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1

Mayer, Michael. Farbe und Konstitution bei H-Chelaten der Pyrazinreihe: Präparative und spektroskopische Untersuchungen. Hartung-Gorre, 1985.

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2

Güven, Alâettin. Potentially tautomeric pyridazino (4,5-b) indolones. University of East Anglia, 1992.

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3

A, Graf Josef. Struktur-Funktionsbeziehungen zwischen Lipidmatrix und Pigment-Protein-Komplexen in Thylakoidmembranen: Physiologische und fluoreszenzspektroskopische Untersuchungen zur Wirkung von Pyridazinonen, Cytokininen und Cerulenin bei Petunia hybrida. [Biologisches Institut der Universität Stuttgart], 1987.

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4

Taylor, Edward C., Peter Wipf, and Desmond J. Brown. Supplement 1, Pyridazines. Wiley-Interscience, 1999.

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5

Castle, Raymond N. Pyridazines. Wiley & Sons, Incorporated, John, 2009.

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6

The pyridazines. Wiley, 2000.

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7

Tétényi, Péter. Polymers and Pyridazines. Jenny Stanford Publishing, 2019. http://dx.doi.org/10.1201/9780429296468.

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8

Tétényi, Péter. Polymers and Pyridazines. Jenny Stanford Publishing, 2019.

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9

Tétényi, Péter. Polymers and Pyridazines. Jenny Stanford Publishing, 2019.

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10

Tétényi, Péter. Polymers and Pyridazines. Jenny Stanford Publishing, 2019.

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11

Taylor, Edward C., Desmond J. Brown, and Jonathan A. Ellman. Pyridazines, Supplement 1. Wiley & Sons, Incorporated, John, 2007.

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12

Tétényi, Péter. Polymers and Pyridazines. Jenny Stanford Publishing, 2019.

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13

Polymers and Pyridazines. Taylor & Francis Group, 2019.

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14

The pyrazines. John Wiley & Sons, 2002.

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15

Castle, Raymond N. Chemistry of Heterocyclic Compounds, Pyridazines. Wiley & Sons, Incorporated, John, 2008.

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16

Liu, Siyu. Antithrombotic/antiplatelet properties and mechanism of action of tetramethylpyrazine, including structure-activity relationship studies. 1991.

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17

Castle, Raymond N. Condensed Pyridazines Including Cinnolines and Phthalazines. Wiley & Sons, Incorporated, John, 2009.

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18

Taylor, Edward C., Peter Wipf, and Desmond J. Brown. Cinnolines and Phthalazines: Chemistry of Heterocyclic Compounds, Supplement II (Chemistry of Heterocyclic Compounds: A Series Of Monographs). Wiley-Interscience, 2005.

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19

Castle, Raymond N. Chemistry of Heterocyclic Compounds, Condensed Pyridazines Including Cinnolines and Phthalazines. Wiley & Sons, Incorporated, John, 2008.

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20

Simpson, J. C. Pyridazine and Pyrazine Rings : (Cinnolines, Phthalazines, and Quinoxalines). Wiley & Sons, Incorporated, John, 2009.

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21

Simpson, J. C. Chemistry of Heterocyclic Compounds, Pyridazine and Pyrazine Rings. Wiley & Sons, Incorporated, John, 2008.

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22

Brown, D. J. Pyrazines, Supplement 1. Wiley & Sons, Incorporated, John, 2003.

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23

Brown, D. J. Pyrazines, Volume 58, Supplement 1. Wiley & Sons, Incorporated, John, 2003.

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24

Wu, Xiao-Feng, and Zechao Wang. Transition Metal Catalyzed Pyrimidine, Pyrazine, Pyridazine and Triazine Synthesis: Transition Metal-Catalyzed Heterocycle Synthesis Series. Elsevier, 2016.

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25

Eland, John H. D., and Raimund Feifel. Conjugated and aromatic molecules. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198788980.003.0006.

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In the vast majority of conjugated and aromatic molecules, the outermost occupied orbitals are either of π‎ character or non-bonding lone pairs belonging to heteroatoms. These are the orbitals from which double ionisation gives rise to most of the distinct bands that can be discerned in their spectra. Double photoionisation spectra of ethylene, butadiene, pyrrole, furan, thiophene, benzene, hexafluorobenzene, toluene, pyridine, pyrazine, pyrimidine, pyridazine, naphthalene, azulene, quinoline, biphenyl, TDME, iron pentacarbonyl, ferrocene, and TMPPD are presented with analysis where possible.
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26

Ansell, Martin F. Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds : Heterocyclic Compounds : Part I: Six-Membered Heterocyclic Compounds with Two Hetero-Atoms from Group V of the Periodic Table: The Pyridazine and Pyrimidine Groups. Elsevier Publishing Company, 1995.

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