Surface-Confined Amorphous Films from Metal-Coordinated Simple Phenolic Ligands

被引：193

作者：

Rahim, Md. Arifur ^{[1
,2
]}

Kempe, Kristian ^{[1
,2
]}

Muellner, Markus ^{[1
,2
]}

Ejima, Hirotaka ^{[1
,2
]}

Ju, Yi ^{[1
,2
]}

van Koeverden, Martin P. ^{[1
,2
]}

Suma, Tomoya ^{[1
,2
]}

Braunger, Julia A. ^{[1
,2
]}

Leeming, Michael G. ^{[3
,4
]}

Abrahams, Brendan F. ^{[3
]}

Caruso, Frank ^{[1
,2
]}

机构：

[1] Univ Melbourne, ARC Ctr Excellence Convergent Bionano Sci & Techn, Parkville, Vic 3010, Australia

[2] Univ Melbourne, Dept Biomol & Chem Engn, Parkville, Vic 3010, Australia

[3] Univ Melbourne, Sch Chem, Parkville, Vic, Australia

[4] Univ Melbourne, Inst Mol Sci & Biotechnol Bio21, Parkville, Vic 3010, Australia

来源：

CHEMISTRY OF MATERIALS | 2015年 / 27卷 / 16期

基金：

澳大利亚研究理事会;

关键词：

ORGANIC FRAMEWORKS; CROSS-LINKING; RESONANCE RAMAN; COMPLEXES; IRON; CATECHOL; IRON(III); CAPSULES; FUNCTIONALITY; NETWORKS;

D O I：

10.1021/acs.chemmater.5b02790

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Coordination chemistry of natural polyphenols and transition metals allows rapid self-assembly of conformal coatings on diverse substrates. Herein, we report that this coordination-driven self-assembly process applies to simple phenolic molecules with monotopic or ditopic chelating sites (as opposed to macromolecular, multitopic polyphenols), leading to surface-confined amorphous films upon metal coordination. Films fabricated from gallic acid, pyrogallol, and pyrocatechol, which are the major monomeric building blocks of polyphenols, have been studied in detail. Pyrocatechol, with one vicinal diol group (i.e., bidentate), has been observed to be the limiting case for such assembly. This study expands the toolbox of available phenolic ligands for the formation of surface-confined amorphous films, which may find application in catalysis, energy, optoelectronics, and the biomedical sciences.

引用

页码：5825 / 5832

页数：8

共 53 条

[1] Molecular diversity in phenolic and polyphenolic precursors of tannin-inspired nanocoatings [J].

Barrett, Devin G. ;

Sileika, Tadas S. ;

Messersmith, Phillip B. .

CHEMICAL COMMUNICATIONS, 2014, 50 (55) :7265-7268

[2] Amorphous Metal-Organic Frameworks [J].

Bennett, Thomas D. ;

Cheetham, Anthony K. .

ACCOUNTS OF CHEMICAL RESEARCH, 2014, 47 (05) :1555-1562

[3] MAGNETIC EXCHANGE INTERACTIONS IN SEMIQUINONE COMPLEXES OF IRON - STRUCTURAL AND MAGNETIC-PROPERTIES OF TRIS(3,5-DI-TERT-BUTYLSEMIQUINONATO)IRON(III) AND TETRAKIS(3,5-DI-TERT-BUTYLSEMIQUINONATO)TETRAKIS(3,5-DI-TERT-BUTYLCATECHOLATO)TETRAIRON(III) [J].

BOONE, SR ;

PURSER, GH ;

CHANG, HR ;

LOWERY, MD ;

HENDRICKSON, DN ;

PIERPONT, CG .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (06) :2292-2299

[4] Use of the di-2-pyridyl ketone/3,5-di-tert-butylcatechol "blend" in iron(III) chemistry:: a cationic tetranuclear cluster and an anionic trinuclear complex [J].

Boudalis, AK ;

Dahan, F ;

Bousseksou, A ;

Tuchagues, JP ;

Perlepes, SP .

DALTON TRANSACTIONS, 2003, (17) :3411-3418

[5] Nanoengineering of inorganic and hybrid hollow spheres by colloidal templating [J].

Caruso, F ;

Caruso, RA ;

Möhwald, H .

SCIENCE, 1998, 282 (5391) :1111-1114

[6] Mussel Inspired Dynamic Cross-Linking of Self-Healing Peptide Nanofiber Network [J].

Ceylan, Hakan ;

Urel, Mustafa ;

Erkal, Turan S. ;

Tekinay, Ayse B. ;

Dana, Aykutlu ;

Guler, Mustafa O. .

ADVANCED FUNCTIONAL MATERIALS, 2013, 23 (16) :2081-2090

[7] Supramolecular Coordination: Self-Assembly of Finite Two- and Three-Dimensional Ensembles [J].

Chakrabarty, Rajesh ;

Mukherjee, Partha Sarathi ;

Stang, Peter J. .

CHEMICAL REVIEWS, 2011, 111 (11) :6810-6918

[8]

Clogston JD, 2011, METHODS MOL BIOL, V697, P63, DOI 10.1007/978-1-60327-198-1_6

[9] Metal-Organic Frameworks and Self-Assembled Supramolecular Coordination Complexes: Comparing and Contrasting the Design, Synthesis, and Functionality of Metal-Organic Materials [J].

Cook, Timothy R. ;

Zheng, Yao-Rong ;

Stang, Peter J. .

CHEMICAL REVIEWS, 2013, 113 (01) :734-777

[10]

Deria P, 2014, CHEM SOC REV, V43, P5896, DOI [10.1039/c4cs00067f, 10.1039/C4CS00067F]

← 1 2 3 4 5 6 →