MRS: Put some chicken feathers in your engine

That is what Richard Wool suggested as apparently, when treated thermally near their melting temperature, the cheratin in the feathers develops tunnels around 7 Angstroms in size, which are very good for hydrogen storage. The material is not very efficient, but at least it is extremely low cost (3000kg waste feathers a year are produced in the US alone).

Wool presented also an interesting technology for prefab roofs. They would be made of recycled cardboard or other natural fibers and soybean oil resin, which is then cross linked by free radical polymerization, started by a cobalt based catalyst. Although this technology has been around for a few years (it was developed to make roofs able to withstand hurricanes) it has been recently picked up by the South African government which will deploy it on 2.2 million homes as an energy efficient substitute for steel and other materials currently used in housing there.

Reactions – Stuart Warren

Stuart Warren is in the Department of Chemistry at The University of Cambridge, and worked on new synthetic methods, particularly those involving phosphorus or sulfur, rearrangements and asymmetric synthesis.

1. What made you want to be a chemist?

I was lucky enough to go to Cheadle Hulme School in Cheshire and be taught chemistry by David Goodison. I had an early love of science and it was not long before David’s thoughtful approach and emphasis on ‘why?’ rather than ‘how?’ led me to prefer chemistry to any other science. I can still picture vividly the day he introduced organic chemistry to us. He used carboxylic acids as examples and I grew angry at this and protested to him that they weren’t acids at all. He smiled and suggested that I wait and see what was to follow. Sometimes people who react quite violently against something come to love it because they are so deeply engaged with it. That was how I came to like organic chemistry. But it was Denis Marrian, Peter Sykes and Malcolm Clark in my undergraduate days at Cambridge who gave organic chemistry the solid intellectual foundation that made me want to do it for the rest of my life.

2. If you weren’t a chemist and could do any other job, what would it be – and why?

I might have wanted to be a professional cricketer, but I wasn’t good enough. I tried biochemistry at Harvard with Frank Westheimer and rejected it in favour of organic chemistry. So no other science. I suppose an actor, a novelist or an Anglican minister.

3. What are you working on now, and where do you hope it will lead?

I no longer have a research group but my writing continues. I am now working on the second edition of the textbook ‘Organic Chemistry’ with Jonathan Clayden for OUP. Paul Wyatt and I have completed the four books in the Organic Synthesis series for Wiley, the last one to be published later this year. Paul and I also do courses in industry including one on ‘Advanced Heterocyclic Chemistry’ and I have hopes that we might produce a book with that title as the next, and for me probably final, project. It seems me that there is a great need for an accessible, mechanistically oriented book on Heterocyclic Chemistry that tries to explain the reactions rather than give lists of them.

4. Which historical figure would you most like to have dinner with – and why?

The Duke of Wellington was a master of the sharp remark, had no patience with administrators, and saw practical results as what really mattered. I want to find out how he got round the British, Spanish and Portuguese administrators in the Peninsular War and what made him persist with the Catholic Emancipation bill when all seemed lost. He would decline the invitation, of course, so maybe it would be Sir Pelham Warner who could describe his very long cricketing career or I could resurrect Charles Rees to continue the many conversations so rudely interrupted by his death.

5. When was the last time you did an experiment in the lab – and what was it?

In about 1973 Robin Shepherd had completed a series of experiments to establish the stereospecificity of Ph2PO migration. He had an X-ray of the starting material but couldn’t crystallise the product. So I did that, got the X-ray from Luigi Nassimbeni and published the result in Nature. F. H. Allen, O. Kennard, L. R. Nassimbeni, R. G. Shepherd, and S. Warren, Nature 248, 670–671 (1974); Stereochemistry of a carbonium ion rearrangement.

6. If exiled on a desert island, what one book and one music album would you take with you?

It would be a very difficult choice between Great Expectations, Pride and Prejudice, Hardy’s or Wordsworth’s collected poems or the Revised New English Bible.

Music is easier: Schubert or Vaughan Williams songs sung by Ian Bostrich or Finzi, Ode on the Intimations of Immortality sung by Ian Partridge. I think I would miss most the wonderful sound of the human voice.

7. Which chemist would you like to see interviewed on Reactions – and why?

Guy Lloyd-Jones (Bristol), as his work seems to me to combine the very best in mechanistic analysis and the latest developments in organo-metalic chemistry and asymmetric catalysis. He is one of the sharpest thinkers in the world of organic chemistry today.

Nobel reflections

Early October saw the announcement of this year’s suite of Nobel Prize recipients and, as has been the case on quite a few occasions in recent years, there was some consternation when it came to the Chemistry prize. Many thoughts were expressed in the blogosphere and twittersphere and Carmen’s post over at C&ENtral Science has a few handy links that you can use as a starting point.

