John E. Bercaw

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John E. Bercaw
John Bercaw 1986.png
Bercaw in 1986
Born (1944-12-03) December 3, 1944 (age 79)[ citation needed ]
NationalityAmerican
Alma mater
Known for Metallocene chemistry
Awards1980 ACS Award in Pure Chemistry
Scientific career
Fields Chemistry
Institutions California Institute of Technology
Thesis Titanocene as a reactive intermediate in the reduction of molecular hydrogen and nitrogen  (1971)
Doctoral advisor Hans-Herbert Brintzinger
Other academic advisors Jack Halpern
Doctoral students Peter T. Wolczanski, Paul Chirik, Barbara Burger
Other notable students Don Tilley, Gregory L. Hillhouse, Gerard Parkin, Christopher W. Jones, Guillermo Bazan
Website www.cce.caltech.edu/content/john-e-bercaw

John E. Bercaw (born December 3, 1944)[ citation needed ] is an American chemist and Centennial Professor of Chemistry, Emeritus at the California Institute of Technology. [1] [2]

Contents

Early life and education

Born in Cincinnati, Ohio,[ citation needed ] Bercaw obtained his bachelor of science in 1967 from North Carolina State University and later his PhD from the University of Michigan in 1971 under the direction of Hans-Herbert Brintzinger, [3] followed by postdoctoral research with Jack Halpern at the University of Chicago. [4]

Career

He joined the faculty at the Caltech in 1972. Bercaw was elected a Fellow of the American Academy of Arts and Sciences in 1991. [5]

He is a member of the National Academy of Sciences (elected 1990), and he has received several national awards from the American Chemical Society (see below). [6]

His research interests are in synthetic, structural and mechanistic organotransition metal chemistry, including most recently catalysts for polymerization and trimerization of olefins and investigations of hydrocarbon hydroxylation; fundamental transformations and thermodynamics of organotransition metal chemistry; catalysts for hydrocarbon partial oxidation; catalysts for olefin trimerization and polymerization; homogeneous transformations of carbon monoxide and dihydrogen to fuels and chemicals.

Prof. Bercaw has greatly enhanced our understanding of the mechanisms of Ziegler-Natta (ZN) olefin polymerizations. This metal-catalyzed polymerization process is operated on a vast scale and produces, worldwide, over 200 billion pounds of polyolefins per year. Bercaw’s work has led to a fundamental understanding of the detailed mechanisms of chain growth in ZN polymerizations and the factors which control syndio- and isotacticities and the degree of comonomer incorporation in copolymerizations; these variables are critical in determining the physical properties of the resultant polymers and copolymers.

Commercial processes have been based on Bercaw’s discoveries. For example, new and superior ethylene/alpha-olefin copolymers are now industrially produced with titanium catalysts utilizing (η5- C5Me4)SiMe2NCMe3 and related ligands devised in Bercaw’s laboratories. These copolymers have proved to have superior properties. These types of systems have also allowed superior methods for production of ethylene/propylene and ethylene/propylene/diene elastomers.

Awards

Source: [7]

YearAwards
1980 ACS Award in Pure Chemistry
1990ACS Award in Organometallic Chemistry
1997ACS Award for Distinguished Service in the Advancement of Inorganic Chemistry
1999ACS George A. Olah Award in Hydrocarbon or Petroleum Chemistry
1999 American Institute of Chemists Chemical Pioneer Award
2000ACS Arthur C. Cope Scholar Award
2005Northwestern University - Chemistry Department's Basolo Medal
2008University of Chicago Chemistry Department Closs Lecturer
2013Southern California Section of the ACS Tolman Medal [8]
2014 Willard Gibbs Award [9]
2017 Gabor A. Somorjai Award for Creative Research in Catalysis [7]

Related Research Articles

<span class="mw-page-title-main">Alkene</span> Hydrocarbon compound containing one or more C=C bonds

In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins.

<span class="mw-page-title-main">Ethylene</span> Hydrocarbon compound (H₂C=CH₂)

Ethylene is a hydrocarbon which has the formula C2H4 or H2C=CH2. It is a colourless, flammable gas with a faint "sweet and musky" odour when pure. It is the simplest alkene.

A Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, is a catalyst used in the synthesis of polymers of 1-alkenes (alpha-olefins). Two broad classes of Ziegler–Natta catalysts are employed, distinguished by their solubility:

<span class="mw-page-title-main">Petrochemical</span> Chemical product derived from petroleum

Petrochemicals are the chemical products obtained from petroleum by refining. Some chemical compounds made from petroleum are also obtained from other fossil fuels, such as coal or natural gas, or renewable sources such as maize, palm fruit or sugar cane.

<span class="mw-page-title-main">Karl Ziegler</span> German chemist (1898–1973)

Karl Waldemar Ziegler was a German chemist who won the Nobel Prize in Chemistry in 1963, with Giulio Natta, for work on polymers. The Nobel Committee recognized his "excellent work on organometallic compounds [which]...led to new polymerization reactions and ... paved the way for new and highly useful industrial processes". He is also known for his work involving free-radicals, many-membered rings, and organometallic compounds, as well as the development of Ziegler–Natta catalyst. One of many awards Ziegler received was the Werner von Siemens Ring in 1960 jointly with Otto Bayer and Walter Reppe, for expanding the scientific knowledge of and the technical development of new synthetic materials.

Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH3CH=CH2. It has one double bond, and is the second simplest member of the alkene class of hydrocarbons. It is a colorless gas with a faint petroleum-like odor.

<span class="mw-page-title-main">Kaminsky catalyst</span> Ethylene polymerization catalyst

A Kaminsky catalyst is a catalytic system for alkene polymerization. Kaminsky catalysts are based on metallocenes of group 4 transition metals activated with methylaluminoxane (MAO). These and other innovations have inspired development of new classes of catalysts that in turn led to commercialization of novel engineering polyolefins.

<span class="mw-page-title-main">Acenaphthylene</span> Chemical compound

Acenaphthylene, a polycyclic aromatic hydrocarbon is an ortho- and peri-fused tricyclic hydrocarbon. The molecule resembles naphthalene with positions 1 and 8 connected by a -CH=CH- unit. It is a yellow solid. Unlike many polycyclic aromatic hydrocarbons, it has no fluorescence.

Amorphous poly alpha olefin is a commodity chemical used in multiple applications.

<span class="mw-page-title-main">Olefin metathesis</span> Organic reaction involving the breakup and reassembly of alkene double bonds

In organic chemistry, olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative organic reactions. For their elucidation of the reaction mechanism and their discovery of a variety of highly active catalysts, Yves Chauvin, Robert H. Grubbs, and Richard R. Schrock were collectively awarded the 2005 Nobel Prize in Chemistry.

Polyketones are a family of high-performance thermoplastic polymers. The polar ketone groups in the polymer backbone of these materials gives rise to a strong attraction between polymer chains, which increases the material's melting point (255 °C for copolymer, 220 °C for terpolymer. Trade names include Poketone, Carilon, Karilon, Akrotek, and Schulaketon. Such materials also tend to resist solvents and have good mechanical properties. Unlike many other engineering plastics, aliphatic polyketones such as Shell Chemicals' Carilon are relatively easy to synthesize and can be derived from inexpensive monomers. Carilon is made with a palladium catalyst from ethylene and carbon monoxide. A small fraction of the ethylene is generally replaced with propylene to reduce the melting point somewhat. Shell Chemical commercially launched Carilon thermoplastic polymer in the U.S. in 1996, but discontinued it in 2000. Hyosung announced that they would launch production in 2015.

Coordination polymerisation is a form of polymerization that is catalyzed by transition metal salts and complexes.

A polyolefin is a type of polymer with the general formula (CH2CHR)n where R is an alkyl group. They are usually derived from a small set of simple olefins (alkenes). Dominant in a commercial sense are polyethylene and polypropylene. More specialized polyolefins include polyisobutylene and polymethylpentene. They are all colorless or white oils or solids. Many copolymers are known, such as polybutene, which derives from a mixture of different butene isomers. The name of each polyolefin indicates the olefin from which it is prepared; for example, polyethylene is derived from ethylene, and polymethylpentene is derived from 4-methyl-1-pentene. Polyolefins are not olefins themselves because the double bond of each olefin monomer is opened in order to form the polymer. Monomers having more than one double bond such as butadiene and isoprene yield polymers that contain double bonds (polybutadiene and polyisoprene) and are usually not considered polyolefins. Polyolefins are the foundations of many chemical industries.

<span class="mw-page-title-main">Constrained geometry complex</span>

In organometallic chemistry, a "constrained geometry complex" (CGC) is a kind of catalyst used for the production of polyolefins such as polyethylene and polypropylene. The catalyst was one of the first major departures from metallocene-based catalysts and ushered in much innovation in the development of new plastics.

