scholarly journals A study of the vacuum pyrolysis of para-substituted diazoacetophenones with He(I) ultraviolet photoelectron spectroscopy

1998 ◽  
Vol 76 (8) ◽  
pp. 1162-1173 ◽  
Author(s):  
Nick H Werstiuk ◽  
Heidi M Muchall ◽  
Jiagong Ma ◽  
Michael TH Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Quantum Chemical ◽  
Laser Power ◽  
Spectroscopic Data ◽  
Power Level ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Wolff Rearrangement ◽  
Vacuum Pyrolysis ◽  
The Subject ◽  
Ab Inito

An ultraviolet photoelectron (PE) spectrometer apparatus that utilizes a tuneable 50 W CW CO2 laser as a directed heat source was used to study the vacuum pyrolysis of diazoacetophenone (1a) and its p-methyl, p-methoxy, p-chloro, and p-nitro analogues 1b, 1c, 1d, and 1e. Analysis of the pyrolysate with He(I) ultraviolet PE spectroscopy shows that at a laser power level of 26 W (500 ± 50°C) 1a, 1b, 1c, and 1d, cleanly yield the corresponding phenylketenes 2a, 2b, 2c, and 2d, respectively, the products of the Wolff rearrangement of the incipient ketocarbenes. Of this group of highly reactive ketenes, which cannot be isolated in the condensed phase at ambient temperature, only 2a has been the subject of a previous PE spectroscopic study. But our work indicates that the sample of 2a prepared in the earlier study was impure. The low volatility of p-nitrodiazoacetophenone (1e) thwarted our attempts to generate 2e and obtain its spectrum. Calculations at semiempirical (AM1) and ab inito (HF/6-31G(d)) levels of theory established that the diazoacetophenones prefer to adopt twisted syn conformations. That the calculated ionization potentials (HAM/3 and Becke3LYP/6-31+G(d)//HF/6-31G(d)) of 1a-1d and the synthesized PE spectra of 1a, 1b, and 1c correlate well with the PE spectroscopic data supports this finding. Shifts observed in the three low-energy ionizations of ketenes 2b, 2c, and 2d induced by the para-substitution can be related to the character of the corresponding occupied molecular orbitals of phenylketene (2a).Key words: diazoacetophenones, phenylketenes, He(I) photoelectron spectroscopy, thermolysis, quantum chemical calculations.

A study of the vacuum pyrolysis of 4-diazoisothiochroman-3-one with Hel ultraviolet photoelectron spectroscopy

1996 ◽  
Vol 74 (12) ◽  
pp. 2536-2539 ◽  
Author(s):  
N.H. Werstiuk ◽  
J. Ma ◽  
C.D. Roy ◽  
A.J. Kresge ◽  
E.A. Jefferson
Keyword(s):  
Heat Source ◽  
Ab Initio ◽  
Photoelectron Spectroscopy ◽  
Laser Power ◽  
Activation Enthalpy ◽  
Power Level ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Wolff Rearrangement ◽  
Vacuum Pyrolysis ◽  
New Compounds

A newly developed ultraviolet photoelectron spectrometer apparatus that utilizes a tunable 50 W CW CO2 laser as a directed heat source is used to study the vacuum pyrolysis of 4-diazoisothiochroman-3-one (1a). Analysis of the pyrolysate with ultraviolet photoelectron spectroscopy shows that 1a undergoes a facile pyrolysis at a laser power level of less than 26 W, yielding two new compounds: thiaketene 3a, the product of a Wolff rearrangement, and benzocyclobutenthione (6a), which can be derived from thiacarbene 4a, the decarbonylation product of 3a. Activation enthalpies/energies calculated at the AM1 and ab initio levels of theory indicate that, unlike the case of 4-diazoisochroman-3-one (1b), the Wolff rearrangement of the incipient carbene may be concerted with loss of nitrogen from 1a. The activation enthalpy/energy calculated for the decarbonylation of 3a is significantly higher (AM1, 20.5 kcal/mol; RHF/6-31G(d), 11.7 kcal/mol; MP2(full)//RHF/6-31G(d), 14.3 kcal/mol) than the activation enthalpy/energy for the decarbonylation of 3b. This result is in keeping with the fact that we detect 3a, but 3b is not found in detectable amounts in the pyrolysate of 1b. Key words: vacuum pyrolysis, 4-diazoisothiochroman-3-one, HeI ultraviolet photoelectron spectroscopy, AM1 and ab initio calculations.

