УДК 547.62:544.183.26
V. A. Babkin, V. V. Trifonov, A. P. Knyazev, V. Yu. Dmitriev,
D. S. Andreev, A. V. Ignatov, E. S.Titova, O. V. Stoyanov, G. E. Zaikov
QUANTUM-CHEMICAL CALCULATION OF THE MODELS OF DEKACENE AND EICOCENE
BY METHOD MNDO WITHIN THE FRAMEWORK OF MOLECULAR GRAPHENE MODEL
Keywords: quantum chemical calculation, method MNDO, dekacene, eicocene, acid strength.
Quantum-chemical calculation of molecules dekacene and eicocene was done by method MNDO. Optimized by all parameters geometric and electronic structures of these compounds was received. Each of these molecular models has a universal factor of acidity equal to 33 (pKa=33). They all pertain to class of very weak Н-acids (рКа>14).
Ключевые слова: квантово-химический расчет, метод MNDO, декацен, эйкоцен, кислотная сила.
Впервые выполнен квантово-химический расчет молекул декацена и эйкоцена методом ММБО с оптимизацией геометрии по всем параметрам стандартным градиентным методом Получено оптимизированное геометрическое и электронное строение этих соединений. Теоретически оценена их кислотная сила (рКа=33). Установлено, что эти близкие к графену соединения относятся к классу очень слабых кислот (рКа>14).
Aims and backgrounds
The aim of this work is a study of electronic structure of molecules dekacene, eicocene and theoretical estimation its acid power by quantum-chemical method MNDO within the framework of molecular graphene model, which was dicovered by Novoselov and Game in 2004 [1].
Methodical part
The calculation was done with optimization of all parameters by standard gradient method built-in in PC GAMES S [2]. The calculation was executed in approach the insulated molecule in gas phase. Program MacMolPlt was used for visual presentation of the model of the molecule. [3].
The results of the calculation and discussion
Geometric and electronic structures, general and electronic energies of moleculaes dekacene, eicocene was received by method MNDO and are shown on fig. 1, fig. 2 and in tab.1-3 . The universal factor of acidity was calculated by formula: pKa = 49,4-134,61*qmaxH+ [4] (where, qmaxH+ - a maximum positive charge on atom of the hydrogen (by Milliken [1]) R=0.97, R- a coefficient of correlations, qmaxH+=+0,06). pKa=33. This formula was successfully used in the following articles: [5, 6, 7].
Quantum-chemical calculation of molecules dekacene, eicocene by method MNDO was executed for the first time. Optimized geometric and electronic structures of these compound was received. Acid power of molecules dekacene, eicocene was theoretically evaluated (pKa=33). These compounds pertain to class of very weak H-acids (pKa>14).
Table 1 - Optimised bond lengths, valent corners and atom charges of dekacene
H52 H44 H37 H31 H26 h»9
HI 4 H8 H58 H64
H 49 H43 НЗЭ H32 H25 H20 НИ H7 Fig. 1 - Geometric and electronic molecular structure of dekacene. (Е0= -550105 kDg/mol, Eel= -4850841 kDg/mol).
