Amao, Yutaka’s team published research in Talanta in 66 | CAS: 596-01-0

Talanta published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Computed Properties of 596-01-0.

Amao, Yutaka published the artcileOptical CO2 sensor of the combination of colorimetric change of α-naphtholphthalein in poly(isobutyl methacrylate) and fluorescent porphyrin in polystyrene, Computed Properties of 596-01-0, the publication is Talanta (2005), 66(4), 976-981, database is CAplus and MEDLINE.

An optical CO2 sensor based on the overlay of the CO2 induced absorbance change of pH indicator dye α-naphtholphthalein in poly(iso-Bu methacrylate) (polyIBM) layer with the fluorescence of tetraphenylporphyrin (TPP) in polystyrene layer is developed. The observed luminescence intensity from TPP at 655 nm increased with increasing the CO2 concentration The ratio I 100/I 0 value of the sensing film consisting of α-naphtholphthalein in polyIBM and TPP in polystyrene layer, where I 0 and I 100 represent the detected luminescence intensities from a layer exposed to Ar and CO2 saturated conditions, resp., that the sensitivity of the sensor, is 192. The response and recovery times of the sensing film are <6.0 s for switching from Ar to CO2, and for switching from CO2 to Ar. The signal changes are fully reversible and no hysterisis is observed during the measurements. The highly sensitive optical CO2 sensor based on fluorescence intensity changes of TPP due to the absorption change of α-naphtholphthalein in polyIBM layer with CO2 is achieved.

Talanta published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Computed Properties of 596-01-0.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Amao, Yutaka’s team published research in Reactive & Functional Polymers in 63 | CAS: 596-01-0

Reactive & Functional Polymers published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Amao, Yutaka published the artcileRapid responsible optical CO2 sensor of the combination of colorimetric change of α-naphtholphthalein in poly(trimethylsiliylpropyne) layer and internal reference fluorescent porphyrin in polystyrene layer, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, the publication is Reactive & Functional Polymers (2005), 63(1), 35-41, database is CAplus.

An optical CO2 sensor based on the overlay of the CO2 induced absorbance change of pH indicator dye α-naphtholphthalein in poly(trimethylsilyl-propyne) (poly(TMSP))layer with the fluorescence of tetraphenylporphyrin (TPP) in polystyrene layer is developed. The observed luminescence intensity from TPP at 655 nm increased with increasing the CO2 concentration The ratio I100/I0 value of the sensing film, where I0 and I100 represent the detected luminescence intensities from a layer exposed to 100% argon and 100% CO2, resp., that the sensitivity of the sensor, is 10.3. The response and recovery times of the sensing film are <3.0 s for switching from argon to CO2, and for switching from CO2 to argon. The signal changes are fully reversible and no hysteresis is observed during the measurements. The highly sensitive and fast responsible optical CO2 sensor based on fluorescence intensity changes of TPP due to the absorption change of α-naphtholphthalein with CO2 is achieved using poly(TMSP) film.

Reactive & Functional Polymers published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Gao, Zhumei’s team published research in Shihua Jishu Yu Yingyong in 28 | CAS: 596-01-0

Shihua Jishu Yu Yingyong published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Recommanded Product: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Gao, Zhumei published the artcileAcidity determination of oxidation solution from phenol production with 1- naphtholphthalein as indicator, Recommanded Product: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, the publication is Shihua Jishu Yu Yingyong (2010), 28(1), 56-57, database is CAplus.

The acidity of oxidation solution from phenol production was determined with 1-naphtholphthalein as indicator instead of phenolphthalein, and the accuracy was investigated. The results showed that when 1-naphtholphthalein was used as indicator, the pH value at end point was 8.69, similar with the theor. pH value at end point 8.70. The determination results of organic acid samples whose acidity was known as 288mg/kg indicated that the deviation for 1-naphtholphthalein was 3 mg/kg, while 102mg/kg for phenolphthalein.

Shihua Jishu Yu Yingyong published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Recommanded Product: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Koganovskii, A. M.’s team published research in Kolloidnyi Zhurnal in 37 | CAS: 596-01-0

Kolloidnyi Zhurnal published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Category: benzofurans.

Koganovskii, A. M. published the artcileAdsorption on silica gel of nonionic surfactants with solubilized substances from aqueous solutions, Category: benzofurans, the publication is Kolloidnyi Zhurnal (1975), 37(3), 560-4, database is CAplus.

