The Sn atom in the title compound, [Sn(CH(3))(2)(NCS)(2)(C(20)H(14)N(4))], is N,N',N''-chelated by the terpyridine part of the N-heterocycle. The Sn atom exists in a trans-C(2)SnN(5) penta-gonal-bipyramidal geometry [C-Sn-C = 173.66 (8)°] with the methyl groups in axial and the N atoms in equatorial positions.

Novel macrocyclic saccharide receptors that possess terpyridine skeletons as a hydrogen-bonding site are presented. On modification of the hydrogen-bonding sites and the macrocyclic bridges, the receptors showed selective bindings for ribofuranosides, deoxyribofuranosides, and glucopyranosides, respectively. The binding affinities of the receptors were very high, so that native monosaccharides ...

Two solvated cobalt(ii) terpyridine complexes, [Co(MeO-terpy)2](BF4)2·H2O (·H2O) and [Co(MeO-terpy)2](BF4)2·acetone (·acetone) were prepared. Annealing each of these complexes resulted in the formation of two desolvated species, and , respectively. ·H2O and exhibited two-step and gradual SCO. The compound ·acetone has high-spin at all temperatures and undergoes a reverse spin transition due to ...

Negative differential resistance (NDR) behaviors of single molecule junctions composed of a thiol-terminated Ru(ii) bis-terpyridine (Ru(tpy-SH)2) molecule sandwiched between two gold electrodes are measured using a specifically modified scanning probe microscope break junction technique (SPMBJ) at room temperature. The low-bias (0.623 ± 0.135 V) NDR observed for one of the three conductance gro...

Terpyridine-based ligands form octahedral complexes with Co(2+) at low cation concentrations to form helical assemblies which provide a supramolecular gel framework. Increasing the Co(2+) concentration above 0.6 equiv. reveals a second, co-existing square pyramidal complex derived assembly, having a distinct helicity. While this geometry dominates at 1 equiv. of Co(2+), we find this unique form...

The title compound, C(33)H(25)N(5), belongs to the family of pyridine-2,6-dicarboxaldehyde Schiff bases which possess a terdentate coordinating site (-N=C-C=N-C-C=N-) similar to terpyridine derivatives. The dihedral angles between pairs of terminal rings are 69.67 (9) and 66.23 (9)°. The shortest distance between the centroids of aromatic rings in neighbouring mol-ecules is 3.8080 (14) Å.

Reaction of the novel thiopropyl-closo-1,2-carborane ligand bearing a pendant glycerol group HS(CH(2))(3)CB(10)H(10)CCH(2)OCH(CH(2)OH)(2)(L) with the labile platinum(ii) precursor [Pt(MeCN)(terpy)](OTf)(2)(terpy = 2,2':6',2''-terpyridine; OTf = trifluoromethanesulfonate) affords the highly water-soluble platinum(ii) complex [PtL(terpy)]OTf, the first example of a metal-carborane complex functio...

The synthesis of several symmetrically 4,4''-functionalized 2,2':6',2''-terpyridines is reported. In addition to the biscarboxylic acid 4,4''-tpy(CO₂H)₂ (3), the anthryl esters 4,4''-tpy(CO₂CH₂Anth) ₂(5a) and 4,4''-tpy(CO₂CH₂CH₂OAnth)₂ (5b) were synthesized. Furthermore, both anthryl esters were used to synthesize symmetric iron(II)-bis(terpyridine)complexes 6a-b. Irradiation experiments were c...

The first series of cyclometalated ruthenium complexes with a CCC-pincer bis-carbene ligand have been obtained as bench-stable compounds. Single-crystal X-ray analysis of one of these complexes with 4'-di-p-anisylamino-2,2':6',2''-terpyridine is presented. The Ru(II/III) redox potentials and MLCT absorptions of these complexes can be varied by attaching an electron-donating or -withdrawing grou...

Conjugate addition of organometallic reagents to enones to form silyl enol ether products is a versatile method to difunctionalize activated olefins, but the organometallic reagents required can be limiting. The reductive cross-electrophile coupling of unhindered primary alkyl bromides with enones and chlorosilanes to form silyl enol ether products is catalyzed by a nickel-complexed ortho-bromi...