Photochemistry and Reactivity of the Phenyl Radical–Water System: A Matrix Isolation and Computational Study

The reaction of the phenyl radical 1 with water has been investigated by using matrix isolation spectroscopy and quantum chemical calculations. The primary thermal product of the reaction between 1 and water is a weakly bound complex stabilized by an OH???π interaction. This complex is photolabile, and visible‐light irradiation (λ>420 nm) results in hydrogen atom transfer from water to radical 1 and the formation of a highly labile complex between benzene and the OH radical. This complex is stable under the conditions of matrix isolation, however, continuous irradiation with λ>420 nm light results in the complete destruction of the aromatic system and formation of an acylic unsaturated ketene. The mechanisms of all reaction steps are discussed in the light of ab initio and DFT calculations.     

Variable-temperature FT-IR studies on the thermodynamics of carbon dioxide adsorption on a faujasite-type H-Y zeolite

Adsorption of carbon dioxide on a faujasite-type H-Y zeolite (Si:Al = 2.6:1) was studied by variable-temperature (200-290 K range) infrared spectroscopy. Adsorbed CO₂ molecules interact with the Brønsted acid Si(OH)Al groups located inside the zeolite supercage, bringing about a characteristic bathochromic shift of the O-H stretching mode from 3645 cm⁻¹ (free OH group) to 3540 cm⁻¹ (hydrogen-bonded CO₂ adsorption complex). Simultaneously, the asymmetric (ν₃) mode of adsorbed CO₂ is observed at 2353 cm⁻¹. From the observed variation of the integrated intensity of the 3645 and 2353 cm⁻¹ IR absorption bands upon changing temperature, corresponding values of standard adsorption enthalpy and entropy were found to be ΔH° = −28.5(±1) kJ mol⁻¹ and ΔS° = −129(±10) J mol⁻¹ K⁻¹. Comparison with the reported values of ΔH° for CO₂ adsorption on other zeolites is briefly discussed.     

Model of an asymmetric DPPC/DPPS membrane: effect of asymmetry on the lipid properties. A molecular dynamics simulation study

The study of asymmetric lipid bilayers is of a crucial importance due to the great number of biological process in which they are involved such as exocytosis, intracellular fusion processes, phospholipid-protein interactions, and signal transduction pathway. In addition, the loss of this asymmetry is a hallmark of the early stages of apoptosis. In this regard, a model of an asymmetric lipid bilayer composed of DPPC and DPPS was simulated by molecular dynamics simulation. Thus, the asymmetric membrane was modeled by 264 lipids, of which 48 corresponded to DPPS- randomly distributed in the same leaflet with 96 DPPC. In the other leaflet, 120 DPPC were placed without DPPS-. Due to the presence of a net charge of -1 for the DPPS- in physiological conditions, 48 Na+ were introduced into the system to balance the charge. To ascertain whether the presence of the DPPS- in only one of the two leaflets perturbs the properties of the DPPC in the other leaflet composed only of DPPC, different properties were studied, such as the atomic density of the different components across the membrane, the electrostatic potential across the membrane, the translational diffusion of DPPC and DPPS, the deuterium order parameters, lipid hydration, and lipid-lipid charge bridges. Thus, we obtained that certain properties such as the surface area lipid molecule, lipid head orientation, order parameter, translational diffusion coefficient, or lipid hydration of DPPC in the leaflet without DPPS remain unperturbed by the presence of DPPS in the other leaflet, compared with a DPPC bilayer. On the other hand, in the leaflet containing DPPS, some of the DPPC properties were strongly affected by the presence of DPPS such as the order parameter or electrostatic potential.     

Locally definable homotopy

In [E. Baro, M. Otero, On o-minimal homotopy, Quart. J. Math. (2009) 15pp, in press (doi:10.1093/qmath/hap011)] o-minimal homotopy was developed for the definable category, proving o-minimal versions of the Hurewicz theorems and the Whitehead theorem. Here, we extend these results to the category of locally definable spaces, for which we introduce homology and homotopy functors. We also study the concept of connectedness in ?-definable groups — which are examples of locally definable spaces. We show that the various concepts of connectedness associated to these groups, which have appeared in the literature, are non-equivalent.     

