Open Access. Powered by Scholars. Published by Universities.®
- Discipline
- Keyword
-
- Nanocomposites (42)
- Polystyrene (25)
- Fire retardancy (22)
- Cone calorimetry (13)
- Spectroelectrochemistry (11)
-
- Poly(methyl methacrylate) (10)
- Thermal stability (10)
- Inelastic scattering (8)
- NMR (8)
- Nanocomposite (8)
- Thermal degradation (8)
- Cobalt (7)
- Fire Retardancy (7)
- Iron (7)
- X-ray structures (7)
- Cross-linking (6)
- Crystal structure (6)
- Cyclic voltammetry (6)
- Electrochemistry (6)
- Ionic liquid (6)
- Layered double hydroxide (6)
- Molecular data (6)
- Oxidation (6)
- Cytochrome P450 (5)
- Kinetics (5)
- Layered double hydroxides (5)
- Polyethylene (5)
- Wave functions (5)
- XPS (5)
- Zinc (5)
- Publication Year
Articles 661 - 690 of 690
Full-Text Articles in Chemistry
Tris(Diethyldithiocarbamato)(4-Methoxyphenyl)Tellurium(Iv), P-Meoc6H4Te(S2Cnet2)3, And The Triclinic Modification Of Tris(Diethyldithiocarbamato)Phenyltellurium(Iv), Phte(S2Cnet2)3, Steinar Husebye, Sergey V. Lindeman
Tris(Diethyldithiocarbamato)(4-Methoxyphenyl)Tellurium(Iv), P-Meoc6H4Te(S2Cnet2)3, And The Triclinic Modification Of Tris(Diethyldithiocarbamato)Phenyltellurium(Iv), Phte(S2Cnet2)3, Steinar Husebye, Sergey V. Lindeman
Chemistry Faculty Research and Publications
No abstract provided.
Benz[4,5]Isoquino[1,2-B]Quinazoline-7,9-Dione And A Rearrangement Product Of Its Hydrolysis, 2-(1,8-Naphthalenedicarboximido)Benzamide, Sergey V. Lindeman, Igor I. Ponomarev, Alexandr L. Rusanov
Benz[4,5]Isoquino[1,2-B]Quinazoline-7,9-Dione And A Rearrangement Product Of Its Hydrolysis, 2-(1,8-Naphthalenedicarboximido)Benzamide, Sergey V. Lindeman, Igor I. Ponomarev, Alexandr L. Rusanov
Chemistry Faculty Research and Publications
No abstract provided.
Cis-(Diethyldithiocarbamato)Diiodo(Phenyl)Tellurium(Iv), Phte(S2Cnet2)I2, And Its Methoxy-Substituted Mixed Br/1 Analogue Cis-Bis(0.4-Bromo/0.6-Iodo)-(Diethyldithiocarbamato)(4-Methoxyphenyl) Tellurium(Iv), P-Meoc6H4Te(S2 Cnet2)(Br0.4I0.6)2, Steinar Husebye, Steffen Kudis, Sergey V. Lindeman, Peter Strauch
Cis-(Diethyldithiocarbamato)Diiodo(Phenyl)Tellurium(Iv), Phte(S2Cnet2)I2, And Its Methoxy-Substituted Mixed Br/1 Analogue Cis-Bis(0.4-Bromo/0.6-Iodo)-(Diethyldithiocarbamato)(4-Methoxyphenyl) Tellurium(Iv), P-Meoc6H4Te(S2 Cnet2)(Br0.4I0.6)2, Steinar Husebye, Steffen Kudis, Sergey V. Lindeman, Peter Strauch
Chemistry Faculty Research and Publications
The TeIV complexes PhTe(S2CNEt2)I2, (1), and p-MeOC6H4Te(S2CNEt2)Br0.4/I0.6) 2, (2), have been synthesized by reacting PhTeI3 with NaS2CNEt2, and p-MeOC6H4Te(S2CNEt2)2I with Br2, respectively. In (2), both I atoms are partially replaced by Br atoms in a 3:2 ratio. The structures display distorted octahedral Te coordination with two symmetrically coordinated S atoms [Te—S 2.550 (2)—2.569 (2) Å in three independent molecules of (1) and 2.523 …
Cis-6-Methoxycarbonyl-2,10-Dioxa-1-Phosphabicyclo[4.4.0]Decane 1-Oxide, Thomas M. Lane, Oscar P Rodriguez, Anthony Gerard Sommese, Sheldon E. Cremer, Dennis W. Bennett
Cis-6-Methoxycarbonyl-2,10-Dioxa-1-Phosphabicyclo[4.4.0]Decane 1-Oxide, Thomas M. Lane, Oscar P Rodriguez, Anthony Gerard Sommese, Sheldon E. Cremer, Dennis W. Bennett
Chemistry Faculty Research and Publications
The crystal structure of the title compound, C9H1505P, is described. The molecule consists of two cis-fused six-membered rings, both in the chair conformation..
