Assessing the negative impact of chlorantraniliprole, isoxaflutole, and simazine pesticides on phospholipid membrane models and tilapia gill tissues.

The indiscriminate and, very often, incorrect use of pesticides in Brazil, as well as in other countries, results in severe levels of environmental pollution and intoxication of human life. Herein, we studied plasma membrane models (monolayer and bilayer) of the phospholipid Dioleoyl-sn-glycerol-3-phosphocholine (DOPC) using Langmuir films, and large (LUVs) and giant (GUVs) unilamellar vesicles, to determine the effect of the pesticides chlorantraniliprole (CLTP), isoxaflutole (ISF), and simazine (SMZ), used in sugarcane. CLTP affects the lipid organization of the bioinspired models of DOPC π-A isotherms, while ISF and SMZ pesticides significantly affect the LUVs and GUVs. Furthermore, the in vivo study of the gill tissue in fish in the presence of pesticides (2.0 × 10-10 mol/L for CLTP, 8.3 × 10-9 mol/L for ISF, and SMZ at 9.9 × 10-9 mol/L) was performed using optical and fluorescence images. This investigation was motivated by the gill lipid membranes, which are vital for regulating transporter activity through transmembrane proteins, crucial for maintaining ionic balance in fish gills. In this way, the presence of phospholipids in gills offers a model for understanding their effects on fish health. Histological results show that exposure to CLTP, ISF, and SMZ may interfere with vital gill functions, leading to respiratory disorders and osmoregulation dysfunction. The results indicate that exposure to pesticides caused severe morphological alterations in fish, which could be correlated with their impact on the bioinspired membrane models. Moreover, the effect does not depend on the exposure period (24h and 96h), showing that animals exposed to pesticides for a short period suffer irreparable damage to gill tissue. In summary, we can conclude that the harm caused by pesticides, both in membrane models and in fish gills, occurs due to contamination of the aquatic system with pesticides. Therefore, water quality is vital for the preservation of ecosystems.

A SA-CASSCF and MS-CASPT2 study on the electronic structure of nitrosobenzene and its relation to its dissociation dynamics.

The photodissociation channels of nitrosobenzene (PhNO) induced by a 255 nm photolytic wavelength have been studied using the complete active space self-consistent method and the multistate second-order multiconfigurational perturbation theory. It is found that there exists a triplet route for photodissociation of the molecule. The reaction mechanism consists of a complex cascade of nonadiabatic electronic transitions involving triple and double conical intersections as well as intersystem crossing. Several of the relevant states (S2, S4, and S5 states) correspond to double excitations. It is worth noting that the last step of the photodissociation implies an internal conversion process. The experimentally observed velocity pattern of the NO fragment is a signature of such a conical intersection.

Conservation of El-Sayed's Rules in the Photolysis of Phenyl Azide: Two Independent Decomposition Doorways for Alternate Direct Formation of Triplet and Singlet Phenylnitrene.

In the present work, we demonstrate that the formation of triplet and singlet phenylnitrene, when arises from the photodissociation of phenyl azide, fulfills El-Sayed's rules or the electronic angular momentum conservation law. It is shown that the singlet-triplet inversion of phenylnitrene via the vibronic coupling mechanism is not an effective process. In contrast, it is found that there exist two independent dissociation channels that yield alternatively singlet and triplet phenylnitrene. Therefore, a proposed mechanism that violates the angular momentum low is avoided. The clue of the photoreaction lies in the conjunction (energetic and spatial) of two crossing points in a very narrow region of the multidimensional space: (i) an intersystem crossing (ISC1) and (ii) a conical intersection (CI1). The geometrical separation between these two crossing geometries is only 0.016 Å measured in Cartesian coordinates, and the respective energy difference is 2 kcal/mol. This work has been performed by application of the complete active space self-consistent field and multiconfigurational second-order perturbation method.

Theoretical Approaches for Modeling the Effect of the Electrode Potential in the SERS Vibrational Wavenumbers of Pyridine Adsorbed on a Charged Silver Surface.

