Physical Sciences and Mathematics Commons^™

Direct Patterning Of Silanized-Biomolecules On Semiconductor Surfaces, Dorjderem Nyamjav, Richard C. Holz

Chemistry Faculty Research and Publications

A novel approach to pattern silanized-biomolecules directly onto glass (SiO_x) substrates via Dip-Pen nanolithography (DPN) and microcontact printing (μCP) is presented. Subsequent hybridization reactions of DPN patterned silanized-DNA with its complementary strands provide “proof-of-concept” that the patterned oligonucleotides maintain their biological activities. The fabrication strategy does not require premodification of substrates and offers a cheap and robust way to immobilize molecules on electronically important semiconductor surfaces.

Study On Intumescent Flame Retarded Polystyrene Composites With Improved Flame Retardancy, Hongdian Lu, Charles A. Wilkie

Chemistry Faculty Research and Publications

The flame retardancy and thermal stability of ammonium polyphosphate/tripentaerythritol (APP/TPE) intumescent flame retarded polystyrene composites (PS/IFR) combined with organically-modified layered inorganic materials (montmorillonite clay and zirconium phosphate), nanofiber (multiwall carbon nanotubs), nanoparticle (Fe₂O₃) and nickel catalyst were evaluated by cone calorimetry, microscale combustion calorimetry (MCC) and thermogravimetric analysis (TGA). Cone calorimetry revealed that a small substitution of IFR by most of these fillers (≤2%) imparted substantial improvement in flammability performance. The montmorillonite clay exhibited the highest efficiency in reducing the peak heat release rate of PS/IFR composite, while zirconium phosphate modified with C₂₁H_{26 …}

Chelate-Assisted Oxidative Coupling Reaction Of Arylamides And Unactivated Alkenes: Mechanistic Evidence For Vinyl C–H Bond Activation Promoted By An Electrophilic Ruthenium-Hydride Catalyst, Ki Hyeok Kwon, Do W. Lee, Chae S. Yi

Chemistry Faculty Research and Publications

The cationic ruthenium hydride complex [(η⁶-C₆H₆)(PCy₃)(CO)RuH]⁺BF₄⁻ was found to be a highly regioselective catalyst for the oxidative C−H coupling reaction of aryl-substituted amides and unactivated alkenes to give o-alkenylamide products. The kinetic and spectroscopic analyses support a mechanism involving a rapid vinyl C−H activation followed by a rate-limiting C−C bond formation step.

The Effect Of Boron-Containing Layered Hydroxy Salt (Lhs) On The Thermal Stability And Degradation Kinetics Of Poly (Methyl Methacrylate), Stephen Majoni, Shengpei Su, Jeanne Hossenlopp

Chemistry Faculty Research and Publications

A boron-containing layered hydroxy salt (LHS), ZHTMDBB, was prepared and compounded with a highly flammable synthetic polymer, poly (methyl methacrylate) {PMMA}, via melt blending: the composite structure was intercalated with poor dispersion. The effect of this LHS on the flammability, thermal stability and degradation kinetics of PMMA was investigated via cone calorimetry and thermogravimetric analysis. The addition of 3-10% by mass of ZHTMDBB to PMMA resulted in significant reduction of peak heat release rate (22-48%) of the polymer and improvements in thermal stability were observed in both air and nitrogen. Effective activation energies for the degradation process were evaluated using …

The Utility Of Nanocomposites In Fire Retardancy, Linjiang Wang, Xuejun He, Charles A. Wilkie

Chemistry Faculty Research and Publications

Nanocomposites have been shown to significantly reduce the peak heat release rate, as measured by cone calorimetry, for many polymers but they typically have no effect on the oxygen index or the UL-94 classification. In this review, we will cover what is known about the processes by which nanocomposite formation may bring this about. Montmorillonite will be the focus in this paper but attention will also be devoted to other materials, including carbon nanotubes and layered double hydroxides. A second section will be devoted to combinations of nanocomposite formation with conventional (and unconventional) fire retardants. The paper will conclude with …