<span class="mw-page-title-main">Robert H. Grubbs</span> American chemist and Nobel Laureate (1942–2021)

Robert Howard GrubbsForMemRS was an American chemist and the Victor and Elizabeth Atkins Professor of Chemistry at the California Institute of Technology in Pasadena, California. He was a co-recipient of the 2005 Nobel Prize in Chemistry for his work on olefin metathesis.

In polymer chemistry, ring-opening metathesis polymerization (ROMP) is a type of chain-growth polymerization involving olefin metathesis. The driving force of the reaction is relief of ring strain in cyclic olefins. A variety of heterogeneous and homogeneous catalysts have been developed. Most large-scale commercial processes rely on the former while some fine chemical syntheses rely on the homogeneous catalysts. Catalysts are based on transition metals such as tungsten, molybdenum, rhenium, rubidium, and titanium.

<span class="mw-page-title-main">James C. Stevens</span> American organometallic chemist

James Carl Stevens, a chemist, was the first Distinguished Fellow, at the Dow Chemical Company, retiring in January 2015. His area of expertise is organometallic chemistry and his primary field of research is in the area of polyolefin catalysis, particularly in the area of polyethylene, polypropylene, ethylene/styrene copolymers, and the combinatorial discovery of organometallic single-site catalysts. Stevens major contributions have come in the discovery and commercial implementation of single-site polyolefin catalysts. He invented and led the commercialization of constrained geometry catalyst for the polymerization of olefins. These have been commercialized by Dow as a number of polymers, elastomers and plostomers.

In polymer chemistry, chain walking (CW) or chain running or chain migration is a mechanism that operates during some alkene polymerization reactions. CW can be also considered as a specific case of intermolecular chain transfer. This reaction gives rise to branched and hyperbranched/dendritic hydrocarbon polymers. This process is also characterized by accurate control of polymer architecture and topology. The extent of CW, displayed in the number of branches formed and positions of branches on the polymers are controlled by the choice of a catalyst. The potential applications of polymers formed by this reaction are diverse, from drug delivery to phase transfer agents, nanomaterials, and catalysis.

Samuel Emmett Horne Jr. was a research scientist at B. F. Goodrich noted for first synthesizing cis-1,4-polyisoprene, the main polymer contained in natural tree rubber, using Ziegler catalysis. Earlier attempts to produce synthetic rubber from isoprene had been unsuccessful, but in 1955, Horne prepared 98 percent cis-1,4-polyisoprene via the stereospecific polymerization of isoprene. The product of this reaction differs from natural rubber only slightly. It contains a small amount of cis-1,2-polyisoprene, but it is indistinguishable from natural rubber in its physical properties.

<span class="mw-page-title-main">Herbert S. Eleuterio</span> American industrial chemist (1927–2022)

Herbert S. Eleuterio was an American industrial chemist noted for technical contributions to catalysis, polymerization, industrial research management, and science education. In particular, he discovered the olefin metathesis reaction and several novel fluoropolymers. Additionally, he explored techniques for research leadership, especially methods for fostering collaboration, globalization, and scientific creativity.

References

  1. "FACULTY ::: Division of Chemistry and Chemical Engineering ::: CALTECH". Archived from the original on October 26, 2009. Retrieved July 15, 2009.
  2. "John e. Bercaw | Caltech Directory".
  3. Bercaw, John Edward (1971). Titanocene as a reactive intermediate in the reduction of molecular hydrogen and nitrogen (Ph.D.). University of Michigan. OCLC   68280047. ProQuest   302503406.
  4. "John e. Bercaw / Chemistry at Illinois". Archived from the original on May 4, 2017. Retrieved March 24, 2010.
  5. "Book of Members, 1780–2010: Chapter B" (PDF). American Academy of Arts and Sciences. Retrieved June 15, 2011.
  6. "MSU Chemistry - Max T. Rogers Lectureship". www2.chemistry.msu.edu. Archived from the original on March 27, 2004.
  7. 1 2 "National Awards". American Chemical Society. November 2, 2022. Retrieved November 19, 2022.
  8. "Tolman Award – SCALACS". SCALACS – Southern California Section of the American Chemical Society. September 5, 1948. Retrieved November 19, 2022.
  9. "Chicago ACS". Chicago ACS. Retrieved November 19, 2022.