Vibrational wavenumbers of pyridine adsorbed on a silver electrode have been correlated to the calculated ones from different theoretical approaches based on DFT methods. The vibrational tuning caused by the electrode potential has been simulated by means of pyridine-silver clusters with different densities of charge or, alternatively, under applied external electric fields. Both methodologies predict correctly a qualitative red-shift of the vibrational wavenumbers at negative potentials. As a result, harmonic frequency calculations performed at the B3LYP/LanL2DZ level of theory by using a linear [Ag n Py] q complex model with different densities of charge (q eff = q/n) have exhibited the best agreement with the experimental observations although the tuning amplitudes are overestimated. Electric fields calculations are unable to account for subtle details observed in the spectra related to the differentiated chemical nature of the metal-molecule bond at positive or negative potentials with respect to the potential of zero charge of the electrode.

Conical intersections and intersystem crossings explain product formation in photochemical reactions of aryl azides.

Photochemistry of 3- and 4-methoxyphenyl azide at 266 nm has been studied by means of the complete active space self-consistent field (CASSCF) and multi-configurational second-order perturbation (MS-CASPT2) methods. Minima and interstate crossing points have been optimized using the CASSCF method. The calculations predict that the key step of the photolysis of both azides is a non-radiative process. However, an important difference is found when we compare the reactivity of both isomers of azide, deactivation of 3-methoxyphenyl azide (1) can occur via two reaction channels (internal conversion or intersystem crossing), which lead to formation of the dimer of 2H-azepine derivative (2a) and 3,3'-dimethoxyazobenzene (2b). In contrast, deactivation of 4-methoxyphenyl azide (3) takes place via a singlet to triplet intersystem crossing, which leads to formation of 4,4'-dimethoxyazobenzene (4). After initial deactivation, both isomers follow a cascade of surface crossings until they reach the final nitrenes, respectively. The reference active space for the two azides is 14 electrons in 13 orbitals and comprises the six π-type orbitals of the aromatic ring plus four σ-(N-N2) and five π-type orbitals of the -N3 moiety.

Application of surface-enhanced resonance Raman scattering (SERS) to the study of organic functional materials: electronic structure and charge transfer properties of 9,10-bis((E)-2-(pyridin-4-yl)vinyl)anthracene.

The electron donor-acceptor properties of 9,10-bis((E)-2-(pyridin-4-yl)vinyl) anthracene (BP4VA) are studied by means of surface-enhanced Raman scattering (SERS) spectroscopy and vibronic theory of resonance Raman spectroscopy. The SERS spectra recorded in an electrochemical cell with a silver working electrode have been interpreted on the basis of resonance Raman vibronic theory assisted by DFT calculations. It is demonstrated that the adsorbate-metal interaction occurs through the nitrogen atom of the pyridyl moiety. Concerning the electron donor-acceptor properties of the adsorbate, it is shown that the charge transfer excited states of BP4VA are not optically active, in contrast, an internal transition to an excited state of BP4VA, which is localized in the anthracene framework, is strongly allowed. The charge transfer states will be populated by an ultrafast non-radiative process, that is, internal conversion. Thus, irradiation of BP4VA interacting with an appropriate surface creates an effective charge separation.

Charge transfer at the nanoscale and the role of the out-of-plane vibrations in the selection rules of surface-enhanced Raman scattering.

