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Andreas Roodt

Publications and source records attributed to Andreas Roodt.

12 recordsLinked to original sources

Rhodium hydride formation in the presence of a bulky monophosphite ligand: a spectroscopic and solid-state investigation.

A study has been carried out on rhodium catalyst preforming when modified with the bulky tris(2,4-di-tert-butylphenyl) phosphite, P(Obtbp)(3). X-Ray crystal structure determinations of a tropolone-type precursor complex [Rh(TropBr(3))(CO){P(Obtbp)(3)}].P(Obtbp)(3).CH(3)COCH(3)(TropBr(3)= 3,5,7-tribromotropolonate) and the free P(Obtbp)(3) ligand are reported. Systematic in situ IR and NMR studies of the particular rhodium phosphite modified catalyst and its precursors have led to the identification of two distinct rhodium hydride species. A {(1)H,(31)P} HMBC NMR experiment afforded clarity on the (31)P NMR spectra observed under hydroformylation conditions. The species were identified as [HRh(CO)(3){P(Obtbp)(3)}] and [HRh(CO)(2){P(Obtbp)(3)}(2)]. Attention was also given to the rate of catalyst formation when starting from different rhodium precursors.

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Carbonyl(5-nitrotropolonato-kappa2O1,O2)(triphenylphosphine-kappaP)rhodium(I).

The molecule of the title complex, [Rh(5-NO2trop)(C18H15P)(CO)] (5-NO2trop is 2-hydroxy-5-nitrocyclohepta-2,4,6-trienone, C7H4NO4), has a distorted square-planar geometry. Strong intramolecular and weak intermolecular hydrogen bonding is observed, with H...O distances of the order of 2.25 and 2.55 A, respectively. The Rh-CO, Rh-O (trans to CO), Rh-O (trans to P) and Rh-P bond distances are 1.775 (7), 2.072 (4), 2.068 (4) and 2.2397 (17) A, respectively, the O-Rh-O angle is 77.09 (16) degrees and the bidentate O-C-C-O torsion angle is 1.5 (7) degrees.

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cis-Diphenylbis(1,3,5-triaza-7-phosphaadamantane-kappaP)platinum(II).

The structure of the title compound, [Pt(C(6)H(5))(2)(C(6)H(12)N(3)P)(2)] or [Pt(Ph)(2)(PTA)(2)] (where Ph is phenyl and PTA is 1,3,5-triaza-7-phosphaadamantane), is discussed. Selected geometric parameters are: Pt-P = 2.2888 (16) and 2.2944 (17) A, Pt-C = 2.052 (5) and 2.064 (6) A, C-Pt-C = 84.6 (2) degrees and P-Pt-P = 99.28 (6) degrees. The effective cone angle for the PTA ligands was calculated as 113 degrees.

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Synthesis, crystal structure and hydroformylation activity of triphenylphosphite modified cobalt catalysts.

The dinuclear complex [Co(2)(CO)(6)[P(OPh)3]2] (2) has been synthesised and was fully characterised. The solid state structure revealed a trans diaxial geometry, no bridging carbonyls, and Co-Co and Co-P bond lengths of 2.6722(4) and 2.1224(4) Angstrom, respectively. Catalysed hydroformylation of 1-pentene with 2 was attempted at temperatures in the range 120 to 210 degrees C and pressures between 34 and 80 bar. High pressure spectroscopy (HP-IR and HP-NMR) was used to detect hydride intermediates. High pressure infrared (HP-IR) studies revealed the formation of [HCo(CO)(3)P(OPh)3] (4) at ca. 110 degrees C, but at higher temperatures absorption bands corresponding to [HCo(CO)(4)]() were observed. The hydride intermediate 4 has also been synthesised and characterised. Upon increased ligand concentration, HP-IR studies showed the formation of new carbonyl absorption bands due to a higher substituted cobalt carbonyl complex-[HCo(CO)(2)[P(OPh)3]2] (5), which is believed to be catalytically less active. Complex 5 has been synthesised independently and was fully characterised. A low temperature crystal structural study of 5 revealed a trigonal bipyramidal structure with a trans H-Co-CO arrangement and two equatorial phosphite ligands, the Co-P bond lengths being 2.1093(8) and 2.1076(8)[Angstrom], respectively.

