Goodbye – and thanks

As Stu announced about 3 months ago, I’m leaving Nature Chemistry – today!

It’s been a real privilege to be involved right from the start – when we hadn’t published any papers and the submission system was even open. The journal was a blank slate. Of course, that blank slate was pretty soon filled with papers, of which I handled my fair share. And that’s where the real privilege comes in: being the first person other than the researchers themselves to read some wonderful pieces of chemistry. The best part of this job is reading papers that make you go “Wow” – and then sharing them with the world!

One of the other highlights is going out to conferences and meeting people. I’ve been fortunate to go to some fantastic conferences, meet some chemistry heroes and visit incredible institutions. Although not quite as personal, I feel like I’ve ‘met’ lots of bloggers and tweeters through their posts and tweets, and having the ‘chore’ of reading tons of blogs so I can write blogroll every month has been extremely enjoyable.

So I’d like to thank all the authors, referees, people I’ve talked to at conferences, people who’ve entertained me in their departments, and all the bloggers and tweeters who make this job as fun as it is!

And of course, I have to thank the rest of the team, who’ve been a pleasure to work with! And that includes the people who aren’t on that webpage, our wonderful production team.

See you all over at Chemistry World!

Neil

Blogroll: Space dinosaurs!

Highly respected organic chemist publishes a Perspective in JACS, chaos ensues.

Ronald Breslow — past president of the ACS and Priestley medallist in 1999 — is a “well-respected research lion”, in the words of SeeArOh at Just Like Cooking. Few would dispute his place in the chemistry firmament. With many achievements behind him, surely he has earned the right to close a Perspective article in JACS on the possible origin of homochirality in biological molecules with a chuckle — suggesting that humans would be better off not meeting the advanced dinosaurs, with amino acids of the opposite chirality, who may populate distant corners of the universe!

Apparently not. At least, not according to some of the dinosaur-focused bloggers/newshounds out there — such as Dinosaur Tracking or Discovery. In their defence, however, they were reacting to the press briefing that the ACS somewhat mystifyingly released. It was mystifying because it ignored the six pages of discussion about the origin of chirality of amino acids to focus on the last two ‘space dino’ sentences.

The combination of Breslow and space dinos proved tempting for some chemistry bloggers, with SeeArrOh covering the paper and its final words in the good-humoured tone in which they were surely intended. Paul Bracher, who blogs at ChemBark, has worked in the origin-of-life field, and actually discussed the scientific content of the paper — how refreshing! But Bracher certainly doesn’t mince his words giving his opinion of the ACS press office.

The final twist in the dinosaur’s tale came in the comments on Just Like Cooking and ChemBark: hasn’t Breslow written something quite similar in Tetrahedron Letters and the Israel Journal of Chemistry? The similarity is such that, at the time of writing, JACS has removed the paper from its website, citing copyright concerns.

[As mentioned in this post, we’re posting the monthly blogroll column here on the Sceptical Chymist. This is June’s article]

Blogroll: Arnie and artemisinin

A chemist who wants to terminate malaria and a calculation to have at your fingertips.

“Malaria. I hate this parasite. I want to kill it.” Imagine these words spoken in a voice similar to Arnold Schwarzenegger’s and you’ll understand why they nearly made Karl Collins fall off his chair, as he explained in a post at A Retrosynthetic Life. Of course, it wasn’t Arnie speaking, but Peter Seeberger of the Max Planck Institute, who discussed his efficient and cheap route to making artemisinin. Seeberger’s development means that “artemisinin factories the size of large cardboard boxes can be made for £10,000”. Overall, the cost of producing this potent antimalarial could fall to “10% of what it is today” — this might go some way to explain why Seeberger’s next appointments were with the UN and the Gates Foundation. Collins explains more about Seeberger’s career in his blogpost and you can read the Angewandte Chemie paper that reports the continuous flow synthesis via https://doi.org/c55rks.

“By the time you finish this sentence, your fingernails will have grown one nanometre.” If you read that sentence with some scepticism, you’re not alone. Zen Faulkes, who blogs at Neurodojo, asked “Is that accurate?”. To start with, his students did some guesstimations, ‘Fermi problem’ style, that showed it might be true, but like any good scientist, Faulkes wanted data. So he measured the growth rate of his fingernails using callipers accurate to 0.01 mm. After five or six measurements on ten fingers he arrived at an average fingernail growth rate of 0.92 nm per second! But wait — Faulkes went a step further and discovered it took him about 3.77 seconds to read that sentence, so his fingernails would have grown a whopping 3.47 nm. Interested readers may like to tackle the problem posed in the comments: How many moles of β-keratin are deposited onto the nail per second?

