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Cited by 4 publications
(12 citation statements)
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“…Figure 1a shows the gas-phase absorption spectra of 8-azasteroid I, normalized to 1.0 as to the maximum of the optical density D of the band λ max = 296 nm, at a constant temperature T up = 270 o C and various temperatures giving the vapor pressure T low . They differ markedly from the absorption spectra of the solutions of this steroid in hexane and ethyl alcohol given in [6]. In the spectra of the above solutions, the corresponding band is shifted toward long waves (λ max = 261 and 265 nm).…”
contrasting
confidence: 63%
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“…Figure 1a shows the gas-phase absorption spectra of 8-azasteroid I, normalized to 1.0 as to the maximum of the optical density D of the band λ max = 296 nm, at a constant temperature T up = 270 o C and various temperatures giving the vapor pressure T low . They differ markedly from the absorption spectra of the solutions of this steroid in hexane and ethyl alcohol given in [6]. In the spectra of the above solutions, the corresponding band is shifted toward long waves (λ max = 261 and 265 nm).…”
contrasting
confidence: 63%
“…The analysis of the absorption, fluorescence, fluorescence excitation spectra, and duration of the excited states of a water solution (pH 7.4) of 2,3-dimethoxy-8-azagona-1,3,5(10),13-tetraene-12,17-dion (hereinafter referred to as 8-azasteroid III) has revealed the existence of two centers emitting a long-wave and a short-wave fluorescence [5]. The fluorescence of 8-azasteroid III and 8-aza-D-homogona-1,3,5(10),13-tetraene-12,17a-dion (hereinafter referred to as 8-azasteroid I) in the neutral solvent hexane has been assigned to three centers of luminescence [6]. Assumptions on the nature of the centers have been made.…”
mentioning
confidence: 99%
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“…Based on analysis of the absorption, fluorescence, fluorescence excitation spectra and the duration of the excited states in aqueous solution (pH 7.4) for 2,3,-dimethoxy-8-azagona-1,3,5(10),13-tetraene-12,17-dione, it has been established that two centers exist that emit long-wavelength and shortwavelength fluorescence [5]. In the neutral solvent hexane, the fluorescence of 2,3-dimethoxy-8-azagona-1,3,5(10), 13-tetraene-12,17-dione and 8-aza-D-homogona-1,3,5(10),13-tetraene-12,17a-dione even appears as three luminescence centers [6].Of special interest are studies of the luminescence of 8-azasteroids in the gas phase, where there is no effect from the surrounding medium and relaxation processes appear in pure form. N. A. Brisevich et al [7] comprehensively studied a number of immunoactive compounds of the 8-azasteroid class in the gas phase, and the presence of three absorption and fluorescence centers was observed.…”
mentioning
confidence: 99%
“…Based on analysis of the absorption, fluorescence, fluorescence excitation spectra and the duration of the excited states in aqueous solution (pH 7.4) for 2,3,-dimethoxy-8-azagona-1,3,5(10),13-tetraene-12,17-dione, it has been established that two centers exist that emit long-wavelength and shortwavelength fluorescence [5]. In the neutral solvent hexane, the fluorescence of 2,3-dimethoxy-8-azagona-1,3,5(10), 13-tetraene-12,17-dione and 8-aza-D-homogona-1,3,5(10),13-tetraene-12,17a-dione even appears as three luminescence centers [6].…”
mentioning
confidence: 99%