Now that the dust has settled somewhat, we’ve taken a look at the issue in our December editorial. The first paragraph is repeated below as a teaser:


Chemistry is often referred to as ‘the central science’ and its associations to all fields are clearly there to behold, but to some these links may stretch too far. Some purists have had their chemical noses put of joint with the recent awarding of the Nobel Prize in Chemistry for ‘studies of the structure and function of the ribosome’ — apparently a topic that, for some, is not chemistry but biology. The arguments over the undeniable biological bent of the Nobel Prize in Chemistry are not new, but they seem to have reached a new level of intensity (or at least visibility) this year with various blogs and tweets doubting its current relevance to chemists. The award certainly leads to questions over the definition of chemistry and whether such ‘structural biology’ can indeed be classified as chemistry.


The rest of the article is available for free on our website to anyone with a nature.com account (and if you don’t have one, it’s easy to sign up for one).

There is also an ‘Editor’s Letter’ (an Editorial?) in the November issue of ACS Chemical Biology that considers the same topic, including whether we need new Nobel Prizes.

Stuart

Stuart Cantrill (Chief Editor, Nature Chemistry)

Your language help required

Do any of our readers speak Korean?? If so, we’d love some help.

Some background…being utterly self-obsessed, we’ve set up Google News alerts that let us know whenever a news website (or blog) publishes a story that mentions ‘Nature Chemistry’. It’s nice to see when our articles get picked up elsewhere, and very useful to get feedback of any kind – it’s less interesting seeing how many cosmetic products are marketed using the awful phrase “nature’s chemistry”! [at least 2 or 3 a week, since you asked]

Anyway, this week we’ve found 3 or 4 webpages, in Korean, that mention Nature Chemistry. One mentions JACS as well.

So what? Well, the unusual thing is that the articles really don’t look like normal science news articles at all! They look a lot more like a celebrity news story, complete with a professional photo of a young chap posing with/without guitar case – check ’em out.

Google Translate doesn’t help – apart from providing a kind of Lear-esque nonsense poetry all of its own – but maybe you can! Is one of our – or JACS’ – authors famous in Korea? Am I missing the point entirely?

Neil

Neil Withers (Associate Editor, Nature Chemistry)

Volume 1 – done!

Today the December issue of Nature Chemistry went live (yes, I know it’s still November and Thanksgiving has not yet arrived for our American cousins, but hey, all the Christmas stuff is already in the shops…!).

Anyway, this represents a fairly significant milestone because it closes out Volume 1 of the journal. Nine issues, lots of pretty covers and some great science to boot! (I guess I’m biased, but you’ll just have to live with that). For those who are fans of metrics, it is these nine issues that will contribute to our first immediacy index (due out in the summer of 2010) and our first impact factor – due one year after that.

But we’re not resting on our laurels, not al all! So begins Volume 2, and the January 2010 issue is not too far from being put to bed as well (short deadlines because of the festive season…). Indeed, two papers from this issue have already been published online in advance of print – with two more following next Sunday.

We will endeavour to continue bringing you the best chemistry from labs around the world in 2010 and hope you enjoy what we have to offer. But now that we can draw a line under Volume 1, for those of you brave enough to leave comments on this post, we’d be keen to hear what you think we’ve got right, what we’ve got wrong – and what your favourite bits were…

Let us know – we’re always looking to improve.

Stuart

Stuart Cantrill (Chief Editor, Nature Chemistry)

Reactions – Maitland Jones

Maitland Jones, Jr, teaches in the Department of Chemistry at New York University.

1. What made you want to be a chemist?

When I was 12 or 13, I met William Doering. I had asked/demanded (remember I was all of 12) of my parents to be allowed to play the 12-year old tennis circuit that summer. My parents properly replied, “Time to get a job, kid.” They met Doering at a party and coerced, or bribed, him into giving their kid what would today be called an internship at Hickrill, a privately funded basic research lab that happened to be near where we lived. There I not only met Doering, for whom I would work for the next ten years or so, but several other wonderful organic chemists, including Larry Knox, for whom I directly worked at Hickrill, washing dishes and being a general gopher. I knew nothing, of course, but the atmosphere was electric, the work intense, and the passion palpable. No one with the slightest interest in science could emerge from that place unchanged.

2. If you weren’t a chemist and could do any other job, what would it be – and why?

All my life I have loved jazz, and I have spent an enormous number of hours in dingy clubs over the last five or six decades. I know a lot about the music and run a jazz series in Princeton, New Jersey. I probably – certainly – could not be a musician, but I could run a club, or maybe be a critic. I still might do that.

