Log in

Relevant bibliographies by topics / Butatrienone / Journal articles

Journal articles on the topic 'Butatrienone'

To see the other types of publications on this topic, follow the link: Butatrienone.

Author: Grafiati

Published: 10 December 2022

Last updated: 29 January 2023

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Butatrienone.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Brown, RFC, KJ Coulston, FW Eastwood, ADE Pullin, and AC Staffa. "Argon Matrix Study of the Infrared Spectrum of Butatrienone." Australian Journal of Chemistry 43, no. 3 (1990): 561. http://dx.doi.org/10.1071/ch9900561.

Full text

Abstract:

Butatrienone, H2C=C=C=C=O, was generated by pyrolysis of each of six different precursors in a stream of argon at temperatures in the range 710-880°C, and the pyrolysate-argon mixture was condensed on a Csl plate at c. 10 K. Infrared spectra were obtained between 4000 and 250 cm-1. Two precursors, buta-2,3-dienoic trifluoracetic anhydride (1) and buta-2,3-dienoyl chloride (2), gave pyrolysates showing a spectrum consisting of six strong bands and five weak bands. Four precursors, bicyclo [2.2.1]hept-5′-en-2′-ylideneacetic trifluoracetic anhydride (3), 5-( bicyclo [2.2.1]hept-5′-en-2′-ylidene)-2,2-dimethyl-1,3-dioxan-4,6- dione (4),2,2-dimethyl-5-(7?-oxabicyclo[2.2.1]hept-5?-en-2?-ylidene)- 1,3-dioxan-4,6-dione (5) and 3,4-diazatricyclo[5.2.1.02,6]deca-3,8-diene-endo-cis-2,6-dicarboxylic anhydride (6) gave pyrolysates showing spectra consisting principally of the six strong bands. The observed bands assigned to matrix-isolated butatrienone were at 3105w, 3035s, 3010w, 2964w, 2242s, 1996w, 1495s, 1456s, 728s, 404w cm-1. Calculated frequencies, using various models, for butatrienone are reported and are used to make plausible assignments. The strongest band (v2) attributed to butatrienone was at 2242 cm-1 which was shifted to 2200 cm-1 in (1-13C) butatrienone.

APA, Harvard, Vancouver, ISO, and other styles

2

Brown, Ronald D., Peter D. Godfrey, Martin J. Ball, Stephen Godfrey, Donald McNaughton, Martin Rodler, Burkhard Kleiboemer, and Robert Champion. "Is butatrienone (H2C:C:C:C:O) kinked?" Journal of the American Chemical Society 108, no. 21 (October 1986): 6534–38. http://dx.doi.org/10.1021/ja00281a015.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Anderson, MR, RFC Brown, NR Browne, FW Eastwood, GD Fallon, DPC Gan, ADE Pullin, and AC Staffa. "The Pyrolysis of Butatrienone Precursors: 3,4-Diazatricyclo[5.2.1.02,6]deca-3,8-diene-endo-cis-2,6-dicarboxylic anhydride and Its 5,5-Diphenyl Derivative." Australian Journal of Chemistry 43, no. 3 (1990): 549. http://dx.doi.org/10.1071/ch9900549.

Full text

Abstract:

Flash vacuum pyrolysis of the title anhydride (4) gave a poor yield of butatrienone , detected by argon matrix isolation infrared spectroscopy. Similar pyrolysis of the 5,5-diphenyl derivative (8) failed to give diphenylbutatrienone ; the red product (16) is considered to have been formed by dimerization of an intermediate 2H-indenylidenemethanone (15). The crystal structure of (16) has been determined.

APA, Harvard, Vancouver, ISO, and other styles

4

Şahin, Sevgi, Erdi A. Bleda, Zikri Altun, and Carl Trindle. "Computational characterization of isomeric C4 H2 O systems: Thermochemistry, vibrational frequencies, and optical spectra for butatrienone, ethynyl ketene, butadiynol, and triafulvenone." International Journal of Quantum Chemistry 116, no. 6 (December 29, 2015): 444–51. http://dx.doi.org/10.1002/qua.25063.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

KATAGIRI, HIDEKI, YUKIHIRO SHIMOI, and SHUJI ABE. "A THEORETICAL STUDY OF BISTABILITY OF POLYDIACETYLENE: TCDU(poly(5,7-dodecadiyne-1,12-diyl-bis-phenylurethane)." International Journal of Modern Physics B 15, no. 28n30 (December 10, 2001): 3821–24. http://dx.doi.org/10.1142/s0217979201008755.

Full text

Abstract:

We performed a first-principles calculation of typical polydiacetylene (PDA), TCDU (poly(5,7-dodecadiyne-1,12-diyl-bis-phenylurethane)). Potential energy curves (PEC's) as a function of two bond lengths of the backbone chain are presented. The present PEC's show that TCDU has only an acetylene-type stable structure and a butatriene-type structure is unstable, consistent with our previous calculations with a geometry optimization procedure. This result is in contrast to the case of a hypothetical hydrogen-substituted PDA where a butatriene-type structure is obtained as a meta-stable structure.

