Alkylpyrrolidiniumtrialkoxysilyl iodides as organic iodide sources for dye-sensitised solar cells.

Two new alkylpyrrolidiniumtriethoxysilyl iodides have been developed as iodide sources for DSSCs; the compound with an undecyl spacer between the siloxane and the pyrrolidinium moieties furnished higher open circuit voltages than the propyl analogue and higher efficiencies at low light intensity.

Bis(acetylacetonato)ruthenium(II) complexes containing alkynyldiphenylphosphines. Formation and redox behaviour of [Ru(acac)2(Ph2PC triple bond CR)2] (R=H, Me, Ph) complexes and the binuclear complex cis-[{Ru(acac)2}2(micro-Ph2PC triple bond CPPh2)}2].

Two equivalents of Ph(2)PC triple bond CR (R=H, Me, Ph) react with thf solutions of cis-[Ru(acac)(2)(eta(2)-alkene)(2)] (acac=acetylacetonato; alkene=C(2)H(4), 1; C(8)H(14), 2) at room temperature to yield the orange, air-stable compounds trans-[Ru(acac)(2)(Ph(2)PC triple bond CR)(2)] (R=H, trans-3; Me=trans-4; Ph, trans-5) in isolated yields of 60-98%. In refluxing chlorobenzene, trans-4 and trans-5 are converted into the yellow, air-stable compounds cis-[Ru(acac)(2)(Ph(2)PC triple bond CR)(2)] (R=Me, cis-4; Ph, cis-5), isolated in yields of ca. 65%.

Catalytic reduction of dinitrogen to ammonia at a single molybdenum center.

Since our discovery of the catalytic reduction of dinitrogen to ammonia at a single molybdenum center, we have embarked on a variety of studies designed to further understand this complex reaction cycle. These include studies of both individual reaction steps and of ligand variations. An important step in the reaction sequence is exchange of ammonia for dinitrogen in neutral molybdenum(III) compounds.

Observation of 1MLCT and 3MLCT excited states in quadruply bonded Mo2 and W2 complexes.

The photophysical properties of the series of quadruply bonded M(2)(O(2)C-Ar)(4) [M = Mo, Ar = phenyl (ph), 1-naphthalene (1-nap), 2-naphthalene (2-nap), 9-anthracene (9-an), 1-pyrene (1-py), and 2-pyrene (2-py); M = W, Ar = ph, 2-nap] complexes were investigated. The lowest energy absorption of the complexes is attributed to a metal-to-ligand charge transfer (1)MLCT transition from the metal-based delta HOMO to the pi* O(2)C-Ar LUMO. The Mo(2)(O(2)C-Ar)(4) complexes exhibit weak short-lived emission (<10 ns) and a nonemissive, long-lived (40-76 mus) excited state detected by transient absorption spectroscopy.

New metal-organic polygons involving MM quadruple bonds: M8(O2CtBu)4(mu-SC4H2-3,4-{CO2}2)6 (M=Mo, W).

The reactions between M2(O2CtBu)4, where M=Mo or W, and thienyl-3,4-dicarboxylic acid (0.5-1.5 equiv) in toluene proceed via a series of detectable intermediates to the compounds M8(O2CtBu)4(mu-SC4H2-3,4-{CO2}2)6, which are isolated as air-sensitive yellow (M=Mo) or red (M=W) powders and show parent molecular ions in their mass spectra (MALDI).

Thienyl carboxylate ligands bound to and bridging MM quadruple bonds, M = Mo or W: models for polythiophenes incorporating MM quadruple bonds.

A series of compounds of the form [M(2)L(4)] and [[((t)()BuCO(2))(3)M(2)](2)(mu-L')] have been made where M = Mo or W, L = a thienyl, bithienyl, or terthienyl carboxylate, and L' = a corresponding thienyl dicarboxylate. The electronic absorption spectra are reported and the electronic structures discussed. Intense metal-to-ligand charge transfer bands traverse the visible and near-IR regions of the electronic absorption spectrum.

9,10-Anthracene dicarboxylate bridged complexes with M2 quadruply bonded dimetal units: [[M2(O2CtBu)3]2(mu-9,10-An(CO2)2)], where M = Mo or W.

From the reactions between [M2(O2CtBu)4] and 9,10-anthracenedicarboxylic acid in toluene, the dicarboxylate bridged complexes [[M2(O2CtBu)3]2(mu-9,10An(CO2)2)], have been obtained as microcrystalline yellow (M = Mo) and red (M = W) powders. The powders are soluble in THF forming intense red (M = Mo) and green (M = W) solutions. The electronic absorption spectra in 2-MeTHF have been recorded as a function of temperature (2-298 K) and show a small bathochromic shift on cooling.

Thienyl carboxylate ligands bound to M2 quadruple bonds involving molybdenum and tungsten. Models for dimetallated polythiophenes.

Thienyl-carboxylate and -dicarboxylate groups attached to dinuclear centers (M = Mo or W) having MM quadruple bonds show interesting electronic properties and provide insight into the probable nature of related dimetallated polythiophenes.