Reactions – Loh Kian Ping

Loh Kian Ping is at the Department of Chemistry, National University of Singapore, and works on the synthesis and modification of functional carbon materials for advanced technological applications.

1. What made you want to be a chemist?

First of all, the study of chemistry as a subject interests me because it is immediately relevant in many ways. There seems to be a set of intuitively easy to understand rules behind the game that chemists play. Chemists explain how the universe operates in a language that is appealing to the pragmatic mind. I believe if the human civilization is destroyed by some natural disasters and need to be rebuilt, the chemists will be the most needed group of people to put the basic infrastructure of human civilization back to place, which is why the first scientist or magician on earth is the alchemist.

I am also inspired by the positive image of the creator in the chemist. A chemist is basically a creator, a cook, an artist and a crafsman combined into one. He can create new molecules from simple building blocks, and some of these molecules can reduce pain and save life, others can be transformed into useful things like plastics and clothings.

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

I would be a lawyer. I think I can be persuasive, since the same set of presentation skills and indirect thinking is needed. As a lawyer I probably would make more money than I make now, too.

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

I am working on how to create geometrically well-defined nanostructures on an atomically-thin sheet of carbon. An atomically-thin sheet of carbon, called graphene, is a two-dimensional material. My team is working on how to create nanoscale periodic corrugations on this material. This has implication for changing the energy gap of graphene as well as increasing its surface area when used as a charge collection platform.

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

I like to have dinner with Dmitri Mendeleev who wrote the volume “Principles of Chemistry” and who was credited with the discovery of periodic table. I am curious what is the thinking process going on in his mind that led him to the discovery, given the very limited information available at that time.

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

I have to confess that now I am a laptop or PC chemist, directing the reactions from a computer. The last time I did an experiment in the laboratory was one year ago when I helped my postdoctoral fellow fix up a furnace needed for the chemical vapor deposition of graphene.

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

I would take with me my diary to write my thoughts down and to record what I have for dinner on that deserted island – like grilled gecko or crab carpacio. For the music album, that would be my favourite oldies like the Carpenters.

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

I would recommend Professor Klaus Mullen, for his wonderful work on the bottom-up synthesis of graphene from designer molecules. This is a good example of the ingenuity of the chemists because they can make almost anything and everything using bottom-up strategy.

Blogroll: What’s in a name?

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

Named reactions represent a fascinating subsection of chemistry, so we eagerly awaited the answers to Derek Lowe’s ‘Name Reactions You’ve Never Run’ blogpost. Lowe starts things off with the confession of a colleague who, despite years of experience, has never run a Diels–Alder reaction and continues with his own admission “I’ve never done a straight aldol condensation”, nor a Fischer indole synthesis. The comments thread was soon filled with people happily admitting which famous reactions have passed them by.

Who could fail to click on a blogpost with the title ‘Is earwax an organocatalyst?’. We certainly couldn’t and were rewarded with an informative post on the Chemistry Blog by Chemjobber, picking up on a Newscripts item by Steve Ritter in Chemical and Engineering News (89, 56; 2011). Way back in 1960 — in the days before blogs — budding chemist Charles Johnson discovered that his earwax accelerated the process of making colourful lake pigments. In his later life, as an undergraduate student, Johnson further found that earwax worked as a catalyst to make trans-stilbene, “although his professor didn’t seem impressed.” Chemjobber reminds us of Dylan Stiles’s blogpost on the now-defunct Tenderbutton in which he took a TLC of his earwax, which Chemjobber describes as “one of the initial triumphs of the chemblogosphere”. Who knew such an unpleasant substance was so interesting?

And finally… Mary Carmichael got so fed up with seeing marketing spiel that uses the phrase ‘chemical-free’ to describe products that she started a blog, ‘F No, “Chemical Free!”’. Among the products named and shamed so far are “chemical free sunblock and bug spray” and even a chemistry set that offers “60 fun activities with no chemicals”. That doesn’t sound like much fun to us.

The art of abstracts

[This post is based on the editorial in the August 2011 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.]