A study of the vacuum pyrolysis of 4-diazo-3-isochromanone with Hel ultraviolet photoelectron spectroscopy

1995 ◽  
Vol 73 (10) ◽  
pp. 1738-1740 ◽  
Author(s):  
N.H. Werstiuk ◽  
J. Ma ◽  
C.D. Roy ◽  
A.J. Kresge ◽  
E. Jefferson
Keyword(s):  
Mass Spectrometry ◽  
Heat Source ◽  
Photoelectron Spectroscopy ◽  
Laser Power ◽  
Ring Opening ◽  
Power Level ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Photoionization Mass Spectrometry ◽  
Cw Laser ◽  
Vacuum Pyrolysis

A newly developed ultraviolet photoelectron spectrometer – CO2 laser instrument that utilizes a 50-W CW laser as a directed heat source was used to study the vacuum pyrolysis of 4-diazo-3-isochromanone (1). Analysis of the pyrolysate with ultraviolet photoelectron spectroscopy and photoionization mass spectrometry established that 1 undergoes a facile, unexpected pyrolysis at a laser power level of 26 W yielding N2, CO, and benzocyclobutenone (6). A multistep mechanism beginning with the formation of 4-carbena-3-isochromanone (2), which rearranges to oxaketene 3, can be written for the reaction. If 3 is an intermediate, it must be unusually thermally labile for it readily decarbonylates to 2-carbena-3,4-benzotetrahydrofuran (4). The ring opening of 4 into the ortho-quininoid ketene 5 and the cyclization of 5 into 6 are possible final steps in the conversion of 1 into 6. Keywords: vacuum pyrolysis, 4-diazo-3-isochromanone, HeI ultraviolet photoelectron spectroscopy.

A study of the vacuum pyrolysis of 6,6-dihalobicyclo[3.1.0]hexanes with Hel ultraviolet photoelectron spectroscopy

1994 ◽  
Vol 72 (12) ◽  
pp. 2537-2539 ◽  
Author(s):  
Nick Henry Werstiuk ◽  
Chandra Deo Roy ◽  
Jiangong Ma
Keyword(s):  
Heat Source ◽  
Gas Phase ◽  
High Power ◽  
Photoelectron Spectroscopy ◽  
Laser Power ◽  
Continuous Wave ◽  
Spectroscopic Studies ◽  
High Yield ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Vacuum Pyrolysis

To establish the utility of using a high-power CW (continuous wave) CO2 laser as a directed heat source for preparing organic transients targeted for gas-phase ultraviolet photoelectron spectroscopic studies, we studied the vacuum pyrolysis of 6,6-dibromobicyclo[3.1.0]hexane (1a), 6,6-dichlorobicyclo[3.1.0]hexane (1b), and exo-6-bromo-endo-6-chlorobicyclo[3.1.0]hexane (1c). While it has already been established that 1a and 1b rearrange to the 2,3-dihalocyclohexenes 3a and 3b, respectively, when heated in the condensed phase, upon vacuum pyrolysis 1a and 1b readily eliminate HX — not the dihalogens — and give the 2-halo-1,3-cyclohexadienes 2a and 2b in high yield. That 2,3-dibromocyclohexene (3a) does not eliminate HBr at the laser power used to pyrolyze 1a and 1b and that bromochloro compound 1c selectively loses HCl to form 2a suggests that the 1,3-elimination of HX occurs in a concerted fashion without isomerization of the cyclopropane.