Bond lengths R,A Valent comers Grad Atom Charge (by Milliken)
1 2 3 4 5 6
C(1)-C(2) 1 46 C(3)-C(2)-C(1) 118 C(1) -0.04
C(2)-C(3) 1 45 C(12)-C(9)-C(1) 122 C(2) -0.04
C(3)-C(4) 1 38 C(4)-C(3)-C(2) 123 C(3) -0.02
C(4)-C(5) 1 47 C(9)-C(1)-C(2) 119 C(4) -0.06
C(5)-C(6) 1 38 C(5)-C(4)-C(3) 119 C(5) -0.06
C(6)-C(1) 1 45 C(10)-C(2)-C(3) 123 C(6) -0.02
H(7)-C(3) 1 09 C(6)-C(5)-C(4) 119 H(7) 0.06
H(8)-C(6) 1 09 C(54)-C(53)-C(4) 123 H(8) 0.06
C(9)-C(12) 1 44 C(1)-C(6)-C(5) 123 C(9) -0.02
C(9)-C(1) 1 39 C(53)-C(4)-C(5) 118 C(10) -0.02
C(10)-C(2) 1 39 C(2)-C(1)-C(6) 118 C(11) -0.04
C(11)-C(10) 1 44 C(9)-C(1)-C(6) 123 C(12) -0.04
C(12)-C(11) 1.46 C(4)-C(3)-H(7) 120 H(13) 0.06
H(13)-C(10) 1.38 C(1)-C(6)-H(8) 117 H(14) 0.06
H(14)-C(9) 1.45 C(11)-C(12)-C(9) 118 C(15) -0.02
C(15)-C(16) 1.42 C(15)-C(12)-C(9) 123 C(16) -0.04
C(15)-C(12) 1.41 C(1)-C(2)-C(10) 119 C(17) -0.04
C(16)-C(17) 1.45 C(18)-C(11)-C(10) 123 C(18) -0.02
С(17)-C(18) 1.42 C(2)-C(10)-C(11) 122 H(19) 0.06
С(18)-C(11) 1.41 C(15)-C(12)-C(11) 119 H(20) 0.06
H(19)-C(15) 1.09 C(10)-C(11)-C(12) 118 C(21) -0.02
H(20)-C(18) 1.09 C(16)-C(15)-C(12) 122 C(22) -0.04
C(21)- C(22) 1.41 C(2)-C(10)-H(13) 120 C(23) -0.04
C(21)-C(16) 1.42 C(12)-C(9)-H(14) 118 C(24) -0.02
C(22)-C(23) 1.46 C(17)-C(16)-C(15) 119 H(25) 0.06
С(23)-C(24) 1.40 C(21)-C(16)-C(15) 123 H(26) 0.06
С(24)-C(17) 1.42 C(18)-C(17)-C(16) 119 C(27) -0.02
H(25)-C(24) 1.09 C(22)-C(21)-C(16) 122 C(28) -0.02
H(26)-C(21) 1.09 C(11)-C(18)-C(17) 122 C(29) -0.04
C(27)-C(30) 1.39 C(21)-C(16)-C(17) 119 C(30) -0.04
C(27)-C(22) 1.44 C(12)-C(11)-C(18) 119 H(31) 0.06
C(28)-c(23) 1.44 C(24)-C(17)-C(18) 123 H(32) 0.06
End table 1
1 2 3 4 5 6
C(29)-C(28) 1.39 C(16)-C(15)-H(19) 118 C(33) -0.02
C(30)-C(29) 1.46 C(11)-C(18)-H(20) 119 C(34) -0.04
H(31)-C(27) 1.09 C(23)-C(22)-C(21) 119 C(35) -0.02
H(32)-C(28) 1.09 C(27)-C(22)-C(21) 123 C(36) -0.04
C(33)-c(29) 1.45 C(24)-C(23)-C(22) 119 H(37) 0.06
C(34)- C(33) 1.38 C(30)-C(27)-C(22) 122 H(38) 0.06
C(35)-C(36) 1.38 C(17)-C(24)-C(23) 122 C(39) -0.02
C(35)-C(30) 1.45 C(27)-C(22)-C(23) 118 C(40) -0.04
C(36)-C(34) 1.47 C(16)-C(17)-C(24) 119 C(41) -0.04
H(37)-C(35) 1.09 C(28)-C(23)-C(24) 123 C(42) -0.02
H(38)-C(33) 1.09 C(17)-C(24)-H(25) 119 H(43) 0.06
C(39)-C(40) 1.38 C(22)-C(21)-H(26) 119 H(44) 0.06