Surface-enhanced Raman scattering (SERS) spectroscopy of pyridazine shows the selective enhancement of the bands recorded at about 1570, 1450 and 380 cm-1, which are assigned to two different types of vibrations. The first two correspond to in-plane 8a;νring and 19b;δ(CH) totally symmetric A1 modes, respectively, while the last band is assigned to the out-of-plane 16b;τring,B1 vibration. The selective enhancement has been analyzed on the basis of a resonant Raman process involving photoexcited metal (M)-to-molecule (A) charge transfer (CT: M-A + hν → M+-A-) states of the metal-adsorbate surface complex, which have also been related to the doublet electronic states of the corresponding radical anion of the adsorbate (A-). According to the selection rules of the electromagnetic/plasmonic SERS enhancement mechanism, the simultaneous enhancement of in-plane and out-of-plane modes could be attributed to different orientations of the adsorbate (perpendicular and parallel, respectively, or tilted) with respect to the metallic surface. The calculated resonance Raman-CT spectra (SERS-CT) and the vibrational wavenumbers of isolated pyridazine and of the pyridazine-Ag2 complex obtained from electronic structure calculations suggest a single type of molecule adsorbed with perpendicular orientation. The relative SERS enhancements of both in-plane and out-of-plane modes are due to Franck-Condon factors related to differences between the equilibrium geometries (A1 vibrations, ΔQ ≠ 0) and gradients (B1 vibrations, Δν ≠ 0 and ΔQ ≠ 0), respectively, of the potential energy surfaces of the involved ground and photoinduced CT electronic states. Therefore, the selective enhancement of the SERS bands of pyridazine is controlled by a general metal-to-molecule resonant CT mechanism. This conclusion supports the usefulness of SERS in studying the subtle electronic structure of charged interfaces as well as key processes such as electron transfer at the nanoscale.

An MS-CASPT2 study of the photodecomposition of 4-methoxyphenyl azide: role of internal conversion and intersystem crossing.

The photochemical decomposition of 4-methoxyphenyl azide (CH3O-Ph-N3) is investigated using multiconfigurational second-order perturbation theory (MS-CASPT2). In addition, the multi-state resonance Raman spectra of the reactant, intermediates, and product are computed with a multi-state version of the vibronic theory of Albrecht. The results support that the key step of the photolysis of the parent azide is a 21A'/23A'' intersystem crossing which in a second step decays through a 23A''/13A'' conical intersection to give directly the formation of triplet 4-methoxyphenyl nitrene (CH3O-Ph-N) in its lowest electronic state, 13A''. It is found that the efficiency of the cited intersystem crossing is enhanced by the close presence of a 21A'/21A'' conical intersection. On the other hand, the calculated spectra suggest that the only two species which would be observed in the gas phase experiments are the triplet nitrene plus 4,4'-dimethoxyazobenzene.

An approach to the electronic structure of molecular junctions with metal clusters of atomic thickness.

TD-DFT calculations predict a linear dependence of the energies of charge transfer states of Agn-pyrazine-Agn molecular junctions on the inverse of the size (1/n) of the linear metal chains. The density of charge (qeff = q/n) in the metal-to-metal charge transfer excited states (CTMM: Agnq-pyrazine-Agn-q) smoothly tunes the electronic structure of the junction, especially the metal-to-molecule charge transfer states (CT0 and CT1) and the first excited singlet of pyrazine (S1,Pz). In enlarged junctions, pyrazine bonds preferably to one of the Agn clusters and this weak adsorption produces a significant unexpected asymmetry for forward and reverse charge transfer processes.

Surface-enhanced Raman scattering of picolinamide, nicotinamide, and isonicotinamide: unusual carboxamide deprotonation under adsorption on silver nanoparticles.

Surface-Enhanced Raman Scattering (SERS) of picolinamide, nicotinamide, and isonicotinamide has been studied on silver colloids at pH⩾7. The wavenumbers of the SERS bands assigned to 1; νring and ν(C-X) vibrational modes show important blue-shifts (ca. +50cm(-1)) with respect to the Raman spectra, whereas the Amide III bands undergo red-shifts up to -50cm(-1). We demonstrate that these shifts are originated by the deprotonation of the carboxamide groups which link to the metal through the nitrogen and oxygen atoms of the respective azanion groups. In order to support this conclusion, theoretical DFT force field calculations have been carried out, confirming that the pyridinecarboxamides interact with the metallic surface in their deprotonated forms as benzamide does.

Evidence of deprotonation of aromatic acids and amides adsorbed on silver colloids by surface-enhanced Raman scattering.