[As mentioned in this post, we’re posting the monthly blogroll column here on the Sceptical Chymist. This is May’s article]

Your Monday answer

On Friday, I asked “What weight could you hang from a chemical bond before it broke? How many atoms [is that]?”

Paul from ChemBark suggested “~350 pN or ~400 nanograms or so” and Ali Moeed guessed “1000+ atoms”.

To be honest, I have no idea what the right answer is! But the fun with these kind of problems is working them out, so here are two methods I used and the answers they gave. Basically, I needed to know/calculate the mechanical force required to break a bond, seamlessly convert that into a force-due-to-gravity, and then work out what mass/how many atoms would give that force (on earth). If there are any mistakes in the following, please let me know in the comments! And if you have a better way to go about it, please do so.

First method (no research): The ball-park figure for the strength of a bond in my head is 100 kJ/mol, or 2 x 10-22 J per bond. Unfortunately, that’s an energy, not a force. But energy is just force x distance, right? So let’s say the bond is broken when you’ve moved one atom 10 Å further away. The force required to do this is (2 x 10-22 J/10 x 10-10 m) = 2 x 10-11 Newtons. A mass of 0.1 kg ‘weighs’ 1 N, so the weight required to break a bond is 2 x 10-12 kg. Which is pretty small in the human-sized world, but pretty massive in the atomic world – but how many atoms? I decided to think about gold atoms, as these make pretty nice nanoparticles. Gold has an atomic weight of ~200 g/mol, or 0.2 kg/mol, so that’s 2 x 10-12 kg / 0.2 kg/mol = 10-11 mol of gold. And finally, 6 x 1023 atoms of gold/mol x 10-11 mol = 6 x 1012 atoms of gold.

Second method: Gav used popular internet-based search engine ‘Google’ to find this paper from Matyjaszewski et al in Nature, the abstract of which says “[C-C bond] strength is evident in the hardness of diamonds [etc]; on the single-molecule level, it manifests itself in the need for forces of several nanonewtons to extend and mechanically rupture one bond.” So repeating the calculations from 10-9 Newtons gives 10-10 kg, or 3 x 1014 atoms of gold.

So my two answers aren’t exactly the same, but I think they’re close enough (what’s a factor of 50 when things are between 10-12 and 1023??) to indicate that it would take a LOT of atoms – one fat ‘nano’particle – to break a bond by their weight alone. I see Paul’s answer is in a similar range, and Ali is technically right with “1000+” but that leaves quite a lot of wiggle room!

What does this teach us? Well, apart from the fact that chemical bonds are strong, perhaps just that physicsgravity is weak, chemistryelectrostatics are strong!

NOTE: As I am just about to press publish, I see John at It’s the Rheothing has tacked the problem too, but (naturally) from a polymer perspective – how long a polymer could a bond support? I won’t spoil the surprise – go and read his post!

Neil

Neil Withers (Associate Editor, Nature Chemistry)

Your weekend problem…

A question struck me yesterday afternoon (editorial discretion prevents me revealing exactly why): what weight could you hang from a chemical bond before it broke? How many atoms?

I asked the rest of the team if they had any ideas, but got no answers I would be comfortable publishing! Still intrigued, I thought about it more while it was my turn on the tea rota.

It’s relatively easy to work out, with a little digging, but might surprise you. I’ll let you all stew on the question over the weekend – and suggest your own answers below – and return with my Fermi-style calculation on Monday!

Neil

Neil Withers (Associate Editor, Nature Chemistry)

Blogroll: Scary chemicals

Sensational chemophobia and the problems with biofuels

‘Are you scared yet?’ This is the title of See Arr Oh’s post on Just Like Cooking but could equally serve as the unspoken subtitle of the news report he’s blogging about. First highlighted on ChemBark the investigative report from US TV channel Fox29 is about “unlocked chemistry labs and the ease with which a terrorist could steal hazardous materials”. So far, so serious. But, as ChemBark says, “the underlying point of securing labs is a valid one, but the presentation is way Way WAAAAAAY over the top”. See Arr Oh takes the presentation to task more than ChemBark, giving us some random quotes that illustrate the chemophobic sensationalism of the report, which breathlessly reveals the presence of 0.1 M HCl and ether. He counted “26 mentions of the word ‘chemical’ (or once every 14.4 seconds)” – mostly “preceded by a sensationalist adjective”. We can’t deny that lab security is an issue for serious discussion, but perhaps it deserves better reporting than it got from Fox29.

