[Pd(IPr*)(3-Cl-pyridinyl)Cl2] : a novel and efficient PEPPSI precatalyst

The preparation of the novel, well-defined [Pd(IPr*)(3-Cl-pyridinyl)Cl-2] complex is described. The steric parameters of the ligand as well as its reactivity in the Buchwald-Hartwig amination were directly compared to other [Pd(NHC)(3-Cl-pyridinyl)Cl-2] and [Pd(IPr*)(LX)Cl)] precatalysts (LX = cinnamyl or acac). The title complex exhibits similar catalytic activity to [Pd(NHC)(3-Cl-pyridinyl)Cl-2] congeners (NHC = IPr and SIPr) at room temperature. However, it also showed improved reactivity at low catalyst loading and high temperature (as low as 0.025 mol %). On the other hand, it proved to be as efficient as the previously reported [Pd(IPr*)(cinnamyl)Cl] complex, pointing to the most likely existence of a similar catalytically active species

A continuum modeling approach to the housing allocation and transportation emissions problem

Paper Session: 675 - paper no. 11-029

Carbon-based two electron sigma-donor ligands beyond classical N-heterocyclic carbenes

Ghadwal R. Carbon-based two electron sigma-donor ligands beyond classical N-heterocyclic carbenes. DALTON TRANSACTIONS. 2016;45(41):16081-16095.N-Heterocyclic carbenes (NHCs) are an important class of compounds that are indeed regarded as most versatile carbon-donor ligands in transition metal and organometallic catalysis. In addition, NHCs are also capable of stabilizing a variety of highly reactive main group compounds with intriguing properties. The enormous success of NHCs prompted the investigation of other carbon-based neutral ligands with additional structural and electronic features. Reactivity studies of NHCs and their complexes unveiled routes to new carbon donor ligands. Such NHC-derived ligands can be grouped into three categories: (i) N-heterocyclic olefins (the donor site is extended by an intervening carbon atom), (ii) ditopic carbanionic-NHCs (an additional coordination site is generated by the deprotonation of an NHC), and (iii) abnormal-NHCs (the carbene center of an NHC is moved to different positions). This article summarizes the recent advances in NHC chemistry of compounds featuring the aforementioned ligands, which are exclusively derived by the functionalization of NHCs, 1,3-bis(2,6-diisopropylphenyl) imidazol-2-ylidene (IPr) in particular