15987197

Source:http://linkedlifedata.com/resource/pubmed/id/15987197

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002508, umls-concept:C0175668, umls-concept:C0233929, umls-concept:C0303920, umls-concept:C0522529, umls-concept:C0597357, umls-concept:C0598447, umls-concept:C0599225, umls-concept:C1177210
pubmed:issue	14
pubmed:dateCreated	2005-6-30
pubmed:abstractText	[reaction: see text] A new fluorescent probe N-butyl-4,5-di[2-(phenylamino)ethylamino]-1,8-naphthalimide 1 senses only Cu(II) among heavy and transition metal (HTM) ions by means of a colorimetric (primrose yellow to pink) method with a large red-shift in emission (green to red) attributed to the deprotonation of the secondary amines as a receptor conjugated to the naphthalimide fluorophore.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1523-7060
pubmed:author	pubmed-author:CuiJingnanJ, pubmed-author:QianXuhongX, pubmed-author:XuZhaochaoZ
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3029-32
pubmed:year	2005
pubmed:articleTitle	Colorimetric and ratiometric fluorescent chemosensor with a large red-shift in emission: Cu(II)-only sensing by deprotonation of secondary amines as receptor conjugated to naphthalimide fluorophore.
pubmed:affiliation	State Key Laboratory of Fine Chemicals, Dalian University of Technology, China.
pubmed:publicationType	Journal Article