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December 26, 2008

Reactions - Luisa De Cola

1. What made you want to be a chemist?

I was always a very curious child and I liked science in general. I guess my first choice would not have been chemistry but biology or medicine and indeed I studied biology for one year before realizing that chemistry was my preferred discipline.

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

I like many very different things. Perhaps a medical doctor, a neurologist, or a musician or perhaps a film director.

3. How can chemists best contribute to the world at large?

Chemists make our world! Everything we eat, drink, any clothes we wear, anything we touch is chemistry! The challenge now is surely to solve the energy crisis, the water problem and to improve early diagnosis of illness.

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

I would love to have dinner with Albert Einstein. I had since I was very young a special admiration for him as a scientist but in some respect also for his turbulent life.

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

I must confess that I am often in the lab, even just to look at my student showing me something... The last time I did manually something myself was about 3 years ago showing one of my student how to separate an iridium complex using an alumina column.

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

This is a very difficult question... perhaps the book would be One Hundred Years of Solitude by Gabriel García Márquez. The CD I alternate jazz and classical music but I also love pop music. I guess would probably be Bill Evans or Keith Jarrett the Köln concert.

Luisa De Cola is Professor in Physics and Chemistry at the Universities of Münster (Germany) and Twente (The Netherlands). Her main interest is luminescent and electroluminescent molecules and nanomaterials.

December 22, 2008

Materials Girl: The bell curve doth toll

Posted on behalf of Materials Girl

Finals are, at last, over and winter break has begun! ‘Tis the season for living at home, sleeping in, catching up on blogging, and checking grades online obsessively! (More precisely, I am procrastinating on studying for the GRE. Ugh. The vocabulary words I’m familiar with nowadays are on par with trimethylxanthine, eigenfunction, and nanorod, not termagant, eleemosynary, and nadir).

As far as grading goes, some form of curving seems standard among non-humanities classes. My science professors tend to aim for “nice” exam averages of 60-80, then curve results so that the wretched students scoring 50% get C's instead of F's. The brilliant engineering profs think everything is completely straightforward and write “easy” exams. Hah!

From a student’s perspective, I generally don’t have problems with curving. It’s nice to not worry about getting +90% on everything and risk having a few arithmetical errors or forgotten arrows kill perceived performance. However, if someone achieves those high scores and stays well above average, an A still isn’t guaranteed. And, that really sucks. It seems to boil down to two choices: battling tests & grading rubrics to score some set percentage, or battling classmates to be at the top of the pack. At the end of the day, it’s just a matter of a little luck and how well you fight (and get back up when beaten down) – regardless of the opponent.

Everyone says to not worry about GPAs, but it can’t be completely written off – especially since some schools give out A’s more easily than others. Experience and recommendations aside, how much do grad schools and companies really factor in what university an applicant comes from? At career fairs, recruiters always, always begin by looking for the GPA on my resume. It does make sense, since a 5-10 minute conversation can’t really tell them how qualified or knowledgeable I might be. But, what if I had a B in a class because my peers were a little bit better that time around, and I could’ve taken the same class the next term and gotten an A? I don’t think the 4.0 from community college will be of much help...

NChem Research Highlights: Biosensing dyes, strong biomimics and levitating beads

So here it is...Research Highlights, everybody's having fun. But before we all disappear for Christmas, here are the final RHs of the year.

I covered a pretty smart idea for a class of biosensors. Reducing cynanine dyes means they don't fluoresce, until they come into contact with the nasty reactive oxygen species that mess around with cells. Even cleverer, the reduced forms can slip in and out cells willy-nilly, whereas the fluorescing ones are trapped inside the cells, showing you where the problem is.

You might well have seen this one elsewhere, but now you can read Tim's take on the biomimetic material that's thin and strong - it's all about the ice templating, you know.

Last, but by no means whatsoever least, it's a nifty idea for what could become 'TLC for solid-supported synthesis'. And it involves magnetically levitating beads!

And finally...unlike the BMJ we haven't got a load of spurious research to make it into the news-light festive season newspapers - watch out for next year though - and we're a week before the RSC releases the same story about hangover cures for the 3rd or 4th year running, so I'll leave you with some mathematical clues to help you wrap presents better!

