化学
分子间力
堆积
磷光
氢键
单体
无定形固体
结晶学
金属间化合物
光化学
分子
聚合物
有机化学
物理
荧光
量子力学
合金
作者
Sebastian Wilde,Darío González‐Abradelo,Constantin Gabriel Daniliuc,Marcus Böckmann,Nikos L. Doltsinis,Cristian Alejandro Strassert
标识
DOI:10.1002/ijch.201800050
摘要
Abstract In this work we describe the synthesis and DFT‐supported photophysical characterization of a series of Pt(II) complexes bearing tetradentate luminophores with increasing degree of fluorination. Aggregation into crystalline phases leads to substitution‐dependent arrangements that in all cases hinder intermetallic coupling, as intermolecular interactions are dominated by hydrogen bonding and π‐stacking. In amorphous matrices, on the other hand, we observed that an increasing level of fluorination favors the tendency towards Pt−Pt interaction upon aggregation, leading to a red‐shifted phosphorescence, if compared with monomeric species in dilute solutions and crystalline solids.
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