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copper phthalocyanine solubility

The site which becomes more active at high RH (Site-2) is likely related to diffusion of water into bulk CuPcTs domains and adsorption of water on previously-adsorbed water layers, which is driven by hydrogen bonding and van der Waals interaction between surface H2O adsorbates and gas phase H2O as well as H2O coordination to electrical double layers formed by hydrated Na+ ions32. [30] The scientists failed to get the desired product but instead got a small quantity of a bright bluish compound that was later known as metal-free phthalocyanine. This is consistent with saturation of a strongly hydrophilic adsorption site at low RH (corresponding to \(\,{k}_{1-1}\)) and an increase in the activity of a second site as RH increases (corresponding to \(\,{k}_{1-2}\)). [7] In 1927, Swiss researchers serendipitously discovered copper phthalocyanine, copper naphthalocyanine, and copper octamethylphthalocyanine in an attempted conversion of o-dibromobenzene into phthalonitrile. Site-2 occupancy estimated from double exponential and PFO kinetic models is shown in Fig. Water-soluble copper phthalocyanine (TSCuPc) was used as probe molecule and its pH value was adjusted with HCl and NaOH solution. Article Copper phthalocyanine-3,4,4,4-tetrasulfonic acid tetrasodium salt (dye content 85%, in water) was purchased from Sigma Aldrich and used without further purification. Google Scholar. Phthalonitrile should be formed here as an intermediate, but it is instantly cyclotetramerizing in the presence of cuprous bromide, a by-product of the reaction, to form semi-bromo copper phthalocyanine. phthalocyanine phthalocyanines tethered situ Copper Phthalocyanine (CPC) pigments, by virtue of their exceptionally brilliant shade, high tinctorial strength, low cost and outstanding fastness properties, have been ruling the colorant industry ever since their commercial introduction in 1935. The r2 values of each fit are shown in the inset bar graph. Zagal, J., Bindra, P. & Yeager, E. A mechanistic study of O2 reduction on water soluble phthalocyanines adsorbed on graphite electrodes. The dye derived from cobalt phthalocyanine and an amine is Phthalogen Dye IBN. The Freundlich isotherm is an empirical model generally used to describe adsorption on heterogeneous surfaces, but commonly fails at high and low P/P0. The images or other third party material in this article are included in the articles Creative Commons license, unless indicated otherwise in a credit line to the material. 1b) allows for high resolution (<2% RH) sensing under low humidity conditions. Use the Previous and Next buttons to navigate the slides or the slide controller buttons at the end to navigate through each slide. N.L. WebCopper phthalocyanine | C32H16CuN8 | CID 475701 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more. 4a bottom panel). The requested specifications are not available. Japanese Journal of Applied Physics UV-Vis spectrum shows that the Q bands of these two derivatives split and shift to the red, which means successive protonation happened and In the approximation \(\,[{M}_{e1}-{M}_{t1}]\approx [{M}_{e2}-{M}_{t2}]\), the pseudo-second order (PSO) rate equation34 becomes \(d{M}_{ad}/dt=\,{k}_{2}{({M}_{e}-{M}_{t})}^{2}\). Another positive aspect of the molecular arrangement in beta is the close association of different molecular stacks. The fitted region was reduced to the 450900nm range to reduce the standard error. The e modification is also gaining popularity because of its pure reddish shade. Figure3a shows extinction coefficient (k) (top panel) and index of refraction (n) (bottom panel) as a function of wavelength () at different RH levels. Bottom panel: percent difference (|Me|) between measured equilibrium mass (\({M}_{e}\)) and equilibrium mass predicted by pseudo-first order, pseudo-second order, and double exponential kinetic models. Rudzinski, W. & Plazinski, W. Kinetics of solute adsorption at solid/solution interfaces: a theoretical development of the empirical pseudo-first and pseudo-second order kinetic rate equations, based on applying the statistical rate theory of interfacial transport. minutes. for more information. Optical thickness of the CuPcTs film was estimated from SPE data. 97, 318324 (2012). Journal of membrane science Figure4b shows electrical (1/R) and optical (op) conductivities and relates them to mass change of CuPcTs as the film undergoes water adsorption. for more information. Structurally larger analogues include naphthalocyanines. Aqueous solubility of copper phthalocyanine-3,4,4,4-tetrasulfonic acid tetrasodium salt (CuPcTs) enables fabrication of flexible electronic devices by low cost inkjet printing. After the completion of the reaction, the solvent is removed by vacuum distillation and the crude product thus obtained is further purified by treatment with dilute acid and alkali solutions to remove basic and acidic impurities present. 