Synthesis, crystal structure, photoluminescence and dielectric properties of a new organic–inorganic compound: tetrachlorocadmate (II) 2.2′-bipyridinium
Single crystals of a new organic–inorganic compound (C 10 H 10 N 2 ) CdCl 4 were grown by the slow evaporation technique and characterized by X-ray diffraction, Hirshfeld surface, Infrared absorption, Solid state 13 C NMR, photoluminescence (PL) properties, differential scanning calorimetry (DSC) an...
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creator | Lassoued, Mohamed Saber Lassoued, Abdelmajid Abdelbaky, Mohammed S. M. Ammar, Salah Gadri, Abdellatif Ben Salah, Abdelhamid García-Granda, Santiago |
description | Single crystals of a new organic–inorganic compound (C
10
H
10
N
2
) CdCl
4
were grown by the slow evaporation technique and characterized by X-ray diffraction, Hirshfeld surface, Infrared absorption, Solid state
13
C NMR, photoluminescence (PL) properties, differential scanning calorimetry (DSC) and dielectric measurements. The title compound belongs to the monoclinic space group P2
1
/c with the following unit cell parameters: a = 7.29420(1), b = 13.9206(3), c = 14.3880(3) Å, β = 100.247(2)° and Z = 4. The structure can be described by the alternation of two different cationic-anionic layers. It consists of isolated [CdCl
4
]
2−
tetrahedral anions and 2.2′ bipyridinium (C
10
H
10
N
2
)
2+
cations, which are connected via N–H⋯Cl hydrogen bonds. The Hirshfeld surface analysis was conducted to investigate intermolecular interactions and associated 2D fingerprint plots, revealing the relative contribution of these interactions in the crystal structure quantitatively. Furthermore, the room temperature infrared (IR) spectrum of the title compound was recorded and analyzed on the basis of detailed vibrational studies found in the literature; the detailed assignment confirms the presence of the organic groups. Solid state
13
C NMR spectrum shows four signals, confirming the solid state structure determined by X-ray diffraction. Besides, photoluminescence measurements showed a strong emission line at 2.95 eV associated with radiative recombinations of excitons confined within the [CdCl
4
]
2−
which were investigated at room temperature. Finally, the thermal analysis studies were performed, and phase transition was found in the temperature range between 300 and 550 K, while the electrical measurements were performed to discuss the phase-transition mechanism. |
doi_str_mv | 10.1007/s10854-017-8507-9 |
format | Article |
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10
H
10
N
2
) CdCl
4
were grown by the slow evaporation technique and characterized by X-ray diffraction, Hirshfeld surface, Infrared absorption, Solid state
13
C NMR, photoluminescence (PL) properties, differential scanning calorimetry (DSC) and dielectric measurements. The title compound belongs to the monoclinic space group P2
1
/c with the following unit cell parameters: a = 7.29420(1), b = 13.9206(3), c = 14.3880(3) Å, β = 100.247(2)° and Z = 4. The structure can be described by the alternation of two different cationic-anionic layers. It consists of isolated [CdCl
4
]
2−
tetrahedral anions and 2.2′ bipyridinium (C
10
H
10
N
2
)
2+
cations, which are connected via N–H⋯Cl hydrogen bonds. The Hirshfeld surface analysis was conducted to investigate intermolecular interactions and associated 2D fingerprint plots, revealing the relative contribution of these interactions in the crystal structure quantitatively. Furthermore, the room temperature infrared (IR) spectrum of the title compound was recorded and analyzed on the basis of detailed vibrational studies found in the literature; the detailed assignment confirms the presence of the organic groups. Solid state
13
C NMR spectrum shows four signals, confirming the solid state structure determined by X-ray diffraction. Besides, photoluminescence measurements showed a strong emission line at 2.95 eV associated with radiative recombinations of excitons confined within the [CdCl
4
]
2−
which were investigated at room temperature. Finally, the thermal analysis studies were performed, and phase transition was found in the temperature range between 300 and 550 K, while the electrical measurements were performed to discuss the phase-transition mechanism.