The surface-enhanced raman scattering (SERS) of benzoic acid/benzamide and salicylic acid/salicylamide on silver colloids show important wavenumber shifts with respect to the Raman spectrum of the band assigned to mode 1;ν(ring) when adsorbed on the metal surface (ca. +50 cm(-1)). In the case of the acids, this shift is originated by the deprotonation of the carboxylic group in agreement with the well-known fact that aromatic acids are adsorbed on silver as carboxylates. However, the main conclusion of this work is that a similar behavior is found for the respective amides that do not behave as acids in water solution. The here studied aromatic amides are adsorbed as azanions on silver nanoparticles even at pH 7 and link to the metal through the nitrogen and oxygen atoms of the ionized carboxamide group. This is a very surprising result given that amides are not significantly ionized even at pH 13-14. The deprotonation of these amides is not determined exclusively by the pH, but it is mainly caused by the strong affinity of the anionic species to the metal. Therefore, the SERS must be cautiously used as a universal pH sensor if the adsorption occurs through the ionizable group. In order to support this conclusion, theoretical DFT force field calculations have been carried out, confirming that deprotonated benzamide and salicylamide interact with the metallic surface.

Percutaneous endoscopic gastrostomy complication rates and compliance with the American Society for Gastrointestinal Endoscopy guidelines for the management of antithrombotic therapy.

BACKGROUND: The American Society for Gastrointestinal Endoscopy (ASGE) has published recommendations in regards to anticoagulant (AC) and antiplatelet (AP) therapy management during endoscopic procedures. So far, no study has assessed either ASGE recommendation compliance during percutaneous endoscopic gastrostomy (PEG) placement or procedure-associated complication rates as related to the observance of these recommendations. The aims of this study were to compare the incidence and type of complications during PEG placement in patients receiving or not receiving AC and/or AP therapy and to determine the compliance with ASGE's AC and AP management guidelines. METHODS: Medical files of patients who underwent PEG placement from January 2004 to December 2008 were reviewed. Clinical and procedure-related data were recorded. Patients were separated into 1 of 2 groups: patients under AP and/or AC therapy prior to PEG placement (n = 51) and a control group of patients (n = 40) not receiving any AP and/or AC treatment at least 6 months prior to the procedure. RESULTS: A total of 91 patients (51 cases) were included. Groups were comparable in demographics and clinical characteristics. No differences in the frequency and type of complications were found between groups. ASGE's recommendations were not followed in any of these patients. CONCLUSIONS: Overall PEG placement complication rate was 13.7%. AP therapy may be safely discontinued closer to the time of endoscopic procedure than the time currently recommended by the ASGE guidelines.

Modelling the effect of the electrode potential on the metal-adsorbate surface states: relevant states in the charge transfer mechanism of SERS.

Quantum mechanical calculations of the ground and excited electronic states of several [Ag(n)-pyridine](q) complexes yield a linear dependence of the energies of the surface states, especially the metal-to-molecule charge transfer states, on q(eff) = q/n. This is the first theoretical approach to modelling the effect of the electrode potential on SERS.

How the electrode potential controls the selection rules of the charge transfer mechanism of SERS.

This communication reports, for the first time, the dependence of the SERS intensities under resonant CT conditions (SERS-CT) on the electrode potential. SERS-CT intensities have been estimated from the properties of S(0)-CT(i) transitions ranging between 200-1200 nm of selected [Ag(n)-pyridine](q) and [Ag(n)-pyrazine](q) complexes.

Comment on "Multiconfigurational perturbation theory can predict a false ground state" by C. Camacho, R. Cimiraglia and H. A. Witek, Phys. Chem. Chem. Phys., 2010, 12, 5058.

Prediction of the true ground state of Sc(2) with multiconfigurational perturbation theory requires a balanced active space in building the reference wave function.

Photochemistry of protonated nitrosamine: chemical inertia of NH2NOH+ versus reactivity of NH3NO+.

