Solvent-free isothermal tuning of viscoelasticity of polymer materials is important for an emerging photochemical molding technology and photoreversible adhesives. In this study we designed a four-armed star-shaped poly(butyl acrylate, BA) oligomer having four coumarin end groups. The irradiation of UV at the wavelength of 365 nm (UV 365 ) to the viscous poly(BA) oligomer under a solvent-free condition produced a solid network material along with the progress of dimerization reaction with coumarin end groups. The subsequent irradiation of UV at the wavelength of 254 nm (UV 254 ) caused dimer dissociation reaction to attain change in the mixing degree of star and network architectures in the material. Moreover, viscoelasticity of the network material was tunable by repetitive UV 365 and UV 254 irradiations. V C 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018, 56, 9-15 KEYWORDS: network polymer; star-shaped polymer; photostimulation; solvent-free isothermal process; viscoelasticity INTRODUCTION Change in the physical state of materials is one of the most fundamental phenomena we experience in everyday life. The change between physical states such as liquid-solid transition is generally caused by the shift in temperature of materials and is industrially important across the broad spectrum of applications such as heat molding plastic materials and hot melt adhesives. However, materials displaying stimuli-triggered isothermal reversible liquid-nonliquid conversion (IRLNC) are quite rare. To cause molecular ordering and disordering as undergone in a thermal phase transition process, utilization of stimuli-responsive molecules holds the key. Some groups have reported isothermal melting and crystallization of azobenzene (Azo)-containing small molecules, relying on trans-cis photoisomerization. [1][2][3] This strategy is preferable for photoreversible adhesive applications, which enables ON-OFF attachment and detachment of surfaces coated by them without using solvent fractions. 4 Although the IRLNC strategy should, in principle, be applicable for tuning viscoelasticity of materials, only two physical states, i.e., solid and liquid ones are allowed for such small molecules. Therefore, the development of materials exhibiting solvent-free IRLNC with tunable viscoelasticity remains a challenge. Recently, Zhou et al. designed acrylate and methacrylate polymers with tunable glass transition temperature