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Hassan Ganjitabar

Researcher at University of Nottingham

Publications -  8
Citations -  83

Hassan Ganjitabar is an academic researcher from University of Nottingham. The author has contributed to research in topics: Photoionization & Circular dichroism. The author has an hindex of 4, co-authored 6 publications receiving 36 citations. Previous affiliations of Hassan Ganjitabar include University of Tehran.

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Vibrationally-resolved photoelectron spectroscopy and photoelectron circular dichroism of bicyclic monoterpene enantiomers

TL;DR: In this article, the photoionization of four chiral bicyclic monoterpene isomers, α-pinene, β-pinenes, 3-carene and sabinene, has been studied using synchrotron radiation and compared to recent findings for the cyclic isomer limonene.
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Intense Vibronic Modulation of the Chiral Photoelectron Angular Distribution Generated by Photoionization of Limonene Enantiomers with Circularly Polarized Synchrotron Radiation

TL;DR: Photoionization of the chiral monoterpene limonene has been investigated using polarized synchrotron radiation between the adiabatic ionization threshold, 8.505 and 23.5 eV, and a rich vibrational structure is seen in the threshold photoelectron spectrum and is interpreted using a variety of computational methods.
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Conformer-dependent vacuum ultraviolet photodynamics and chiral asymmetries in pure enantiomers of gas phase proline

TL;DR: In this paper, the conformer-specific photoelectron circular dichroism (PECD) was measured in the vacuum ultraviolet (VUV) photoionization of proline, as well as a conformerdependent cation fragmentation behavior.
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Decoupling vibration and electron energy dependencies in the photoelectron circular dichroism of a terpene, 3-carene.

TL;DR: This paper investigates the PECD of a rigid chiral monoterpene, 3-carene, using single-photon vacuum ultraviolet ionization by polarized synchrotron radiation and selecting energies from the ionization threshold up to 19.0 eV, finding that the reported chiral asymmetry from the randomly oriented 3-Carene enantiomers reaches a maximum of over 21%.
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The role of the intermediate state in angle-resolved photoelectron studies using (2 + 1) resonance-enhanced multiphoton ionization of the chiral terpenes, α-pinene and 3-carene

TL;DR: In this article, photoelectron angular distributions (PADs) ranging up to the maximum 6th order Legendre polynomial term set by the Yang theorem have been recorded for the (2'+'1) resonance enhanced multiphoton i...