Ting Tang

Xiamen University

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Tiandi Tang

Changzhou University

Zhongxue Fang

Yancheng Teachers University

Wenqian Fu

Changzhou University

Yu Feng

Changzhou University

Andrew M. Harned

Deciphera Pharmaceuticals (United States)

Hai Dong

Huazhong University of Science and Technology

Quanyong Yu

Changzhou University

Cheng Wang

Xiamen University

Lei Zhang

Jinzhou Medical University

Qun Chen

Changzhou University

Cooperative Institutions

Collaborative Innovation Center of Chemistry for Energy Materials

Xiamen University

Changzhou University

ASML (United States)

ASML (Netherlands)

Wenzhou University

Tan Kah Kee Innovation Laboratory

Nanjing Tech University

Catalytic Materials (United States)

Huazhong University of Science and Technology

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Preparation of Bismuth-Lanthanum Composite Oxide and its Photocatalytic Performance

Advanced materials research (2012)

Ting Tang Hong Deng Qi Jiang Ji Chuan Huo Shun Hua Hu

Bi-La composite oxide was prepared by thermal decomposition of molecular precursor of BiLa(dtpa)(NO 3 )•3.5H 2 O (dtpa=Diethylene triaminepentaacetic). The effect of calcinated temperature on structure was discussed by X-ray powder diffraction, scanning electron microscopy and UV-vis diffuse reflectance spectroscopy. The photocatalytic performance of samples prepared was discussed through the degradation of methyl orange. The results show that Bi-La composite oxide prepared at 500°C exhibits the best photocatalytic activity for the degradation of methyl orange (20mg/L) and the optimum amount of photocatalyst is 1.0 g/L.

Methyl orange

Lanthanum

Bismuth

Lanthanum oxide

10.4028/www.scientific.net/amr.616-618.1667

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Citations (1)

Organic template-free synthesis of zeolite Y nanoparticle assemblies and their application in the catalysis of the Ritter reaction

RSC Advances (2017)

Ting Tang Lei Zhang Hai Dong Zhongxue Fang Wenqian Fu

Zeolite Y nanoparticle assemblies with mesoporous structure has good catalytic performance in the Ritter reaction.

Ritter reaction

10.1039/c6ra27129d

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Citations (43)

Zeolite Y nanoparticle assemblies with high activity in the direct hydration of terminal alkynes

RSC Advances (2016)

Shuling Xu Zhi Yun Yu Feng Ting Tang Zhongxue Fang

A strong acidic zeolite Y nanoparticle assembly (HNANO-Y) with a micro–meso–macroporous structure was synthesized and used as a highly efficient heterogeneous catalyst for the hydration of alkynes to prepare ketone compounds.

10.1039/c6ra11489j

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Citations (15)

Adsorption Equilibrium of Ethylene-Carbon Dioxide Mixture on Zeolite ZSM5

Studies in surface science and catalysis (1986)

Wang Jin-gu Yang-Chun Chang Yi Hua Haiqing Li Ting Tang

10.1016/s0167-2991(09)60919-8

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Citations (4)

Experimental evidence for the formation of cationic intermediates during iodine(iii)-mediated oxidative dearomatization of phenols

Organic & Biomolecular Chemistry (2018)

Ting Tang Andrew M. Harned

Hammett analysis reveals iodine(iii)-mediated oxidative dearomatization reactions proceed through cationic intermediates and not direct nucleophilic attack on an activated phenol.

Cationic polymerization

10.1039/c8ob01652f

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Citations (22)

Design and synthesis of the basic Cu-doped zeolite X catalyst with high activity in oxidative coupling reactions

Journal of Catalysis (2016)

Sheng‐Chun Chen Zhen Shao Zhongxue Fang Qun Chen Ting Tang

Cinnamic acid

Coupling reaction

Oxidative addition

10.1016/j.jcat.2016.01.030

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Citations (46)

Ionic Current Saturation Enabled by Cation Gating Effect in Metal–Organic-Framework Membranes

Nano Letters (2024)

Han Zhou Ting Tang Rong Hu Yu Jiang Gang Yuan

Ion transport through nanoporous two-dimensional (2D) membranes is predicted to be tunable by controlling the charging status of the membranes' planar surfaces, the behavior of which though remains to be assessed experimentally. Here we investigate ion transport through intrinsically porous membranes made of 2D metal-organic-framework layers. In the presence of certain cations, we observe a linear-to-nonlinear transition of the ionic current in response to the applied electric field, the behavior of which is analogous to the cation gating effect in the biological ion channels. Specifically, the ionic currents saturate at transmembrane voltages exceeding a few hundreds of millivolts, depending on the concentration of the gating cations. This is attributed to the binding of cations at the membranes' surfaces, tuning the charging states there and affecting the entry/exit process of translocating ions. Our work also provides 2D membranes as candidates for building nanofluidic devices with tunable transport properties.

Saturation (graph theory)

Ion Exchange Membranes

10.1021/acs.nanolett.4c00991

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Holistic EPE measurement and qualification by large field of view (LFOV) contour-based metrology

Jing Guo Ting Tang Shu-Yu Lai Pooya Sharifani Amir Nojoomi

10.1117/12.3051568

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Supported Fe Ions on Different Zr-Based Metal–Organic Frameworks for Alkane Oxidation

ACS Applied Engineering Materials (2023)

Ting Tang Yiheng Dai Jiaxing Liu Jiawei Chen Bingling Dai

The catalytic activation of C–H(sp3) bonds in saturated alkanes is an important process, and Fe-supported metal–organic frameworks (MOFs) have shown promise in this area. In this study, we investigated a series of Zr-based MOFs with different secondary building units (SBUs) and pore sizes as the Fe support and found that MIL140-BPDC-Fe exhibited the highest photocatalytic oxidation of cyclohexane under visible light irradiation (TONcyclohexane = 6914, conversion = 26.2%, apparent quantum yield (AQY) = 5%). Interestingly, we observed significant differences in the catalytic activity of these Zr-MOFs in activating saturated C–H(sp3) bonds, which may be attributed to differences in the substrate concentration within the MOF channels due to substrate–SBU interactions. Notably, the presence or absence of hydroxyl groups on the SBUs appeared to play a role in this preconcentration effect, as MOFs with SBUs lacking hydroxyl groups tended to concentrate more alkane substrates in the MOF channel as revealed by substrate adsorption measurement.

SBus

Alkane

10.1021/acsaenm.3c00287

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Citations (1)

New Strategy To Access Enantioenriched Cyclohexadienones: Kinetic Resolution of para-Quinols by Organocatalytic Thiol-Michael Addition Reactions

ACS Omega (2018)

Ting Tang Nicholas G. Moon Lydia McKay Andrew M. Harned

Existing stereoselective routes to 2,5-cyclohexadienones involve either desymmetrization of an achiral substrate or have attempted to perform an asymmetric dearomatization of a phenol. Herein, we report proof-of-principle experiments aimed at developing a kinetic resolution as an alternative method for accessing enantioenriched 2,5-cyclohexadienones. More specifically, chiral bifunctional thiourea catalysts were used to promote the addition of 2-thionapthalene into unsymmetric para-quinols. The selectivity of the kinetic resolution was found to be quite sensitive to substitution around the substrate.

Desymmetrization

Kinetic resolution

Michael reaction

Thiol

10.1021/acsomega.8b01787

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Citations (13)