See you all in the New Year - thanks for all the comments in 2008!

Neil


Neil Withers (Associate Editor, Nature Chemistry)

December 19, 2008

Reactions - Ivan Dmochowski

1. What made you want to be a chemist?

For almost as long as I can remember, I’ve loved math and applying math to understanding the physical world. I grew up near Woods Hole, MA, which meant that there were high-quality local science fairs and “real scientists” as judges. My experiences of designing and performing independent science projects whet my appetite for science research. My interest in chemistry started in high school, where I had two very good chemistry teachers. However, I didn’t know many chemists, and I never really considered a career in chemistry.

As an undergraduate at Harvard, I gravitated towards the chemistry major, somewhat through a process of elimination. In my Junior year, I worked in the labs of Prof. George Whitesides, and was amazed at the breadth of interesting projects going on in his lab, and the range of activities in which he was involved. This was my first real exposure to university research chemistry, and I was hooked! The idea of being able to solve difficult and interesting real-world problems using a scientific discipline — chemistry — appealed to me very much. It also appealed to me to “spend the rest of my life in school” and to have opportunities to travel widely, and to make friends and pursue scientific collaborations around the world. And, even as a college student, it seemed great to be able to pursue problems of one’s choosing, and to have very little oversight in the form of a boss. I had so much fun doing chemistry research in college that it became clear to me that I should continue. I applied to chemistry graduate school and found a great mentor in Prof. Harry Gray at Caltech, who inspired me to pursue a career in chemistry.

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

I would love to try many different careers, but one of my first loves was baseball. I think it would be fun to be a Major League baseball pitcher. I played Little League as a kid, and always particularly looked forward to game days when I was pitching. The pitcher has the opportunity to control the outcome of the game, and time slows down when you’re on the mound. I love the feeling of needing to make every pitch count, and all of the mental challenges of trying to compete and win. In the off-season, baseball players also have the opportunity to do a lot of good in their communities.

3. How can chemists best contribute to the world at large?

That’s a great question. One of the things I love most about a career in chemistry is how many different doors it opens. Indeed, chemistry is great training for many undertakings. The general public forgets, I think, that science can be a wealth- and health-creating enterprise. Chemists have improved the lives of millions of people by developing new drugs, and chemists have created many thriving companies. Chemists are also great educators--of students in the classroom and citizens at large. Many university presidents are chemists, perhaps due to the administrative aspects of running a lab. Collectively, chemists can do a lot of good by designing new drugs, new materials, and new processes that will make the world a cleaner, healthier, and more sustainable place, and in the process employ millions of people. But, the world also desperately needs chemistry representatives to go into politics, and fill positions at the highest levels of government. The planet is facing major challenges in energy and healthcare, and chemists must take the lead in addressing these problems, both individually and collectively.

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

I love studying history, particularly the history of science. I think it would be wonderful to have dinner with Albert Einstein, and get some insight into how he observed the world and solved problems. It also seems like he had a great sense of humor, and I suspect the dinner would be very entertaining.

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

I occasionally perform experiments using my lab’s confocal microscope. For example, I’ve done some experiments recently that involve developing a fluorescent probe to study how anesthetics work. Research is great fun, but I find that it can be frustrating when I don’t have much time to devote to it. I generally have more fun these days watching my graduate students and postdocs conduct experiments in lab. When things go well, I get to see lots of good data!

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

Assuming I didn’t need to learn a new language or unusual skills to survive, I would probably take a copy of Shakespeare’s complete works, as there would be a play for every occasion — sad, funny, historical, or strange. It’s unlikely that I would bring a CD. When I’m alone, I usually enjoy the peace and quiet. If I were in exile, it’s likely I would try to keep doing whatever it was that had led to my exile!

Ivan Dmochowski is in the Department of Chemistry at The University of Pennsylvania and works on developing chemical tools for addressing long-standing problems in biology and materials science.

