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1.
Fictitious hydrogen atoms H*A of variable nuclear charge 0.5 ≤ ZA ≤ 2 (and thus of variable electronegativity) are used to study the intrinsic dependency of chemical bonding on electronegativity. Dissociation energy and equilibrium distance are reported for symmetrical 1‐, 2‐ and 3‐electron H*AH*A systems and 2‐electron dissymmetrical H*A‐H ones. Dealing with symmetrical systems, the strongest two‐electron bonds are found for ZA ≈ 1.2. Oneelectron and three‐electron strongest bonds occur respectively with low (ca. 0.7) and high (ca. 1.7) ZA values and can become stronger than the corresponding 2‐electron system. Comparison with data on real systems leads to conclude that electronegativity is a prevailing atomic property in the control of the dissociation energy of symmetrical 1‐, 2‐ and 3‐electron bonds. A simplified mathematical model at Hartree‐Fock or Heitler‐London level with a minimal basis set reproduces these trends semi‐quantitatively and provides the overall shape of the dissociation curves. Finally some points are qualitatively discussed from MO analysis, which emphasize the dependence of the bonding/antibonding properties on the nucleus charge ZA and their occupancy number. © 2011 Wiley Periodicals, Inc. Int J Quantum Chem, 2011 相似文献
2.
Zhengbiao Zhang Wei Zhang Xiulin Zhu Zhenping Cheng Jian Zhu 《Journal of polymer science. Part A, Polymer chemistry》2007,45(24):5722-5730
A metal complex, cobalt(II) 2‐ethylhexanoate (CEH), was added to the system of thermal‐initiated reversible addition‐fragmentation chain transfer (RAFT) polymerization of methyl methacrylate (MMA) with 2‐cyanoprop‐2‐yl 1‐dithionaphthalate (CPDN) as the RAFT agent at 115 °C. The polymerization rate was remarkably enhanced in the presence of CEH in comparison with that in the absence of CEH, and the increase of the CPDN concentration also accelerated the rate of polymerization. The polymerization in the concurrence of CPDN and CEH demonstrated the characters of “living”/controlled free radical polymerization: the number‐average molecular weights (Mn) increasing linearly with monomer conversion, narrow molecular weight distributions (Mw/Mn) and obtained PMMA end‐capped with the CPDN moieties. Meanwhile, CEH can also accelerate the rate of RAFT polymerization of MMA using the PMMA as macro‐RAFT agent instead of CPDN. Similar polymerization profiles were obtained when copper (I) bromide (CuBr)/N,N,N′,N′′,N′′‐pentamethyldiethylenetriamine was used instead of CEH. Extensive experiments in the presence of butyl methacrylate, bis(cyclopentadienyl) cobalt(II) and cumyl dithionaphthalenoate were also conducted; similar results as those of MMA/CPDN/CEH system were obtained. A transition of the polymerization mechanism, from RAFT process without CEH addition to atom transfer radical polymerization in the presence of CEH, was possibly responsible for polymerization profiles. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5722–5730, 2007 相似文献
3.
Paola Gramatica Simona Kovarich Partha Pratim Roy 《Journal of computational chemistry》2013,34(20):1796-1796
We appreciate the interest of Dr. Rayne on our article and we completely agree that the dataset of (benzo‐)triazoles, which were screened by the hydroxyl radical reaction quantitative structure‐activity relationship (QSAR) model, 1 was not only composed of benzo‐triazoles but also included some simpler triazoles (without the condensed benzene ring), such as the chemicals listed by Dr. Rayne, as well as some related heterocycles (also few not aromatic). We want to clarify that in this article 1 (as well as in other articles 2 - 5 in which the same dataset was screened), for conciseness, the abbreviations (B)TAZs and BTAZs were used as general (and certainly too simplified) notations meaning an extended dataset of benzo‐triazoles, triazoles, and related compounds. © 2013 Wiley Periodicals, Inc. 相似文献