J. Perry, S. Marder, L. Cheng, G. Bourhill, K. Mansour, C. Gorman, S. Gilmour, B. Tiemann
{"title":"Nonlinear Polarizabilities of Symmetric and Non-symmetric Polyene and Cyanine-Like Organic Molecules","authors":"J. Perry, S. Marder, L. Cheng, G. Bourhill, K. Mansour, C. Gorman, S. Gilmour, B. Tiemann","doi":"10.1364/nlo.1992.fa7","DOIUrl":null,"url":null,"abstract":"There is considerable interest in understanding the origin of the molecular nonlinear polarizabilities. Recently, the important role of bond alternation (difference in the carbon-carbon double bond and single bond lengths) in influencing the second order polarizability, β, of asymmetric conjugated dyes has been pointed out.[1] It was suggested that there is an optimal degree of alternation needed to maximize β. The connection between bond-alternation and the electronic, optical and chemical properties of conjugated molecules has also been recognized previously.[2] These studies as well as the results of prior experimental studies[3] have led us to investigate the affect of bond alternation on the third-order polarizability, γ. One aim of the present work is to gain insight into the differences between the magnitude and signs of γ for simple polyenes and cyanines. For moderate length to long polyenes, nonresonant electronic γ is positive, whereas for comparable cyanines γ is negative.","PeriodicalId":219832,"journal":{"name":"Nonlinear Optics: Materials, Fundamentals, and Applications","volume":"490 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nonlinear Optics: Materials, Fundamentals, and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1364/nlo.1992.fa7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
There is considerable interest in understanding the origin of the molecular nonlinear polarizabilities. Recently, the important role of bond alternation (difference in the carbon-carbon double bond and single bond lengths) in influencing the second order polarizability, β, of asymmetric conjugated dyes has been pointed out.[1] It was suggested that there is an optimal degree of alternation needed to maximize β. The connection between bond-alternation and the electronic, optical and chemical properties of conjugated molecules has also been recognized previously.[2] These studies as well as the results of prior experimental studies[3] have led us to investigate the affect of bond alternation on the third-order polarizability, γ. One aim of the present work is to gain insight into the differences between the magnitude and signs of γ for simple polyenes and cyanines. For moderate length to long polyenes, nonresonant electronic γ is positive, whereas for comparable cyanines γ is negative.