Photocycloaddition of Zero-Dimensional Metal Halide Hybrids with Reversible Photochromism.

In this work, two zero-dimensional (0D) metal halide hybrids L 2 ZnBr 4 [ 1 , L = ( E )-4-(2-(1 H -pyrrol-3-yl)vinyl)-1-methylpyridin-1-ium] and L 6 Pb 3 Br 12 ( 2 ) were prepared, which demonstrated photochromism and photoinduced cracking. Upon irradiation at 450 nm, a single crystal-to-single crystal transformation occurred as a result of the [2 + 2] photocycloaddition of L . Interestingly, compared to the complete photocycloaddition of L in 1 , only two-thirds of L monomers could be photodimerized in 2 because of the difference in L orientation. 1 shows reversible photochromic behavior including rapid response time, few cracks, high conversion rate, and good reaction reversibility, while 2 exhibits no significant color change but distinct photoinduced cracking because of the large local lattice strain induced by inhomogeneous and anisotropic deformation. Moreover, the photocycloaddition of L results in the distinct shift of photoluminescence of 1 and 2 , attributed to the variation in conjugation of π electrons and distortion of metal halide clusters. As a proof-of-concept, reversible optical writing is demonstrated for 1 . These findings provide new insights into the design of stimuli-responsive multifunctional materials.