Ken Raymond

Last updated
Ken Raymond
Kenraymond.jpg
Born (1942-01-07) January 7, 1942 (age 82)
Alma mater Reed College (B.S.) (1964)
Northwestern University (Ph.D) (1968)
Scientific career
Fields Inorganic Chemistry, Bioinorganic Chemistry
Institutions University of California, Berkeley
Doctoral advisor Fred Basolo, James A. Ibers
Doctoral students Keith Hodgson, Rebecca Abergel,
Other notable students Vy Maria Dong (postdoc)
Website www.cchem.berkeley.edu/knrgrp/home.html

Kenneth Norman Raymond (born January 7, 1942) is a bioinorganic and coordination chemist. He is Chancellor's Professor of Chemistry at the University of California, Berkeley, [1] Professor of the Graduate School, the Director of the Seaborg Center in the Chemical Sciences Division at Lawrence Berkeley National Laboratory, and the President and Chairman of Lumiphore. [2] [3]

Contents

Biography

Early life and education

Raymond was born on January 7, 1942, in Astoria, Oregon, and was raised in various towns in Oregon. [4] After graduating from Clackamas High School in 1959, he spent a year in Germany where he worked as a test-driver for Volkswagen and developed a taste for German culture. He then attended Reed College in Portland, Oregon, where he majored in Chemistry and earned a Bachelor of Arts in 1964. [4] Raymond then attended Northwestern University where he studied coordination chemistry and crystallography under Fred Basolo and also worked closely with James A. Ibers, earning his Ph.D. degree in 1968.

Academic career

Raymond received an appointment to the faculty in the Department of Chemistry at the University of California, Berkeley in 1967 as an assistant professor. He became an associate professor in 1974 and a full professor of chemistry in 1978. [5] He has served as Vice Chair for the Berkeley Chemistry Department (1982−1984) and Chair (1993−1996). [5] He was Chair of the ACS Division of Inorganic Chemistry in 1996. [5]

Research from the Raymond group has covered a wide range of topics in inorganic chemistry, including actinide and lanthanide chemistry, microbial iron transport, and metal-based supramolecular assemblies. At the heart of his research throughout his career is a basic interest in metal-ligand specificity as understood through crystallography and solution thermodynamics.

Raymond, now a UC Berkeley Chancellor's Professor and the Director of the Glenn T. Seaborg Center at Lawrence Berkeley National Laboratory, continues to make strides in fundamental research in the fields of metals in biology and physical inorganic chemistry.

Scientific achievements

Uranocene

One of the first great achievements of Raymond's independent research career was the determination of the crystal structure of uranocene (di-π-(cyclooctatetraene)uranium). [6] This structure was a seminal discovery in the study of f-block sandwich complexes. Since this discovery, the analogous structures of several other f-block metals have been explored (including thorium and cerium from the Raymond lab). [7] [8]

Microbial iron transport

The study of iron transport systems in microbes and the coordination chemistry of siderophores is one of the longest running projects in the Raymond group. Several generations of students have studied the structures and solution behaviors of some of the most notable siderophores including enterobactin, desferrioxamine B, alcaligin and bacillibactin. Recently, the project has begun to explore siderophore interactions with the innate immune system during bacterial infections. [9] Throughout the years the iron project has continued to thrive and has been said to have "more twists and turns than an Agatha Christie novel."[ citation needed ] Studies in siderophore structure, and especially ligand specificity, have inspired several other projects in the Raymond group.

Actinide sequestration

Raymond's early interest in actinides (including plutonium, uranium and others), along with his expertise with siderophores, has led to the development of actinide decorporation agents. This project is based on a fundamental understanding of coordination chemistry, in order to design ligands that are selective for and support the geometry constraints of these elements.

