Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2012Modulation of Metallophilic Bonds146citations
  • 2012Intensely Luminescent Homoleptic Alkynyl Decanuclear Gold(I) Clusters and Their Cationic Octanuclear Phosphine Derivatives51citations

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Karttunen, Antti J.
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Haukka, Matti
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Chang, Yuh-Chia
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Pakkanen, Tapani
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Chou, Pi-Tai
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Selivanov, Stanislav I.
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Janis, Janne
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Tunik, Sergey P.
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2012

Co-Authors (by relevance)

  • Karttunen, Antti J.
  • Haukka, Matti
  • Chang, Yuh-Chia
  • Pakkanen, Tapani
  • Chou, Pi-Tai
  • Pakkanen, Tapani A.
  • Selivanov, Stanislav I.
  • Janis, Janne
  • Tunik, Sergey P.
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article

Modulation of Metallophilic Bonds

  • Karttunen, Antti J.
  • Haukka, Matti
  • Koshevoy, Igor O.
  • Chang, Yuh-Chia
  • Pakkanen, Tapani
  • Chou, Pi-Tai
Abstract

<p>We report a homoleptic Au-Cu alkynyl cluster that represents an unexplored class of luminescent materials with stimuli-responsive photophysical properties. The bimetallic complex formulated as [Au2Cu2(C2OHC5H8)(4)] efficiently self-assembles from Au(SC4H8)Cl, Cu(NCMe)(4)PF6, and 1-ethynylcyclopentanol in the presence of NEt3. This compound shows remarkably diverse polymorphism arising from the modulation of metallophilic interactions by organic solvents. Four crystalline forms, obtained from methanol (1a); ethanol, acetone, or choloroform (1b); toluene (1c); and diethyl ether or ethyl acetate (1d), demonstrate different photoluminescent characteristics. The solid-state quantum yields of phosphorescence (Phi) vary from 0.1% (1a) to 25% (1d), depending on the character of intermetallic bonding. The structures of 1b-d were determined by single-crystal X-ray diffraction. The ethanol (1b, Phi = 2%) and toluene (1c, Phi = 10%) solvates of [Au2Cu2(C2OHC5H8)(4)](n) adopt octanuclear isomeric structures (n = 2), while 1d (Phi = 25%) is a solvent-free chain polymer built from two types of Au4Cu4 units. Electronic structure calculations show that the dramatic enhancement of the emission intensity is correlated with the increasing role of metal-metal bonding. The latter makes the emission progressively more metal-centered in the order 1b &lt;1c &lt;1d. The metallophilic contacts in 1a-d show high sensitivity to the vapors of certain solvents, which effectively induce unusual solid-state isomerization and switching of the absorption and luminescence properties via non-covalent interactions. The reported polymorphic material is the first example of a gold(I) alkynyl compound demonstrating vapochromic behavior.</p>

Topics
  • impedance spectroscopy
  • compound
  • cluster
  • polymer
  • x-ray diffraction
  • gold
  • intermetallic
  • phosphorescence