2013
DOI: 10.1016/j.snb.2012.08.020
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Understanding the VOC sorption processes on fluoro alkyl substituted phthalocyanines using ATR FT-IR spectroscopy and QCM measurements

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Cited by 23 publications
(21 citation statements)
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“…Furthermore, the band at 3066 cm −1 attributed to the aromatic C H groups is very small in intensity and has also the shape of a derivative function, which is interpreted as a weak interaction between the acetonitrile molecules and the aromatic C H groups. The type of interaction was also observed in the previous experiments with fluoropropoxy Pcs [13]. However, the intensity of the bands is relatively low in the case of tosylamido substituted phthalocyanine indicating that the number of aromatic C H groups interacting with the system of acetonitrile is lower.…”
Section: Acetonitrile Sorptionsupporting
confidence: 78%
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“…Furthermore, the band at 3066 cm −1 attributed to the aromatic C H groups is very small in intensity and has also the shape of a derivative function, which is interpreted as a weak interaction between the acetonitrile molecules and the aromatic C H groups. The type of interaction was also observed in the previous experiments with fluoropropoxy Pcs [13]. However, the intensity of the bands is relatively low in the case of tosylamido substituted phthalocyanine indicating that the number of aromatic C H groups interacting with the system of acetonitrile is lower.…”
Section: Acetonitrile Sorptionsupporting
confidence: 78%
“…The coating process, the characterization of the films in various atmospheres using ATR and QCM techniques as well as the automated gas mixing system to produce the gas vapours are described in detail in [13].…”
Section: Transducer Coating and Characterization Of The Sorption Phenmentioning
confidence: 99%
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“…Regarding humidity effects, Bohrer et al observed electrical current changes on cobalt and metal-free phthalocyaninebased chemiresistors due to the device exposure to water vapor, whereas Karimov and co-workers registered capacitance changes on copper phthalocyanine-coated electrodes for different RH values [51,52]. According to Bohrer et al vapor molecules in general interact at phthalocyanine free sites but can also compete for O 2 -bound sites [51,[53][54][55] and Karimov et al expect that water molecules can act as p-type dopants in MPcs similar to the O 2 effect [52]. Harbeck et al, using quartz crystal microbalance sensors and Fourier transform infrared (FTIR) spectroscopy, observed that water sorption in fact occurs at the core of substituted MPcs as well as weak hydrogen bonds in N-H groups of metal-free phthalocyanines [54].…”
Section: Resultsmentioning
confidence: 99%