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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1.080 Topics available

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977 Locations available

693.932 PEOPLE
693.932 People People

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Naji, M.
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Buchard, Antoine

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (15/15 displayed)

  • 2023Variations around the presence and position of sulfur in sugar-derived cyclic monomers: influence on polymerisation thermodynamics, polymer sequence and thermal properties8citations
  • 2023Chemical Recycling of Commercial Poly(l-lactic acid) to l-Lactide Using a High-Performance Sn(II)/Alcohol Catalyst System64citations
  • 2023A molecular dynamics approach to modelling oxygen diffusion in PLA and PLA clay nanocomposites3citations
  • 2020Polymers from sugars and unsaturated fatty acids: ADMET polymerisation of monomers derived from D-xylose, D-mannose and castor oil41citations
  • 2019Divergent Catalytic Strategies for the Cis/Trans Stereoselective Ring-Opening Polymerization of a Dual Cyclic Carbonate/Olefin Monomer62citations
  • 2019Copolymerization of Cyclic Phosphonate and Lactide: Synthetic Strategies toward Control of Amphiphilic Microstructure14citations
  • 2018Bipyrrolidine salan alkoxide complexes of lanthanides: synthesis, characterisation, activity in the polymerisation of lactide and mechanistic investigation by DOSY NMR8citations
  • 2017Di-Zinc Aryl Complexes41citations
  • 2017Polymers from sugars and CO271citations
  • 2017Di-Zinc Aryl Complexes:CO2 Insertions and Applications in Polymerization Catalysis41citations
  • 2014Preparation of stereoregular isotactic poly(mandelic acid) through organocatalytic ring-opening polymerization of a cyclic O-carboxyanhydride95citations
  • 2012Recent developments in catalytic activation of renewable resources for polymer synthesis39citations
  • 2012Phosphasalen yttrium complexes: Highly active and stereoselective initiators for lactide polymerization106citations
  • 2012Experimental and computational investigation of the mechanism of carbon dioxide/cyclohexene oxide copolymerization using a dizinc catalyst126citations
  • 2010Iminophosphorane neodymium(III) complexes as efficient initiators for lactide polymerization76citations

Places of action

Chart of shared publication
Kociok-Köhn, Gabriele
5 / 38 shared
Hardy, Craig
1 / 1 shared
Williams, Charlotte
1 / 2 shared
Mcguire, Thomas M.
2 / 2 shared
Parker, Stephen C.
1 / 33 shared
Castro Dominguez, Bernardo
1 / 6 shared
Lightfoot, Jasmine
1 / 1 shared
Piccini, Marco
1 / 1 shared
Chuck, Christopher
1 / 3 shared
Leak, David J.
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Castaing, Rémi
1 / 2 shared
Pérale, Cécile
1 / 1 shared
Markwart, Jens C.
1 / 3 shared
Wurm, Frederik R.
1 / 42 shared
Wolf, Thomas
1 / 10 shared
Beament, James
2 / 2 shared
Jones, Matthew D.
2 / 18 shared
Williams, Charlotte Katherine
2 / 2 shared
Romain, Charles
2 / 4 shared
White, Andrew J. P.
3 / 6 shared
Trott, Gemma
2 / 2 shared
Garden, Jennifer A.
2 / 3 shared
Gregory, Georgina L.
1 / 1 shared
Davidson, Matthew G.
1 / 10 shared
Jeffery, Ben J.
1 / 1 shared
Carbery, David R.
1 / 2 shared
Ivanova, Petya K.
1 / 1 shared
Lowe, John P.
1 / 6 shared
Williams, Charlottek.
1 / 1 shared
Weiner, Jonathan
1 / 1 shared
Bakewell, Clarem.
1 / 1 shared
Goff, Xavier F. Le
2 / 2 shared
Williams, Charlotte K.
3 / 5 shared
Auffrant, Audrey
2 / 2 shared
Cao, Thi-Phuong-Anh
1 / 1 shared
Kember, Michael R.
1 / 1 shared
Rzepa, Henry S.
1 / 1 shared
Jutz, Fabian
1 / 1 shared
Floch, Pascal Le
1 / 1 shared
Platel, Rachel H.
1 / 1 shared
Chart of publication period
2023
2020
2019
2018
2017
2014
2012
2010

Co-Authors (by relevance)

  • Kociok-Köhn, Gabriele
  • Hardy, Craig
  • Williams, Charlotte
  • Mcguire, Thomas M.
  • Parker, Stephen C.
  • Castro Dominguez, Bernardo
  • Lightfoot, Jasmine
  • Piccini, Marco
  • Chuck, Christopher
  • Leak, David J.
  • Castaing, Rémi
  • Pérale, Cécile
  • Markwart, Jens C.
  • Wurm, Frederik R.
  • Wolf, Thomas
  • Beament, James
  • Jones, Matthew D.
  • Williams, Charlotte Katherine
  • Romain, Charles
  • White, Andrew J. P.
  • Trott, Gemma
  • Garden, Jennifer A.
  • Gregory, Georgina L.
  • Davidson, Matthew G.
  • Jeffery, Ben J.
  • Carbery, David R.
  • Ivanova, Petya K.
  • Lowe, John P.
  • Williams, Charlottek.
  • Weiner, Jonathan
  • Bakewell, Clarem.
  • Goff, Xavier F. Le
  • Williams, Charlotte K.
  • Auffrant, Audrey
  • Cao, Thi-Phuong-Anh
  • Kember, Michael R.
  • Rzepa, Henry S.
  • Jutz, Fabian
  • Floch, Pascal Le
  • Platel, Rachel H.
OrganizationsLocationPeople

article

Di-Zinc Aryl Complexes

  • Williams, Charlotte Katherine
  • Romain, Charles
  • White, Andrew J. P.
  • Trott, Gemma
  • Buchard, Antoine
  • Garden, Jennifer A.
Abstract

Two new di-zinc aryl complexes, [LZn2Ph2] and [LZn2(C6F5)2], coordinated by a diphenol tetraamine macrocyclic ligand are prepared and fully characterized, including by single crystal X-ray diffraction experiments. The complexes' reactivities with monomers including carbon dioxide, cyclohexene oxide, phthalic anhydride, iso-propanol and phenol are investigated using both experimental studies and density functional theory calculations. In particular, [LZn2Ph2] readily inserts carbon dioxide to form a carboxylate, at 1 bar pressure, whereas [LZn2(C6F5)2] does not react. Under these conditions [LZn2Ph2] shows moderate activity in the ring-opening copolymerisation of cyclohexene oxide / carbon dioxide (TOF = 20 h-1); cyclohexene oxide / phthalic anhydride (TOF = 33 h-1) and the ring opening polymerisations of rac-lactide (TOF = 99 h-1) and ε-caprolactone (TOF = 5280 h-1).

Topics
  • density
  • single crystal X-ray diffraction
  • single crystal
  • Carbon
  • theory
  • experiment
  • zinc
  • density functional theory