Ferrer García, MontserratGomez-Bautista, DanielGutiérrez i Currius, AlbertOrduña Marco, GuillermoOro, Luis A.Pérez Torrente, Jesús J.Rossell Alfonso, OriolRuiz Sabín, Eliseo2019-02-122019-02-122016-02-080276-7333https://hdl.handle.net/2445/128170New titanocene pyridinethiolate compounds [(RCp)(2)Ti(4-Spy)(2)] (R = H (1), Me (2); Cp = cyclo-pentadienyl; 4-Spy = pyridine-4-thiolate) and [Cp2Ti(2-Spy)(2)] (3; 2-Spy = pyridine-2-thiolate) have been prepared by reaction of the corresponding Li(Spy) salt with the appropriate compound [(RCp)(2)TiCl2]. Compounds 1 and 2 have been used as metalloligands in self-assembly reactions with the acceptor late-transition-metal compounds [M(H2O)(2)(dppp)]-(OTf)(2) (M = Pd (a) Pt (b); dppp = 1,3-bis-(diphenylphosphino)propane), and the series of early-late tetranuclear metallamacrocycles [{(RCp)(2)Ti(4-Spy)(2)}{M-(dppp)}](2)(OTf)(4) (R = H, M = Pd (1(2)a(2)); R = H, M = Pt (1(2)b(2)); R = Me, M = Pd (2(2)a(2)); R = Me, M = Pt (2(2)b(2))) arising from the anti isomer of the titanocene metalloligands have been obtained. Only ligand transfer reactions from Ti to either Pd or Pt atoms have been observed when the pyridine-2-thiolate derivative 3 has been assayed in self-assembly processes. The obtained species have been characterized by NMR spectroscopy and ESI(+) mass spectrometry. The supramolecular assemblies have shown to be nonrigid in solution, and their fluxional behavior has been studied by VT H-1 NMR spectroscopy. A DFT study including ab initio molecular dynamics in order to elucidate the structures and the relative stability of the isomers has been performed.34 p.application/pdfeng(c) American Chemical Society , 2016LligandsMetallsEspectroscòpia de ressonància magnètica nuclearEspectrometria de masses amb ionització per electroespraiQuímica supramolecularLigandsMetalsNuclear magnetic resonance spectroscopyElectrospray ionization mass spectrometrySupramolecular chemistryinfo:eu-repo/semantics/article6670012019-02-12info:eu-repo/semantics/openAccess