A Prize for Crossing Boundaries

English
 
skeletal proteins prgressively constrict an artificial membrane
 
 

 

 

 

 

 

 

 

 

 

A doctoral student with a degree in physics, who conducts research on biological systems in the Faculty of Chemistry, has received an award given by the Faculty of Mathematics. To Roie Shlomovitz, a student in the group of Prof. Nir Gov of the Chemical Physics Department and the 2010 recipient of the Lee A. Segel Memorial Prize in Theoretical Biology, this makes perfect sense. Prof. Segel, a member of the Weizmann Institute’s Mathematics and Computer Science Faculty for many years who passed away in 2005, was one of the first to cross the boundaries between the disciplines of mathematics and the life sciences, showing that mathematics could be used to describe the dynamics of biological systems and teaching biologists to think “mathematically.” “My work fits right in with Segel’s approach,” says Shlomovitz.

Shlomovitz and Gov investigate proteins that form the cell’s internal skeleton. These proteins – actin and myosin – make up the fibers that enable our muscles to contract and are involved in cell movement and cell division. When a cell moves, actin filaments gather on the leading side, forming a bulge that propels the cell onward. In cell division, actin and myosin proteins create a ring encircling the cell’s midriff, squeezing the membrane tightly and pinching it in two.

What causes these proteins to push the cell membrane outward in one case and constrict it in another? How do they “know” when and where to apply pressure? To address such questions, Shlomovitz and Gov observe what happens to these proteins in cells, turn the data into mathematical models and, finally, test the predictions of their models in such biological systems as yeast. According to their model, actin and myosin proteins get their directions from the shapes of molecules in the cell’s membrane. When the cell is about to move, the membrane points the way by exaggerating its outward curve on one side. The convex membrane molecules “invite” the actin to gather round; large amounts of these molecules and the actin flock to the site to drive the edge forward. In the early stages of cell division, on the other hand, the membrane’s center takes on an inward curve. Investigating bacterial proteins, the researchers found that concave curves attract these proteins, as well: A circular network of actin and myosin marks the division line.

The mathematical model they developed borrowed an equation from physics that describes the free energy of a system. Using this equation, they calculated the distribution of proteins in the membrane and revealed how this distribution relies on the membrane’s shape. The researchers showed exactly how the bowed segment induces the proteins to encircle the membrane right at the center, how the growing inward bend of the membrane continuously attracts more proteins to the spot to increase the constriction, and how the distance between one protein and the next determines whether they’ll become a part of the tightening band or form separate rings.

Their model not only predicted the behavior of these proteins on artificial membrane bulges and indents; an experimental group in Taiwan found it could also explain the wavy shapes of living cell membranes. Shlomovitz: “We describe the complex biological processes occurring within a single cell by constructing chemical and physical models. Mathematics is the ‘language’ we use to analyze them.”


Prof. Nir Gov’s research is supported by the Helen and Milton A. Kimmelman Center for Biomolecular Structure and Assembly.

 
Distribution of skeletal proteins in an artificial membrane resembling a long bacteria: The spontaneous curvature of the proteins (purple) drives them to move together to form rings that coalesce, increasingly constricting the membrane
Chemistry
English

Local Color

English
Prof. Valeri Krongauz and his team. self-tinting glasses in all colors
 
 

 

Prof. Valeri Krongauz is not content with seeing life only through rose-tinted glasses. His research has made it possible to manufacture self-tinting eyeglasses that, upon exposure to the sun, darken and assume any color of the spectrum, from yellow to red to blue.
 
Krongauz, a professor emeritus in the Weizmann Institute’s Organic Chemistry Department, is one of the world’s leading experts on organic photochromic materials – carbon-based substances that change color when exposed to bright light. One of his inventions has led to the establishment of Chromtech Ltd., a company in the Rabin Science Park adjacent to the Institute that sells photochromic materials to manufacturers of self-tinting eyeglasses.
 
