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Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
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Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
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Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron

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Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron
Journal Article

Synthesis and X-ray structures of amidinate, oxoamidate, and thioamidate complexes of boron

2000
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Overview
The reactions of PhBCl 2 with Li[CE(N t Bu)( n Bu)] or Li[CS(N t Bu)(NH t Bu)] (1:1 molar ratio) in toluene at 23°C produced the heterocycles Ph(Cl)B( -N t Bu)( -E)C( n Bu) ( 1a , E = N t Bu; 1b , E = O; 1c , E = S) or Ph(Cl)B( -N t Bu)( -S)C(NH t Bu) ( 2 ), which were characterized by 1 H, 11 B and 13 C NMR and by mass spectra. X-ray structural determinations revealed that 1a , 1c and 2 contain four-membered rings. In 2 the thioamidate ligand adopts an N,S bonding mode. Crystal data: 1a , monoclinic, space group P2 1 , a = 8.816(3), b = 11.311(2), c = 10.168(3) Å, = 98.86(3)°, V = 1001.7(5) Å 3 , Z = 2, R = 0.042, and R w = 0.020; 1c , monoclinic, space group P2 1 /n, a = 7.617(2), b = 11.200(1), c = 19.568(2), = 90.74(2)°, V = 1669.1(5) Å 3 , Z = 4, R = 0.046, and R w = 0.059; 2 , monoclinic, space group P2 1 /a, a = 11.357(2), b = 12.289(2), c = 12.620(3) Å, = 95.43(2)°, V = 1753.4(5) Å 3 , Z = 4, R = 0.043, and R w = 0.027. Key words: boron, amidinate, oxoamidate, thioamidate, X-ray structures.
Publisher
NRC Research Press,Canadian Science Publishing NRC Research Press