2012
DOI: 10.1107/s1600536812033582
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[2,7-Dimethoxy-8-(4-propylbenzoyl)naphthalen-1-yl](4-propylphenyl)methanone

Abstract: In the title compound, C32H32O4, the 4-propylbenzoyl groups at the 1- and 8-positions of the naphthalene ring system are aligned almost antiparallel, and their benzene rings make a dihedral angle of 8.64 (10)°. The dihedral angles between the naphthalene ring system and the benzene rings are 69.37 (8) and 69.45 (8)°. In the crystal, C—H...O interactions link adjacent molecules via their aroyl groups

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Cited by 2 publications
(2 citation statements)
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“…For details of the formation reaction of aroylated naphthalene compounds via electrophilic aromatic substitution of naphthalene derivatives, see: Okamoto & Yonezawa (2009); Okamoto et al (2011). For the structures of closely related compounds, see: Hijikata et al (2010); Muto et al (2010); Sasagawa, Hijikata et al (2011); Sasagawa, Muto et al (2011); Sasagawa et al (2012). Data collection: PROCESS-AUTO (Rigaku, 1998); cell refinement: PROCESS-AUTO; data reduction: PROCESS-AUTO; program(s) used to solve structure: SIR2004 (Burla et al, 2005); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEPIII (Burnett & Johnson, 1996); software used to prepare material for publication: SHELXL97.…”
Section: Related Literaturementioning
confidence: 99%
“…For details of the formation reaction of aroylated naphthalene compounds via electrophilic aromatic substitution of naphthalene derivatives, see: Okamoto & Yonezawa (2009); Okamoto et al (2011). For the structures of closely related compounds, see: Hijikata et al (2010); Muto et al (2010); Sasagawa, Hijikata et al (2011); Sasagawa, Muto et al (2011); Sasagawa et al (2012). Data collection: PROCESS-AUTO (Rigaku, 1998); cell refinement: PROCESS-AUTO; data reduction: PROCESS-AUTO; program(s) used to solve structure: SIR2004 (Burla et al, 2005); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEPIII (Burnett & Johnson, 1996); software used to prepare material for publication: SHELXL97.…”
Section: Related Literaturementioning
confidence: 99%
“…The curious reversible aroylation behavior of the naphthalene derivative [16] and chemospecific and regioselective ethereal alkyl-oxygen bond cleavage reaction of aroylated naphthalenes [19] can be explained on the basis of the structural features of the aroylated naphthalenes. Under these circumstances, the authors have undertaken the structural studies of the aroylnaphthalne compounds [20][21][22][23][24][25][26] with investigation of the formation and the related reaction behaviors.…”
Section: Introductionmentioning
confidence: 99%