My first encounters with McGill University
came when I was still in a baby carriage. My mother used to wheel
me about the campus when we lived in that neighborhood and, as
she recounted years later, she would tell me that I would go to
McGill. There was some precedent for my going there, since two of
my father's brothers received their M.D.'s at McGill.
I have always loved going to school. Since neither of my parents
had a higher education, my academic "idols" were these two
paternal uncles and one of their uncles, my great-uncle, Henrik
Steen (né Markus). My admiration for him, living in faraway
Sweden, was not because of a teol.dr. (which he received from the
University of Uppsala in 1915) nor because of the
many books he wrote - I knew nothing of that - but rather because
he was reputed to speak 13 languages. I learned decades later
that the number was only 9! Growing up, mostly in Montreal, I was
an only child of loving parents. I admired my father's athletic
prowess - he excelled in several sports - and my mother's
expressive singing and piano playing.
My interest in the sciences started with mathematics in the very
beginning, and later with chemistry in early high school and the
proverbial home chemistry set. My education at Baron Byng High
School was excellent, with dedicated masters (boys and girls were
separate). I spent the next years at McGill University, for both
undergraduate and, as was the custom of the time, graduate study.
Our graduate supervisor, Carl A. Winkler, specialized in rates of
chemical reactions. He himself had received his Ph.D. as a
student of Cyril Hinshelwood at
Oxford.
Hinshelwood was later the recipient of the Nobel Prize for his
work on chemical kinetics. Winkler brought to his laboratory an
enthusiastic joyousness in research and was much loved by his
students.
During my McGill years, I took a number of math courses, more
than other students in chemistry. Upon receiving a Ph.D. from
McGill University in 1946, I joined the new post-doctoral program
at the National Research Council of Canada in Ottawa. This
program at NRC later became famous, but at the time it was still
in its infancy and our titles were Junior Research Officers. The
photochemistry group was headed by E.W.R. Steacie, an
international figure in the study of free-radical reactions and a
major force in the development of the basic research program at
NRC. I benefitted from the quality of his research on gas phase
reaction rates. Like my research on chemical reaction rates in
solution at McGill (kinetics of nitration), it was experimental
in nature. There were no theoretical chemists in Canada at the
time, and as students I don't think we ever considered how or
where theories were conceived.
About 1948 a fellow post-doctoral at NRC, Walter Trost, and I
formed a two-man seminar to study theoretical papers related to
our experimental work. This adventure led me to explore the
possibility of going on a second post-doctoral, but in
theoretical work, which seemed like a radical step at the time. I
had a tendency to break the glass vacuum apparatus, due to a
still present impetuous haste, with time-consuming consequences.
Nevertheless, the realization that breaking a pencil point would
have far less disastrous consequences played little or no role, I
believe, in this decision to explore theory!
I applied in 1948 to six well-known theoreticians in the U.S. for
a postdoctoral research fellowship. The possibility that one of
them might take on an untested applicant, an applicant hardly
qualified for theoretical research, was probably too much to hope
for. Oscar K. Rice at the University of North Carolina alone
responded favorably, subject to the success of an application he
would make to the Office of Naval Research for this purpose. It
was, and in February 1949 I took the train south, heading for the
University of North
Carolina in Chapel Hill. I was impressed on arrival there by
the red clay, the sandy walks, and the graciousness of the
people.
After that, I never looked back. Being exposed to theory,
stimulated by a basic love of concepts and mathematics, was a
marvelous experience. During the first three months I read
everything I could lay my hands on regarding reaction rate
theory, including Marcelin's classic 1915 theory which came
within one small step of the Transition State Theory of 1935. I
read numerous theoretical papers in German, a primary language
for the "chemical dynamics" field in the 1920s and 1930s,
attended my first formal course in quantum mechanics, given by
Nathan Rosen in the Physics Department, and was guided by Oscar
in a two-man weekly seminar in which I described a paper I had
read and he pointed out assumptions in it that I had overlooked.
My life as a working theorist began three months after this
preliminary study and background reading, when Oscar gently
nudged me toward working on a particular problem.
Fortunately for me, Oscar's gamble paid off. Some three months
later, I had formulated a particular case of what was later
entitled by B. Seymour Rabinovitch, RRKM theory
("Rice-Ramsperger-Kassel-Marcus"). In it, I blended statistical
ideas from the RRK theory of the 1920s with those of the
transition state theory of the mid-1930s. The work was published
in 1951. In 1952 I wrote the generalization of it for other
reactions. In addition, six months after arrival in Chapel Hill,
I was also blessed by marriage to Laura Hearne, an attractive
graduate student in sociology at UNC. She is here with me at this
ceremony. Our three sons, Alan, Kenneth and Raymond, and two
daughters-in-law are also present today.
In 1951, I attempted to secure a faculty position. This effort
met with little success (35 letters did not yield 35 no's, since
not everyone replied!). Very fortunately, that spring I met Dean
Raymond Kirk of the Polytechnic Institute of Brooklyn at an
American Chemical Society meeting in Cleveland, which I was
attending primarily to seek a faculty position. This meeting with
Dean Kirk, so vital for my subsequent career, was arranged by
Seymour Yolles, a graduate student at UNC in a course I taught
during Rice's illness. Seymour had been a student at Brooklyn
Poly and learned, upon accidentally encountering Dr. Kirk, that
Kirk was seeking new faculty. After a subsequent interview at
Brooklyn Poly, I was hired, and life as a fully independent
researcher began.
