Frankland, Edward
Frankland, Edward
(b. Catterall, near Churchtown, Lanscashire, England, 18 January 1825 d. Golaa, Gudbrandalen, Norway, 9 August 1899)
Chemistry
Frankland was the illegitimate son of Peggy frankland, the daughter of a calico printer. After education in seven schools, including Lancaster Grammar School, Frankland was apprenticed by his stepfather, William Helm, to a Lancaster druggist, Stephen Ross. The drudgery of the years from 1840 to 1845, during which Ross taught him little, haunted Frankland’s dreams for the remainder of his life. Through the efforts of two local doctors, Christopher and James Johnson, he was given facilities to perform chemical experiments in his spare time, and in 1845 they found him employment in Lyon Playfair’s laboratory at the government’s Museum of Economic Geology in London. There he met the brilliant German chemist A. W. H. Kolbe, who taught him Robert Bunsen’s methods of gas analysis—a technique Frankland exploited in his later researches.
In 1846 Frankland became Playfair’s assistant at the Civil Engineering College at Putney, London. and during the summer of 1847 he accompanied Kolbe to Marburg in order to study with Bunsen. From 1847 to 1848 he taught science with John Tyndall at the progressive Quaker school run by George Edmondson at Queenwood, Hampshire. Frankland completed his training with Bunsen at Marburg from 1848 to 1849, obtained his doctorate, and briefly studied with Justus Liebig at Giessen before returning to London to take Playfair’s chair of chemistry at Putney from 1850 to 1851. He became professor of chemistry at Owens College, Manchester, in 1851, but this position proved unsatisfactory. In 1857 he returned to London, where, until 1864, he was lecturer in chemistry at St. Bartholomew’s Hospital.
Frankland also indulged in the pluralism of a lectureship in science at Addiscombe Military College from 1859 to 1863, and from 1863 to 1869 he was professor of chemistry at the Royal Institution. Finally, in 1865, he succeeded A. W. Hofmann as professor of chemistry at the Royal College of Chemistry, a position he retained through the college’s many transformations until his retirement in 1885. From 1865, Frankland made official monthly analyses of the water supplies of London, and from 1868 to 1874 he served on the important Royal Commission on Rivers Pollution. For these services he was knighted in 1897.
At the age of eighteen Frankland underwent an extreme form of evangelical conversion, but after 1848 he lapsed into skepticism. Together with Tyndall, T. H. Huxley, J. D. Hooker, and others he was an active member of an informal scientific pressure group which called itself the X Club. Yet the club was unable to gain for Frankland the presidency of the Royal Society or of the British Association for the Advancement of Science, owing to his modesty and poor ability in public debate. But he did serve as president of the Chemical Society from 1871 to 1873 and was the founder and first president of the Institute of Chemistry (the society for professional chemists) from 1877 to 1880.
Frankland is an outstanding example of a pure scientist who was deeply conscious of the significance and importance of applied science; but his public service in the improvement of water and gas supplies and his contributions to the development of British scientific education await proper assessment. Frankland possessed a voracious appetite for travel, which he combined with mountaineering, yachting, and fishing. He was also a keen gardener, music lover, and amateur astronomer. In 1874, following the death of his first wife, Sophie Fick, by whom he had three sons and two daughters, he married Ellen Grenside, by whom he had two daughters.
Frankland’s extraordinary practical and manipulative ability, as well as his power, like Bunsen’s, to combine physics with chemistry, was exemplified in all three of the broad categories of his research: organic, physical, and applied chemistry. In 1844 H. Fehling had obtained a new compound, benzonitrile, C7 H5 N (i.e., phenyl cyanide), by the dry distillation of ammonium benzoate. Following A. Schlieper’s preparation of valeronitrile, C5 H9 N (i.e., butyl cyanide), in 1846, Kolbe and Frankland noted that both nitriles were easily hydrolyzed to their corresponding acids (i.e., benzoic and valeric acids). In their joint work of 1847 they pointed out that if these so-called nitriles were really cyanides, then their hydrolysis would agree with Berzelius’ iconoclastic suggestion that acetic acid was a methyl radical conjugated with oxalic acid (C2 H3. C2 O3. HO, C = 6, O = 8). If both these assumptions were made, it followed that the homologues of acetic acid (e.g., propionic acid) arose from the conjugation of oxalic acid with ethyl (alkyl) radicals. Their production of propionic acid from ethyl cyanide in 18471 led Frankland and Kolbe to attempt separately the isolation of alkyl radicals from acids: Kolbe by the electrolysis of acids (1849) and Frankland by using a reaction between alkyl iodides and zinc based on analogy with Bunsen’s celebrated isolation of cacodyl in 1837. But after much controversy and the reform of atomic weights, Frankland was forced to admit that the formulas of the radicals he prepared between 1848 and 1851 had to be doubled and that the radicals were in fact inert hydrocarbons of the paraffin series.
