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Pregled bibliografske jedinice broj: 41816

Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol


Pavlović, Gordana; Lapić, Jasmina; Rapić, Vladimir
Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol // Structural chemistry, 11 (2000), 6; 355-360 (međunarodna recenzija, članak, znanstveni)


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Naslov
Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol

Autori
Pavlović, Gordana ; Lapić, Jasmina ; Rapić, Vladimir

Izvornik
Structural chemistry (1040-0400) 11 (2000), 6; 355-360

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
ferrocene compounds; 2-(ferrocenylmethyl)propane-1; 3-diol; spectroscopic characterization; X-ray analysis
(ferrocene compounds; 2-(ferrocenylmethyl)propane-1; spectroscopic characterization; X-ray analysis 3-diol)

Sažetak
The title compound was obtained by reduction of diethyl (ferrocenylmethyl)malonate with lithium aluminium hydride in diethyl ether. The structure of this novel ferrocene derivative was assigned by means of elemental analysis, IR, 1^H NMR, and 13^C NMR spectroscopy. The structure was also confirmed by a single crystal X-ray study. The compound crystallizes in monoclinic P 2--_1/a space group with unit cell dimensions: a = 9.7360(6), b = 27.040(5), c = 14.767(3) A, beta = 103.835(6)^o, V = 3774.8(11) A^ 3, Z = 12. The asymmetric unit contains three crystallographically independent molecules. In the ferrocenyl moieties, the Fe-C bond distance values are in the range 2.006(5) - 2.051(3) A and C-C distances in the range 1.366(7) - 1.425(4) A. The cyclopentadienyl rings in each of the molecules are mutually twisted by about 13o from the eclipsed conformation. The hydroxyl groups are involved in the intermolecular O-H...O hydrogen bond formation with O...O distances in the range 2.686(3) - 2.801(4) A forming infinite two-dimensional network in a (0 0 1) plane. The crystal structure is additionally stabilized by C-H...O weak intermolecular hydrogen bonds.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
058102
119408

Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Profili:

Avatar Url Jasmina Lapić (autor)

Avatar Url Gordana Pavlović (autor)

Avatar Url Vladimir Rapić (autor)


Citiraj ovu publikaciju:

Pavlović, Gordana; Lapić, Jasmina; Rapić, Vladimir
Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol // Structural chemistry, 11 (2000), 6; 355-360 (međunarodna recenzija, članak, znanstveni)
Pavlović, G., Lapić, J. & Rapić, V. (2000) Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol. Structural chemistry, 11 (6), 355-360.
@article{article, author = {Pavlovi\'{c}, Gordana and Lapi\'{c}, Jasmina and Rapi\'{c}, Vladimir}, year = {2000}, pages = {355-360}, keywords = {ferrocene compounds, 2-(ferrocenylmethyl)propane-1, 3-diol, spectroscopic characterization, X-ray analysis}, journal = {Structural chemistry}, volume = {11}, number = {6}, issn = {1040-0400}, title = {Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol}, keyword = {ferrocene compounds, 2-(ferrocenylmethyl)propane-1, 3-diol, spectroscopic characterization, X-ray analysis} }
@article{article, author = {Pavlovi\'{c}, Gordana and Lapi\'{c}, Jasmina and Rapi\'{c}, Vladimir}, year = {2000}, pages = {355-360}, keywords = {ferrocene compounds, 2-(ferrocenylmethyl)propane-1, spectroscopic characterization, X-ray analysis 3-diol}, journal = {Structural chemistry}, volume = {11}, number = {6}, issn = {1040-0400}, title = {Ferrocene compounds. XXVII. Synthesis and structure of 2-(ferrocenylmethyl)propane-1, 3-diol}, keyword = {ferrocene compounds, 2-(ferrocenylmethyl)propane-1, spectroscopic characterization, X-ray analysis 3-diol} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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