• Issue

    Chinese Journal of Chemistry: Volume 33, Issue 9

    993-1095
    September, 2015

Cover Picture

Free Access

Cover Picture: Bromine Bonding Induced Selective Recognition of Different Guests for Hexaphenylbenzene Bromides in the Solid State (Chin. J. Chem. 9/2015)

  • Page: 993
  • First Published: 17 September 2015
Cover Picture: Bromine Bonding Induced Selective Recognition of Different Guests for Hexaphenylbenzene Bromides in the Solid State (Chin. J. Chem. 9/2015)

The cover picture shows the recognition of CH2Cl2 molecules for hexaphenylbenzene bromide HBH in solid state (Atom colors: C, gray; Br, red; Cl, green; H, white). With propeller-like shape, hexaphenylbenzene bromides display different recognition abilities for guest molecules in solid state. HBH can encapsulate CH2Cl2 or Et2O molecules selectively from different solvent systems. For DBH, the recognition pattern is dominated between themselves. In CH2Cl2/toluene/Et2O system, toluene molecule can be encapsulated selectively by MBH. In these supramolecular assemblies, bromine bonding plays an important role. More details are discussed in the article by Zhang et al. on page 1031–1036.

Contents

Free Access

Contents: Chin. J. Chem. 9/2015

  • Pages: 995-999
  • First Published: 17 September 2015

Review

Gold Nanoparticles for Cancer Theranostics

  • Pages: 1001-1010
  • First Published: 12 August 2015
Gold Nanoparticles for Cancer Theranostics

Gold nanoparticles have seen unprecedented development in biomedical field, particularly for caner theranostics. This review introduces methods for preparing various shapes of gold nanoparticles and describes their current applications in the field of cancer treatment. Moreover, the review presents the development routes and current issues of gold nanoparticles in clinical theranostics.

Communications

Ruthenium Trichloride Catalyzed Highly Efficient Deoximation of Oximes to the Carbonyl Compounds and Nitriles without Acceptors

  • Pages: 1011-1014
  • First Published: 29 June 2015
Ruthenium Trichloride Catalyzed Highly Efficient Deoximation of Oximes to the Carbonyl Compounds and Nitriles without Acceptors

An acceptor-free catalysis protocol for the deoximation of ketoximes and aldoximes using RuCl3 as the catalyst has been developed. Under the optimized conditions, various oximes were converted to ketones and nitriles with excellent isolated yields.

Highly Efficient Synthesis of Arylpyrrole Derivatives via Rh(III)-Catalyzed Direct CH Arylation with Aryl Boronic Acids

  • Pages: 1015-1018
  • First Published: 12 August 2015
Highly Efficient Synthesis of Arylpyrrole Derivatives via Rh(III)-Catalyzed Direct C<span class='icomoon'></span>H Arylation with Aryl Boronic Acids

A highly efficient Rh(III)-catalyzed direct CH arylation of pyrrole derivatives with aryl boronic acids under mild conditions has been developed. The methodology features wide substrate scope and excellent functional group compatibility (20 examples, up to 98% yield).

4-OH-TEMPO/TCQ/TBN/HCl: A Metal-Free Catalytic System for Aerobic Oxidation of Alcohols under Mild Conditions

  • Pages: 1019-1023
  • First Published: 12 August 2015
4-OH-TEMPO/TCQ/TBN/HCl: A Metal-Free Catalytic System for Aerobic Oxidation of Alcohols under Mild Conditions

A green and economical catalyst system, 4-OH-TEMPO/TCQ/TBN/HCl, for the aerobic oxidation of a broad range of primary and secondary alcohols to the corresponding carbonyl compounds has been developed. These reactions proceed without transition-metals under mild conditions with excellent yields.

Full Papers

Synthesis of Hydroxyapatite Nanorods under Mild Conditions and Their Drug Release Properties

  • Pages: 1024-1030
  • First Published: 12 August 2015
Synthesis of Hydroxyapatite Nanorods under Mild Conditions and Their Drug Release Properties

Hydroxyapatite (HAp) nanorods with high aspect ratio have been successfully synthesized via the hydrolysis of the precursor CaHPO4 at 60°C at atmospheric pressure. The as-prepared CaHPO4 sample using CTAB as surfactant is well crystallized at the first precipitation step. At the second hydrolysis step, the CTA+ and OH act to control the formation and growth of HAp nanorods. The HAp nanorods modified with suitable surfactants are of great potential applications in drug delivery system.

Bromine Bonding Induced Selective Recognition of Different Guests for Hexaphenylbenzene Bromides in the Solid State

  • Pages: 1031-1036
  • First Published: 22 July 2015
Bromine Bonding Induced Selective Recognition of Different Guests for Hexaphenylbenzene Bromides in the Solid State

Selective recognition of different guests for hexaphenylbenzene bromides in the solid state.