Magnetic resonance imaging

Efforts toward the development of siderophore-inspired gadolinium(III) chelates began in the 1980s and have led to several promising compounds for magnetic resonance imaging. These compounds are both more stable and have a higher relaxivity than commercially available compounds and are the subject of several patents. Hexadentate hydroxypyridinone (HOPO) and terephthalamide (TAM) oxygen donor chelators allow for high thermodynamic stability of complexes while allowing for two-three water molecules to be directly coordinated to the lanthanide. Research has focused on macromolecular conjugation in recent years, including a collaboration with Jean Fréchet and dendrimers developed in his laboratory. [10] [11]

Lanthanide luminescence

Other lanthanide coordination compounds have been developed to serve as luminescent reporters in time-resolved bioassays. As experts in ligand design, the Raymond group has been able to develop ligands that optimize the luminescence of several lanthanides (particularly terbium and europium), leading to an array of brilliantly emissive complexes. Due to their remarkable properties, these compounds have been commercialized by Lumiphore. [12]

Supramolecular assemblies

Naphthalene-M4L6 cluster Logo-supra.jpg
Naphthalene-M4L6 cluster

Based on a predictive strategy, the Raymond group has developed several self-assembled, metal-ligand clusters of high symmetry. Some of these clusters, including the naphthalene-M4L6 workhorse cluster (see image), have a cavity within the cluster that can encapsulate a variety of guest molecules. In collaboration with Robert G. Bergman, the unique reaction chemistry of these host–guest assemblies has been explored. Recent work on this project, which led to a paper in Science , [13] has demonstrated unprecedented host–guest reaction rate accelerations reminiscent of enzyme kinetics.

Honors

Related Research Articles

<span class="mw-page-title-main">Coordination complex</span> Molecule or ion containing ligands datively bonded to a central metallic atom

A coordination complex is a chemical compound consisting of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents. Many metal-containing compounds, especially those that include transition metals, are coordination complexes.

<span class="mw-page-title-main">Inorganic chemistry</span> Field of chemistry

Inorganic chemistry deals with synthesis and behavior of inorganic and organometallic compounds. This field covers chemical compounds that are not carbon-based, which are the subjects of organic chemistry. The distinction between the two disciplines is far from absolute, as there is much overlap in the subdiscipline of organometallic chemistry. It has applications in every aspect of the chemical industry, including catalysis, materials science, pigments, surfactants, coatings, medications, fuels, and agriculture.

Uranocene, U(C8H8)2, is an organouranium compound composed of a uranium atom sandwiched between two cyclooctatetraenide rings. It was one of the first organoactinide compounds to be synthesized. It is a green air-sensitive solid that dissolves in organic solvents. Uranocene, a member of the "actinocenes," a group of metallocenes incorporating elements from the actinide series. It is the most studied bis[8]annulene-metal system, although it has no known practical applications.

<span class="mw-page-title-main">Sandwich compound</span> Chemical compound made of two ring ligands bound to a metal

In organometallic chemistry, a sandwich compound is a chemical compound featuring a metal bound by haptic, covalent bonds to two arene (ring) ligands. The arenes have the formula CnHn, substituted derivatives and heterocyclic derivatives. Because the metal is usually situated between the two rings, it is said to be "sandwiched". A special class of sandwich complexes are the metallocenes.

<span class="mw-page-title-main">Organoactinide chemistry</span> Study of chemical compounds containing actinide-carbon bonds

Organoactinide chemistry is the science exploring the properties, structure, and reactivity of organoactinide compounds, which are organometallic compounds containing a carbon to actinide chemical bond.

Gregory S. Girolami is the William H. and Janet G. Lycan Professor of Chemistry at the University of Illinois Urbana-Champaign. His research focuses on the synthesis, properties, and reactivity of new inorganic, organometallic, and solid state species. Girolami has been elected a fellow of the American Association for the Advancement of Science, the Royal Society of Chemistry, and the American Chemical Society.