An M-Carboranedicarboxylic Acid Dianilide, Sergey V. Lindeman, Georgii A. Kats, Lyudmila G. Komarova
An M-Carboranedicarboxylic Acid Dianilide, Sergey V. Lindeman, Georgii A. Kats, Lyudmila G. Komarova
Chemistry Faculty Research and Publications
The crystal structure of the 'non hydrogen-bonded' (according to IR data) polymorph of 1,7-bis(phenylcarbamoyl)-1,7-dicarba-closo-dodecaborane(12), C16-H22B10N2O2, has been determined. The two phenylamide groups have a Z configuration [the torsion angles 0-C-N-C are -2.3 (5) and -3.0 (5)°]. As a result both 'active' protons of these groups are almost completely shielded by other H atoms of the neighbouring carborane nucleus and phenyl substituents, and, therefore, no hydrogen-bonding contacts are found.
N1-Acetyl-3'-Methylandrosta-4,16-Dieno[16,17-D]Pyrazole-3-One, Sergey V. Lindeman, Alexandr I. Yanovsky, Ezequiel Huipe Nava, Alexey V. Kamernitzky, Alina V. Skorova, Irina V. Vesela
N1-Acetyl-3'-Methylandrosta-4,16-Dieno[16,17-D]Pyrazole-3-One, Sergey V. Lindeman, Alexandr I. Yanovsky, Ezequiel Huipe Nava, Alexey V. Kamernitzky, Alina V. Skorova, Irina V. Vesela
Chemistry Faculty Research and Publications
In an attempt to find the structural features promoting the thermal isomerization of the N-acylated steroid [16,17-d]pyrazoles into [17,16-c]pyrazole derivatives,the X-ray structure analysis of the title compound, C23H30N2O3, (1), has been carried out. The steroid moiety of (I) has the usual conformation. The dihedral angle between the planar pyrazole ring and the N-acetyl group is very small [5.6 (2)°], but the amide C-N bond seems to be substantially elongated [1.404 (3) Å ]. The d-pyrazole ring junction via a double bond leads to deformations of …
5-Acetyl[2.2]Paracyclophane, Sergey V. Lindeman, Yuri T. Struchkov, Vyacheslav N. Guryshev
5-Acetyl[2.2]Paracyclophane, Sergey V. Lindeman, Yuri T. Struchkov, Vyacheslav N. Guryshev
Chemistry Faculty Research and Publications
The title compound 5-acetyltricyclo[8.2.2.24,7]hexa-deca-4,6,10,12,13,15-hexaene, C18H18O,is the first example of a mono-π-substituted [2.2]paracyclophane to be structurally characterized. The average bending angles are α = 13.2 and β = 9.9°. The distance between the 'bottoms' of the practically parallel boat-like benzene nuclei is 3.098(2) Å. The π conjugation between the acetyl group and the substituted benzene cycle is negligible (rotation angle ca 45°) because of steric hindrance.
Β-Homopipitzolone, Ezequiel Huipe Nava, V. A. Igonin, Sergey V. Lindeman, Yuri T. Struchkov, V. Mendoza, G. Garcia, J. A. Guzman
Β-Homopipitzolone, Ezequiel Huipe Nava, V. A. Igonin, Sergey V. Lindeman, Yuri T. Struchkov, V. Mendoza, G. Garcia, J. A. Guzman
Chemistry Faculty Research and Publications
The structure of β-homopipitzolone (one of the two isomers of an intermediate product in the homocedrole synthesis) has been unequivocally established as 1 O-hydroxy-2,6,9-trimetbyltricyclo[6.3.1.01,6] dodeca-9-ene-5, II, 12-trione with relative IR,2R,6R,8S configuration.