1 and 2.The IR of compound BS exhibited characteristic hydroxide solubility oxide The DC resistance increases linearly with mass during H2O adsorption (FigureS8). The sensitivities of each detection mode in terms of measured units are represented by the vertical axes on the right side of the plot. Google Scholar. Box 2008, Oak Ridge, TN, 37831-6496, USA, Eric S. Muckley,Christopher B. Jacobs,Keith Vidal,Nickolay V. Lavrik,Bobby G. Sumpter&Ilia N. Ivanov, Bredesen Center, University of Tennessee Knoxville, 444 Greve Hall, 821 Volunteer Blvd, Knoxville, TN, 37996-3394, USA, Computer Science and Mathematics Division, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA, You can also search for this author in Many phthalocyanine compounds are, thermally, very stable and do not melt but can be sublimed. the rising edge of the mass change becomes more rounded at higher pressures. 1 represents 2 distinct sequentially-occurring PFO reactions. Park, J. H., Lee, S. & Kummel, A. C. Domain fracture and recovery process of metal phthalocyanine monolayers via NO2 and H2O. The relative arrangements of these stacks, as well as the stacking overlap of the adjacent molecules, are different in different modifications. Both porphyrins and phthalocyanines function as planar tetradentate dianionic ligands that bind metals through four inwardly projecting nitrogen centers. McGarvey, M.; McKay, R.B. The Temkin model is particularly well-suited for predicting gas phase equilibrium with surfaces that contain a distribution of binding energies and explicitly accounts for adsorbate-adsorbate interactions by acknowledging that the heat of adsorption decreases linearly with adsorbate coverage27, 28. CU-PCIN-02-P , CU-PCIN-03-P , CU-PCIN-04-P , CU-PCIN-05-P CAS #: 147-14-8 Relevant identified uses of the substance: Scientific research and development Supplier details: American Elements 10884 (d) Top panel: comparison of Site-2 occupancy (\({\theta }_{2}\)) as estimated from pseudo-first order kinetic and double exponential models. The mono-protonated and di-protonated forms of copper phthalocyanine (CuPc) were obtained by increasing concentrations of trifluoroacetic acid (TFA) solution to a fixed concentration of CuPc solutions. Tosun, . Gul Hassan, Memoon Sajid & Changhwan Choi, Muhammad Awais, Muhammad Umair Khan, Tahseen Elahi Chattha, Soobin Park, Jinmyeong Seo, Bongyoung Yoo, A. Rambabu, Deependra Kumar Singh, S. B. Krupanidhi, Chaudhry Muhammad Furqan, Muhammad Umair Khan, Hoi-Sing Kwok, Muhammad Umair Khan, Gul Hassan, Jinho Bae, Laura Ascherl, Emrys W. Evans, Florian Auras, Scientific Reports WebCopper phthalocyanine (CuPc), also called phthalocyanine blue, phthalo blue and many other names, is a bright, but soluble in concentrated sulfuric acid. 156, 210 (2010). Changes in the slopes of n and k with RH (FigureS5a) indicate the presence of a 2-step process. 1 and 2.The IR of compound BS exhibited characteristic Both ratios \({{\rm{\tau }}}_{2}/{{\rm{\tau }}}_{1}\) and \({k}_{1-2}/{k}_{1-1}\) increase linearly from ~0.03 to ~0.1 as RH increases from 10% to 95%, which suggests that the double exponential behavior modelled in Fig. Unfortunately, the scientists failed to recognize the significance of their discovery. CU-PCIN-02-P , CU-PCIN-03-P , CU-PCIN-04-P , CU-PCIN-05-P CAS #: 147-14-8 Relevant identified uses of the substance: Scientific research and development Supplier details: American Elements 10884 During the first step, H2O molecules undergo rapid adsorption at hydrophilic sulfonyl/salt groups near CuPcTs domain surfaces. At RH>60%, the formation of H2O layers containing mobile Na+ ions can increase the effective contact area at electrodes and result in improved electronic transport by allowing charge carriers to hop between hydrated ionic structures consisting of coordinated Na+ and dipolar H2O, leading to a decrease in R2. Journal of Photonics for Energy Characterizing the optical response of CuPcTs to humidity is important for studying performance of CuPcTs-based optoelectronic devices under changing humidity conditions and development of optical humidity sensors. & Garca-Valenzuela, A. Adsorption kinetics of optochemical NH 3 gas sensing with semiconductor polyaniline films. The Journal of Physical Chemistry B The fit parameters correspond to the simplified two-site adsorption model, where the fraction of adsorbates present at each site are estimated by \({\theta }_{1}={A}_{1}/({A}_{1}+{A}_{2})\) and \(\,{\theta }_{2}=1-{\theta }_{1}={A}_{2}/({A}_{1}+{A}_{2})\). Exponential heterogeneous (multi-site) adsorption kinetic models are of the form \(\,{\rm{\Delta }}M={M}_{{\rm{0}}}+{\sum }_{i=1}^{n}{A}_{i}{{\rm{e}}}^{-t/{{\rm{\tau }}}_{i}}\), where \(n\) is the number of active sites, \({A}_{i}\) corresponds to the relative amount of mass adsorbed at Site-i, and \({{\rm{\tau }}}_{i}\,\,\)is the inverse of the adsorption rate constant at Site-i. The choice of the solvent is very important, as it plays a significant role in the generation of impurities. The inset bar graph displays r2 values for each of the fits. Thus, overall the copper phthalocyanine molecule consists of both hydrophilic and hydrophobic areas. Journal of Molecular Liquids 3d). Woollam Co. 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