<span class="mw-page-title-main">Actinocene</span> Class of chemical compounds

Actinocenes are a family of organoactinide compounds consisting of metallocenes containing elements from the actinide series. They typically have a sandwich structure with two dianionic cyclooctatetraenyl ligands (COT2-, which is C
8
H2−
8
) bound to an actinide-metal center (An) in the oxidation state IV, resulting in the general formula An(C8H8)2.

<span class="mw-page-title-main">Thorium compounds</span> Chemical compounds

Many compounds of thorium are known: this is because thorium and uranium are the most stable and accessible actinides and are the only actinides that can be studied safely and legally in bulk in a normal laboratory. As such, they have the best-known chemistry of the actinides, along with that of plutonium, as the self-heating and radiation from them is not enough to cause radiolysis of chemical bonds as it is for the other actinides. While the later actinides from americium onwards are predominantly trivalent and behave more similarly to the corresponding lanthanides, as one would expect from periodic trends, the early actinides up to plutonium have relativistically destabilised and hence delocalised 5f and 6d electrons that participate in chemistry in a similar way to the early transition metals of group 3 through 8: thus, all their valence electrons can participate in chemical reactions, although this is not common for neptunium and plutonium.

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

Neptunocene, Np(C8H8)2, is an organoneptunium compound composed of a neptunium atom sandwiched between two cyclooctatetraenide (COT2-) rings. As a solid it has a dark brown/red colour but it appears yellow when dissolved in chlorocarbons, in which it is sparingly soluble. The compound is quite air-sensitive.

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

Plutonocene, Pu(C8H8)2, is an organoplutonium compound composed of a plutonium atom sandwiched between two cyclooctatetraenide (COT2-) rings. It is a dark red, very air-sensitive solid that is sparingly soluble in toluene and chlorocarbons. Plutonocene is a member of the actinocene family of metallocenes incorporating actinide elements in the +4 oxidation state.

<span class="mw-page-title-main">Jaqueline Kiplinger</span> American inorganic chemist

Jaqueline Kiplinger is an American inorganic chemist who specializes in organometallic actinide chemistry. Over the course of her career, she has done extensive work with fluorocarbons and actinides. She is currently a Fellow of the Materials Synthesis and Integrated Devices group in the Materials Physics and Applications Division of Los Alamos National Laboratory (LANL). Her current research interests are focused on the development of chemistry for the United States’ national defense and energy needs.

William J. Evans is a Distinguished Professor at the University of California, Irvine, who specializes in the inorganic and organometallic chemistry of heavy metals, specifically the rare earth metals, actinides, and bismuth. He has published over 500 peer-reviewed research papers on these topics.

<span class="mw-page-title-main">Rebecca Abergel</span> French inorganic chemist

Rebecca Abergel is a professor of nuclear engineering and of chemistry at University of California, Berkeley. Abergel is also a senior faculty scientist in the chemical sciences division of Lawrence Berkeley National Laboratory, where she directs the Glenn T. Seaborg Center and leads the Heavy Element Chemistry research group. She is the recipient of several awards for her research in nuclear and inorganic chemistry.

T. Don Tilley is a professor of chemistry at the University of California, Berkeley.

<span class="mw-page-title-main">Marinella Mazzanti</span> Italian chemist

Marinella Mazzanti is an Italian inorganic chemist specialized in coordination chemistry. She is a professor at EPFL and the head of the group of Coordination Chemistry at EPFL's School of Basic Sciences.

Curium compounds are compounds containing the element curium (Cm). Curium usually forms compounds in the +3 oxidation state, although compounds with curium in the +4, +5 and +6 oxidation states are also known.

Cerium compounds are compounds containing the element cerium (Ce), a lanthanide. Cerium exists in two main oxidation states, Ce(III) and Ce(IV). This pair of adjacent oxidation states dominates several aspects of the chemistry of this element. Cerium(IV) aqueous solutions may be prepared by reacting cerium(III) solutions with the strong oxidizing agents peroxodisulfate or bismuthate. The value of E(Ce4+/Ce3+) varies widely depending on conditions due to the relative ease of complexation and hydrolysis with various anions, although +1.72 V is representative. Cerium is the only lanthanide which has important aqueous and coordination chemistry in the +4 oxidation state.