Due to the complexity and the costs involved in making self-tinting plastic lenses, only a handful of large companies worldwide possess the necessary technology. Other lens manufacturers – along with manufacturers of self-tinting films for car windows – can now purchase self-tinting material from Chromtech in powder form.
 
A major advantage of Chromtech’s photochromic materials is that, thanks to their intense tinting ability, they can be either dissolved within the plastic lens or used as a component of a thin coating. The coating, which is stable and highly sensitive, can be easily applied to the surface of any plastic lens. Its darkening results from a relatively minor molecular event: A photochromic structure changes its color when it absorbs a photon of light, which breaks just one of its chemical bonds; once the light disappears, the bond bounces back into place and the structure returns to its original color.
 
Organic photochromic materials were discovered at the Weizmann Institute in 1952. At the height of the Cold War, the substances attracted the attention of Soviet scientists, who sought to use them for making protective goggles against the blinding radiation emitted after the explosion of an atomic bomb. Krongauz, who worked at the time in a large physical chemistry institute in Moscow, stayed clear of the military research because, like many other Soviet Jews, he was concerned that knowledge of military secrets might later prevent him from leaving the country. Besides, he was drawn to basic research, and he focused on fundamental studies of photochromic materials, which, apart from posing interesting scientific questions, attracted him by their aesthetic beauty.
 
After immigrating to Israel and joining the Weizmann Institute in 1976, he made groundbreaking contributions to the theory of photochromism and other areas of organic chemistry, and conducted pioneering research in an area today known as nanoscience. One of his applied projects led to the establishment of Chromtech, which Krongauz, now its chief technology officer, founded in 1999 together with Amram Masad, the company’s president and CEO, under a license from Weizmann’s Yeda Research and Development Co. Ltd.
 
Chromtech today employs half a dozen chemists, all from Russia and all holding Ph.D. degrees. One of the company’s potential future projects is to develop self-tinting intraocular lenses, the implants inserted during eye surgery when the eye’s natural lens is clouded by a cataract. Another promising development is the plasma technology for applying a very thin layer of the self-tinting material as a vapor under vacuum conditions. Chromtech’s sales have been growing steadily over the past few years and seem likely to continue to grow – a good reason for optimism, even without wearing rose-tinted glasses.
 
Amram Masad, Dr. Boris Perlmutter, Dr. Alexander Shif, Prof. Valeri Krongauz and Drs. Judith Ratner, Lev Pinkin and Dmitry Fridland. Bright future
Chemistry
English

The First Molecular Keypad Lock

English
 
Molecular keypad works on chemical reactions
 
 
 
 
 
 
 
 
 
 

 
Keypad locks, such as those for preventing auto theft, allow an action to take place only when the right “password” is entered: a series of numbers punched in a pre-set sequence. Now a team of scientists at the Weizmann Institute of Science has created a molecule that can function as an ultra-miniaturized version of a keypad locking mechanism. Their work appeared in the Journal of the American Chemical Society.
 
The molecule, synthesized in the lab of Prof. Abraham Shanzer of the Organic Chemistry Department, is composed of two small linked units, or fluorescent probes, separated by a molecular chain to which iron can bind. One of these probes can shine a bright fluorescent blue and the other a fluorescent green, but only if the surrounding conditions are right. Instead of the electric pulses of an electronic keypad, the molecular keypad inputs consist of iron ions, acids, bases and ultraviolet light. Shanzer and his group – which included Drs. David Margulies, Galina Melman and Clifford Felder – were thus able to produce a molecule-size device that lights up only when the correct chemical “passwords” are introduced. “It’s just like a tiny ATM banking machine,” says Shanzer.
 
He believes this molecular keypad lock – the first of its kind – will lead to new ideas and inventions in such areas as information security: “Faster and more powerful molecular locks could serve as the smallest ID tags, providing the ultimate defense against forgery.” In the future, molecular keypads might also prove valuable in designing “smart” diagnostic equipment to detect the release of biological molecules or disease-indicative changes in the body.
 