An abridged version of the editorial is usually featured in these posts, but I thought I’d tell a little of the story behind the story in this case (and after you’ve read this, you can go and read the editorial!). The team here at Nature Chemistry follow the literature predominantly through RSS feeds and so we’re quick to see (and comment on) graphical abstracts that catch the eye – particularly those that confuse and/or amuse rather than instruct.

I’ve also seen a few blog posts here and there in the last year or so lauding the introduction of this wonderful new publishing innovation (I’m paraphrasing here, but that was the general gist). Now, graphical abstracts might be new in some fields, but they’ve been in chemistry journals for quite some time. And this got me thinking — just how long have they been around and who started the trend? Now, the internet is a marvellous thing, but I thought I might find out more if I went to a real chemistry library at a university; one with real journals and real books.

I’m now going to sound like I am very old to some of you, but e-mail only really became a popular and widespread tool during my undergraduate years. Looking something up in the scientific literature meant leaving the chemistry department, walking to the library in the middle of the campus (remembering to take my photocopying card with me) and flipping through bound volumes of journals. During my PhD, more and more scientific literature found its way on to the web, but trips to the library were still necessary. So, fondly reminiscing about my student days, I set off to the chemistry library at the University of Cambridge (with thanks to Oren for arranging access).

I spent a happy morning browsing row upon row of nicely bound journals and occasionally lifting one from its home on a shelf. There were quite a few other people in the library, but in the two or three hours I was there, I don’t recall seeing anyone else venture over to the journals. Students appeared to be studying or surfing the web to find the objects of their desire — scientific journals or otherwise. I had a fairly complete set of the chemistry literature all to myself, and I could browse — sure, I was doing some targeted searching, but I was also browsing… looking for nothing in particular other than things that happened to catch my eye. (Such as this article by Ian Rae from New J. Chem. in 1990 (vol. 14, pp. 3–4): ‘Why can’t we have element Q?’ — which, incidentally, I can’t find online anywhere…).

Anyway, it was nice to be back in a library — the smell and feel of the books is something you obviously don’t get from searching through the literature online, and that’s a shame (well, it is for me — for all you youngsters out there who don’t even know where your university library is, you probably wouldn’t miss what you’ve never experienced). The chronology of the appearance of graphical abstracts in a broader range of journals is something that didn’t quite make it into the editorial, so here it is for those of you who are interested:

As far as I can tell, Angewandte Chemie was first (in 1976!) and then Tetrahedron Letters joined the party in 1986 (some of you reading this still might not have been born by this point…). Tetrahedron itself followed suit in 1990. The first RSC journal to include graphical abstracts was not Chem. Commun., but J. Chem. Soc., Perkin Trans. 2 in 1993. Chem. Commun. did start soon after in mid 1994. The ACS was a little late to the game and graphical abstracts did not make their debut in JACS until 2002. The trail had, nonetheless, already been blazed by JOC in 1996 and Org. Lett. from its inception in 1999. After a bit more sleuthing, however, I did discover that from 1992 onwards, Inorg. Chem. included graphical abstracts for some of its Communications. It took a while for the physical chemists to join in (at ACS journals at least) with J. Phys. Chem. A and B getting graphical in 2006. If I’m wrong about any of this, or you have anything else interesting you wish to share about graphical abstracts, then please do comment.

So, the point of the editorial… I do believe that graphical abstracts do bring back some of the browsability that we’ve lost by moving away from paper journals. Not all of it, but a little flavour at least. We’ve also taken the opportunity to point out in the editorial what we think makes a good graphical abstract — something every publishing chemist should take a little time to think about.

You can read the editorial here (registration is free).

Stuart

Stuart Cantrill (Chief Editor, Nature Chemistry)

Reactions – Ed Constable

Edwin (Ed) Constable works in the Department of Chemistry at the University of Basel, and works on applied coordination and supramolecular chemistry.

1. What made you want to be a chemist?

Honestly, it was the gift of a chemistry set when I was 14. Although I had inspirational teachers, chemistry had never clicked with me until I could play with chemicals on my own. Almost certainly not an aproved strategy today! I went from the bottom of the class to the top in the space of one term. Before that, I wanted to be a writer or a historian.

