Wang Xuefei, Leng Xudong, Kuk Yunseung, Lee Jihyun, Jing Qun, Ok Kang Min
Department of Chemistry, Sogang University, Seoul, 04107, Republic of Korea.
Xinjiang Key Laboratory of Solid State Physics and Devices, School of Physical Science and Technology, Xinjiang University, 777 Huarui Road, Urumqi, 830017, China.
Angew Chem Int Ed Engl. 2024 Jan 25;63(5):e202315434. doi: 10.1002/anie.202315434. Epub 2023 Nov 27.
Enhancing anisotropy through the controlled arrangement of anionic groups is essential for improving the nonlinear optical (NLO) performance of non-π-conjugated NLO materials. In this study, we present the successful synthesis of the first examples of mixed alkali metal-alkaline earth metal sulfamate materials, including noncentrosymmetric Cs Mg(NH SO ) ⋅ 4H O (1), as well as centrosymmetric K Ca(NH SO ) (2) and Rb Ca(NH SO ) (3). All three compounds feature promising deep ultraviolet cut-off edges, notably 1 with a cut-off edge below 180 nm. The synergy of Cs and Mg cations in 1 facilitated the successful alignment of polar [NH SO ] tetrahedra in a uniform orientation. Remarkably, 1 stands as the sole instance among reported sulfamate compounds with a co-parallel anionic arrangement, yielding a very large dipole moment compared to other non-π-conjugated NLO materials. Moreover, the substantial dipole moment of 1 yields an enhanced second harmonic generation response, approximately 2.3 times that of KH PO , and a large birefringence of 0.054 at 546.1 nm. The approach of regulating the arrangement of anionic groups using aliovalent cations holds promise for advancing the exploration of non-π-conjugated NLO materials.
通过控制阴离子基团的排列来增强各向异性对于提高非π共轭非线性光学(NLO)材料的非线性光学性能至关重要。在本研究中,我们成功合成了首例混合碱金属-碱土金属氨基磺酸盐材料,包括非中心对称的CsMg(NH₂SO₃)₂·4H₂O(1),以及中心对称的K₂Ca(NH₂SO₃)₂(2)和Rb₂Ca(NH₂SO₃)₂(3)。所有这三种化合物都具有良好的深紫外截止边,特别是1的截止边低于180 nm。1中Cs和Mg阳离子的协同作用促进了极性[NH₂SO₃]四面体以均匀取向成功排列。值得注意的是,1是已报道的氨基磺酸盐化合物中唯一具有共平行阴离子排列的实例,与其他非π共轭NLO材料相比,产生了非常大的偶极矩。此外,1的大偶极矩产生了增强的二次谐波产生响应,约为KH₂PO₄的2.3倍,并且在546.1 nm处具有0.054的大双折射。使用异价阳离子调节阴离子基团排列的方法有望推动非π共轭NLO材料的探索。