People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Burrows, Andrew D.
University of Bath
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (17/17 displayed)
- 2023Vanillin cross-linked chitosan film with controlled release of green tea polyphenols for active food packagingcitations
- 2022Coupling Postsynthetic High-Temperature Oxidative Thermolysis and Thermal Rearrangements in Isoreticular Zinc MOFscitations
- 2022Coupling Postsynthetic High-Temperature Oxidative Thermolysis and Thermal Rearrangements in Isoreticular Zinc MOFscitations
- 2021Solvent Sorption-Induced Actuation of Composites Based on a Polymer of Intrinsic Microporositycitations
- 2019Polymer of Intrinsic Microporosity (PIM-7) Coating Affects Triphasic Palladium Electrocatalysiscitations
- 2018Polymer of intrinsic microporosity (PIM-7) coating affects triphasic palladium electrocatalysiscitations
- 2017Mechanical characterisation of polymer of intrinsic microporosity PIM-1 for hydrogen storage applicationscitations
- 2017AFM imaging and nanoindentation of polymer of intrinsic microporosity PIM-1citations
- 2015Manufacturing of metal-organic framework monoliths and their application in CO 2 adsorptioncitations
- 2015PIM-MOF Composites for Use in Hybrid Hydrogen Storage Tanks
- 2015Manufacturing of metal-organic framework monoliths and their application in CO2 adsorptioncitations
- 2015The synthesis and characterisation of coordination and hydrogen-bonded networks based on 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoic acidcitations
- 2013Supercritical hydrogen adsorption in nanostructured solids with hydrogen density variation in porescitations
- 2013Supercritical hydrogen adsorption in nanostructured solids with hydrogen density variation in porescitations
- 2008Subtle structural variation in copper metal-organic frameworks: Syntheses, structures, magnetic properties and catalytic behaviourcitations
- 2006Incorporation of dyes into hydrogen-bond networks: The structures and properties of guanidinium sulfonate derivatives containing ethyl orange and 4-aminoazobenzene-4 '-sulfonate
- 2003The influence of functional group orientation on the structure of zinc 1,1,4-trimethylthiosemicarbazide dicarboxylates: Probing the limits of crystal engineering strategies
Places of action
Organizations | Location | People |
---|
article
The influence of functional group orientation on the structure of zinc 1,1,4-trimethylthiosemicarbazide dicarboxylates: Probing the limits of crystal engineering strategies
Abstract
The reaction of [Zn(tmtsc)(2)](NO3)(2) [tmtsc = 1,1,4-trimethylthiosemicarbazide, MeNHC(S)NHNMe2] with a range of sodium dicarboxylates has been shown to lie on the borderline between commonly used crystal engineering strategies. The products exhibit a wide range of structural diversity with the main driving force being the relative orientation of the carboxylate groups. Thus, fumarate leads to the hydrogen-bonded aggregate [Zn(tmtsc)(2)(OH2)][fumarate] (2) in which cations and anions are linked by hydrogen bond donor-donor acceptor-acceptor (DD:AA) interactions, whereas isophthalate and (+)-camphorate lead to coordination polymers [Zn(tmtsc)(mu-isophthalate)] (3a) and [Zn(tmtsc)(mu-camphorate)] (4) with the metal centres linked by bridging dicarboxylate ligands. In the case of isophthalate, a hydrated product [Zn(tmtsc)(mu-isophthalate)].H2O (3b) was also characterised, although microanalysis and powder X-ray diffraction revealed this to be a minor product. Incorporation of water was shown to lead to a change in carboxylate coordination mode from eta(1) in 3a to 112 in 3b. Use of terephthalate leads to the compound [{Zn(tmtsc)(OH2)}(2)(mu-terephthalate)]-[terephthalate].2H(2)O (5), in which half of the terephthalates bridge metal centres, to form dimers, and the remainder link the dimeric cations through DD:AA hydrogen bond interactions. Homophthalate leads to discrete dimers [Zn(tmtsc)(mu-homophthalate)12 (6), whereas acetylenedicarboxylate yields the unexpected compound [Zn(tmtsc)(2)(OH2)][O2CCH= CC(O)N(Me)C(=NNMe2)S](2).H2O (7) in which the dicarboxylate has reacted with tmtsc to give a 2-hydrazono-4-oxo1,3-thiazolidineacetate, which is subsequently trapped in the solid state by DDAA hydrogen bonding interactions with [Zn(tMtSO(2)(OH2)](2+). All products were characterised by single crystal X-ray crystallography, and the representational nature of these crystal structures to the bulk materials was confirmed by microanalysis and powder diffraction. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.