The use of tpy'(tpy'= 4,4',4''-tri-tert-butyl-terpyridine) as a ligand for nickel allows for the isolation of a Ni(I)-alkyl complex and a Ni(II)-alkyl halide complex, both of which can be used as mechanistic probes of key steps in alkyl cross-coupling reactions.

We report the first Hg(2+) selective hydrogelation by 4'-[4-(4-aminophenyl)phenyl]-2,2':6',2''-terpyridine. The gel showed remarkable response towards specific chemical agents such as benzo-18-crown-6 ether and K(+) which enabled extensive modulation of the gel morphology.

We report the analysis of a novel terpyridine based supramolecular hydrogel which shows fluorescent properties in the gel but not in the sol form; the gel forms in a narrow pH range in aqueous solutions specifically in the presence of sodium ions, and contains between 98% and 99.2% water.

Resonant X-ray Emission Spectroscopy (RXES) is used to characterize the ligand field states of the prototypic self-assembled square-planar complex, [Pt(tpy)Cl]Cl (tpy=2,2':6',2''-terpyridine), and determine the effect of weak metal-metal and π-π interactions on their energy.

Multicomponent, self-assembled rhomboidal constructs are reported, in which bis-terpyridines possessing 120° or 60° directionality and Zn(II) or Cd(II) in a stoichiometric ratio (1 : 1 : 2) initially form rhomboid and triangle mixtures; whereas, a tris-terpyridine reacts with the 60°-based bis-ligand and metal to quantitatively form a heteroleptic, centrally fused, rhomboidal structure.

Dye-sensitized solar cells have been assembled using a sequential approach: a TiO(2) surface was functionalized with an anchoring ligand, followed by metallation with Zn(OAc)(2) or ZnCl(2), and subsequent capping with a chromophore functionalized 2,2':6',2''-terpyridine; the DSCs exhibit surprisingly good efficiencies confirming the effectiveness of the new strategy for zinc-based DSC fabrication.

A 9 ps (3)MLCT lifetime was achieved by a Fe(II) complex based on C(NHC)^N(py)^C(NHC) pincer ligands. This is the longest known so far for any kind of complexes of this abundant metal, and increased by almost two orders of magnitude compared to the reference Fe(II) bis-terpyridine complex.

Due to its special coordination ability to Cu(II)-terpyridine complexes, a simple and straightforward visual recognition of p-DMAP out of its analogues has been realized via selective metallogel collapse. In combination with the selective gel collapse and the self-healing properties of metallohydrogel , its potential application towards chemo-switch is also demonstrated.

Activation of the relatively inactive polypyridine backbone with strong electrophilic fluorine, originating from acetyl hypofluorite (AcOF) enables attack of the acetoxy moiety at the α position to the heteroatom. Derivatives of bipyridine, phenanthroline and terpyridine systems have been acetoxylated or oxygenated within a few minutes usually in very good yields.

{[Ru(CH3CN)3]2(tppz)}(4+) (tppz = tetra-2-pyridylpyrazine) undergoes photoinduced CH3CN exchange with λirr ≥ 610 nm in H2O. In contrast, cis-{[Ru(tpy)(L)]2(bpm)}(4+) (tpy = 2,2':6',2''-terpyridine, bpm = 2,2'-bipyrimidine, L = CH3CN) is not reactive, but the complex with L = DMSO is photoactive. These complexes are potentially useful for the release of multiply caged drugs.