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Volumn 341, Issue 3, 1999, Pages 228-236

Synthesis of Macrocyclic Phenanthrolines with Exotopic Binding Sites. Probing Their Complexation Behavior with Copper(I) and Iron(II)

Author keywords

Copper; Iron; Macromolecules; Supramolecular chemistry; Synthetic methods

Indexed keywords


EID: 0347711874     PISSN: 16154150     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1521-3897(199904)341:3<228::aid-prac228>3.0.co;2-f     Document Type: Article
Times cited : (13)

References (49)
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    • M. Schmittel, C. Michel, unpublished results: 3-Bromo-1,10-phenanthroline was treated in a Sonogashira coupling with trimethylsilylacetylene and arylated in 2,9-position with mesityl lithium. Subsequent deprotection of the trimethyIsilyl group and Sonogashira coupling with p-diiodobenzene furnished the desired linear bisphenanthroline
    • M. Schmittel, C. Michel, unpublished results: 3-Bromo-1,10-phenanthroline was treated in a Sonogashira coupling with trimethylsilylacetylene and arylated in 2,9-position with mesityl lithium. Subsequent deprotection of the trimethyIsilyl group and Sonogashira coupling with p-diiodobenzene furnished the desired linear bisphenanthroline.
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    • Quaternary carbons are not cited since the proper assignment could not be established despite long lasting data collection at a DMX 600 NMR instrument because of solubility problems
    • Quaternary carbons are not cited since the proper assignment could not be established despite long lasting data collection at a DMX 600 NMR instrument because of solubility problems.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.