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3,7-dibromohinokitiol: a redetermination.

The structure of the title compound (systematic name: 3,7-dibromo-2-hydroxy-6-isopropylcyclohepta-2,4,6-trien-1-one), C(10)H(10)Br(2)O(2), previously described by Ito, Fukazawa & Iitaka [Tetrahedron Lett. (1972), 13, 745-749], has been redetermined. Strong inter- and intramolecular hydrogen bonds, with H.O distances of 2.17 (9) and 2.06 (6) A, respectively, are observed. There are also two short Br...Br and two short Br.(ring centroid) interactions. Important dimensions include C--O(carbonyl) = 1.252 (5) A, C--O(hydroxyl) = 1.355 (5) A, C-Br(3-position) = 1.904 (4) A and C--Br(7-position) = 1.905 (4) A, and an O--C--C--O ring torsion angle of -6.7 (6) degrees.

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Trans-bis(3,5-diaza-1-azonia-7-phosphaadamantane-kappaP)bis(thiocyanato-kappaS)palladium(II) bis(thiocyanate).

The crystal structure of the title compound, trans-[Pd(NCS)(2)(C(6)H(13)N(3)P)(2)](NCS)(2), is one of the few palladium(II) complexes containing two protonated water-soluble 1,3,5-triaza-7-phosphaadamantane (PTA) ligands reported to date. The compound displays a distorted square-planar geometry, with the Pd atom on an inversion centre and with the S atoms of the thiocyanate counter-ions occupying the axial positions above and below the equatorial plane described by the phosphine and thiocyanate ligands. Geometric parameters for the formal coordination polyhedron include a Pd--P distance of 2.2940 (8) A, a Pd--S distance of 2.3509 (8) A and a P--Pd--S angle of 89.45 (3) degrees. The effective cone angle for the PTA ligands was calculated as 114.5 degrees.

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trans-Carbonyliodotris(triphenylstibine-kappaSb)rhodium(I).

The crystal structure of the title compound, [RhI(C(18)H(15)Sb)(3)(CO)], represents a rare example of a crystallographically characterized five-coordinate Rh(I)-SbPh(3) complex. The compound crystallizes with the I-Rh-CO core on a threefold rotation axis, with three crystallographically equivalent triphenylstibine ligands. Selected geometric parameters are: Rh-I = 2.7159 (8), Rh-Sb = 2.5962 (4), Rh-C(CO) = 1.825 (6) and C(CO)-O 1.153 (6) A, and Sb-Rh-I = 89.374 (10) and Sb-Rh-C(CO) = 90.626 (10) degrees. The cone angle of the SbPh(3) ligand was determined as 137 degrees, according to the Tolman model.

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Reaction Mechanism for Olefin Exchange at Chloro Ethene Complexes of Platinum(II).

