86 research outputs found
SYNTHESIS OF THE MACROCYCLIC THIOCROWN ETHERS 1,4,7,10,13,16,19-HEPTATHIAHENEICOSANE (21-S-7) AND 1,4,7,10,13,16,19,22-OCTATHIATETRAEICOSANE (24-S-8)
The synthesis and characterization of the two macrocyclic sulfides, 1,4,7,10,13,16,19-heptathiaheneicosane (21-S-7) and 1,4,7,10,13,16,19,22-octathiatetraeicosane (24-S-8), are described starting from different combinations of dithiols and dichlorides of differing chain lengths. Cs2CO3 is used for the cyclizations.</p
SYNTHESIS OF THE MACROCYCLIC THIOCROWN ETHERS 1,4,7,10,13,16,19-HEPTATHIAHENEICOSANE (21-S-7) AND 1,4,7,10,13,16,19,22-OCTATHIATETRAEICOSANE (24-S-8)
SYNTHESIS OF THE MACROCYCLIC THIOCROWN ETHERS 1,4,7,10,13,16,19-HEPTATHIAHENEICOSANE (21-S-7) AND 1,4,7,10,13,16,19,22-OCTATHIATETRAEICOSANE (24-S-8)
The synthesis and characterization of the two macrocyclic sulfides, 1,4,7,10,13,16,19-heptathiaheneicosane (21-S-7) and 1,4,7,10,13,16,19,22-octathiatetraeicosane (24-S-8), are described starting from different combinations of dithiols and dichlorides of differing chain lengths. Cs2CO3 is used for the cyclizations
SYNTHESIS OF THE MACROCYCLIC THIOCROWN ETHERS 1,4,7,10,13,16,19-HEPTATHIAHENEICOSANE (21-S-7) AND 1,4,7,10,13,16,19,22-OCTATHIATETRAEICOSANE (24-S-8)
SYNTHESIS OF THE MACROCYCLIC THIOCROWN ETHERS 1,4,7,10,13,16,19-HEPTATHIAHENEICOSANE (21-S-7) AND 1,4,7,10,13,16,19,22-OCTATHIATETRAEICOSANE (24-S-8)
SYNTHESIS AND X-RAY STRUCTURE OF THE 1ST DINUCLEAR HOMOLEPTIC CHROMIUM(II) AMIDE, ([I-PR)2N]CR[MU-(I-PR)2N])2
SYNTHESIS AND X-RAY STRUCTURE OF THE 1ST DINUCLEAR HOMOLEPTIC CHROMIUM(II) AMIDE, ([I-PR)2N]CR[MU-(I-PR)2N])2
PREPARATION AND CHARACTERIZATION OF [V3CL5(N,N,N',N'-TETRAMETHYLETHYLENEDIAMINE)3][V(NPH2)4] - A V(II)-V(III) MIXED-VALENCE COMPLEX
PREPARATION AND CHARACTERIZATION OF [V3CL5(N,N,N',N'-TETRAMETHYLETHYLENEDIAMINE)3][V(NPH2)4] - A V(II)-V(III) MIXED-VALENCE COMPLEX
DIVALENT VANADIUM AND DINITROGEN FIXATION - THE PREPARATION AND X-RAY STRUCTURE OF (MU-N2)([(O-ME2NCH2)C6H4]2V(PY))2(THF)2
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