J Terence Blaskovits, Clémence Corminboeuf, Marc H Garner
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引用次数: 0
摘要
在低位单重态和三重态之间违反亨德规则的分子可能会催生新一代的荧光发光体。然而,目前已知的具有这种特性的分子只有几类。在这里,我们利用 FORMED 数据库的高通量筛选算法,发现了一类第一激发态违反亨德规则的化合物。我们研究了这类桥[10]-和[14]环烯周边饱和桥,并将它们与违反 Hund 规则的已知共轭多环系统联系起来。尽管与相关的非互变多环烃类在结构上有相似之处,但这些桥联环烯周圈的机理却有所不同。在这里,每个激发态都有两个分子轨道构型。因此,只能根据最低激发态的单重态和三重态的对称性来确定是否违反了亨德规则。通过几个合成现实分子的例子,桥接[10]-和[14]环烯类为已知的违反 Hund 规则的非互变和互变(氮杂萘)类分子提供了结构上的联系。这些设计原理可能为鉴定光物理相关的第一激发单重态和三重态顺序颠倒的新型分子开辟了道路。
Excited-State Hund's Rule Violations in Bridged [10]- and [14]Annulene Perimeters.
Molecules with Hund's rule violations between low-lying singlet and triplet states may enable a new generation of fluorescent emitters. However, only a few classes of molecules are known with this property at the current time. Here, we use a high-throughput screening algorithm of the FORMED database to uncover a class of compounds where the first excited state violates Hund's rule. We examine this class of bridged [10]- and [14]annulene perimeters with saturated bridges, and relate them to known conjugated polycyclic systems with Hund's rule violations. Despite the structural similarities with the related class of nonalternant polycyclic hydrocarbons, the mechanism is different in these bridged annulene perimeters. Here, two molecular orbital configurations contribute to each excited state. Consequently, a Hund's rule violation can only be unambiguously assigned based on the symmetry of the lowest excited singlet and triplet states. With several examples of synthetically realistic molecules, the class of bridged [10]- and [14]annulenes thus provides a structural link between the known nonalternant and alternant (azaphenalene) classes of molecules violating Hund's rule. These design principles may open avenues for the identification of new types of molecules where the order of the photophysically relevant first excited singlet and triplet states are inverted.
期刊介绍:
The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.