Chain-Selective And Regioselective Ethylene And Styrene Dimerization Reactions Catalyzed By A Well-Defined Cationic Ruthenium-Hydride Complex: New Insights On The Styrene Dimerization Mechanism, Do W. Lee, Chae S. Yi

Chemistry Faculty Research and Publications

The cationic ruthenium hydride complex [(η⁶-C₆H₆)(PCy₃)(CO)RuH]⁺BF₄⁻ was found to be a highly regioselective catalyst for the ethylene dimerization reaction to give 2-butene products (TOF = 1910 h⁻¹, >95% selectivity for 2-butenes). The dimerization of styrene exclusively produced the head-to-tail dimer (E)-PhCH(CH₃)CH═CHPh at an initial turnover rate of 2300 h⁻¹. A rapid and extensive H/D exchange between the vinyl hydrogens of styrene-d₈ and 4-methoxystyrene was observed within 10 min without forming the dimer products at room temperature. The inverse …

X-Ray Structure Of Mer-[Mo(Co)3(Pph3)(Κ2-Dppm)], Shishir Ghosh, Shariff E. Kabir, Faranza K. Camellia, Md. Kamal Hossain, Daniel T. Haworth, Sergey V. Lindeman, Tasneem A. Siddiquee, Dennis W. Bennett

Chemistry Faculty Research and Publications

Treatment of [Mo(CO)₃(NCMe)₃] with bis(diphenylphosphino)methane (dppm) and triphenylphosphine (PPh₃) at 50 °C afforded mer-[Mo(CO)₃(PPh₃)(κ²-dppm)] (1) in 55% yield which has been characterized by single crystal X-ray diffraction studies and spectroscopic measurements. Compound 1 crystallizes in the triclinic space group P−1 with a = 10.3449(6), b = 11.1570(6), c = 17.8961(10) Å, β = 80.8400(10)°, Z = 2 and V = 1959.8(2) ų.

De Novo Synthesis Of Polyhydroxyl Aminocyclohexanes, Anobick Sar, Sergey Lindeman, William Donaldson

Chemistry Faculty Research and Publications

The syntheses of 12 stereochemically diverse polyhydroxyl aminocyclohexane (“aminocyclitols”) derivatives are described. These short syntheses require 2–5 steps from N-(2,4-cyclohexadien-1-yl)phthalimide, which is prepared in two steps from tricarbonyl(cyclohexadienyl)iron(1+). The relative stereochemistries of the aminocyclitols were assigned by ¹H NMR spectroscopy as well as X-ray diffraction analysis.

Regioselective Formation Of Α-Vinylpyrroles From The Ruthenium-Catalyzed Coupling Reaction Of Pyrroles And Terminal Alkynes Involving C–H Bond Activation, Ruili Gao, Chae S. Yi

Chemistry Faculty Research and Publications

The cationic ruthenium catalyst Ru₃(CO)₁₂/NH₄PF₆ was found to be highly effective for the intermolecular coupling reaction of pyrroles and terminal alkynes to give gem-selective α-vinylpyrroles. The carbon isotope effect on the α-pyrrole carbon and the Hammett correlation from a series of para-substituted N-arylpyrroles (ρ = −0.90) indicate a rate-limiting C−C bond formation step of the coupling reaction.

Mixed-Metal Cluster Synthesis: [Re(Co)3(Μ-S2Nc7H4)]2 As A Precursor For Tri- And Tetranuclear 2-Mercaptobenzothiolato Capped Clusters, Shishir Ghosh, Kamrun N. Khanam, Md. Kamal Hossain, G. M. Golzar Hossain, Daniel T. Haworth, Sergey V. Lindeman, Graeme Hogarth, Shariff E. Kabir

Chemistry Faculty Research and Publications

The readily prepared [Re₂(CO)₆(μ-S₂NC₇H₄)₂] (1) reacts with Group 8 trimetallic carbonyl clusters to yield new mixed-metal tri- and tetranuclear clusters. With [Os₃(CO)₁₀(NCMe)₂] at 80 °C the tetranuclear mixed-metal cluster [Os₃Re(CO)₁₃(μ₃-C₇H₄NS₂)] (2) is the only isolated product. With Ru₃(CO)₁₂ products are dependent upon the reaction temperature. At 80 °C, a mixture of tetranuclear mixed-metal [Ru₃Re(CO)₁₃(μ₃-C₇H₄NS₂)] (5) …

