Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 121 (1990), S. 371-375 
    ISSN: 1434-4475
    Keywords: Photosensibilization ; Electron transfer ; 2,4,6-Triphenylpyrylium tetrafluoroborate ; 3-Phenylpropiophenones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Photolyse der 3-Phenylpropiophenone1 a–d in Gegenwart von 2,4,6-Triphenyl-pyrylium-tetrafluoroborat (TPT) ergeben die entsprechenden α,β-ungesättigten Ketone2 a–c und1 d (aus1 c), neben Acetophenon (3), Benzophenon (4), Benzoesäure (5) und Benzaldehyd (6), vermutlich durch Fragmentierung des Radikal-Kations1 + ·, das mittels Übertragung eines Elektrons von1 zuTPT im angeregten Zustand erzeugt wird.
    Notes: Summary Photolysis of 3-phenylpropiophenones1 a–d in the presence of 2,4,6-triphenylpyrylium tetrafluoroborate (TPT) yields the corresponding α,β-unsaturated ketones2 a–c and1 d (from1 c), together with acetophenone (3), benzophenone (4), benzoic acid (5) and benzaldehyde (6), presumably by fragmentations of the radical cation1 + ·, generated via a single electron transfer process from1 to the excitedTPT.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1434-1948
    Keywords: Terpyridine ; Copper sensing ; Cyclam ; Fluorescence ; Solution studies ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A synthetic strategy has been devised for the preparation of new compounds in which terpyridyl fragments are linked to 1,4,8,11-tetraazacyclotetradecane (cyclam). Reaction of excess cyclam with 4′-[(4-bromomethyl)phenyl]-2,2′:2″,6′-terpyridine afforded the ligand 1-[4′-p-tolyl-(2,2′:6′,2″-terpyridyl)]-1,4,8,11-tetraazacyclotetradecane (L1) in which the tetraaza macrocycle was covalently attached to one benzyl-terpyridyl fragment. Under similar conditions reaction of cyclam with excess 4′-[(4-bromomethyl)phenyl]-2,2′:2″,6′-terpyridine gave the tetra substituted cyclam derivative 1,4,8,11-[4′-p-tolyl-(2,2′:6′,2″-terpyridyl)]-1,4,8,11-tetraazacyclotetradecane (L2). The multidentate ligand L2 was crystallographically characterised by single-crystal X-ray diffraction techniques. Reaction of L1 with [Ru(mtpy)Cl3] gave the heteroleptic ruthenium(II) complex [Ru(L1)(mtpy)][PF6]2 (mtpy = 4′-methyl-2,2′:6′2″-terpyridine). The fluorescent intensity of the metallo-receptor [Ru(L1)(mtpy)][PF6]2 was quenched selectively in the presence of copper(II) in an aqueous environment. To gain insight into the nature of this interaction, potentiometric titrations on [Ru(L1)(mtpy)]2+ in the presence of Cu2+ were carried out. The quenching of the emission intensity was associated with the presence of the copper {Cu[Ru(L1)(mtpy)]}4+ complex in solution. The receptor 1-[4′-methyl-(2,2′:6′,2″-terpyridyl)]-1,4,8,11-tetraazacyclotetradecane (L3), in which the cyclam fragment is separated from the terpyriyl by a methylene group, has also been synthesised by reaction of 4′-bromomethyl-2,2′:2″,6′-terpyridine and cyclam. With L3 as starting material, the ruthenium complex [Ru(L3)(mtpy)]2+ was prepared in order to evaluate the effect that the nature of the spacer has on the quenching of the fluorescence upon addition of Cu2+.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...