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Yves C. Zimmermann

Researcher at Uppsala University

Publications -  5
Citations -  297

Yves C. Zimmermann is an academic researcher from Uppsala University. The author has contributed to research in topics: Self-assembled monolayer & Alkylation. The author has an hindex of 5, co-authored 5 publications receiving 282 citations. Previous affiliations of Yves C. Zimmermann include University of Basel.

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Development of supramolecular structure through alkylation of pendant pyridyl functionality

TL;DR: The complex 12+ as discussed by the authors is a metal-containing analogue of 4,4′-bipyridine and undergoes N-alkylation reactions with a variety of alkylating agents to give more highly functionalised tetracationic complexes which may be termed metalloviologens.
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Redistribution of terpy ligands—approaches to new dynamic combinatorial libraries

TL;DR: Mixing solutions of homoleptic cobalt(II) complexes [CoA2]2+ and [CoB2] 2+ results in the establishment of a combinatorial library containing the heteroleptic complex [CoAB]2+. By using enantiomorphic ligands A and B the reactions may be followed by 1H NMR spectroscopy as mentioned in this paper.
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Electrochemical probing of ground state electronic interactions in polynuclear complexes of a new heteroditopic ligand

TL;DR: The investigation of the electronic absorption and emission spectra reveals an energy transfer in the excited state from the terminating bipy-boundMetal centres to the central terpy-bound metal centre, which indicates that the bridge is able to facilitate energyTransfer in the exciting state between the metal centres despite the lack of interactions in the ground state.
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Self-Assembled Monolayers of Ruthenium and Osmium Bis-Terpyridine ComplexesInsights of the Structure and Interaction Energies by Combining Scanning Tunneling Microscopy and Electrochemistry

TL;DR: Self-Assembled Monolayers of Ruthenium and Osmium Bis-Terpyridine Complexes-Insights of the Structure and Tnteraction Energies by Combining Scanning Tunneling Microscopy and Electrochemistry as discussed by the authors.
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Self-assembled monolayers of Ru/Os dinuclear complexes: probing monolayer structure and interaction energies by electrochemical means.

TL;DR: It was shown that the tpy coordination sites of the dinuclear complexes interact more strongly within the SAM than the bipyridine-coordinated fragments, supported by peak potential shifts, which are due to interaction forces in SAMs.