Campagnolo Filippo, Aneggi Eleonora, Baratta Walter, Munir Talha, Zuccaccia Daniele
Dipartimento di Scienze Agroalimentari, Ambientali e Animali, Sezione di Chimica, Università di Udine, Via Cotonificio 108, I-33100 Udine, Italy.
Molecules. 2024 Jun 26;29(13):3018. doi: 10.3390/molecules29133018.
The amount of free ions, ion pairs, and higher aggregate of the possible species present in a solution during the gold(I)-catalyzed alkoxylation of unsaturated hydrocarbon, i.e., ISIP (inner sphere ion pair) [(NHC)AuX] and OSIP (outer sphere ion pairs) [(NHC)Au(TME)X] [NHC 1,3-bis(2,6-di-isopropylphenyl)-imidazol-2-ylidene; TME = tetramethylethylene (2,3-bis methyl-butene); X = Cl, BF, OTf; and OTs BArF (ArF = 3,5-(CF)CH)], has been determined. The H and F DOSY NMR measurements conducted in catalytic conditions indicate that the dissociation degree (α) of the equilibrium ion pair/free ions {[(NHC)Au(TME)X] [(NHC)Au(TME)] + X} depends on the nature of the counterion (X) when chloroform is the catalytic solvent: while the compounds containing OTs and OTf as the counterion gave a low α (which means a high number of ion pairs) of 0.13 and 0.24, respectively, the compounds containing BF and BArF showed higher α values of 0.36 and 0.32, respectively. These results experimentally confirm previous deductions based on catalytic and theoretical data: the lower the α value, the greater the catalytic activity because the anion that can activate methanol during a nucleophilic attack, although the lower propensity to activate methanol of BF and BArF, as suggested by the DFT calculations, cannot be completely overlooked. As for the effect of the solvent, α increases as the dielectric constant increases, as expected, and in particular, green solvents with high dielectric constants show a very high α (0.90, 0.84, 0.80, and 0.70 for propylene carbonate, γ-valerolactone, acetone, and methanol, respectively), thus confirming that the moderately high activity of NHC-Au-OTf in these solvents is due to the specific effect of polar functionalities (O-H, C=O, O-R) in activating methanol. Finally, the DOSY measurements conducted in p-Cymene show the formation of quadrupole species: under these conditions, the anion can better exercise its 'template' and 'activating' roles, giving the highest TOF.
已测定在金(I)催化不饱和烃的烷氧基化反应过程中,溶液中可能存在的游离离子、离子对以及更高聚集体的量,即内球离子对(ISIP)[(NHC)AuX]和外球离子对(OSIP)[(NHC)Au(TME)X] [NHC = 1,3-双(2,6-二异丙基苯基)-咪唑-2-亚基;TME = 四甲基乙烯(2,3-双甲基-丁烯);X = Cl、BF、OTf;以及OTs BArF(ArF = 3,5-(CF)CH)]。在催化条件下进行的H和F DOSY NMR测量表明,当氯仿为催化溶剂时,平衡离子对/游离离子{[(NHC)Au(TME)X] [(NHC)Au(TME)] + X}的解离度(α)取决于抗衡离子(X)的性质:以OTs和OTf作为抗衡离子的化合物分别给出了较低的α值(这意味着离子对数量较多),分别为0.13和0.24,而含有BF和BArF的化合物显示出较高的α值,分别为0.36和0.32。这些结果通过实验证实了基于催化和理论数据的先前推断:α值越低,催化活性越高,因为在亲核攻击过程中能够活化甲醇的阴离子,尽管如DFT计算所表明的,BF和BArF活化甲醇的倾向较低,但也不能完全被忽视。至于溶剂的影响,正如预期的那样,α随着介电常数的增加而增加,特别是具有高介电常数的绿色溶剂显示出非常高的α值(碳酸丙烯酯、γ-戊内酯、丙酮和甲醇的α值分别为0.90、0.84、0.80和0.70),从而证实了NHC-Au-OTf在这些溶剂中的适度高活性是由于极性官能团(O-H、C=O、O-R)在活化甲醇方面的特定作用。最后,在对异丙基苯中进行的DOSY测量显示形成了四极物种:在这些条件下,阴离子能够更好地发挥其“模板”和“活化”作用,给出最高的TOF。