December 18, 2008

Top 10 Research Highlights of 2008

So, with 2008 drawing to a close, we thought we'd select our favourites from the chemistry we've covered this year. The five of us editors had two picks each, so here's our top 10 (in no particular order):

Gav
Ion transport: Testing the water
Eigen complexes, Zundel complexes, Grotthuss mechanism: there’s some great terminology related to water structure but we still don’t fully understand it! This paper was a good example of how fancy spectroscopic techniques can be used to understand just what is going on with the seriously speedy diffusion of hydroxide ions in water.

Catalytic hydrogenation: Guided by theory
The importance of heterogeneous catalysis to the chemical industry really can’t be overstated, so one of my favourites this year was this theoretical paper by Jens Nørskov and friends. They use computational methods to seek out the best (and economically viable) alternatives to expensive industry-standard hydrogenation catalysts. Watch out for a review in this area next year!

Stu
Nobel Prize 2008: Green fluorescent protein
Over the past few years GFP has been a favourite pick in the numerous 'what will win the Nobel Prize in Chemistry this year' lists. And now it has — and deservingly so. The question is, what will be the consensus pick for the next few years?

Coordination polymers: Ringing the changes
A research highlight that combines two of my favourite things — beer and football...no wait, I mean coordination polymers and Borromean rings.

Steve
Organocatalysis: Making light work of it
Most organocatalytic reactions involve typical polar reactions between one nucleophilic and one electrophilic partner. Not only is this approach radical, solving a long-standing problem in asymmetric synthesis, it was also the easiest headline I wrote all year.

Enzyme catalysis: Enantioselectivity evolved
Everyone knows that enzymes are good catalysts, but the search for the right enzyme can be a long one. I love the idea of training an enzyme to do what you want – and biasing evolution by using a clever reaction design is probably the ultimate way of achieving this.

Anne
Chirality: Handed over
Chirality can be a somewhat tricky property to introduce in materials. Here, the chirality of organic linkers is preserved and passed on to the bulk of an organosilicate material directly during the synthesis — a very elegant chirality transfer.

Molecular network: Random order
Check out these molecules that, when adsorbed onto a surface, form hexagonal ‘holes’ in a regular array regardless of how they arrange themselves. This leads to an ordered — yet aperiodic — molecular network.

Neil
Protein chemistry: Handy crystallization
The combination of painstaking chemical synthesis of both forms of the protein, followed by the conceptual leap to crystallise both of them in order to get the X-ray structure, made these two papers extremely impressive. And when you add the cool application – antifreeze proteins to help preserve donated organs — it adds up to work that made me say ‘I wish we’d published it!’

Superconductivity: The good samarium
It's solid state inorganic chemistry, it's superconductivity — I love it. This is just a sample of the 'gold rush' of work that was triggered by the pnictide superconductors.

And slightly less seriously, here are our top 10 Research Highlight headlines of the year:

Come on silene
The magnificent seven
Cage closed
The good samarium
Heterogeneous chemistry on Mars
All features great and small
Knot your usual molecules
Supersize sandwich
The 39 steps
Caught in a trap

And many thanks to Jane for copy-editing and Dipti for publishing everything for us all year!

Neil


Neil Withers (Associate Editor, Nature Chemistry)

December 17, 2008

All I want from Santa...

One year in high school I was a 'secret Santa', where I was anonymously responsible for getting presents for another person. Last year in the NPG office we had a gift exchange where people randomly got silly things and then we played an elaborate game to decide who got what. There are many kinds of these little holiday adventures, yet none to do with science. Why not?

I could imagine a lab surprising another lab by cleaning all their glassware, or the delivery of a big drum of silica with a red bow on top. What about people getting each other gilded, monogrammed pipettes? Or making up those paper coupons that are alternately endearing and/or scream out 'I didn't know what to get you' that are good for one hour of literature searching, or one extraction, or the use of the last unbroken, unscratched 50 mL RBF (if there is even such a precious, precious thing)? Perhaps graduate students could arrive to find tiny presents in their lab coat pockets from the science Santa? Maybe that only works if you leave them by the hood...

Anyway, I was thinking recently about what science presents I wanted for the holidays, and suddenly realized

"What could be better than the January issue of Nature Chemical Biology?!?"