At 20°, the adsorption of nonionogenic surfactants C10H21O(C2H4O)17H, C12H25O(C2H4O)17H, C12H25O(C2H4O)23H, and OP-10 from aqueous solutions containing solubilized α-naphtholphthalein (I) or naphthalene (II) on large-pore silica gel was higher than from solutions without the solubilized compounds The aqueous solutions of the surfactants were saturated with I or II by shaking at constant temperature for 15 days. The I and II did not adsorb from diethylene glycol, aqueous saturated solution of poly(ethylene glycol), or undecane solutions without surfactants. These compounds adsorb in the surface layer of the adsorbed surfactants making the outer-adsorbed layer more hydrophobic which results in an addnl. adsorption of the surfactants.

Kolloidnyi Zhurnal published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Category: benzofurans.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Fan, Huiru’s team published research in ChemPlusChem in 83 | CAS: 596-01-0

ChemPlusChem published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Fan, Huiru published the artcileSulfur (VI) Fluoride Exchange Polymerization for Large Conjugate Chromophores and Functional Main-Chain Polysulfates with Nonvolatile Memory Performance, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, the publication is ChemPlusChem (2018), 83(5), 407-413, database is CAplus and MEDLINE.

Sulfur (VI) fluoride exchange (SuFEx) reactions can be applied not only in organic click synthesis, but also in the preparation of functional main-chain polymers. In this work, four functional main-chain polysulfates (PNT-PS, NPNT-PS, PHF-PS, and TPE-PS) are synthesized in high yield using the SuFEx reaction at room temperature The polysulfates exhibit satisfactory thermal stability and solution processability. They are used as the active layer for memory devices (ITO/PNT-PS/Al, ITO/NPNT-PS/Al, ITO/PHF-PS/Al, and ITO/TPE-PS/Al). I-V measurements show that ITO/PNT-PS/Al and ITO/NPNT-PS/Al exhibit stable flash-memory (write-read-erase) behavior, while ITO/PHF-PS/Al and ITO/TPE-PS/Al exhibit WORM (write once read many) behavior. Our studies provide a feasible and efficient synthetic methodol. for the preparation of new memory materials.

ChemPlusChem published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Ghoneim, M. M.’s team published research in Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical in 18A | CAS: 596-01-0

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Application In Synthesis of 596-01-0.

Ghoneim, M. M. published the artcileInfrared spectra of some derivatives of phenolphthalein and sulfonphthalein, Application In Synthesis of 596-01-0, the publication is Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical (1979), 18A(4), 349-50, database is CAplus.

The comparison of the IR of phenolphthalein, sulfonphthalein and their derivatives, observed in KBr, indicates that the phenolphthaleins exist mainly in the lactone form; sulfonphthaleins have the quinone-like structure. This behavior is attributed to the higher tendency of sulfonphthalein to form the sulfonate ion than the phenolphthalein to attain the carboxylic structure.

Indian Journal of Chemistry, Section A: Inorganic, Physical, Theoretical & Analytical published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Application In Synthesis of 596-01-0.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Cai, Yaqi’s team published research in Yejin Fenxi in 11 | CAS: 596-01-0

Yejin Fenxi published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Related Products of benzofurans.

Cai, Yaqi published the artcileStudy on the flow injection-catalytic photometric determination of rhodium, Related Products of benzofurans, the publication is Yejin Fenxi (1991), 11(1), 34-6, database is CAplus.

In this paper, a new method is recommended for the determination of rhodium by flow injection anal. The proposed method is based on the catalytic action of Rh(III) on the oxidation of α-naphtholphthalein with KIO4. The method is sensitive, rapid, and simple. In the concentration range of 0.020-0.40 μg/mL, rhodium can be determined at the rate of 64 per h.

Yejin Fenxi published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Related Products of benzofurans.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Cai, Yaqi’s team published research in Fenxi Huaxue in 17 | CAS: 596-01-0

Fenxi Huaxue published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Cai, Yaqi published the artcileStudies on flow injection analysis of platinum metals. III. Ruthenium(III)-potassium periodate (KIO4)-α-naphtholphthalein system, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, the publication is Fenxi Huaxue (1989), 17(3), 213-16, 212, database is CAplus.

A method was developed for the determination of trace Ru(III) by flow-injection anal. based on the catalytic effect of Ru(III) on the oxidation of α-naphtholphthalein with KIO4 in borate buffer (pH 9-11.5). The decoloration was monitored. The proposed method is rapid, simple, and sensitive. The detection limit for Ru(III) is 0.010 μg/mL and 65 determinations can be achieved in 1 h. The method was applied to determine Ru in refined ores and slags; good results were obtained.