Preparation and Intramolecular CC Coupling Reaction for Bis-benzimidazolium Salt

  • Pages: 1037-1040
  • First Published: 22 July 2015
Preparation and Intramolecular C<span class='icomoon'></span>C Coupling Reaction for Bis-benzimidazolium Salt

One new compound 2 containing two boat-like seven-membered rings was prepared through intramolecular CC coupling reaction under the catalysis of Pd(OAc)2.

Non-Flat Bisbenzylisoquinoline Alkaloid Fangchinoline As a Class of Potent G-Quadruplex Stabilizer with Anti-cancer Activity

  • Pages: 1041-1048
  • First Published: 29 June 2015
Non-Flat Bisbenzylisoquinoline Alkaloid Fangchinoline As a Class of Potent G-Quadruplex Stabilizer with Anti-cancer Activity

Novel non-flat G-quadruplex ligands exhibit good stabilization to G-quadruplex structure. The ligand and the G-quadruplex form a 2:1 complex.

One-pot Two-Step Cycloaddition Reaction for Convenient Synthesis of Polycyclic Spirooxindole-fused [1,3]Oxazines

  • Pages: 1049-1056
  • First Published: 12 August 2015
One-pot Two-Step Cycloaddition Reaction for Convenient Synthesis of Polycyclic Spirooxindole-fused [1,3]Oxazines

Three-component reactions of substituted pyridines, isatins with methyl propiolate, or dimethyl acetylenedicarboxylate afforded spiro[3H-indole-3,2′-[2H,9aH-pyrido[2,1-b][1,3]oxazines], which in turn reacted with N-arylmaleamide to give novel spirooxindoline fused [1,3]oxazines in good yields.

Preparation of ZSM-5 Coated on Monolithic Interconnected Macroporous Al2O3 Using Cheap n-Butylamine as Template

  • Pages: 1057-1063
  • First Published: 22 July 2015
Preparation of ZSM-5 Coated on Monolithic Interconnected Macroporous Al2O3 Using Cheap n-Butylamine as Template

The irregular ZSM-5 zeolites were formed and coated on monolithic interconnected macroporous Al2O3 after seeding progress and impregnated, aged and hydrothermal reaction in the crystallization solution using n-butylamine as template.

A Fluorescent Probe for Hg2+ Based on Gold(I) Complex with An Aggregation-Induced Emission Feature

  • Pages: 1064-1068
  • First Published: 12 August 2015
A Fluorescent Probe for Hg2+ Based on Gold(I) Complex with An Aggregation-Induced Emission Feature

We designed and synthesized a gold(I) complex that exhibited aggregation-induced emission in acetonitrile-water mixtures. It showed high selectivity and sensitivity for Hg2+ in acetonitrile-water (1:1, V:V) solution. Dynamic light scattering measurements were conducted to verify that the addition of Hg2+ changed the particle size and induced fluorescence quenching.

Mechanism of Incompatible Herb Pairs, Panax ginseng and Veratrum nigrum L.: Material Basis and Metabolic Profiles of Ginsenosides in Rat Intestinal Bacteria

  • Pages: 1069-1076
  • First Published: 12 August 2015
Mechanism of Incompatible Herb Pairs, Panax ginseng and Veratrum nigrum L.: Material Basis and Metabolic Profiles of Ginsenosides in Rat Intestinal Bacteria

The mechanism of incompatibility of P. ginseng and V. nigrum L. was studied from the aspects of substance basis and metabolic profiles using ESI-MS and UPLC-MSn.

TMSCl Promoted Direct sp3 C-H Alkenylation to Construct (E)-2-Styryl-tetrahydrobenzo[d]thiazoles

  • Pages: 1077-1083
  • First Published: 22 July 2015
TMSCl Promoted Direct sp3 C-H Alkenylation to Construct (E)-2-Styryl-tetrahydrobenzo[d]thiazoles

A high-efficient and stereo-specific approach for synthesizing (E)-2-styryl-tetrahydrobenzo[d]thiazoles via TMSCl-catalyted direct sp3 C-H alkenylation of 2-methyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one under metal-free conditions has been developed.

Enhancing the Structural Diversity and Bioactivity of Natural Products by Combinatorial Modification Exemplified by Total Tanshinones

  • Pages: 1084-1088
  • First Published: 22 July 2015
Enhancing the Structural Diversity and Bioactivity of Natural Products by Combinatorial Modification Exemplified by Total Tanshinones

Six new quinoxlinetanshinones 16 were isolated from the combinatorial modified semi-synthetic mixture. These quinoxlinetanshinones demonstrated strong DNA binding properties.

Note

Identification and Fibrinolytic Evaluation of an Isoindolone Derivative Isolated from a Rare Marine Fungus Stachybotrys longispora FG216

  • Pages: 1089-1095
  • First Published: 10 June 2015
Identification and Fibrinolytic Evaluation of an Isoindolone Derivative Isolated from a Rare Marine Fungus Stachybotrys longispora FG216

An isoindolone derivative, Fungi fibrinolytic compound (FGFC1), was isolated from a rare marine microorganism strain Stachybotrys longispora FG216 and also evaluated for fibrinolytic activity in vitro and in vivo. FGFC1 is a potential thrombolytic activity agent in the future.