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calix[4]resorcinarene
CHROMATOGRAPHIA · 2021 ·Vol. 84 ·期 4 ·325-333 · IF 2.044

A New Stationary Phase for Capillary Gas Chromatography: Calix[4]resorcinarene Functionalized with Imidazolium Cationic Units

Shuai Xiaomin,Cai Zhiqiang,Zhao Xinyu,Chen Yujie,Zhang Qian,Ma Ziwei,Hu Junjie,Sun Tao,Hu Shaoqiang

In this work, a novel calix[4]resorcinarene-based ionic liquid (C4RA-2IL) was synthesized, structurally characterized, and statically coated on capillary column as stationary phase for capillary gas chromatography (GC). The column efficiency of the C4RA-2IL column is 3345 plates m −1 , which are determined by n -dodecane at 120 °C. Based on its McReynolds constants, the C4RA-2IL column showed moderate polarity. Particularly, the C4RA-2IL column show high separation performance for a wide range of analytes and some difficult separation of meta/para-isomers. Moreover, it exhibited excellent selectivity for critical aromatic isomers of chloroaniline, bromaniline, iodoaniline, toluidine and xylidine isomers and shows advantageous separation capability over the commercial polysiloxane stationary phase. This work presents a promising future of calixarene-based ionic liquid as a new type of stationary phase in GC separations.

研究领域: 分析化学 · 色谱技术
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CHINESE SCIENCE BULLETIN · 2014 ·Vol. 59 ·期 11 ·1097-1103 · IF 1.365

Single-component chemically amplified i-line molecular glass photoresist based on calix[4]resorcinarenes

Liu Juan,Liu Zhengping,Wang Liyuan,Sun Haiyan

Calix[4]resorcinarene, prepared by the acid-catalyzed condensation of resorcinol and paraldehyde, was used as the core of the molecular glass compound. The hydroxyl groups of calix[4]resorcinarene were partly protected by tert-butoxycarbonyl ( t -BOC) and then esterified with 2-diazo-1-naphthoquinone-4-sulfonyl chloride (2,1,4-DNQ-Cl). Upon irradiation to 365 nm light, the 2,1,4-DNQ groups undergo photolysis to generate a small quantity of sulfonic acid other than indene carboxylic acid. The generated sulfonic acid can further catalyze the deprotection of the t -BOC group. So, a new type of single-component chemically amplified i-line positive photoresist can be formed by the molecular glass compounds. The lithographic performance of the resist was evaluated with high resolution and photosensitivity with an i-line stepper.

研究领域: 材料科学 · 化学工程
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FUEL · 2022 · IF 8.035

A fully-organic polymerization carrier calix[4]resorcinarene supported cobalt ionic liquid catalyst with oxone for desulfurization

Hang Xu,Shaokang Wang,Fengmin Wu,Qinlin Yuan,Yafei Guo,Yinke Zhang,Xuefeng Wei,Jun Zhang

One of the disadvantages of using inorganic solid catalysts is the formation of solid waste. The use of fully-organic solid catalysts can reduce secondary pollution by simple combustion or bio-degradation. Here, an organic polymerization carrier, calix[4]resorcinarene, with polyhydroxyl characteristics, was synthesized. A cobalt containing ionic liquid was successfully chemically bonded to the hydroxyl groups on the carrier surface using 3-chloropropyltrimethoxysilane as linking agent. The resulting fully-organic supported ionic liquid catalyst was coupled with oxone for desulfurization. The micro-structure of the catalyst was composed of a porous spatial network structure. The reaction system exhibited excellent dibenzothiophene (DBT) removal (93.3%) after 90 min under the optimum experimental conditions (20 °C, 6 g of model oil with an initial sulfur content of 1000 ppm, 0.2 g of 20 wt% oxone solution with a dosage frequency of three, 15% of CoCl 2 , 0.15 g of catalyst, and 2 g of [Bmim]BF 4 ). After six regeneration cycles, the sulfur removal remained above 90%. The desulfurization kinetics and mechanism were also discussed, and it was found that the hyperbolic model provided a better fit to the experimental data compared to the pseudo first-order model. The likely mechanism involves DBT being extracted using the ionic liquid [Bmim]BF 4 before being oxidized by the catalyst/oxone system to form DBTO 2 , which is easily removed from the system using polar solvents.

