Literature DB >> 24288138

Self-assembled selenium monolayers: from nanotechnology to materials science and adaptive catalysis.

Leonid V Romashov1, Valentine P Ananikov.   

Abstract

Self-assembled monolayers (SAMs) of selenium have emerged into a rapidly developing field of nanotechnology with several promising opportunities in materials chemistry and catalysis. Comparison between sulfur-based self-assembled monolayers and newly developed selenium-based monolayers reveal outstanding complimentary features on surface chemistry and highlighted the key role of the headgroup element. Diverse structural properties and reactivity of organosulfur and organoselenium groups on the surface provide flexible frameworks to create new generations of materials and adaptive catalysts with unprecedented selectivity. Important practical utility of adaptive catalytic systems deals with development of sustainable technologies and industrial processes based on natural resources. Independent development of nanotechnology, materials science and catalysis has led to the discovery of common fundamental principles of the surface chemistry of chalcogen compounds.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  catalysis; material science; nanotechnology; selenium; self-assembled monolayers; sulfur

Mesh:

Substances:

Year:  2013        PMID: 24288138     DOI: 10.1002/chem.201302115

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  7 in total

1.  Case studies on the formation of chalcogenide self-assembled monolayers on surfaces and dissociative processes.

Authors:  Yongfeng Tong; Tingming Jiang; Azzedine Bendounan; Makri Nimbegondi Kotresh Harish; Angelo Giglia; Stefan Kubsky; Fausto Sirotti; Luca Pasquali; Srinivasan Sampath; Vladimir A Esaulov
Journal:  Beilstein J Nanotechnol       Date:  2016-02-17       Impact factor: 3.649

2.  Triptycene-terminated thiolate and selenolate monolayers on Au(111).

Authors:  Jinxuan Liu; Martin Kind; Björn Schüpbach; Daniel Käfer; Stefanie Winkler; Wenhua Zhang; Andreas Terfort; Christof Wöll
Journal:  Beilstein J Nanotechnol       Date:  2017-04-20       Impact factor: 3.649

3.  Electrophilic trifluoromethylselenolation of terminal alkynes with Se-(trifluoromethyl) 4-methylbenzenesulfonoselenoate.

Authors:  Clément Ghiazza; Anis Tlili; Thierry Billard
Journal:  Beilstein J Org Chem       Date:  2017-12-07       Impact factor: 2.883

4.  Electrophilic Trifluoromethylselenolation of Boronic Acids.

Authors:  Clément Ghiazza; Anis Tlili; Thierry Billard
Journal:  Molecules       Date:  2017-05-19       Impact factor: 4.411

5.  Metal-free nucleophilic trifluoromethylselenolation via an iodide-mediated umpolung reactivity of trifluoromethylselenotoluenesulfonate.

Authors:  Kevin Grollier; Alexis Taponard; Arnaud De Zordo-Banliat; Emmanuel Magnier; Thierry Billard
Journal:  Beilstein J Org Chem       Date:  2020-12-10       Impact factor: 2.883

Review 6.  Preparation of Hybrid Sol-Gel Materials Based on Living Cells of Microorganisms and Their Application in Nanotechnology.

Authors:  Olga A Kamanina; Evgeniya A Saverina; Pavel V Rybochkin; Vyacheslav A Arlyapov; Anatoly N Vereshchagin; Valentine P Ananikov
Journal:  Nanomaterials (Basel)       Date:  2022-03-25       Impact factor: 5.076

7.  Thermally Driven Structural Order of Oligo(Ethylene Glycol)-Terminated Alkanethiol Monolayers on Au(111) Prepared by Vapor Deposition.

Authors:  Young Ji Son; Hungu Kang; Sicheon Seong; Seulki Han; Nam-Suk Lee; Jaegeun Noh
Journal:  Molecules       Date:  2022-08-23       Impact factor: 4.927

  7 in total

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