Photoluminescent Green Emission Band Induced by the Systematic Change of -CH3, -OCH3 and Naphthyl Groups in Chiral Imines
Herein, we report the morphological, optical, and structural modifications induced by the change of different functional groups in the para-position of the benzene ring in a series of chiral imines. These organic compounds were examined using scanning electron microscopy (SEM), optical absorption, X...
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Veröffentlicht in: | Crystal growth & design 2018-02, Vol.18 (2), p.660-668 |
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creator | Moreno, O. Portillo Bustamante, F. J. Meléndez Portillo, M. Chávez Morales, G. E. Moreno Téllez, G. Hernández Sánchez, A. Sosa García, M. E. Araiza Rosas, E. Rubio Sharma, P Pérez, R. Gutiérrez |
description | Herein, we report the morphological, optical, and structural modifications induced by the change of different functional groups in the para-position of the benzene ring in a series of chiral imines. These organic compounds were examined using scanning electron microscopy (SEM), optical absorption, X-ray diffraction, and photoluminescence (PL) techniques. SEM images showed drastic morphological changes, and the absorbance results showed significant changes in the bands located in the ∼200–400 nm range, associated with π → π*, δ → δ*, and n → π* transitions. An optical behavior similar to that of semiconductors (in the UV region), with two transitions in the ∼3.3–4.3 eV range was observed for the compounds. The results obtained by PL spectra exhibited changes in intensity, with gradually shifting increases in the green band emission. However, it is more intense with the crystals of the imine bearing the -OCH3 functional group, considering that the aforementioned green band is associated with the different morphology in these crystals. |
doi_str_mv | 10.1021/acs.cgd.7b00851 |
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Portillo ; Bustamante, F. J. Meléndez ; Portillo, M. Chávez ; Morales, G. E. Moreno ; Téllez, G. Hernández ; Sánchez, A. Sosa ; García, M. E. Araiza ; Rosas, E. Rubio ; Sharma, P ; Pérez, R. Gutiérrez</creator><creatorcontrib>Moreno, O. Portillo ; Bustamante, F. J. Meléndez ; Portillo, M. Chávez ; Morales, G. E. Moreno ; Téllez, G. Hernández ; Sánchez, A. Sosa ; García, M. E. Araiza ; Rosas, E. Rubio ; Sharma, P ; Pérez, R. Gutiérrez</creatorcontrib><description>Herein, we report the morphological, optical, and structural modifications induced by the change of different functional groups in the para-position of the benzene ring in a series of chiral imines. These organic compounds were examined using scanning electron microscopy (SEM), optical absorption, X-ray diffraction, and photoluminescence (PL) techniques. SEM images showed drastic morphological changes, and the absorbance results showed significant changes in the bands located in the ∼200–400 nm range, associated with π → π*, δ → δ*, and n → π* transitions. An optical behavior similar to that of semiconductors (in the UV region), with two transitions in the ∼3.3–4.3 eV range was observed for the compounds. The results obtained by PL spectra exhibited changes in intensity, with gradually shifting increases in the green band emission. 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These organic compounds were examined using scanning electron microscopy (SEM), optical absorption, X-ray diffraction, and photoluminescence (PL) techniques. SEM images showed drastic morphological changes, and the absorbance results showed significant changes in the bands located in the ∼200–400 nm range, associated with π → π*, δ → δ*, and n → π* transitions. An optical behavior similar to that of semiconductors (in the UV region), with two transitions in the ∼3.3–4.3 eV range was observed for the compounds. The results obtained by PL spectra exhibited changes in intensity, with gradually shifting increases in the green band emission. 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Gutiérrez</creatorcontrib><jtitle>Crystal growth & design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno, O. Portillo</au><au>Bustamante, F. J. Meléndez</au><au>Portillo, M. Chávez</au><au>Morales, G. E. Moreno</au><au>Téllez, G. Hernández</au><au>Sánchez, A. Sosa</au><au>García, M. E. Araiza</au><au>Rosas, E. Rubio</au><au>Sharma, P</au><au>Pérez, R. Gutiérrez</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoluminescent Green Emission Band Induced by the Systematic Change of -CH3, -OCH3 and Naphthyl Groups in Chiral Imines</atitle><jtitle>Crystal growth & design</jtitle><addtitle>Cryst. Growth Des</addtitle><date>2018-02-07</date><risdate>2018</risdate><volume>18</volume><issue>2</issue><spage>660</spage><epage>668</epage><pages>660-668</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>Herein, we report the morphological, optical, and structural modifications induced by the change of different functional groups in the para-position of the benzene ring in a series of chiral imines. These organic compounds were examined using scanning electron microscopy (SEM), optical absorption, X-ray diffraction, and photoluminescence (PL) techniques. SEM images showed drastic morphological changes, and the absorbance results showed significant changes in the bands located in the ∼200–400 nm range, associated with π → π*, δ → δ*, and n → π* transitions. An optical behavior similar to that of semiconductors (in the UV region), with two transitions in the ∼3.3–4.3 eV range was observed for the compounds. The results obtained by PL spectra exhibited changes in intensity, with gradually shifting increases in the green band emission. However, it is more intense with the crystals of the imine bearing the -OCH3 functional group, considering that the aforementioned green band is associated with the different morphology in these crystals.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.cgd.7b00851</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1269-7768</orcidid></addata></record> |
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title | Photoluminescent Green Emission Band Induced by the Systematic Change of -CH3, -OCH3 and Naphthyl Groups in Chiral Imines |
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