3. What are you working on now, and where do you hope it will lead?

Well, I closed the research lab when I moved from Princeton to NYU, so I can only answer that in retrospect. My group worked on the chemistry of reactive intermediates, carbenes, benzynes, and the like. We also expanded into the chemistry of boron cage compounds, and the interactions of reactive intermediates with those three-dimensionally aromatic compounds. We hoped only that it would lead to a better understanding of how molecules react – and of how “electrons talk to each other.”

4. Which historical figure would you most like to have dinner with – and why?

Thelonious Monk. I saw and heard Monk when I was a kid. Indeed, I was at the Five Spot for a few of the times Monk played with John Coltrane. I didn’t have a good enough understanding of the music then, and I’d like to talk to Monk about his music, or, better, to see him play again, nowI have a deeper appreciation of it.

5. When was the last time you did an experiment in the lab – and what was it?

A long long ago, probably in the 1970’s – or even 1960’s. Peter Gaspar was visiting Princeton for a semester, and we happened on a result of Bill (Florida) Jones’s that had, we thought, important implications for the chemistry of phenylcarbenes. So I ran the experiments, evaporating p-tolyl diazomethane through a hot pyrolysis tube and collecting the products, styrene and benzocyclobutene, as Peter and I expected/hoped. Write it out – it is a remarkable transformation. Then work out a mechanism. It’s wonderful chemistry. It turns out that a student of Harold Shechter’s had run similar experiment but for some reason Harold never published them at the time and they languished in Dissertation Abstracts.

6. If exiled on a desert island, what one book and one music album would you take with you?

It has to be a book I’ve read because one can’t take chances on a desert island, so I might pick Thomas Pynchon’s Gravity’s Rainbow, for sheer flat-out virtuosity. Even if one doesn’t get all the references – or even if one doesn’t get the point at all – one can read it page by page, sentence by sentence, just for the brilliancy of the writing. And it’s long. If I am allowed another, I’d take David Foster Wallace’s Infinite Jest – for much the same reasons. Or maybe Vikram Seth’s A Suitable Boy. Or….

Music is easy: Charlie Parker, the Collected Dials and Savoys.

7. Which chemist would you like to see interviewed on Reactions – and why?

There are only a small number of the great physical organic chemists left – Doering and Roberts, I guess. Few know them now, I’m afraid, as the discipline has fallen so far out of favor. It would be nice to let them have a chance to make the case again.

Tateshina 2009: Behind closed doors

I spent last week-end at the 9th Tateshina Conference on Organic Chemistry in Nagano, a couple of hours east of Tokyo on the train (from which I enjoyed a superb view of Mt Fuji on the way back).

This meeting is the Asian sister of the EUCHEM Conference on Stereochemistry, better known as the ‘Bürgenstock Conference’. At a time when there are many – and varied – conferences, these two adopt a very particular format (you can read our editorial on ‘meeting matters’ here, no subscription is required but you need a nature.com account).

Limited to around 60-70 invited participants, mostly from Japan, China, Singapore and Korea, the Tateshina Conference is designed to favour communication. Delegates gather in a secluded location (rendered particularly beautiful by the autumn leaves) for 48 hours, with about half a day left free so that they can engage in scientific chats, or make the most of the venue, or combine both. A large chunk of time is devoted to dialogue: a 25 minute presentation is followed by at least 15 minutes of discussion – rather than the mere 5 minutes allocated in most meetings – leading to some lively exchanges. And, this isn’t chemistry-related but I cannot not mention that we were treated to a fantastic clavichord recital, including a guest appearance from our chairman, Eiichi Nakamura, for a clavichord-flute ensemble.

This all contributed to a unique atmosphere — but I won’t tell you about the science because in order to encourage open and stimulating communication, it is agreed that any information presented isn’t for public use. Judging from the wide range of topics discussed I can reveal, however, that many areas of chemistry come under the umbrella of organic chemistry.

Anne

Anne Pichon (Associate Editor, Nature Chemistry)

The role of referees

One of the most fundamental aspects of our job here at the Nature research journals is overseeing the peer-review process. In making our decisions on whether to accept a manuscript for publication, the advice given to us by experts on the topic in question is absolutely crucial. And we get a wide range of responses from referees – sometimes we get very lengthy and detailed reports (some of which even rival the word count of the original manuscript being evaluated – yes, really), and sometimes we get very short reports of just a sentence or two.

What do we want? Well, Nature Physics have written a wonderfully lucid editorial explaining just that. If you referee for any journal, but especially those in the Nature stable, this is required reading. You can find the editorial here – it is freely available, but you do need to have a nature.com account.

I’ll leave you with one of the most important sentences from the editorial to whet your appetite and encourage you to go and read it – Whatever you think about a paper, it is vital to explain to us exactly why you think it.

Stuart

Stuart Cantrill (Chief Editor, Nature Chemistry)