Structure Of 2-Methyl-5,6,7-Triphenyl-6,7-Dihydropyrazolo[2,3-A]Pyrimidine, Sergey V. Lindeman, Yuri T. Struchkov, O. V. Shishkin, S. M. Desenko, V. V. Lipson, V. D. Orlov
Structure Of 2-Methyl-5,6,7-Triphenyl-6,7-Dihydropyrazolo[2,3-A]Pyrimidine, Sergey V. Lindeman, Yuri T. Struchkov, O. V. Shishkin, S. M. Desenko, V. V. Lipson, V. D. Orlov
Chemistry Faculty Research and Publications
C25H21N3, Mr = 363.46, monoclinic, P21/n, a = 9.245 (2), b = 23.502 (5), c = 9.340 (2) Å, β= 103.50(3)°, V=1973.3(2) Å3, Z=4, Dx= 1.220 (2) g cm-3, λ (Mo Kα )= 0.71069 Å, μ = 0.068 cm-1, F(000) = 768, T= 292 K, R = 0.091 for 1442 unique observed reflections. The dihydropyrimidine ring adopts a distorted sofa conformation. The aryl substituents on the saturated C atoms have an axial orientation.
Structure Of 3-(3,5-Dimethylpiperidino)-N-(P-Chlorophenyl)Succinimide, V. A. Igonin, Sergey V. Lindeman, Yuri T. Struchkov, Ezequiel Huipe Nava, V. Mendoza
Structure Of 3-(3,5-Dimethylpiperidino)-N-(P-Chlorophenyl)Succinimide, V. A. Igonin, Sergey V. Lindeman, Yuri T. Struchkov, Ezequiel Huipe Nava, V. Mendoza
Chemistry Faculty Research and Publications
In the title molecule, 3-(3,5-dimethylpiperidino )-1-(4-chlorophenyl)-2,5-pyrrolidinedione (1), the N-(p-chlorophenyl) substituent is rotated by 68.8° relative to the succinimide plane. The piperidinyl ring has a chair conformation with all substituents in equatorial positions; the conformation around the piperidino-succinimide C--N bond is staggered.
Structure Of (22S)-3Β-Acetoxy-20-(3-Isopropylisoxazolin-5-Yl)-4,4,14 Α-Trimethylpregn-8(9)-Ene, Sergey V. Lindeman, Mikael S. Alexanyan, Yuri T. Struchkov, Rajesh Kumar Thaper, Irina G. Reshetova, Alexey V. Kamernitzky
Structure Of (22S)-3Β-Acetoxy-20-(3-Isopropylisoxazolin-5-Yl)-4,4,14 Α-Trimethylpregn-8(9)-Ene, Sergey V. Lindeman, Mikael S. Alexanyan, Yuri T. Struchkov, Rajesh Kumar Thaper, Irina G. Reshetova, Alexey V. Kamernitzky
Chemistry Faculty Research and Publications
C32H51NO3, Mr = 497·7, orthorhombic, P212121, a = 7·577 (2), b = 10·510 (2), c = 35·399 (7) Å, V = 2819 (1) Å3, Z = 4, Dx = 1·173 g cm-3, λ (Mo Kα) = 0·71073 Å, μ = 0·69 cm-1, F(000) = 1096, T = 153 K, R = 0·0497 for 2235 observed reflections. The compound investigated is found to be a (22S)-epimer.
Structure Of 2,9-Dimethyl-1,10-Phenanthroline Hemihydrate, Doyle Britton, Larry C. Thompson, Richard C. Holz
Structure Of 2,9-Dimethyl-1,10-Phenanthroline Hemihydrate, Doyle Britton, Larry C. Thompson, Richard C. Holz
Chemistry Faculty Research and Publications
C14H12N2•½H2O, Mr = 217•27, tetragonal I41/a, a = 14•258 (3), c = 22•286 (4) Å, V = 4531 (3) Å3, Z = 16, Dx = 1•274 (1) g cm-3, Mo Kα radiation λ = 0•71073 Å, µ = 0•74 cm-1, F(000) = 1840, T = 297 K, R = 0•041 for 1196 unique observed reflections with I > 2σ(I). Pairs of dimethylphenanthroline molecules related by a twofold axis are bridged by water molecules lying on the twofold …
A Strategy For The Design Of Flame Retardants: Cross-Linking Processes, Charles A. Wilkie, Sunil J. Sirdesai, Thitivat Suebsaeng
A Strategy For The Design Of Flame Retardants: Cross-Linking Processes, Charles A. Wilkie, Sunil J. Sirdesai, Thitivat Suebsaeng
Chemistry Faculty Research and Publications
Cross-linking is identified as an effective means for flame retardation of polymers and schemes for the cross-linking of poly(ethylene terephthalate) and poly(methyl methacrylate) are presented. For poly(ethylene terephthalate) the scheme involves polymerization of the initially produced vinyl ester. This is followed by chain-stripping, producing a polyene, and cyclization of this polyene. For poly(methyl methacrylate) the scheme entails the formation of anhydride linkages between adjacent polymer strands. Evidence is presented to show the efficacy of these processes and information is produced to aid in the identification of new flame retardants.