I undertook an experimental research program on both gas phase
and solution reaction rates, wrote the 1952 RRKM papers, and
wondered what to do next in theoretical research. I felt at the
time that it was pointless to continue with RRKM since few
experimental data were available. Some of our experiments were
intended to produce more.
After some minor pieces of theoretical study that I worked on, a
student in my statistical mechanics class brought to my attention
a problem in polyelectrolytes. Reading everything I could about
electrostatics, I wrote two papers on that topic in 1954/55. This
electrostatics background made me fully ready in 1955 to treat a
problem I had just read about on electron transfers. I comment on
this next period on electron transfer research in my Nobel
Lecture. About 1960, it became clear that it was best for me to
bring the experimental part of my research program to a close -
there was too much to do on the theoretical aspects - and I began
the process of winding down the experiments. I spent a year and a
half during 1960-61 at the Courant Mathematical Institute at
New York
University, auditing many courses which were, in part, beyond
me, but which were, nevertheless, highly instructive.
In 1964, I joined the faculty of the University of Illinois in
Urbana-Champaign and I never undertook any further
experiments there. At Illinois, my interests in electron transfer
continued, together with interests in other aspects of reaction
dynamics, including designing "natural collision coordinates",
learning about action-angle variables, introducing the latter
into molecular collisions, reaction dynamics, and later into
semiclassical theories of collisions and of bound states, and
spending much of my free time in the astronomy library learning
more about classical mechanics, celestial mechanics,
quasiperiodic motion, and chaos. I spent the academic year of
1975-76 in Europe, first as Visiting Professor at the University
of Oxford and later as a Humboldt Awardee at the Technical University
of Munich, where I was first exposed to the problem of electron
transfer in photosynthesis.
In 1978, I accepted an offer from the California Institute of
Technology to come there as the Arthur Amos Noyes Professor
of Chemistry. My semiclassical interlude of 1970-80 was
intellectually a very stimulating one, but it involved for me
less interaction with experiments than had my earlier work on
unimolecular reaction rates or on electron transfers.
Accordingly, prompted by the extensive experimental work of my
colleagues at Caltech in these fields of unimolecular reactions,
intramolecular dynamics and of electron transfer processes, as
well as by the rapidly growing experimental work in both broad
areas world-wide, I turned once again to those particular topics
and to the many new types of studies that were being made. Their
scope and challenge continues to grow to this day in both fields.
Life would be indeed easier if the experimentalists would only
pause for a little while!
There was a time when I had wondered about how much time and
energy had been lost doing experiments during most of my stay at
Brooklyn Poly- experiments on gas phase reactions, flash
photolysis, isotopic exchange electron transfer, bipolar
electrolytes, nitration, and photoelectrochemistry, among
others-and during all of my stay at NRC and at McGill. In
retrospect, I realized that this experimental background heavily
flavored my attitude and interests in theoretical research. In
the latter I drew, in most but not all cases, upon experimental
findings or puzzles for theoretical problems to study. The growth
of experiments in these fields has served as a continually
rejuvenating influence. This interaction of experiment and
theory, each stimulating the other, has been and continues to be
one of the joys of my experience.
Honors received for the theoretical work include the Irving
Langmair and the Peter Debye Awards of the American Chemical
Society (1978, 1988), the Willard Gibbs, Theodore William
Richards, and Pauling Medals, and the Remsen and Edgar Fahs Smith
Awards, from various sections of the ACS, (1988, 1990, 1991,
1991, 1991), the Robinson and the Centenary Medals of the Faraday
Division of the Royal Society of Chemistry (1982, 1988), Columbia
University's Chandler Medal (1983) and Ohio State's William Lloyd
Evans Award (1990), a Professorial Fellowship at University
College, Oxford (1975 to 1976) and a Visiting Professorship in
Theoretical Chemistry at Oxford during that period, the Wolf
Prize in Chemistry (1985), the National Medal of Science (1989),
the Hirschfelder Prize in Chemistry (1993), election to the
National Academy of Sciences (1970), the American Academy of Arts
and Sciences (1973), the American Philosophical Society (1990),
honorary membership in the Royal Society of Chemistry (1991), and
foreign membership in the Royal Society (London) (1987) and in
the Royal Society of Canada (1993). Honorary degrees were
conferred by the University of Chicago and by Goteborg,
Polytechnic, McGill, and Queen's Universities and by the
University of New Brunswick (1983, 1986, 1987, 1988, 1993, 1993).
A commemorative issue of the Journal of Physical Chemistry was
published in 1986.
From Les Prix Nobel. The Nobel Prizes 1992, Editor Tore Frängsmyr, [Nobel Foundation], Stockholm, 1993
This autobiography/biography was written at the time of the award and later published in the book series Les Prix Nobel/Nobel Lectures. The information is sometimes updated with an addendum submitted by the Laureate. To cite this document, always state the source as shown above.
Copyright © The Nobel Foundation 1992