Mission Statement

The Asian Chemical Editorial Society (ACES) is an organization of 13 major chemical societies in Asia and the Pacific. It was founded in 2005 as a conglomeration of chemical societies with the mutual aim of creating a modern publishing forum for research in Asia and coordinating future publishing activities.

The participating societies share a commitment to scientific excellence, to publishing ethics, and to the highest standards in publication, which are the basis for the success of Chemistry—An Asian Journal and its associated journals.

Publications

Chemistry—An Asian Journal

A sister journal of Angewandte Chemie and Chemistry—A European Journal

Supporting Organizations: ChemPubSoc Europe, Gesellschaft Deutscher Chemiker (German Chemical Society, GDCh), Federation of Asian Chemical Societies (FACS).

Asian Journal of Organic Chemistry

A sister journal of the European Journal of Organic Chemistry

For the publication of the AsianJOC, ACES is joined by the Korean Society of Organic Synthesis.

Supporting Organization: ChemPubSoc Europe

ACES supports the publication of the ChemPubSoc Europe journals Chemistry—A European Journal, the European Journal of Organic Chemistry, and ChemSusChem.

© Wiley-VCH 2012

Journals

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Chem Asian J

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ChemAsianJ for iPad

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Asian J Org Chem

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AsianJOC for iPad

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Sister
Journals

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Angew Chem

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Chem Eur J

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Eur J Org Chem

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Associated
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ChemSusChem

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Related
Journals

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Chem Rec

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Chin J Chem

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J Chin Chem Soc

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News

Editorials: New Developments

Chemistry - An Asian Journal Theresa Kueckmann
A Good Year
Chem. Asian J. 2014 9, 4.

Asian Journal of Organic ChemistryRichard Threlfall
There's an App for That
Asian J. Org. Chem. 2014 3, 3.

 

Research of the DayEditors' Choice: Spotlights

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A Base-Free Neutral Phase-Transfer Reaction System

A Base-Free Neutral Phase-Transfer Reaction System

In and out of phase: The mechanism of a novel base-free neutral phase-transfer reaction system was investigated (see scheme). The aqueous–organic biphasic reaction system with lipophilic tetraalkylammonium bromide was essential to promote the neutral phase-transfer reactions. The base-free reaction system could be applied to several asymmetric reactions.

[Full Paper]
Seiji Shirakawa, Lijia Wang, Rongjun He, Satoru Arimitsu, Keiji Maruoka
Chem. Asian J., Apr 15, 2014, DOI: 10.1002/asia.201402194. Read article.

Donor–Acceptor-Type Copolymers Based on a Naphtho[1,2-c:5,6-c]bis(1,2,5-thiadiazole) Scaffold for High-Efficiency Polymer Solar Cells

Donor–Acceptor-Type Copolymers Based on a Naphtho[1,2-c:5,6-c]bis(1,2,5-thiadiazole) Scaffold for High-Efficiency Polymer Solar Cells

Walking on sunshine: Four donor–acceptor-type low-bandgap conjugated polymers based on a naphtho[1,2-c:5,6-c]bis(1,2,5-thiadiazole) acceptor and different donors with a bithiophene spacer have been synthesized. The best device performance was achieved by PF-C12NT, with Voc=0.87 V, Jsc=12.19 mA cm−2, FF=61.36 %, and PCE=6.51 % (100 mW cm−2, AM 1.5G).

[Full Paper]
Li-Qian Liu, Gui-Chuan Zhang, Peng Liu, Jie Zhang, Sheng Dong, Ming Wang, Yu-Guang Ma, Hin-Lap Yip, Fei Huang
Chem. Asian J., Apr 15, 2014, DOI: 10.1002/asia.201402019. Read article.