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通过阳离子-阴离子协同相互作用策略实现草酸锑双折射的显著增强。

Sharp Enhancement of Birefringence in Antimony Oxalates Achieved by the Cation-Anion Synergetic Interaction Strategy.

作者信息

Zhang Die, Wang Qiang, Ren Liying, Cao Liling, Huang Ling, Gao Daojiang, Bi Jian, Zou Guohong

机构信息

College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610066, P. R. China.

College of Chemistry, Sichuan University, Chengdu 610065, P. R. China.

出版信息

Inorg Chem. 2022 Aug 8;61(31):12481-12488. doi: 10.1021/acs.inorgchem.2c02262. Epub 2022 Jul 27.

DOI:10.1021/acs.inorgchem.2c02262
PMID:35894629
Abstract

Birefringent materials with large birefringence play an important role in in laser science and technology owing to their ability to modulate polarized light. However, the lack of systematic and effective synthesis strategies severely hinders the development of novel superior birefringent materials. Herein, the cation-anion synergetic interaction strategy was proposed to successfully synthesize two excellent UV birefringent materials, RbSb(CO)F·HO and [C(NH)]Sb(CO)F·HO. Both compounds feature unprecedented [Sb(CO)F] anionic chains composed of planar π-conjugated [CO] units and a distorted SbOF complex with stereochemically active lone pairs, which induce a large optical anisotropy. Remarkably, further enhancement of birefringence in [C(NH)]Sb(CO)F·HO was achieved via cation-anion synergetic interactions between the [C(NH)] cationic groups and [Sb(CO)F] anionic chains. It exhibited a giant birefringence of 0.323@546 nm, twice larger than that of its analogue RbSb(CO)F·HO (0.162@546 nm). A detailed structural analysis and theoretical calculations revealed that the cation-anion synergetic interaction strategy is an effective strategy for the efficient exploration of superior birefringent materials, which will guide the further exploration of new structure-driven functional materials.

摘要

具有大双折射的双折射材料由于其调制偏振光的能力,在激光科学和技术中发挥着重要作用。然而,缺乏系统有效的合成策略严重阻碍了新型优质双折射材料的发展。在此,提出了阳离子 - 阴离子协同相互作用策略,成功合成了两种优异的紫外双折射材料,RbSb(CO)F·H₂O 和 [C(NH₂)₃]Sb(CO)F·H₂O。这两种化合物都具有由平面π共轭[CO]单元组成的前所未有的[Sb(CO)F]阴离子链以及带有立体化学活性孤对电子的扭曲SbOF络合物,这会诱导出大的光学各向异性。值得注意的是,通过[C(NH₂)₃]阳离子基团与[Sb(CO)F]阴离子链之间的阳离子 - 阴离子协同相互作用,[C(NH₂)₃]Sb(CO)F·H₂O 的双折射进一步增强。它在546nm处表现出0.323的巨大双折射,是其类似物RbSb(CO)F·H₂O(在546nm处为0.162)的两倍。详细的结构分析和理论计算表明,阳离子 - 阴离子协同相互作用策略是有效探索优质双折射材料的有效策略,这将指导对新的结构驱动功能材料的进一步探索。

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