UV-photoelectron Spectroscopy of Unhindered Germylenes and Carbon-arsenic Multiple-bonded Species

2010 ◽  
Vol 63 (12) ◽  
pp. 1608 ◽  
Author(s):  
Anna Chrostowska ◽  
Alain Dargelos ◽  
Alain Graciaa
Keyword(s):  
Experimental Data ◽  
Gas Phase ◽  
Photoelectron Spectroscopy ◽  
Quantum Chemical ◽  
Group Iv ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Fundamental Information ◽  
Structure And Bonding ◽  
Uv Photoelectron Spectroscopy ◽  
Established Technique

Ultraviolet photoelectron spectroscopy (UV-PES) is a well established technique that provides ionization energies of molecules in the gas phase. Flash vacuum thermolysis or vacuum gas-solid reactions coupled with UV-PES are especially suited for the generation and analysis of small amounts of short-lived species in real-time. These experimental data, supported by quantum chemical calculations for the consistency of the assignments of PES spectra, provide fundamental information about electronic structure and bonding that is obtained by no other technique. This paper aims to give some representative original examples chosen from Pau’s research group that illustrate the advantages and wide applicability of these techniques. These examples show the selected data and conclusions which focus on the reactivity of low-coordinated of Main Group IV and V elements. Germylenes and simplest carbon-arsenic multiple bonded species ware successfully characterized using UV photoelectron spectroscopy – a very powerful, direct characterization instrument.

Surface potential of liquid microjet investigated using extreme ultraviolet photoelectron spectroscopy

2020 ◽  
Vol 152 (14) ◽  
pp. 144503
Author(s):  
Junichi Nishitani ◽  
Shutaro Karashima ◽  
Christopher W. West ◽  
Toshinori Suzuki
Keyword(s):  
Surface Potential ◽  
Photoelectron Spectroscopy ◽  
Extreme Ultraviolet ◽  
Ultraviolet Photoelectron Spectroscopy

Vacuum ultraviolet photoelectron spectroscopy of transient species

1981 ◽  
Vol 44 (5) ◽  
pp. 1059-1066 ◽  
Author(s):  
J.M. Dyke ◽  
N.B.H. Jonathan ◽  
A. Morris ◽  
M.J. Winter
Keyword(s):  
Photoelectron Spectroscopy ◽  
Vacuum Ultraviolet ◽  
Ultraviolet Photoelectron Spectroscopy ◽  
Transient Species

scholarly journals Synthesis and Characterisation of Molecular Polarised-Covalent Thorium-Rhenium and -Ruthenium Bonds

Inorganics ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 30
Author(s):  
Joseph P. A. Ostrowski ◽  
Ashley J. Wooles ◽  
Stephen T. Liddle
Keyword(s):  
Quantum Chemical Calculations ◽  
Quantum Chemical ◽  
Spectroscopic Data ◽  
Raman Spectroscopic ◽  
Ir And Raman ◽  
Alkane Elimination

Separate reactions of [Th{N(CH2CH2NSiMe2But)2(CH2CH2NSi(Me)(But)(μ-CH2)]2 (1) with [Re(η5-C5H5)2(H)] (2) or [Ru(η5-C5H5)(H)(CO)2] (3) produced, by alkane elimination, [Th(TrenDMBS)Re(η5-C5H5)2] (ThRe, TrenDMBS = {N(CH2CH2NSiMe2But)3}3-), and [Th(TrenDMBS)Ru(η5-C5H5)(CO)2] (ThRu), which were isolated in crystalline yields of 71% and 62%, respectively. Complex ThRe is the first example of a molecular Th-Re bond to be structurally characterised, and ThRu is only the second example of a structurally authenticated Th-Ru bond. By comparison to isostructural U-analogues, quantum chemical calculations, which are validated by IR and Raman spectroscopic data, suggest that the Th-Re and Th-Ru bonds reported here are more ionic than the corresponding U-Re and U-Ru bonds.

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