</description><identifier>ISSN: 0957-4522</identifier><identifier>EISSN: 1573-482X</identifier><identifier>DOI: 10.1007/s10854-017-8507-9</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Cations ; Characterization and Evaluation of Materials ; Chemistry and Materials Science ; Crystal structure ; Dielectric properties ; Diffraction ; Electrical measurement ; Excitons ; Hydrogen bonds ; Infrared absorption ; Infrared analysis ; Materials Science ; NMR ; Nuclear magnetic resonance ; Optical and Electronic Materials ; Phase transitions ; Photoluminescence ; Single crystals ; Solid state ; Studies ; Surface analysis (chemical) ; Thermal analysis ; X-ray diffraction</subject><ispartof>Journal of materials science. Materials in electronics, 2018-04, Vol.29 (7), p.5413-5426</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Journal of Materials Science: Materials in Electronics is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-b1096fc19645977fc3fbda9c3ffb442b8b15fc4df2e32a680baf32d64a4a46103</citedby><cites>FETCH-LOGICAL-c316t-b1096fc19645977fc3fbda9c3ffb442b8b15fc4df2e32a680baf32d64a4a46103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10854-017-8507-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10854-017-8507-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Lassoued, Mohamed Saber</creatorcontrib><creatorcontrib>Lassoued, Abdelmajid</creatorcontrib><creatorcontrib>Abdelbaky, Mohammed S. M.</creatorcontrib><creatorcontrib>Ammar, Salah</creatorcontrib><creatorcontrib>Gadri, Abdellatif</creatorcontrib><creatorcontrib>Ben Salah, Abdelhamid</creatorcontrib><creatorcontrib>García-Granda, Santiago</creatorcontrib><title>Synthesis, crystal structure, photoluminescence and dielectric properties of a new organic–inorganic compound: tetrachlorocadmate (II) 2.2′-bipyridinium</title><title>Journal of materials science. Materials in electronics</title><addtitle>J Mater Sci: Mater Electron</addtitle><description>Single crystals of a new organic–inorganic compound (C
10
H
10
N
2
) CdCl
4
were grown by the slow evaporation technique and characterized by X-ray diffraction, Hirshfeld surface, Infrared absorption, Solid state
13
C NMR, photoluminescence (PL) properties, differential scanning calorimetry (DSC) and dielectric measurements. The title compound belongs to the monoclinic space group P2
1
/c with the following unit cell parameters: a = 7.29420(1), b = 13.9206(3), c = 14.3880(3) Å, β = 100.247(2)° and Z = 4. The structure can be described by the alternation of two different cationic-anionic layers. It consists of isolated [CdCl
4
]
2−
tetrahedral anions and 2.2′ bipyridinium (C
10
H
10
N
2
)
2+
cations, which are connected via N–H⋯Cl hydrogen bonds. The Hirshfeld surface analysis was conducted to investigate intermolecular interactions and associated 2D fingerprint plots, revealing the relative contribution of these interactions in the crystal structure quantitatively. Furthermore, the room temperature infrared (IR) spectrum of the title compound was recorded and analyzed on the basis of detailed vibrational studies found in the literature; the detailed assignment confirms the presence of the organic groups. Solid state
13
C NMR spectrum shows four signals, confirming the solid state structure determined by X-ray diffraction. Besides, photoluminescence measurements showed a strong emission line at 2.95 eV associated with radiative recombinations of excitons confined within the [CdCl
4
]
2−
which were investigated at room temperature. Finally, the thermal analysis studies were performed, and phase transition was found in the temperature range between 300 and 550 K, while the electrical measurements were performed to discuss the phase-transition mechanism.</description><subject>Cations</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry and Materials Science</subject><subject>Crystal structure</subject><subject>Dielectric properties</subject><subject>Diffraction</subject><subject>Electrical measurement</subject><subject>Excitons</subject><subject>Hydrogen bonds</subject><subject>Infrared absorption</subject><subject>Infrared analysis</subject><subject>Materials Science</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Optical and Electronic Materials</subject><subject>Phase transitions</subject><subject>Photoluminescence</subject><subject>Single crystals</subject><subject>Solid state</subject><subject>Studies</subject><subject>Surface analysis (chemical)</subject><subject>Thermal analysis</subject><subject>X-ray diffraction</subject><issn>0957-4522</issn><issn>1573-482X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kcFKHTEUhoMo9Nb2AboLuLFgbJLJzGS6K6L1gtCFCt2FTObEG5lJxiSD3J3v0G2foo_kkxi5LrqRs_jP4vv_w-FH6Aujp4zS9ltiVNaCUNYSWdOWdHtoxeq2IkLy3_toRbu6JaLm_AP6mNI9pbQRlVyhv9dbnzeQXDrBJm5T1iNOOS4mLxFO8LwJOYzL5DwkA94A1n7Ag4MRTI7O4DmGGWJ2kHCwWGMPjzjEO-2deX764_zbjk2Y5rD44TvOkKM2mzHEYPQw6Qz4eL3-ivkpf376R3o3b6MbnHfL9AkdWD0m-Pymh-j24vzm7JJc_fq5PvtxRUzFmkx6RrvGGtY1ou7a1prK9oPuitheCN7LntXWiMFyqLhuJO21rfjQCF2mYbQ6REe73PLNwwIpq_uwRF9OKtbJgkhJm0KxHWViSCmCVXN0k45bxah6LUHtSlClBPVaguqKh-88qbD-DuJ_ye-aXgAD-pAC</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Lassoued, Mohamed Saber</creator><creator>Lassoued, Abdelmajid</creator><creator>Abdelbaky, Mohammed S. M.