The work on radicals also led Frankland in 1849 to the isolation of a new reactive organometallic compound, zinc methyl; this, together with the alkyl alkyltin compounds which he prepared in 1850 by the action of sunlight on alkyl halides in the presence of tin, produced the following problem. If, as the conjugation theories of Berzelius and Liebig held, the different alkyl groups associated with oxalic acid (i.e., a carboxylic group) had little or no influence on the combining properties of the acid, why did alkylconjugated metals have combining powers different from those of the metals alone? For example, tin diethyl (stanethylium) formed only one oxide, whereas tin itself formed at least two oxides. Zinc methyl, on the other hand, seemed to possess the same singular combining power as zinc. Here was the seed of the concept of valance, which, with international agreement on atomic weight values, was to unite the rival theoretical schools of chemistry during the 1860’s into the common aim of structural chemistry.
On 10 May 1852 Frankland read to the Royal Society a paper on organic metallic compounds in which he made the empirical observation that elements possessed fixed combining powers, or “only room, so to speak, for the attachment of a fixed and definite number of the atoms of other elements”.2 The expression “valence” or “valency” began to be used by other chemists only after 1865, whereas Frankland tended to use the misleading term “atomicity”. Although the development of valence as an architectural concept for linking atoms together within a molecule owed more to the work of Kekulé in the 1850’s and 1860’s, Franklank’s teaching position at the Royal College of Chemistry and his influence on the Department of Science and Art science examinations enabled him to spread the idea through the younger generation of British chemists. In 1866 he published an influential textbook, Lecture Notes, in which he adopted Crum Brown’s graphic (structural) formulas and argued (against Kekulé) that elements could exhibit more than one valence below a fixed upper maximum. He also developed a special shorthand structural notation3, but it proved confusing and its use did not persist into the twentieth century.
Frankland was quick to see that the analytical techniques he had developed and the organometallic compounds he had prepared would be powerful aids to synthesis, by which he meant the chemist’s ability to build up compounds “stone by stone” with a view to understanding their atomic configurations. From 1863 to 1870 he and Baldwin Duppa exploited zinc ethyl and other organic reagents, including ethyl acetate, in the synthesis of ethers, dicarboxylic acids, unsaturated monocarboxylic acids, and hydroxy acids. This meticulous work revealed clearly the structure and relationship of these compounds, and of course its methodology had great bearing on the growth of the chemical industry.
Intermittent work on combustion during the 1860’s was initiated by a memorable ascent of, and nighton, Mont Blanc with Tyndall in 1859. Frankland found that Humphry Davy’s views on the nature of flame were unsound and that pressure variations produced striking changes in the illuminating power of flames4. He showed the relevance of this finding to the supply of domestic illuminating gas and, in 1868, to stellar spectroscopy. During the latter brief investigation in collaboration with the astronomer J. N. Lockyer, lines of helium were first observed in the sun; but Frankland did not agree with Lockyer’s interpretation that helium was a new element5.
Frankland’s wide interests included biology. In 1865, together with Adolf Fick and Johannes Wislicenus, he designed an experiment to test Liebig’s theory that the source of muscular energy was the oxidation of nitrogenous muscular tissue. The two Germans performed this experiment by ascending Mt. Faulhorn in Switzerland while on a protein-free diet, then measuring the nitrogen output in their urine6. That confirmed their suspicion that muscular energy comes principally from the oxidation of nonnitrogenous materials. It remained for Frankland to confirm in the laboratory that the oxidation of carbohydrates and fats produces sufficient energy to account for the mechanical work of an organism7. His calorimetric experiments of 1866 on the energy values of common foodstuffs laid the foundation for quantitative dietetics.