研究领域: 化学工程 · 环境科学
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2024 · IF 4.9

Tetrasulfonatomethyl-n-hexyl calix[4]resorcinarene tetrasodium assisted preparation of ZnFe2O4/ZnO composites with enhanced photodegradation performance for organic contaminants

Bin Du,Haoran Ye,Yincheng Wang,Ming Shen,Hui Zhou

The limited optical adsorption range and rapid recombination of photoexcited electron-hole pairs have severely hindered the development of ZnO-based photocatalysts . As macromolecular compounds, calixarenes become potential photocatalyst modifiers owing to their special molecular structures. In this work, ZnFe 2 O 4 /ZnO heterojunction photocatalysts which consist of ZnFe 2 O 4 nanoparticles and ZnO nanosheets were fabricated by simple hydrothermal reaction with the introduction of tetrasulfonatomethyl-n-hexyl calix[4]resorcinarene tetrasodium (THCRT 1 ). The synthesized ZnFe 2 O 4 /ZnO nanocomposite possesses a larger specific surface area , broader-spectrum absorption and an electronegative surface due to the addition of THCRT. Furthermore, the successful construction of ZnFe 2 O 4 /ZnO heterojunction leads to low charge transfer resistance and enhanced photocurrent density. Therefore, the THCRT-capped ZnFe 2 O 4 /ZnO composite exhibited superior adsorptive performance and removal efficiency towards Rhodamine B (RhB) and Levofloxacin hydrochloride (LH). The calcined nanocomposite degraded 95.80 % of RhB (10 mg L −1 ) and 97.86 % of LH (20 mg L −1 ) after 120 min under simulated sunlight illumination at a minimal catalyst dosage of 0 .1 g L −1 . Additionally, to determine the band structures , the band gaps, valence band positions and the Fermi levels were measured by Tauc plot, valence band x-ray photoelectron spectroscopy (XPS-Vb) and Mott-Schottky plot, respectively. Finally, based on the band structure results, we proposed a potential photocatalytic mechanism of n-n heterojunction. This work offers a promising prospect in the treatment of sewage containing organic contaminants.

CAS / MDL: 3317-61-1 rp174455
研究领域: 材料科学 · 环境科学 · 化学工程
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DYES AND PIGMENTS · 2018 · IF 3.767

A calix[4]resorcinarene-based hyper-structured molecule bearing disperse red 1 as the chromophore with enhanced photorefractive performance under non-electric field

Wansheng Zong,Lixin Wang,Qing Guo,Juan Li,Wenbo Wu,Yingliang Liu,Shengang Xu,Shaokui Cao

A hyper-structured molecule (HSM) CRA-DR1 and a model molecule Ph-DR1 for photorefractive (PR) application under non-electric field were designed and synthesized via highly reactive “click” reaction between alkynyl derivatives of calix [4]resorcinarene (CRA) or resorcinol and an azide derivative of disperse red 1 (DR1) in satisfactory yields. XRD pattern and UV–Vis absorption spectra indicated that the CRA-DR1 with three-dimensional (3D) CRA core could effectively decrease the aggregation, packing and crystallization of the nonlinear optical (NLO) chromophores . AFM images showed a smooth and pinhole-free morphology of the CRA-DR1 film. Two-beam coupling (TBC) experiment was used to test the photorefractive performance in optically transparent films of Ph-DR1 and CRA-DR1 doped with [6,6]-phenyl-C 61 -butyric acid methyl ester (PCBM) as a photosensitizer and N -ethyl-carbazole (ECz) as a plasticizer . Without poling and without external electric filed, the coupling gain coefficient obtained in the CRA-DR1-based composite is 147.4 cm −1 , which is higher than that of Ph-DR1-based composite (132.6 cm −1 ) owing to its asymmetrical 3D CRA core. Coupled with its convenient synthesis and commercial DR1, CRA-DR1 could serve as a good candidate for PR application.

研究领域: 材料科学 · 光学 · 化学
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