Abstract
The translational diffusion of many transient radicals has been revealed to be different from that expected from the stable closed shell molecules. The origin of the slower diffusion of the radicals was investigated. In particular, participation of the hydrogen bonding to the diffusion process was considered from view points of excess friction and the solvent dependence.
Original language | English |
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Pages (from-to) | 419-422 |
Number of pages | 4 |
Journal | Chemical Physics Letters |
Volume | 372 |
Issue number | 3-4 |
DOIs | |
Publication status | Published - Apr 29 2003 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Physics and Astronomy(all)
- Physical and Theoretical Chemistry