醋酸锰催化合成萘并噻唑衍生物研究型综合实验

设计了“醋酸锰（Ⅲ）催化合成2-邻氯苯甲酰氨基萘并[1，2-d]噻唑”研究型综合化学实验，以自制的醋酸锰（Ⅲ）为催化剂，催化氧化1-萘基-3-邻氯苯甲酰基硫脲合成2-邻氯苯甲酰氨基萘并[1，2-d]噻唑。通过该实验项目的教学，可使学生掌握醋酸锰（Ⅲ）、1-萘基-3-邻氯苯甲酰基硫脲和2-邻氯苯甲酰氨基萘并[1，2-d]噻唑的合成方法，掌握有机化合物结构表征的方法，可以培养学生的实践动手能力、科研创新能力以及综合运用知识的能力。该实验项目集无机合成实验、有机合成实验和仪器分析实验于一体，具有较强的可操作性和实用性，可作为基础化学研究型综合化学实验或开放性实验开设。     

Manganese(II) tetrasulfophthalocyanine covalently supported on natural silk: A new highly active catalyst for synthesis of benzoxazepine derivatives in water

Natural silk as a biodegradable, biocompatible, renewable, green and abundant biomaterial was used as a support for chemical immobilization of a water‐soluble manganese(II) complex with a phthalocyanine ligand possessing covalent binding ability. The prepared manganese(II) tetrasulfophthalocyanine complex supported on natural silk revealed efficient catalytic activity and reusability for the synthesis of benzoxazepine derivatives in water at room temperature.     

Interaction of Cationic Manganese Porphyrins with DNA. A Binding Model

The DNA cleavage properties of two cationic manganese porphyrins possessing different peripheral substituents were compared. The identical nature of the strand scission patterns of the porphyrins on a 139 base pair restriction fragment of pBR-322 DNA, along with other evidence, suggests that the porphyrin is end-on bound via the minor groove in a melted or partially melted region of DNA. This unusual binding mode underscores the potential of outisde binding cationic metalloporphyrins as probes for low melting regions of DNA     

Effect of manganese addition on physical properties of Co0.6Zn0.4MnxFe2-xO4 system

X-ray analysis and magnetic properties have been studied for the system Co_0.6Zn_0.4Mn_xFe_2-xO₄. The bulk density, X-ray density and porosity were also studied. It was found that the lattice constant decreased with increasing manganese concentration x. The X-ray density, the bulk density and porosity do depend on the manganese content. The magnetic susceptibility and the activation energies were found to be increased with increasing percentage of the manganese ions while the dc conductivity decreased.     

Vibrational Spectra of Magnesium Hydrogenphosphate Trihydrate and of its Manganese Analogue

Abstract

The infrared (IR) and Raman spectra of MgHPO₄. 3H₂O and of a series of partially deuterated analogues as well as the IR spectra of MnHPO₄. 3H₂O have been recorded and interpreted. The analysis of the IR spectra in the HOD bending region rules out the possibility of existence of H₃OC⁺ ions in the structure.     

Facile Access to 3-Alkyl-Substituted 3-Hydroperoxy-2,4-pyrrolidinediones Using Manganese(III)-Catalyzed Aerobic Oxidation

Abstract

3-Alkyl-substituted 2,4-pyrrolidinediones were directly oxidized under very mild manganese(III)-catalyzed aerobic oxidation conditions to give the corresponding 3-hydroperoxy-2,4-pyrrolidinediones in quantitative yields. The scope and limitations for the synthesis of the hydroperoxyprrolidinediones are described.     

Effect of Manganese Valence on Specific Capacitance in Supercapacitors of Manganese Oxide Microspheres

Manganese oxides have attracted great interest in electrochemical energy storage due to high theoretical specific capacitance and abundant valence states. The multiple valence states in the redox reactions are beneficial for enhancing the electrochemical properties. Herein, three manganese microspheres were prepared by a one-pot hydrothermal method and subsequent calcination at different temperatures using carbon spheres as templates. The trivalent manganese of Mn₂O₃ exhibited multiple redox transitions of Mn³⁺/Mn²⁺ and Mn⁴⁺/Mn³⁺ during the intercalation/deintercalation of electrolyte ions. The possible redox reactions of Mn₂O₃ were proposed based on the cyclic voltammetry and differential pulse voltammogram results. Mn₂O₃ microsphere integrated the advantages of multiple redox couples and unique structure, demonstrating a high specific capacitance and long cycling stability. The symmetric Mn₂O₃//Mn₂O₃ device yielded a maximum energy density of 29.3 Wh kg⁻¹ at 250 W kg⁻¹.     

Investigation of the manganese stress on wheat plant by attenuated total reflectance Fourier transform infrared spectroscopy

ABSTRACT

The present paper deals with the investigation of the changes in chemical contents of the leaf of wheat seedling stressed by excess manganese using attenuated total reflectance Fourier transform infrared spectroscopy (FTIR) technique. The infrared spectra of the leaves of control and manganese-treated wheat plants have been recorded in the spectral region 485–4000?cm^?1 at a resolution of 4?cm^?1. The recorded spectrum has been analyzed with the help of curve-fitting method for the quantitative estimation of chemical contents and conformational changes. The study indicated changes arising in the polysaccharide, lignin, amino acid, secondary structure of protein, and lipid in the leaves of control and manganese-treated wheat plants. Manganese treatment increased the amount of cellulose, lignin, and amide II till 200?μM concentration, while a decrease was observed at 1000?µM concentration. Manganese induced conformational changes in the secondary structure of protein which was indicated by shifting of the bands to the higher wavenumber and change in the β sheet/α helix ratio. In addition, manganese stress decreased lipid content in the leaves of the wheat seedlings. The study demonstrates the potential of attenuated total reflectance FTIR for the non-invasive and rapid monitoring of the plants stressed with heavy metals.     

2,6-吡啶二亚胺基锰(Ⅲ)配合物的合成、晶体结构及催化性能

由三齿含氮配体2,6-二[1-(2,6-二甲基苯基亚胺)乙基]吡啶(L1)、2,6-二[1-(2,6-二乙基苯基亚胺)乙基]吡啶(L2)和2,6-二[1-(2,4,6-三甲基苯基亚胺)乙基]吡啶(L3)分别与MnCl2·4H2O在乙腈中反应,合成了3个新的具有较大空间位阻的2,6-吡啶二亚胺基氯化锰配合物L1Mn(Ⅱ)...