Das Pooja, Halder Soumi, Ray Partha Pratim, Jana Narayan Ch, Sahu Priyanka, Isab Anvarhusein A, Dandela Rambabu, Natarajan Ramalingam, Dinda Joydev
Department of Chemistry, Utkal University, VaniVihar Bhubaneswar-751004 Odisha India
Department of Physics, Jadavpur University Kolkata-700032 WB India.
RSC Adv. 2025 Apr 23;15(17):13086-13094. doi: 10.1039/d5ra00684h. eCollection 2025 Apr 22.
Two supramolecular complex assemblies, [Ag(1)][PF]·4MeCN 2 and Ag(i)-Au(i) mixed metal complex [AgAu(1)][PF]·4MeCN 3, have been prepared from 3-(pyridylmethyl)imidazo[1,5-]pyridin-4-ylium hexafluorophosphate (1 HPF), which is the precursor of N-heterocyclic carbene (NHC). These complexes were subsequently analyzed using various spectroscopic techniques to confirm their structural and chemical properties. Transmetallation of Au(i) onto the Ag macrocycle results in the formation of an AgAu macrocyclic assembly. Au(i) selectively binds with the soft donor C, whereas Ag(i) binds with comparatively hard donor N (py = pyridine). The geometries of 2 and 3 were established by single-crystal X-ray diffraction studies. Both molecules form a 2D network through M-M and several non-covalent interactions. Electrical conductivity measurements revealed that Ag(i) complex 2 is better conductor than Au(i) complex 3. Optoelectronic studies revealed the utility of complexes 2 and 3 as photovoltaic devices. Furthermore, MS-junction potential measurements show that they are suitable for semiconductor devices, with complex 2 being more efficient than complex 3. Finally, in this study, we aimed to explore the scope of (i) the development of heterobimetallic supramolecular organometallic complexes (SOC), (ii) the charge transport behaviour of SOCs, and (iii) the modification of intrinsically conductive SOCs-based electronics.
两种超分子配合物组装体,[Ag(1)][PF]·4MeCN 2和Ag(i)-Au(i)混合金属配合物[AgAu(1)][PF]·4MeCN 3,由3-(吡啶甲基)咪唑并[1,5 - ]吡啶-4-鎓六氟磷酸盐(1 HPF)制备而成,1 HPF是N-杂环卡宾(NHC)的前体。随后使用各种光谱技术对这些配合物进行分析,以确认其结构和化学性质。Au(i)向Ag大环的金属转移导致形成AgAu大环组装体。Au(i)选择性地与软供体C结合,而Ag(i)与相对硬的供体N结合(py =吡啶)。通过单晶X射线衍射研究确定了2和3的几何结构。两个分子通过M-M和几种非共价相互作用形成二维网络。电导率测量表明,Ag(i)配合物2比Au(i)配合物3是更好的导体。光电研究揭示了配合物2和3作为光伏器件的用途。此外,MS结电势测量表明它们适用于半导体器件,配合物2比配合物3更有效。最后,在本研究中,我们旨在探索(i)异双金属超分子有机金属配合物(SOC)的开发范围,(ii)SOC的电荷传输行为,以及(iii)基于本征导电SOC的电子器件的改性。