Unlike rubber bands, molecular bonds may not break faster when pulled

June 17, 2009

From balloons to rubber bands, things always break faster when stretched. Or do they? University of Illinois scientists studying chemical bonds now have shown this isn't always the case, and their results may have profound implications for the stability of proteins to mechanical stress and the design of new high-tech polymers.

"Our findings contradict the intuitive notion that molecules are like rubber bands in that when we pull on a , it should always break faster," said chemistry professor Roman Boulatov, who led the study. "When we stretch a sulfur-sulfur bond, for example, how fast it breaks depends on how the nearby atoms move."

The findings also contradict the conventional interpretation of experimental results obtained by other researchers studying the fragmentation rate of certain proteins containing sulfur-sulfur bonds when stretched with a microscopic force probe. In those experiments, as the force increased, the proteins fragmented faster, leading the researchers to conclude that as the sulfur-sulfur bond was stretched, it reacted faster and broke faster.

"Our experiments suggest a different conclusion," Boulatov said. "We believe the acceleration of the fragmentation was caused by a change in the protein's structure as it was stretched, and had little or nothing to do with increased reactivity of a stretched sulfur-sulfur bond."

In their experiments, the researchers use stiff stilbene as a molecular force probe to generate well-defined forces on atom by atom.

The probe allows reaction rates to be measured as a function of the restoring force. Similar to the force that develops when a rubber band is stretched, the molecular restoring force contains information about how much the molecule was distorted, and in what direction.

In previous work, when Boulatov's team pulled on carbon-carbon bonds with the same force they would later apply to sulfur-sulfur bonds, they found the carbon-carbon bonds broke a million times faster than when no force was applied.

"Because the sulfur-sulfur bond is much weaker than the carbon-carbon bond, you might think it would be much more sensitive to being pulled on," Boulatov said. "We found, however, that the sulfur-sulfur bond does not break any faster when pulled."

Boulatov and his team report their findings in a paper accepted for publication in Angewandte Chemie, and posted on the journal's Web site.

"When we pulled on the sulfur-sulfur bond, the nearby methylene groups prevented the rest of the molecule from relaxing," Boulatov said, "thus eliminating the driving force for the sulfur-sulfur bond to break any faster."

Chemists must bear in mind that even in simple chemical reactions, such as a single bond dissociation, "we must take into account other structural changes in the molecule," Boulatov said. "The elongation alone, which occurs when a bond is stretched, does not represent the full picture of what happens when the reaction occurs."

The good news, Boulatov said, is that not every polymer that is stretched will break faster. "We might be able to design polymers, for example, that would resist fragmentation under modest mechanical stresses," he said, "or will not break along the stretched direction, but in some other desired direction."

Source: University of Illinois at Urbana-Champaign (news : web)


print this article email this article download pdf blog this article bookmark this article     Stumble it Digg this share on Facebook retweet share on Reddit add to delicious
Rate this story - 5 /5 (1 vote)


June 17, 2009 all stories

Comments: 0

5 /5 (1 vote)
  • Stumble this up

  • Digg this

  • share this

  • hide
  • Related Stories

  • New molecular force probe stretches molecules, atom by atom
    created Mar 29, 2009 | popularity not rated yet | comments 0
  • 'Impossible' Molecular Chain Reaction on Metal is Demonstrated
    created Dec 12, 2008 | popularity not rated yet | comments 0
  • EPA says sulfur dioxide emissions are down
    created Nov 17, 2007 | popularity not rated yet | comments 0
  • 'Yanking' Chemical Bonds with Molecular Wires Speeds Reactions
    created Mar 15, 2006 | popularity not rated yet | comments 0
  • New Direction for Hydrogen Atom Transfers
    created Oct 19, 2005 | popularity not rated yet | comments 0



  • hide
  • Relevant PhysicsForums posts

  • Zinc Oxide reduction
    created 5 hours ago
  • depolymerization of HDPE
    created 21 hours ago
  • Question, whats the best chemistry software for a college student?
    created Nov 08, 2009
  • Why only opposite spin electrons in an orbital ?
    created Nov 08, 2009
  • More from Physics Forums - Chemistry

Other News

Toward home-brewed electricity with 'personalized solar energy'

Toward home-brewed electricity with 'personalized solar energy'

Chemistry / Materials Science

created Nov 04, 2009 | popularity 3.4 / 5 (9) | comments 4

New scientific discoveries are moving society toward the era of "personalized solar energy," in which the focus of electricity production shifts from huge central generating stations to individuals in their ...


Scientists Reproduce a Building Block of Life in Laboratory

Scientists Reproduce a Building Block of Life in Laboratory

Chemistry / Biochemistry

created Nov 06, 2009 | popularity 4.8 / 5 (23) | comments 0

(PhysOrg.com) -- NASA scientists studying the origin of life have reproduced uracil, a key component of our hereditary material, in the laboratory.


Newly Discovered Fat Molecule: An Undersea Killer with an Upside

Newly Discovered Fat Molecule: An Undersea Killer with an Upside

Chemistry / Biochemistry

created Nov 05, 2009 | popularity 4.8 / 5 (10) | comments 0

(PhysOrg.com) -- A chemical culprit responsible for the rapid, mysterious death of phytoplankton in the North Atlantic Ocean has been found by collaborating scientists at Rutgers University and the Woods Hole ...


CU-Boulder map of human bacterial diversity shows wide interpersonal differences

Map of Human Bacterial Diversity Shows Wide Interpersonal Differences

Chemistry / Biochemistry

created Nov 05, 2009 | popularity 4.7 / 5 (11) | comments 0

(PhysOrg.com) -- A University of Colorado at Boulder team has developed the first atlas of bacterial diversity across the human body, charting wide variations in microbe populations that live in different ...


Mimicking nature, scientists can now extend redox potentials

Mimicking nature, scientists can now extend redox potentials

Chemistry / Biochemistry

created Nov 04, 2009 | popularity 4.8 / 5 (5) | comments 0

(PhysOrg.com) -- New insight into how nature handles some fundamental processes is guiding researchers in the design of tailor-made proteins for applications such as artificial photosynthetic centers, long-range ...