{REIIICl3} core complexes with bifunctional single amino acid chelates

Sangeeta Ray Banerjee; Lihui Wei; Murali K. Levadala; Neva Lazarova; Vladimir O. Golub; Charles J. O'Connor; Karin A. Stephenson; John F. Valliant; John W. Babich; Jon Zubieta

doi:10.1021/ic020391d

{RE^IIICl₃} core complexes with bifunctional single amino acid chelates

Sangeeta Ray Banerjee, Lihui Wei, Murali K. Levadala, Neva Lazarova, Vladimir O. Golub, Charles J. O'Connor, Karin A. Stephenson, John F. Valliant, John W. Babich, Jon Zubieta

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

20 Scopus citations

Abstract

The reactions of the Re(V) starting material [ReO(PPh₃)₂Cl₃] with ligands of the type XN(Y)Z [X = Y = 2-pyridylmethyl, Z = -CH₂CO₂Et (L¹Et), -CH₂CH₂CO₂Et (L²Et), -CH₂CH₂CH₂CH₂CH (NHCO₂Bu^t)CO₂H (L³H); X = 2-pyridylmethyl, Y = 2-(1-methylimidazolyl)methyl, Z = -CH₂CO₂Et (L⁴Et)] yielded the Re(III) trichloride complexes of the type [ReCl₃(LⁿR)]. The complexes are mononuclear, paramagnetic species with a facial geometry of the chloride ligands. The nitrogen donors of the tridentate LⁿR ligands complete the distorted octahedral coordination spheres of the complexes. Crystal data: [ReCl₃(L¹Et)] (1), monoclinic, C2/m, a = 16.088(3) Å, b = 9.980(2) Å, c = 12.829(2) Å, β = 91.384(3)°, Z = 4, D_calc = 1.967 g/cm^-3; [ReCl₃(L⁴Et)] (4), monoclinic, C2/c, a = 22.880(1) Å, b = 7.4926(4) Å, c = 22.560(1) Å, β = 94.186(1)°, Z = 8, D_calc = 2.001 g/cm^-3.

Original language	English (US)
Pages (from-to)	5795-5802
Number of pages	8
Journal	Inorganic Chemistry
Volume	41
Issue number	22
DOIs	https://doi.org/10.1021/ic020391d
State	Published - Nov 4 2002

ASJC Scopus subject areas

Physical and Theoretical Chemistry
Inorganic Chemistry

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@article{cec344ca997044b3b2d6b2209b677a4b,

title = "{REIIICl3} core complexes with bifunctional single amino acid chelates",

abstract = "The reactions of the Re(V) starting material [ReO(PPh3)2Cl3] with ligands of the type XN(Y)Z [X = Y = 2-pyridylmethyl, Z = -CH2CO2Et (L1Et), -CH2CH2CO2Et (L2Et), -CH2CH2CH2CH2CH (NHCO2But)CO2H (L3H); X = 2-pyridylmethyl, Y = 2-(1-methylimidazolyl)methyl, Z = -CH2CO2Et (L4Et)] yielded the Re(III) trichloride complexes of the type [ReCl3(LnR)]. The complexes are mononuclear, paramagnetic species with a facial geometry of the chloride ligands. The nitrogen donors of the tridentate LnR ligands complete the distorted octahedral coordination spheres of the complexes. Crystal data: [ReCl3(L1Et)] (1), monoclinic, C2/m, a = 16.088(3) {\AA}, b = 9.980(2) {\AA}, c = 12.829(2) {\AA}, β = 91.384(3)°, Z = 4, Dcalc = 1.967 g/cm-3; [ReCl3(L4Et)] (4), monoclinic, C2/c, a = 22.880(1) {\AA}, b = 7.4926(4) {\AA}, c = 22.560(1) {\AA}, β = 94.186(1)°, Z = 8, Dcalc = 2.001 g/cm-3.",

