Materials Map

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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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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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Bag, Ranjit

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University of South Wales

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2019Synthesis, Structures and Chemistry of the Metallaboranes of Group 4-9 with M2B5 Core Having a Cross Cluster M-M Bond14citations
  • 2019Synthesis, Structures and Chemistry of the Metallaboranes of Group 4–9 with M2B5 Core Having a Cross Cluster M–M Bond14citations

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Ghosh, Sundargopal
1 / 2 shared
Saha, Suvam
2 / 2 shared
Mondal, Bijan
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Borthakur, Rosmita
2 / 2 shared
Dorcet, Vincent
2 / 27 shared
Halet, Jean-François
2 / 29 shared
Roisnel, Thierry
2 / 54 shared
Chart of publication period
2019

Co-Authors (by relevance)

  • Ghosh, Sundargopal
  • Saha, Suvam
  • Mondal, Bijan
  • Borthakur, Rosmita
  • Dorcet, Vincent
  • Halet, Jean-François
  • Roisnel, Thierry
OrganizationsLocationPeople

article

Synthesis, Structures and Chemistry of the Metallaboranes of Group 4–9 with M2B5 Core Having a Cross Cluster M–M Bond

  • Bag, Ranjit
  • Saha, Suvam
  • Mondal, Bijan
  • Borthakur, Rosmita
  • Dorcet, Vincent
  • Halet, Jean-François
  • Roisnel, Thierry
Abstract

<jats:p>In an attempt to expand the library of M2B5 bicapped trigonal-bipyramidal clusters with different transition metals, we explored the chemistry of [Cp*WCl4] with metal carbonyls that enabled us to isolate a series of mixed-metal tungstaboranes with an M2{B4M’} {M = W; M’ = Cr(CO)4, Mo(CO)4, W(CO)4} core. The reaction of in situ generated intermediate, obtained from the low temperature reaction of [Cp*WCl4] with an excess of [LiBH4·thf], followed by thermolysis with [M(CO)5·thf] (M = Cr, Mo and W) led to the isolation of the tungstaboranes [(Cp*W)2B4H8M(CO)4], 1–3 (1: M = Cr; 2: M = Mo; 3: M = W). In an attempt to replace one of the BH—vertices in M2B5 with other group metal carbonyls, we performed the reaction with [Fe2(CO)9] that led to the isolation of [(Cp*W)2B4H8Fe(CO)3], 4, where Fe(CO)3 replaces a {BH} core unit instead of the {BH} capped vertex. Further, the reaction of [Cp*MoCl4] and [Cr(CO)5·thf] yielded the mixed-metal molybdaborane cluster [(Cp*Mo)2B4H8Cr(CO)4], 5, thereby completing the series with the missing chromium analogue. With 56 cluster valence electrons (cve), all the compounds obey the cluster electron counting rules. Compounds 1–5 are analogues to the parent [(Cp*M)2B5H9] (M= Mo and W) that seem to have generated by the replacement of one {BH} vertex from [(Cp*W)2B5H9] or [(Cp*Mo)2B5H9] (in case of 5). All of the compounds have been characterized by various spectroscopic analyses and single crystal X-ray diffraction studies.</jats:p>

Topics
  • compound
  • single crystal X-ray diffraction
  • cluster
  • single crystal
  • chromium
  • thermolysis