Effect of molecular structure on the infrared signatures of astronomically relevant PAHs
Emission bands from polycyclic aromatic hydrocarbons (PAHs) dominate the mid-infrared spectra of a wide variety of astronomical sources, encompassing nearly all stages of stellar evolution. Despite their similarities, details in band positions and shapes have allowed a classification of PAH emission...
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description | Emission bands from polycyclic aromatic hydrocarbons (PAHs) dominate the mid-infrared spectra of a wide variety of astronomical sources, encompassing nearly all stages of stellar evolution. Despite their similarities, details in band positions and shapes have allowed a classification of PAH emission to be developed. It has been suggested that this classification is in turn associated with the degree of photoprocessing of PAHs. Over the past decade, a more complete picture of the PAH interstellar life-cycle has emerged, in which a wide range of PAH species are formed during the later stages of stellar evolution. After this they are photoprocessed, increasing the relative abundance of the more stable (typically larger and compact) PAHs. For this work we have tested the effect of the symmetry, size, and structure of PAHs on their fragmentation pattern and infrared spectra by combining experiments at the free electron laser for infrared experiments (FELIX) and quantum chemical computations. Applying this approach to the cations of four molecular species, perylene (C20H12), peropyrene (C26H14), ovalene (C32H14) and isoviolanthrene (C34H18), we find that a reduction of molecular symmetry causes the activation of vibrational modes in the 7–9 μm range. We show that the IR characteristics of less symmetric PAHs can help explain the broad band observed in the class D spectra, which are typically associated with a low degree of photoprocessing. Such large, nonsymmetrical irregular PAHs are currently largely missing from the NASA Ames PAH database. The band positions and shapes of the largest more symmetric PAH measured here, show the best resemblance with class A and B sources, representative of regions with high radiation fields and thus heavier photoprocessing. Furthermore, the dissociation patterns observed in the mass spectra hint to an enhanced stability of the carbon skeleton in more symmetric PAHs with respect to the irregular and less symmetric species, which tend to loose carbon containing units. Although not a direct proof, these findings are fully in line with the grandPAH hypothesis, which claims that symmetric large PAHs can survive as the radiation field increases, while their less symmetric counterparts are destroyed or converted to symmetric PAHs. |
doi_str_mv | 10.1051/0004-6361/201834130 |
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G. G. M.</creator><creatorcontrib>Bouwman, J. ; Castellanos, P. ; Bulak, M. ; Terwisscha van Scheltinga, J. ; Cami, J. ; Linnartz, H. ; Tielens, A. G. G. M.</creatorcontrib><description>Emission bands from polycyclic aromatic hydrocarbons (PAHs) dominate the mid-infrared spectra of a wide variety of astronomical sources, encompassing nearly all stages of stellar evolution. Despite their similarities, details in band positions and shapes have allowed a classification of PAH emission to be developed. It has been suggested that this classification is in turn associated with the degree of photoprocessing of PAHs. Over the past decade, a more complete picture of the PAH interstellar life-cycle has emerged, in which a wide range of PAH species are formed during the later stages of stellar evolution. After this they are photoprocessed, increasing the relative abundance of the more stable (typically larger and compact) PAHs. For this work we have tested the effect of the symmetry, size, and structure of PAHs on their fragmentation pattern and infrared spectra by combining experiments at the free electron laser for infrared experiments (FELIX) and quantum chemical computations. Applying this approach to the cations of four molecular species, perylene (C20H12), peropyrene (C26H14), ovalene (C32H14) and isoviolanthrene (C34H18), we find that a reduction of molecular symmetry causes the activation of vibrational modes in the 7–9 μm range. We show that the IR characteristics of less symmetric PAHs can help explain the broad band observed in the class D spectra, which are typically associated with a low degree of photoprocessing. Such large, nonsymmetrical irregular PAHs are currently largely missing from the NASA Ames PAH database. The band positions and shapes of the largest more symmetric PAH measured here, show the best resemblance with class A and B sources, representative of regions with high radiation fields and thus heavier photoprocessing. Furthermore, the dissociation patterns observed in the mass spectra hint to an enhanced stability of the carbon skeleton in more symmetric PAHs with respect to the irregular and less symmetric species, which tend to loose carbon containing units. 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G. G. M.</creatorcontrib><title>Effect of molecular structure on the infrared signatures of astronomically relevant PAHs</title><title>Astronomy and astrophysics (Berlin)</title><description>Emission bands from polycyclic aromatic hydrocarbons (PAHs) dominate the mid-infrared spectra of a wide variety of astronomical sources, encompassing nearly all stages of stellar evolution. Despite their similarities, details in band positions and shapes have allowed a classification of PAH emission to be developed. It has been suggested that this classification is in turn associated with the degree of photoprocessing of PAHs. Over the past decade, a more complete picture of the PAH interstellar life-cycle has emerged, in which a wide range of PAH species are formed during the later stages of stellar evolution. After this they are photoprocessed, increasing the relative abundance of the more stable (typically larger and compact) PAHs. For this work we have tested the effect of the symmetry, size, and structure of PAHs on their fragmentation pattern and infrared spectra by combining experiments at the