Details of Grant 

EPSRC Reference:	EP/E038522/1
Title:	State-resolved studies of the vibronic structure and reaction dynamics of molecular dications
Principal Investigator:	Price, Professor SD
Other Investigators:
Researcher Co-Investigators:
Project Partners:
Department:	Chemistry
Organisation:	UCL
Scheme:	Standard Research
Starts:	01 October 2007	Ends:	30 September 2011	Value (£):	390,194
EPSRC Research Topic Classifications:	Gas & Solution Phase Reactions Instrumentation Eng. & Dev.
EPSRC Industrial Sector Classifications:	Chemicals
Related Grants:
Panel History:
Summary on Grant Application Form
Molecules which carry two positive charges, molecular dications, possess unusual properties. Firstly, due to the repulsion of the two like-charges the molecules are highly energetic. This high energy means that they react differently to singly-charged ions. Secondly, the repulsion between the two positive charges means than many of these doubly charged molecules are very short-lived and they fragment to form a pair of singly-charged ions. However, for most small molecules, certain arrangements of their electrons give strong enough chemical bonds to hold the molecule together despite the repulsion between the pair of positive charges. These arrangements of the electrons generate so-called long-lived ( metastable ) electronic states of molecular dications. In these metastable states many small molecular dications can live for long enough to collide with a neutral molecule and undergo chemical reactions. This application proposes an extensive upgrade to a piece of apparatus developed by the applicant to study the chemical reactions of molecular dications. The apparatus operates by identifying both of the charged products that usually are formed in a dication chemical reaction. The apparatus uses a specially designed mass spectrometer to detect and identify both of the charged products from reaction of an individual dication; a so-called coincidence experiment. Using a position-sensitive detector in the mass spectrometer allows the experiment to precisely determine how both of the product ions are moving following an individual reactive event. Such studies of the motion of the product ions, the so-called dynamics of a reactive process, provide a powerful probe of the mechanism of the chemical reaction. In it's current configuration the experiment has revealed the reactivity of a wide-range of dications and shown that dication reactions proceed by unusual pathways. However, the accuracy with which the experiment can probe the energies of the reaction products is currently limited and this application proposes significant developments to the spectrometer to dramatically improve this energy resolution. We propose to install a larger area detector and improved timing electronics, together the incorporation of a more controlled and constrained inlet (a molecular beam ) for the neutral molecules. These improvements, together with a new design of mass spectrometer which incorporates a velocity imaging methodology, will improve the energy resolution of the spectrometer so that the energies and reactivity of individual vibrational levels of diatomic dications can be determined. Velocity imaging is a technique developed for laser spectroscopy, involving a special arrangement of electric fields in the mass spectrometer, which allows the product ion velocities to be determined accurately. To implement velocity imaging in our experiment, which does not use a laser to ionize the products of the reaction, involves a new design of mass spectrometer, which we have developed, which still gives accurate product ion velocities but does not degrade the ability of the mass spectrometer to identify different species. We propose to use the upgraded apparatus to study the energy levels of diatomic dications which cannot be probed by existing techniques and also to study the reactivity and reaction mechanisms of the molecular dications which have recently been implicated as key species in the chemistry of planetary ionospheres.
Key Findings
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Potential use in non-academic contexts
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Project URL:	http://www.ucl.ac.uk/chemistry/staff/academic_pages/stephen_price
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