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LiO_(4)tetrahedra lock the alignment of π-conjugated layers to maximize optical anisotropy in metal hydroisocyanurates
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作者 Xianghe Meng Fei Liang +6 位作者 Jian Tang Kaijin Kang Wenlong Yin Tixian Zeng Bin Kang Zheshuai Lin Mingjun Xia 《Inorganic Chemistry Frontiers》 2019年第10期2850-2854,共5页
Parallel and compact alignments ofπ-conjugated anions in a crystal are of importance to maximize the optical anisotropy of crystalline materials.Our attempts to design colossal birefringence in metal hydroisocyanurat... Parallel and compact alignments ofπ-conjugated anions in a crystal are of importance to maximize the optical anisotropy of crystalline materials.Our attempts to design colossal birefringence in metal hydroisocyanurates M2N(H_(2)C_(3)N_(3)O_(3))4·6H_(2)O(M/N=Li/Ca and Na/Ba)were successful using cation coordination control.In particular,Li_(2)Ca(H_(2)C_(3)N_(3)O_(3))4·6H_(2)O(LCHCY)shows the largest birefringence(Δn=0.407@800 nm)among all the reported metal cyanurates and hydroisocyanurates,even larger than that of 2D BN layers,due to the reinforced lock effect of basal oxygens from LiO_(4)tetrahedra.LCHCY is a novel promising ultraviolet birefringent crystal with a short ultraviolet cut-off and a wide transmission range. 展开更多
关键词 crystalline materialsour tetrahedra maximize optical anisotropy parallel compact alignments metal cyanurates cation coordination controlin conjugated layers optical anisotropy
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