Adam J. Matzger | |
---|---|
Born | |
Nationality | American |
Alma mater | Oberlin College, University of California, Berkeley, California Institute of Technology |
Scientific career | |
Fields | Chemistry |
Institutions | University of Michigan |
Doctoral advisor | Peter C. Vollhardt |
Other academic advisors | Robert H. Grubbs and Nathan S. Lewis |
Website | http://umich.edu/~ajmgroup/ |
Adam J. Matzger, a researcher in polymers and crystals, is the Charles G. Overberger Collegiate Professor of Chemistry at the University of Michigan.
This section of a biography of a living person does not include any references or sources .(July 2021) |
Matzger is a native of Piedmont, California but moved to Ohio to complete his undergraduate career at Oberlin College, where he graduated with a Bachelor of Arts in Chemistry in 1992. From there he moved back to California for his graduate work at the University of California at Berkeley where he studied under Professor Peter C. Vollhardt. In 1997 he earned his Ph. D. degree with a thesis titled "Synthetic, Theoretical, and Structural Studies on Dehydrobenzoannulenes and Phenylenes."
He then was a Postdoctoral Researcher at California Institute of Technology (co-mentored by Robert H. Grubbs and Nathan S. Lewis) until 2000 when he was appointed Assistant Professor of Chemistry and of Macromolecular Science and Engineering at the University of Michigan. In 2006 he became an Associate Professor and finally a full Professor in 2009; in 2013 he was appointed as the Charles G. Overberger Collegiate Professor of Chemistry. His group researches a range of topics in organic materials, specifically porous materials, polymorphism and metal organic frameworks (MOFs). He is also leading a Multi-University Research Initiative (MURI), funded by the US Army, for improving material properties through cocrystallization.
While traditionally polymorphs are discovered or selectively made through manipulation of growth conditions, such as temperature or solvent, Matzger's group has instead found the ability to control polymorphs by employing different polymers to induce heteronucleation. He first showed this ability with the control over the monoclinic and orthorhombic forms of acetaminophen, a widely used pharmaceutical. [1] This is the only polymorph discovery technique invented in the last 100 years to substantially increase the range of polymorphs accessible;[ citation needed ]
Matzger has pioneered the use of cocrystallization for development of energetic materials. His group has made numerous cocrystals with increased power and decreased sensitivity. Among these are a 2:1 cocrystal of CL-20:HMX and a 1:1 CL20:TNT(2,4,6-trinitro-toluene). [2] [3] CL-20 (2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaiso-wurtzitane) is a powerful explosive that is too sensitive to be viable in military use and HMX (1,3,5,7-tetranitro-1,3,5,7-tetrazacyclooctane) is a standard military explosive. Previous to his work, only aromatic energetic materials were able to form cocrystals because of their ability to pi-stack. Cocrystals that his group have formed are realized through CH hydrogen bonding with the oxygen atoms from the nitro groups, thus opening cocrystallization to the more powerful non-aromatic energetics.
His group uses scanning tunneling microscopy to investigate the spontaneous self-assembly of physisorbed monolayers at atmospheric conditions, two-dimensional crystallization. From this they have created a two-dimensional structural database (2DSD) which has helped unify the view of interfacial self-assembly making it possible to draw comparisons to bulk crystals. [4] This allows the investigation of the differences that arise due to the presence of an interface or reduced dimensionality.
His lab synthesized metal-organic frameworks (MOFs) with high surface areas. Through a collaboration with Michael O'Keeffe and Omar M. Yaghi, they developed MOF-177, or Zn4O(1,3,5-benzenetribenzonate)2, which has a very large surface area, 4,500 m2g−1 and extra large pores which allow the binding of large guest molecules, such as polycyclic organic molecules, the combination of which was not possible in a single material prior to this. [5] Developments from this have included the introduction of coordination copolymerization for producing high surface area materials from simple feedstocks. [6]
HMX, also called octogen, is a powerful and relatively insensitive nitroamine high explosive chemically related to RDX. The compound's name is the subject of much speculation, having been variously listed as High Melting Explosive, High-velocity Military Explosive, or High-Molecular-weight RDX.
