Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics

The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5...
Ausführliche Beschreibung

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Autor*in:	Moinul Karim [verfasserIn] Yurngdong Jahng [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2014

Schlagwörter:	Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence

Übergeordnetes Werk:	In: Molecules - MDPI AG, 2003, 19(2014), 8, Seite 12842-12851
Übergeordnetes Werk:	volume:19 ; year:2014 ; number:8 ; pages:12842-12851

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/molecules190812842

Katalog-ID:	DOAJ020838662

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520			\|a The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied.
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allfields	10.3390/molecules190812842 doi (DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013 DE-627 ger DE-627 rakwb eng QD241-441 Moinul Karim verfasserin aut Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied. Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry Yurngdong Jahng verfasserin aut In Molecules MDPI AG, 2003 19(2014), 8, Seite 12842-12851 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:19 year:2014 number:8 pages:12842-12851 https://doi.org/10.3390/molecules190812842 kostenfrei https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 kostenfrei http://www.mdpi.com/1420-3049/19/8/12842 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 19 2014 8 12842-12851
spelling	10.3390/molecules190812842 doi (DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013 DE-627 ger DE-627 rakwb eng QD241-441 Moinul Karim verfasserin aut Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied. Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry Yurngdong Jahng verfasserin aut In Molecules MDPI AG, 2003 19(2014), 8, Seite 12842-12851 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:19 year:2014 number:8 pages:12842-12851 https://doi.org/10.3390/molecules190812842 kostenfrei https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 kostenfrei http://www.mdpi.com/1420-3049/19/8/12842 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 19 2014 8 12842-12851
allfields_unstemmed	10.3390/molecules190812842 doi (DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013 DE-627 ger DE-627 rakwb eng QD241-441 Moinul Karim verfasserin aut Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied. Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry Yurngdong Jahng verfasserin aut In Molecules MDPI AG, 2003 19(2014), 8, Seite 12842-12851 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:19 year:2014 number:8 pages:12842-12851 https://doi.org/10.3390/molecules190812842 kostenfrei https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 kostenfrei http://www.mdpi.com/1420-3049/19/8/12842 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 19 2014 8 12842-12851
allfieldsGer	10.3390/molecules190812842 doi (DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013 DE-627 ger DE-627 rakwb eng QD241-441 Moinul Karim verfasserin aut Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied. Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry Yurngdong Jahng verfasserin aut In Molecules MDPI AG, 2003 19(2014), 8, Seite 12842-12851 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:19 year:2014 number:8 pages:12842-12851 https://doi.org/10.3390/molecules190812842 kostenfrei https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 kostenfrei http://www.mdpi.com/1420-3049/19/8/12842 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 19 2014 8 12842-12851
allfieldsSound	10.3390/molecules190812842 doi (DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013 DE-627 ger DE-627 rakwb eng QD241-441 Moinul Karim verfasserin aut Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics 2014 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied. Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry Yurngdong Jahng verfasserin aut In Molecules MDPI AG, 2003 19(2014), 8, Seite 12842-12851 (DE-627)311313132 (DE-600)2008644-1 14203049 nnns volume:19 year:2014 number:8 pages:12842-12851 https://doi.org/10.3390/molecules190812842 kostenfrei https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 kostenfrei http://www.mdpi.com/1420-3049/19/8/12842 kostenfrei https://doaj.org/toc/1420-3049 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 19 2014 8 12842-12851
language	English
source	In Molecules 19(2014), 8, Seite 12842-12851 volume:19 year:2014 number:8 pages:12842-12851
