The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes
Само за регистроване кориснике
1997
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документуАпстракт
The octahedral copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid (H(4)1,3-pddadp) prepared in the region of pH 2 to 7 are hexadentates. Only one (trans(O-6)) of the three geometrical isomers was found to dominate. The trans(O-6)-Na-2[Cu(1,3-pddadp)] . NaNO3 . 2H(2)O complex crystallizes in the space group P2/c of the monoclinic crystal system with a = 9.231(2), b = 11.736(14), c = 10.150(2) Angstrom, beta = 109.33(2)degrees and Z = 2. The conformations of the chelate rings are found to be envelope for the glycinate and skew-boat for the beta-alaninate and 1,3-propanediamine rings, The complex is a tetragonally elongated octahedron (T similar to 0.8) with C-2 molecular symmetry. IR (carboxylate region) and electronic absorption spectra are assigned and discussed in relation to the structure of complexes. For hexadentate Cu(II) edta-type complexes of known structures the strain analysis is also discussed.
Кључне речи:
crystal structures / copper complexes / Edta-type complexesИзвор:
Inorganica Chimica Acta, 1997, 262, 2, 203-211Финансирање / пројекти:
- Serbian Ministry for Science and Technology
- US–YU Joint Fund for Scientific and Technological Cooperation from the National Science Foundation [Grant No. 8818818].
DOI: 10.1016/S0020-1693(97)05524-2
ISSN: 0020-1693
WoS: A1997XX42300012
Scopus: 2-s2.0-0001114620
Колекције
Институција/група
VinčaTY - JOUR AU - Radanović, Dušan J. AU - Prelesnik, Bogdan V. AU - Radanović, Dušanka D. AU - Matović, Zoran AU - Douglas, Bodie PY - 1997 UR - https://vinar.vin.bg.ac.rs/handle/123456789/2087 AB - The octahedral copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid (H(4)1,3-pddadp) prepared in the region of pH 2 to 7 are hexadentates. Only one (trans(O-6)) of the three geometrical isomers was found to dominate. The trans(O-6)-Na-2[Cu(1,3-pddadp)] . NaNO3 . 2H(2)O complex crystallizes in the space group P2/c of the monoclinic crystal system with a = 9.231(2), b = 11.736(14), c = 10.150(2) Angstrom, beta = 109.33(2)degrees and Z = 2. The conformations of the chelate rings are found to be envelope for the glycinate and skew-boat for the beta-alaninate and 1,3-propanediamine rings, The complex is a tetragonally elongated octahedron (T similar to 0.8) with C-2 molecular symmetry. IR (carboxylate region) and electronic absorption spectra are assigned and discussed in relation to the structure of complexes. For hexadentate Cu(II) edta-type complexes of known structures the strain analysis is also discussed. T2 - Inorganica Chimica Acta T1 - The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes VL - 262 IS - 2 SP - 203 EP - 211 DO - 10.1016/S0020-1693(97)05524-2 ER -
@article{ author = "Radanović, Dušan J. and Prelesnik, Bogdan V. and Radanović, Dušanka D. and Matović, Zoran and Douglas, Bodie", year = "1997", abstract = "The octahedral copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid (H(4)1,3-pddadp) prepared in the region of pH 2 to 7 are hexadentates. Only one (trans(O-6)) of the three geometrical isomers was found to dominate. The trans(O-6)-Na-2[Cu(1,3-pddadp)] . NaNO3 . 2H(2)O complex crystallizes in the space group P2/c of the monoclinic crystal system with a = 9.231(2), b = 11.736(14), c = 10.150(2) Angstrom, beta = 109.33(2)degrees and Z = 2. The conformations of the chelate rings are found to be envelope for the glycinate and skew-boat for the beta-alaninate and 1,3-propanediamine rings, The complex is a tetragonally elongated octahedron (T similar to 0.8) with C-2 molecular symmetry. IR (carboxylate region) and electronic absorption spectra are assigned and discussed in relation to the structure of complexes. For hexadentate Cu(II) edta-type complexes of known structures the strain analysis is also discussed.", journal = "Inorganica Chimica Acta", title = "The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes", volume = "262", number = "2", pages = "203-211", doi = "10.1016/S0020-1693(97)05524-2" }
Radanović, D. J., Prelesnik, B. V., Radanović, D. D., Matović, Z.,& Douglas, B.. (1997). The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes. in Inorganica Chimica Acta, 262(2), 203-211. https://doi.org/10.1016/S0020-1693(97)05524-2
Radanović DJ, Prelesnik BV, Radanović DD, Matović Z, Douglas B. The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes. in Inorganica Chimica Acta. 1997;262(2):203-211. doi:10.1016/S0020-1693(97)05524-2 .
Radanović, Dušan J., Prelesnik, Bogdan V., Radanović, Dušanka D., Matović, Zoran, Douglas, Bodie, "The favored trans(O-6) geometry in hexadentate copper(II) complexes of 1,3-propanediamine-N,N-diacetic-N,N-di-3-propionic acid. Crystal structure of trans(O-6)-Na-2[Cu(1,3-pddadp)]center dot NaNO3 center dot 2H(2)O. Strain analysis and spectral assignments of complexes" in Inorganica Chimica Acta, 262, no. 2 (1997):203-211, https://doi.org/10.1016/S0020-1693(97)05524-2 . .