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

Probably a wildlife photographer or science journalist. I have always felt that communication of what we are doing, why we are doing it and why it is important is an essential and often underrated part of our job. And wildlife photography? Because it is fun.

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

Our primary work at present concentrates upon the major problem facing mankind in the upcoming hundred years – namely the development of sustainable and environmentally acceptable energy policies. We have large programmes in the development of photovoltaic cells, specifically dye sensitzed solar cells and OLED and light emitting electrochemical cells for efficient next generation lighting. Our aim is to replace scarce and expensive elements such as ruthenium and iridium by earth-abundant first row transition metals.

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

Another good question. I thought long and hard about this and finally decided on Paracelsus (Philippus Aureolus Theophrastus Bombastus von Hohenheim). Not only was he a predecessor of mine at the University of Basel, but he was active at the cusp between alchemy, magic and science. He is arguably one of the first medicinal chemists and I would like to know what drove him. He was also apparently a very difficult person, so it would be an interesting dinner.

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

A very quick and dirty preparation of [Ru(dmso)4Cl2] about six months ago. Simply heating RuCl3.3H2O in dmso and collecting the crystals!

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

Oh dear, I never was one for Desert Island Disks! The book would need to be one that I could read repeatedly and always find something new. Disregarding the Bible and Shakespeare which are always present on desert islands according to my sources, I would chose the complete works of “Saki” ( H.H. Munro). He is a wickedly funny and often cruel writer of short stories from the Edwardian period who was one of the many talents lost in the global conflict 1914-1918. For music, it is much more difficult. Certainly nothing classical. I guess I am not allowed my iPod, so the choice ends up between Leonard Cohen, Dory Previn, Al Stewart, The Smiths and Pink Floyd. Very difficult to decide, but on balance it would be Pink Floyd “The Wall”.

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

Achim Mueller. I know Achim well and suspect that his answers would provide a unique insight to a unique mind!

A chemistry reference resolver

Editor’s note: The following is posted on behalf of Alex Zhurakovskyi, who introduces us to his search interface for chemistry publications.


Chemistry is fast-paced nowadays. We use online databases to do sub-structure searches, download NMR spectra in just a few clicks, and it no longer takes a whole day in the library to get just a couple of papers. Publishing houses, for the most part, did a tremendous job of scanning and publishing their archives on the web. But finding and downloading a paper for a given citation can still be a cumbersome and time-consuming task.

First, one might google the website of the corresponding journal (although many of us keep numerous bookmarks or have a dedicated ‘links’ page on a group website). Then, one would look for a citation-based search form — and hopefully this is not buried somewhere on the page. If the volume number is absent, screening through the whole archive may be necessary. Depending on a journal, all of this may take quite a while — sometimes longer that the actual reading!

So, I asked myself if I could simplify this process and make it faster? I envisioned a system that would accept a citation in any format (such as the traditional ‘J. Org. Chem., 2010, 75, 4657’, my favourite type of citation ‘joc 2010 4657’, or a simple DOI) and redirect the user to the paper — in a single click. And also be capable of resolving references where only the year is provided and the volume number is absent.

The alpha version of the Organic Chemistry Reference Resolver was developed in early 2010 for private use. Later on, the project was made available on the web at https://chemsearch.kovsky.net under the Creative Commons license.

In addition to the web-interface I have developed a couple of browser extensions (Safari/Chrome/Firefox 3) as well as a tiny widget that can be added to any webpage. Interestingly, it is the widgets on the Japanese chemistry portals Chem-Station and ChemPort that provide two thirds of the users.

In the future, I plan to extend the scope of supported publications, upgrade the extensions, and implement the year search for all titles (now it works with about 70% of journals).

Element of the month: Selenium stories

It was while making sulfuric acid that Jöns Jacob Berzelius — ‘the father of Swedish chemistry’ — noticed a red residue which he first took for tellurium, as Russell Boyd from Dalhousie University notes in this month’s ‘in your element’ article (subscription required). A more meticulous investigation, however, revealed that the residue displayed different properties, resembling those of sulfur. The new element fell into place between tellurium and sulfur in the chalcogen family of the periodic table, and Berzelius named it selenium (after the Greek word for Moon) owing to its similarity with tellurium (named after the Latin word for Earth).

