Please use this identifier to cite or link to this item: http://repository.ipb.ac.id/handle/123456789/74336
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dc.contributor.advisorIrawadi, Tun Tedja
dc.contributor.advisorDarmawan, rer nat Noviyan
dc.contributor.authorNurmeilia, Ika
dc.date.accessioned2015-02-27T06:34:03Z
dc.date.available2015-02-27T06:34:03Z
dc.date.issued2014
dc.identifier.urihttp://repository.ipb.ac.id/handle/123456789/74336
dc.description.abstractIn this study, hemicyanine-based chemosensor was successfully synthesized from 3-(carboxymethyl)-2-methylbenzotiazolium bromide (kmb salt) and 4- diethylamino-2-hydroxybenzaldehyde through condensation reaction. Hemicyanine product was (E)-2-(2-(4-(diethylamino)-2-hydroxystyryl)benzo[d] thiazol-3-ium-3-yl)acetate (hemicyanine 1). Kmb salt and hemicyanine 1 were characterized using 1H nuclear magnetic resonance and Fourier transform infrared spectroscopy. The presence of Hg(II) ions shifted the maximum absorption wavelength from 541 to 462.5 nm. The ability of hemicyanine 1 to selectively recognize Hg(II) ions was evidenced by solution color change from red to yellowish green. The role of –OH group on selectivity and sensitivity of hemicyanine 1 toward Hg(II) ions was proven by synthesizing another hemicyanine compound without –OH group, that was (E)-2-(2-(4- (dimethylamino)styryl)benzo[d]thiazol-3-ium-3-yl)acetate (hemicyanine 2). Ultraviolet-visible spectrum of hemicyanine 2 with Hg(II) ions did not shift the maximum absorption wavelength and did not change the color of hemicyanine solution. As the result, hemicyanine 2 cannot be used as chemosensor for Hg(II) ions.en
dc.language.isoid
dc.subject.ddcBogor-Jawa Baraten
dc.subject.ddc2014en
dc.subject.ddcIon Hg (II)en
dc.subject.ddcChemistryen
dc.titleSintesis Kemosensor Ion Hg(II) Berbasis Hemisianinen
dc.subject.keywordBogor Agricultural University (IPB)en
dc.subject.keywordHg(II)en
dc.subject.keywordhemicyanineen
dc.subject.keywordchemosensoren
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