Engineering of gold surface work function by electrodeposition of spirobifluorene donor–acceptor bipolar systems

Charge separation in gold/spirobifluorene-based donor (triphenylamine)–acceptor (cyano) bipolar systems has been investigated by contact potential difference and surface photovoltage spectroscopy. Organic films were formed on gold electrode by electrochemical polymerization and by dipping in dye solution. The gold surface work function has been changed over more than 0.4 eV depending on the numbers of electrochemical deposition cycles. Photovoltage effects were analyzed in terms of internal photoemission from Au into organic film, and organic layer light absorption. The energetic differences between the Fermi-level of Au and HOMO levels of organic systems were obtained. The results showed that the electrodeposition is a versatile tool for electrode surface work function tuning.     

A new titanium building block for early-late heterometallic complexes; preparation of a new tetrameric metallomacrocycle by self assembly

The new titanium dicarboxylate complex Cp*TiMe(OOC)2py (2) [Cp*=eta5-C5Me5; (OOC)2py = 2,6-pyridinedicarboxylate] has been synthesized. The reaction of complex 2 with water renders [Cp*Ti(OOC)2py]2O (3). The molecular structure of 3 has been studied by X-ray diffraction methods. Complex 2 reacts with isocyanides to yield the respective iminoacyl derivatives Cp*Ti(eta2-MeCNR)(OOC)2py [R=tBu (4), 2,6-dimethylphenyl (xylyl) (5)]. The molecular structure of complex4 has been established by X-ray diffraction. Compound 2 has been employed as a new building block for the preparation of new early-late heterometallic compounds; it reacts with [M(mu-OH)(COD)]2 (M = Rh, Ir) to give the corresponding tetranuclear metallomacrocycle derivatives [Cp*Ti{(OOC)(2)py}(mu-O)M(COD)]2 [M = Rh (6); Ir (7)]. The molecular structure of 6 has been established by X-ray diffraction.     

Chiral close-packing of achiral star-shaped molecules on solid surfaces

From the interplay of scanning tunneling microscopy and theoretical calculations, we study the chiral self-assembly of achiral HtB-HBC molecules upon adsorption on the Cu(110) surface. We find that chirality is expressed at two different levels: a +/-5 degrees rotation of the molecular axis with respect to the close-packed direction of the Cu(110) substrate and a chiral close-packed arrangement expected for star-shaped molecules in 2D. Out of the four possible chiral expressions, only two are found to exist due the effect of van der Waals (vdW) interactions forcing the molecules to simultaneously adjust to the atomic template of the substrate geometry and self-assemble in a close-packed geometry.     

Combined theoretical and FTIR spectroscopic studies on hydrogen adsorption on the zeolites Na-FER and K-FER

The interaction between molecular hydrogen and the alkali-metal-exchanged zeolites Na-FER and K-FER at a low temperature was investigated by combining variable-temperature infrared spectroscopy and theoretical calculations by using a periodic DFT model. The experimentally determined values of standard adsorption enthalpy, DeltaH degrees , were -6.0 (+/-0.8) and -3.5 (+/-0.8) kJ mol(-1) for Na-FER and K-FER, respectively. These results were found to be in agreement with corresponding DeltaH degrees values obtained from calculations on the periodic model. Two types of alkali-metal cation sites in FER were found: channel intersection sites and channel wall sites. Calculations showed a similar interaction energy for both site types, and similar structures of adsorption complexes. Up to two dihydrogen molecules can be physisorbed on the alkali-metal cation located on the intersection of two channels, while only one H2 molecule is physisorbed on the cation at the channel wall site. The adsorption enthalpies of H2 on alkali-metal-exchanged FER are significantly smaller than those found previously for the MFI-type zeolites Na-ZSM-5 and K-ZSM-5, which is likely due to a difference in the alkali-metal cation coordination in the two zeolite frameworks.     

Solar Energy Conversion Using a Semiconductor Electrode Photosensitized by Tetraphenylporphyrin

The synthesis of meso-tetraphenylporphyrin (TPP) and its application in a solar- energy conversion device are described as an undergraduate laboratory experiment. In the first part of the exercise, a convenient procedure for the synthesis of TPP is presented. In the second section of the experiment, the construction of a high-efficiency photoelectrode that utilizes the light harvesting capacity of the porphyrin is presented. The spectral sensitization of a wide-band-gap semiconductor is achieved using TPP as an efficient photoreceptor, This mimics the role of the tetrapyrrolic macrocycle in natural photosynthesis.