The photochemical behavior of the protonated simplest nitrosamine [NH2NO-H](+) has been addressed by means of the CASPT2//CASSCF methodology in conjunction with the ANO-L basis sets. The relative stability of the different tautomers, namely, (1) NH2NOH(+), (2) NH3NO(+), and (3) NH2NHO(+), has been considered, and the corresponding tautomerization transition states have been characterized. With respect to the most chemically relevant species, it has been found that NH2NOH(+) corresponds to a bound structure, while NH3NO(+) corresponds to an adduct between NH3 and NO(+) at both CASSCF and CASPT2 levels of theory. Vertical transition calculations and linear interpolations on the homolytic dissociation of NH3NO(+) in combination with previous results on neutral nitrosamine [J. Chem. Phys. 2006, 125, 164311] and neutral N,N-dimethylnitrosamine [J. Org. Chem. 2007, 72, 4741] indicate that, in acidic diluted solutions, the protonation of nitrosamine takes place on the excited surface. The N-N dissociation channels have been studied both in ground and first excited singlet state. An S1/S0 conical intersection is found to be responsible for the photostability of NH2NOH(+). On the contrary, NH3NO(+) is photochemically unstable as its first excited state is purely dissociative. The latter species is characterized by a twofold reactivity: the formation of nitrosyl cation (NO(+)) in the ground state and the photorelease of physiologically relevant nitric oxide radical (NO) in its first excited state.

Gallbladder carcinoma: intraoperative imprint cytology, a helpful and valuable screening procedure.

BACKGROUND/PURPOSE: A major problem arises when a tumor is not readily recognized at the time of cholecystectomy. A carcinoma at early stages or one hidden by acute or chronic inflammation can be overlooked during surgery, and the diagnosis would then be made only after microscopic examination of paraffin-embedded tissue. The purpose of the present report is to communicate the results of 10 years' experience with the use of imprint cytology for the intraoperative diagnosis of gallbladder carcinoma. METHODS: During the period June 1994 to June 2004, 525 imprint cytologies of gallbladder mucosa were performed after 160 open cholecystectomies and 365 laparoscopic cholecystectomies. The patients had been operated on for acute or chronic cholecystitis due to lithiasis. Only 18 patients had a preoperative diagnosis of gallbladder carcinoma. The sensitivity, specificity, predictive values, accuracy, and their confidence intervals (95% CIs), of intraoperative imprint cytology for the diagnosis of carcinoma were analyzed. RESULTS: The average time employed for each procedure was 10 min. Patients' mean age was 69.2 years with a range of 24 to 92 years. Three hundred and forty-two patients (65.1%) were women and 183 (34.9%) were men. The imprint cytology method was positive in 44 of 58 gallbladder carcinomas diagnosed, with a sensitivity of 75.9% (44/58 patients) and a specificity of 99.8% (466/467). Only 1 case (1/525; 0.2%) was a false-positive; this was due to reactive changes. The positive predictive value was 97.8% (44/45; 95% CI = 86.8-99.9), negative predictive value was 97.1% (466/480; 95% CI = 95.0-98.3), and accuracy was 97.1% ([44 + 466]/525; 95% CI = 95.2-98.3). There was insufficient or inadequate material in 4 cases. CONCLUSIONS: Imprint cytology of the gallbladder mucosa is an easy, rapid, and high-quality method for detecting gallbladder carcinoma.

Raman study of the rigidity of penta-p-phenylene derivatives used as legs in molecular tripods.

Molecular planarity of penta-p-phenylene (P5P) and several substituted derivatives with four side chains of various lengths, including deca(ethylene glycol) groups, is discussed by considering the changes in the intensity ratio between the Raman bands recorded at 1280 and 1220 cm(-1). The intensity ratio between both bands I(1280)/I(1220) shows a small increase with the size of the substituent, indicating a high rigidity for all these compounds, even those with long oligo(ethylene glycol) side chains. This result is important given that these phenylene derivatives are versatile building blocks for the construction of nanometric tripod-shaped adsorbates for biological applications since the side chains should prevent the nonspecific interaction with proteins.