Porphyrins at interfaces

被引:575
作者
Auwaerter, Willi [1 ]
Ecija, David [1 ,2 ]
Klappenberger, Florian [1 ]
Barth, Johannes V. [1 ]
机构
[1] Tech Univ Munich, Phys Dept E20, James Franck Str, D-85748 Garching, Germany
[2] IMDEA Nanosci, Madrid 28049, Spain
基金
加拿大自然科学与工程研究理事会; 欧洲研究理事会;
关键词
SCANNING-TUNNELING-MICROSCOPY; SINGLE-MOLECULE; CYTOCHROME-C; FE-PHTHALOCYANINE; SOLAR-CELLS; SURFACE; METALATION; MANIPULATION; COORDINATION; SPIN;
D O I
10.1038/nchem.2159
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porphyrins and other tetrapyrrole macrocycles possess an impressive variety of functional properties that have been exploited in natural and artificial systems. Different metal centres incorporated within the tetradentate ligand are key for achieving and regulating vital processes, including reversible axial ligation of adducts, electron transfer, light-harvesting and catalytic transformations. Tailored substituents optimize their performance, dictating their arrangement in specific environments and mediating the assembly of molecular nanoarchitectures. Here we review the current understanding of these species at well-defined interfaces, disclosing exquisite insights into their structural and chemical properties, and also discussing methods by which to manipulate their intramolecular and organizational features. The distinct characteristics arising from the interfacial confinement offer intriguing prospects for molecular science and advanced materials. We assess the role of surface interactions with respect to electronic and physicochemical characteristics, and describe in situ metallation pathways, molecular magnetism, rotation and switching. The engineering of nanostructures, organized layers, interfacial hybrid and bio-inspired systems is also addressed.
引用
收藏
页码:105 / 120
页数:16
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