Prof. Abraham Shanzer’s research is supported by the Nella and Leon Benoziyo Center for Neurological Diseases; the J & R Center for Scientific Research; the Helen and Martin Kimmel Center for Molecular Design; the Schmidt Minerva Center for Supramolecular Architectures; and Mr. and Mrs. Mordechai Glikson, Israel. Prof. Shanzer is the incumbent of the Siegfried and Irma Ullmann Professorial Chair.
 A certain sequence of letters, EBU, creates chemical conditions in which an iron atom disconnects itself from an organic molecule (on the right), activating it and causing it to emit green fluorescent light. The sequence EUB leads to the emission of blue light. Other sequences of letters do not cause light emission
Chemistry
English

Live Wire

English

Evaporation pond bacteria use sunlight for energy

 

 
Nature may be the ultimate designer, using evolution to precisely engineer each biological component to fit a unique function. So the discovery by a team of Weizmann Institute scientists that a protein in a cell wall excels at a function it apparently never performs in living organisms - conducting electricity - was as surprising as finding that hooking up a keyboard could turn a washing machine into a computer.
 
Prof. Mordechai Sheves, Dean of the Institute's Faculty of Chemistry, Prof. David Cahen of the Materials and Interfaces department, and Drs. Yongdong Jin and Noga Friedman of the Organic Chemistry Department, made their discovery in a series of experiments on a membrane protein isolated from a salt-water microorganism that, like plants, uses sunlight for energy. This protein, known as bacteriorhodopsin (or bR for short), captures the sunlight, which is converted inside the cell to chemical energy for storage. When sunlight hits the protein, protons are ejected and pumped across the cell membrane to energy conversion machinery on the other side. Our eyes contain similar proteins, rhodopsins, which also capture light but convert it to optic nerve signals rather than energy. Both bacterial and mammalian proteins contain a segment called retinal, a vitamin A derivative needed for eyesight. 
 
Distinguished by its deep purple color, bR changes to yellow following light absorption. Sheves and Cahen found this protein an ideal subject both because of its light activity and because of its unusual stability. Since it has been extensively studied, they had access to a vast fund of knowledge on the protein's structure and function, allowing them to manipulate various parts in their experiments. 
 
Their findings showed that bR can pass a current that is tens of thousands of times stronger than that which would be expected to pass through a protein - the difference is comparable to that between a room heater on at full blast and the electricity used by the little red LED on the side that tells you the heater's on. The retinal portion of the protein turned out to be a crucial component for passing current.  
 
The scientists found that the electron transfer is affected by light absorption. The protein's ability to capture sunlight activates a chemical switch: A retinal double bond changes the molecule's shape, flipping a part of the molecule from one side of the bond to the other. After this switchover takes place, the ability of the protein to pass current improves twofold. When the scientists carefully substituted a different molecule for the retinal segment - one that can't undergo the chemical change wrought by light absorption - the photosensitive effect was gone. 
 
The study raises interesting questions about evolution, says Sheves: "Why would nature create and maintain such an efficient system for conducting electricity, and then not use it? Is it simply an accident of biology, or did evolution abandon electron transport early on in favor of other kinds of energy? And if so, why?"    
  
Prof. Mordechai Sheves's research is supported by the Helen and Milton A. Kimmelman Center for Biomolecular Structure and Assembly; the Joseph and Ceil Mazer Center for Structural Biology; the A.M.N. Fund for the Promotion of Science, Culture and Arts in Israel; Samuel T. Cramer, Beverly Hills, CA; and the estate of Klara and Max Seidman, Israel. Prof. Sheves is the incumbent of the Ephraim Katzir-Rao Makineni Professorial Chair in Chemistry.

bacteriorhodopsin and retinal segment

 

 

Bacteriorhodopsin-containing microorganisms give these evaporation ponds near San Francisco their color
Chemistry
English

Sensing Trouble

English

A tiny sensor that uses organic molecules to detect problems – from asthma to hidden explosives – has been developed at the Weizmann Institute by Prof. Ron Naaman of the Chemical Physics Department, along with Prof. David Cahen of the Materials and Interfaces Department and Prof. Abraham Shanzer of the Organic Chemistry Department. 

