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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/BF01165804</subfield>
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   <subfield code="a">Coordination chemistry of polyoxomolybdates: The versatile behavior of amidoximes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Soo-Gyun Roh, Anna Proust, Francis Robert, Pierre Gouzerh]</subfield>
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   <subfield code="a">The reactions of 2-thienylamidoxime and 2-thienylmethylamidoxime with [MoO2(acae)2] or x-(NBu4 [Mo8O26]. in alcohols or acetonitrile, yield a number of compounds with different nuclearities and various molybdenum cores, such as the compact {Mo4O10(OMe)2}2+ the cyclic {Mo4O12}, and the open {Mo11On211-1}2+ (n= 2 or 4) cores. Addition of NH2OH to the reaction mixtures results in the formation of nitrosyl complexes containing either the Mo(NO)3 or the Mo(NO) 2 2 units. The amidoxime component may be present either as RC(NH2)NHO. RC(NHi2), RC(NH)NHO or RC(NH)NO2: ligands, or as hydrogen-bonded RC(NH2)NOH molecules. The crystal structures of [MoO(acac)RIC'(NH2)NO] {RJC(NH)NO}](1), [Mo(NO)(acae)2 {RIC(NH2)NO}] (4), (NBu4)2[Mo4O10(OMe)2{RIC(NH) NO}2] (12a),(NBu4)2(H3O)[Mo5O13(OMe)4(NO)].2R1C(NH2)NOH(13b) and [R1C(NH2)2)]3[Mo5O13(OEt)4(NO)] (14) (R1=2-thienyl) are reported. The cryslallographic data for these compounds are as follows:1, mono-clinic. P21 a.a=24.547(4)A. b=8.188(4)A. c=9.607(3)A, ß=96.18(3)c, R=0.046. R10=0.050: 4. monoclinic, P21c.a=8.265(2)A, b=9.381(2)A,c=24.770(4)A, c = 24.7701(4) A, ß=93.99(2). R=0.039. R=0.042;12a, monoclinic, C2/c, a= 19.570(5)A. b=16.883(4)A, c = 19.82(l)A. ß= 114.36(5)°, R=0.064,R.=0.074;13b monoclinic;. P21 c.a=18.197(5)A, b=15.857(14) A, c = 23.075(17) A, β=93.20(3). R=O.050. Rw=0.057;14, trictinic PI, a = 9.871(3),b= 14.138(3).c= 14.781(8)A. α=92.67(2)c β=99.36(1)° γ=90.52(2)°. R = 0.044. Rw = 0.049. Particular attention is focused on the various coordination modes that the different ligand forms adopt: µ- κO, κ2N,O, κ2N',O, µ-κN: κ2O. and μ3- κN:κN:κ2O.</subfield>
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   <subfield code="a">Plenum Publishing Corporation, 1996</subfield>
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   <subfield code="a">Molybdenum</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">polyoxometalates</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">metal oxide analogs</subfield>
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   <subfield code="a">amidoximes</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">hydroxylaminc</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">nitrosyl complexes</subfield>
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   <subfield code="a">Roh</subfield>
   <subfield code="D">Soo-Gyun</subfield>
   <subfield code="u">KyungPook National University, Republic of Korea</subfield>
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   <subfield code="a">Proust</subfield>
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   <subfield code="u">Laboratoire de Chimic des Metaux de Transition, URA-CNRS, No. 419, Unversité Pierre et Marie Curie,, Case 42. 4 Place Jussieu, 75252, Paris Cedex 05, France</subfield>
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   <subfield code="a">Robert</subfield>
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   <subfield code="t">Journal of Cluster Science</subfield>
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   <subfield code="g">7/4(1996-12-01), 593-627</subfield>
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