Structural Basis For Catalysis By The Mono- And Dimetalated Forms Of The Dape-Encoded N-Succinyl-L,L-Diaminopimelic Acid Desuccinylase, Boguslaw P. Nocek, Danuta Gillner, Yao Fan, Richard C. Holz, Andzrej Joachimiak

Chemistry Faculty Research and Publications

Biosynthesis of lysine and meso-diaminopimelic acid in bacteria provides essential components for protein synthesis and construction of the bacterial peptidoglycan cell wall. The dapE operon enzymes synthesize both meso-diaminopimelic acid and lysine and, therefore, represent potential targets for novel antibacterials. The dapE-encoded N-succinyl-l,l-diaminopimelic acid desuccinylase functions in a late step of the pathway and converts N-succinyl-l,l-diaminopimelic acid to l,l-diaminopimelic acid and succinate. Deletion of the dapE gene is lethal to Helicobacter pylori and Mycobacterium smegmatis, indicating that DapE's are essential for cell growth and proliferation. Since there are no similar pathways in humans, inhibitors …

Synergistic Effect Of Carbon Nanotubes And Decabromodiphenyl Oxide/Sb2O3 In Improving The Flame Retardancy Of Polystyrene, Hongdian Lu, Charles A. Wilkie

Chemistry Faculty Research and Publications

Brominated flame retardant polystyrene composites were prepared by melt blending polystyrene, decabromodiphenyl oxide, antimony oxide, multi-wall carbon nanotubes and montmorillonite clay. Synergy between carbon nanotubes and clay and the brominated fire retardant was studied by thermogravimetric analysis, microscale combustion calorimetry and cone calorimetry. Nanotubes are more efficient than clay in improving the flame retardancy of the materials and promoting carbonization in the polystyrene matrix. Comparison of the results from the microscale combustion calorimeter and the cone calorimeter indicate that the rate of change of the peak heat release rate reduction in the microscale combustion calorimeter was slower than that in …

Inhibitors Of NΑ-Acetyl-L-Ornithine Deacetylase: Synthesis, Characterization And Analysis Of Their Inhibitory Potency, J. Hlavacek, J. Picha, V. Vanek, J. Jiracek, J. Slaninova, V. Fucik, M. Budesinsky, Danuta M. Gillner, Richard C. Holz

Chemistry Faculty Research and Publications

A series of N ^α-acyl (alkyl)- and N ^α-alkoxycarbonyl-derivatives of l- and d-ornithine were prepared, characterized, and analyzed for their potency toward the bacterial enzyme N ^α-acetyl-l-ornithine deacetylase (ArgE). ArgE catalyzes the conversion of N ^α-acetyl-l-ornithine to l-ornithine in the fifth step of the biosynthetic pathway for arginine, a necessary step for bacterial growth. Most of the compounds tested provided IC₅₀ values in the μM range toward ArgE, indicating that they are moderately strong inhibitors. N ^α-chloroacetyl-l-ornithine (1g) was the best inhibitor tested toward ArgE providing an IC₅₀ value of 85 …

Investigation Of The Thermal Degradation Of Polyurea: The Effect Of Ammonium Polyphosphate And Expandable Graphite, Walid Awad, Charles A. Wilkie

Chemistry Faculty Research and Publications

Polyurea was compounded with ammonium polyphosphate and expandable graphite and the morphology was studied by atomic force microscopy. The thermal degradation of polyurea and polyurea compounded with the additives has been investigated using thermogravimetry coupled with Fourier Transform infrared spectroscopy and mass spectrometry. The study of the thermal degradation and the parameters affecting the thermal stability of PU is essential in order to effectively design flame retarded polyurea. In general, thermal decomposition of polyurea occurs in two steps assigned to the degradation of the hard segment and soft segment, respectively. Adding these additives accelerates the decomposition reaction of polyurea. However, …

