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用其他大体积取代基取代均三甲苯基对[Pt(1,3-双(4-均三甲苯基-吡啶-2-基)-4,6-二氟-苯)氯]发光性能的影响

Effect of the Substitution of the Mesityl Group with Other Bulky Substituents on the Luminescence Performance of [Pt(1,3-bis(4-Mesityl-pyridin-2-yl)-4,6-difluoro-benzene)Cl].

作者信息

De Soricellis Giulia, Guerchais Véronique, Colombo Alessia, Dragonetti Claudia, Fagnani Francesco, Roberto Dominique, Marinotto Daniele

机构信息

Dipartimento di Chimica, Università degli Studi di Milano, UdR INSTM di Milano, Via C. Golgi 19, I-20133 Milan, Italy.

Dipartimento di Chimica, Università di Pavia, Via Taramelli 12, I-27100 Pavia, Italy.

出版信息

Molecules. 2025 Mar 27;30(7):1498. doi: 10.3390/molecules30071498.

Abstract

The synthesis and characterization of two new complexes, namely [Pt(bis(4-(4-(tert-butyl)phenyl)-pyridin-2-yl)-4,6-difluorobenzene)Cl] and [Pt(bis(4-(3,5-di-tert-butylphenyl)-pyridin-2-yl)-4,6-difluorobenzene)Cl], are reported. Both are highly luminescent in the blue region (Φlum = 0.89-0.95 at 478-480 nm), like the parent complex [Pt(1,3-bis(4-mesityl-pyridin-2-yl)-4,6-difluoro-benzene)Cl] in degassed diluted dichloromethane solution. An increase in concentration leads to the formation of bi-molecular emissive excited states, as evidenced by a growing structureless band that peaked at 690-697 nm. This formation is more facile for the complex with one tert-butyl group in para of the phenyl group. It appears that the introduction of two tert-butyls in positions 3 and 5 of the phenyl group hampers the neighboring of the monomeric species, although less efficiently than the introduction of methyls in positions 2 and 6.

摘要

报道了两种新配合物,即[Pt(双(4-(4-(叔丁基)苯基)-吡啶-2-基)-4,6-二氟苯)Cl]和[Pt(双(4-(3,5-二叔丁基苯基)-吡啶-2-基)-4,6-二氟苯)Cl]的合成与表征。在脱气稀释二氯甲烷溶液中,这两种配合物在蓝色区域均具有高发光性(在478 - 480 nm处,Φlum = 0.89 - 0.95),与母体配合物[Pt(1,3-双(4-均三甲苯基-吡啶-2-基)-4,6-二氟苯)Cl]类似。浓度增加会导致双分子发射激发态的形成,这由在690 - 697 nm处达到峰值的无结构谱带的增长所证明。对于苯基对位带有一个叔丁基的配合物,这种形成更容易。似乎在苯基的3和5位引入两个叔丁基会阻碍单体物种的相邻,尽管效率不如在2和6位引入甲基。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8eeb/11990200/ed47aea4ae6b/molecules-30-01498-sch001.jpg

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