Known as MOCSER (MOle-cular Controlled SEmiconductor Resistor), the sensor can detect minuscule amounts of substances, as little as just a few hundred molecules. These tiny quantities, however, can yield mountains of information. Levels of nitrous oxide (NO) molecules in exhaled breath, for instance, can reveal whether a person is having an asthma attack. The NO sensor has recently been developed as an easy-to-use, accurate asthma detector that can help diagnose the disease or predict attacks.

The sensor is so small that 28 can fit onto a standard electronic chip. MOCSER sensors can be produced inexpensively and might be designed to detect all sorts of substances, including harmful pollutants that are hard to monitor, banned materials and biological molecules.  
   
Prof. Ron Naaman’s research is supported by the Nancy and Stephen Grand Research Center for Sensors and Security; the Fritz Haber Center for Physical Chemistry; the Ilse Katz Institute for Material Sciences and Magnetic Resonance Research; the Wolfson Advanced Research Center for Bio Micro Technology; and the Philip M. Klutznick Fund for Research. Prof. Naaman is the incumbent of the Aryeh and Mintze Katzman Professorial Chair.
Chemistry
English

Going Magnetic

English

Prof. Ron Naaman. Magnetic and organic

When Itai Carmeli first came to his Ph.D. adviser with his results, he was gently told to get back to work. “I told him there was no such physics,” recalls a smiling Prof. Ron Naaman of the Institute’s Chemical Physics Department. “A year later he was back - with similar findings.”


Carmeli had been tinkering around with organic molecules, which he used to create extremely thin, single-layered films on a gold substrate. The surprise was that the films were behaving like a powerful magnet.


There are different types of magnets, Naaman explains, from the common fridge magnets we all played with as kids, which always display magnetic behavior; to temporary magnets such as paperclips and nails, which only work when exposed to a strong magnetic field; to magnets powered by an electric current. Nearly all of these contain one or more components with magnetic properties. The twist in our case was that the films lacked any magnetic materials.


In their study, recently published in Physical Review Letters and the Journal of Chemical Physics, the Institute team experimented with films made of three types of organic molecules. The molecules each had a positive and negative pole, and they were tightly packed, such that their negative poles faced the gold substrate, while their positive poles faced away. And this, says Naaman, might have been the trick: while opposite charges are known to attract, like charges repel, particularly when in close proximity on the surface of the film. The team - which included physicist Prof. Zeev Vager and materials scientists Prof. Shimon Reich and Dr. Gregory Leitus - believes that this repulsion force causes electrons to flow from the gold substrate to neutralize charged sites on the molecules in an attempt to stabilize the system. This extremely thin layer of flowing electrons in turn induces an electric current - forming a leading type of magnet dubbed an electromagnet (see box).


“We believe that the electrons are behaving as if in a co-op,” says Vager. “Electrons usually orbit in small circles, around individual molecules; but in this case they may be orbiting domains in the film containing hundreds of thousand of molecules, thus creating an electric current that transforms the system into a powerful magnet. Films of this sort might feature in electromagnets used in futuristic high-density discs and other electronics.”


Magnetic moments


Birds do it, bees do it, so do whales, salmon and, according to a new study, even Caribbean spiny lobsters - all use the Earth’s magnetic field as a navigating compass.

Magnetism was first discovered by the ancient Greeks and Chinese. Experimenting with the materials of their natural environment, they found that certain rare stones, called lodestones, attract small pieces of iron. Adding to their “magic,” these stones were found to always point in a north-south direction when suspended on a string. They quickly became invaluable to navigators, fortune-tellers and builders.