Although often eclipsed by sulfur in textbooks, selenium has a reactivity of its own. I particularly like the fact that its grey allotrope, the most stable form, conducts electricity better in the light than in the dark, and converts electric current from AC to DC — properties which have not gone unnoticed in the fabrication of photovoltaic cells and rectifiers, respectively. Its red tint also went on to account for a worldwide application: selenium dioxide (which adopts a one-dimensional chain structure) imparts vibrant reds and pinks to glass.

It was only much, much later (140 years after its discovery) that the role of selenium in biological systems was identified. It replaces sulfur in some proteins, which in recent years have been shown to help the prevention of cancer, by hindering radical attacks on cells or possibly also by slowing tumour growth. It is introduced in the body by ingestion — dietary recommendations however follow a fine line between too little and too much, both with potentially very serious consequences. While ingesting too little can lead to a weakened immune system or heart problems, selenium poisoning comes with unpleasant skin or breath odour side effects, can affect mental awareness, and can even be life-threatening at high doses. Around 55 micrograms per day sounds just right — I was very surprised to read that it is contained in a single dried Brazil nut!

Have a look at the article to find out more, but I wouldn’t recommend daily Brazil nut fests.

Anne

Anne Pichon (Associate Editor, Nature Chemistry)

Reactions – Panče Naumov

Panče Naumov is at the Department of Material and Life Science at Osaka University, Japan, holds a position from the external staff of Ss Cyril and Methodius University in Macedonia, works on solid-state chemistry and photochemistry, and is particularly interested in unstable and “exotic” molecular species.

1. What made you want to be a chemist?

More than anything else, it was pure and simple curiosity that initially led me to chemistry. As a nerdy kid, this raw drive to find out about things compelled me to spend countless hours in a makeshift lab that I created out of my family’s storehouse. And throughout my entire career, my curiosity has never really waned. It grew stronger during my school days, when I managed the school lab, and remains just as strong even to this day in my very own laboratory. One particular quote by E. Einstein has always resonated with me ― “Curiosity has its own reason for existing.” To that I would add, “…and it will never cease to exist.”

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

I would most likely be an astronomer. As broad as the fields of biology, chemistry, and physics are, we can only begin to explore one side of the spectrum of infinity. We examine organisms, cells, tissues, molecules, atoms, quarks, and even tinier “particles”. However, there is a whole other side that is equally exciting and technically challenging. If I were an astronomer, the possibilities to study planets, stars, galaxies, galaxy clusters, and certainly much more beyond that would quite literally be endless.

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

Throughout history, the problems that our world has had to deal with have been numerous and varied. However, it has become increasingly clear that our society today is faced with these three major problems: security, the environment, and energy. In my research group, we are interested in the molecular mechanisms underlying the processes of conversion among the light, chemical, thermal, and mechanical energies in the solid state. By elucidating the details of these mechanisms, we hope to arrive at a deeper understanding of the structural factors that govern energy transformation and improve its efficacy in the future.

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

Actually, I would love to break bread with two historical figures. Having both Alexander the Great and Nikola Tesla at the dinner table would make for an exciting and incredibly stimulating evening. At the mere age of 30, Alexander the Great succeeded in uniting most of the known world at that time with his visionary approach. The wisdom that he displayed beyond his years and beyond his time has made our Macedonian nation very proud. In my view, Alexander the Great’s strategy of “conquer and unite” instead of “divide and conquer” was really a progressive concept not unlike the ones seen in contemporary unions such as the United States and the European Union. Perhaps along with Thomas Edison, Nikola Tesla should have been awarded the Nobel Prize. If in 1893 Tesla could demonstrate a wireless energy transfer, there is no doubt in my mind that he would be able to make a profound contribution to our society’s endeavors today and even to our future undertakings, such as teleportation. He could change the world as we know it. I’d love to ask him how.

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

A couple of months ago, I was trying to crystallize an important antiviral compound. Unfortunately, being a group leader has prevented me from dedicating the time necessary to be directly involved in experiments of late.

