Mechanism and selectivity of X− + CH3ONO2 (X = NCCH2, CH3C(O)CH2, and PhCH2) multichannel gas phase reactions

Abstract The mechanisms and ionic product distributions related to multiple channels of the X −  + CH 3 ONO 2 (X = NCCH 2 , CH 3 C(O)CH 2 , and PhCH 2 ) gas phase reactions were investigated at the B2PLYP/6–311 + G(3df,2p)//MP2/6–31 + G(d,p) level of theory. The reaction channels are bimolecular nucleophilic displacements at either the carbon (S N 2@C) or nitrogen (S N 2@N) centers and a proton abstraction followed by dissociation (E CO 2). For the ambident NCCH 2 − and CH 3 C(O)CH 2 − nucleophiles, two additional pathways for each reaction channel become available through attacks via the methylenic carbon or nitrogen/oxygen centers. The large number of reaction channels for these ambident nucleophiles precludes the unique determination of the E CO 2:S N 2@C:S N 2@N ratios and of the carbon or nitrogen/oxygen regioselectivity by mass spectrometry measurements. Thus, the relevance of performing detailed, accurate and reliable computational modeling, including determination of unimolecular rate constants with the RRKM theory. The nucleophilic displacements have the largest rate constants, which are: S N 2@C for the NCCH 2 − and CH 3 C(O)CH 2 − nucleophiles via methylenic carbon and oxygen centers attacks, respectively, and S N 2@N for the PhCH 2 − anion. The ionic products distributions 10:82:8, 2:97:1, and 0:18:82 related to the E CO 2:S N 2@C:S N 2@N reaction pathways were calculated for the reactions with NCCH 2 − , CH 3 C(O)CH 2 − , and PhCH 2 − , respectively, which are in excellent quantitative agreement with the experimental data. These agreements suggest that these reactions with large nucleophiles and/or (de)localized charge have a statistical behavior, unlike the same reaction with smaller and localized charge nucleophiles (F − and OH − ).