When Nobel Laureates talk, people listen — and when they write provocative editorials, people read closely. So when we spotted the editorial in Angewandte Chemie by Hartmut Michel (1988 Laureate) titled ‘The Nonsense of Biofuels‘, we sat up. And so did Ash Jogalekar at The Curious Wavefunction, where he took us through the photosynthesis expert’s arguments. First among these is the lack of efficiency of photosynthesis itself — a 4% upper limit — which is exacerbated by the energy needed to grow, harvest and transform the biomass into useful fuels. Finally, when it comes to fuelling transportation, only 20% of the energy produced by a combustion engine is used to propel the vehicle. Michel suggests that either photosynthesis needs to be improved, or photovoltaics and batteries pursued with more vigour — solar cells are around 15% efficient, and vehicles can usefully use 80% of the battery’s energy.

[As mentioned in this post, we’re posting the monthly blogroll column here on the Sceptical Chymist. This is April’s article]

Blogroll: Better by design

The differences between planes and drugs, engineers and medicinal chemists … and Jimmy Stewart.

Have you ever wondered about the similarities and differences between drug design and aeroplane design? If not, don’t worry because Ashutosh Jogalekar at the Curious Wavefunction has blogged about a paper that does just that. Both of these design processes use modelling, but “compared with the aeronautical industry where modelling has been applied to airplane design for decades, why has it taken so long for modelling to catch on in the pharmaceutical industry?” Jogalekar takes us through the three reasons he sees: the complexity of biological systems compared with aeronautical ones; the natural inclination of engineers to learn programming and modelling is generally not shared by the mix of people who work in pharma; and the lack of a “comprehensive knowledge base for validating modelling techniques”. As a molecular modeller himself, Jogalekar finds the paper upbeat and hopes that “the pharmaceutical industry makes a concerted effort to test, refine, retain and discard modelling approaches to drug design at all levels”.

Derek Lowe blogged his own thoughts on the paper, noting that, in biological systems, “there are so many nonlinear effects, so many crazy little things that can add up to so much more than you’d ever think”. The “Andy Grove fallacy” — which is what Lowe calls the propensity of engineers and other outsiders to underestimate the complexity of drug discovery — is a favourite topic on In The Pipeline, so a lot of comments came from both sides of the fence — from engineers and biologists.

And finally … after pursuing exciting research on artificial photosynthesis, he left college and became a banker. A modern-day tale of the priorities of under-funded young scientists? No! It’s a scene from the Jimmy Stewart movie You Can’t Take it with You, released in 1938, which Nick Uhlig shared the clip on the Chemistry Blog.

[As mentioned in this post, we’re posting the monthly blogroll column here on the Sceptical Chymist. This is February’s article]

In praise of posters

Can you imagine scientific meetings without poster sessions?

The busiest — and loudest — areas of any conference are most likely to be the poster sessions. This is surely testament to the power of the humble poster: they are the places to see the newest science and talk to the people who actually do the work in the lab. The Nature Chemistry editors are frequently to be found inspecting and discussing posters (with or without a beer in hand…) that catch their eye at the conferences they attend throughout the year.

But once upon a time there must have been meetings without posters. So when was the first poster and who came up with the idea? Sadly, it looks as though history has not recorded the exact moment for us to celebrate. As far as we can tell, however, the idea originated in Europe before spreading to North America in 1974 at the Biochemistry/Biophysics Meeting in Minneapolis. The American Chemical Society then introduced poster sessions for the fall national meeting, in Chicago in 1975, a move that was seen as a ‘trail blazer’.

Since those early days of poster pioneers, the rise of personal computing alongside desktop publishing and graphical design software has further driven the evolution and development of posters. Of course, having the right tools to hand does not guarantee that the perfect poster will be produced every time.

So what makes a good poster? Fortunately for the more graphically challenged presenter, there are books, websites, blogs and even a Flickr photo group devoted to academic posters. From the combined experience of the Nature Chemistry team (which includes one first and two third prizes from our student days), we can also offer some advice. Clarity and content are key. Can all the text be read from a reasonable distance? Imagine that your poster is the highlight of the session: your ideal collaborator (or an interested editor) could be struggling to make out your conclusions at the back of the adoring crowd!

As with any presentation meant for an external audience, considering who makes up that audience and suitably tailoring your poster is critical. The amount of background material needed for a small subject-specific meeting will be very different from that needed for an ACS meeting with many thousands of attendees. When presenting your poster to other delegates, finding out what level of background knowledge they have will mean you pitch it at the right level and gives you the chance to create a dialogue.