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

I would undoubtedly take “The Little Prince,” a book that amazes me with its simplicity of narration. I love it now, but I haven’t always held it in such high esteem. When I was 7, I hated it. At 14, I still considered it a very ho-hum read. Then, at 21, something clicked and it became my favorite book. Eventually, at 28, I made sure most of my friends had a copy. If you don’t already have one, I highly recommend it.

As far as music is concerned, I would need something to soothe the soul. The Best of Nina Simone would probably do the trick with her “blue” moments under the “blue” skies. But, how would I play it on a deserted island? I guess the album could double as a fan or placemat!

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

Bart E. Kahr from New York University in New York would make an excellent choice for the innovative methods he uses in furthering our knowledge of solid state chemistry and supramolecular chemistry. I find his work enlightening and timeless.

Speaking Frankly: Critically acclaimed

Frank Leibfarth is a graduate student trying to make his way through the academic maze. Find him contributing to the Sceptical Chymist or continue the conversation on Twitter @Frank_Leibfarth.


“If we charged a dollar per mistake, I’d be a lot richer after this presentation.” This was my advisor’s comment after my first group meeting presentation in graduate school. This did not instill confidence, but I didn’t feel too bad — mostly because of prior experience being the subject of criticism. I was a kicker on my college football team (the American kind), the one position where the game stops and everyone watches you succeed or fail. In a weird sort of way, this was somewhat of a relief. I always knew where I stood and I got used to taking criticism, sometimes with a not–so-constructive delivery.

After this, transitioning into the scientific arena was easy; everyone seemed so encouraging and uplifting when giving me suggestions. As I have progressed, however, I have not been satisfied. I want to be a better scientist (sometimes I must admit that too much of my self-worth is tied up in the discipline) and I want others to help me get there. Unfortunately, I have been intermittently frustrated with the congeniality of my elders. At times, I have specifically asked for criticism and still do not receive it.

Criticism is a necessary and inherent part of the growth and development of scientists. In fact, we have a number of built-in mechanisms for such criticisms, including the graduate qualifying exam, thesis defense, paper reviews, and grant proposals. Academia takes this mechanism to an extreme, with tenure being the constructive and/or destructive criticism that culminates in either ultimate job security or unemployment. From my point of view, the system seems set up to work well, with chances to evaluate and improve at many stages along the way.

In my experience, however, the process routinely breaks down when people don’t know how to properly give or take criticism. Further complicating matters, the simultaneous competitive and creative nature of our discipline makes criticism inherently subjective, leading to a sometimes under- or over indulgence in these decisive remarks. Lastly, in our international field, we always need to consider the approaches of different cultures toward criticism.

So how do we balance the difficulty in giving criticism with its necessity to our discipline? First, we must always remember that providing good constructive criticism takes effort. Whether reviewing a paper or sitting on a thesis committee, active engagement and significant time are required. More important, however, is an understanding of the intimate link between empathy and criticism. The scientific system is designed to improve our collective experience by improving the quality of our individual members. So be critical! Make my generation into great, thick-skinned scientists! But remember we all have our own insecurities and doubts, so show us the human side of science every once in a while.

Reactions – Wilhelm Huck

Wilhelm Huck is at the Institute for Molecules and Materials at the Radboud University Nijmegen in the Netherlands and works on picoliter droplets that can be used as artificial cells to study the influence that the crowded environment commonly found in living cells has on the ‘chemistry of life’.

1. What made you want to be a chemist?

I was fascinated by the way chemistry could present a molecular picture of how our body works. At the same time, I grew up next to one of the largest chemical sites in the Netherlands (DSM) and saw that this molecular picture can also be applied to the synthetic world around us.

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

Perhaps it would be fun to be a banker for a while. It can’t be that difficult, and if I turn out to be any good, I could go back to chemistry and wouldn’t have to write any grant proposals any more.