</creator><creator>Ammar, Salah</creator><creator>Gadri, Abdellatif</creator><creator>Ben Salah, Abdelhamid</creator><creator>García-Granda, Santiago</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>L7M</scope><scope>P5Z</scope><scope>P62</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0W</scope></search><sort><creationdate>20180401</creationdate><title>Synthesis, crystal structure, photoluminescence and dielectric properties of a new organic–inorganic compound: tetrachlorocadmate (II) 2.2′-bipyridinium</title><author>Lassoued, Mohamed Saber ; Lassoued, Abdelmajid ; Abdelbaky, Mohammed S. M. ; Ammar, Salah ; Gadri, Abdellatif ; Ben Salah, Abdelhamid ; García-Granda, Santiago</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-b1096fc19645977fc3fbda9c3ffb442b8b15fc4df2e32a680baf32d64a4a46103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Cations</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry and Materials Science</topic><topic>Crystal structure</topic><topic>Dielectric properties</topic><topic>Diffraction</topic><topic>Electrical measurement</topic><topic>Excitons</topic><topic>Hydrogen bonds</topic><topic>Infrared absorption</topic><topic>Infrared analysis</topic><topic>Materials Science</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Optical and Electronic Materials</topic><topic>Phase transitions</topic><topic>Photoluminescence</topic><topic>Single crystals</topic><topic>Solid state</topic><topic>Studies</topic><topic>Surface analysis (chemical)</topic><topic>Thermal analysis</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lassoued, Mohamed Saber</creatorcontrib><creatorcontrib>Lassoued, Abdelmajid</creatorcontrib><creatorcontrib>Abdelbaky, Mohammed S. M.</creatorcontrib><creatorcontrib>Ammar, Salah</creatorcontrib><creatorcontrib>Gadri, Abdellatif</creatorcontrib><creatorcontrib>Ben Salah, Abdelhamid</creatorcontrib><creatorcontrib>García-Granda, Santiago</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>DELNET Engineering & Technology Collection</collection><jtitle>Journal of materials science. Materials in electronics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lassoued, Mohamed Saber</au><au>Lassoued, Abdelmajid</au><au>Abdelbaky, Mohammed S. M.</au><au>Ammar, Salah</au><au>Gadri, Abdellatif</au><au>Ben Salah, Abdelhamid</au><au>García-Granda, Santiago</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, crystal structure, photoluminescence and dielectric properties of a new organic–inorganic compound: tetrachlorocadmate (II) 2.2′-bipyridinium</atitle><jtitle>Journal of materials science. Materials in electronics</jtitle><stitle>J Mater Sci: Mater Electron</stitle><date>2018-04-01</date><risdate>2018</risdate><volume>29</volume><issue>7</issue><spage>5413</spage><epage>5426</epage><pages>5413-5426</pages><issn>0957-4522</issn><eissn>1573-482X</eissn><abstract>Single crystals of a new organic–inorganic compound (C
10
H
10
N
2
) CdCl
4
were grown by the slow evaporation technique and characterized by X-ray diffraction, Hirshfeld surface, Infrared absorption, Solid state
13
C NMR, photoluminescence (PL) properties, differential scanning calorimetry (DSC) and dielectric measurements. The title compound belongs to the monoclinic space group P2
1
/c with the following unit cell parameters: a = 7.29420(1), b = 13.9206(3), c = 14.3880(3) Å, β = 100.247(2)° and Z = 4. The structure can be described by the alternation of two different cationic-anionic layers. It consists of isolated [CdCl
4
]
2−
tetrahedral anions and 2.2′ bipyridinium (C
10
H
10
N
2
)
2+
cations, which are connected via N–H⋯Cl hydrogen bonds. The Hirshfeld surface analysis was conducted to investigate intermolecular interactions and associated 2D fingerprint plots, revealing the relative contribution of these interactions in the crystal structure quantitatively. Furthermore, the room temperature infrared (IR) spectrum of the title compound was recorded and analyzed on the basis of detailed vibrational studies found in the literature; the detailed assignment confirms the presence of the organic groups. Solid state
13
C NMR spectrum shows four signals, confirming the solid state structure determined by X-ray diffraction. Besides, photoluminescence measurements showed a strong emission line at 2.95 eV associated with radiative recombinations of excitons confined within the [CdCl
4
]
2−
which were investigated at room temperature. Finally, the thermal analysis studies were performed, and phase transition was found in the temperature range between 300 and 550 K, while the electrical measurements were performed to discuss the phase-transition mechanism.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10854-017-8507-9</doi><tpages>14</tpages></addata></record> |
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subjects | Cations Characterization and Evaluation of Materials Chemistry and Materials Science Crystal structure Dielectric properties Diffraction Electrical measurement Excitons Hydrogen bonds Infrared absorption Infrared analysis Materials Science NMR Nuclear magnetic resonance Optical and Electronic Materials Phase transitions Photoluminescence Single crystals Solid state Studies Surface analysis (chemical) Thermal analysis X-ray diffraction |
title | Synthesis, crystal structure, photoluminescence and dielectric properties of a new organic–inorganic compound: tetrachlorocadmate (II) 2.2′-bipyridinium |
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