Intermolecular Dehydrative Coupling Reaction Of Arylketones With Cyclic Alkenes Catalyzed By A Well-Defined Cationic Ruthenium-Hydride Complex: A Novel Ketone Olefination Method Via Vinyl C–H Bond Activation, Chae S. Yi, Do W. Lee

Chemistry Faculty Research and Publications

The cationic ruthenium−hydride complex [(η⁶-C₆H₆)(PCy₃)(CO)RuH]⁺BF₄⁻ was found to be a highly effective catalyst for the intermolecular olefination reaction of aryl ketones with cycloalkenes. The preliminary mechanistic analysis revealed that an electrophilic ruthenium−vinyl complex is the key species for mediating both vinyl C−H bond activation and the dehydrative olefination steps of the coupling reaction.

Nmr Dynamics Investigation Of Ligand-Induced Changes Of Main And Side-Chain Arginine N-H’S In Human Phosphomevalonate Kinase, Andrew L. Olson, Sheng Cai, Timothy J. Herdendorf, Henry M. Miziorko, Daniel S. Sem

Chemistry Faculty Research and Publications

Phosphomevalonate kinase (PMK) catalyzes phosphoryl transfer from adenosine triphosphate (ATP) to mevalonate 5-phosphate (M5P) on the pathway for synthesizing cholesterol and other isoprenoids. To permit this reaction, its substrates must be brought proximal, which would result in a significant and repulsive buildup of negative charge. To facilitate this difficult task, PMK contains 17 arginines and eight lysines. However, the way in which this charge neutralization and binding is achieved, from a structural and dynamics perspective, is not known. More broadly, the role of arginine side-chain dynamics in binding of charged substrates has not been experimentally defined for any protein to …

Thermal Degradation Of High-Temperature Fluorinated Polyimide And Its Carbon Fiber Composite, Andrea D. Adamczak, Adam A. Spriggs, Danielle M. Fitch, Walid Awad, Charles A. Wilkie, Jaime C. Grunlan

Chemistry Faculty Research and Publications

No abstract provided.

An In Vitro Spectroscopic Analysis To Determine Whether Para-Chloroaniline Is Produced From Mixing Sodium Hypochlorite And Chlorhexidine, John Thomas, Daniel S. Sem

Chemistry Faculty Research and Publications

Introduction: The purpose of this in vitro study was to determine whether para-chloroaniline (PCA) is formed through the reaction of mixing sodium hypochlorite (NaOCl) and chlorhexidine (CHX).

Methods: Initially, commercially available samples of chlorhexidine acetate (CHXa) and PCA were analyzed with ¹H nuclear magnetic resonance (NMR) spectroscopy. Two solutions, NaOCl and CHXa, were warmed to 37ºC, and when mixed they produced a brown precipitate. This precipitate was separated in half, and pure PCA was added to 1 of the samples for comparison before they were each analyzed with ¹H NMR spectroscopy.

Results: The peaks in …

Anion Exchange Kinetics Of Nanodimensional Layered Metal Hydroxides: Use Of Isoconversional Analysis, Stephen Majoni, Jeanne Hossenlopp

Chemistry Faculty Research and Publications

Anion exchange reactions of nanodimensional layered metal hydroxide compounds are utilized to create materials with targeted physical and chemical properties and also as a means for controlled release of intercalated anions. The kinetics of this important class of reaction are generally characterized by model-based approaches. In this work, a different approach based on isothermal, isoconversional analysis was utilized to determine effective activation energies with respect to extent of reaction. Two different layered metal hydroxide materials were chosen for reaction with chloride anions, using a temperature range of 30−60 °C. The concentrations of anions released into solution and the changes in …

Breaking The Cycle: Impact Of Sterically-Tailored Tetra(Pyrazolyl)Lutidines On The Self-Assembly Of Silver(I) Complexes, Tyler James Morin, Andrew Merkel, Sergey V. Lindeman, James R. Gardinier

