Yadav Inderpal, Shanu Mohd, Acharyya Jitendra Nath, Prakash G Vijaya, Sankar Muniappan
Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee247667, India.
Nanophotonics Lab, Department of Physics, Indian Institute of Technology Delhi, Hauz Khas110016, New Delhi, India.
Inorg Chem. 2022 Dec 5;61(48):19289-19301. doi: 10.1021/acs.inorgchem.2c03064. Epub 2022 Nov 20.
A new series of nonplanar and unsymmetrically β-functionalized "push-pull" copper corroles, CuTPC(CHO)R [R = H, Br, Ph, Me, or 2-thienyl (Th)], were synthesized and characterized to elucidate the effect of β-functionalization and nonplanarity on the photophysical, redox, and nonlinear optical (NLO) properties on the corrole ring. The synthetic route to unsymmetrically β-octasubstituted copper corroles includes bromination of CuTPC(CHO) to get CuTPC(CHO)Br in 80% yield, which was further subjected to the Pd-catalyzed Suzuki reaction. CuTPC(CHO)Br exhibited a large red shift in the Soret band (Δλ = 35-40 nm) and both the Q bands (Δλ = 10-50 nm), as compared to CuTPC and CuTPC(CHO). CuTPC(CHO)Br was 510 and 290 mV anodically shifted in the first oxidation and the first reduction compared to CuTPC owing to the strong -I effect of CHO and Br groups. Density functional theory studies revealed that all the β-octasubstituted copper corroles exhibited highly nonplanar saddle-shape conformation of the corrole ring. Very high torsional saddling was observed for CuTPC(CHO)Th (79-83°) than that for CuTPC (49-53°), even larger than that for CuTPCBr (67-70°). Femtosecond laser-induced third-order NLO studies from these copper corroles showed strong two-photon absorption cross-sections (0.48-6.98 × 10 GM) and self-focusing-type positive nonlinear refraction behavior. The observed structure-dependent two-photon absorption coefficients (β) are in the range of ∼2.7-20.9 × 10 m/W, and the values are in the range of ∼0.64-6.45 × 10 m/W. The present results may facilitate a new window for these copper corroles in nonlinear optical devices, femtosecond optical limiters, and many other ultrafast photonic applications.
合成并表征了一系列新型的非平面且不对称β-官能化的“推-拉”型铜卟吩配合物CuTPC(CHO)R [R = H、Br、Ph、Me或2-噻吩基(Th)],以阐明β-官能化和非平面性对卟吩环的光物理、氧化还原和非线性光学(NLO)性质的影响。不对称β-八取代铜卟吩配合物的合成路线包括将CuTPC(CHO)溴化以80%的产率得到CuTPC(CHO)Br,然后将其进一步进行钯催化的铃木反应。与CuTPC和CuTPC(CHO)相比,CuTPC(CHO)Br在Soret带(Δλ = 35-40 nm)以及两个Q带(Δλ = 10-50 nm)中均表现出较大的红移。由于CHO和Br基团的强-I效应,与CuTPC相比,CuTPC(CHO)Br在第一次氧化和第一次还原过程中阳极位移分别为510和290 mV。密度泛函理论研究表明,所有β-八取代铜卟吩配合物的卟吩环均呈现高度非平面的鞍形构象。观察到CuTPC(CHO)Th的扭转鞍形角(79-83°)比CuTPC的(49-53°)高,甚至比CuTPCBr的(67-70°)还要大。对这些铜卟吩配合物进行的飞秒激光诱导三阶NLO研究显示出很强的双光子吸收截面(0.48-6.98×10 GM)和自聚焦型正非线性折射行为。观察到的结构依赖性双光子吸收系数(β)在~2.7-20.