S
Simon R. L. Everitt
Researcher at University of Reading
Publications - 9
Citations - 284
Simon R. L. Everitt is an academic researcher from University of Reading. The author has contributed to research in topics: Sulfoxide & Bipyridine. The author has an hindex of 9, co-authored 9 publications receiving 278 citations. Previous affiliations of Simon R. L. Everitt include University of Birmingham.
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Journal ArticleDOI
Inclusion complexation of (cyclo)alkanes and (cyclo) alkanols with 6-O-modified cyclodextrins
Yoshihisa Inoue,Keiko Yamamoto,Takehiko Wada,Simon R. L. Everitt,Xing Ming Gao,Zhi Jie Hou,Lin Hui Tong,Shao Kai Jiang,Hou Ming Wu +8 more
TL;DR: In this article, the free energy of inclusion complexation has been shown to increase linearly to a certain limit with extending chain length or ring size of the guests, giving unit increments per methylene (dΔG°/dNC).
Journal ArticleDOI
Diastereoselective preparation and characterization of ruthenium bis(bipyridine) sulfoxide complexes.
Dusan Hesek,Yoshihisa Inoue,Simon R. L. Everitt,Hitoshi Ishida,Mieko Kunieda,Michael G. B. Drew +5 more
TL;DR: This represents the first process by which a sigma-bonded ligand occupying only a single coordination site has had such an important influence on the stereochemical outcome of a ruthenium bis(bipyridine) complex formation.
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Preparation and structural elucidation of novel cis ruthenium(II) bis(bipyridine) sulfoxide complexes
Dusan Hesek,Yoshihisa Inoue,Simon R. L. Everitt,Hitoshi Ishida,Mieko Kunieda,Michael G. B. Drew +5 more
TL;DR: In this article, four novel cis-ruthenium bis(bipyridine) sulfoxide complexes with the general formula cis-[Ru(A)2(B)(Cl)]X (2, A = 2,2,2′-biprithmidine (bpy), B = TMSO; 3, A= 4,4,4′-dimethyl-2.2, 2.2′-, Bπ, B = DMSO, DMP; 4, A. = DMP, B.= TMS
Journal ArticleDOI
The first asymmetric synthesis of chiral ruthenium tris(bipyridine) from racemic ruthenium bis(bipyridine) complexes
TL;DR: In this paper, the first asymmetric synthesis of ruthenium trisbipyridine derivatives starting from corresponding racemic RRThenium bis(bibyridine) complexes is described, which can be easily converted to the products with a retention of configuration at the metal center.
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Conversion of a new chiral reagent Δ-[Ru(bpy)2 (dmso)Cl]PF6 to Δ-[Ru(bpy)2(dmbpy)]PF6Cl with 96.8% retention of chirality (dmbpy = 4,4′-dimethyl-2,2′-bipyridine)
Dusan Hesek,Yoshihisa Inoue,Simon R. L. Everitt,Hitoshi Ishida,Mieko Kunieda,Michael G. B. Drew +5 more
TL;DR: In this paper, the new chiral ruthenium bis(bpy) sulfoxide reagent Δ-cis-[Ru( bpy)2(dmso)Cl]PF6 (100% ee following HPLC resolution) is used to prepare Δ-[Ru (bpy)-2(dmbpy)][PF6]Cl in excellent yield (97%) with almost complete retention of absolute configuration (96.8%), as confirmed by X-ray crystallographic studies on a single enantiomer.