Low energy (

A 7-Tesla Fourier transform ion-cyclotron resonance (FTICR) mass spectrometer was modified to insert a surface inside the cell for ion-surface collisions leading to the dissociation of impacting ions. Modifications were made to the software/hardware to collide the ions brought into the cell and trap the resulting fragment and undissociated primary ions inside the cell. The trapping plates were also ramped to determine kinetic energy distributions of these ions. The surface-induced dissociation (SID) of benzene and chromium hexacarbonyl ions was first studied as test cases for the instrument. Then a systematic study of the SID of small protonated peptides formed by electrospray ionization was begun. A series of small alanine(A)-containing peptides, viz., AA, AAA, AAAA, AAAAA, and PAAAA were used in the study. In the absence of any direct comparisons of the SID processes with the commonly used technique of tandem mass spectrometry of collision-induced dissociations (CID) via collisions with a neutral gas, a comparative study of CID and SID using the same protonated peptides was made. Since multiple collisions are often used to enhance dissociation efficiency in CID, the CID was performed under single as well as multiple collisional activation conditions. Both on-resonance and sustained off-resonance irradiation excitation were used for CID experiments. Kinetic energy of the ions was varied by changing peak-to-peak voltage applied to the excitation plates. Results are shown in a series of graphs, and a simple theoretical model is presented. This direct comparison of the two activation techniques on the same instrument provided insights into the similarities and differences between these two. The results suggest that internal energy distributions of ions activated by ion-surface collision and multiple collision ion-gaseous neutral collisions are quite comparable. The results also suggest that, in ion-surface collisions, the ion collides with only a small fraction of th e self-assembled monolayer chain, making it effectively a process very similar to CID.

This first volume in the series brings together the latest developments in solid surface photochemistry, providing insights into the most up to date research activities on light-initiated chemical reactions. The book offers a comprehensive study of the photochemical and photophysical properties of molecules on various surfaces like zeolites, metals and metal oxides. Chapter 1 discusses the nature of the photochemical and photophysical reactions occurring on solid surfaces. Subsequent chapters deal with a description of the dynamical aspects of surface photohemistry, a study of the specific nature of photochemistry of molecules included within zeolite cavities and a comprehensive study of the reactivities of photo-generated electron-hole pair states involved in photo-induced and photocatalytic reactions. The book also investigates many possible and actual key applications of solid surface photochemistry, such as molecular photo-devices, photo-chemical vapour deposition of thin layered semiconductors, sensitive optical media and control of photochemical reaction paths as well as efficient photocatalytic reaction processes which will be indispensable for ecologically clean and safe chemical systems. Surface Photochemistry will be of interest to researchers in surface science and also to graduate students interested in catalysis or photo-chemistry. It will be valuable as a reference book for academics in many aspects of materials science.

Time-of-flight secondary ion mass spectrometry (ToF-SIMS) is the most versatile of the surface analysis techniques that have been developed during the last 30 years. This is the Second Edition of the first book ToF-SIMS: Surface analysis by Mass Spectrometry to be dedicated to the subject and the treatment is comprehensive

Begins with a historical overview by Henry Taube. Overviews the advances pioneered by Taube, including mechanisms of electron transfer reactions, charge transfer complexes, and *p back bonding effects in metal-ligand interactions. Discusses applications of principles of electron transfer to diverse areas of chemistry and biology such as the selective and controlled oxidation of organic functional groups, polymerization catalysis, metal biological interactions with DNA, biological electron transfer reactions, and new imaging agents in diagnostic medicine.

On three occasions and at different locations, conferences were held to honor the eightieth birthday of Professor Herbert Frohlich: on the 18th December, 1985, in Liverpool, England; on the 14th February, 1986, in Stuttgart, Germany; and on the 8th March, 1986, on the Palm Coast, Florida. This Festschrift is a compilation of the papers of those conferences. Frohlich's choice of problems, from the earliest days, was couched in the phy sics of intrinsically interacting systems of excitation. One example, in which he set the course of research which is still followed, concerned dielectric breakdown, developed from the 1930's over several decades. The interacting systems are the electrons (receiving energy from an electric field) and lattice atom motion (taking energy from the electrons via "electron-phonon" interaction, hence heat dissipa tion). There is a threshold field above which the latter cannot keep up with the former, and the combined system (electrons plus phonons) "runs away"; that is to say, collectively it switches to a new state.