Synlett 2024; 35(07): 789-800
DOI: 10.1055/a-2095-5164
account

Pt(II)-Bisacetylide ‘Roller Wheels’: Molecular Engineering towards Small Bandgap, High Crystallinity, and Controlled Triplet Exciton Processes

Yang Qin
Y.Q. would like to thank National Science Foundation (CHE-2101535) for financial support of this research.


Abstract

Triplet excitons are ubiquitous in organic chromophores and possess intrinsically longer lifetimes than their singlet exciton counterparts, and thus potentially larger diffusion lengths that have been considered beneficial for organic solar cells (OSCs). However, existing triplet-generating materials rarely possess low bandgap, high triplet energy and yield, and good crystallinity and charge mobility within a single compound. In this Account, I first describe the rationales behind our ‘roller-wheel’-type molecular structural designs through a brief literature survey and our initial attempt in Pt-containing conjugated polymers. Then, a series of novel Pt-bisacetylide-containing small molecules will be discussed. I mainly focus on the thought process for selecting the building blocks and detail their synthetic strategies, as well as their solid-state structures, especially that of the single crystals, confirming the effectiveness of our structural designs. Next, photophysical properties of these compounds are discussed in the context of optical spectroscopy and transient absorption spectroscopy, which is corroborated by theoretical calculations. Organic solar cells employing these compounds are introduced next, one of which displayed record-setting performance among Pt-containing materials. I end this Account with an outlook on future works with a focus on molecular engineering to control triplet excited-state energetics and dynamics.

1 Introduction

2 Initial Attempt

3 Rationale of Design

4 Synthesis of ‘Roller Wheels’

5 Solid-State Structures of ‘Roller Wheels’

6 Photophysical Studies

7 Theoretical Investigation

8 Device Application

9 Outlook – Managing Triplet Excited States



Publication History

Received: 02 May 2023

Accepted after revision: 17 May 2023

Accepted Manuscript online:
17 May 2023

Article published online:
06 July 2023

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