C(39)-C(36) 1.46 C(29)-C(30)-C(27) 119 C(45) -0.04
C(40)-C(41) 1.48 C(35)-C(30)-C(27) 123 C(46) -0.06
C(41)- C(42) 1.38 C(22)-C(23)-C(28) 118 C(47) -0.06
C(42)-C(34) 1.46 C(33)-C(29)-C(28) 123 C(48) -0.04
H(43)-C(42) 1.09 C(23)-C(28)-C(29) 122 H(49) 0.06
H(44)-C(39) 1.09 C(35)-C(30)-C(29) 118 H(50) 0.06
C(45)- C(46) 1.36 C(28)-C(29)-C(30) 119 H(51) 0.06
C(45)- C(40) 1.47 C(36)-C(35)-C(30) 124 H(52) 0.06
C(46)-C(47) 1.45 C(30)-C(27)-H(31) 120 C(53) -0.02
C(47)-C(48) 1.36 C(23)-C(28)-H(32) 118 C(54) -0.04
C(48)-C(41) 1.47 C(30)-C(29)-C(33) 118 C(55) -0.04
H(49)-C(48) 1.09 C(42)-C(34)-C(33) 123 C(56) -0.02
H(50)-C(47) 1.09 C(29)-C(33)-C(34) 123 H(57) 0.06
H(51)-C(46) 1.09 C(39)-C(36)-C(34) 118 H(58) 0.06
H(52)-C(45) 1.09 C(34)-C(36)-C(35) 119 C(59) -0.04
C(53)-C(54) 1.38 C(39)-C(36)-C(35) 123 C(60) -0.06
C(53)-C(4) 1.46 C(33)-C(34)-C(36) 119 C(61) -0.06
C(54)- C(55) 1.48 C(40)-C(39)-C(36) 123 C(62) -0.04
C(55)-C(56) 1.38 C(36)-C(35)-H(37) 120 H(63) 0.06
C(56)-C(5) 1.46 C(29)-C(33)-H(38) 117 H(64) 0.06
H(57)-C(53) 1.09 C(41)-C(40)-C(39) 119 H(65) 0.06
H(58)-C(56) 1.09 C(45)-C(40)-C(39) 123 H(66) 0.06
C(59)- C(60) 1.36 C(42)-C(41)-C(40) 119
C(59)-C(54) 1.47 C(46)-C(45)-C(40) 122
C(60)-C(61) 1.45 C(34)-C(42)-C(41) 123
C(61)- C(62) 1.36 C(45)-C(40)-C(41) 118
C(62)-C(55) 1.47 C(36)-C(34)-C(42) 118
H(63)-C(59) 1.09 C(48)-C(41)-C(42) 123
H(64)-C(62) 1.09 C(34)-C(42)-H(43) 117
H(65)-C(61) 1.09 C(40)-C(39)-H(44) 120
H(66)-C(60) 1.09 C(47)-C(46)-C(45) 121
C(48)-C(47)-C(46) 121
C(41)-C(48)-C(47) 122
C(40)-C(41)-C(48) 118
C(41)-C(48)-H(49) 118
C(48)-C(47)-H(50) 121
C(47)-C(46)-H(51) 118
C(46)-C(45)-H(52) 120
C(55)-C(54)-C(53) 119
C(3)-C(4)-C(53) 123
C(56)-C(55)-C(54) 119
C(60)-C(59)-C(54) 122
C(5)-C(56)-C(55) 123
C(59)-C(54)-C(55) 118
C(4)-C(5)-C(56) 118
C(6)-C(5)-C(56) 123
C(54)-C(53)-H(57) 120
C(5)-C(56)-H(58) 117
C(61)-C(60)-C(59) 121
C(53)-C(54)-C(59) 123
C(62)-C(61)-C(60) 121
C(55)-C(62)-C(61) 122
C(54)-C(55)-C(62) 118
C(56)-C(55)-C(62) 123
C(60)-C(59)-H(63) 120
C(55)-C(62)-H(64) 118
C(62)-C(61)-H(65) 121
C(61)-C(60)-H(66) 118
Fig. 2 - Geometric and electronic molecular structure of eicocene. (E0= -1069853 kDg/mol, Ee,= -11719827 kDg/mol)
Table 2 - Optimised bond lengths, valent corners and atom charges of eicocene