Anti-Cancer Action Of Metal Complexes: Electron Transfer And Oxidative Stress?, Peter Kovacic, William J. Popp, James R. Ames, Michael D. Ryan
Anti-Cancer Action Of Metal Complexes: Electron Transfer And Oxidative Stress?, Peter Kovacic, William J. Popp, James R. Ames, Michael D. Ryan
Chemistry Faculty Research and Publications
Evidence is presented in support of an electron transfer mechanism for various metal complexes possessing anti-neoplastic properties. Cyclic voltammetry was performed on several metallocenes, bis(acetato)bis(imidazole)Cu(II), and coordination compounds (Cu or Fe) of the anti-tumor agents, bipyridine, phenanthroline, hydroxyurea, diethyldithiocarbamate, and α, α1-bis(8-hydroxyquinolin-7-yl)-4-methoxytoluene. The favorable reduction potentials ranged from +0.5 to -0.5 V. Electrochemical behavior is correlated in some cases with structure and physiological activity. Relevant literature data are discussed.
Interactions Of Water-Soluble Metalloporphyrins With Nucleic Acids Studied By Resonance Raman Spectroscopy, Jinghua H. Schneider, Junichi Odo, Kazuo Nakamoto
Interactions Of Water-Soluble Metalloporphyrins With Nucleic Acids Studied By Resonance Raman Spectroscopy, Jinghua H. Schneider, Junichi Odo, Kazuo Nakamoto
Chemistry Faculty Research and Publications
The resonance Raman spectra of water-soluble porphyrins, M(TMpy-P4) (M = Cu(II), Ni(II) and Co(III)) and their mixtures with poly(dG-dC)2, poly(dA-dT)2 and calf thymus and salmon DNAs were measured using a divided rotating cell to determine the magnitudes of frequency shift and intensity variation resulting from M(TMpy-P4)-nucleic acid interactions. Bands II(Cβ-H bending, ˜ 1100 cm-1) and VIII(Cβ-Cβ stretch, ˜ 1570 cm-1) show a large and small upward shift, respectively, when Cu(TMpy-P4) and Ni(TMpy-P4) are intercalated at the G-C sites. In contrast, these bands show a small upward and downward shift, respectively, when Co(TMpy-P4) is groove-bound at the A-T …
Electron Transfer-Oxy Radical Mechanism For Anti-Cancer Agents: 9-Anilinoacridines, Peter Kovacic, James R. Ames, Michael D. Ryan
Electron Transfer-Oxy Radical Mechanism For Anti-Cancer Agents: 9-Anilinoacridines, Peter Kovacic, James R. Ames, Michael D. Ryan
Chemistry Faculty Research and Publications
A possible mode of action involving electron transfer is advanced for the 9- anilinoacridines. The mechanism entails formation of toxic oxy radicals which destroy the neoplasm. Cyclic voltammetry was performed on iminium type ions derived by protonation of the acridines. Reductions were generally reversible with potentials of about - 0.60 V. Involvement of quinoidal metabolites is also a possibility. The relationship of electrochemical behavior to structure and physiological activity is addressed.
Structure Of L,L-Diphenylarsenanium Bromide Monohydrate, J. A. Campbell, R. Larsen, C. Campana, Sheldon E. Cremer, A. Gamliel
Structure Of L,L-Diphenylarsenanium Bromide Monohydrate, J. A. Campbell, R. Larsen, C. Campana, Sheldon E. Cremer, A. Gamliel
Chemistry Faculty Research and Publications
No abstract provided.
Structure Of L-Benzyl-2,2,3,3-Tetramethyl-L-Phenylphosphetanium Bromide, A Cyelobutane Derivative, J. A. Campbell, R. Larsen, C. Campana, Sheldon E. Cremer
Structure Of L-Benzyl-2,2,3,3-Tetramethyl-L-Phenylphosphetanium Bromide, A Cyelobutane Derivative, J. A. Campbell, R. Larsen, C. Campana, Sheldon E. Cremer
Chemistry Faculty Research and Publications
No abstract provided.
