Performance of a chirped-pulse Fourier transform millimeter wave spectrometer in the range of 75-110 GHz.

We present a home-built chirped-pulse Fourier transform millimeter wave (CP-FTMMW) spectrometer. The setup is devoted to the sensitive recording of high-resolution molecular spectroscopy in the W band between 75 and 110 GHz. We describe the experimental setup in detail, including a characterization of the chirp excitation source, the optical beam path, and the receiver. The receiver is a further development of our 100 GHz emission spectrometer. The spectrometer is equipped with a pulsed jet expansion and a DC discharge. Spectra of methyl cyanide as well as hydrogen cyanide (HCN) and hydrogen isocyanide (HNC) products from the DC discharge of this molecule are recorded to characterize the performance of the CP-FTMMW instrument. The formation of the HCN isomer is favored by a factor of 63 with respect to HNC. Hot/cold calibration measurements enable a direct comparison of the signal and noise levels of the CP-FTMMW spectra to those of the emission spectrometer. For the CP-FTMMW instrument, we find many orders of magnitude of signal enhancement and a much stronger noise reduction due to the coherent detection scheme.

Structure-property relationship of donor-acceptor acridones - an optical, electrochemical and computational study.

The synthesis of two neutral acridone derivatives was carried out to design media sensitive chromophores by taking advantage of intramolecular charge transfer (ICT) features. The molecules comprised two different donor-acceptor-donor triads, with absorption maxima at 425 nm and 520 nm, for the ketone and dicyanomethylene derivatives, respectively. The ketone variant exhibited fluorescence at room temperature, whereas the dicyanomethylene derivative was only emissive in frozen hexane. The ketone emission was highly solvatochromic, with Stokes shifts that ranged from 5000 cm(-1) to 10 000 cm(-1). Electrochemically, both compounds displayed similar oxidation potentials at approximately 0.35 V versus ferrocene/ferrocenium, which was anticipated since both systems employ the same ethynylaniline donor portion of the molecule, whereas only the 9-dicyanomethylene derivative showed a reduction peak at -1.5 V vs. Fc/Fc(+). Additional spectroelectro-chemical experiments supported a delocalized cationic charge on the ethynylaniline fragments during oxidation and that during electrochemical reduction the dicyanomethylene moieties show localized anionic charge. All of the experimental observations are finally compared to DFT, TDDFT and NICS(0) computations to gain insight into the transitions involved and deduce the role of the acridone core in stabilizing its oxidized and reduced forms.

Photophysics and photochemistry of aflatoxins B1 and B2.

Aflatoxins are mycotoxins produced by fungi of the genus Aspergillus, which is widely spread in the tropics and subtropics. To date, aflatoxin phototoxicity has been recognized, but the mechanism responsible for this phototoxicity has not been fully characterized. In the present paper, nanosecond laser flash photolysis studies allowed us to elucidate the photochemical processes undergone by two mycotoxins, namely aflatoxin B(1) and B(2), upon UV irradiation. In brief, photolysis (308 nm) of the aflatoxins leads to intersystem crossing, giving rise to their triplet excited state. The triplet state can readily be quenched by indole and hydroquinone, and also by molecular oxygen yielding singlet oxygen (singlet oxygen quantum yields of 0.51 and 0.59 were found for aflatoxin B(1) and B(2), respectively). In addition, our data indicate the ability of the two aflatoxins to photoionize upon 248 nm excitation. The photoionization quantum yield for aflatoxin B(1) and B(2) have been estimated to be 0.11 and 0.29, respectively.

Photochemistry of 2,6-diisopropylphenol (propofol).

The photochemistry of the anaesthetic agent propofol (PPF) was investigated in three different solvents of quite different polarity (cyclohexane, methanol and phosphate buffer pH 7) by means of nanosecond laser flash photolysis and absorption spectroscopy. GC-MS spectrometry measurements of PPF in cyclohexane have revealed the formation of two major products upon low intensity UV continuous irradiation of PPF in aerated solution: the diphenol derivative of PPF and 2,6-diisopropyl-p-benzoquinone (PPFQ). Only the diphenol compound was obtained in anaerobic solution. PPF phenoxyl radical (PPF ) generation has been assigned as the original step leading to the formation of both the diphenol compound and PPFQ in cyclohexane as revealed by laser flash photolysis at 266 nm and by electron paramagnetic resonance spectroscopy as well. Investigation of PPF by nanosecond flash photolysis at 266 nm in the other solvents revealed the occurrence of different photochemical processes depending on the nature and the polarity of the solvent. A reaction scheme is proposed in order to discuss the mechanism of reaction of PPF in all media.

Reactivity towards singlet oxygen of propofol inside liposomes and neuronal cells.

Singlet oxygen (1O2), a reactive oxygen species, has been found to be implicated in many cellular events and pathological disorders. Herein, we investigated the reactivity of 1O2 towards the anaesthetic agent propofol (PPF) encapsulated within DMPC liposomes. By time resolved luminescence, the rate constant of 1O2 quenching by PPF was evaluated, depending on the location of the sensitizer, with following values: 1.35+/-0.05x10(7) M(-1) s(-1) for deuteroporphyrin (as embedded source) and 0.8+/-0.04x10(7) M(-1) s(-1) for uroporphyrin (as external source), respectively. The nature of the oxidation product, resulting from the reaction of 1O2 with PPF, was determined using absorption and HPLC techniques. Finally, the in vitro protective effect of PPF towards the 1O2-induced neuronal cell toxicity was evaluated in terms of cell viability.

Suicide? Accident? Predictable? Avoidable? The psychological autopsy in jail suicides.

The psychological autopsy is a timely adjunct to the suicide detection and prevention efforts emerging in many jails. These efforts can only be enhanced by a thorough review of what went right or wrong for a particular inmate. Conducted in a nonthreatening spirit of peer review, the psychological autopsy can provide staff with closure and new knowledge which will allow them to proceed more effectively and confidently in safeguarding other inmates.