In 1867, together with H. E. Armstrong, Frankland devised a method for analyzing water by combustion analysis of organic carbon and nitrogen in vacuo 8. A rival method developed by J. A. Wanklyn in the same year9, which identified nitrogen content as ammonia, led to acrimonious disputes between the two men over the respective merits of their systems. Frankland’s method, although extremely accurate, proved too cumbersome and difficult for the unskilled, so Wanklyn’s simpler but less reliable technique was usually preferred by public analysts. Frankland’s humanitarian and scientific interest in water analysis was continued by his son Percy.
NOTES
1. E. Frankland and H. Kolbe, “On the Chemical Constitution of Metacetonic Acid, and Some Other Bodies Related to It”, in Memories of the Chemical Society, 3 (1845–1848), 386–391.
2. E. Frankland. “On a New Series of Organic Bodies Containing Metals”, in Philosophical Transactions of the Royal Society, 142 (1852), 417–444, sec p. 440. Publication of this paper was delayed by the oversight of the Society’s secretary, G. Stokes (see Frankland’s autobiography, 1902 ed., p. 187).
3. E. Frankland, “Contributions to the Notation of Organic and Inorganic Bodies”, in Journal of the Chemical Society, 4 (1866). 372–395.
4. E. Frankland, “On the Influence of Atmospheric Pressure Upon Some of the Phenomena of Combustion”, in Philosophical Transcations of the Royal Society, 151 (1861), 629–653.
5. Letter to Lockyer, 9 Sept. 1872, in the archives of the Sir J. N. Lockyer Obsernatory, Sidmouth, Devonshire.
6. A. Fick and J. Wislicenus, “On the Origin of Muscular Power”, in Philosophical Magazine, 4th ser., 31 (1866), 485–503.
7. E. Frankland, “On the Origin of Muscular Power”, ibid., 32 (1866), 182–199.
8. E. Frankland and H. E. Armstrong, “On the Analysis of Potable Waters”, in Journal of the Chemical Society, 6 (1868), 77–108.
9. J. A. Wanklyn, E. T. Chapman, and M. H. Smith, “Water Analysis: Determination of the Nitrogenous Organic Matter”, ibid, 5 , 445–454.
BIBLIOGRAPHY
1. Original Works. Frankland published over 130 papers, of which the Royal Society Catalogue of Scientific Papers (London, 1867–1925) lists 107; see II, 699–700, VII, 700–701, IX, 918, and XV, 101; sixty-four were republished, some in a revised form, by Frankland in his 1877 book. To these should be added “A Course of Ten Lectures at the Royal Institution”, in Chemical News, 3 (1861), 99–104, 118–122, 132–136, 166–170, 185–187, 201–203, 215–219, 291–299, 377–381, and 4 (1861), 51–54, 65–68, 93–97; “Chemical Research in England”, in Nature, 3 (1870–1871), 445; an untitled paper on chemical apparatus read to the Kensington Science Conferences of 1876, in Nature, 14 (1876), 73–76 — see also South Kensington Museum. Conferences Held in Connection With the Special Loan Collection of Scientific Apparatus, 3 unnumbered vols. (London, 1876), “Chemistry, Biology”, pp. 1–13; the presidential addess to the Institute of Chemistry, in Chemical News, 37 (1878), 57–59; reply to Lockyer’s attack on the Institute of Chemistry, ibid, 52 (1885), 305–306. Note also Frankland’s important evidence to the Select Committee on Scientific Instruction for Industrial Classes, 1867–1868, in Parliamentary Papers 1867–1868, XV (432), pars. 8033–8177; and to the Devonshire Commission on Scientific Instruction and the Advancement of Science, 1871–1875, ibid., 1872, XXV (C.536); 1874, XXII (C.1087); and 1875, XXVIII (C.1298), pars. 40–47, 516–518, 758–835, 980–982, 2473–2488, 5667–5896, 11,053–11,108, and index. Finally, note Frankland’s influence in George S. Newth, Chemical Lecture Experiments. Non-metallic Elements (London, 1892, 1896).
