Morris, D. G. Recent advances in the chemistry of ylides. Surv. Progress Chem. 10, 189–257 (1983).Article
Google Scholar
Bachrach, S. M. Molecular structure of phosphonium ylides. J. Org. Chem. 57, 4367–4373 (1992).Article
Google Scholar
Chauvin, R. & Canac, Y. Transition Metal Complexes of Neutral Eta1-Carbon Ligands. Vol. 30 (Springer Science & Business Media, 2010).Johnson, A. with special contributions by WC Kaska, KAO Statzewski and DA Dixon, Ylides and Imines of Phosphorus. Wiley, New York, chapters 6, 153-220 (1993).Coyne, E., Gilheany, D., Katritzky, A., Meth-Cohn, O. & Rees, C. Comprehensive Organic Functional Group Transformation (Pergamon Press, Elsevier, Oxford, 1995).
Google Scholar
Clark, J. S., Dossetter, A. G. & Whittingham, W. G. Stereoselective synthesis of the bicyclic core structure of the highly oxidised sesquiterpene neoliacinic acid. Tetrahedron Lett. 37, 5605–5608 (1996).Article
Google Scholar
Krohnke, F. & Timmler, H. Ber. 69, 674 (1930).Navarro, R. & Urriolabeitia, E. P. α-Stabilized phosphoylides as versatile multifunctional ligands. J. Chem. Soc. Dalton Trans. 23, 4111–4122 (1999).Article
Google Scholar
Spannenberg, A., Baumann, W. & Rosenthal, U. Palladium (II) complexes of α-stabilized phosphorus ylides. Organometallics 19, 3991–3993 (2000).Article
Google Scholar
Ebrahim, M. M., Stoeckli-Evans, H. & Panchanatheswaran, K. Reactivity of mercury (II) halides with the unsymmetrical phosphorus ylide Ph2PCH2CH2PPh2C(H)C(O)Ph: Crystal structure of {HgI2 [PPh2CH2CH2PPh2C(H)C(O)Ph]}n. Polyhedron 26, 3491–3495 (2007).Article
Google Scholar
Sabounchei, S. J. et al. Synthesis and characterization of novel simultaneous C and O-coordinated and nitrate-bridged complexes of silver (I) with carbonyl-stabilized sulfonium ylides and their antibacterial activities. Dalton Trans. 42, 2520–2529 (2013).Article
PubMed
Google Scholar
Sabounchei, S. J. et al. Pd(II) and Pt(II) complexes of α-keto stabilized sulfur ylide: Synthesis, structural, theoretical and catalytic activity studies. J. Mol. Struct. 1135, 174–185 (2017).Article
ADS
Google Scholar
Bravo, P., Fronza, G., Ticozzi, C. & Gaudiano, G. Palladium (II) complexes with sulphonium ylides. J. Organomet. Chem. 74, 143–154 (1974).Article
Google Scholar
Deuerlein, S., Leusser, D., Flierler, U., Ott, H. & Stalke, D. [(thf)Li2{H2CS(Nt-Bu)2}]2: Synthesis, polymorphism, and experimental charge density to elucidate the bonding properties of a lithium sulfur ylide. Organometallics 27, 2306–2315 (2008).Article
Google Scholar
Sabounchei, S. J. et al. Reactivity of mercury(II) halides with the α-keto stabilized sulfonium ylides: Crystal structures of two new polymer and binuclear complexes and in vitro antibacterial study. Polyhedron 53, 1–7 (2013).Article
Google Scholar
Pearson, R. G. Hard and soft acids and bases. J. Am. Chem. soc. 85, 3533–3539 (1963).Article
Google Scholar
Fronza, G., Bravo, P. & Ticozzi, C. Carbon-13 nuclear magnetic resonance studies of some phosphonium, arsonium, sulfonium and pyridinium keto-stabilized salts, and ylides and of their palladium(II) complexes. J. Organomet. Chem. 157, 299–310 (1978).Article
Google Scholar
Dega-Szafran, Z. et al. Experimental and quantum chemical evidences for C-H⋯ N hydrogen bonds involving quaternary pyridinium salts and pyridinium ylides. J. Mol. Struct. 555, 31–42 (2000).Article
ADS
Google Scholar
Sabounchei, S. et al. A new Pd(II) complex of a sulfur ylide; Synthesis, X-ray characterization, theoretical study and catalytic activity toward the Suzuki-Miyaura reaction. Polyhedron 117, 273–282 (2016).Article
Google Scholar
Sabounchei, S. J., Gharacheh, M. A. & Hosseinzadeh, M. Synthesis and multinuclear NMR study of novel complexes of Zn(II) and Hg(II) containing phosphorus ylides. Asian J. Chem. 22, 1949–1956 (2010).