Fenxi Huaxue published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Rottman, Claudio’s team published research in Journal of the American Chemical Society in 121 | CAS: 596-01-0

Journal of the American Chemical Society published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Related Products of benzofurans.

Rottman, Claudio published the artcileSurfactant-Induced Modification of Dopants Reactivity in Sol-Gel Matrixes, Related Products of benzofurans, the publication is Journal of the American Chemical Society (1999), 121(37), 8533-8543, database is CAplus.

Organically and bio-organically doped sol-gel materials have attracted much attention due to their ability to reproduce solution mol. activities within the ceramic environment. We take now this methodol. one step forward and explore conditions under which the dopant properties can be modified by the matrix. Specifically we report that the co-entrapment of the surfactant cetyltrimethylammonium bromide (CTAB, the modifier) at low concentrations, with an extensive series of pH indicators representing several key mol. families (the primary dopant) within tetramethoxysilane (TMOS)-derived silica sol-gel matrixes, greatly modifies the indicating performance of the primary dopant. Thus, very large pKi shifts of up to 3-4 orders of magnitude obtained upon the co-entrapment cause methyl orange (MO) to become an indicator for higher acidities and phenolphthalein for higher basicities, compared to their solution behavior. In another example, the ΔpKi between the two indicating transitions of alizarin increased from ∼4.5 pH units in solution to ∼10.5 pH units (!) in the glass, transforming it into an indicator for both the high acidic and high basic pH ranges. In yet another example, the two indicating transitions of phenol red were shifted to a more acidic pH range, pushing the tail of the more acidic titration branch into the neg. pH values range. These and other effects were found to be more pronounced by the co-entrapment than by the use of CTAB solutions or of sol-gel matrixes without CTAB, pointing to a synergetic effect between the surfactant and the silica cage. The indicators also proved highly sensitive in revealing the properties of the local environment created by the surfactant. Thus, the indicator mols. were shown to migrate and reorient within the hydrophobic and the hydrophilic regions of micellar environment, according to their acquired charge upon pH changes. The concentration-dependent and humidity-dependent surfactant aggregation processes within the silica cage were probed with MO, and the results were compared with the behavior of entrapped MO in sol-gel matrixes of varying hydrophobicities, obtained by the copolymerization of CH3Si(OCH3)3 with TMOS at various ratios, with and without CTAB. Of practical importance have been the observations that the dopant/surfactant co-entrapment greatly improves the leaching profiles: half-lives, ranging from several months to several years, were found for MO and methyl red; and using SAXS, surface area and porosity measurements, it was shown that CTAB can be used to stabilize the microscopic structure of the material upon heat-drying. This provides a potential solution to the problem of continuing structural changes, which take place with sol-gel materials long after the completion of their synthesis.

Journal of the American Chemical Society published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Related Products of benzofurans.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem

Escobedo, P.’s team published research in Nature Communications in 13 | CAS: 596-01-0

Nature Communications published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Escobedo, P. published the artcileSmart facemask for wireless CO2 monitoring, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, the publication is Nature Communications (2022), 13(1), 72, database is CAplus and MEDLINE.

The use of facemasks by the general population is recommended worldwide to prevent the spread of SARS-CoV-2. Despite the evidence in favor of facemasks to reduce community transmission, there is also agreement on the potential adverse effects of their prolonged usage, mainly caused by CO2 rebreathing. Herein we report the development of a sensing platform for gaseous CO2 real-time determination inside FFP2 facemasks. The system consists of an opto-chem. sensor combined with a flexible, battery-less, near-field-enabled tag with resolution and limit of detection of 103 and 140 ppm resp., and sensor lifetime of 8 h, which is comparable with recommended FFP2 facemask usage times. We include a custom smartphone application for wireless powering, data processing, alert management, results displaying and sharing. Through performance tests during daily activity and exercise monitoring, we demonstrate its utility for non-invasive, wearable health assessment and its potential applicability for preclin. research and diagnostics.

Nature Communications published new progress about 596-01-0. 596-01-0 belongs to benzofurans, auxiliary class Benzofuran,Naphthalene,Alcohol,Ester, name is 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one, and the molecular formula is C28H18O4, Name: 3,3-Bis(4-hydroxynaphthalen-1-yl)isobenzofuran-1(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Benzofuran,
Benzofuran | C8H6O – PubChem