Archive for the ‘Themed Issue’ Category

Green Chemistry 15 years on…

In January 1999 the first issue of Green Chemistry was published with an Editorial written by James Clark, setting out his vision for the Journal.

GC 1999 Issue 1 Cover jpg

1999: First cover of Green Chemistry

Green Chemistry, 2013, Vol. 15, issue 1 front cover

GC, Vol. 15, issue 1 front cover

To mark the occasion of the Journal entering it’s fifteenth year of publication in 2013 we will be having a number of interesting articles asking those scientists who have contributed to the Journal strategy to reflect on how the subject has changed over the last 15 years and asking them for their vision on the subject in the future. 

We will also be highlighting those papers that have been most cited over the years – the papers that you as readers have been citing the most. 

Details about all of these activities will be posted on the Green Chemistry blog throughout 2013.

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Green Chemistry Themed Issue on Green Solvents Marks the International Year of Chemistry

Graphical abstract: The echoes of green chemistryTo mark the International Year of Chemistry in 2011, Green Chemistry has published a themed issue on green solvents for synthesis.  This themed issue is online now and contains articles by world-leading chemists detailing the recent advances and challenges faced in this area. It has been approved as an official IYC Activity.

The issue showcases the innovative research towards the substitution of volatile organic solvents in solution phase synthesis. The series of articles presented in this themed issue are based on the keynote presentations at an international conference organised by Dechema, held in October 2010 in Berchtesgaden, Germany. 

You can read Guest Editor Walter Leitner’s editorial online here and the full issue online here.

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Read the best ionic liquid research from the Asia-Pacific region

Green Chemistry has collated a number of ionic liquid research presented at the recent 2nd Asia Pacific Conference on Ionic Liquids and Green Processes held in Dalian, China, on 7-10 September 2010. The selection of articles below represents some of the best ionic liquid research from the Asia-Pacific region. You can access the web-themed issue online.

Fangmin Jin and co-workers demonstrate the reduction of NaHCO3 to formate using isopropanol as a reducing agent. Yields of about 70% were acheived.

Read more about Fangmin Jin’s work:

From NaHCO3 into formate and from isopropanol into acetone: Hydrogen-transfer reduction of NaHCO3 with isopropanol in high-temperature water
Zheng Shen, Yalei Zhang and Fangming Jin
Green Chem., 2011, DOI:10.1039/C0GC00627K , Advanced Article

A fruitful collaboration between the teams led by Changping Li and Urs Welz-Biermann resulted in the development of a microwave-assisted extraction of bioactive lactones from chinese herbal medicines using protic ionic liquids.  The Dalian scientists concluded that the extraction mechanism of microwave-assisted ionic liquid extraction is the similar to traditional organic solvent extraction.

Read the full paper:

Microwave-assisted extraction of lactones from Ligusticum chuanxiong Hort. using protic ionic liquids
Chi Yansheng, Zhang Zhida, Li Changping, Liu Qingshan, Yan Peifang and Urs Welz-Biermann
Green Chem., 2011, 13, 666-670

In this web-themed issue, Li and Welz-Biermann also report a room-temperature method to desulfurise fuels employing an oxidation method combined with extraction using acidic ionic liquids. The method shows some promise level of sulfur removal from the model oil reached 99% in 180 min.

Interested in finding out more? Read the full article here:

Desulfurization by oxidation combined with extraction using acidic room-temperature ionic liquids

Chi Yansheng, Li Changping, Jiao Qingzhu, Liu Qingshan, Yan Peifang, Liu Xiumei and Urs Welz-Biermann
Green Chem., 2011, DOI: 10.1039/C0GC00745E, Advanced Article

 Liu et al. showed that double SO3H-functionalized ionic liquids exhibited better catalytic activity for the esterification of glycerol compared to non-functionalizeds ionic liquids. Glycerol conversion was achieved in 95% within 30 min by using catalytic amounts of ionic liquids (only 0.1 mol% based on glycerol).

You can read the full paper online:

Esterification of glycerol with acetic acid using double SO3H-functionalized ionic liquids as recoverable catalysts

Xiumei Liu, Huiyuan Ma, Yue Wu, Chang Wang, Miao Yang, Peifang Yan and Urs Welz-Biermann
Green Chem., 2011, 13, 697-701

Kim et al. demonstrate an eco-friendly way of making polymers. The Korean scientists synthesized double metal cyanide (DMC) catalysts for the ring opening polymerization of propylene oxide, employing nontoxic lactate esters as complexing agents. “Highly pure polyol products that can be raw materials for high performance polymers like polyurethane are produced by using the resulting catalysts,” claim Kim and co-workers.

Double metal cyanide catalysts bearing lactate esters as eco-friendly complexing agents for the synthesis of highly pure polyols
Ji Hwan Yoon, In Kyu Lee, Hye Yoon Choi, Eun Ji Choi, Ju Ho Yoon, Sang Eun Shim and Il Kim
Green Chem., 2011, 13, 631-639

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Inviting submissions from the Asia Pacific Conference on Ionic Liquids and Green Processes

We invite you to contribute to a web-themed issue on ionic liquid and green processes.

Contributors to the 2nd Asia Pacific Conference on Ionic Liquids and Green Processes (APCIL-2) are invited to submit their work to Green Chemistry and those that are accepted for publication will be collated in a Green Chemistry SCI-indexed web themed issue dedicated to the conference.

We welcome the submission of primary research full papers, communications, critical reviews or perspectives within the scope of the Journal. If you would like to submit a review article based on the work presented at the conference, please do contact us to discuss this further.

The deadline for the submission of articles for the themed issue is 30th of September2010.

All articles will be peer-reviewed and will be published as Advance Articles online as soon as they are ready. All manuscripts will have a conference footnote added upon publication and all accepted papers will be collated as a web-themed issue dedicated to the conference. 

If you have any questions regarding the submission process please contact us: green-rsc@rsc.org.

Manuscripts can be submitted online: http://mc.manuscriptcentral.com/gc .

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