Bond lengths R,A Valence corners Grad Atom Charge (by Milliken)
1 2 3 4 5 6
C(2)-C(1) 1.46 C(5)-C(6)-C(1) 122 C(1) -0.03
C(3)-C(2) 1.44 C(11)-C(10)-C(2) 122 C(2) -0.04
C(4)-C(3) 1.39 C(1)-C(2)-C(3) 118 C(3) -0.02
C(4)-C(5) 1.47 C(10)-C(2)-C(3) 123 C(4) -0.04
C(5)-C(54) 1.46 C(5)-C(4)-C(3) 119 C(5) -0.04
C(6)-C(5) 1.39 C(2)-C(3)-C(4) 122 C(6) -0.02
C(6)-C(1) 1.44 C(54)-C(5)-C(4) 118 H(7) +0.06
H(7)-C(3) 1.09 C(6)-C(5)-C(4) 119 H(8) +0.06
H(8)-C(6) 1.09 C(53)-C(54)-C(5) 123 C(9) -0.02
C(9)-C(1) 1.40 C(54)-C(5)-C(6) 123 C(10) -0.02
C(10)-C(2) 1.40 C(2)-C(1)-C(6) 118 C(11) -0.03
C(10)-C(11) 1.43 C(2)-C(3)-H(7) 118 C(12) -0.03
C(11)-C(18) 1.42 C(5)-C(6)-H(8) 120 H(13) +0.06
C(11)-C(12) 1.45 C(1)-C(6)-H(8) 118 H(14) +0.06
C(12)-C(9) 1.43 C(2)-C(1)-C(9) 119 C(15) -0.02
H(13)-C(10) 1.09 C(1)-C(2)-C(10) 119 C(16) -0.04
H(14)-C(9) 1.09 C(18)-C(11)-C(10) 123 C(17) -0.04
C(15)-C(12) 1.42 C(12)-C(11)-C(10) 119 C(18) -0.02
C(16)-C(15) 1.41 C(17)-C(18)-C(11) 122 H(19) +0.06
C(16)-C(17) 1.45 C(9)-C(12)-C(11) 119 H(20) +0.06
C(17)-C(24) 1.44 C(15)-C(12)-C(11) 119 C(21) -0.02
C(18)-C(17) 1.41 C(1)-C(9)-C(12) 122 C(22) -0.04
H(19)-C(15) 1.09 C(18)-C(11)-C(12) 119 C(23) -0.04
H(20)-C(18) 1.09 C(2)-C(10)-H(13) 119 C(24) -0.02
C(21)-C(16) 1.44 C(11)-C(10)-H(13) 118 H(25) +0.06
C(22)-C(21) 1.39 C(1)-C(9)-H(14) 119 H(26) +0.06
C(23)-C(22) 1.46 C(9)-C(12)-C(15) 123 C(27) -0.02
C(24)-C(23) 1.39 C(17)-C(16)-C(15) 119 C(28) -0.02
H(25)-C(24) 1.09 C(12)-C(15)-C(16) 122 C(29) -0.04
H(26)-C(21) 1.09 C(24)-C(17)-C(16) 118 C(30) -0.04
Continuation table 2
1 2 3 4 5 6
C(27)-C(22) 1.45 C(18)-C(17)-C(16) 119 H(31) +0.06
C(28)-C(23) 1.45 C(23)-C(24)-C(17) 122 H(32) +0.06
C(29)-C(28) 1.38 C(24)-C(17)-C(18) 123 C(33) -0.02
C(29)-C(30) 1.47 C(12)-C(15)-H(19) 119 C(34) -0.04
C(30)-C(27) 1.38 C(17)-C(18)-H(20) 119 C(35) -0.02
H(31)-C(27) 1.09 C(15)-C(16)-C(21) 123 C(36) -0.04
H(32)-C(28) 1.09 C(17)-C(16)-C(21) 118 H(37) +0.06
C(33)-C(29) 1.46 C(16)-C(21)-C(22) 122 H(38) +0.06
C(34)-C(33) 1.38 C(21)-C(22)-C(23) 119 C(39) -0.02
C(34)-C(36) 1.48 C(27)-C(22)-C(23) 118 C(40) -0.04
C(34)-C(42) 1.46 C(22)-C(23)-C(24) 119 C(41) -0.04
C(35)-C(30) 1.46 C(28)-C(23)-C(24) 123 C(42) -0.02
C(36)-C(35) 1.38 C(23)-C(24)-H(25) 120 H(43) +0.06
