biostudies-literatureUnknown9(22)Zhang SLThis study theoretically determines the effect of substituents on the stability of the triple-bonded L-E₁₃[triple bond, length as m-dash]N-L (E₁₃ = B, Al, Ga, In, and Tl) compound using the M06-2X/Def2-TZVP, B3PW91/Def2-TZVP, and B3LYP/LANL2DZ+dp levels of theory. Five small substituents (F, OH, H, CH₃ and SiH₃) and four large substituents (SiMe(Si<i>t</i>Bu₃)₂, Si<i>i</i>PrDis₂, Tbt ([double bond, length as m-dash] C₆H₂-2,4,6-{CH(SiMe₃)₂}₃) and Ar* ([double bond, length as m-dash]C₆H₃-2,6-(C₆H₂-2,4,6-i-Pr₃)₂)) are used. Unlike other triply bonded L-E₁₃[triple bond, length as m-dash]P-L, L-E₁₃[triple bond, length as m-dash]As-L, L-E₁₃[triple bond, length as m-dash]Sb-L and L-E₁₃[triple bond, length as m-dash]Bi-L molecules that have been studied, the theoretical findings for this study show that both small (but electropositive) ligands and bulky substituents can effectively stabilize the central E₁₃[triple bond, length as m-dash]N triple bond. Nevertheless, these theoretical observations using the natural bond orbital and the natural resonance theory show that the central E₁₃[triple bond, length as m-dash]N triple bond in these acetylene analogues must be weak, since these E₁₃[triple bond, length as m-dash]N compounds with various ligands do not have a real triple bond.RSC advances12195-12208https://www.ebi.ac.uk/biostudies/studies/S-EPMC9063501biostudies-literatureA computational study to determine whether substituents make E₁₃[triple bond, length as m-dash]nitrogen (E₁₃ = B, Al, Ga, In, and Tl) triple bonds synthetically accessible.PMC9063501Su MDZhang SLYang MCfalseA computational study to determine whether substituents make E₁₃[triple bond, length as m-dash]nitrogen (E₁₃ = B, Al, Ga, In, and Tl) triple bonds synthetically accessible.This study theoretically determines the effect of substituents on the stability of the triple-bonded L-E₁₃[triple bond, length as m-dash]N-L (E₁₃ = B, Al, Ga, In, and Tl) compound using the M06-2X/Def2-TZVP, B3PW91/Def2-TZVP, and B3LYP/LANL2DZ+dp levels of theory. Five small substituents (F, OH, H, CH₃ and SiH₃) and four large substituents (SiMe(Si<i>t</i>Bu₃)₂, Si<i>i</i>PrDis₂, Tbt ([double bond, length as m-dash] C₆H₂-2,4,6-{CH(SiMe₃)₂}₃) and Ar* ([double bond, length as m-dash]C₆H₃-2,6-(C₆H₂-2,4,6-i-Pr₃)₂)) are used. Unlike other triply bonded L-E₁₃[triple bond, length as m-dash]P-L, L-E₁₃[triple bond, length as m-dash]As-L, L-E₁₃[triple bond, length as m-dash]Sb-L and L-E₁₃[triple bond, length as m-dash]Bi-L molecules that have been studied, the theoretical findings for this study show that both small (but electropositive) ligands and bulky substituents can effectively stabilize the central E₁₃[triple bond, length as m-dash]N triple bond. Nevertheless, these theoretical observations using the natural bond orbital and the natural resonance theory show that the central E₁₃[triple bond, length as m-dash]N triple bond in these acetylene analogues must be weak, since these E₁₃[triple bond, length as m-dash]N compounds with various ligands do not have a real triple bond.2019-01-01T00:00:00Z2019 Apr2025-04-04T20:50:57.902Z2025-04-04T20:50:57.902ZS-EPMC90635013551584310.1039/c9ra00318e