693.932 PEOPLE
| People | Locations | Statistics |
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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Petrov, R. H. | Madrid |
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| Azevedo, Nuno Monteiro |
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Jones, Matthew D.
University of Bath
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (18/18 displayed)
- 2019Copolymerization of Cyclic Phosphonate and Lactide: Synthetic Strategies toward Control of Amphiphilic Microstructurecitations
- 2018Bipyrrolidine salan alkoxide complexes of lanthanides: synthesis, characterisation, activity in the polymerisation of lactide and mechanistic investigation by DOSY NMRcitations
- 2017Synthesis of PLGA using a C3-symmetric Zr (IV) amine tris(phenolate) alkoxide initiator and the effects of gamma radiation on its propertiescitations
- 2017Zirconium amine tris(phenolate):A more effective initiator for biomedical lactidecitations
- 2017Zirconium amine tris(phenolate)citations
- 2017Zn<sup>II</sup> Chlorido Complexes with Aliphatic, Chiral Bisguanidine Ligands as Catalysts in the Ring‐Opening Polymerisation of <i>rac</i>‐Lactide Using FT‐IR Spectroscopy in Bulkcitations
- 2016Aminopiperidine based complexes for lactide polymerisationcitations
- 2013Synergistic empirical and theoretical study on the stereoselective mechanism for the aluminum salalen complex mediated polymerization of rac-Lactidecitations
- 2011Homopiperazine and piperazine complexes of Zr(IV) and Hf(IV) and their application to the ring-opening polymerisation of lactidecitations
- 2011Salalen aluminium complexes and their exploitation for the ring opening polymerisation of rac-lactidecitations
- 2009Synthesis and structure of aluminium amine-phenolate complexescitations
- 2009Novel Ti(IV) and Zr(IV) complexes and their application in the ring-opening polymerisation of cyclic esterscitations
- 2006Synthesis and X-ray structures of new titanium(IV) aryloxides and their exploitation for the ring opening polymerization of epsilon-caprolactonecitations
- 2003trans-bis[(S)-(-)-2-aminomethyl-1-ethylpyrrolidine-kappa N-2]palladium(II) dichloride methanol trisolvate
- 2003(η3-Allyl)[(S)-(+)-(2-pyrrolidinylmethyl)-pyrrolidine] palladium(II) trifluoromethane-sulfonatecitations
- 2003(eta(3)-allyl)[(S)-(+)-(2-pyrrolidinylmethyl)pyrrolidine]palladium(II) trifluoromethanesulfonate
- 2003[1,1 '-bis(diphenylphosphino)ferrocene-kappa P-2,P '](1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate dichloromethane disolvatecitations
- 2003(eta(3)-Allyl)[(R)-(+)-2,2 '-bis(diphenylphosphino)-1,1 '-binaphthyllpalladium(II) trifluoromethanesulfonate dichloromethane solvatecitations
Places of action
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article
(η3-Allyl)[(S)-(+)-(2-pyrrolidinylmethyl)-pyrrolidine] palladium(II) trifluoromethane-sulfonate
Abstract
<p>The title compound, [Pd(C<sub>3</sub>H<sub>5</sub>)(C<sub>9</sub>H <sub>18</sub>N<sub>2</sub>)]CF<sub>3</sub>SO<sub>3</sub>, crystallizes in the non-centrosymmetric space group P2<sub>1</sub>2<sub>1</sub>2<sub>1</sub> and contains only one crystallographically unique Pd metal centre, showing a pseudo-square-planar geometry. (S)-(+)-(2-Pyrrolidinylmethyl)pyrrolidine (pmp, C<sub>9</sub>H<sub>18</sub>N<sub>2</sub>) acts as an N,N′-bidentate chelating ligand, leading to the formation of the chiral [Pd(η<sup>3</sup>- allyl)(pmp)]<sup>+</sup> complex cation, which is hydrogen bonded to the trifluoromethanesulfonate anion.</p>