Citation: Shi-Tao Han, Hong-Ying Duan, Tian-Guang Zhan, Xiao-Bo Hu, Li-Chun Kong, Kang-Da Zhang. Light-fueled dissipative self-assembly at molecular and macro-scale enabled by a visible-light-responsive transient hetero-complementary quadruple hydrogen bond[J]. Chinese Chemical Letters, ;2023, 34(3): 107639. doi: 10.1016/j.cclet.2022.06.062 shu

Light-fueled dissipative self-assembly at molecular and macro-scale enabled by a visible-light-responsive transient hetero-complementary quadruple hydrogen bond

Shi-Tao Han ^a ,
Hong-Ying Duan ^a ,
Tian-Guang Zhan ^a ,
Xiao-Bo Hu ^{a, *,} ,
Li-Chun Kong ^a ,
Kang-Da Zhang ^{a, b, *,}

a.
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China
b.
Key Laboratory of Precise Synthesis of Functional Molecules of Zhejiang Province, School of Science, Westlake University, Hangzhou 310024, China

xiaobo.hu@zjnu.edu.cn

Kangda.Zhang@zjnu.cn

Received Date: 6 May 2022
Revised Date: 21 June 2022
Accepted Date: 23 June 2022
Available Online: 30 June 2022

Figures(7)

The development of out-of-equilibrium self-assembly systems using light as input fuel is highly desirable and promising for the fabrication of smart supramolecular materials. Herein, we report the construction of new artificial light-fueled dissipative molecular and macroscopic self-assembly systems based on a visible-light-responsive transient quadruple H-bonding array, which consists of an azobenzene-modified ureidopyrimidinone (UPy) module (Azo-O-UPy) and a nonphotoactive diamidonaphthyridine (DAN) derived competitive binder (Napy-1). The visible light (410 nm) irradiation can induce the E to Z isomerization of the azobenzene unit of E-Azo-O-UPy to produce Z-Azo-O-UPy with an opened UPy binding site, which can complex with Napy-1 to form a quadruply H-bonded heterodimer. The heterodimer is metastable and can be quickly disassembled in dark, owing to the fast thermal relaxation of Z-Azo-O-UPy to E-Azo-O-UPy. While introducing such transient quadruple H-bonding interaction into a linear polymer system or a polymeric gel system, light-fueled out-of-equilibrium polymeric assembly both at molecular and macro-scale can be achieved.
- Dissipative self-assembly,
- Macroscopic self-assembly,
- Photo-responsiveness,
- Quadruple hydrogen bonds,
- Supramolecular chemistry
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