کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1311161 975296 2010 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis, spectroscopic and structural characterization of the high-spin Fe(II) cyanato-N and thiocyanato-N “picket fence” porphyrin complexes
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Synthesis, spectroscopic and structural characterization of the high-spin Fe(II) cyanato-N and thiocyanato-N “picket fence” porphyrin complexes
چکیده انگلیسی

Two new iron(II) five-coordinated porphyrin complexes [Na(2,2,2-crypt)] [FeII(TpivPP)(NCO)] (1) (TpivPP = α,α,α,α-tetrakis(o-pivalamidophenyl) porphyrin known as picket fence porphyrin and 2,2,2-crypt is the cryptand-222) and [K(2,2,2-crypt)][FeII(TpivPP)(NCS)] (2) have been prepared and characterized. The UV–Vis and IR spectroscopic data are consistent with a cyanato-N and thiocyanato-N ferrous porphyrinates. The Mössbauer data and the X-ray structural analysis indicate that the Fe(II) cation in 1 and 2 is high-spin (S = 2) and has the (dxy)2(dxz)1(dyz)1(dz2)1(dx2-y2)1(dxy)2(dxz)1(dyz)1(dz2)1(dx2-y2)1 ground state electronic configuration.For complex 1, the average equatorial iron-pyrrole N bond length (Fe–Np = 2.120(2) Å), the distance between the iron and the 24-atom mean plane of the porphyrin ring (Fe–PC = 0.6805(7) Å) and the distance between the iron and the plane made by the four pyrrole nitrogens (Fe–PN = 0.5923(12) Å) are longer than those of complex 2 and similar five-coordinated Fe(II) high-spin porphyrinates. This is probably due to the significant electronic repulsion of the dx2-y2dx2-y2 and dxy orbitals by the negative charge of the pyrrole N atoms in case of 1.

Two new iron(II) five-coordinated porphyrin complexes [Na(2,2,2-crypt)] [FeII(TpivPP)(NCO)] (TpivPP = α,α,α,α-tetrakis(o-pivalamidophenyl) porphyrin known as picket fence porphyrin and 2,2,2-crypt is the cryptand-222) and [K(2,2,2-crypt)][FeII(TpivPP)(NCS)] have been prepared. Both NCS− and NCO− iron(II) porphyrinates were characterized by UV–Vis, IR spectroscopy and elemental analysis.The Mössbauer data and the X-ray structural analysis indicate that the Fe(II) cation in the two pseudo-halide derivatives is high-spin (S = 2) and has the (dxy)2(dxz)1(dyz)1(dz2)1(dx2-y2)1(dxy)2(dxz)1(dyz)1(dz2)1(dx2-y2)1 ground state electronic configuration.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Inorganica Chimica Acta - Volume 363, Issue 13, 25 October 2010, Pages 3208–3213
نویسندگان
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