Sterically demanding aryloxides as supporting ligands in organoactinide chemistry. Synthesis, structural characterization, and reactivity of Th(O-2,6-t-Bu(2)C(6)H(3))(2)(CH(2)SiMe(3))(2) and formation of the trimeric thorium hydride Th3H6(O-2,6-t-Bu(2)C(6)H(3))(6)

被引:44
作者
Clark, DL
Grumbine, SK
Scott, BL
Watkin, JG
机构
[1] Chem. Sci. and Technology Division, Los Alamos National Laboratory, Los Alamos
关键词
D O I
10.1021/om950654u
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of ThBr4(THF)(4) with 2 equiv of KOAr (Ar = 2,6-t-Bu(2)C(6)H(3)) produces the bis(aryloxide) complex ThBr2(OAr)(2)(THF)(2) (1) in 67% yield. Alkylation of 1 with 2 equiv of Me(3)SiCH(2)MgCl allows the isolation of Th(OAr)2(CH(2)SiMe(3))(2) (2) in 61% yield. Thermolysis of 2 (benzene, 60 degrees C, 36 h) in the presence of NEt(3) results in the formation of the cyclometalated ligand redistribution product Th(OC6H3-t-BuCMe(2)CH(2))(OAr)(2) (3). Reaction of 2 with 1 equiv of 2,6-dimethylphenyl isocyanate leads to insertion into the Th-C bond to yield (ArO)(2)Th[OC(=NR)CH(2)SiMe(3)](CH(2)SiMe(3)) (4; R = 2,6-Me(2)C(6)H(3)) Aminolysis of 2 with 2 equiv of 2,6-diisopropylaniline allows the isolation of the bls(amido) species Th(OAr)(2)(NH2,6-i-Pr2C6H3)(2) (5) in 92% yield. 2 reacts with dihydrogen (1.5 atm) over a period of 7 days to form the trimeric dihydride complex Th-3(mu(3)-H)(2)(mu(2)-H)(4)(OAr)(6) (6) In the presence of 1 equiv of [HNMe(2)Ph][B(C6F5)(4)], 2 catalyzes the hydrogenation of 1-hexene (N-t = 1 h(-1)), while 6 is found to be a single-component catalyst for the analogous process (N-t = 3 h(-1)). Complexes 1-6 have been characterized by H-1 NMR and IR spectroscopy, microanalysis, and, in the case of 2 and 6, by single-crystal X-ray diffraction studies. 2 comprises a pseudotetrahedral thorium metal center bearing two aryloxide and two alkyl ligands. The O-Th-O angle between the aryloxide ligands (119.2(4)degrees) is significantly larger than the C-Th-C angle (101.4(6)degrees). Th-O and Th-C distances average 2.137(11) and 2.462(18)% respectively, while Th-C-Si angles are 125.9(8) and 122.8(8)degrees. The alkyl groups of 2 also display a reduced C-H coupling constant (J(CH) = 98 Hz), suggestive of cl-agostic interaction between the methylene group and the Th metal center. 6 exhibits a triangular arrangement of three thorium metal centers, each bearing two terminal aryloxide ligands. Two sides of the trimetallic core (Th-Th distances 3.781(1) and 3.818(1) Angstrom) are bridged by single mu(2)-hydride ligands, while the third side is bridged by two mu(2)-hydride ligands (Th-Th distance 3.588(1) Angstrom). Each face of the trimer is capped by a mu(3)-hydride ligand to produce a structurally unique M(3)(mu(3)-X)(2)(mu(2)-X)(4)X(6) geometry. Th-(mu(2)-H) and Th-(mu(3)-H) distances lie in the ranges 2.0(1)-2.3(1) and 2.3(1)-2.6(1) Angstrom, respectively, while Th-O distances range from 2.126(7) to 2.164(7) Angstrom.
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页码:949 / 957
页数:9
相关论文
共 91 条
[1]   ISOLATION OF A NEW SERIES OF 7-COORDINATE HYDRIDE COMPOUNDS OF TANTALUM(V) AND THEIR INVOLVEMENT IN THE CATALYTIC-HYDROGENATION OF ARENE RINGS [J].
ANKIANIEC, BC ;
FANWICK, PE ;
ROTHWELL, IP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1991, 113 (12) :4710-4712
[2]  
ARLIGUIE T, 1991, NEW J CHEM, V15, P569
[3]   SYNTHESIS AND STRUCTURE OF HIGH-VALENT ORGANOURANIUM COMPLEXES CONTAINING TERMINAL MONOOXO FUNCTIONAL-GROUPS [J].
ARNEY, DSJ ;
BURNS, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (21) :9840-9841
[4]   OXIDATION CHEMISTRY OF A URANIUM(III) ARYLOXIDE [J].
AVENS, LR ;
BARNHART, DM ;
BURNS, CJ ;
MCKEE, SD ;
SMITH, WH .
INORGANIC CHEMISTRY, 1994, 33 (19) :4245-4254
[5]   POLYNUCLEAR METAL HYDRIDO ALKOXIDES - REACTIONS OF W-4(H)(2)(O-I-PR)(14) AND W-2(H)(O-C-C5H9)(7)(HNME(2)) WITH CARBON-CARBON, CARBON-OXYGEN, AND CARBON-NITROGEN MULTIPLE BONDS [J].
BARRY, JT ;
CHACON, ST ;
CHISHOLM, MH ;
HUFFMAN, JC ;
STREIB, WE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (07) :1974-1990
[6]   EARLY ACTINIDE ALKOXIDE CHEMISTRY - SYNTHESIS, CHARACTERIZATION, AND MOLECULAR-STRUCTURES OF TH(IV) AND U(IV) ARYLOXIDE COMPLEXES [J].
BERG, JM ;
CLARK, DL ;
HUFFMAN, JC ;
MORRIS, DE ;
SATTELBERGER, AP ;
STREIB, WE ;
VANDERSLUYS, WG ;
WATKIN, JG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (27) :10811-10821
[7]   HALF-SANDWICH AND MIXED-RING URANIUM COMPLEXES [J].
BERTHET, JC ;
LEMARECHAL, JF ;
EPHRITIKHINE, M .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1994, 480 (1-2) :155-161
[8]   SYNTHESIS AND CRYSTAL AND MOLECULAR-STRUCTURES OF M(OAR')2(CH2-PY-6ME)2 (M = HF, TH - OAR' = 2,6-DI-TERT-BUTYLPHENOXIDE - CH2-PV-6ME = 2-(6-METHYLPYRIDYL)METHYL) - COMPLEXES CONTAINING 2 C,N-CHELATING PYRIDYL METHYL LIGANDS [J].
BESHOURI, SM ;
FANWICK, PE ;
ROTHWELL, IP ;
HUFFMAN, JC .
ORGANOMETALLICS, 1987, 6 (12) :2498-2502
[9]  
BOERSMA J, 1968, ORGANOZINC COORDINAT, P61
[10]   CATALYTIC ACTIVITY OF SUPPORTED F-ELEMENT ORGANOMETALLIC COMPLEXES [J].
BOWMAN, RG ;
NAKAMURA, R ;
FAGAN, PJ ;
BURWELL, RL ;
MARKS, TJ .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1981, (06) :257-258