Search

The IR and UV absorption spectra of CO 2 + isolated in solid neon were studied by using our newly built mass-selective matrix isolation system. The IR absorption spectrum revealed the formation of CO2 in both cationic and anionic forms in solid Ne, since neutral CO2 was also used to serve as an electron scavenger in this study. Subsequently, we recorded the UV absorption spectrum of the same matrix sample in the spectral region 270−400 nm, encompassing the electronic transitions of CO 2 + from the ground state to the first two electronic excited states. Notably, the observation of the electronic transition A 2 Π u ← X 2 Π g was dominated by the vibrational progression of the symmetric CO stretching mode, while a single sharp band was observed in the electronic transition B 2 Σ u + ← X 2 Π g. The presented spectra might be useful for future studies on terrestrial and astrochemical conjunctions. [ABSTRACT FROM AUTHOR]

Phenoxide anions (PhO−) and phenoxy radicals (PhO) were generated by the electron bombardment of a phenol/argon sample during matrix deposition. Further irradiation of the matrix sample at 365 nm led to the detachment of the electron from PhO− and afforded its neutral counterpart PhO in solid Ar. In a separate experiment, the photolysis of a phenol/Ar matrix at 160 nm mainly afforded PhO, phenyl (Ph) radicals, and various open‐chain ketenes, but no PhO−. The Infrared (IR) lines of PhO− were assigned on the basis of the observed photochemical behaviors and the prediction of the vibrational wavenumbers with the corresponding IR intensities predicted by the B3LYP/aug‐cc‐pVTZ theory. [ABSTRACT FROM AUTHOR]

A questionnaire which provides desirable reliability and validity has been previously developed to assess the disease awareness of diagnosed chronic kidney disease (CKD) patients. However, conventional paper questionnaires often have disadvantages, including recall bias. To substantially improve this, we therefore aimed to explore the feasibility of developing a smartphone-based electronic version (e-version) based upon its original paper version and subsequently tested its validity, reliability, and applicability. A pilot study was conducted at Guangdong Provincial Hospital of Chinese Medicine in Guangzhou, China, during August 2019. The e-version had identical content to the paper version and was adapted in terms of layout and assisted functions via the Wechat-incorporated Wen-Juan-Xing platform. Eligible patients with diagnosed CKD were invited to participate and were assigned the e-version. Randomly selected respondents received a test-retest of the same e-version 2 weeks after their first completion. In some instances, psychometric properties, including validity and reliability of the e-version, were examined. In others, its clinical application was also tested, which included comparisons among the clinical profiles of patients who had/had not responded to the questionnaire as well as patients with above or below average questionnaire scores. Of the 225 patients screened, 217 were enrolled to participate, with a response rate of 52.5%. Desirable reliability (Cronbachα = 0.962, ICC for total scores = 0.948), while good convergent validity (Cronbachα = 0.962) and low discriminant validity (one extracted component), of the e-version were detected. Performing inter-group comparisons highlighted statistical differences in terms of higher education level (z = −2.436, P = 0.015) and earlier CKD stages (z = −1.978, P = 0.048), with these patients often preferring to respond. No significant differences were detected in the clinical profiles between respondents who obtained an above or below average questionnaire score. The e-version is reliable but was not shown to be a valid approach. Audiences with higher education levels and less advanced disease condition may prefer to respond to the e-version. Adaptation of this e-questionnaire, from its original paper version, may not be a direct transition and meticulous modifications may be required during the transition process. Chinese Clinical Trial Registry (ChiCTR1900024633). [ABSTRACT FROM AUTHOR]