Sy. Wang et al., Tetranuclear manganese carboxylate complexes with a trigonal pyramidal metal topology via controlled potential electrolysis, INORG CHEM, 39(7), 2000, pp. 1501-1513
Controlled potential electrolysis (CPE) procedures are described that provi
de access to complexes with a [Mn-4(mu(3)-O)(3)(mu(3)-O2CR)](6+) core (3Mn(
III),Mn-IV) and a trigonal pyramidal metal topology, starting from species
containing the [Mn-4(mu(3)-O)(2)](8+) core (4Mn(III)). [Mn4O2(O2CMe)(6)(py)
(2)(dbm)(2)] (6): triclinic, P (1) over bar, a = 10.868(3) Angstrom, b = 13
.864(3) Angstrom, c = 10.625(3) Angstrom, alpha = 108.62(1)degrees, beta =
118.98(1)degrees, gamma = 89.34(2)degrees, V= 1307 Angstrom(3), Z = 1, T =
-131 degrees C, R (R-w) = 3.24 (3.70%)%. [Mn4O2(O2CPh)(6)(py)(dbm)(2)] (8):
monoclinic, P2(1)/c, a = 14.743(6) Angstrom, b = 15.536(8) Angstrom, c = 3
0.006(13) Angstrom, beta = 102.79(1)degrees, V = 6702 Angstrom(3), Z = 4, T
= -155 degrees C, R(R-w) = 4.32 (4.44)%. Both 6 and 8 contain a [Mn4O2](8) core; 8 only has one py group, the fourth Mn-III site being five-coordina
te. (NBu4II)[Mn4O2(O2CPh)(7)(dbm)(2)] (10) is available from two related pr
ocedures. CPE of 10 at 0.65 V vs ferrocene in MeCN leads to precipitation o
f [Mn4O3(O2CPh)(4)(dbm)(3)] (11); similarly, CPE of 6 at 0.84 V in MeCN/CH2
Cl2 (3:1 v/v) gives [Mn4O3(O2CMe)(4)(dbm)(3)] (12). Complier 11: monoclinic
, P2(1)/n, a = 15.161(3) Angstrom, b = 21.577(4) Angstrom, c = 22.683(5) An
gstrom, beta = 108.04(3)degrees, V = 7056 Angstrom(3), Z = 4, T = -100 degr
ees C, R (wR2) = 8.63 (21.80)%. Complex 12: monoclinic, P2(1)/n, a = 13.549
(2) Angstrom, b = 22.338(4) Angstrom, c = 16.618(2) Angstrom, beta = 103.74
(1)degrees, V = 4885 Angstrom(3), Z = 4, T = -171 degrees C, R (R-w) = 4.63
(4.45)%. Both 11 and 12 contain a [Mn-4(mu(3)-O)(3)(mu-O2CR)] core with a
Mn-4 trigonal pyramid (Mn-IV at the apex) and the RCO2- bridging the Mn-3(I
II) base. However, in 11, the carboxylate is eta(2),mu(3) with one O atom t
erminal to one Mn-III and the other O atom bridging the other two Mn-III io
ns, whereas in 12 the carboxylate is eta(1),mu(3), a single O atom bridging
three Mn-III ions. Variable-temperature, solid-state magnetic susceptibili
ty studies on 11 and 12 show that, for both complexes, there are antiferrom
agnetic exchange interactions between Mn-III/Mn-IV pairs, and ferromagnetic
interactions between Mn-III/Mn-III pairs. In both cases, the resultant gro
und state of the complex is S = 9/2, confirmed by magnetization vs field st
udies in the 2.00-30.0 K and 0.50-50 kG temperature and field ranges, respe
ctively.