RESUMO
Low-valent main group compounds that fluoresce in the solid-state were previously unknown. To address this, we investigated room-temperature photoluminescence from a series of crystals of germylenes 3-8 in this article; they exhibited emissions nearly reaching the NIR. Germylene carboxylates (3-8) were synthesized by reacting dipyrromethene stabilized germylene pyrrolide (2) with carboxylic acids such as acetic acid, trifluoroacetic acid, benzoic acid, p-cyanobenzoic acid, p-nitrobenzoic acid, and acetylsalicylic acid.
RESUMO
The paper reports the charge transfer mechanism between poly (3,4-ethylenedioxythiophene) (PEDOT) and high energy materials such as RDX, HMX and TNT, respectively in terms of ratios of anti-stokes (AS) and stokes(S) Raman lines of NO2 bands. Generally it works as an effective sensing medium for the detection of explosives when mixed in an equal proportion and are subjected to 532 nm wavelength without any chemical treatment [1]. The pristine PEDOT is less sensitive to 532 nm wavelength (2.33 eV) but influences the Raman S and AS lines of explosives in the mixture. The study also reveals that a small quantity (one milligram) of PEDOT is sufficient to initiate the positive charge transfer mechanism between its oxidized state to the lone pairs of electrons on the oxygen atoms of the nitro group of the explosive molecules. Consequently, the intensity of the Raman spectra of RDX, HMX and TNT is dropped by an order of 22.5, 11.45 and 17.2 times, respectively along with the shift of the NO2 vibrational modes. It is also attributed to Photon-electron-phonon interaction. Finally, we have estimated the reduced mass of the functional group to ascertain the force constant and the intensity ratios of AS /S lines to confirm the charge transfer mechanism. The effect of charge transfer mechanism is also reflected in drastic change in transmission /absorption characteristics of FTIR spectra of same PEDOT and explosive mixtures.
