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731.
This paper will compare the mechanism and kinetics of living carbocationic polymerization of isobutylene (IB) and styrene (St), initiated by the 2-chloro-2,4,4-trimethyl-pentane (TMPCl) / TiCl4) system in 60/40 (v/v) methylcyclohexane / methyl chloride mixed solvent at −80 and −75 °C. The rate of initiation was found to be first order in TiCl4 in both systems. While initiation is instantaneous in IB polymerization at [TiCl4]0 ⩾ [TMPCl]0, it is slow in St polymerization. Kinetic derivation showed that initiating efficiency is dependent on [M] in this latter system, which was also demonstrated experimentally. The apparent initiation rate constant was determined from initiator consumption rate data and was found to be ki,app = 1.39 l2/mol2sec. The rate of St consumption measured using a real time fibre-optic mid-FTIR monitoring technique compared well with gravimetric data and was found to be closer to first order in TiCl4 at [TiCl4]0 < [TMPCl]0. However, the rate followed a close to second order in TiCl4 at [TiCl4]0 ⩾ [TMPCl]0. The mechanistic model proposed earlier for living carbocationic IB polymerization, which yielded good agreement with experimental data, seems to apply to carbocationic St polymerization as well. This model reconciles the discrepancy between rate constants published for carbocationic IB and St polymerizations, and accounts for shifting TiCl4 orders. However, independent investigations are necessary to verify the proposed mechanistic model. Optimized conditions led to living carbocationic St polymerization producing high molecular weight PS with 100% initiating efficiency. 相似文献
732.
Ghulam Murtaza Majid Khan Saba Farooq M. Iqbal Choudhary Sammer Yousuf 《Acta Crystallographica. Section C, Structural Chemistry》2023,79(6):237-248
Many heterocycles have been developed as drugs due to their capacity to interact productively with biological systems. The present study aimed to synthesize cocrystals of the heterocyclic antitubercular agent pyrazinamide ( PYZ , 1 , BCS III) and the commercially available anticonvulsant drug carbamazepine ( CBZ , 2 , BCS class II) to study the effect of cocrystallization on the stability and biological activities of these drugs. Two new cocrystals, namely, pyrazinamide–homophthalic acid (1/1) ( PYZ:HMA , 3 ) and carbamazepine–5-chlorosalicylic acid (1/1) ( CBZ:5-SA , 4 ), were synthesized. The single-crystal X-ray diffraction-based structure of carbamazepine–trans-cinnamic acid (1/1) ( CBZ:TCA , 5 ) was also studied for the first time, along with the known cocrystal carbamazepine–nicotinamide (1/1) ( CBZ:NA , 6 ). From a combination drug perspective, these are interesting pharmaceutical cocrystals to overcome the known side effects of PYZ ( 1 ) therapy, and the poor biopharmaceutical properties of CBZ ( 2 ). The purity and homogeneity of all the synthesized cocrystals were confirmed by single-crystal X-ray diffraction, powder X-ray diffraction and FT–IR analysis, followed by thermal stability studies based on differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Detailed intermolecular interactions and the role of hydrogen bonding towards crystal stability were evaluated quantitatively via Hirshfeld surface analysis. The solubility of CBZ at pH 6.8 and 7.4 in 0.1 N HCl and H2O were compared with the values of cocrystal CBZ:5-SA ( 4 ). The solubility of CBZ:5-SA was found to be significantly improved at pH 6.8 and 7.4 in H2O. All the synthesized cocrystals 3 – 6 exhibited a potent urease inhibition (IC50 values range from 17.32 ± 0.89 to 12.3 ± 0.8 µM), several times more potent than standard acetohydroxamic acid (IC50 = 20.34 ± 0.43 µM). PYZ:HMA ( 3 ) also exhibited potent larvicidal activity against Aedes aegypti. Among the synthesized cocrystals, PYZ:HMA ( 3 ) and CBZ:TCA ( 5 ) were found to possess antileishmanial activity against the miltefosine-induced resistant strain of Leishmania major, with IC50 values of 111.98 ± 0.99 and 111.90 ± 1.44 µM, respectively, in comparison with miltefosine (IC50 = 169.55 ± 0.20 µM). 相似文献
733.
Amin Al-Fakih Zakaria Mohamed Nor Shaik Inayath Basha M. Nasiruzzaman Shaikh Shamsad Ahmad Mohammed A. Al-Osta Md. Abdul Aziz 《Chemical record (New York, N.Y.)》2023,23(5):e202300039
The disposal of red mud (RM), a waste material generated by the aluminum industry, remains a global environmental concern because of its high alkalinity and smaller particle size, which have the potential to pollute air, soil, and water. Recently, efforts have been made to develop a strategy for reusing industrial byproducts, such as RM, and turning waste into value-added products. The use of RM as (i) a supplementary cementitious material for construction and building materials, such as cement, concrete, bricks, ceramics, and geopolymers, and (ii) a catalyst is discussed in this review. Furthermore, the physical, chemical, mineralogical, structural, and thermal properties of RM, as well as its environmental impact, are also discussed in this review. It is possible to conclude that using RM in catalysis, cement, and construction industries is the most efficient way to recycle this byproduct on a large scale. However, the low cementitious properties of RM can be attributed to a reduction in the fresh and mechanical properties of composites incorporating RM. On the other hand, RM can be used as an efficient active catalyst to synthesize organic molecules and reduce air pollution, which not only makes use of solid waste but also lowers the price of the catalyst. The review provides basic information on the characterization of RM and its suitability in various applications, paving the way for more advanced research on the sustainable disposal of RM waste. Future research perspectives on the utilization of RM are also addressed. 相似文献