During the 13th century, French-man Pierre de Maricourt discovered that magnets had two magnetic poles - north and south - and in the 1600s, England’s Sir William Gilbert concluded that Earth itself was a giant magnet with north and south poles - which explains the wonder of animal migration treks.


The 1800s saw the first connection made between electricity and magnetism, when Danish physicist Hans Christian discovered that running an electric current through a wire creates a magnetic field - a phenomenon that quickly became known as electromagnetism. And today, this form of magnetism is everywhere - in the electric motors in refrigerators, washing machines and racecars; the read/write heads of discs and videotape players, and far more.


Prof. Naaman’s research is supported by the Fritz Haber Center for Physical Chemistry; the Ilse Katz Institute for Material Sciences and Magnetic Resonance Research; the Wolfson Advanced Research Center; the Philip M. Klutznick Fund for Research, Chicago, IL; and Dr. Pamela Scholl, Northbrook, IL. He is the incumbent of the Aryeh and Mintze Katzman Professorial Chair.

 
Prof. Ron Naaman. Electrons in a co-op
Space & Physics
English

Gaining Momentum

English
 
An accidental discovery 40 years ago led to an improvement in firefighting techniques: When polymers (long chains of molecules) were added to the water pumped through firehoses, that water projected over greater distances - of critical importance to those living and working in high-rise buildings.

But the why behind this finding remained a mystery until it was recently solved by a group of scientists of the Weizmann Institute’s Chemical Physics Department that included Prof. Itamar Procaccia, Dr. Victor L’vov, Dr. Anna Pomyalov and postdoctoral fellow Dr. Vasyl Tyberkevych.

Intuition told them that adding polymers should slow the flow of water through the hose by raising the water’s viscosity. The scientists noted that the normally folded up polymer molecules became stretched out like long strings of beads in the rushing stream, which did, indeed increase water viscosity.

However, a stronger counter-effect was also noted. The pressure produced in the pumps creates momentum, some of which carries water out of the end of the hose and some of which flows to the pipe walls. The polymers interfere with the flow of momentum to the pipe walls, and since the total momentum in the hose remains constant, a reduction in flow of momentum in one direction increases it in the other. The effect, therefore, is to raise the momentum, and thus the speed, of the water exiting the hose.

Institute scientists are currently testing the possibility of replacing the long-chain polymers with tiny air bubbles, an approach that may have relevance for transporting oil in pipelines and reducing drag on the bows of ships.
 
Prof. Procaccia’s research is supported by the Minerva Center for Nonlinear Physics of Complex Systems; the Naftali and Anna Backenroth-Broniki Fund for Complexity established by Mr. Yehuda Broniki of Israel; and the late Mr. Simon Pupko. He is the incumbent of the Barbara and Morris L. Levinson Professorial Chair in Chemical Physics.
Chemistry
English

NMR - the Movie

English

Prof. Lucio Frydman. Magnetism

 

 

Lucio Frydman devotes much of his time to one of the oldest traditions of humankind - making tools and using them to explore the world that surrounds us. But things have changed quite a bit since early blade-shaping, fire-making and glass-blowing attempts. “The goal is to craft ever-sensitive recording methods for peering into the heart of matter,” says Frydman, a professor in the Institute’s Chemical Physics Department.


The tool he is working to perfect is called nuclear magnetic resonance (NMR), which, since its development in the 1940s, has proven invaluable to studying the structure of molecules, designing new drugs and even exploring the human brain (see box).


The key to NMR is magnetism. All matter is made up of atoms, and each atom contains a nucleus. When exposed to electromagnetic radiation, nuclei “get excited” - they start spinning, creating their own electromagnetic sounds. The nucleus of each type of atom emits a sound that is entirely unique. The challenge facing NMR scientists is to study the dispersion patterns of the sound waves produced by the excited molecules - in other words, to work backward from the resulting “nuclear symphony” to reconstruct a precise three-dimensional picture of the molecule.