sourceStr	In Molecules 19(2014), 8, Seite 12842-12851 volume:19 year:2014 number:8 pages:12842-12851
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topic_facet	Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence Organic chemistry
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container_title	Molecules
authorswithroles_txt_mv	Moinul Karim @@aut@@ Yurngdong Jahng @@aut@@
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callnumber-first	Q - Science
author	Moinul Karim
spellingShingle	Moinul Karim misc QD241-441 misc Friedländer reactions misc benzo[g]quinoline misc 2-phenylbenzo[g]quinoline misc 2-(pyrid-2-yl)benzo[g]quinoline misc 1,3-di(benzo[g]quinolin-2-yl)benzene misc 1,3,5-tri(benzo[g]quinolin-2-yl)benzene misc N,C-bidentate misc photoluminescence misc Organic chemistry Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics
authorStr	Moinul Karim
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topic_title	QD241-441 Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics Friedländer reactions benzo[g]quinoline 2-phenylbenzo[g]quinoline 2-(pyrid-2-yl)benzo[g]quinoline 1,3-di(benzo[g]quinolin-2-yl)benzene 1,3,5-tri(benzo[g]quinolin-2-yl)benzene N,C-bidentate photoluminescence
topic	misc QD241-441 misc Friedländer reactions misc benzo[g]quinoline misc 2-phenylbenzo[g]quinoline misc 2-(pyrid-2-yl)benzo[g]quinoline misc 1,3-di(benzo[g]quinolin-2-yl)benzene misc 1,3,5-tri(benzo[g]quinolin-2-yl)benzene misc N,C-bidentate misc photoluminescence misc Organic chemistry
topic_unstemmed	misc QD241-441 misc Friedländer reactions misc benzo[g]quinoline misc 2-phenylbenzo[g]quinoline misc 2-(pyrid-2-yl)benzo[g]quinoline misc 1,3-di(benzo[g]quinolin-2-yl)benzene misc 1,3,5-tri(benzo[g]quinolin-2-yl)benzene misc N,C-bidentate misc photoluminescence misc Organic chemistry
topic_browse	misc QD241-441 misc Friedländer reactions misc benzo[g]quinoline misc 2-phenylbenzo[g]quinoline misc 2-(pyrid-2-yl)benzo[g]quinoline misc 1,3-di(benzo[g]quinolin-2-yl)benzene misc 1,3,5-tri(benzo[g]quinolin-2-yl)benzene misc N,C-bidentate misc photoluminescence misc Organic chemistry
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title	Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics
ctrlnum	(DE-627)DOAJ020838662 (DE-599)DOAJ81abbf1da26942f0a31cad6dca915013
title_full	Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics
author_sort	Moinul Karim
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author_browse	Moinul Karim Yurngdong Jahng
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class	QD241-441
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author-letter	Moinul Karim
doi_str_mv	10.3390/molecules190812842
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title_sort	unusual product distribution from friedländer reaction of di- and triacetylbenzenes with 3-aminonaphthalene-3-carbaldehyde and properties of new benzo[g]quinoline-derived aza-aromatics
callnumber	QD241-441
title_auth	Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics
abstract	The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied.
abstractGer	The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied.
abstract_unstemmed	The Friedländer reactions of acetylbenzenes and 2-acetylpyridine with 3-aminonaphthalene-2-carbaldehyde afforded the corresponding 2-phenylbenzo[g]quinoline and 2-(pyrid-2-yl)benzo[g]quinoline, respectively. The same reactions of 3-aminonaphthalene-2-carbaldehyde with 1,2-, 1,3-, 1,4-di- and 1,3,5-triacetylbenzenes, however, afforded a series of corresponding (benzo[g]quinolin-2-yl)benzenes as new N,C-bidentate and unexpected benzo[g]quinoline. Crystallinity, thermal properties, absorption and emission spectral properties of the products were studied.
collection_details	GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700
container_issue	8
title_short	Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics
url	https://doi.org/10.3390/molecules190812842 https://doaj.org/article/81abbf1da26942f0a31cad6dca915013 http://www.mdpi.com/1420-3049/19/8/12842 https://doaj.org/toc/1420-3049
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doi_str	10.3390/molecules190812842
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up_date	2024-07-03T17:18:37.390Z
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Unusual Product Distribution from Friedländer Reaction of Di- and Triacetylbenzenes with 3-Aminonaphthalene-3-Carbaldehyde and Properties of New Benzo[g]quinoline-Derived Aza-aromatics

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