Zinc acetate is a salt with the formula Zn(CH3CO2)2, which commonly occurs as the dihydrate Zn(CH3CO2)2·2H2O. Both the hydrate and the anhydrous forms are colorless solids that are used as dietary supplements. When used as a food additive, it has the E number E650.
1,3,5,7-Cyclooctatetraene (COT) is an unsaturated derivative of cyclooctane, with the formula C8H8. It is also known as [8]annulene. This polyunsaturated hydrocarbon is a colorless to light yellow flammable liquid at room temperature. Because of its stoichiometric relationship to benzene, COT has been the subject of much research and some controversy.
A coordination polymer is an inorganic or organometallic polymer structure containing metal cation centers linked by ligands. More formally a coordination polymer is a coordination compound with repeating coordination entities extending in 1, 2, or 3 dimensions.
Hexanitrohexaazaisowurtzitane, also called HNIW and CL-20, is a polycyclic nitroamine explosive with the formula C6H6N12O12. It has a better oxidizer-to-fuel ratio than conventional HMX or RDX. It releases 20% more energy than traditional HMX-based propellants.
Crystal engineering studies the design and synthesis of solid-state structures with desired properties through deliberate control of intermolecular interactions. It is an interdisciplinary academic field, bridging solid-state and supramolecular chemistry.
Metal–organic frameworks (MOFs) are a class of porous polymers consisting of metal clusters coordinated to organic ligands to form one-, two- or three-dimensional structures. The organic ligands included are sometimes referred to as "struts" or "linkers", one example being 1,4-benzenedicarboxylic acid (BDC).
Omar M. Yaghi is the James and Neeltje Tretter Chair Professor of Chemistry at the University of California, Berkeley, an affiliate scientist at Lawrence Berkeley National Laboratory, the Founding Director of the Berkeley Global Science Institute, and an elected member of the US National Academy of Sciences as well as the German National Academy of Sciences Leopoldina.
Covalent organic frameworks (COFs) are a class of porous polymers that form two- or three-dimensional structures through reactions between organic precursors resulting in strong, covalent bonds to afford porous, stable, and crystalline materials. COFs emerged as a field from the overarching domain of organic materials as researchers optimized both synthetic control and precursor selection. These improvements to coordination chemistry enabled non-porous and amorphous organic materials such as organic polymers to advance into the construction of porous, crystalline materials with rigid structures that granted exceptional material stability in a wide range of solvents and conditions. Through the development of reticular chemistry, precise synthetic control was achieved and resulted in ordered, nano-porous structures with highly preferential structural orientation and properties which could be synergistically enhanced and amplified. With judicious selection of COF secondary building units (SBUs), or precursors, the final structure could be predetermined, and modified with exceptional control enabling fine-tuning of emergent properties. This level of control facilitates the COF material to be designed, synthesized, and utilized in various applications, many times with metrics on scale or surpassing that of the current state-of-the-art approaches.
In crystallography, a periodic graph or crystal net is a three-dimensional periodic graph, i.e., a three-dimensional Euclidean graph whose vertices or nodes are points in three-dimensional Euclidean space, and whose edges are line segments connecting pairs of vertices, periodic in three linearly independent axial directions. There is usually an implicit assumption that the set of vertices are uniformly discrete, i.e., that there is a fixed minimum distance between any two vertices. The vertices may represent positions of atoms or complexes or clusters of atoms such as single-metal ions, molecular building blocks, or secondary building units, while each edge represents a chemical bond or a polymeric ligand.
In materials science, cocrystals are "solids that are crystalline, single-phase materials composed of two or more different molecular or ionic compounds generally in a stoichiometric ratio which are neither solvates nor simple salts." A broader definition is that cocrystals "consist of two or more components that form a unique crystalline structure having unique properties." Several subclassifications of cocrystals exist.
