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7-芳亚甲基异长叶烷酮类化合物的合成及其紫外吸收特征

芮坚 徐徐 杨益琴 黄建峰 王石发

南京林业大学学报(自然科学版)2016,Vol.40Issue(2):88-94,7.
南京林业大学学报(自然科学版)2016,Vol.40Issue(2):88-94,7.DOI:10.3969/j.issn.1000-2006.2016.02.015

7-芳亚甲基异长叶烷酮类化合物的合成及其紫外吸收特征

Synthesis and ultraviolet absorption characteristics of 7-arylidene-isolongifolanene

芮坚 1徐徐 1杨益琴 2黄建峰 3王石发4

作者信息

  • 1. 南京林业大学化学工程学院,江苏 南京 210037
  • 2. 江苏省生物质绿色燃料与化学品重点实验室,江苏 南京 210037
  • 3. 南京林业大学江苏省林业资源高效加工利用协同创新中心,江苏 南京 210037
  • 4. 南京林业大学轻工科学与工程学院,江苏 南京 210037
  • 折叠

摘要

Abstract

A series of 7⁃arylidene⁃isolongifolanone a—j were synthesized by condensation of isolongifolanone with aro⁃matic aldehydes including 4⁃bromobenzaldehyde, 4⁃fluorobenzaldehyde, 3⁃nitrobenzaldehyde, 2,4⁃dichlorobenzaldehyde under catalyzation of potassium tert⁃butoxide. The structures of compounds a—j were identified by means of 1 H NMR, 13 C NMR, GC⁃MS and FT⁃IR, and their ultraviolet absorption characteristics as well as light stabilities were also investi⁃gated. The results showed that compounds a, b, c, d and j exhibited good absorbency as the medium⁃wave ultraviolet ( UVB) type absorbents,and compounds e, f, g, h and i had both functions as long⁃wave ultraviolet ( UVA) and UVB absorbents. The light stability sequence of those compounds was h>g>e>c>a>d>b>f>i>j. The UV absorption intensity was d>i>e>h>g>f>b>c>j>a.

关键词

异长叶烷酮/7-芳亚甲基异长叶烷酮/紫外吸收/光稳定性

Key words

isolongifolanone/7-arylidene-isolongifolanone/ultraviolet absorption/lightstability

分类

化学化工

引用本文复制引用

芮坚,徐徐,杨益琴,黄建峰,王石发..7-芳亚甲基异长叶烷酮类化合物的合成及其紫外吸收特征[J].南京林业大学学报(自然科学版),2016,40(2):88-94,7.

基金项目

江苏省高校自然科学研究重大项目(14KJA220001);国家自然科学基金项目(31170538,31470592);江苏省生物质能源与材料重点实验室开放基金 ()

南京林业大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1000-2006

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