化学
溶剂变色
光化学
接受者
乙腈
溶剂
发色团
荧光
晶体结构
吸收(声学)
电子结构
电子受体
密度泛函理论
结晶学
计算化学
有机化学
物理
量子力学
凝聚态物理
声学
作者
Roslyn S. Butler,Pamela Cohn,Phillip A Tenzel,Khalil A. Abboud,Ronald K. Castellano
摘要
“Push−pull” purines have been synthesized by the introduction of electron-accepting functional groups (A = CN, CO2Me, and CONHR) to the heterocyclic C(8) position to complement typical electron-donating substituents at C(2) (D1) and C(6) (D2). The donor−acceptor purines show significantly altered, and overall improved photophysical properties relative to their acceptor-free precursors (A = H); these include red-shifted (20−50 nm) absorption maxima, highly solvatochromic emission profiles (em λmax from 355−466 nm depending on substitution pattern and solvent) with excellent linear correlations between emission energy and solvent polarity (ETN), improved photochemical stability upon continuous irradiation, and enhanced (up to 2500%) fluorescence quantum yields. Comprehensive structure−property studies show how the absorption/emission maxima and quantum yields depend on donor and acceptor structure, relative donor position (C(2) or C(6)), and solvent (1,4-dioxane, dichloromethane, acetonitrile, methanol, and in some cases water). Further insight regarding electronic structure comes from a quantitative treatment of the solvent-dependent emission data (that provides Δμge values ranging from 1.9 to 3.4 D) and DFT (B3LYP/6-311++G**) electronic structure calculations. X-ray crystal structures of several derivatives showcase the molecular recognition capabilities of the donor−acceptor chromophores that overall have photophysical and structural properties suitable for applications in biosensing and materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI