†Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.
‡State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, People's Republic of China.
J Am Chem Soc. 2015 Jul 8;137(26):8572-83. doi: 10.1021/jacs.5b04156. Epub 2015 Jun 25.
Research on stable open-shell singlet diradicaloids recently became a hot topic because of their unique optical, electronic, and magnetic properties and promising applications in materials science. So far, most reported singlet diradicaloid molecules have a symmetric structure, while asymmetric diradicaloids with an additional contribution of a dipolar zwitterionic form to the ground state were rarely studied. In this Article, a series of new push-pull type oligo(N-annulated perylene)quinodimethanes were synthesized. Their chain length and solvent-dependent ground states and physical properties were systematically investigated by various experimental methods such as steady-state and transient absorption, two-photon absorption, X-ray crystallographic analysis, electron spin resonance, superconducting quantum interference device, Raman spectroscopy, and electrochemistry. It was found that with extension of the chain length, the diradical character increases while the contribution of the zwitterionic form to the ground state becomes smaller. Because of the intramolecular charge transfer character, the physical properties of this push-pull system showed solvent dependence. In addition, density functional theory calculations on the diradical character and Hirshfeld charge were conducted to understand the chain length and solvent dependence of both symmetric and asymmetric systems. Our studies provided a comprehensive understanding on the fundamental structure- and environment-property relationships in the new asymmetric diradicaloid systems.
最近,由于具有独特的光学、电子和磁学性质以及在材料科学中的广阔应用前景,稳定的开壳 singlet 双自由基的研究成为了热点。到目前为止,大多数报道的 singlet 双自由基分子都具有对称的结构,而对于具有额外偶极双极性 zwitterionic 形式贡献的不对称双自由基研究较少。在本文中,我们合成了一系列新型的推拉型寡聚(N-稠合苝)醌二亚甲基。通过稳态和瞬态吸收、双光子吸收、X 射线晶体学分析、电子顺磁共振、超导量子干涉装置、拉曼光谱和电化学等各种实验方法,系统地研究了它们的链长和溶剂依赖性基态和物理性质。研究发现,随着链长的增加,双自由基特征增加,而基态中 zwitterionic 形式的贡献变小。由于分子内电荷转移特性,该推拉体系的物理性质表现出溶剂依赖性。此外,我们还进行了双自由基特征和 Hirshfeld 电荷的密度泛函理论计算,以了解对称和不对称体系的链长和溶剂依赖性。我们的研究为新的不对称双自由基体系的基本结构-和环境-性质关系提供了全面的理解。