Controlling the Dimensionality of On-Surface Coord... - BV FAPESP
Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Controlling the Dimensionality of On-Surface Coordination Polymers via Endo- or Exoligation

Full text
Author(s):
Show less -
Shchyrba, Aneliia [1] ; Waeckerlin, Christian [2] ; Nowakowski, Jan [2] ; Nowakowska, Sylwia [1] ; Bjoerk, Jonas [3] ; Fatayer, Shadi [1] ; Girovsky, Jan [2] ; Nijs, Thomas [1] ; Martens, Susanne C. [1, 4] ; Kleibert, Armin [5] ; Stoehr, Meike [6] ; Ballav, Nirmalya [7] ; Jung, Thomas A. [2] ; Gade, Lutz H. [4]
Total Authors: 14
Affiliation:
[1] Univ Basel, Dept Phys, CH-4056 Basel - Switzerland
[2] Paul Scherrer Inst, Lab Micro & Nanotechnol, CH-5232 Villigen, PSI - Switzerland
[3] Linkoping Univ, IFM, Dept Phys Chem & Biol, S-58183 Linkoping - Sweden
[4] Heidelberg Univ, Inst Anorgan Chem, D-69120 Heidelberg - Germany
[5] Paul Scherrer Inst, CH-5232 Villigen, PSI - Switzerland
[6] Univ Groningen, Zernike Inst Adv Mat, NL-9747 AG Groningen - Netherlands
[7] Indian Inst Sci Educ & Res, Dept Chem, Pune 411008, Maharashtra - India
Total Affiliations: 7
Document type: Journal article
Source: Journal of the American Chemical Society; v. 136, n. 26, p. 9355-9363, JUL 2 2014.
Web of Science Citations: 36
Abstract

The formation of on-surface coordination polymers is controlled by the interplay of chemical reactivity and structure of the building blocks, as well as by the orientating role of the substrate registry. Beyond the predetermined patterns of structural assembly, the chemical reactivity of the reactants involved may provide alternative pathways in their aggregation. Organic molecules, which are transformed in a surface reaction, may be subsequently trapped via coordination of homo- or heterometal adatoms, which may also play a role in the molecular transformation. The amino-functionalized perylene derivative, 4,9-diaminoperylene quinone-3,10-diimine (DPDI), undergoes specific levels of dehydrogenation (-1 H-2 or -3 H-2) depending on the nature of the present adatoms (Fe, Co, Ni or Cu). In this way, the molecule is converted to an endo- or an exoligand, possessing a concave or convex arrangement of ligating atoms, which is decisive for the formation of either ID or 2D coordination polymers. (AU)

FAPESP's process: 13/04855-0 - Study of self-assembly of terpyridyl molecules on metallic surfaces
Grantee:Shadi Passam Fatayer
Support Opportunities: Scholarships abroad - Research Internship - Master's degree