What Is the Main Feature Distinguishing the Through-Space Interactions in Cyclophanes from Their Aliphatic Analogues?
暂无分享,去创建一个
[1] T. Dziembowska,et al. Substituent effect on inter-ring interaction in paracyclophanes , 2019, Molecular Diversity.
[2] R. Herges,et al. Cyclic tris-[5]helicenes with single and triple twisted Möbius topologies and Möbius aromaticity , 2018, Chemical science.
[3] J. Lahann,et al. Planar chiral [2.2]paracyclophanes: from synthetic curiosity to applications in asymmetric synthesis and materials. , 2018, Chemical Society reviews.
[4] Caio L. Firme,et al. Revisiting electronic nature and geometric parameters of cyclophanes and their relation with stability – DFT, QTAIM and NCI study , 2018, Computational and Theoretical Chemistry.
[5] A. Hesselmann,et al. On the Stability of Cyclophane Derivates Using a Molecular Fragmentation Method. , 2016, Chemphyschem : a European journal of chemical physics and physical chemistry.
[6] T. Dziembowska,et al. Aromaticity and Through-Space Interaction between Aromatic Rings in [2.2]Paracyclophanes. , 2016, The journal of physical chemistry. A.
[7] J. Hernández‐Trujillo,et al. Electron density analysis of bent aromatic molecules: intramolecular interactions in small paracyclophanes , 2016, Theoretical Chemistry Accounts.
[8] Vladimír Lukes,et al. Theoretical study of substituent effects on the geometry and strain enthalpy in [2,2]paracyclophanes , 2016 .
[9] Paul Geerlings,et al. Understanding the fundamental role of π/π, σ/σ, and σ/π dispersion interactions in shaping carbon-based materials. , 2014, Chemistry.
[10] L. Vaccaro,et al. Organic Small Molecules for Photonics and Electronics from the [2.2]Paracyclophane Scaffold , 2012 .
[11] S. Grimme,et al. Accurate Computation of Structures and Strain Energies of Cyclophanes with Modern DFT Methods , 2012 .
[12] M. Nishio,et al. The CH/π hydrogen bond in chemistry. Conformation, supramolecules, optical resolution and interactions involving carbohydrates. , 2011, Physical chemistry chemical physics : PCCP.
[13] S. Bachrach. DFT study of [2.2]-, [3.3]-, and [4.4]paracyclophanes: strain energy, conformations, and rotational barriers. , 2011, The journal of physical chemistry. A.
[14] D. Ramaiah,et al. Functional cyclophanes: promising hosts for optical biomolecular recognition. , 2010, Chemical Society reviews.
[15] S. Grimme,et al. A consistent and accurate ab initio parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu. , 2010, The Journal of chemical physics.
[16] Julia Contreras-García,et al. Revealing noncovalent interactions. , 2010, Journal of the American Chemical Society.
[17] Heidi M. Muchall,et al. New insights into the use of (TD-)DFT for geometries and electronic structures of constrained pi-stacked systems: [n.n]paracyclophanes. , 2008, The journal of physical chemistry. A.
[18] H. Hopf. [2.2]Paracyclophanes in polymer chemistry and materials science. , 2008, Angewandte Chemie.
[19] S. Galembeck,et al. A computational study of tetrafluoro-[2.2]cyclophanes. , 2008, The journal of physical chemistry. A.
[20] R. Parthasarathi,et al. Chemical reactivity patterns of [n]paracyclophanes , 2007 .
[21] S. Galembeck,et al. Computational study about through-bond and through-space interactions in [2.2]cyclophanes. , 2007, The journal of physical chemistry. A.
[22] M. Ostrowski,et al. Planarization of the cyclohexane ring by its incorporation into a cyclophane cage : Hexahydrosuperphane , 2006 .
[23] D. Quiñonero,et al. Ab initio study of [n.n]paracyclophane (n = 2, 3) complexes with cations: unprecedented through-space substituent effects. , 2006, The journal of physical chemistry. A.
[24] V. I. Rozenberg,et al. Novel multichiral diols and diamines by highly stereoselective pinacol coupling of planar chiral [2.2]paracyclophane derivatives. , 2005, Chemistry.
[25] K. Laali,et al. A computational study of [2.2]cyclophanes. , 2005, The Journal of organic chemistry.
[26] T. Friščić,et al. Cyclophanes and Ladderanes: Molecular Targets for Supramolecular Chemists , 2005 .
[27] S. Grimme. On the importance of electron correlation effects for the pi-pi interactions in cyclophanes. , 2004, Chemistry.
[28] M. Palusiak,et al. Are the O-H...H-C intramolecular systems of 2-cyclopropyl ethenol and its derivatives classified as dihydrogen bonds? Ab initio and DFT study , 2004 .
[29] K. Lyssenko,et al. The transannular interaction in [2.2]paracyclophane: repulsive or attractive? , 2003, Chemphyschem : a European journal of chemical physics and physical chemistry.
[30] E. Molins,et al. About the evaluation of the local kinetic, potential and total energy densities in closed-shell interactions , 2001 .
[31] Rainer Herges and,et al. Delocalization of Electrons in Molecules , 2001 .
[32] Paul L. A. Popelier,et al. Characterization of a Dihydrogen Bond on the Basis of the Electron Density , 1998 .
[33] S. Lin,et al. Preparation of 3e,4,5,6e,7,8-hexahydro[2.2]paracyclophane , 1997 .
[34] R. Bader,et al. Identifying and Analyzing Intermolecular Bonding Interactions in van der Waals Molecules , 1996 .
[35] D. Schomburg,et al. Cyclophanes, XXXIX. The Structure of the Dicyanoacetylene Adducts of [2.2]Paracyclophane , 1995 .
[36] K. Rissanen,et al. The First Clamped and Strongly Deformed Adamantane , 1990 .
[37] M. Ziegler,et al. Structure of 4,7,12,15-tetrahydro[2.2]paracyclophane; a molecule with interdeck through-space interaction , 1986 .
[38] Y. Chujo,et al. Optically active cyclic compounds based on planar chiral [2.2]paracyclophane: extension of the conjugated systems and chiroptical properties , 2015 .
[39] R. Gleiter,et al. Modern cyclophane chemistry , 2004 .
[40] F. Bickelhaupt,et al. Structures and strain energies of small [n]metacyclophanes , 2000 .
[41] R. Bader. Atoms in molecules : a quantum theory , 1990 .