H(37)-C(35) 1.09 C(16)-C(21 )-H(26) 118 H(44) +0.06
H(38)-C(33) 1.09 C(21)-C(22)-C(27) 123 C(45) -0.02
C(39)-C(36) 1.46 C(22)-C(23)-C(28) 118 C(46) -0.03
C(40)-C(39) 1.38 C(30)-C(29)-C(28) 119 C(47) -0.03
C(40)-C(41) 1.48 C(23)-C(28)-C(29) 123 C(48) -0.02
C(41)-C(48) 1.45 C(27)-C(30)-C(29) 119 H(49) +0.05
C(42)-C(41) 1.38 C(35)-C(30)-C(29) 118 H(50) +0.05
H(43)-C(42) 1.09 C(22)-C(27)-C(30) 123 C(51) -0.02
H(44)-C(39) 1.09 C(22)-C(27)-H(31) 117 C(52) -0.04
C(45)-C(40) 1.45 C(23)-C(28)-H(32) 117 C(53) -0.04
C(46)-C(45) 1.39 C(28)-C(29)-C(33) 123 C(54) -0.02
C(47)-C(46) 1.49 C(30)-C(29)-C(33) 118 H(55) +0.06
C(48)-C(47) 1.39 C(36)-C(34)-C(33) 120 H(56) +0.06
H(49)-C(48) 1.09 C(42)-C(34)-C(33) 123 C(57) -0.04
H(50)-C(45) 1.09 C(29)-C(33)-C(34) 123 C(58) -0.06
C(51)-C(4) 1.46 C(35)-C(36)-C(34) 120 C(59) -0.06
C(52)-C(51) 1.38 C(41)-C(42)-C(34) 123 C(60) -0.04
C(52)-C(53) 1.48 C(39)-C(36)-C(34) 118 H(61) +0.06
C(53)-C(60) 1.47 C(27)-C(30)-C(35) 123 H(62) +0.06
C(54)-C(53) 1.38 C(30)-C(35)-C(36) 123 H(63) +0.06
H(55)-C(51) 1.09 C(42)-C(34)-C(36) 118 H(64) +0.06
H(56)-C(54) 1.09 C(30)-C(35)-H(37) 117 C(65) -0.04
C(57)-C(52) 1.47 C(29)-C(33)-H(38) 117 C(66) -0.04
C(58)-C(57) 1.36 C(35)-C(36)-C(39) 123 C(67) -0.02
C(59)-C(58) 1.45 C(41)-C(40)-C(39) 119 C(68) -0.04
C(60)-C(59) 1.36 C(36)-C(39)-C(40) 123 C(69) -0.04
H(61)-C(57) 1.09 C(48)-C(41)-C(40) 118 C(70) -0.02
H(62)-C(60) 1.09 C(42)-C(41)-C(40) 119 H(71) +0.06
H(63)-C(59) 1.09 C(47)-C(48)-C(41) 124 H(72) +0.06
H(64)-C(58) 1.09 C(48)-C(41)-C(42) 123 C(73) -0.02
C(65)-C(70) 1.46 C(41)-C(42)-H(43) 120 C(74) -0.02
C(66)-C(65) 1.47 C(36)-C(39)-H(44) 117 C(75) -0.04
C(67)-C(66) 1.46 C(39)-C(40)-C(45) 123 C(76) -0.04
C(68)-C(67) 1.37 C(41)-C(40)-C(45) 118 H(77) +0.06
C(68)-C(69) 1.48 C(40)-C(45)-C(46) 124 H(78) +0.06
C(69)-C(120) 1.46 C(45)-C(46)-C(47) 119 C(79) -0.02
C(70)-C(69) 1.38 C(124)-C(46)-C(47) 118 C(80) -0.04
H(71)-C(67) 1.09 C(46)-C(47)-C(48) 119 C(81) -0.04
H(72)-C(70) 1.09 C(123)-C(47)-C(48) 123 C(82) -0.02
C(73)-C(65) 1.38 C(47)-C(48)-H(49) 119 H(83) +0.06
C(74)-C(66) 1.38 C(40)-C(45)-H(50) 117 H(84) +0.06
C(75)-C(74) 1.46 C(3)-C(4)-C(51) 123 C(85) -0.02
C(75)-C(76) 1.47 C(5)-C(4)-C(51) 118 C(86) -0.03
C(76)-C(73) 1.46 C(53)-C(52)-C(51) 119 C(87) -0.04
H(77)-C(74) 1.09 C(4)-C(51)-C(52) 123 C(88) -0.02
H(78)-C(73) 1.09 C(60)-C(53)-C(52) 118 H(89) +0.06
C(79)-C(76) 1.39 C(54)-C(53)-C(52) 119 H(90) +0.06
C(80)-C(79) 1.45 C(59)-C(60)-C(53) 122 C(91) -0.02
C(80)-C(81) 1.46 C(60)-C(53)-C(54) 123 C(92) -0.02
C(81)-C(82) 1.45 C(4)-C(51)-H(55) 117 C(93) -0.04
C(82)-C(75) 1.39 C(53)-C(54)-H(56) 120 C(94) -0.04
H(83)-C(79) 1.09 C(51)-C(52)-C(57) 123 H(95) +0.06
H(84)-C(82) 1.09 C(53)-C(52)-C(57) 118 H(96) +0.06
C(85)-C(80) 1.40 C(52)-C(57)-C(58) 122 C(97) -0.02
C(86)-C(85) 1.43 C(57)-C(58)-C(59) 121 C(98) -0.04
C(86)-C(87) 1.45 C(58)-C(59)-C(60) 121 C(99) -0.02
C(87)-C(88) 1.43 C(52)-C(57)-H(61) 118 C(100) -0.04
C(88)-C(81) 1.40 C(59)-C(60)-H(62) 120 H(101) +0.06
H(89)-C(88) 1.09 C(58)-C(59)-H(63) 118 H(102) +0.06
H(90)-C(85) 1.09 C(57)-C(58)-H(64) 121 C(103) -0.02
C(91)-C(86) 1.42 C(69)-C(70)-C(65) 123 C(104) -0.04
C(92)-C(87) 1.42 C(70)-C(65)-C(66) 118 C(105) -0.04
C(93)-C(92) 1.41 C(73)-C(65)-C(66) 119 C(106) -0.02
C(93)-C(94) 1.45 C(65)-C(66)-C(67) 118 H(107) +0.06
C(94)-C(91) 1.41 C(74)-C(66)-C(67) 123 H(108) +0.06
H(95)-C(91) 1.09 C(69)-C(68)-C(67) 120 C(109) -0.04
H(96)-C(92) 1.09 C(66)-C(67)-C(68) 123 C(110) -0.06
C(97)-C(93) 1.44 C(120)-C(69)-C(68) 118 C(111) -0.06
C(98)-C(97) 1.39 C(70)-C(69)-C(68) 120 C(112) -0.04
C(98)-C(100) 1.46 C(119)-C(120)- 123 H(113) +0.06
C(69)
C(98)-C(106) 1.45 C(120)-C(69)-C(70) 123 H(114) +0.06
C(99)-C(94) 1.44 C(66)-C(67)-H(71) 117 H(115) +0.06
C(100)-C(99) 1.39 C(69)-C(70)-H(72) 120 H(116) +0.06
H(101)-C(99) 1.09 C(70)-C(65)-C(73) 123 C(117) -0.02
H(102)-C(97) 1.09 C(65)-C(66)-C(74) 119 C(118) -0.04
C(103)- C(100) 1.45 C(76)-C(75)-C(74) 118 C(119) -0.04
C(104)-C(103) 1.38 C(66)-C(74)-C(75) 123 C(120) -0.02
C(104)-C(105) 1.47 C(73)-C(76)-C(75) 118 H(121) +0.05
C(105)- C(112) 1.47 C(79)-C(76)-C(75) 119 H(122) +0.05
C(106)-C(105) 1.38 C(65)-C(73)-C(76) 123 C(123) -0.02
H(107)-C(106) 1.09 C(66)-C(74)-H(77) 120 C(124) -0.02
H(108)-C(103) 1.09 C(65)-C(73)-H(78) 120 H(125) +0.05
C(109)-C(104) 1.47 C(73)-C(76)-C(79) 123 H(126) +0.05
C(110)-C(109) 1.36 C(81)-C(80)-C(79) 118
C(111)-C(110) 1.45 C(76)-C(79)-C(80) 122
C(112)-C(111) 1.36 C(82)-C(81)-C(80) 118
H(113)-C(112) 1.09 C(88)-C(81)-C(80) 119
H(114)-C(111) 1.09 C(75)-C(82)-C(81) 122
H(115)-C(110) 1.09 C(74)-C(75)-C(82) 123
H(116)-C(109) 1.09 C(76)-C(75)-C(82) 119
C(117)-C(68) 1.46 C(76)-C(79)-H(83) 120
C(118)-C(117) 1.38 C(75)-C(82)-H(84) 120
C(118)-C(119) 1.49 C(79)-C(80)-C(85) 123
C(118)-C(123) 1.44 C(81)-C(80)-C(85) 119
C(119)-c(124) 1.44 C(87)-C(86)-C(85) 119
C(120)-C(119) 1.38 C(80)-C(85)-C(86) 122
H(121)-C(117) 1.09 C(88)-C(87)-C(86) 119
H(122)-C(120) 1.09 C(92)-C(87)-C(86) 119
C(123)-C(47) 1.42 C(81)-C(88)-C(87) 122
C(124)-C(46) 1.42 C(82)-C(81)-C(88) 123
H(125)-C(123) 1.09 C(81 )-C(8 8)-H(89) 119
H(126)-C(124) 1.09 C(80)-C(85)-H(90) 119
C(85)-C(86)-C(91) 123
C(87)-C(86)-C(91) 119
C(88)-C(87)-C(92) 123
C(94)-C(93)-C(92) 119
C(87)-C(92)-C(93) 122
C(91)-C(94)-C(93) 119
C(99)-C(94)-C(93) 118
C(86)-C(91)-C(94) 122
C(86)-C(91 )-H(95) 119
C(87)-C(92)-H(96) 119
C(92)-C(93)-C(97) 123
C(94)-C(93)-C(97) 118
C(100)-C(98)-C(97) 119
C(106)-C(98)-C(97) 123
C(93)-C(97)-C(98) 122
C(99)-C(100)-C(98) 119
C(105)-C(106)-C(98) 123
C(103)-C(100)-C(98) 118
C(91)-C(94)-C(99) 123
C(94)-C(99)-C(100) 122
C(106)-C(98)-C(100) 118
C(94)-C(99)-H(101) 118
C(93)-C(97)-H(102) 118
C(99)-C(100)-C(103) 123
C(105)-C(104)-C(103) 119
End table 2
1 2 3 4 5 6
C(100)-C(103)-C(104) 123
C(112)-C(105)-C(104) 118
C(106)-C(105)-C(104) 119
C(111)-C(112)-C(105) 122
C(112)-C(105)-C(106) 123
C(105)-C(106)-H(107) 120
C(100)-C(103)-H(108) 117
C(103)-C(104)-C(109) 123
C(105)-C(104)-C(109) 118
C(104)-C(109)-C(110) 122
C(109)-C(110)-C(111) 121
C(110)-C(111)-C(112) 121
C(111)-C(112)-H(113) 120
C(110)-C(111)-H(114) 118
C(109)-C(110)-H(115) 121
C(104)-C(109)-H(116) 118
C(67)-C(68)-C(117) 123
C(69)-C(68)-C(117) 118
C(119)-C(118)-C(117) 119
C(123)-C(118)-C(117) 123
C(68)-C(117)-C(118) 123
C(124)-C(119)-C(118) 118
C(47)-C(123)-C(118) 124
C(120)-C(119)-C(118) 119
C(46)-C(124)-C(119) 124
C(123)-C(118)-C(119) 118
C(124)-C(119)-C(120) 123
C(68)-C(117)-H(121) 117
C(119)-C(120)-H(122) 120
C(46)-C(47)-C(123) 118
C(45)-C(46)-C(124) 123
C(47)-C(123)-H(125) 118
C(46)-C(124)-H(126) 118
Table 3 - Total energy (E0), maximal charge on the hydrogen atom (qmaxH+ ) and universal factor of acidity (pKa) of molecules dekacene and eicocene
Molecules Eq (kDg/mol) a H+ Hmax pKa
Dekacene -550105 +0.06 33
Eicocene -1069853 +0.06 33
References
