naphthoquinone (Lawsone) and different substituted aromatic primary amines. Furthermore, author developed push-pull chromophores of A- π -D- π -A type containing an electron-withdrawing azo core, phenazine moieties, and a hydroxyl group as electron donor. The benzo[a]quinoxalino[2,3-i]phenazin-5-ol moiety was introduced to make the system planer as well as to increase the π -conjugation. The optical properties of these dyes were studied in N,N -dimethylformamide (DMF).","PeriodicalId":447757,"journal":{"name":"Current Trends in Fashion Technology & Textile Engineering","volume":"2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Trends in Fashion Technology & Textile Engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.19080/ctftte.2019.04.555649","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
This chapter provides a general overview and information on near-infrared (NIR) absorbing azo dyes. In this work, we have developed an efficient and simple protocol for the synthesis of novel A- π -D- π -A NIR azo dyes. The near-infrared absorbing azo dyes were synthesized by using 2-hydroxy-1,4 naphthoquinone (Lawsone) and different substituted aromatic primary amines. Furthermore, author developed push-pull chromophores of A- π -D- π -A type containing an electron-withdrawing azo core, phenazine moieties, and a hydroxyl group as electron donor. The benzo[a]quinoxalino[2,3-i]phenazin-5-ol moiety was introduced to make the system planer as well as to increase the π -conjugation. The optical properties of these dyes were studied in N,N -dimethylformamide (DMF).