Fully sp2-Carbon-Linked Crystalline Two-Dimensional Conjugated Polymers: Insight into 2D Poly(phenylenecyanovinylene) Formation and its Optoelectronic Properties

被引:46
作者
Becker, Daniel [1 ]
Biswal, Bishnu P. [1 ]
Kalenczuk, Paula [1 ]
Chandrasekhar, Naisa [1 ]
Giebeler, Lars [2 ]
Addicoat, Matthew [3 ]
Paasch, Silvia [4 ]
Brunner, Eike [4 ]
Leo, Karl [5 ]
Dianat, Arezoo [6 ]
Cuniberti, Gianaurelio [6 ]
Berger, Reinhard [1 ]
Feng, Xinliang [1 ]
机构
[1] Tech Univ Dresden, Ctr Advancing Elect Dresden, Fac Chem & Food Chem, D-01062 Dresden, Germany
[2] Leibniz Inst Solid State & Mat Res Dresden, Dept Chem Funct Mat, Helmholtzstr 20, D-01069 Dresden, Germany
[3] Nottingham Trent Univ, Sch Sci & Technol, Clifton Lane, Nottingham NG11 8NS, England
[4] Tech Univ Dresden, Chair Bioanalyt Chem, D-01069 Dresden, Germany
[5] Dresden Integrated Ctr Appl Phys & Photon Mat IAP, Nothnitzer Str 61, D-01187 Dresden, Germany
[6] Tech Univ Dresden, Inst Mat Sci, D-01062 Dresden, Germany
关键词
2D conjugated polymers; density functional calculations; optoelectronics; polyphenylene vinylene; post-synthetic modification; COVALENT ORGANIC FRAMEWORK; EFFECTIVE IONIC-RADII; LIGHT-EMITTING DIODE; OPTICAL-PROPERTIES; CARBON; TECHNOLOGY; VINYLENE); GRAPHENE; LINKAGE; SYSTEMS;
D O I
10.1002/chem.201806385
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyano-substituted polyphenylene vinylenes (PPVs) have been the focus of research for several decades owing to their interesting optoelectronic properties and potential applications in organic electronics. With the advent of organic two-dimensional (2D) crystals, the question arose as to how the chemical and optoelectronic advantages of PPVs evolve in 2D compared with their linear counterparts. In this work, we present the efficient synthesis of two novel 2D fully sp(2)-carbon-linked crystalline PPVs and investigate the essentiality of inorganic bases for their catalytic formation. Notably, among all bases screened, cesium carbonate (Cs2CO3) plays a crucial role and enables reversibility in the first step with subsequent structure locking by formation of a C=C double bond to maintain crystallinity, which is supported by density functional theory (DFT) calculations. A quantifiable energy diagram of a "quasi-reversible reaction" is proposed, which allows the identification of further suitable C-C bond formation reactions for 2D polymerizations. Moreover, the narrowing of the HOMO-LUMO gap is delineated by expanding the conjugation into two dimensions. To enable environmentally benign processing, the postmodification of 2D PPVs is further performed, which renders stable dispersions in the aqueous phase.
引用
收藏
页码:6562 / 6568
页数:7
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