Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Michael T. Hay is active.

Publication


Featured researches published by Michael T. Hay.


Inorganic Chemistry Communications | 2003

Synthesis and characterization of a novel iron (III) silsesquioxane compound

Michael T. Hay; Brandan J. Hainaut; Steven J. Geib

Abstract A new iron (III) containing silsesquioxane compound, [Bu4N][((CH3)2CHCH2)7Si7O12FeCl] (4) was prepared by reacting [Bu4N][FeCl4] (3) with the isobutyl substituted silsesquioxane trisilanol, ((CH3)2CHCH2)7Si7O12H3, (1) in the presence of three equivalents of triethylamine, Et3N (2). The magnetic susceptibility of 4 was measured by Evans method, and the effective magnetic moment, μeff, is consistent with a high spin Fe (III) center. The composition and molecular structure of 4 was fully determined by IR, elemental analysis, APCI mass spec, and X-ray crystal analyses, and its potential as a precursor to a model of the structure and chemistry of the Fe-ZSM-5 catalyst is discussed.


Inorganica Chimica Acta | 2003

New Fe(III) and Os(VI) silsesquioxanes

Patricia A. Shapley; W.Stuart Bigham; Michael T. Hay

Abstract The high-spin iron(III) silsesquioxane complexes [N( n Bu) 4 ][( cyclo -C 5 H 9 ) 7 Si 7 O 12 FeCl] and [N( n Bu) 4 ][( cyclo -C 5 H 9 ) 7 Si 7 O 12 Fe(OSiMe 3 )] result from the reaction of ( cyclo -C 5 H 9 ) 7 Si 7 O 9 (OH) 3 with either [N( n Bu) 4 ][FeCl 4 ] or [N( n Bu) 4 ][Fe(OSiMe 3 ) 4 ]. Substitution of the terminal chloride or (trimethyl)silanolate ligands with tert -butoxide produces [N( n Bu) 4 ][( cyclo -C 5 H 9 ) 7 Si 7 O 12 Fe(OCMe 3 )]. Similar substitution reactions with the methyl ester of N -acetylcysteine produce [N( n Bu) 4 ][( cyclo -C 5 H 9 ) 7 Si 7 O 12 Fe{SCH 2 CH(NHCOCH 3 )CO 2 Me}]. A dimeric complex, [( cyclo -C 5 H 9 ) 7 Si 7 O 12 Fe(NEt 3 )] 2 , forms in the reaction of ( cyclo -C 5 H 9 ) 7 Si 7 O 9 (OH) 3 with NEt 3 and FeCl 3 . The reaction between ( cyclo -C 5 H 9 ) 7 Si 7 O 9 (OH) 2 (OSiMe 3 ) and [Ph 4 P][Os(N)Cl 4 ] forms [PPh 4 ][( cyclo -C 5 H 9 ) 7 Si 7 O 11 (OSiMe 3 )Os(N)Cl 2 ], a square-pyramidal Os(VI) complex with a bidentate siloxy ligand.


Acta Crystallographica Section E: Crystallographic Communications | 2005

Tetrabutyl­ammonium tetrachloro­ferrate(III)

Michael T. Hay; Steven J. Geib

In the title compound, [(C4H9)4N][FeCl4], the central FeIII atom in the anion is tetrahedrally coordinated by four Cl atoms, while the cation exists as a central N atom bonded to four n-butyl groups, also in a tetrahedral arrangement. Both the cation and anion lie on crystallographic twofold axes.


Water Environment Research | 2015

Analytical Methods for Pesticide Residues in the Water Environment.

Liang Hc; Bilon N; Michael T. Hay

A review of literature published in 2014 focusing on analytical methods for pesticides in the water environment is presented here. The review includes publications on extraction methods and on analytical methods such as biochemical assays and immunoassays, electrochemical methods, chromatographic or mass spectrometric techniques, spectrophotometric techniques, fluorescence, and chemiluminescence techniques.


Acta Crystallographica Section E-structure Reports Online | 2012

Tetra-butyl-ammonium tetra-kis-(trimethyl-silanolato-κO)ferrate(III).

Michael T. Hay; Richard J. Staples; Andre Lee

In the title salt, (C16H36N)[Fe(C3H9OSi)4], the cation contains a central N atom bonded to four n-butyl alkyl groups in a tetrahedral arrangement, while the anion contains a central FeIII atom tetrahedrally coordinated by four trimethylsilanolate ligands.


Journal of the American Chemical Society | 1998

SPECTROSCOPY OF MIXED-VALENCE CUA-TYPE CENTERS : LIGAND-FIELD CONTROL OF GROUND-STATE PROPERTIES RELATED TO ELECTRON TRANSFER

Daniel R. Gamelin; David W. Randall; Michael T. Hay; Robert P. Houser; Ton C. Mulder; Gerard W. Canters; Simon de Vries; William B. Tolman; Yi Lu; Edward I. Solomon


Proceedings of the National Academy of Sciences of the United States of America | 1996

Construction and characterization of an azurin analog for the purple copper site in cytochrome c oxidase

Michael T. Hay; John H. Richards; Yi Lu


Biochemistry | 1999

Structural basis of electron transfer modulation in the purple CuA center.

Howard Robinson; Marjorie C. Ang; Yi Gui Gao; Michael T. Hay; Yi Lu; Andrew H.-J. Wang


Inorganic Chemistry | 1998

Spectroscopic Characterization of an Engineered Purple CuA Center in Azurin

Michael T. Hay; Marjorie C. Ang; Daniel R. Gamelin; Edward I. Solomon; William E. Antholine; Martina Ralle; Ninian J. Blackburn; Priscilla D. Massey; Xiaotang Wang; and Angela H. Kwon; Yi Lu


Journal of the American Chemical Society | 1995

Engineered Cupredoxins and Bacterial Cytochrome c Oxidases Have Similar CuA Sites: Evidence from Resonance Raman Spectroscopy

Colin R. Andrew; Pekka Lappalainen; Matti Saraste; Michael T. Hay; Yi Lu; C. Dennison; Gerard W. Canters; James A. Fee; Nobuhumi Nakamura; Joann Sanders-Loehr

Collaboration


Dive into the Michael T. Hay's collaboration.

Top Co-Authors

Avatar

Steven J. Geib

University of Pittsburgh

View shared research outputs
Top Co-Authors

Avatar

Andre Lee

Michigan State University

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

James A. Fee

Scripps Research Institute

View shared research outputs
Top Co-Authors

Avatar

John H. Richards

California Institute of Technology

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge