Enantioselective control of lattice and shape chirality in inorganic nanostructures using chiral biomolecules

被引:0
|
作者
Assaf Ben-Moshe
Sharon Grayer Wolf
Maya Bar Sadan
Lothar Houben
Zhiyuan Fan
Alexander O. Govorov
Gil Markovich
机构
[1] Raymond and Beverly Sackler Faculty of Exact Sciences,Department of Chemistry
[2] School of Chemistry,Department of Physics and Astronomy
[3] Tel Aviv University,undefined
[4] Electron Microscopy Unit,undefined
[5] Weizmann Institute of Science,undefined
[6] Ben Gurion University of the Negev,undefined
[7] Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons,undefined
[8] Forschungszentrum Jülich GmbH,undefined
[9] Ohio University,undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
A large number of inorganic materials form crystals with chiral symmetry groups. Enantioselectively synthesizing nanostructures of such materials should lead to interesting optical activity effects. Here we report the synthesis of colloidal tellurium and selenium nanostructures using thiolated chiral biomolecules. The synthesis conditions are tuned to obtain tellurium nanostructures with chiral shapes and large optical activity. These nanostructures exhibit visible optical and chiroptical responses that shift with size and are successfully simulated by an electromagnetic model. The model shows that they behave as chiral optical resonators. The chiral tellurium nanostructures are transformed into chiral gold and silver telluride nanostructures with very large chiroptical activity, demonstrating a simple colloidal chemistry path to chiral plasmonic and semiconductor metamaterials. These materials are natural candidates for studies related to interactions of chiral (bio)molecules with chiral inorganic surfaces, with relevance to asymmetric catalysis, chiral crystallization and the evolution of homochirality in biomolecules.
引用
收藏
相关论文
共 33 条
  • [21] Deformation control method for active shape morphing lattice structure using topology optimization approach
    Xu, Bo
    Gu, Xiaojun
    Wang, Jun
    Zhang, Yahui
    Zhu, Jihong
    Zhang, Weihong
    [J]. SMART MATERIALS AND STRUCTURES, 2024, 33 (02)
  • [22] Size and shape control of a variety of metallic nanostructures using tilted, rotating evaporation and lithographic lift-offtechniques
    Eschimese, Damien
    Vaurette, Francois
    Troadec, David
    Leveque, Gaetan
    Melin, Thierry
    Arscott, Steve
    [J]. SCIENTIFIC REPORTS, 2019, 9 (1)
  • [23] Synthesis of (formylferrocenyl)bismuthanes. A way to control the stereochemistry at the chiral bismuth centre using hypervalent bond formation and planar chirality of ferrocene
    Murafuji, T
    Mutoh, T
    Sugihara, Y
    [J]. CHEMICAL COMMUNICATIONS, 1996, (14) : 1693 - 1694
  • [24] Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality
    Martinez, Jose I.
    Uria, Uxue
    Muniz, Maria
    Reyes, Efram
    Carrillo, Luisa
    Vicario, Jose L.
    [J]. BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 2015, 11 : 2577 - 2583
  • [25] Independent control of size and shape of GaAs nanostructures during droplet epitaxy using ultra-low arsenic flux
    Balakirev, S. V.
    Lakhina, E. A.
    Kirichenko, D. V.
    Chernenko, N. E.
    Shandyba, N. A.
    Eremenko, M. M.
    Solodovnik, M. S.
    [J]. ST PETERSBURG POLYTECHNIC UNIVERSITY JOURNAL-PHYSICS AND MATHEMATICS, 2022, 15 (03): : 315 - 319
  • [26] Size and shape control of a variety of metallic nanostructures using tilted, rotating evaporation and lithographic lift-off techniques
    Damien Eschimese
    François Vaurette
    David Troadec
    Gaëtan Leveque
    Thierry Melin
    Steve Arscott
    [J]. Scientific Reports, 9
  • [27] Chiral Compounds of Essential Oils. Part XII. Authenticity Control of Rose Oils, Using Enantioselective Multidimensional Gas Chromatography
    Kreis, Peter
    Mosandl, Armin
    [J]. FLAVOUR AND FRAGRANCE JOURNAL, 1992, 7 (04) : 199 - 203
  • [28] Axial Chirality Control by 2,4-Pentanediol for the Alternative Synthesis of C3*-TunePhos Chiral Diphosphine Ligands and Their Applications in Highly Enantioselective Ruthenium-Catalyzed Hydrogenation of β-Keto Esters
    Sun, Xianfeng
    Li, Wei
    Hou, Guohua
    Zhou, Le
    Zhang, Xumu
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2009, 351 (16) : 2553 - 2557
  • [29] Enhanced electrocatalytic activity of Pt-nanostructures prepared by electrodeposition using poly(vinyl pyrrolidone) as a shape-control agent
    Ye, Feng
    Hu, Weiwei
    Zhang, Tierui
    Yang, Jun
    Ding, Yulong
    [J]. ELECTROCHIMICA ACTA, 2012, 83 : 383 - 386
  • [30] Chiral aminoalcohol NOBIN for instantaneous chirality control of racemic but tropos BIPHEP-Rh(I)-complexes:: highly enantioselective ene-type cyclization of 1,6-enynes catalyzed by the Rh(I)-complexes without use of acid
    Mikami, Koichi
    Kataoka, Shohei
    Wakabayashi, Kazuki
    Aikawa, Kohsuke
    [J]. TETRAHEDRON LETTERS, 2006, 47 (36) : 6361 - 6364