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Adolf von Baeyer
Johann Friedrich Wilhelm Adolf von Baeyer (German: [ˈaːdɔlf fɔn ˈbaɪɐ] ⓘ; 31 October 1835 – 20 August 1917) was a German chemist who synthesised indigo and developed a nomenclature for cyclic compounds (that was subsequently extended and adopted as part of the IUPAC organic nomenclature). He was ennobled in the Kingdom of Bavaria in 1885 and was the 1905 recipient of the Nobel Prize in Chemistry.
Baeyer was born in Berlin as the son of the noted geodesist and captain of the Royal Prussian Army Johann Jacob Baeyer and his wife Eugenie Baeyer née Hitzig (1807–1843). Both his parents were Lutherans at the time of his birth and he was raised in the Lutheran religion. His mother was the daughter of Julius Eduard Hitzig and a member of the originally Jewish Itzig family, and had converted to Christianity before marrying his father, who was of non-Jewish German descent. Baeyer had four sisters: Clara (born 1826) Emma (born 1831), Johanna (Jeanette) (born 1839), Adelaide (died 1843) and two brothers: Georg (born 1829) and Edward (born 1832). Baeyer lost his mother at a young age while she was giving birth to his sister Adelaide.
Although his birth name was Johann Friedrich Wilhelm Adolf Baeyer, he was known simply as Adolf throughout most of his life. The poet Adelbert von Chamisso and the astronomer Friedrich Wilhelm Bessel were his godparents. On his 50th birthday he was raised to the hereditary nobility by King Ludwig II of Bavaria, conferring on him the "von" distinction.
Baeyer became interested in science early, performing experiments on plant nutrition at his paternal grandfather's Müggelsheim farm as a boy. In Berlin he began chemical experimentation at the age of nine. Three years later, he synthesized a previously unknown chemical compound -double carbonate of copper and sodium. On his 13th birthday, he initiated his lifework, buying a chunk of indigo worth two Thalers for his first dye experiments.
When a schoolboy, his chemistry teacher at the Friedrich Wilhelm Gymnasium appointed him as his assistant. After graduating from secondary school in 1853, he entered the Berlin University to study physics and mathematics. A stint in the Prussian army interrupted his study until 1856, when he returned to academia at the University of Heidelberg, intending to study chemistry under Robert Bunsen.[citation needed] After an argument with the renowned chemist he changed his mentor to August Kekulé. He continued to collaborate with Kekulé even after he returned to Berlin in 1858 for the completion of his doctorate on arsenic methyl chloride, or cacodylic chloride.
After completing his doctorate, he followed Kekulé to the University of Ghent, when Kekulé became professor there. He became a lecturer at the Gewerbeinstitut Berlin (Royal Trade Academy) in 1860 and a professor at the University of Strasbourg in 1871. In 1875, he succeeded Justus von Liebig as Chemistry Professor at the University of Munich.
Baeyer's chief achievements include the synthesis and description of the plant dye indigo, the discovery of the phthalein dyes, and the investigation of polyacetylenes, oxonium salts, nitroso compounds (1869) and uric acid derivatives (1860 and onwards) (including the discovery of barbituric acid (1864), the parent compound of the barbiturates). He was the first to propose the correct formula for indole in 1869, after publishing the first synthesis three years earlier. His contributions to theoretical chemistry include the 'strain' (Spannung) theory of triple bonds and strain theory in small carbon rings.
In 1871 he discovered the synthesis of phenolphthalein by condensation of phthalic anhydride with two equivalents of phenol under acidic conditions (hence the name). That same year he was the first to obtain synthetic fluorescein, a fluorophore pigment which is similar to naturally occurring pyoverdin that is synthesised by microorganisms (e.g., by some fluorescent strains of Pseudomonas). Baeyer named his finding "resorcinphthalein" as he had synthesised it from phthalic anhydride and resorcinol. The term fluorescein would not start to be used until 1878.