A two-dimensional polymer (2DP) is a sheet-like monomolecular macromolecule consisting of laterally connected repeat units with end groups along all edges. This recent definition of 2DP is based on Hermann Staudinger's polymer concept from the 1920s. According to this, covalent long chain molecules ("Makromoleküle") do exist and are composed of a sequence of linearly connected repeat units and end groups at both termini.
Solid sorbents for carbon capture include a diverse range of porous, solid-phase materials, including mesoporous silicas, zeolites, and metal-organic frameworks. These have the potential to function as more efficient alternatives to amine gas treating processes for selectively removing CO2 from large, stationary sources including power stations. While the technology readiness level of solid adsorbents for carbon capture varies between the research and demonstration levels, solid adsorbents have been demonstrated to be commercially viable for life-support and cryogenic distillation applications. While solid adsorbents suitable for carbon capture and storage are an active area of research within materials science, significant technological and policy obstacles limit the availability of such technologies.
Adel F. Halasa is an American scientist noted for his contributions to the development of rubber, particularly in the area of tire tread polymers for the Goodyear AquaTred tire. In 1997, he won the Charles Goodyear Medal, bestowed by the American Chemical Society, Rubber Division to individuals who "have been the principal inventor(s), innovator(s), or developer(s) of a significant change or contribution to the rubber industry".
Hong-Cai (Joe) Zhou is a Chinese–American chemist and academic. He is the Davidson Professor of Science and Robert A. Welch Chair in Chemistry at Texas A&M University. He is also the associate editor of the journal Inorganic Chemistry.
Susumu KitagawaForMemRS is a Japanese chemist working in the field of coordination chemistry, with specific focus on the chemistry of organic–inorganic hybrid compounds, as well as chemical and physical properties of porous coordination polymers and metal-organic frameworks in particular. He is currently distinguished professor at Kyoto University's institute for integrated cell-material sciences (iCeMS), of which he is co-founder and current director.
Kumar Biradha is a researcher in the field of crystal engineering. He was born on 15 June 1968 in Relangi, Andhra Pradesh. He is a professor at the Department of Chemistry, Indian Institute of Technology, Kharagpur, and a member of Editorial Advisory board of Crystal Growth & Design, an American Chemical Society Journal.
Tomislav Friščić holds the Leverhulme International Professorship and Chair in Green and Sustainable chemistry at the University of Birmingham. His research focus is at the interface of green chemistry and materials science, developing solvent-free chemistry and mechanochemistry for the cleaner, efficient synthesis of molecules and materials, including organic solids such as pharmaceutical cocrystals, coordination polymers and Metal-Organic Frameworks (MOFs), and a wide range of organic targets such as active pharmaceutical ingredients. He is a Fellow of the Royal Society of Chemistry (RSC), member of the College of New Scholars, Artists and Scientists of the Royal Society of Canada and a corresponding member of the Croatian Academy of Sciences and Arts. He has served on the Editorial Board of CrystEngComm, the Early Career Board of the ACS journal ACS Sustainable Chemistry & Engineering, and was an Associate Editor for the journal Molecular Crystals & Liquid Crystals as well as for the journal Synthesis. He was a Topic Editor and Social Media Editor, and is currently a member of the Editorial Advisory Board of the journal Crystal Growth & Design published by the American Chemical Society (ACS). He famously has a dog named Zizi.
Carboxylate–based metal–organic frameworks are metal–organic frameworks that are based on organic molecules comprising carboxylate functional groups.
Metal–organic nanotubes (MONTs) are a class of crystalline coordination polymers consisting of organic ligands bonded to a metal or metal cluster that form single-walled one-dimensional porous structures. The usage of organic ligands allows the properties of the resulting material to be tuned, as in the parent class of metal-organic frameworks (MOFs), but like carbon nanotubes, MONTs are anisotropic structures.