free electron laser for infrared experiments (FELIX) and quantum chemical computations. Applying this approach to the cations of four molecular species, perylene (C20H12), peropyrene (C26H14), ovalene (C32H14) and isoviolanthrene (C34H18), we find that a reduction of molecular symmetry causes the activation of vibrational modes in the 7–9 μm range. We show that the IR characteristics of less symmetric PAHs can help explain the broad band observed in the class D spectra, which are typically associated with a low degree of photoprocessing. Such large, nonsymmetrical irregular PAHs are currently largely missing from the NASA Ames PAH database. The band positions and shapes of the largest more symmetric PAH measured here, show the best resemblance with class A and B sources, representative of regions with high radiation fields and thus heavier photoprocessing. Furthermore, the dissociation patterns observed in the mass spectra hint to an enhanced stability of the carbon skeleton in more symmetric PAHs with respect to the irregular and less symmetric species, which tend to loose carbon containing units. Although not a direct proof, these findings are fully in line with the grandPAH hypothesis, which claims that symmetric large PAHs can survive as the radiation field increases, while their less symmetric counterparts are destroyed or converted to symmetric PAHs.</description><subject>Abundance</subject><subject>Astrochemistry</subject><subject>Banded structure</subject><subject>Carbon</subject><subject>Cations</subject><subject>Celestial bodies</subject><subject>Classification</subject><subject>Emission</subject><subject>Free electron lasers</subject><subject>Infrared astronomy</subject><subject>Infrared lasers</subject><subject>Infrared signatures</subject><subject>Infrared spectra</subject><subject>Interstellar</subject><subject>ISM: molecules</subject><subject>Mass spectra</subject><subject>methods: laboratory: molecular</subject><subject>molecular processes</subject><subject>Molecular structure</subject><subject>Organic chemistry</subject><subject>photon-dominated region</subject><subject>Polycyclic aromatic hydrocarbons</subject><subject>Quantum chemistry</subject><subject>Radiation</subject><subject>Relative abundance</subject><subject>Stellar evolution</subject><subject>Symmetry</subject><issn>0004-6361</issn><issn>1432-0746</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNo9kEFPAjEQhRujiYj-Ai9NPK-02267HAlBkJDoQdFbU7tTXVy22HaJ_Hu7wXCazMz33kweQreU3FNS0BEhhGeCCTrKCS0Zp4ycoQHlLM-I5OIcDU7EJboKYZPaPIED9D6zFkzEzuKta8B0jfY4RN-Z2HnArsXxC3DdWq89VDjUn63uN6FX6AS61m1ro5vmgD00sNdtxM-TRbhGF1Y3AW7-6xC9Psxepots9TR_nE5WmWGCxAyMHI8lE1xURNqqtCXQQqcJLWRF0_NQ5jnTDCgTWhfEsNIa4FLaD1kZADZEd0ffnXc_HYSoNq7zbTqpcip5nqxKmih2pIx3IXiwaufrrfYHRYnqI1R9QKoPSJ0iTKrsqKpDhN-TRPtvJSSThSrJm6LL9XzNl1IV7A8sXHLn</recordid><startdate>20190101</startdate><enddate>20190101</enddate><creator>Bouwman, J.</creator><creator>Castellanos, P.</creator><creator>Bulak, M.</creator><creator>Terwisscha van Scheltinga, J.</creator><creator>Cami, J.</creator><creator>Linnartz, H.</creator><creator>Tielens, A. 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M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of molecular structure on the infrared signatures of astronomically relevant PAHs</atitle><jtitle>Astronomy and astrophysics (Berlin)</jtitle><date>2019-01-01</date><risdate>2019</risdate><volume>621</volume><spage>A80</spage><pages>A80-</pages><issn>0004-6361</issn><eissn>1432-0746</eissn><abstract>Emission bands from polycyclic aromatic hydrocarbons (PAHs) dominate the mid-infrared spectra of a wide variety of astronomical sources, encompassing nearly all stages of stellar evolution. Despite their similarities, details in band positions and shapes have allowed a classification of PAH emission to be developed. It has been suggested that this classification is in turn associated with the degree of photoprocessing of PAHs. Over the past decade, a more complete picture of the PAH interstellar life-cycle has emerged, in which a wide range of PAH species are formed during the later stages of stellar evolution. After this they are photoprocessed, increasing the relative abundance of the more stable (typically larger and compact) PAHs. For this work we have tested the effect of the symmetry, size, and structure of PAHs on their fragmentation pattern and infrared spectra by combining experiments at the free electron laser for infrared experiments (FELIX) and quantum chemical computations. Applying this approach to the cations of four molecular species, perylene (C20H12), peropyrene (C26H14), ovalene (C32H14) and isoviolanthrene (C34H18), we find that a reduction of molecular symmetry causes the activation of vibrational modes in the 7–9 μm range. We show that the IR characteristics of less symmetric PAHs can help explain the broad band observed in the class D spectra, which are typically associated with a low degree of photoprocessing. Such large, nonsymmetrical irregular PAHs are currently largely missing from the NASA Ames PAH database. The band positions and shapes of the largest more symmetric PAH measured here, show the best resemblance with class A and B sources, representative of regions with high radiation fields and thus heavier photoprocessing. Furthermore, the dissociation patterns observed in the mass spectra hint to an enhanced stability of the carbon skeleton in more symmetric PAHs with respect to the irregular and less symmetric species, which tend to loose carbon containing units. 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subjects | Abundance Astrochemistry Banded structure Carbon Cations Celestial bodies Classification Emission Free electron lasers Infrared astronomy Infrared lasers Infrared signatures Infrared spectra Interstellar ISM: molecules Mass spectra methods: laboratory: molecular molecular processes Molecular structure Organic chemistry photon-dominated region Polycyclic aromatic hydrocarbons Quantum chemistry Radiation Relative abundance Stellar evolution Symmetry |
title | Effect of molecular structure on the infrared signatures of astronomically relevant PAHs |
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