Direct transformation of n-alkane into all-trans conjugated polyene via cascade dehydrogenation

Author:

Li Xuechao1,Niu Kaifeng12,Zhang Junjie1,Yu Xiaojuan3ORCID,Zhang Haiming1,Wang Yuemin3,Guo Qing4,Wang Pengdong5,Li Fangsen5ORCID,Hao Zhengming1,Xu Chaojie1,Tang Yanning1,Xu Zhichao1,Lu Shuai15,Liu Peng4,Xue Guigu4,Wei Yen6,Chi Lifeng1

Affiliation:

1. Jiangsu Key Laboratory for Carbon Based Functional Materials & Devices, Institute of Functional Nano & Soft Materials, Soochow University, Suzhou 215123, China

2. Department of Physics, Chemistry and Biology, IFM, Linköping University, 58183 Linköping, Sweden

3. Institute of Functional Interfaces, Karlsruhe Institute of Technology, Eggenstein-Leopoldshafen 76344, Germany

4. Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, China

5. Vacuum Interconnected Nanotech Workstation (Nano-X), Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China

6. Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084, China

Abstract

Abstract Selective C(sp3) −H activation is of fundamental importance in processing alkane feedstocks to produce high-value-added chemical products. By virtue of an on-surface synthesis strategy, we report selective cascade dehydrogenation of n-alkane molecules under surface constraints, which yields monodispersed all-trans conjugated polyenes with unprecedented length controllability. We are also able to demonstrate the generality of this concept for alkyl-substituted molecules with programmable lengths and diverse functionalities, and more importantly its promising potential in molecular wiring.

Funder

Ministry of Science and Technology

National Natural Science Foundation of China

German Research Foundation

Publisher

Oxford University Press (OUP)

Subject

Multidisciplinary

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