Google Scholar
Sabounchei, S. J. et al. Structural, theoretical and multinuclear NMR study of mercury (II) and silver (I) complexes with two new ambidentate phosphorus ylides. Polyhedron 38, 131–136 (2012).Article
Google Scholar
van der Bondi, A. Waals volumes and radii. J. Phys. Chem. 68, 441–451 (1964).Article
Google Scholar
Morokuma, K. Molecular orbital studies of hydrogen bonds. III. C=O··· H-O hydrogen bond in H2CO···H2O and H2CO···2H2O. J. Phys. Chem. 55, 1236–1244 (1971).Article
Google Scholar
Ziegler, T., Rauk, A. & Baerends, A. J. Theor. Chim. Acta. (1977).Article
Google Scholar
Bayat, M. & Soltani, E. Stabilization of group 14 tetrylene compounds by N-heterocyclic carbene: A theoretical study. Polyhedron 123, 39–46 (2017).Article
Google Scholar
Bayat, M. & Hatami, M. Nature of the metal–ligand bond in some [(CO)4M←BIIM (R)]{M= Cr, Mo, W; R= H, F, Cl, Br} complexes: A theoretical study. Polyhedron 110, 46–54 (2016).Article
Google Scholar
Sabounchei, S. et al. A new Pd (II) complex of a sulfur ylide; Synthesis, X-ray characterization, theoretical study and catalytic activity toward the Suzuki-Miyaura reaction. Polyhedron 117, 273–282 (2016).Article
Google Scholar
Frenking, G. et al. Towards a rigorously defined quantum chemical analysis of the chemical bond in donor–acceptor complexes. Coord. Chem. Rev. 238, 55–82 (2003).Article
Google Scholar
Lein, M. & Frenking, G. in Theory and Applications of Computational Chemistry 291–372 (Elsevier, 2005).Bayat, M. & Kamali, S. Computational landscape of the formation and nature of bond in the “1+1” versus “1+2” nano-sized complexes of some adducts of N-heterocyclic carbenes (NHC) with heavy elements of group II (Ca, Sr, Ba) metallocenes. J. Mol. Liq. 222, 953–962 (2016).Article
Google Scholar
Aidi, M. et al. Coordination chemistry of some new Mn(II), Cd(II) and Zn(II) macrocyclic Schiff base complexes containing a homopiperazine head unit. Spectral, X-ray crystal structural, theoretical studies and anticancer activity. Inorganica Chim. Acta 490, 294–302 (2019).Article
Google Scholar
Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. & Puschmann, H. OLEX2: A complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 42, 339–341 (2009).Article
ADS
Google Scholar
Sheldrick, G. M. Crystal structure refinement with SHELXL. Acta Crystallogr. Sect. A: Found. Adv 71, 3–8 (2015).Article
ADS
Google Scholar
Sheldrick, G. M. SHELXT–Integrated space-group and crystal-structure determination. Acta Crystallogr. A Found. Adv. 71, 3–8 (2015).Article
ADS
PubMed
PubMed Central
Google Scholar
Zhao, Y. & Truhlar, D. G. A new local density functional for main-group thermochemistry, transition metal bonding, thermochemical kinetics, and noncovalent interactions. J. Chem. Phys. https://doi.org/10.1063/1.2370993 (2006).Article
PubMed
Google Scholar
Wang, Y., Jin, X., Yu, H. S., Truhlar, D. G. & He, X. Revised M06-L functional for improved accuracy on chemical reaction barrier heights, noncovalent interactions, and solid-state physics. Proc. Natl. Acad. Sci. 114, 8487–8492 (2017).Article
ADS
PubMed
PubMed Central
Google Scholar
Zhao, Y. & Truhlar, D. G. The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: Two new functionals and systematic testing of four M06-class functionals and 12 other functionals. Theor. Chem. Acc. 120, 215–241 (2008).Article
Google Scholar
Wang, Y., Verma, P., Jin, X., Truhlar, D. G. & He, X. Revised M06 density functional for main-group and transition-metal chemistry. Proc. Natl. Acad. Sci. 115, 10257–10262 (2018).Article
ADS
PubMed
PubMed Central
Google Scholar
Austin, A. et al. A density functional with spherical atom dispersion terms. J. Chem. Theory Comput. 8, 4989–5007 (2012).Article
PubMed
Google Scholar
Autschbach, J., Ziegler, T., van Gisbergen, S. J. & Baerends, E. J. Chiroptical properties from time-dependent density functional theory. I. Circular dichroism spectra of organic molecules. J. Chem. Phys. 116, 6930–6940 (2002).Article
ADS
Google Scholar
Barone, V. et al. Implementation and validation of a multi-purpose virtual spectrometer for large systems in complex environments. Phys. Chem. Chem. Phys. 14, 12404–12422 (2012).Article
PubMed
Google Scholar
Frisch, M. et al. Gaussian 09, Revision a. 02, 200, gaussian. Inc., Wallingford, CT 271 (2009).Weinhold, F., Landis, C. & Glendening, E. What is NBO analysis and how is it useful?. Int. Rev. Phys. Chem. 35, 399–440 (2016).Article
Google Scholar
Baerends, E.J. et al. ADF2017, SCM, Theoretical Chemistry, Vrije Universiteit, Amsterdam, The Netherlands. ADF. Available online: http://www.scm.com (accessed on 20 April 2020) (2014).Balouiri, M., Sadiki, M. & Ibnsouda, S. K. Methods for in vitro evaluating antimicrobial activity: A review. J. Pharma. Anal. 6, 71–79 (2016).Article
Google Scholar