Ergosterol (provitamin D2) triplet state: an efficient sensitiser of singlet oxygen, O2(1 delta g), formation

The triplet state of ergosterol (provitamin D2) has been produced in benzene by pulse radiolysis and characterised in terms of absorption spectrum, lifetime, self-quenching properties and relaxed triplet energy. The amount of singlet oxygen, O₂(¹Δ_g), produced as a consequence of the oxygen quenching of this species has been determined by kinetic infrared emission spectroscopy. Ergosterol is significantly more efficient as a singlet oxygen sensitiser in benzene than is naphthalene, the absolute standard employed in this work.     

Determination of rate constants for charge transfer and the distribution of semiconductor and electrolyte electronic energy levels in dye-sensitized solar cells by open-circuit photovoltage decay method

A combination of electron lifetime measurement in nanoparticles as a function of the Fermi level position at high resolution in the potential scale with a new model to describe this dependence provides a powerful tool to study the microscopic processes and parameters governing recombination in dye-sensitized solar cells. This model predicts a behavior divided in three domains for the electron lifetime dependence on open-circuit voltage that is in excellent agreement with the experimental results: a constant lifetime at high photovoltage, related to free electrons; an exponential increase due to internal trapping and detrapping and an inverted parabolla at low photovoltage that corresponds to the density of levels of acceptor electrolyte species, including the Marcus inverted region.     

Efficiency of the photoprocesses leading to singlet oxygen (1 delta g) generation by alpha-terthienyl: optical absorption, optoacoustic calorimetry and infrared luminescence studies

The triplet energy of alpha-terthienyl has been determined by heavy atom-induced optical absorption: the value of 39.7 +/- 1.5 kcal/mol is consistent with earlier energy transfer work. Combining this result with calorimetric data from optoacoustic calorimetry indicates that intersystem crossing occurs with at least 90% efficiency in polar and non-polar solvents. The quantum yields for singlet oxygen formation via energy transfer from triplet alpha-terthienyl have been obtained from time-resolved measurements of its IR phosphorescence: these yields are in the 0.6-0.8 range in non-polar and polar (hydroxylic and non-hydroxylic) solvents.     

Thermal-lensing and phosphorescence studies of the quantum yield and lifetime of singlet molecular oxygen (1 delta g) sensitized by hematoporphyrin and related porphyrins in deuterated and non-deuterated ethanols

Time-resolved thermal-lensing was used to measure the absolute quantum yield (φ_Δ) of singlet molecular oxygen, O₂(¹Δ_g), produced by hematoporphyrin photosensitization in ethanol. Deuteration of the solvent did not affect the value of φ_Δ. The value of φΔ= 0.53 was then used as reference to evaluate φΔ in O₂ (¹Δ_g) phosphorescence experiments with the related porphyrins, monohydroxyethylvinyl deuteroporphyrin and dihematoporphyrin ether. The φ_Δ values, in conjunction with the respective quantum yields of intersystem crossing (measured using a nanosecond laser flash photolysis technique) served to evaluate efficiencies, S_Δ, of O₂ (¹Δ_g) production from the porphyrin triplet states. The lifetime T_Δ in monodeuterated ethanol was measured as 29 ± 3 μs and 30 ± 1 (xs by time-resolved thermal lensing and phosphorescence detection, respectively. T_Δ in ethanol and fully deuterated ethanol were in good agreement with values reported in the literature.     

Quantum real wave-packet dynamics of the N(4S)+NO(X2Pi)-->N2(X1Sigma(g)+)+O(3P) reaction on the ground and first excited triplet potential energy surfaces: rate constants, cross sections, and product distributions

The reaction N+NO-->N(2)+O was studied by means of the time-dependent real wave-packet (WP) method and the J-shifting approximation. We consider the ground 1 (3)A(") and first excited 1 (3)A(') triplet states, which correlate with both reactants and products, using analytical potential energy surfaces (PESs) recently developed in our group. This work extends our previous quantum dynamics study, and probabilities, cross sections, and rate constants were calculated and interpreted on the basis of the different shapes of the PESs (barrierless 1 (3)A(") and with barrier 1 (3)A(') surfaces, respectively). The WP rate constant (k(1)) shows a weak dependence on T(200-2500 K), as the dominant contribution to reactivity is provided by the barrierless ground PES. There is a good agreement of WP k(1) with the measurements and variational transition state theory (VTST) data, and also between the WP and VTST k(1)(1 (3)A(")) results. Nevertheless, there is a large discrepancy between the WP and VTST k(1)(1 (3)A(')) results. Product state distributions were also calculated for the much more reactive 1 (3)A(") PES. There is an excellent agreement with the experimental average fraction of vibrational energy in N(2)(25+/-3%), the only measured dynamics property of this reaction.     

Theoretical study of the C6H3 potential energy surface and rate constants and product branching ratios of the C2H(2Sigma+) + C4H2(1Sigma(g)+) and C4H(2Sigma+) + C2H2(1Sigma(g)+) reactions

Ab initio CCSD(T)cc-pVTZ//B3LYP6-311G(**) and CCSD(T)/complete basis set (CBS) calculations of stationary points on the C(6)H(3) potential energy surface have been performed to investigate the reaction mechanism of C(2)H with diacetylene and C(4)H with acetylene. Totally, 25 different C(6)H(3) isomers and 40 transition states are located and all possible bimolecular decomposition products are also characterized. 1,2,3- and 1,2,4-tridehydrobenzene and H(2)CCCCCCH isomers are found to be the most stable thermodynamically residing 77.2, 75.1, and 75.7 kcal/mol lower in energy than C(2)H + C(4)H(2), respectively, at the CCSD(T)/CBS level of theory. The results show that the most favorable C(2)H + C(4)H(2) entrance channel is C(2)H addition to a terminal carbon of C(4)H(2) producing HCCCHCCCH, 70.2 kcal/mol below the reactants. This adduct loses a hydrogen atom from the nonterminal position to give the HCCCCCCH (triacetylene) product exothermic by 29.7 kcal/mol via an exit barrier of 5.3 kcal/mol. Based on Rice-Ramsperger-Kassel-Marcus calculations under single-collision conditions, triacetylene+H are concluded to be the only reaction products, with more than 98% of them formed directly from HCCCHCCCH. The C(2)H + C(4)H(2) reaction rate constants calculated by employing canonical variational transition state theory are found to be similar to those for the related C(2)H + C(2)H(2) reaction in the order of magnitude of 10(-10) cm(3) molecule(-1) s(-1) for T = 298-63 K, and to show a negative temperature dependence at low T. A general mechanism for the growth of polyyne chains involving C(2)H + H(C[triple bond]C)(n)H --> H(C[triple bond]C)(n+1)H + H reactions has been suggested based on a comparison of the reactions of ethynyl radical with acetylene and diacetylene. The C(4)H + C(2)H(2) reaction is also predicted to readily produce triacetylene + H via barrierless C(4)H addition to acetylene, followed by H elimination.