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In this paper, a rigid scaffold imposes the photophysics of chromophores with a benzylidene imidazolidinone core by mimicking the β-barrel structure of the green fluorescent protein (GFP) and its analogs. The designed artificial frameworks maintain fluorescence responses and, therefore, conformational rigidity of typically non-emissive GFP-related chromophores. To replicate a small weight percent of the chromophore inside the natural GFP, two synthetic approaches were utilized: coordinative immobilization and non-coordinative inclusion. Despite low chromophore loading in the rigid matrix, both approaches resulted in formation of photoluminescent hybrid materials. Furthermore, the rigid scaffold dictates chromophore fluorescence by replicating its behavior in solution or the solid state. The presented results open an avenue for utilization of rigid scaffolds in the engineering of materials with tunable photoluminescence profiles for a variety of practical applications.

This paper reports for the first time in situ crystal growth of ZIF-8 on electrospun polyurethane (PU) nanofibers. In SEM images, continuous and compact ZIF-8 nanocrystals grow along electrospun PU nanofibers. The highest loading capacity of ZIF-8 on PU reaches 63%. By N2 adsorption-desorption, ZIF-8-PU shows a high surface area of 566 cm(2) g(-1). Combining the good flexibility of PU with the high adsorption properties of ZIF-8, ZIF-8-PU can be easily tailored into clothes or other forms as adsorption material. Furthermore, the gas adsorption ability of ZIF-8-PU was measured for H2, N2, O2 and CO2 at room temperature (20 °C) under different pressure gradients. The results show that the adsorption capacity of ZIF-8-PU for CO2 is nearly 11 times that for H2, 50 times that for O2 and 75 times that for N2 at 800 mmHg.