45 research outputs found
C−Cl Bond Activation of <i>ortho</i>-Chlorinated Imine with Iron Complexes in Low Oxidation States
The ortho-chelated iron(II) complexes [FeCl(PMe3)3((C6H3Cl-ortho)CHN-R)] (R = Me, Ph) (3, 4) and [FeCl(PMe3)3(C6H4-CHN-R)] (R = Ph, n-Bu) (7, 8) were prepared through oxidative addition of the C−Cl bond of ortho-chlorinated imine using iron(0) complexes, [Fe(PMe3)4]. The reactions of 3, 4, and 8 with CO delivered the carbonyl Fe(II) complexes 9−11. A one-pot reaction of [FeMe2(PMe3)4] with (C6H3Cl2-2,6)CHN-Ph in CO atmosphere resulted in carbonyl Fe(II) complexes [FeMe(CO)(PMe3)2((C6H3Cl-ortho)CHN-Ph)] (12). The crystal and molecular structures of complexes 3, 4, 7−9, and 12 were determined by X-ray diffraction
C−Cl Bond Activation of <i>ortho</i>-Chlorinated Imine with Iron Complexes in Low Oxidation States
The ortho-chelated iron(II) complexes [FeCl(PMe3)3((C6H3Cl-ortho)CHN-R)] (R = Me, Ph) (3, 4) and [FeCl(PMe3)3(C6H4-CHN-R)] (R = Ph, n-Bu) (7, 8) were prepared through oxidative addition of the C−Cl bond of ortho-chlorinated imine using iron(0) complexes, [Fe(PMe3)4]. The reactions of 3, 4, and 8 with CO delivered the carbonyl Fe(II) complexes 9−11. A one-pot reaction of [FeMe2(PMe3)4] with (C6H3Cl2-2,6)CHN-Ph in CO atmosphere resulted in carbonyl Fe(II) complexes [FeMe(CO)(PMe3)2((C6H3Cl-ortho)CHN-Ph)] (12). The crystal and molecular structures of complexes 3, 4, 7−9, and 12 were determined by X-ray diffraction
Fig 2 -
Forest plots of the relationship between the PNI and survival outcomes: A. OS B. DMFS C. PFS.</p
C−Cl Bond Activation of <i>ortho</i>-Chlorinated Imine with Iron Complexes in Low Oxidation States
The ortho-chelated iron(II) complexes [FeCl(PMe3)3((C6H3Cl-ortho)CHN-R)] (R = Me, Ph) (3, 4) and [FeCl(PMe3)3(C6H4-CHN-R)] (R = Ph, n-Bu) (7, 8) were prepared through oxidative addition of the C−Cl bond of ortho-chlorinated imine using iron(0) complexes, [Fe(PMe3)4]. The reactions of 3, 4, and 8 with CO delivered the carbonyl Fe(II) complexes 9−11. A one-pot reaction of [FeMe2(PMe3)4] with (C6H3Cl2-2,6)CHN-Ph in CO atmosphere resulted in carbonyl Fe(II) complexes [FeMe(CO)(PMe3)2((C6H3Cl-ortho)CHN-Ph)] (12). The crystal and molecular structures of complexes 3, 4, 7−9, and 12 were determined by X-ray diffraction
The baseline characteristics of the included studies.
The baseline characteristics of the included studies.</p
C−Cl Bond Activation of <i>ortho</i>-Chlorinated Imine with Iron Complexes in Low Oxidation States
The ortho-chelated iron(II) complexes [FeCl(PMe3)3((C6H3Cl-ortho)CHN-R)] (R = Me, Ph) (3, 4) and [FeCl(PMe3)3(C6H4-CHN-R)] (R = Ph, n-Bu) (7, 8) were prepared through oxidative addition of the C−Cl bond of ortho-chlorinated imine using iron(0) complexes, [Fe(PMe3)4]. The reactions of 3, 4, and 8 with CO delivered the carbonyl Fe(II) complexes 9−11. A one-pot reaction of [FeMe2(PMe3)4] with (C6H3Cl2-2,6)CHN-Ph in CO atmosphere resulted in carbonyl Fe(II) complexes [FeMe(CO)(PMe3)2((C6H3Cl-ortho)CHN-Ph)] (12). The crystal and molecular structures of complexes 3, 4, 7−9, and 12 were determined by X-ray diffraction
Comparison of coronary lesions traits in IVUS between the 2 groups.
<p>Comparison of coronary lesions traits in IVUS between the 2 groups.</p
Comparison of clinical data and coronary lesions between the 2 groups.
<p>Comparison of clinical data and coronary lesions between the 2 groups.</p