We've got not one, but now two pages of research highlights. We've got 10 crystal structures, 8 protein blobs, and 2 mice on our table of contents. We've got single amino acids, peptides both short and long, and proteins doing all kinds of cool stuff. Not only is the issue full of goodies, but we give you a couple of other things to look forward to in the year to come.

With all this inspiration, I think it's time to look for packages of reagents that will fit on a sleigh...
Catherine (associate editor, Nature Chemical Biology)

December 16, 2008

They'd none of them be missed – why 20 amino acids and not 15?

Posted on behalf of Retread

Making DNA is metabolically expensive. 4 ATPs are consumed making adenine (and that's even when you start with 5 phosphoribosyl alpha pyrophosphate – PPRP). This is why parasites living inside cells have such small genomes. As soon as they figure out a way to get the host to do their metabolic work, they jettison the (now redundant) DNA. The leprosy organism which lives inside cells sheathing nerve processes has only two-thirds the DNA of its cousin, the tuberculosis organism. There are many similar examples and not all are bacterial.

As you know, 'the' genetic code is made of nucleotides which come in four varieties (abbreviated A, T, G, C). There are 16 possible combinations when nucleotides are taken 2 at a time, 64 combinations taken 3 at a time. 64 combinations is clearly is overkill for just 20 amino acids. So most amino acids have multiple combinations of 3 nucleotides (called codons) which code for them – these are the synonymous codons. Two amino acids (leucine, arginine) have 6 synonymous codons, 2 have none (e.g., just one codon – methionine and tryptophan), the rest fall inbetween.

If proteins contained only 15 amino acids, you could cut genome size by one-third – that's 4 billion or so ATPs/cell if the 3 other nucleotides are as expensive to make as adenine. As the late senator Dirksen used to say – a billion here, a billion there, pretty soon you're talking real money (this was in a older, happier pre-bailout time).

Why 15 and not 16 amino acids? Because you need a codon to tell the machinery when to stop – such codons were known as 'nonsense', back in the day when all the genome was thought to do was code for protein.

Look at the side chains of the 20 amino acids with your chemist's eye. Some are so similar as to be redundant. Glutamic acid and aspartic acid are chemically the same, differing only by a methylene group – get rid of one. Glutamine and asparagine are just the amides of the two acids (why they aren't called glutamide and asparamide is beyond me). Get rid of one of them. Similarly threonine and serine differ only by an extra methyl group. Not only that but the several hundred different enzymes which add phosphate to them (inappropriately called kinases) don't bother to tell them apart – get rid of one. Do we really need 4 different hydrocarbon side chains (methyl, isopropyl, sec-butyl, isobutyl)? Maddeningly sec-butyl belongs to isoleucine, and isobutyl belongs to leucine. Get rid of two of them – probably a long one and a short one. Other chemists might choose different amino acids to let go.

Removing these 5 amino acids from the total cuts the DNA required to code for them down by one-third, saving all that synthetic ATP. Of course, synonymous codons disappear in the process. Nonetheless, we should be able to build pretty decent proteins from the 15 amino acids we have left. No chemical functionality present in the original 20 has been lost.

Clearly this hasn't happened in the real world. Just why not is probably a matter of history, and an endless source of armchair speculation (like this post). Could there be a reason for all this coding redundancy, or at least could there be mechanisms to keep it in place?

I think such mechanisms exist, but you'll have to give up the protein-centric notion that all DNA does is code for protein. Even better, there is excellent recent hard experimental data to back this up. But that's the subject of the next post.

December 15, 2008

Crosspost: What element do you want for Christmas?

Pop over to the Big Nature news blog The Great Beyond to see what element people want for Christmas...there's a video too.

Personally, I'd like some helium, to keep everyone entertained with squeaky voices while we're waiting for the turkey to cook.

NChem Research Highlights: Chiral alcohols, entrapment and nanotube motors

I'm dreaming of...Research Highlights.

Making tertiary alcohols (ones without any hydrogen atoms attached to the carbon) with controlled chirality is a lot trickier than making other chiral species like secondary alcohols — those methods often rely on the difference in size between hydrogen and the other substituent. But now, using a simple method allows the choice of two achiral reagents to control which enantiomer is formed. And don't forget to check out the News and Views article that Andy sold his soul so you can read it for FREE (for a week).