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

I just started on a very new topic in my new lab at the Radboud University Nijmegen. I think that at a fundamental level, we don’t understand how a cell functions as a chemical reactor. We might have a complete ‘parts list’ and know where everything goes, but we don’t know much about how coupled chemical reactions behave in the crowded, stochastic environment in the interior of the cell. Using living cells is extremely fruitful, but will not allow us to retrieve kinetic and thermodynamic data because we can’t dilute or heat the cells. Therefore, I want to use picoliter droplets in microfluidic devices as artificial cells that can contain the machinery required to transcribe and translate DNA into RNA into proteins, and follow these processes with physical organic chemistry techniques.

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

Fred Sanger. I would like to know how he conceived his strategies to tackle the daunting projects he worked on. In many cases, his chemistry is so deceivingly simple but works so amazingly well. He must be the most naturally gifted chemist ever.

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

I generally need someone to help me…. but we are currently building a new set-up to sort single cells in droplets and occasionally I help aligning the lasers…

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

Difficult question. Assuming I will be marooned for a long time, would I really like to read that one book over and over again? Perhaps it will give me time to finally read the Molecular Biology of the Cell. It is a gripping read!

As for the music: I can’t concentrate when listening to music. The background noise of the ocean will be fine.

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

Bartosz Grzybowski. He is working on some really clever chemistry, but most importantly, I would like to read what historical figure he would like to have dinner with.

ICCOSS XX: Growing crystals in all shapes -and sizes

All good things come to an end… Among the many, and varied, aspects discussed at ICCOSS over the past few days, I wanted to bring your attention to halogen–halogen bonding, which seems to be becoming quite popular. When a halogen atom engages in such a bond, its charge distribution changes a little, leading to a ‘polar flattening’ of the atom. The more electronegative side of one atom naturally engages in a halogen–halogen bond with what has become the more electropositive side of the other. Can these interactions be relied on to assemble building blocks? Can they be tuned in a controllable manner by judicious choice of the halogen?

But the good old hydrogen bond was far from being left out. I enjoyed E. Arunan’s presentation about giving atoms a hydrogen bond radius. After all, covalent, ionic or van der Waals interactions have their covalent, ionic or van der Waals radii counterparts, so although by no means easy it may well be possible to do that for the hydrogen bond too.

Another exciting feature of the solid state is chirality – which turns out to be a lot more widespread that one might think. Bart Kahr had some surprising numbers for us: 8% of organic compounds naturally crystallise in a helical form, and about 25% can be made to do so! He showed a very nice movie of a crystal growing helically — but with an optical axis that moves during the growth process: twisting occurs at the tip, and at the same time the bulk untwists. This, he suggested, is probably associated with strains and stresses that are caused by the presence of an impurity.

From a theoretical perspective, R. Ramasesha showed us how he goes about modelling molecular materials for electronic applications – in a JACS paper from 1911 (very possibly the oldest paper cited at the conference) Moore and McCoy wrote that “it is possible to prepare composite metallic substances from non-metallic constituent elements”. This is exactly what organic electronics are.

But I’m not going to list all the topics discussed. Why not come and see for yourself at the next ICCOSS, held in Cardiff in July 2013!

I did want to mention the presentation by Hitoshi Kanazawa, Professor at Fukushima University, about 60 km from the Daichi nuclear power plant, who reported on the situation and how he and his group went around measuring radioactivity after the accident (this is not easy, as the values measured depend on where exactly you take the measurement, how far above the ground, the winds at that moment and so on). He also tried to find a way to rinse the radioisotopes but all attempts have so far remained unsuccessful. As we know, this accident has been a disaster, and sadly cleaning up will take for ever.

Hitoshi Kanazawa also had a very interesting poster – but I’ll refrain from telling you all about it, as the results are unpublished. I will only say that admiring some sample materials that he’d brought involved a syringe and a band aid, which certainly made for an enhanced poster experience.

And finally… for all of you out there who just love pretty crystals – I know it’s not just me – I have good news: our Ali Baba’s cave does exist. It is in Chihuahua State, Mexico – aptly named the Crystal Cave – connected to the NAICA mines. Dario Braga showed striking pictures throughout his presentation – these caves shelter crystals as big as trees! How did they form? You can find out at the website of the team of scientists and explorers who are studying – and protecting – these amazing crystals.

Anne

Anne Pichon (Associate Editor, Nature Chemistry)