Chen Chong-An, Li Yang, Huang Hongbo, Jin Congcong, Zhang Bingbing, Ok Kang Min
Center for Noncentrosymmetric Materials, Department of Chemistry, Sogang University, Seoul, 04107, Republic of Korea.
College of Chemistry and Materials Science, Hebei University, Baoding, 071002, China.
Angew Chem Int Ed Engl. 2025 Jul;64(27):e202506625. doi: 10.1002/anie.202506625. Epub 2025 May 5.
Birefringent crystals are essential for polarized optical devices, yet achieving large birefringence through rational design remains challenging. The key lies in constructing birefringence-active groups (BAGs) with giant polarization anisotropy and optimal spatial arrangements. Here, we report the successful construction of linear interhalogen BAGs, IX (X = Cl, Br), enabling giant polarization anisotropy. This was accomplished by simple halogenation of IO groups in an aqueous solution. Four novel birefringent crystals were synthesized: [H-4AP][ICl] (1, 4AP = 4-aminopyridine), [HDMA][ICl]·Cl (2, DMA = dimethylamine), [H-4AP][IBr] (3), and [HDMA][IBr]·Br (4). In all these compounds, the linear IX BAG adopts parallel arrangements, effectively maximizing synergistic polarization anisotropy. As a result, compounds 1-4 exhibit giant birefringence values in both the visible (0.647, 0.585, 0.836, and 0.782 at 546 nm) and near-infrared (NIR) regions (0.510, 0.356, 0.762, and 0.509 at 1064 nm), surpassing commercial birefringent crystals and many state-of-the-art materials. Furthermore, these compounds achieve an optimal balance between giant birefringence and moderate bandgap among linear BAG-based materials. Detailed theoretical calculations confirm that the IX BAGs play a dominant role in this exceptional birefringence. This study demonstrates the remarkable potential of linear interhalogen anions for developing high-performance birefringent crystals.
双折射晶体对于偏振光学器件至关重要,但通过合理设计实现大双折射仍然具有挑战性。关键在于构建具有巨大偏振各向异性和最佳空间排列的双折射活性基团(BAGs)。在此,我们报告了线性卤间化合物BAGs(IX ,X = Cl,Br)的成功构建,实现了巨大的偏振各向异性。这是通过在水溶液中对IO 基团进行简单卤化来完成的。合成了四种新型双折射晶体:[H-4AP][ICl](1,4AP = 4-氨基吡啶)、[HDMA][ICl]·Cl(2,DMA = 二甲胺)、[H-4AP][IBr](3)和[HDMA][IBr]·Br(4)。在所有这些化合物中,线性IX BAG采用平行排列,有效最大化协同偏振各向异性。结果,化合物1-4在可见光(546 nm处为0.647、0.585、0.836和0.782)和近红外(NIR)区域(1064 nm处为0.510、0.356、0.762和0.509)均表现出巨大的双折射值,超过了商业双折射晶体和许多先进材料。此外,这些化合物在基于线性BAG的材料中实现了巨大双折射与适度带隙之间的最佳平衡。详细的理论计算证实,IX BAG在这种优异的双折射中起主导作用。这项研究证明了线性卤间阴离子在开发高性能双折射晶体方面的巨大潜力。