Germanium is an element in the no-man's land of semi-metals between metallic and non-metallic elements, but it's still not really a metal. And non-metals have rarely been observed as dications without a lot of accompanying ligands. But now dicationic germanium has been trapped inside a cryptand cage and caught with no clothes on. Which is a great amount of effort to go to in order to let Gav use the headline Caught in a trap.

And my prayers have been answered: a paper with supplementary info movies that show what's going on. So, go and read Tim's highlight about nanocapsules shuttling up and down inside carbon nanotubes, then watch the videos.

And finally...even though we haven't published any issues yet, and won't have an impact factor until about 2011, when we're out and about we still get asked what we think Nature Chemistry's magic number will be. Who knows?? Perhaps by then Thompson ISI will be using the corrected impact factor, as suggested by our heroes over at PHD comics.

Neil


Neil Withers (Associate Editor, Nature Chemistry)

December 12, 2008

Reactions - Hilary Crichton

1. What made you want to be a chemist?

I liked to set things on fire and make pretty colours. It was also the thing that I was best at at school so it seemed sensible to continue with it.

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

That’s easy – run a coffee and cake shop. I could quite happily spend all day baking and would love to have the time to experiment with new flavour combinations and textures. I also love to meet new people and chat.

3. How can chemists best contribute to the world at large?

Chemists should continue to strive to make things that will help people, be it health, energy or environmentally related. However, I think the main thing is the people should do chemistry (and science in general) because they want to know why things happen. Essentially that is how science began and why new ideas form.

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

This is quite tricky, probably someone like Michael Faraday, Richard Feynman, Niels Bohr, Werner Heisenberg. I would also like to meet my Grandad; he died before I was born and sounds like a good bloke. His wife lived until she was 89 and was still running for buses!!

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

Around February/March 2004. I was looking at the collisional depolarisation of rotational angular momentum in OH radicals.

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

I would probably take the Bible. I am not religious but was sent to church when I was wee so have read bits. It would be nice to read the whole lot. It is very long and given the number of people who get solace from it it might help keep me sane. The CD is quite tricky. If I had to pick one it would be If You’re Feeling Sinister by Belle and Sebastian.

Hilary Crichton is an Associate Editor for Nature Materials

December 11, 2008

Free News & Views!

I’ve managed to wangle free access for everyone to a News & Views article about a chemistry paper in this week’s issue of Nature. You can access the News & Views article here, but hurry, because it’s only available for one week, starting today.

The article is written by Karl Hansen, one of the Directors of Process Chemistry at Amgen, and describes a great piece of organic methodology from Varinder Aggarwal’s group. Briefly, the work describes a simple enantioselective method for making chiral tertiary alcohols. The really cool thing about it is that both enantiomers of the target alcohol can be made easily from the same starting material, without using any fancy catalysts or weird reagents. As Hansen points out, the method should be extremely useful for medicinal chemists in particular.

This free-access thing is a bit of an experiment, so do take advantage – if it’s a success, then I should be able to persuade the powers that be to provide more News & Views articles for free in the future. The paper itself is available by subscription only; but if you are a subscriber, then you can access the paper here.

Andy


Andrew Mitchinson (Senior Editor, Nature)

December 09, 2008

The Sceptical Twitterer?

One of the most frequent questions I am asked at conferences is 'what do you do all day?' It's always hard to envision what someone else's job is like; this is probably particularly true with me because I'm outside of the 'normal' scientific careers of academia and industry. I thought one simple way to try to tell you all what my day is like would be to give you a blow-by-blow account. So, here goes! Hope it's not too boring...

8:53 - Sorting through some random notes, trying to figure out what I need to tackle first. I'm putting together an agenda for a meeting tomorrow, so that probably takes priority.

9:24 - Got distracted answering an email from someone who disagrees with a decision we made. Also, Josh just got back in the office and is telling us the news from London.

9:57 - Finished email, working on agenda.

10:26 - Finished agenda. Now I've got to send an email about a review I had sort-of commissioned and then need to read several papers.