It’s not an easy task. To date, scientists wishing to obtain a full NMR picture of complex molecules needed to perform numerous measurements: hundreds or thousands of one-dimensional scans, which could only be performed one after the other. These scans were then combined to create a unified three-dimensional picture. While a single scan took a fraction of a second, the multidimensional procedures leading to the overall picture of the molecule could last several hours or even days.


Now Frydman and his team have developed an approach called ultrafast multidimensional NMR that significantly expedites the analysis of the electromagnetic sounds produced, making it possible to acquire complete multidimensional NMR spectra within a fraction of a second.


Their approach, described in the Proceedings of the National Academy of Sciences (PNAS), USA, “slices up” the molecular sample into numerous thin layers and then simultaneously performs all the measurements required on every one of these slices. The protocol then integrates these measurements according to their precise location, generating an image that amounts to a full multidimensional spectrum from the entire sample.


Thanks to the speed with which the new method collects the data, scientists will now be able to observe rapid changes taking place in molecules, such as the folding of proteins. In a sense, the method amounts to a transition from taking NMR “stills” to making NMR “movies.”


Frydman’s team is applying the techniques they’ve developed to study a variety of molecular structures and their potential interactions with their surroundings. One of their projects examines how nucleic acids and other biological molecules bind to metal ions (metals play vital roles in a range of systems, including serving as catalysts, which speed up reactions or enable them to occur). Additional projects aim to facilitate the efficient use of NMR in pharmaceutical and biochemical studies.


The team’s approach should make it possible to examine molecular and biological systems with a much higher time resolution than was previously possible, yielding detailed insights into molecular-level interactions. These, in turn, might advance the design of new drugs as well as industrial catalysts and novel materials.


Contributing to this research were Dr. Adonis Lupulescu of the Chemical Physics Department and Dr. Tali Scherf of Chemical Services at the Weizmann Institute of Science.


Prof. Frydman’s research is supported by the Fritz Haber Center for Physical Chemistry; the Henri Gutwirth Fund for Research; the estate of Ilse Katz, Switzerland; the Philip M. Klutznick Fund for Research; the Minerva Stiftung Gesellschaft fuer die Forschung m.b.H.; and the Abraham and Sonia Rochlin Foundation.


First magnetic steps


Research using nuclear magnetic resonance dates back to the 1940s, when Felix Bloch of Stanford University and Harvard’s Edward Purcell first applied NMR to examine solids and liquids, earning themselves the 1952 Nobel Prize in Physics. Weizmann Institute scientists Shlomo Alexander and Shaul Meiboom built one of the world’s first high-resolution NMR spectrometers in the early 1950s. They and other Institute scientists later developed an NMR approach for measuring the behavior of molecules in crystals and solutions. Since then NMR and its daughter technique, MRI, have evolved into what is arguably the most commonly used analytical and diagnostic tool in scientific research, spanning the fields of medicine, structural biology, pharmaceutical chemistry, condensed matter physics and earth sciences.

 

Making of a toolmaker


Argentinean-born Prof. Frydman received a Ph.D. in chemistry from the University of Buenos Aires. Following a postdoctoral period at the University of California, Berkeley he joined the faculty of the University of Chicago, where after seven years he became a full professor. He and his family settled in Rehovot, Israel, in 2001, when he joined the Institute’s Chemical Physics Department.


And why choose NMR research? “This field is unique in the way it combines quantum mechanical principles with instrumental and computational challenges,” says Frydman. “Moreover, its importance as a diagnostic tool in a variety of scientific fields means that there’s always a new question just waiting to be explored.”

 

Prof. Lucio Frydman. Ultrafast NMR
Chemistry
English

Light Lends a Hand

English
Prof. Moshe Shaprio and Dr. Petr Kral. visiting physicist
 
 

 

Scientists are often attracted to either the very large or the very small. For Dr. Petr Kral, visiting theoretical physicist at the Weizmann Institute of Science, the fascination lies at the Lilliputian end of the spectrum. He has a longstanding interest in transport through tiny bodies -  how an electron, for example, gets through a molecule attached to two electrical contacts. Recently he has attracted attention with his theoretical work on optical and frictional methods of sending electrons through nanotubes -  tiny molecular cylinders -  to perform specific tasks.

