SCOPUS 정보 검색 플랫폼

Volumn 74, Issue 7, 2009, Pages 2804-2810

Effect of aromatic-aromatic interactions on the conformational stabilities of macrocycle and preorganized structure during macrocyclization

(5) Katagiri, Kosuke a Tohaya, Taichi a Masu, Hyuma a Tominaga, Masahide a Azumaya, Isao a

a TOKUSHIMA BUNRI UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-CONFORMATIONS; AROMATIC AMIDES; AROMATIC-AROMATIC INTERACTIONS; BENZENE RINGS; CONFORMATIONAL STABILITIES; DIAMIDE; DYNAMIC BEHAVIORS; MACRO-CYCLIZATION; MACROCYCLE; MACROCYCLES; MACROCYCLIZATION REACTIONS; MOLECULAR SHAPES; NMR MEASUREMENTS; PHENYLENE RINGS; PLANAR CONFORMATIONS; SYNTHETIC YIELDS; TERPHENYL; TERPHENYL MOIETIES; TWISTED CONFORMATIONS; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

ACIDS; AMIDES; AMINES; AROMATIZATION; BENZENE;

AROMATIC COMPOUNDS;

AMIDE; AROMATIC AMIDE; AROMATIC COMPOUND; BENZENE; DIAMINE; MACROCYCLIC COMPOUND; N,N' DIETHYL N,N' DITERPHENYL 1,3 BENZENEDICARBOXAMIDE; N,N' DIETHYL N,N' DITERPHENYL 1,4 BENZENEDICARBOXAMIDE; TEREPHTHALIC ACID; TERPHENYL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CONFORMATION; CRYSTAL STRUCTURE; CYCLIZATION; MOLECULAR INTERACTION; NUCLEAR MAGNETIC RESONANCE; X RAY CRYSTALLOGRAPHY;

CRYSTALLOGRAPHY, X-RAY; CYCLIZATION; MACROCYCLIC COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; TEMPERATURE;

EID: 64249114939 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo802801n Document Type: Article

Times cited : (24)

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- Crystal data of 2: C48H40N2O 2; M, 676.82, triclinic, space group P1, a, 10.391(2) Å, b, 19.155(4) Å, c, 19.178(4) Å, α, 107.102(2) deg, β, 93.505(3)°. y, 91.272(2)°, V, 3638.3(12) Å3, Z, 4, D cafcd, 1.236 Mg m3, T= 120 K, α(MoKα, 0.075 mm-1, GOF on F2, 0.807, 17831 reflections measured, 13718 unique (Rint, 0.0236) which were used in all calculations. The final R1 and wR2 (F2) were 0.0529 and 0.1302 [I>2σI, Additional material comprising full details of the X-ray data collection and final refinement parameters including anisotropic thermal parameters and a full list of the bond lengths and angles have been deposited with the Cambridge Crystallograph
- 2) were 0.0529 and 0.1302 [I>2σ(I)]. Additional material comprising full details of the X-ray data collection and final refinement parameters including anisotropic thermal parameters and a full list of the bond lengths and angles have been deposited with the Cambridge Crystallographic Data Center in CIF format as supplementary Publication No. CCDC-712723. Copies of the data can be obtained free of charge on application to CCDC. 12 Union Road, Cambridge, CB21EZ, UK, (fax +44 1223 336 033; deposit@ccdc.cam.ac.uk).

46
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- Crystal data of 3: C48H40N2O 2.2CHCl3; M, 915.56, monoclinic, space aroup C2/c, α, 30.709(5) Å, b, 8.472(1) Å, c= 18.198(3) Å, β, 111.575(2)°, V= 4402(1) Å3, Z, 4, Dcalcd= 1.381 Mg m -3, T= 150 K, μ((MoKα, 0.434 mm, GOF on F2, 1.129, 10371 reflections measured, 4405 unique (R int, 0.0319) which were used in all calculations. The final RI and wR2 (F2) were 0.0638 and 0.1687 [I > 2σI, Cambridge Crystallographic Data Center Publication No. CCDC-712724
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51
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- Crystal data of 5: C60H52N4O 4; M, 893.06, monoclinic, space group P21 in, a, 7.765(2) Å, b, 24.472(7) Å, c, 13.084(4) Å, β, 101.834(5)°, V, 2433.5(12) Å3, Z= 2, Dcalcd, 1.219 Mg m -3, T= 150 K, μ(MoKα, 0.077 mm-1, GOF on F2, 0.946, 14448 reflections measured, 5493 unique (Rint, 0.0980) which were used in all calculations. The final R1 and wR2 (F2) were 0.0874 and 0.2175 [I > 2σI, Cambridge Crystallographic Data Center Publication No. CCDC-688290
- 2) were 0.0874 and 0.2175 [I > 2σ(I)]. Cambridge Crystallographic Data Center Publication No. CCDC-688290.

52
- 64249105191
- Crystal data of 6: C64H64N4O 9; M, 1033.19, monoclinic, space group P2 1/c, a =l6.925(3) Å, b, 15.637(3) Å, c, 22.381(4) Å, β= 103.617(4)°, V, 5756.8(19) Å3, Z, 4, Dcalcd, 1.192 Mg m -3, T, 150 K, μ(MoKα, 0.080 mm-1, GOF on F2, 0.986, 17239 reflections measured, 5188 unique (Rint, 0.1071) which were used in all calculations. The final R1 and wR2 (F2) were 0.0797 and 0.2193 [I > 2σI, Cambridge Crystallographic Data Center Publication No. CCDC-688291
- 2) were 0.0797 and 0.2193 [I > 2σ(I)]. Cambridge Crystallographic Data Center Publication No. CCDC-688291.

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