Chemistry Faculty Research and Publications

A improved preparation of the pentadentate ligand α,α,α′,α′-tetra(pyrazolyl)lutidine, pz₄lut, and the syntheses of three new alkyl-substituted pyrazolyl derivatives pz^4′₄lut (pz4′ = 4-methylpyrazolyl), pz*₄lut (pz* = 3,5-dimethylpyrazolyl), and pz^DIP₄lut (pzDIP = 3,5-diisopropylpyrazolyl) are described. The silver(I) complexes of these ligands were studied to ascertain the impact of pyrazolyl substitution, if any, on their binding modes and on solubility issues. In the solid state, [Ag(pz₄lut)](BF₄) (1), [Ag(pz^4′4lut)](BF4) (2), and [Ag(pz*₄lut)](BF4) (3 …

A Shortened Synthesis Of Optically Pure Tricarbonyl[Methyl (2e,4e)-6-Oxo-2,4-Hexadienoate]Iron Leading To Improved Yield, Rajesh K. Pandey, Sergey Lindeman, William Donaldson

Chemistry Faculty Research and Publications

The (+)- and (–)-enantiomers of tricarbonyl[methyl (2E,4E)-6-oxo-2,4-hexadienoate]iron are prepared in 4 steps from commercially available hexadienal (26% and 25% yields, respectively).

Infrared Spectroelectrochemical Reduction Of Iron Porphyrin Complexes, Zhongcheng Wei, Michael D. Ryan

Chemistry Faculty Research and Publications

The spectroelectrochemistry of iron porphinones and their nitrosyl complexes were examined by infrared spectroscopy, as well as ferrous octaethylporphyrin nitrosyl. With the use of d₈-THF, the solvent was transparent down to 1200 cm⁻¹. For the porphinones, the reduction of the macrocycle ring could be observed by the changes in the ν_CO band and, for the nitrosyl complex, the changes in the nitrosyl ligand were directly observable from the ν_NO band. Formation of the ferrous complexes led to a small downshift in the ν_CO band. Further reduction to the formal Fe(“I”) complex led to …

Resin-Modified Glass-Ionomer Setting Reaction Competition, David W. Berzins, S. Abey, M. C. Costache, Charles A. Wilkie, H. W. Roberts

Chemistry Faculty Research and Publications

Resin-modified glass ionomers (RMGI) set by at least 2 mechanisms dependent upon reactant diffusion prior to gelation. Each reaction’s kinetics and setting mechanism may rely on and/or compete with the other. In this study, we investigated RMGI setting reaction interactions using differential scanning calorimetry (DSC) by varying light-cure initiation times. A RMGI was analyzed with isothermal and dynamic temperature scan DSC with light-curing occurring immediately, or at 5 or 10 minutes after mixing as well as without light-activation. Results show that as time allowed for the acid-base reaction increased, the light-activation polymerization exotherm decreased. Conversely, analysis of DSC data suggests …

Isomerization As A Key Path To Molecular Products In The Gas-Phase Decomposition Of Halons, Aimable Kalume, Lisa George, Scott Reid

Chemistry Faculty Research and Publications

The decomposition of halons remains controversial concerning the branching between radical and molecular products. The latter channel, where it has been found, is presumed to occur via a constrained symmetric multicenter transition state. Isomerization pathways in the gas-phase chemistry of halons have rarely been considered, despite the fact that the iso-halons, which feature a halogen−halogen bond, are widely recognized as important reactive intermediates in condensed phases. In this Letter, detailed calculations and modeling of the unimolecular decomposition of several important halons, including CF₂Cl₂, CF₂Br₂, and CHBr₃, reveal that isomerization is …

Immobilization Of Motile Bacterial Cells Via Dip-Pen Nanolithography, Dorjderem Nyamjav, Sergey Rozhok, Richard C. Holz

Chemistry Faculty Research and Publications

A strategy to bind bacterial cells to surfaces in a directed fashion via dip-pen nanolithography (DPN) is presented. Cellular attachment to pre-designed DPN generated microarrays was found to be dependent on the shape and size of the surface feature. While this observation is likely due in part to a dense, well formed mercaptohexadecanoic acid (MHA) monolayer generated via DPN, it may also simply be due to the physical shape of the surface structure. Motile Pseudomonas aeruginosa bacterial cells were observed to bind to DPN generated mercaptohexadecanoic acid/poly-L-lysine (MHA/PLL) line patterns, 'blocks' made up of eight lines with 100 nm spacings, …