The prefix "nano"means one billionth. A nanotube, despite its diminutive transversal size (the tube's length is thousands of times longer than its diameter), could, in principle, be made of almost any layered material. In Kral's laser pump research, he has shown that laser beams -  otherwise known as coherent light -  can be used to excite electrons inside carbon nanotubes so that they move in a single direction. As the electrons make their way through the tube, they push forward movable molecules inside it.

This pumping technique could give rise to such applications as a nano pen, in which atomic "ink"(a chain of atoms) is pushed through the nanotube to write on a surface. The nano pen could also be used for biomedical purposes: By virtue of its tiny size, it could deposit molecules into an individual cell. Recently Kral suggested a scheme in which circularly polarized light could be used to rotate nanotubes with frequencies of billions of times per second -  an idea that could potentially be applied in nanomotors and nanopropellors.


Separating lefts from rights


Kral, who is working in Prof. Moshe Shapiro's group at the Materials and Interfaces Department, is also looking for ways in which laser beams can be harnessed to perform practical tasks in molecules.

One particularly intriguing innovation the team is pursuing is a way of employing lasers to separate the left and right versions of a chiral molecule. Any mirror-image pair -  such as our hands, ears, or feet -  is said to be "chiral"(chir is Greek for "hand"). Molecules can also exhibit this kind of relationship. But left and right molecules, though similar in many respects, can exhibit very different behavior patterns. Aspartame, for example, is a sweet molecule, but its mirror molecule is bitter.

Because only one chiral form may be desired in a biological application, the lefts and rights have to be separated from each other. Theoptical separation of lefts and rights depends, according to Shapiro and Kral's theory, on their asymmetry. Molecules exist in discrete energy states called "quantum levels,"and light can be used to couple different quantum levels. But while non-chiral molecules are subject to certain "selection rules"that dictate conditions for these couplings, chiral (or asymmetric) molecules are largely free of these limitations.

This greater freedom implies that chiral molecules can theoretically be transported across a wider variety of quantum levels. Kral has devised a method, using three laser pulses, that can transfer chiral molecules either directly from one quantum level to another or via anintermediate level. The innovative technique involves a cyclical movement between levels (for example, from level 1 to level 2, from level 2 to level 3, and from level 3 back to level 1).

The next step is to separate the lefts from the rights. The cyclical excitation of molecules by lasers creates interference. The interference conditions that are generated for left and right molecules are different. This determines which molecules go to which level -  lefts to 2, rights to 3,or vice versa, depending on the lasers'phases -  which in turn makes the moleculesdistinguishable from one another. Once the groups have been sorted out by left and right orientation, it becomes possible to pull them apart.

Shapiro and Kral believe it might be possible to use light not only to sift out the desired versions of individual molecules but even to convert the undesirables directly and efficiently into their more beneficial counterparts. The conversion, says Kral, can be done in a few nano-seconds only by using light -  a considerable improvement over all other methods attempted to date.

Right and Left molecules

Prof. Shapiro's research is supported by Mr. Bram Appel, Canada; the Estate of Dr. David Salmon, UK; and the Fritz Haber Center for Physical Chemistry. He holds the Jacques Mimran Professorial Chair.

 

 
illustration: Separating molecules with light
Chemistry
English

Seeking A Low-Energy Position

English

Prof. Sam Safran and Dr. Tsvi Tlusty. energy cost

'The Lord above gave man an arm of iron, so he could do his job and never shirk,' sings Alfred Doolittle in the musical My Fair Lady. 'But with a little bit o' luck,... someone else will do the blinkin' work.' Doolittle was lazy; but the dislike for wasting energy, or more precisely the desire to reach a goal with a minimum investment of energy, is a universal phenomenon common to humans and molecular particles alike. In the case of simple molecules, it drives them to create dense structures (such as solids or liquids), characterized by a large number of bonds between molecules 'costing' a minimum of energy per bond.