Complex equilibria in methanol/chloroform/dichloromethane solutions containing Zeise's anion, [PtCl(3)(C(2)H(4))](-) (1), the solvento species, trans-[PtCl(2)(C(2)H(4))(MeOH)] (2), and the dinuclear complex, trans-[PtCl(2)(C(2)H(4))](2) (3), have been studied by UV-vis, (1)H, and (195)Pt NMR spectroscopy, giving average values of K(Cl) = (1.6 +/- 0.2)10(3) M(-)(1) and K(S) = (0.16 +/- 0.02) M(-)(1) for the equilibrium constants between 2 and 1 and 3 and 2, respectively. The bridged complex 3 is completely split into monomeric solvento complexes 2 in methanol and in chloroform or dichloromethane solutions with [MeOH] > 0.5 M. Ethene exchange at the mononuclear complexes 1 and 2 was studied by (1)H NMR line-broadening experiments in methanol-d(4). Observed overall exchange rate constants decrease with an increase in free chloride concentration due to the displacement of the rapid equilibrium between 1 and 2 toward the more slowly exchanging parent chloro complex 1. Ethene exchange rate constants at 298 K for complexes 1 and 2 are k(ex1) = (2.1 +/- 0.1)10(3) M(-)(1) s(-)(1)and k(ex2) = (5.0 +/- 0.2)10(5) M(-)(1) s(-)(1), respectively, with corresponding activation parameters DeltaH(1)() = 19.1 +/- 0.3 kJ mol(-)(1), DeltaS(1)() = -117 +/- 1 J K(-)(1) mol(-)(1), DeltaH(2)() = 10.2 +/- 0.4 kJ mol(-)(1), and DeltaS(2)() = -102 +/- 2 J K(-)(1) mol(-)(1). The activation process is largely entropy controlled; the enthalpy contributions only amounting to approximately 30% of the free energy of activation. Ethene exchange takes place via associative attack by the entering olefin at the labile site trans to the coordinated ethene, which is either occupied by a chloride or a methanol molecule in the ground state. The intimate mechanism might involve a two-step process via trans-[PtCl(2)(C(2)H(4))(2)] in steady state or a concerted process via a pentacoordinated transition state with two ethene molecules bound to the platinum(II).

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13C and (15)N NMR Mechanistic Study of Cyanide Exchange on Oxotetracyanometalate Complexes of Re(V), Tc(V), W(IV), Mo(IV), and Os(VI).

A range of complexes with general formula [MO(X)(CN)(4)](n)()(-) of W(IV), Mo(IV), Re(V), Tc(V), and Os(VI) were prepared and characterized by (13)C, (15)N, (17)O, and (99)Tc NMR, utilizing (13)C- and (15)N-enriched cyano complexes. A correlation between M-O and M-CN bond strength from X-ray crystallographic data and |(1)J((183)W-(13)C)| coupling is reported. The cyanide (HCN/CN(-)) exchange kinetics on the trans-dioxotetracyanometalate complexes and protonated/substituted ([MO(X)(CN)(4)](n)()(-)) forms thereof were studied in aqueous medium. The dioxotetracyano complexes show a trend of reactivity M(IV) > M(V) >M(VI), which is in agreement with the increase in M-L bond strength (L = O(2)(-) or CN(-)) and a dissociative activation for the cyanide and the oxygen exchange in these complexes. Rate constants (X, k(Xc)) in s(-)(1) at 298 K for the [MO(X)(CN)(4)](n)()(-) complexes are as follows for Mo(IV): O(2)(-), >0.4; OH(-), (1.7 +/- 0.1) x 10(-)(2); H(2)O, (1.5 +/- 0.1) x 10(-)(2); CN(-), (9.6 +/- 0.8) x 10(-)(3). For W(IV): O(2)(-), (4.4 +/- 0.4) x 10(-)(3); OH(-), (9.6 +/- 0.9) x 10(-)(5); H(2)O, (1.1 +/- 0.1) x 10(-)(4); CN(-), (1.1 +/- 0.1) x 10(-)(2); N(3)(-), (3.1 +/- 0.2) x 10(-)(4); F(-), (4.8 +/- 0.1) x 10(-)(5). For Tc(V): O(2)(-), (4.8 +/- 0.4) x 10(-)(3); H(2)O, <4 x 10(-)(5); NCS(-), <4 x 10(-)(5). For Re(V): O(2)(-), (3.6 +/- 0.3) x 10(-)(6) and (1.2 +/- 0.1) x 10(-)(4) for CN(-) and HCN, respectively; OH(2), <4 x 10(-)(8). For Os(VI): O(2)(-), <4 x 10(-)(9) and (1.2 +/- 0.1) x 10(-)(4) for CN(-) and HCN, respectively. The cyanide exchange kinetics were correlated with previously determined proton and oxygen exchange, spanning a kinetic domain of more than 12 orders of magnitude for the five metal centers studied.

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