Charge Transfer-Oxy Radical Mechanism For Anti-Cancer Agents, Peter Kovacic, James R. Ames, Paavo Lumme, Hannu Elo, O. Cox, Michael D. Ryan
Charge Transfer-Oxy Radical Mechanism For Anti-Cancer Agents, Peter Kovacic, James R. Ames, Paavo Lumme, Hannu Elo, O. Cox, Michael D. Ryan
Chemistry Faculty Research and Publications
The proposal is advanced that anti-cancer drugs generally function by charge transfer resulting in formation of toxic oxy radicals which destroy the neoplasm. Electrochemical studies were performed with some of the main types of agents: iminium ions (adenine iminium from alkylating species, iminium metabolite of 6-mercaptopurine, nitidine, other polynuclear iminiums) and metal complexes (Pt(II)diaquodiammine-guanosine, copper salicylaldoximes). Reduction potentials ranged from -0.4 to -1.2 V. Literature data for quinones are presented and radiation is discussed. Based on the theoretical framework, a rationale is offered for the carcinogen-anti-cancer paradox and the role of antioxidants.
Structure Of L,L-Diphenylphosphorinanium Bromide Monohydrate, J. A. Campbell, R. Larsen, R. Ekeland, Sheldon E. Cremer
Structure Of L,L-Diphenylphosphorinanium Bromide Monohydrate, J. A. Campbell, R. Larsen, R. Ekeland, Sheldon E. Cremer
Chemistry Faculty Research and Publications
No abstract provided.
Structure Of A Solvated Nickel(Ii) Complex Of (S)-2'-(N-Benzylprolyl)Aminoacetophenone And (R)-Valine Schiff Base, C25H29N3Nio3.1/2c4H8O. Conformational Calculation Of Diastereomeric Complexes Of (R)-Valine And (S)-Valine, Sergey V. Lindeman, T. V. Timofeeva, V. I. Maleyev, Yuri N. Belokon, M. G. Ryzhov, V. M. Belikov, Yuri T. Struchkov
Structure Of A Solvated Nickel(Ii) Complex Of (S)-2'-(N-Benzylprolyl)Aminoacetophenone And (R)-Valine Schiff Base, C25H29N3Nio3.1/2c4H8O. Conformational Calculation Of Diastereomeric Complexes Of (R)-Valine And (S)-Valine, Sergey V. Lindeman, T. V. Timofeeva, V. I. Maleyev, Yuri N. Belokon, M. G. Ryzhov, V. M. Belikov, Yuri T. Struchkov
Chemistry Faculty Research and Publications
No abstract provided.
The Structure Of 1-Tert-Butyl-2,2,3,4,4-Pentamethylphosphetane 1-Oxide, C12H25Op, J. A. Campbell, C. N. Caughlan, A. Fitzgerald, C. Campana, Sheldon E. Cremer
The Structure Of 1-Tert-Butyl-2,2,3,4,4-Pentamethylphosphetane 1-Oxide, C12H25Op, J. A. Campbell, C. N. Caughlan, A. Fitzgerald, C. Campana, Sheldon E. Cremer
Chemistry Faculty Research and Publications
No abstract provided.