author = "Banerjee, {Sangeeta Ray} and Lihui Wei and Levadala, {Murali K.} and Neva Lazarova and Golub, {Vladimir O.} and O'Connor, {Charles J.} and Stephenson, {Karin A.} and Valliant, {John F.} and Babich, {John W.} and Jon Zubieta",

year = "2002",

month = nov,

day = "4",

doi = "10.1021/ic020391d",

language = "English (US)",

volume = "41",

pages = "5795--5802",

journal = "Inorganic Chemistry",

issn = "0020-1669",

publisher = "American Chemical Society",

number = "22",

}

TY - JOUR

T1 - {REIIICl3} core complexes with bifunctional single amino acid chelates

AU - Banerjee, Sangeeta Ray

AU - Wei, Lihui

AU - Levadala, Murali K.

AU - Lazarova, Neva

AU - Golub, Vladimir O.

AU - O'Connor, Charles J.

AU - Stephenson, Karin A.

AU - Valliant, John F.

AU - Babich, John W.

AU - Zubieta, Jon

PY - 2002/11/4

Y1 - 2002/11/4

N2 - The reactions of the Re(V) starting material [ReO(PPh3)2Cl3] with ligands of the type XN(Y)Z [X = Y = 2-pyridylmethyl, Z = -CH2CO2Et (L1Et), -CH2CH2CO2Et (L2Et), -CH2CH2CH2CH2CH (NHCO2But)CO2H (L3H); X = 2-pyridylmethyl, Y = 2-(1-methylimidazolyl)methyl, Z = -CH2CO2Et (L4Et)] yielded the Re(III) trichloride complexes of the type [ReCl3(LnR)]. The complexes are mononuclear, paramagnetic species with a facial geometry of the chloride ligands. The nitrogen donors of the tridentate LnR ligands complete the distorted octahedral coordination spheres of the complexes. Crystal data: [ReCl3(L1Et)] (1), monoclinic, C2/m, a = 16.088(3) Å, b = 9.980(2) Å, c = 12.829(2) Å, β = 91.384(3)°, Z = 4, Dcalc = 1.967 g/cm-3; [ReCl3(L4Et)] (4), monoclinic, C2/c, a = 22.880(1) Å, b = 7.4926(4) Å, c = 22.560(1) Å, β = 94.186(1)°, Z = 8, Dcalc = 2.001 g/cm-3.

AB - The reactions of the Re(V) starting material [ReO(PPh3)2Cl3] with ligands of the type XN(Y)Z [X = Y = 2-pyridylmethyl, Z = -CH2CO2Et (L1Et), -CH2CH2CO2Et (L2Et), -CH2CH2CH2CH2CH (NHCO2But)CO2H (L3H); X = 2-pyridylmethyl, Y = 2-(1-methylimidazolyl)methyl, Z = -CH2CO2Et (L4Et)] yielded the Re(III) trichloride complexes of the type [ReCl3(LnR)]. The complexes are mononuclear, paramagnetic species with a facial geometry of the chloride ligands. The nitrogen donors of the tridentate LnR ligands complete the distorted octahedral coordination spheres of the complexes. Crystal data: [ReCl3(L1Et)] (1), monoclinic, C2/m, a = 16.088(3) Å, b = 9.980(2) Å, c = 12.829(2) Å, β = 91.384(3)°, Z = 4, Dcalc = 1.967 g/cm-3; [ReCl3(L4Et)] (4), monoclinic, C2/c, a = 22.880(1) Å, b = 7.4926(4) Å, c = 22.560(1) Å, β = 94.186(1)°, Z = 8, Dcalc = 2.001 g/cm-3.

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UR - http://www.scopus.com/inward/citedby.url?scp=20244368918&partnerID=8YFLogxK

U2 - 10.1021/ic020391d

DO - 10.1021/ic020391d

M3 - Article

C2 - 12401085

AN - SCOPUS:20244368918

SN - 0020-1669

VL - 41

SP - 5795

EP - 5802

JO - Inorganic Chemistry

JF - Inorganic Chemistry

IS - 22

ER -

{RE^IIICl₃} core complexes with bifunctional single amino acid chelates

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