Frankland’s books were Ueber die Isolirung des Radicales Aethyl (Marburg-Brunswick, 1849), his Ph.D. diss.; Lecture Notes for Chemical Students (Embracing Mineral and Organic Chemistry ) (London, 1866), the 2nd ed., 2 vols., published as I, Inorganic Chemistry (1870), and II, Organic Chemistry (1872), and a 3rd ed. of II, rev. by F. R. Japp (1881) — see below for the 3rd ed. of I; Reports of the Rivers Pollution Commission (1868), 6 vols. (London, 1870–1874), also in Parliamentary Papers, 1871, XXV, XXVI; 1872 XXXIV; and 1874, XXXIII; Experimental Researches in Pure, Applied, and Physical Chemistry (London, 1877), Frankland’s edited version of his papers, dedicated to Bunsen; How to Teach Chemistry; Hints to Science Teachers and Students, George Chaloner, ed. (London-Philadelphia, 1875); Water Analysis for Sanitary Purposes (London, 1880, 1890); Inorganic Chemistry, rev. by J. R. Japp, 3rd. ed. of Lecture Notes, I; Shetches From the Life of Edward Frankland (London, 1901); and Sketches From the Life of Sir Edward Frankland, edited and completed by M. N. W. [West] and S. J. C. [Colenco] (Frankland’s daughters)
For Kekulé’s claim to priority in valence theory, see his unpublished MS “Zur Geschichte der Valenztheorie”, in R. Anschütz, August Kekulé, I (Berlin, 1929), 555–569, repr. in facs. in R. Kuhn, ed., Cassirte Kapitel aus der Abhandlung: Über die Catboxytartronsäure und die Constitution des Benzols (Weinheim, 1965). frankland’s polemics with Wanklyn may be traced from Chemical News, 17 (1868), 45, 79, 97; 33 (1876), 85, 104–106; and 66 (1892), 103, 119. On the X Club, see Frankland’s autobiography.
MS material is located in London in the Royal Institution (where the Tyndall papers may also be found), the Royal Society, and Imperial College archives. Other archives containing MS papers are those at Liverpool University (the Reade papers), the Lancaster Public Library (the Lancastrian Frankland Society), and the Sir J. N. Lockyer Observatory, Sidmouth. Unlisted papers held by the Frankland family are not yet available for study. Oddments of Frankland’s apparatus are to be found at the Royal Institution and the City of Lancaster Museum.
II. Secondary Literature. The best obituaries are J. Wislicenus, in Berichte der Deutschen chemischen Gesellschaft, 33 (1900), 3847–3874, with photograph and list of papers; H. McLeod, in Journal of the Chemical Society 87 (1905), 574–590; and [J. R. Japp], in Minutes of Proceedings of the Institution of Civil Engineers, 139 (1900), 343–349. A full version of H. E. Armstrong’s Frankland memorial lecture to the Chemical Society was never published, but see his interesting “First Frankland Memorial Oration to the Lancastrian Frankland Society”, in Journal of the Society of Chemical Industry, 53 (1934), 459–466. See also Sir W. Tilden, Famous Chemists (London, 1921), pp. 216–227; and J. R. Partington, A History of Chemistry, IV (London-New York, 1964), ch. 16. For an extremely thorough analysis of Frankland’s contributions to valence theory, see C. A. Russell, History of Valency (Leicester, 1971). Frankland’s period as a schoolteacher is sketched in D. Thompson, “Queenwood College, Hampshire”, in Annals of Science, 11 (1955), 246–254; and his contribution to biochemistry in E. McCollum, A History of Nutrition (Boston, 1957), pp. 127–129. For Frankland’s activities on behalf of professional chemists, see R. B. Pilcher, The Institute of Chemistry of Great Britain and Ireland, History of the Institute, 1877–1914 (London, 1914), passim.
W. H. Brock
Cite this article
Pick a style below, and copy the text for your bibliography.
|
Pistil Factors Controlling Pollination
Magazine article from: Plant Cell; 1/1/2004; ; 700+ words
; ...and Neiland, 2002). The pistil, the pollen-accepting organ...carpels that bear the ovules. Pistil development initiates with...fusion occurs very early in pistil development. Even in species with single pistils, fusion of the carpel margins...
|
|
Class III pistil-specific extensin-like proteins from tobacco have characteristics of Arabinogalactan proteins
Magazine article from: Plant Physiology; 4/1/2001; ; 700+ words
; ...encoding for the class III pistil-- specific extensin...accumulation of PELPIII in the pistil transmitting tissue begins during the early stages of pistil maturation. At flower anthesis...stylar IM of non-pollinated pistils. After pollination the...
|
|
A Selfish Gene Governing Pollen-Pistil Compatibility Confers Reproductive Isolation Between Maize Relatives
Magazine article from: Genetics; 1/1/2006; ; 700+ words
; ...the six is present in the pistil, pollen not having that...effect. On Gal-s Gal-s pistils, gal pollen fails to effect...generically P for pollen-pistil recognition) is illustrated...PP offspring since their pistils are unreceptive to p pollen...