The Electrochemical Oxidation Of Substituted Catechols, Michael D. Ryan, Alice Yueh, Wen-Yu Chen
The Electrochemical Oxidation Of Substituted Catechols, Michael D. Ryan, Alice Yueh, Wen-Yu Chen
Chemistry Faculty Research and Publications
The oxidation of substituted catechols was studied by cyclic voltammetry, chronoamperometry, rotating ring‐disk electrode, and coulometry. The results showed that the quinones that were formed from the oxidation of substituted catechols reacted with the basic forms of the starting material to yield the dimeric product. These products were generally unstable and rapidly polymerized or underwent some other irreversible reaction to form an electroinactive product. For 3,4‐dihydroxyacetophenone and propriophenone, the intermediate was stable long enough to be observed in cyclic voltammetry. The rate of the coupling reaction was found to correlate well with the Hammett ρ‐σ parameters and indicated that there …
The Solid State 13C-Nmr And 19F-Nmr Spectra Of Some Graphite Fluorides, Charles A. Wilkie, Gong-Yu Lin, Daniel T. Haworth
The Solid State 13C-Nmr And 19F-Nmr Spectra Of Some Graphite Fluorides, Charles A. Wilkie, Gong-Yu Lin, Daniel T. Haworth
Chemistry Faculty Research and Publications
The solid state 13C nuclear magnetic resonance spectra of fluorinated graphites show two resonances, one of which is assigned to aromatic carbon and the other to aliphatic carbon. The resonances are very broad with the high-field resonance centered at about 35 ppm below tetramethylsilane (TMS) and a low-field resonance centered at about 160 ppm below tetramethylsilane. The high-field resonance is typical of an sp3-like carbon and the low-field resonance is assigned to sp2-like carbons. It is found that the aromatic resonance in graphite decreases with an increase in fluorination of the graphite fluorides examined in …
The Effect Of Slow Two‐Electron Transfers And Disproportionation On Cyclic Voltammograms, Michael D. Ryan
The Effect Of Slow Two‐Electron Transfers And Disproportionation On Cyclic Voltammograms, Michael D. Ryan
Chemistry Faculty Research and Publications
The EE mechanism (two‐electron transfer) for cyclic voltammetry was investigated in considerable detail along with the effect of disproportionation. The theory was developed for either the first or second electron transfer being slow while the other one was reversible. It was possible to develop generalized working curves for the height and shape of the wave regardless of the difference in Eo's and the values of α and Ks. This theory was then applied to the analysis of the reduction of benzil in the presence of alkaline earth ions in dimethylformamide.
The Solid State 13C-Nmr Spectra Of Some Carbides, Daniel T. Haworth, Charles A. Wilkie
The Solid State 13C-Nmr Spectra Of Some Carbides, Daniel T. Haworth, Charles A. Wilkie
Chemistry Faculty Research and Publications
The utility of NMR spectroscopy to the study of liquids or solids dissolved in liquids is well known. This technique has been used infrequently to studies in the solid state[I,2]. Work has been done on diamond, graphite and coa113-6]. The 13C-NMR of ebony and ivory have been studied by the magic angle technique[7]. The solid state 13C-NMR spectra of graphite and diamond can be interpreted in terms of tetrahedral (sp3) and trigonal planar (sp2) carbon atoms[8]. We now report our investigations using solid state 13C-NMR spectroscopy to study various types of carbides.
A Solid State 13C-Nmr Study Of Diamonds And Graphites, Charles A. Wilkie, Thomas C. Ehlert, Daniel T. Haworth
A Solid State 13C-Nmr Study Of Diamonds And Graphites, Charles A. Wilkie, Thomas C. Ehlert, Daniel T. Haworth
Chemistry Faculty Research and Publications
The 13C-NMR spectra of gem quality and industrial diamonds show two resonances with the more intense resonance at high field. Two resonances are also shown in 13C-NMR spectra of various graphites; however, the low field resonance is of greater intensity than the high field resonance in the graphites. The resonances are very broad and they are assigned to graphite type (sp2) carbon and diamond type (sp3) carbon.
The 13C-Nmr Solid State Spectroscopy Of Various Classes Of Coals, Charles A. Wilkie, Daniel T. Haworth
The 13C-Nmr Solid State Spectroscopy Of Various Classes Of Coals, Charles A. Wilkie, Daniel T. Haworth
Chemistry Faculty Research and Publications
The 13C-NMR spectra of various classes of coal obtained in the solid state show two resonances, one of which is assigned to aromatic carbon and the other to aliphatic carbon. The resonances are very broad with the high field resonance centered at about 7 ppm below tetramethylsilane and a low field resonance centered at about 140 ppm below tetramethysilane. Based on our previous solid state 13C-NMR studies of graphite and diamond, the high field resonance is typical of a sp3 carbon whereas the low fields resonance is assigned to a sp2 carbon whereas the low fields …
A 13C-Nmr Study Of Cis-Ti(Ac Ac)2Cl2, Daniel T. Haworth, Charles A. Wilkie
A 13C-Nmr Study Of Cis-Ti(Ac Ac)2Cl2, Daniel T. Haworth, Charles A. Wilkie
Chemistry Faculty Research and Publications
No abstract provided.
Effect Of Sodium Ions On The Electrochemical Reduction Of Diethyl Fumarate In Dimethylsulfoxide And Acetonitrile, Michael D. Ryan, Dennis H. Evans
Effect Of Sodium Ions On The Electrochemical Reduction Of Diethyl Fumarate In Dimethylsulfoxide And Acetonitrile, Michael D. Ryan, Dennis H. Evans
Chemistry Faculty Research and Publications
No abstract provided.