11:00 - Sent email. Then I talked to Joanne about PubChem and what conferences we might go to next year. Really time to read papers!

11:31 - Debating the merits of a paper. Initial feeling is that sugars are cool.

11:58 - A mini-rant: If there is an article that compromises the novelty of your work, please don't wait until the final paragraph of your 18 page paper to mention it. Needless to say, I recommended rejection. Now reading a second one.

12:28 - Got an awesome review outline from an author for my upcoming focus issue. Very excited! Also had to answer some questions about proofs of an article, and read a couple of papers as possible research highlights. One is not super exciting, one has potential.

1:01 - having lunch; heading to editorial team meeting.

1:57 - lots of stuff to talk about! Now headed to QC meeting of December issue.

3:03 - QC meeting is done, and we continued the editorial meeting. We had to decide what meetings to go to next year and it's hard to pick! Now done with meetings for the day.

3:37 - Hopefully commissioned a News & Views, and did some other random things. Time flies!

4:02 - Making some notes on the review outline from earlier. Also wrote back to someone who has a cool story they want to submit to us.

4:33 - Drowning in production details. It would be better if our production team was in the same office with us.

5:04 - Looking for companies that might want to sponsor a new thing we're doing. Also reading a paper. It would go faster if I picked one instead of doing both, probably!

5:39 - Computer malfunction + working on the last form I have to prepare for that meeting tomorrow. Phew!

6:00 - Sent an email to yet another person about something they're writing for us. And, it's nearly time to go home so I can pretend to have a 'real' life. So, in terms of whether this was a typical day: today was very productive in terms of doing long-term stuff, and working on some projects, but I really didn't make much progress on the manuscripts, or get to look for referees at all. As a result, I'll take some papers home to read overnight and plan to devote much more time to our submissions tomorrow.

Pretty glamorous, huh?!

Catherine (associate editor, Nature Chemical Biology)

December 08, 2008

NChem Research Highlights: Bryostatin, dendrimers and rowing microparticles

A busy week in the Nature Chemistry office: Anne has just returned from a tour of Japanese universities, Stu is about to head off to Bath for Catalysis and Sensing for our Environment 08, Gav's already in Grenoble for ElecMol 08, Steve's visiting Harvard tomorrow and I'm off to a symposium in honour of Professor the Lord Lewis of Newnham at the Royal Society on Thursday and Friday. Phew! But we've still time to bring you a dose of Research Highlights.

Total synthesis can be mind-bogglingly difficult, so why not just go and marvel at bryostatin 16?

Dendrimers, I imagine, are probably normally a big writhing mass of chemistry, but these pyrene dendrimers sound a lot more...staid. Thanks to the stiffness of the dendron units themselves, the whole thing is pretty rigid.

Another article that really needs a movie...swimming microparticles! Although rowing is quite a good way to get your head round it. A big particle (the boat) is linked to a smaller one (the oar). They're magnetic, so a precessing magnetic field makes them rotate (errr, the rower? Bear with me!). In a bulk solvent, they'd just happily rotate, but when they're close to a surface, the viscosity gradient means that the oar 'grips' the the gloopier liquid and the particle/boat moves.

And finally...some shameless slapping of our own backs. According to this post over at Nascent, we almost totally rule! Well, we're in joint second place for the chemistry blog most linked from the blogs registered at nature.com blogs.

Thanks for linking,
Neil


Neil Withers (Associate Editor, Nature Chemistry)

December 05, 2008

Reactions - Cristina Lagunas

1. What made you want to be a chemist?

A fascination for discovering new things. I remember watching, at an early age, an old movie about Marie Curie, and I was hooked by her passion for research. I had a very good chemistry teacher in secondary school and I really enjoyed learning about the structure of the atom and MO theory. As an undergraduate, I enjoyed the inorganic and coordination chemistry labs and my supervisors further inspired me to do research.

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

I’d probably had done a maths degree, which was the other subject I loved in secondary school. With a maths degree, I think I would still have pursued an academic career.

3. How can chemists best contribute to the world at large?

Energy and the environment are our two very challenging issues at the moment. Chemistry and chemists are central to both.