As mentioned in the first paragraph, one of the key attractions of most poster sessions is the opportunity to talk to the people — typically graduate students or postdocs — who have actually performed the experiments. Getting the inside track on how the project really developed in the lab, rather than how it is presented in the finished research article, can often be fascinating. As networking events, poster sessions are unequalled at most scientific meetings: relaxed and full of opportunities to bump into people who might make the ideal advisor for that post-doctoral position you were looking for — and vice versa.

Posters are often a scientist’s first presentation or even publication, and can represent the first step on their journey to public scrutiny, feedback and peer review. This alone should be enough to raise them in people’s estimation, and not be treated as an afterthought by conference organisers or attendees.

[This post is an abridged version of the editorial in the February 2012 issue — the full text can be accessed here, available for free to all registered users. We welcome feedback on our editorials in the comments section below.]

Neil

Neil Withers (Associate Editor, Nature Chemistry)

PS This editorial was inspired by a conversation I had with Steve Koch at ICBIC last year

Blogroll – A hot topic

[As mentioned in this post, we’re posting the monthly blogroll column here on the Sceptical Chymist. This is January’s article]

Looking closely at pepper spray and an explosive mouthful.

People may think that blogs — even those about chemistry — only cover what the blogger had for breakfast and the occasional picture of cute kittens. Hopefully this column has dispelled some of those thoughts in the past few years, but if anyone still needs persuading, Deborah Blum’s post About Pepper Spray should do the trick. Written shortly after a “shocking incident involving peacefully protesting students at the University of California-Davis”, Blum took her readers through the chemistry behind the innocuously named weapon. For those familiar with the Scoville scale, pepper spray is about 1,000 times hotter than jalapeños and up to 25 times hotter than habaneros. But if you think that the effect is similar to the stinging eyes you may have experiences after not being careful in the kitchen, Blum warns “we’re not talking about cookery but a potent blast of chemistry”. Capsaicins, the compounds that confer heat on both chillies and pepper spray, “inflame the airways, causing swelling and restriction” making it particularly dangerous “to people with asthma and other respiratory conditions”. So dangerous, in fact, that it has been linked to around 75 deaths.

Blum’s post about such a newsworthy topic gathered so much attention it’s been re-posted in many venues, including Scientific American where it was the most popular item on the site for days. She even appeared on the Rachel Maddow show on MSNBC to discuss pepper spray (the segment can be found via this link).

On a less controversial, although slightly more explosive, topic, Derek Lowe treated us to another thing he won’t work with, hexanitrohexaazaisowurtzitane. Hiding behind that mouthful are six nitrogen atoms, each bonded to one of six nitro groups. If you dare to even imagine making it, Lowe suggests that you “picture a bunch of guys wheeling around drums of fuming nitric acid while singing the Anvil Chorus from Il Trovatore”.

A new look

Welcome to the new-look Sceptical Chymist! Of course, if you’re just reading this in your RSS reader, then things will look pretty familiar (unless you’re logging on to Google Reader for the first time in a few months — but then you probably can’t see through the tears of frustration you’re weeping).

All the other nature.com blogs are having a re-vamp, meaning this will be cross-posted here and there, so we’ve been asked to do a post to introduce the blog to any new readers. Regular readers may even learn something too — or you can skip the next two paragraphs to see what’s new!

We’ve been blogging at the Sceptical Chymist since March 2006 — the first post even handily explained the name (it’s from the book written by Robert Boyle in 1661, which is a useful point to consider as when chemistry started emerging from alchemy;). It started out with contributions from editors from Nature, Nature Chemical Biology and Nature Nanotechnology, but has since evolved to mainly us, the editors of Nature Chemistry — which was just a twinkle in a publisher’s eye back in 2006! Since then, it’s been a great way to communicate with readers less formally than in an editorial or other journal article, plus a wonderful means of generating discussion and receiving feedback.

You can expect to read interviews with chemists around the world in our Reactions series, reports from conferences we attend, ‘edited highlights’ of editorials and In Your Element, our monthly Blogroll column, as well as the occasional post inspired by almost anything. We also have a brave cadre of guest columnists: our two current guests are both graduate students negotiating the academic maze.

That’s the old blog; what’s new? Well, apart from lots of behind-the-scenes improvements that will make blogging much easier for us, you can see that it’s more seamlessly incorporated in the Nature Chemistry website. The side navigation is a bit less cluttered too. Hopefully the main improvement will be in the commenting: now, once your first comment has been approved, your subsequent ones will go live immediately. This should make discussions a bit more dynamic, and remove the wait while we fish every single comment (including our own!) out of the spam filter.

So have a look round, make yourself at home, test out the comments and let us know what you think!

The Nature Chemistry team.