Hemilabile and reversible carbon monoxide binding properties of iron(II), cobalt(II) and nickel(II) complexes containing a new tridentate P-S-N ligand

TY - JOUR

T1 - Hemilabile and reversible carbon monoxide binding properties of iron(II), cobalt(II) and nickel(II) complexes containing a new tridentate P-S-N ligand

AU - Tate, Christopher W.

AU - deMello, Andrew

AU - Gee, Antony D.

AU - Kealey, Steven

AU - Vilar, Ramon

AU - White, Andrew J. P.

AU - Long, Nicholas J.

PY - 2012/1/7

Y1 - 2012/1/7

N2 - Several first-row transition metal complexes of the formulation [M(1)(2)](X)(2) {where 1 = Ph(2)PCH(2)CH(2)S(2-C(6)H(4)NH(2)); M = Fe(II), X = BF(4)(-) (2); M = Co(II), X = BF(4)(-) (3), Ni(II), X = ClO(4)(-) (4)} have been prepared by reaction of two equivalents of the new P-S-N ligand Ph(2)PCH(2)CH(2)S(2-C(6)H(4)NH(2)) 1 with one equivalent of the appropriate [M(OH(2))(6)](X)(2) precursor in acetonitrile. In the solid state, complexes 2-4 exist as distorted centrosymmetric octahedral structures featuring facially capping ligands in an all-trans arrangement. Reaction of 2 and 3 with a stream of carbon monoxide (1 atm.) for 5 min in acetonitrile generates iron(II) monocarbonyl species of formulation [Fe(CO)(1)(2)](BF(4))(2)2a, and a cobalt(II) dicarbonyl complex, [Co(CO)(2)(1)(2)](BF(4))(2)3a, which can be isolated in the solid state. Complete removal of CO is achieved by either heating to reflux samples of 2a in acetonitrile for 5 min or by heating solid samples of 3a at 120 °C in vacuo over a period of 4 h. The binding of carbon monoxide is fully reversible for 2 and 3 and can be repeated over multiple cycles. When the same trapping reactions were carried out with very low radiochemical (11)CO concentrations, metal carbonyl species were no longer formed. It is likely that the kinetics of (11)CO adduct formation are too slow to allow for effective trapping under the applied radiochemical conditions.

AB - Several first-row transition metal complexes of the formulation [M(1)(2)](X)(2) {where 1 = Ph(2)PCH(2)CH(2)S(2-C(6)H(4)NH(2)); M = Fe(II), X = BF(4)(-) (2); M = Co(II), X = BF(4)(-) (3), Ni(II), X = ClO(4)(-) (4)} have been prepared by reaction of two equivalents of the new P-S-N ligand Ph(2)PCH(2)CH(2)S(2-C(6)H(4)NH(2)) 1 with one equivalent of the appropriate [M(OH(2))(6)](X)(2) precursor in acetonitrile. In the solid state, complexes 2-4 exist as distorted centrosymmetric octahedral structures featuring facially capping ligands in an all-trans arrangement. Reaction of 2 and 3 with a stream of carbon monoxide (1 atm.) for 5 min in acetonitrile generates iron(II) monocarbonyl species of formulation [Fe(CO)(1)(2)](BF(4))(2)2a, and a cobalt(II) dicarbonyl complex, [Co(CO)(2)(1)(2)](BF(4))(2)3a, which can be isolated in the solid state. Complete removal of CO is achieved by either heating to reflux samples of 2a in acetonitrile for 5 min or by heating solid samples of 3a at 120 °C in vacuo over a period of 4 h. The binding of carbon monoxide is fully reversible for 2 and 3 and can be repeated over multiple cycles. When the same trapping reactions were carried out with very low radiochemical (11)CO concentrations, metal carbonyl species were no longer formed. It is likely that the kinetics of (11)CO adduct formation are too slow to allow for effective trapping under the applied radiochemical conditions.

U2 - 10.1039/c1dt11248a

DO - 10.1039/c1dt11248a

M3 - Article

C2 - 22011880

SN - 1477-9226

VL - 41

SP - 83

EP - 89

JO - DALTON TRANSACTIONS (2003)

JF - DALTON TRANSACTIONS (2003)

IS - 1

ER -