Journal of Analytical & Bioanalytical Techniques
Like us on:
Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.
Matrix-assisted laser desorption/ionization (MALDI) is one of the ?soft ionization? methods which do not decompose analyte
during ionization process. MALDI combined with time-of-flight mass spectrometry (MALDI-MS) has been widely used
in many research fields since it enables observation of analyte ions in terms of their molecular weights. Regardless of voluminous
applications in MALDI-MS, the mechanism of MALDI is not fully understood. MALDI includes two important processes;
ionization and desorption. Although knowledge of the ionization process in MALDI has accumulated by several efforts, the
mechanism of desorption process remains unclear. This hinders the detection of many kinds of molecules by this method. In
this study, we have investigated desorption dynamics by using newly developed femtosecond time-resolved mass spectrometry.
To simplify the roles of matrix and analyte, tetracene-doped anthracene crystals (TDA), in which efficient energy transfer
from anthracene to tetracene occurs, were used as a model system and the desorption dynamics of tetracene ions ([tetracene]
from the anthracene crystals was observed. The rise time of the peak intensity of tetracene ions is determined 94.7 ps. According
to the time-resolved fluorescence study, it was observed that the tetracene molecules are excited to the S
state after the 9.4 ps
delay of pumping, and the S
tetracene can be ionized immediately by the irradiation of time-delayed probe pulses. However, the
mass intensity of the tetracene ions grows at 94.7 ps after the pumping, suggesting the observation of the slow desorption of the
tetracene ions in the mass spectrum. Our results reveal that desorption of tetracene ions is triggered by the electronic relaxation
of anthracene leading to the vibrational excitation of lattice phonon modes in the crystals. The delayed growth of the mass signal
implies that the time required for the intermolecular dissociative modes to be excited by the relaxation.
Tatsuya Fujino, attained his Doctor of science from Tokyo Institute of Technology in 1998. He worked as a postdoctoral researcher of Japan Society
for the Promotion of Science (JSPS) at Institute of Molecular Science (IMS) 1998-2002 and as a special postdoctoral researcher at RIKEN, 2002-
2005. Since 2005-till date, he is an Associate Professor at Tokyo Metropolitan University. He got New Century Award from the Japan Society for
Analytical Chemistry (JSAC) in 2006. Best presentation awards from the Spectroscopical Society of Japan (SPSJ) in 2004 and from the Kanto
branch of Chemical Society of Japan (CSJ) in 2007.
Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals