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Discovery of Non-linear Optical Materials by Function-Based Screening of Multi-component Solids

机译:通过基于功能的筛选的非线性光学材料发现多组分固体

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SummaryNon-centrosymmetric arrangement in the solid state is a prerequisite for a molecule to exhibit second harmonic generation (SHG), yet the majority of achiral molecules crystallize in centrosymmetric lattices. Despite advances in circumventing the molecular preference for centrosymmetric structures, current screening methods of discovering SHG active materials need large quantities of parent material. Here, we present a function-based screening method that is designed to consume small quantities of parent material for screening a large pool of coformers that enhance the probability of discovering SHG active materials. With this method, ~30?mg of a non-linear optical (NLO) chromophore,N-(2-aminoethyl)-4-nitro-2-ansidine (1), was sufficient for screening 50 coformers, resulting in five SHG active compounds. Crystal-structure analysis revealed that non-covalent interactions influence the disposition of NLO-phore dipoles and thus affect the bulk SHG properties. Quantum chemical calculations highlighted the coformer contribution toward the second-order susceptibility coefficients, providing a deeper understanding of the structure-property relationships in these SHG materials.Graphical Display OmittedHighlights?High-throughput experimental setup enabling early-stage application?Discovered SHG active salts exhibitingχ(2)values up to 30 times that of urea?Non-covalent interactions and coformer contribution control bulk SHG activityThe Bigger PictureAddressing the increasing demand for efficient non-linear optical (NLO) materials for technologically relevant applications is a challenge because of the current unsustainable models of discovery. The ineffectiveness of these methods in accelerating the discovery of materials with the requisite non-centrosymmetry and ideal chromophore alignment for high performance in applications such as second harmonic generation (SHG) is now recognized as a challenge for the field. In order to optimize this discovery process, we present a high-throughput screening experimental approach. Unlike current experimental methods, this approach is neither sample nor labor intensive and selects hits on the basis of a functional assay. We have successfully demonstrated the practical utility of this method by using an organic NLO chromophore, which resulted in five SHG active salts. Testing the adaptability of this technique with other NLO chromophores will establish whether this becomes the frontline experimental method for discovering NLO materials.Current experimental methods for discovering non-linear optical (NLO) materials are sample intensive, resulting in a slow pace of discovering new materials with large bulk SHG activity. Matzger and colleagues demonstrate a simple, functionally guided high-throughput screening approach that consumes a very small amount of parent NLO-phore to screen large numbers of coformers, maximizing the chances of finding efficient SHG active materials. They successfully discovered five new NLO active salts with only ~30?mg of parent compound.
机译:SublaseNoN-亚离子物质布置在固态中是分子表现出第二次谐波产生(SHG)的先决条件,但大多数成立分子在邻摩尔晶格中结晶。尽管避免了用于离心机结构的分子偏好,但发现SHG活性材料的电流筛选方法需要大量的母体材料。这里,我们介绍了一种基于功能的筛选方法,该方法设计用于消耗少量的母材,用于筛选大量的共焦,增强了SHG活性材料的概率。用这种方法,〜30?Mg的非线性光学(NLO)发色团,N-(2-氨基乙基)-4-硝基-2-吖啶(1)足以筛选50个CoFormers,导致五个SHG活性化合物。晶体结构分析表明,非共价相互作用影响了Nlo-Phore偶联的布置,从而影响散装SHG性能。量子化学计算突出了CoFormer对二阶易感系数的贡献,提供了对这些SHG材料中的结构性质关系的更深理解。图形显示省略了高灯?高通量实验设置能够进行早期应用?发现SHG活性盐展出(2)值高达30倍的尿素的30倍?非共价相互作用和Coformer贡献控制批量SHG活性更大的Pictureaddressing对技术相关应用的高效非线性光学(NLO)材料的增加需求是一个挑战,因为目前的不可持续性是挑战发现模型。这些方法在加速利用必要的非中心对称和理想的发色团对准的基础上的高性能在诸如第二谐波生成(SHG)的高性能方面,这些方法的无效性现在被认为是对该领域的挑战。为了优化这一发现过程,我们提出了一种高吞吐量筛选实验方法。与当前的实验方法不同,这种方法既不是样本也不是劳动密集,并根据功能测定选择命中。我们通过使用有机NLO发色团成功地证明了这种方法的实用实用性,从而导致五个SHG活性盐。用其他NLO发色团测试该技术的适应性将确定这是否成为发现NLO材料的前线实验方法。用于发现非线性光学(NLO)材料的电流实验方法是样本密集型,导致发现新材料的缓慢速度缓慢大量散装活动。 Matzger及其同事展示了一种简单,功能引导的高通量筛选方法,消耗了非常少量的父母NLO-PHORE,以筛选大量的COFORMERS,最大化寻找高效SHG活性材料的机会。他们成功发现了五种新的NLO活性盐,仅具有〜30毫克的母体化合物。

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