1. K. S. Novoselov, et al. Electric Field Effect in Atomically Thin Carbon Films, Science 306, 666 (2004);DOI:10.1126/science.1102896
2. M.W.Shmidt, K.K.Baldrosge, J.A. Elbert, M.S. Gordon, J.H. Enseh, S.Koseki, N.Matsvnaga., K.A. Nguyen, S. J. Su, And Anothers. J. Comput. Chem.14, 1347-1363, (1993).
3. Bode, B. M. and Gordon, M. S. J. Mol. Graphics Mod., 16, 1998, 133-138
4. Babkin V.A., Fedunov R.G., Minsker K.S. and anothers. Oxidation communication, 2002, №1, 25, 21-47.
5. V.A. Babkin, A.V. Ignatov, A.N. Ignatov, M.N. Gulyukin, V.Yu. Dmitriev, O.V. Stoyanov, G.E. Zaikov. Quantum-chemical Calculation of some molecules of triboratols. Kazan. "Vestnik" of Kazan State Technological University. 2013., Vol. 16, N2, p. 15-17
6. V.A. Babkin, A.V. Ignatov, O.V. Stoyanov, G.E. Zaikov. Quantum-chemical Calculation of some monomers of cationic polymerisation with small cycles. Kazan. "Vestnik" of Kazan State Technological University. 2013., Vol. 16, N 4, p.21-22
7. V.A. Babkin, V.V. Trifonov В.В., N.G. Lebedev, V.Yu. Dmitriev, D.S. Andreev, O.V. Stoyanov, G.E. Zaikov. Quantum-chemical Calculation of tetracene and pentacene by MNDO in approximation of the linear molecular model of graphene. Kazan. "Vestnik" of Kazan State Technological University. 2013., Vol. 16, N 7, p.16-18.
© V. А. БаЪкш - д-р хим. наук, проф. нач. научн. отдела Себряковского филиала Волгоградского государственного архитектурно-строительного университета, [email protected]; V. V. ТгНЪпоу - студ. того же вуза, [email protected]; А. Р. Кпуа/еу - канд. геогр. наук, доц. каф. ОТД того же вуза, [email protected]; V. Уи. Бшкпеу - асп. Волгоградского госуд.о архитектурно-строительного университета, [email protected]; Б. 8. Ап^ееу - асп. Волгоградского госуд.о архитектурно-строительного университета, [email protected]; А. V. 1§па1оу - студ. Себряковского филиала Волгоградского государственного архитектурно-строительного университета, [email protected]; Е. 8. Ткоуа - д.х.н. доц. каф. органической химии Волгоградского госуд.о технического университета, [email protected]; О. V. 81оуапоу - д-р техн. наук, проф., зав. каф. технологии пластических масс КНИТУ; С. Е. 2а1коу - д-р, хим. наук, проф. Института биохимической физики РАН, [email protected].