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

Given my answer to question 1, it’ll have to be Marie Curie. She was a truly remarkable woman at a time when women weren’t even allowed to vote: two Nobel prizes (Physics, shared with husband Pierre and H. Becquerel, in 1903; and Chemistry in 1911) for her research on radiation and the discovery of elements such as radium and polonium; first female professor at the Sorbonne. The Curies believed in sharing scientific knowledge freely and never patented anything; and they warned about the danger of radioactive substances in the wrong hands. Marie relentlessly promoted the use of x-rays in medicine, but overlooked the dangers of radioactivity to health. I would like to know if she had done anything different, given what we know today.

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

I haven’t done a full experiment from beginning to end for three or four years, but I do get into the lab and ‘help’ my students with their work now and then. The last time: a couple of weeks ago, helping a new PhD student to set up a reaction with nBuLi.

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

I think I’ll take the Spanish classic El ingenioso hidalgo Don Quijote de la Mancha (or Don Quijote for short), by Cervantes. It has tragedy, comedy and adventure in equal quantities; and I haven’t actually read it properly (only in ‘bits’ in secondary school). A desert island will be a good place to cross it from the ‘to read’ books. Besides, it’s set in my native region of La Mancha, so it’ll remind me of home. As for a CD, I may take Unplugged by Eric Clapton. I don’t seem to get tired of listening to the songs.

Cristina Lagunas is in the School of Chemistry and Chemical Engineering at Queen’s University Belfast, and works on luminescent metal complexes, in particular gold, and on molecular sensors. She is also involved in multidisciplinary research in electrochemistry and catalysis in ionic liquids.

December 03, 2008

Materials Girl: Old school, new school

Posted on behalf of Materials Girl

Fourth year as an undergrad reminds me of being a high-school senior, only more complicated with the wider range of post-graduation options. Still, the ultimate goal generally remains the same: to secure a source of income while pursuing personal interests. (This poses an interesting question regarding why people even go to college – to get a better job, for the pure joy of learning, because it’s expected, to avoid the real world? Aside from the last part, I fell in the category of “all of the above”).

In the high school days, seniors were expected to spend their time applying to colleges, taking standardized tests (ugh), battling senioritis, and trying not stress out over academics and the future. Now, it seems that continuing education past a Bachelor’s is less expected outside of scientific circles – even to the point of being looked down on by uninformed individuals. “You’re graduating already?! Are you going to work or do grad school?” is posed almost as an afterthought. Apparently, old, moldy college students aren’t interesting to the general public. They’re interested in what school I attend (meaning the accompanying sports teams), and perhaps my major. Upon hearing, “chemistry and materials science” I am often written off as just another nerd or pre-med. Nevermind the organic concentration!

The hardships of graduate school and research go tragically unnoticed by the masses. However, what really matters is that we exist, we do good work, we make a difference, and we are happy. Or so I tell myself...

December 01, 2008

NChem Research Highlights: Twisting, diversity and order from disorder

Monday = Research Highlights.

What actually happens when molecules isomerise? How do the atoms really move? I've never really thought about how little I know about it, so it was interesting to read how stilbene (two benzene rings linked by double-bonded carbon atoms) twists as it changes from cis to trans. It's just a shame there's no movie with the article!

As I'm sure many of you know (and as more organic colleagues have told me), making complicated organic molecules can, apparently, be a rather time-consuming and tricky business. Removing tongue from cheek, being able to sample as large a portion of 'chemical space' as possible is crucially important in drug discovery. Now, using only 6 simple reactions (hence Steve's 'Six degrees of separation' headline) a team at Leeds have been able to generate over 80 different scaffolds.

Molecules adsorbed on a surface are unlikely to align themselves in periodic, crystalline array. But using a molecule that can bond in defined ways resulted in a hexagonal 'hole' appearing no matter how the molecules themselves were arranged. This resulted in the holes forming an ordered array while the actual molecules had no order.

I'm afraid the chemistry blogosphere/world of news has run dry for the "And finally..." section this week, so you'll have to put up with this shocking joke:
Why do white bears dissolve in water?
Because they're polar.

I do apologise - any better ones gratefully received!

Neil


Neil Withers (Associate Editor, Nature Chemistry)

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