Neptunium compounds are compounds containing the element neptunium (Np). Neptunium has five ionic oxidation states ranging from +3 to +7 when forming chemical compounds, which can be simultaneously observed in solutions. It is the heaviest actinide that can lose all its valence electrons in a stable compound. The most stable state in solution is +5, but the valence +4 is preferred in solid neptunium compounds. Neptunium metal is very reactive. Ions of neptunium are prone to hydrolysis and formation of coordination compounds.

Americium compounds are compounds containing the element americium (Am). These compounds can form in the +2, +3, and +4, although the +3 oxidation state is the most common. The +5, +6 and +7 oxidation states have also been reported.

<span class="mw-page-title-main">Organothorium chemistry</span> Study of the carbon-thorium bond

Organothorium chemistry describes the synthesis and properties of organothorium compounds, chemical compounds containing a carbon to thorium chemical bond.

References

  1. http://www.cchem.berkeley.edu/knrgrp/KNR_CV.pdf [ bare URL PDF ]
  2. "Lumiphore". Archived from the original on 2018-10-02. Retrieved 2011-07-16.
  3. "Seth Cohen". cohenlab.ucsd.edu. Retrieved 2021-05-18.
  4. 1 2 3 "Bailar Lecturer 2009-10 - Kenneth N. Raymond | Chemistry at Illinois". chemistry.illinois.edu. Retrieved 2021-05-18.
  5. 1 2 3 4 5 6 7 Caulder, Dana L.; Raymond, Kenneth N. (1999-07-28). "Supermolecules by Design". Accounts of Chemical Research. 32 (11): 975–982. doi:10.1021/ar970224v. ISSN   0001-4842.
  6. Zalkin, Allan; Raymond, Kenneth N. (1969-09-01). "Structure of di-.pi.-cyclooctatetraeneuranium (uranocene)". Journal of the American Chemical Society. 91 (20): 5667–5668. doi:10.1021/ja01048a055. ISSN   0002-7863.
  7. Avdeef, Alex; Raymond, Kenneth N.; Hodgson, Keith O.; Zalkin, Allan (1972-05-01). "Two isostructural actinide .pi. complexes. Crystal and molecular structure of bis(cyclooctatetraenyl)uranium(IV), U(C8H8)2, and bis(cyclooctatetraenyl)thorium(IV), Th(C8H8)2". Inorganic Chemistry. 11 (5): 1083–1088. doi:10.1021/ic50111a034. ISSN   0020-1669.
  8. Hodgson, Keith O.; Raymond, Kenneth N. (1972-12-01). "Ion pair complex formed between bis(cyclooctatetraenyl)cerium(III) anion and an ether-coordinated potassium cation. Crystal and molecular structure of [K(CH3OCH2CH2)2O][Ce(C8H8)2]". Inorganic Chemistry. 11 (12): 3030–3035. doi:10.1021/ic50118a031. ISSN   0020-1669.
  9. (2) Raymond, K. N. Proc. Natl. Acad. Sci.2006, 103, 58499-18503.
  10. Raymond, K. N. J. Am. Chem. Soc.1995, 117, 7245-7246.
  11. Conjugation Effects of Various Linkers on Gd(III) MRI Contrast Agents with Dendrimers: Optimizing the Hydroxypyridinonate (HOPO) Ligands with Nontoxic, Degradable Esteramide (...
  12. Lumiphore
  13. Raymond, K. N. Science2007, 316 (5821), 85–88.
  14. John Simon Guggenheim Foundation | Kenneth N. Raymond
  15. "Kenneth Raymond". www.nasonline.org. Retrieved 2021-05-18.
  16. C&EN, 21 January 2008, page 59.