Cationic or Neutral: Dependence of Photophysical Properties of Bis-Alkynylphosphonium Pt(II) Complexes on Ancillary Ligand.

A series of D-π-A alkynylphosphonium salts with different linker between donor and acceptor groups was used to synthesize two series of trans-bis-alkynylphosphonium Pt(II) complexes with different ancillary ligands (triphenylphosphine, P series, and cyanide, CN series). The nature of the ancillary ligand manages the overall charge and emission properties of the complexes obtained. In addition, the variation of the linker in alkynylphosphonium ligands allows fine-tuning the luminescence wavelength.

Homoleptic Alkynylpyridinium Au(I) Complexes as Organometallic 'D-π-A' Chromophores.

A series of terminal acetylenes bearing methylpyridinium acceptor group attached to the alkynyl unit with different π-conjugated aromatic linker have been synthetized. These alkynylpyridinium salts are efficient 'push-pull' chromophores demonstrating bright UV-vis fluorescence with quantum yields up to 70 %. The homoleptic bis-alkynyl Au(I) complexes based on these alkynylpyridinium ligands demonstrate complicated photophysical behavior including dual emission in solution.

Homoleptic Alkynylphosphonium Au(I) Complexes as Push-Pull Phosphorescent Emitters.

A series of compounds - bearing terminal alkynyl sites connected with a phosphonium group via different π-conjugated linkers have been synthesized. The compounds themselves are efficient push-pull emitters and exhibit bright fluorescence in blue and near-UV regions. - were used as alkynyl ligands to obtain a series of homoleptic bis-alkynyl Au(I) complexes -.

Influence of hypomagnetic field on the heartbeat in zebrafish embryos.

The magnetic environment may influence the functioning of the cardiovascular system. It was reported that low-frequency and static magnetic fields affect hemodynamics, heart rate, and heart rate variability in animals and humans. Moreover, recent data suggest that magnetic fields affect the circadian rhythms of physiological processes.

Hexavanadate-Organogold(I) Hybrid Compounds: Synthesis by the Azide-Alkyne Cycloaddition and Density Functional Theory Study of an Intriguing Electron Density Distribution.

The fully oxidized Lindqvist-type hexavanadate compounds decorated by phosphine-derivatized Au(I) moieties oriented in a fashion (-BuN)[VO{(OCH)CCH(NCCH)AuP(CHOMe)}] () and (-BuN)[VO{(OCH)CCHOCH(CNH)AuP(CHOMe)}] () have been prepared by azide-alkyne cycloaddition reactions and characterized by various techniques, including NMR, IR, and UV/vis spectroscopy and electrospray ionization mass spectrometry. Electronic structure calculations unveil the potential of these model hybrid junctions for application in controlled charge-transport experiments on substrate surfaces.