 

But molecular particles (and perhaps people as well) have another, conflicting characteristic that is just as important: under certain conditions they prefer a state of maximum disorder (entropy). The key factor influencing these conflicting tendencies is temperature: at very high temperatures entropy wins and the particles assume a gaseous state, the freest and most disorderly state possible. For example, at high temperatures, water turns to steam. But when the particles are cooled, the energy-saving tendency begins to dominate, causing them to reorganize into more orderly structures. Thus water vapor, when cooled, condenses into a liquid or a solid.

 

These tendencies apply to simple liquids, called isotropic liquids, composed of particles in which the energy 'cost' of bonding between the particles is independent of their orientation. But what about anisotropic systems, which are made up of particles whose bonding energy is highly dependent on their mutual orientation? Can cooling cause these systems to condense?

 

This is a fundamental physics question, but one that may also have important applications, since anisotropic liquids play an important role in modern technology. Dr. Tsvi Tlusty and Prof. Sam Safran, his doctoral adviser and Dean of the Weizmann Institute's Feinberg Graduate School decided to tackle this challenge.

 

In the past, most scientists believed that the answer to this question depended on the nature of the mutual attraction between the particles constituting a liquid. That is, if the mutual attraction is strong enough, it can 'compensate' for the loss of entropy (the loss of disorder involved in the process of condensing matter from gas to liquid).

 

One of the most striking examples of anisotropic liquids is that of magnetic liquids, characterized by magnetic particles that 'float' within a simple liquid, such as water or oil. In ordinary isotropic liquids, the condensed state of matter is formed by the clustering of particles, each clinging to a relatively large number of other particles (between 6 and 12). In contrast, magnetic liquids in dilute solutions form chains where each particle adheres to only two other particles at most, in a north-south-north-south structure. The bonding energy between these particles is highly dependent on their magnetic orientation. When two such magnets are aligned (i.e. their poles are positioned north to north or south to south) they repel each other; but when the nearby poles are of opposite orientation, the magnets mutually attract - which results in the north-south pole structure. This chaining structure in magnetic liquids prevents the usual type of condensation; because each of the particles is in contact with only two of its neighbors, it has less bonding energy. Therefore, until recently, the accepted scientific wisdom was that magnetic liquids could not undergo the usual gas-to-liquid condensation.

 

Safran and Tlusty's research sheds new light on this belief. Using a theoretical model, the scientists have shown that magnetic liquids can undergo condensation. Their conclusion seems from the fact that the magnetic chains 'prefer' to form Y-like junctions that bring together three chains (the energy 'cost' of this state is lower than the 'cost' of having both ends of a chain free). Thus magnetic chains in a dilute solution tend to form large and complex networks. In their study, recently published in Science, the researchers suggest that these network junctions strive for a balance between a state that 'costs' a minimum of energy and a state of maximum entropy. The network finds it 'worthwhile' to create more and more junctions, thus increasing its entropy while making the network denser and more complex. When the system of junctions making up the network is dilute, the material is in the gaseous phase; but when the network becomes more dense, the substance condenses to increase the junction entropy and makes the transition from a gas to a liquid.

 

This finding overturns the previously accepted view that the condensation of magnetic liquids is impossible without the involvement of additional, isotropic forces. In these systems, it is actually the increase in network entropy that stabilizes the condensed liquid state. No other forces are necessary. Further experimentation, resulting in confirmation of the scientists' 'network model,' might lead to the emergence of an entirely new field of technological applications. For instance, a better understanding of the physical properties of anisotropic liquids, and especially of their great sensitivity to changes in magnetic or electric fields, is important for developing advanced computers and other micro-machines.

 

Prof. Safran holds the Fern and Manfred Steinfeld Professorial Chair.

 

 

Prof. Sam Safran and Dr. Tsvi Tlusty
Chemistry
English

Pages