Thermal Degradation Studies On Pmma–Het Acid Based Oligoesters Blends, Thangamani Rajkumar, Chinnaswamy Thangavel Vijayakumar, Palanichamy Sivasamy, Bojja Sreedhar, Charles A. Wilkie

Chemistry Faculty Research and Publications

Imparting thermal stability to polymethyl methacrylate (PMMA) without affecting its optical clarity is attempted by incorporating HET acid based oligoesters. Pure PMMA and PMMA containing five and 20 wt% of four different oligoesters are separately prepared using bulk polymerization. The thermal properties of the materials studied using DSC, TG, TG–FTIR and Pyr–GC–MS are presented. The main volatile degradation products identified are CO, HCl, CO₂, H₂O, hexachlorocyclopentadiene, hexachloroendomethylene tetrahydrophthalic acid/anhydride and methyl methacrylate. A detailed mechanism for the influence of the degradation products of HET acid based oligoesters on the thermal degradation of PMMA is also presented.

Tricarbonylrhenium(I) And Manganese(I) Complexes Of 2-(Pyrazolyl)-4-Toluidine, Brendan J Liddle, Sarath Wanniarachchi, Sergey V. Lindeman, James R. Gardinier

Chemistry Faculty Research and Publications

A series of tricarbonyl rhenium(I) and manganese(I) complexes of the electroactive 2-(pyrazolyl)-4-toluidine ligand, H(pzAn^Me), has been prepared and characterized including by single crystal X-ray diffraction studies. The reactions between H(pzAn^Me) and M(CO)₅Br afford fac-MBr(CO)₃[H(pzAn^Me)] (M = Mn, 1a; Re, 1b) complexes. The ionic species {fac-M(CH₃CN)(CO)₃[H(pzAn^Me)]}(PF₆) (M = Mn, 2a; Re, 2b) were prepared by metathesis of 1a or 1b with TlPF₆ in acetonitrile. Complexes 1a and 1b partly ionize to {M(CH₃CN)(CO)₃[H(pzAn^Me)]^{+ …}

Affinity Capillary Electrophoretic Study Of K+/Na+ Selectivity Of Hexaarylbenzene-Based Polyaromatic Receptor, Sille Ehala, Rajendra Rathore, Emanuel Makrlik, Petr Toman, Václav Kašička

Chemistry Faculty Research and Publications

Affinity capillary electrophoretic (ACE) study has proved the selectivity of hexaarylbenzene-based polyaromatic receptor (R) for K+ ion over Na+ ion. The apparent binding constants of the R complexes with K+ and Na+ ions were determined from the dependence of effective electrophoretic mobility of R on the concentration of the above alkali metal ions in the background electrolyte using a non-linear regression analysis. The apparent binding constants (Kb) of the K-R+ and Na–R+ complexes in methanolic medium were evaluated as log Kb = 3.20 ± 0.22 for the K–R+ complex, and log Kb≅−0.7 for the Na–R+ complex.

Immobilization Of The Aminopeptidase From Aeromonas Proteolytica On Mg2+/Al3+ Layered Double Hydroxide Particles, Steven T. Frey, Stephanie L. Guilmet, Richard G. Egan Iii, Alyssa Bennett, Sarah R. Soltau, Richard C. Holz

Chemistry Faculty Research and Publications

A novel biomaterial formed by the immobilization of the Aminopeptidase from Aeromonas proteolytica (AAP) on synthetic Mg²⁺ and Al³⁺ ion-containing layered double hydroxide (LDH) particles was prepared. Immobilization of AAP on the LDH particles in a buffered, aqueous mixture is rapid such that the maximum loading capacity, 1 × 10⁻⁹ moles of AAP/mg LDH, is achieved in a few minutes. X-ray powder diffraction of LDH samples before and after treatment with AAP indicates that the enzyme does not intercalate between the layers of LDH, but instead binds to the surface. Treatment of AAP/LDH with various amounts of …