|
|
STIG1 Controls Exudate Secretion in the Pistil of Petunia and Tobacco1[w]
Magazine article from: Plant Physiology; 5/1/2005; ; 700+ words
; ...Many interactions between pollen and pistil have evolved to ensure successful sexual...grains and enables successful pollen-pistil interactions (Wolters-Arts et al...other components present in the pollen-pistil environment, such as the exudate, may...
|
|
Portland's Pistils Nursery.(shopping)
Magazine article from: Country Living; 3/1/2006; ; 700+ words
; ...says Megan. In 2002, Megan opened Pistils Nursery and set out to create a sustainable...seeds & more Come springtime, Pistils overflows with perennials, vegetable...ILLUSTRATION OMITTED] getting to Pistils Located just north of downtown Portland...
|
|
Genome-Wide Identification of Genes Expressed in Arabidopsis Pistils Specifically along the Path of Pollen Tube Growth1[w]
Magazine article from: Plant Physiology; 6/1/2005; ; 700+ words
; ...development is dependent on successful pollen-pistil interactions. In crucifers, the pollen...high degree of specificity in pollen-pistil interactions and the precision of directional...pollen/pollen tubes and cells of the pistil that line their path. However, with...
|
|
Pistil attraction. (ocular proof).(Brief Article)
Magazine article from: Look Japan; 12/1/2001; 700+ words
; Pistil attraction In flowering plants, guidance...pollen tube completed its journey down the pistil to reach the embryo sac. The University...tube as the final step of guidance in the pistil. Higashiyama and his group used Torenia...
|
|
Pollen-pistil interactions result in reproductive isolation between Sorghum bicolor and divergent Sorghum species.
Magazine article from: Crop Science; 7/1/2005; ; 700+ words
; ...of this research were to observe pollen germination and tube growth of divergent Sorghum species in sorghum pistils to determine if pistil-pollen interactions are reproductive barriers to producing interspecific hybrids. MATERIALS AND METHODS...
|
|
Pistil-Packing Thieves Just Uproot and Leave
Newspaper article from: The Washington Post; 4/29/2006; ; 700+ words
; You hear of caladiums being snatched from the soil in Silver Spring and junipers getting hijacked from a Beltsville nursery; you check out the crime report in Fairfax County and, just about every week this spring, you read where some dirtbag has purloined plants or lifted leafy things. Plantnapping
|
|
`Marigolds': Hot as a Pistil
Newspaper article from: The Washington Post; 3/22/1996; ; 661 words
; Beatrice Hunsdorfer, the sad monster of a mother at the center of Paul Zindel's "The Effect of Gamma Rays on Man-in-the-Moon Marigolds," is one of those roles into which an actress can really sink her choppers. Sada Thompson's chilling portrayal of Beatrice in the 1970 off-Broadway production made
|
|
pistil
Book article from: The Columbia Encyclopedia, Sixth Edition
...s) in the ovule. A pistil is composed of one or...have one or more simple pistils, each a separate organ...higher orders, a compound pistil, formed of several fused...that has one or more pistils but no stamens (or nonfunctional...flower, in which the pistil is nonfunctional or absent...
|
|
Flower
Encyclopedia entry from: UXL Encyclopedia of Science
...living organisms. Ovary: Base part of the pistil that bears ovules and develops into a...inside the sepals that is often colored. Pistil: Female reproductive organ of flowers...and filament. Stigma: Top part of the pistil upon which pollen lands and germinates...
|
|
stamen
Book article from: The Columbia Encyclopedia, Sixth Edition
...It is typically located between the central pistil and the surrounding petals. A stamen consists...pollination; e.g., they may be longer than the pistil or may be so placed in relation to the pistil (as in the mountain laurel and the lady...
|
|
Fruits
Book article from: Biology
...SIMPLE From a single pistil DRY INDEHISCENT...fusion of several separate pistils of one flower Raspberry...fusion of several separate pistils of several grouped flowers...the lower region of the pistil and the female sex organ...fruits derived from single pistils. In contrast to ...
|
|
fruit
Book article from: The Columbia Encyclopedia, Sixth Edition
...to form, the surrounding ovule (see pistil ) develops into a seed and the ovary wall...A flower may have one or more simple pistils or a compound pistil made up of two or more fused simple pistils (each called a carpel); different arrangements...
|