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σ-Alkenyl endo-palladacycle formation via regiospecific functionalisation of an unreactive NHC-tethered C(sp2)–H bond
National licenceRoyal Society of Chemistry | 2015| -
σ-Acceptor, Z-type ligands for transition metals
National licenceRoyal Society of Chemistry | 2010| -
π–π* Emission from a tetrazine derivative complexed with zinc ion in aqueous solution: a unique water-soluble fluorophore
National licenceRoyal Society of Chemistry | 2011| -
π–π Aggregation in metalloporphyrins: causative factors
National licenceRoyal Society of Chemistry | 1976| -
π-Stacking interactions in some crystalline cisoid E,E-1,4-diaryl-1,3-butadienes
National licenceRoyal Society of Chemistry | 2003| -
π-Stacking and hydrogen bonding direct diastereoselectivity in one-pot syntheses of octahedral iron(ii) complexes
National licenceRoyal Society of Chemistry | 2010| -
π Participation in addition reactions of endo-3,3-diphenyltricyclo[3.2.1.02,4]oct-6-ene
National licenceRoyal Society of Chemistry | 1989| -
π-Mediated rearrangements and 1,2-H shifts of indanylcarbenes
National licenceRoyal Society of Chemistry | 1999| -
π-Interactions in pentafluorophenylfluorophosphonitriles
National licenceRoyal Society of Chemistry | 1968| -
π-Hole/n→π* interactions with acetonitrile in crystal structures
Royal Society of Chemistry | 2018| -
π-Facial selectivity in Diels–Alder reactions of C-2-vinyl glycals. Stereocontrolled route to annulated C-glycopyranosides
National licenceRoyal Society of Chemistry | 1990| -
π Facial hydrogen bonding in the chiral resolving agent (S)-2,2,2-trifluoro-1-(9-anthryl)ethanol and its racemic modification
National licenceRoyal Society of Chemistry | 1991| -
π-Facial diastereoselectivity in the electrophilic and electrophilic–nucleophilic additions to dimethyl (1R,2R,3S,4S)-bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylate
National licenceRoyal Society of Chemistry | 1993| -
π-Face donor properties of N-heterocyclic carbenes
National licenceRoyal Society of Chemistry | 2005| -
π-Extended tetrathiafulvalene BODIPY (ex-TTF-BODIPY): a redox switched “on–off–on” electrochromic system with two near-infrared fluorescent outputs
National licenceRoyal Society of Chemistry | 2014|
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