Zobrazeno 1 - 10
of 130
pro vyhledávání: '"G. W. A. Fowles"'
Autor:
E. Cartmell, G. W. A. Fowles
Las sucesivas ediciones de libros de texto para universitarios son cada vez más voluminosas. Es tanto lo sucedido en Química desde que apareció hace 20 años la primera edición de este libro, que incita a ampliarlo, pero contra esta tendencia gen
Autor:
G. W. A. Fowles
Publikováno v:
Journal of Wine Research. 5:103-112
This review discusses the sources of the sulphur compounds found in beverages. It summarises the nomenclature of these compounds and gives typical values for their threshold values in beers and wines. Practical observations on the reasons for the for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3467938400d2d8ff3d71558e85ed2982
https://doi.org/10.1080/09571269408717989
https://doi.org/10.1080/09571269408717989
Autor:
G. W. A. Fowles
Publikováno v:
Journal of Wine Research. 3:25-41
This paper reviews the evidence for the role of acids in wine. It begins with an overview of the influence of temperature, canopy management and grape variety on the types and levels of acid in grapes. This is followed by examinations of changes in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb8013783f1155204b09f692551f9766
https://doi.org/10.1080/09571269208717912
https://doi.org/10.1080/09571269208717912
Autor:
G. W. A. Fowles
Publikováno v:
Progress in Inorganic Chemistry
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5f8654641e314fecfcffe530dd28db6
https://doi.org/10.1002/9780470166079.ch1
https://doi.org/10.1002/9780470166079.ch1
Publikováno v:
Inorganic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78a1863efc255975a826344e407e2662
https://doi.org/10.1002/9780470132432.ch32
https://doi.org/10.1002/9780470132432.ch32
Publikováno v:
Inorganic Syntheses, Volume 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ee36ee9897618dc2be46d46c65155bc
https://doi.org/10.1002/9780470132432.ch38
https://doi.org/10.1002/9780470132432.ch38
The preparation of WMeCl3Y (Y = S OR Se) and some coordination compounds of WMeCl3Y (Y = O, S OR Se)
Publikováno v:
Journal of Organometallic Chemistry. 170:203-208
The reaction of WCl 4 Y (Y = S or Se) with Me 2 Mg leads to the formation of WMeCl 3 Y. The compounds WMeCl 3 Y (Y = O, S or Se) are very reactive and attempts to isolate them in pure form failed. However, a range of complexes which they form with so
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15de6828b0243ba62f3d2e4770126409
https://doi.org/10.1016/s0022-328x(00)81084-0
https://doi.org/10.1016/s0022-328x(00)81084-0
Publikováno v:
Journal of Inorganic and Nuclear Chemistry. 36:31-34
BBr3, BCl3, AlCl3 and GaCl3 have been found to react with CCl3CN to give 1:1 complexes. I.R. and Raman spectra suggest that the AlCl3 and GaCl3 complexes are simple adducts with CCl3CN bonded through the nitrogen atom, but that with the BX3 adducts d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49b3f2c234ab84f67d46022884214d0c
https://doi.org/10.1016/0022-1902(74)80652-4
https://doi.org/10.1016/0022-1902(74)80652-4
Publikováno v:
J. Chem. Soc., Dalton Trans.. :2409-2413
The salt [PPh3(CH2Ph)][WCl5S] is formed when WCl4S is treated with [PPh3(CH2Ph)]Cl (1 : 1 molar ratio) in Ch2Cl2 solution. Crystals are monoclinic, space group P21/c, with a= 10.572(9), b= 18.413(13), c= 14.250(11)A, and β= 104.20(8)°. The salt con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b4342dc804325012f0e0bed8023704c
https://doi.org/10.1039/dt9810002409
https://doi.org/10.1039/dt9810002409
Publikováno v:
Journal of Organometallic Chemistry. 76:349-353
Phenylzirconium trichloride has been isolated as its tetrahydrofuran adduct PhZrCl 3 ·3thf (I). The reaction of I with a range of nitrogen, phophorus and sulphur ligands gave products of stoichiometry PhZrCl 3 ·thf·L (L = 2,2′-bipyridyl, 4,4′-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61afe0e14ff6a64f987d21e0a7b4e658
https://doi.org/10.1016/s0022-328x(00)87382-9
https://doi.org/10.1016/s0022-328x(00)87382-9