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Xiao-Jun Peng

Publications and source records attributed to Xiao-Jun Peng.

4 recordsLinked to original sources

Design of highly active binary catalyst systems for CO2/epoxide copolymerization: polymer selectivity, enantioselectivity, and stereochemistry control.

Asymmetric, regio- and stereoselective alternating copolymerization of CO(2) and racemic aliphatic epoxides proceeds effectively under mild temperature and pressure by using a binary catalyst system of a chiral tetradentate Schiff base cobalt complex [SalenCo(III)X] as the electrophile in conjunction with an ionic organic ammonium salt or a sterically hindered strong organic base as the nucleophile. The substituent groups on the aromatic rings, chiral diamine backbone, and axial X group of the electrophile, as well as the nucleophilicity, leaving ability, and coordination ability of the nucleophile, all significantly affect the catalyst activity, polymer selectivity, enantioselectivity, and stereochemistry. A bulky chiral cyclohexenediimine backbone complex [SalcyCo(III)X] with an axial X group of poor leaving ability as the electrophile, combined with a bulky nuclephile with poor leaving ability and low coordination ability, is an ideal binary catalyst system for the copolymerization of CO(2) and a racemic aliphatic epoxide to selectively produce polycarbonates with relatively high enantioselectivity, >95% head-to-tail connectivity, and >99% carbonate linkages. A fast copolymerization of CO(2) and epoxides was observed when the concentration of the electrophile or/and the nucleophile was increased, and the number of polycarbonate chains was proportional to the concentration of the nucleophile. Electrospray ionization mass spectrometry, in combination with a kinetic study, showed that the copolymerization involved the coordination activation of the monomer by the electrophile and polymer chain growth predominately occurring in the nucleophile. Both the enantiomorphic site effect resulting from the chiral electrophile and the polymer chain end effect mainly from the bulky nucleophile cooperatively control the stereochemistry of the CO(2)/epoxide copolymerization.

Journal Article↗

A DFT study of Diels-Alder reactions of o-quinone methides and various substituted ethenes: selectivity and reaction mechanism.

The Diels-Alder (DA) reactions of various substituted ethenes (methyl vinyl ether (MVE), styrene, and methyl vinyl ketone (MVK)) with o-quinone methides (o-QM) are studied by means of density functional theory (DFT) at the B3LYP/6-31G(d,p) level. On the basis of analysis for frontier molecular orbital and comparison of the activation energies for different reaction pathways, the ortho attack modes present transition structures more stable than the meta ones. The reactivity, ortho selectivity, and asynchronicity are enhanced with the increase of the electron-releasing character of the substitute on ethene fragment. The discussions for the charge distribution and charge transfer on different transition states indicate that there are different molecular mechanisms for the different substituted ethenes. The calculations show that the effect of solvent decreases the activation energy and increases the asynchronicity. The results also indicate that the hydrogen-bond formation between chloroform and the carbonyl oxygen of the o-QM lowers the activation energies and increases the asynchronicity.

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[Cloning of human telomerase reverse transcriptase promoter for targeted cancer therapy].

OBJECTIVE: An human telomerase reverse transcriptase (hTERT) promoter was cloned to investigate the effect of simplex virus-thymidine kinase (HSV-tk) gene-ganciclovir (GCV) system under control of this promoter on lung cancer cells A549. METHODS: Specific primers were designed to amplify the core hTERT promoter from HepG2 genome. A set of expression vectors encoding LacZ or tk gene under control of hTERT or hCMV promoter was constructed through standard molecular cloning methods. After the transfection with lipofectamine 2000, reverse transcriptional PCR (RT-PCR) and beta-Gal staining were performed to examine the activity of the hTERT promoter. The cytotoxic effects of GCV/tk on A549 and MRC5 cells transfected with the plasmids encoding tk gene were evaluated by MTT assay. RESULTS: The hTERT promoter containing -208-+40 bp of the upstream sequence of human telomerase was successfully cloned. beta-Gal staining and RT-PCR were used to detect the expression of Lac Z and the transcription of tk gene under control of the hTERT promoter, respectively, in A549 rather than MRC5 cells. Cyototoxic effect of GCV was observed only in the A549 but not MRC5 cells after the transfection with pDC511 hTERT/tk, and the effect was dose-dependent. The effect, however, was observed in cells transfected with pDC518 hCMV/tk. CONCLUSION: The hTERT promoter cloned in this study can specifically control the target gene expression in telomerase-positive tumor cells but not the normal cells, suggesting that the HSV-tk/GCV system under control of the hTERT promoter is a promising targeted gene therapy for malignant tumors.

Cloning, Molecular↗

mu-Oxo-bis{[(6-hydroxymethyl-2-pyridylmethyl)bis(2-pyridylmethyl)amine-kappa)N,N',N'',N''',O]iron(III)} tetrakis(perchlorate).

The novel mu-oxo-diiron complex [Fe2O(BPHPA)2](ClO4)4 [BPHPA is (6-hydroxymethyl-2-pyridylmethyl)bis(2-pyridylmethyl)amine, C19H20N4O], contains a binuclear centrosymmetric [Fe2O(BPHPA)2]4+ cation (the bridging O atom lies on an inversion centre) and four perchlorate anions. Each iron ion is coordinated by four N atoms [Fe-N = 2.117 (5)-2.196 (5) A] and one O atom [Fe-O = 2.052 (5) A] from a BPHPA ligand, and by one bridging oxo atom [Fe-O = 1.7896 (9) A], forming a distorted octahedron. There are hydrogen bonds between the hydroxy group and perchlorate O atoms [O-H...O = 2.654 (7) A].

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