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Adolf von Baeyer
Johann Friedrich Wilhelm Adolf von Baeyer (German: [ˈaːdɔlf fɔn ˈbaɪɐ] ⓘ; 31 October 1835 – 20 August 1917) was a German chemist who synthesised indigo and developed a nomenclature for cyclic compounds (that was subsequently extended and adopted as part of the IUPAC organic nomenclature). He was ennobled in the Kingdom of Bavaria in 1885 and was the 1905 recipient of the Nobel Prize in Chemistry.
Baeyer was born in Berlin as the son of the noted geodesist and captain of the Royal Prussian Army Johann Jacob Baeyer and his wife Eugenie Baeyer née Hitzig (1807–1843). Both his parents were Lutherans at the time of his birth and he was raised in the Lutheran religion. His mother was the daughter of Julius Eduard Hitzig and a member of the originally Jewish Itzig family, and had converted to Christianity before marrying his father, who was of non-Jewish German descent. Baeyer had four sisters: Clara (born 1826) Emma (born 1831), Johanna (Jeanette) (born 1839), Adelaide (died 1843) and two brothers: Georg (born 1829) and Edward (born 1832). Baeyer lost his mother at a young age while she was giving birth to his sister Adelaide.
Although his birth name was Johann Friedrich Wilhelm Adolf Baeyer, he was known simply as Adolf throughout most of his life. The poet Adelbert von Chamisso and the astronomer Friedrich Wilhelm Bessel were his godparents. On his 50th birthday he was raised to the hereditary nobility by King Ludwig II of Bavaria, conferring on him the "von" distinction.
Baeyer became interested in science early, performing experiments on plant nutrition at his paternal grandfather's Müggelsheim farm as a boy. In Berlin he began chemical experimentation at the age of nine. Three years later, he synthesized a previously unknown chemical compound -double carbonate of copper and sodium. On his 13th birthday, he initiated his lifework, buying a chunk of indigo worth two Thalers for his first dye experiments.
When a schoolboy, his chemistry teacher at the Friedrich Wilhelm Gymnasium appointed him as his assistant. After graduating from secondary school in 1853, he entered the Berlin University to study physics and mathematics. A stint in the Prussian army interrupted his study until 1856, when he returned to academia at the University of Heidelberg, intending to study chemistry under Robert Bunsen.[citation needed] After an argument with the renowned chemist he changed his mentor to August Kekulé. He continued to collaborate with Kekulé even after he returned to Berlin in 1858 for the completion of his doctorate on arsenic methyl chloride, or cacodylic chloride.
After completing his doctorate, he followed Kekulé to the University of Ghent, when Kekulé became professor there. He became a lecturer at the Gewerbeinstitut Berlin (Royal Trade Academy) in 1860 and a professor at the University of Strasbourg in 1871. In 1875, he succeeded Justus von Liebig as Chemistry Professor at the University of Munich.
Baeyer's chief achievements include the synthesis and description of the plant dye indigo, the discovery of the phthalein dyes, and the investigation of polyacetylenes, oxonium salts, nitroso compounds (1869) and uric acid derivatives (1860 and onwards) (including the discovery of barbituric acid (1864), the parent compound of the barbiturates). He was the first to propose the correct formula for indole in 1869, after publishing the first synthesis three years earlier. His contributions to theoretical chemistry include the 'strain' (Spannung) theory of triple bonds and strain theory in small carbon rings.
In 1871 he discovered the synthesis of phenolphthalein by condensation of phthalic anhydride with two equivalents of phenol under acidic conditions (hence the name). That same year he was the first to obtain synthetic fluorescein, a fluorophore pigment which is similar to naturally occurring pyoverdin that is synthesised by microorganisms (e.g., by some fluorescent strains of Pseudomonas). Baeyer named his finding "resorcinphthalein" as he had synthesised it from phthalic anhydride and resorcinol. The term fluorescein would not start to be used until 1878.