2011
DOI: 10.2298/jsc101201062v
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New Cu (II) and Co(II) octaazamacrocyclic complexes with 2-amino-3-phenyl-propanoic acid

Abstract: New cationic Cu(II) and Co (II) complexes with N,N',N",4,8, and the anion of 2-amino-3-phenylpropanoic acid (S-phenylalanine) were prepared. The complexes were analyzed and characterized by elemental analysis, conductometric, polarimetric, magnetic and cyclic voltammetric measurements, as well as by spectroscopic data (UV/Vis, IR). Both complexes are binuclear with the general formula [M 2 (S-Phe)tpmc](ClO 4 ) 3 ·nH 2 O; S-PheH = S-phenylalanine, M(II) = Cu, n = 7; Co, n = 0. Based on previously reported data … Show more

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Cited by 5 publications
(11 citation statements)
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“…22 In similar 5-coordinated Cu(II) complexes with carboxylate co-ligands the values of the magnetic moments are in the range of 1.75-2.20 μ B /Cu(II). 14,[23][24][25] However, similar values are reported for binuclear Cu(II) complexes with no magnetic interaction between the copper(II) ions as well. [23][24][25] 642 D R A Ž I Ć et al…”
Section: Resultssupporting
confidence: 76%
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“…22 In similar 5-coordinated Cu(II) complexes with carboxylate co-ligands the values of the magnetic moments are in the range of 1.75-2.20 μ B /Cu(II). 14,[23][24][25] However, similar values are reported for binuclear Cu(II) complexes with no magnetic interaction between the copper(II) ions as well. [23][24][25] 642 D R A Ž I Ć et al…”
Section: Resultssupporting
confidence: 76%
“…The large width of the spectral bands, the position of λ max , and the shapes correspond to d-d transitions of the Cu(II) complexes. 26 The similarity of these spectra to the spectra of the related aminocarboxylate complex with S-phenylalanine and with numerous carboxylate Cu(II) complexes 14,[23][24][25] additionally supports the proposed five-coordinate geometry of Cu(II). There is a bathochromic shift of the absorption maximum in the case of complex 2 in comparison to complex 1.…”
Section: Spectroscopic Propertiesmentioning
confidence: 66%
“…A sharp band at 1589.4 cm -1 , ascribed to pyridine ring skeletal vibration in the spectrum of free tpmc (Fig. 3a) is displaced to 1610 cm -1 upon coordination [4]. Strong broad bands at 1361.4-1295.3 cm -1 and 1021.3 cm -1 are assigned to coordinated nitrate [35].…”
Section: Resultsmentioning
confidence: 94%
“…In recent years, interest in macrocyclic polyamines has been on the increase as a result of their attractive structures and their possible applications in many different fields [1][2][3]. The reason for that is their possibility to react or coordinate with many different metal ions as well as organic molecules via by nitrogen atoms [4][5][6][7].…”
Section: Introductionmentioning
confidence: 99%
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