conformational behaviors of trans-2,3-bis(methylthio)-1,4-dioxane, -dithiane and –diselenane. a hybrid-dft study and nbo interpretations

نویسندگان

davood nori-shargh

department of chemistry, science faculty, arak branch, islamic azad university, arak, iran zahra mahmoodi

department of chemistry, science faculty, arak branch, islamic azad university, arak, iran nasrin masnabadi

department of chemistry, roudehen branch, islamic azad university, roudehen, iran hooriye yahyaei

department of chemistry, islamic azad university, zanjan branch, p.o.box 49195.467,zanjan, iran seiedeh negar mousavi

چکیده

the conformational behaviors of 2,3-bis(methylthio)-1,4-dioxane (1), 2,3-bis(methylthio)-1,4-dithiane (2) and 2,3-bis(methylthio)-1,4-diselenane (3) have been analyzed by means ofhybrid-density functional theory (b3lyp/def2-tzvpp) based method and nbo interpretation.b3lyp/def2-tzvpp results showed that the axial conformations of compounds 1-3 are morestable than their equatorial conformations. the calculated gibbs free energy difference (geq–gax)values (i.e. δgeq-ax) at 298.15 k and 1 atm between the axial and equatorial conformationsdecrease from compound 1 to compound 3. the nbo analysis of donor-acceptor (lp→σ*)interactions showed that the anomeric effects (ae) decrease from compound 1 to compound 3.on the other hand, the calculated dipole moment values between the axial and equatorialconformations [δ(μeq - μax)] increase from compound 1 to compound 2 but decrease fromcompound 2 to compound 3. however, the variations of the calculated δ(μeq - μax) values are notin the same trend observed for the corresponding ae and δg values. therefore, the calculatedδμ values do not seem to be sufficient to account for the axial preferences in compounds 1-3.these findings led to the proposal that the ae, due to donor→acceptor hyperconjugation effect,is more significant for the explanation of the axial conformational preferences of compounds 1-3than the electrostatic effect.

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Conformational behaviors of trans-2,3-bis(methylthio)-1,4-dioxane, -dithiane and –diselenane. A hybrid-DFT study and NBO interpretations

The conformational behaviors of 2,3-bis(methylthio)-1,4-dioxane (1), 2,3-bis(methylthio)-1,4-dithiane (2) and 2,3-bis(methylthio)-1,4-diselenane (3) have been analyzed by means ofhybrid-density functional theory (B3LYP/Def2-TZVPP) based method and NBO interpretation.B3LYP/Def2-TZVPP results showed that the axial conformations of compounds 1-3 are morestable than their equatorial conformations. ...

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عنوان ژورنال:
journal of the iranian chemical research

جلد ۳، شماره ۳، صفحات ۱۷۹-۱۸۹

کلمات کلیدی
[ ' a n o m e r i c e f f e c t s ' , ' s t e r e o e l e c t r o n i c i n t e r a c t i o n s ' , ' m o l e c u l a r m o d e l i n g ' , ' a b i n i t i o ' , ' n b o ' , 2 , 3 , ' b i s ( m e t h y l t h i o ) ' , 1 , 4 , ' d i t h i a n e ' ]

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