Supramolecular design of pi-electron functional materials

π电子功能材料的超分子设计

• 批准号: RGPIN-2018-06500
• 负责人: Perepichka, Dmitrii
• 金额: $ 13.7万
• 依托单位: McGill University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-01-01 至 2023-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=748044
• 关键词: Supramolecular; design; pi; electron; functional

Design and synthesis of new pi-electron functional materials allows answering fundamental physical chemistry questions, and play an enabling role in a wide spectrum of applications from pigments and fluorescent labels, to semiconducting devices and electrochemical energy storage media. Our current understanding of optoelectronic properties of such materials is very advanced at the level of single molecules, but is rather limited in situations when the interaction of the molecules with each other and with interfaces are important. Our goal is to understand how electronic properties of organic matter arise and can be controlled at supramolecular level, and use this understanding to create novel types of semiconducting materials where an electronic conductivity arises as a result of programmable molecular self-assembly.This discovery grant will continuously involve 5 graduate students and w undergraduates in research towards this goal through the following short-term 4 projects/objectives. We will:1) Develop novel dynamic covalent chemistry suitable for self-assembly of ordered pi-conjugated polymers and covalent organic frameworks (COFs) under thermodynamic equilibrium. Our first target is aldol cyclization of cyclic ketones leading to rigid conjugated systems with dipole-dipole stabilization.2) Develop omniconjugated building blocks that provide efficient electronic communication in several direction (no “cross-conjugation”). This will be accomplished by the use of (i) sexitopic and (ii) stable pi-radicals “nodes”, which will used as monomers for highly conjugated COFs and as cores for star-shaped molecular materials.3) Gaining control of electronic properties in organic semiconductors via complementary hydrogen bonding. Coassembly of p- and n-type semiconductors and electronic polarization due to H-bonding will lead to strong band-gap modulation (giving rise to intrinsic semiconductors) and can lead to conducting channels that can be turned-on by interaction with H-bonding complementary pairs (including biomolecules).4) Understanding the role of external factors (other than molecular or crystal structure) in controlling the charge transport through organic semiconductors. This will have an immediate impact on the current field of organic field effect transistors (FET), and is a critical step for the future development of self-assembled electronic devices.The scientific impact of this work will be (a) new knowledge at the interface of organic chemistry and solid state physics, that will help stirring the current field of organic electronics along our long term vision and (b) novel electronically functional materials that will advance the current device technologies (FETs, solar cells), can enable novel applications, and will foster collaborations with materials physics and biochemistry groups.

新型π电子功能材料的设计和合成可以回答基本的物理化学问题，并在从颜料和荧光标签到半导体器件和电化学储能介质的广泛应用中发挥促进作用。此类材料在单分子水平上非常先进，但在分子彼此之间以及分子与界面之间的相互作用很重要的情况下却相当有限。我们的目标是了解有机物的电子特性如何产生以及如何控制。超分子水平，并利用这种理解来创造新型半导体材料，其中通过可编程分子自组装产生电子传导性。这项发现补助金将持续吸引 5 名研究生和 2 名本科生通过以下短期研究来实现这一目标：第 4 学期的项目/目标：1) 开发适合热力学平衡下有序 π 共轭聚合物和共价有机骨架 (COF) 自组装的新型动态共价化学。环酮的羟醛环化产生具有偶极-偶极稳定性的刚性共轭系统。2) 开发全共轭结构单元，在多个方向上提供有效的电子通信（无“交叉共轭”）。这将通过使用 (i) 来实现。六位基和（ii）稳定的π自由基“节点”，将用作高度共轭COF的单体和星形分子材料的核心。3）获得电子控制通过 p 型和 n 型半导体的互补氢键共组装以及氢键导致的电子极化，可以改变有机半导体的特性，从而产生强带隙调制（产生本征半导体），并可以形成导电通道。通过与氢键互补对（包括生物分子）的相互作用而开启。4）了解外部因素（分子或晶体结构除外）在控制有机半导体电荷传输中的作用这将对电流产生直接影响。有机领域场效应晶体管（FET），是自组装电子器件未来发展的关键一步。这项工作的科学影响将是（a）有机化学和固态物理学界面的新知识，这将有助于沿着我们的长期愿景搅动当前的有机电子领域；(b) 新型电子功能材料将推进当前的器件技术（FET、太阳能电池），可以实现新颖的应用，并将促进与材料物理和生物化学小组的合作。