APA, Harvard, Vancouver, ISO, and other styles

6

Herges, Rainer, and Christoph Hoock. "A Novel Butatriene Synthesis." Synthesis 1991, no. 12 (1991): 1151–52. http://dx.doi.org/10.1055/s-1991-28408.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Märkl, Gottfried, Hans Sejpka, S. Dietl, Bernd Nuber, and Manfred L. Ziegler. "1-Phospha-1,2,3-butatriene." Angewandte Chemie 98, no. 11 (November 1986): 1020–21. http://dx.doi.org/10.1002/ange.19860981124.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Märkl, Gottfried, Hans Sejpka, Stefan Dietl, Bernd Nuber, and Manfred L. Ziegler. "1-Phospha-1,2,3-butatriene." Angewandte Chemie International Edition in English 25, no. 11 (November 1986): 1003–4. http://dx.doi.org/10.1002/anie.198610031.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Ibis, Cemil, Cigdem Sayil, and N. Gulsah Deniz. "Crystal Structures of Tetrakis‐(4‐chlorophenylthio)‐butatriene and Tetrakis‐(tert‐butylthio)‐butatriene." Spectroscopy Letters 39, no. 4 (August 1, 2006): 299–309. http://dx.doi.org/10.1080/00387010600779146.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Herges, Rainer, and Christoph Hoock. "Butatriene durch Desulfurierung cyclischer Trithiocarbonate." Angewandte Chemie 104, no. 12 (December 1992): 1652–54. http://dx.doi.org/10.1002/ange.19921041223.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Saalfrank, Rolf W., Andreas Welch, and Martin Haubner. "Butatriene durch Cumuhomologisierung von Propadienen." Angewandte Chemie 107, no. 23-24 (December 15, 1995): 2937–38. http://dx.doi.org/10.1002/ange.19951072339.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

HERGES, R., and C. HOOCK. "ChemInform Abstract: A Novel Butatriene Synthesis." ChemInform 23, no. 26 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199226105.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Pollack, Steven K., Ashebir Fiseha, and Babu Narayanswamy. "Butatriene-Based Polymer Chemistry. 2. Synthesis and Characterization of Poly[1,1,4,4-bis(pentamethylene)-1,2,3-butatriene]†,1." Macromolecules 30, no. 18 (September 1997): 5265–70. http://dx.doi.org/10.1021/ma9703766.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Sekiguchi, Akira, Masanobu Tanaka, and Tsukasa Matsuo. "Reduction of tetrakis(trimethylsilyl)butatriene by lithium: Monomeric and dimeric structures of the dilithium butatriene dianion." Silicon Chemistry 1, no. 5/6 (September 2002): 345–50. http://dx.doi.org/10.1023/b:silc.0000025572.57106.48.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Tokitoh, Norihiro, Hiroshi Hayakawa, Midori Goto, and Wataru Ando. "Molecular Structure of Novel 1,2,3-Butatriene Episulfides." Chemistry Letters 17, no. 6 (June 5, 1988): 961–64. http://dx.doi.org/10.1246/cl.1988.961.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Mizuno, Kazuhiko, Hajime Maeda, Hikaru Sugita, Shogo Nishioka, Takayoshi Hirai, and Akira Sugimoto. "Photorearrangement of Vinylidenecyclopropanes to 1,2,3-Butatriene Derivatives." Organic Letters 3, no. 4 (February 2001): 581–84. http://dx.doi.org/10.1021/ol000379u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Leroyer, Léo, Valérie Maraval, and Remi Chauvin. "Synthesis of the Butatriene C4Function: Methodology and Applications." Chemical Reviews 112, no. 3 (October 31, 2011): 1310–43. http://dx.doi.org/10.1021/cr200239h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Deniz, N. G., C. M. Sayil, and C. Ibis. "Crystal structure of a tetrakis(4-chlorophenylthio) butatriene compound." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (August 23, 2005): c290. http://dx.doi.org/10.1107/s0108767305087635.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Tokitoh, Norihiro, Hiroshi Hayakawa, and Wataru Ando. "New aspects in the tautomerism of 1,2,3-butatriene episulfides." Tetrahedron Letters 29, no. 40 (January 1988): 5161–64. http://dx.doi.org/10.1016/s0040-4039(00)80708-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Märkl, G., and U. Herold. "1-phospha-1,2-butadiene - 1-phospha- 1,2, 5-butatriene." Tetrahedron Letters 29, no. 24 (January 1988): 2935–38. http://dx.doi.org/10.1016/0040-4039(88)85051-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

ISLAM, NAZRUL, MASAO TSUKAYAMA, and YASUHIKO KAWAMURA. "CHARGE-TRANSFER REACTION OF BUTATRIENE: FORMATION OF DIHYDRONAPHTHALENE DERIVATIVE." International Journal of Modern Physics B 20, no. 25n27 (October 30, 2006): 4619–24. http://dx.doi.org/10.1142/s0217979206041781.

Full text

Abstract:

The charge-transfer reaction of tetraarylbutatriene 1 with tetracyanoethene (TCNE) in dichloromethane at room temperature was studied and we found a novel addition reaction. A red crystalline material 2 was isolated as an intermediate product which is converted slowly into dihydronaphthalene derivative 3 in dichloromethane but rapidly in protic solvent. The structure of the compounds was determined by X-ray crystallography. The detailed structure and the plausible reaction mechanism have also been discussed.

APA, Harvard, Vancouver, ISO, and other styles

22

Mirejovsky, D., W. Drenth, and F. B. van Duijneveldt. "MO-SCF calculations on protonated butatriene and 1,2,3-pentatriene." Recueil des Travaux Chimiques des Pays-Bas 98, no. 6 (September 2, 2010): 388–92. http://dx.doi.org/10.1002/recl.19790980604.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Suzuki, Noriyuki, Hidekazu Tezuka, Yoshiyuki Fukuda, Hajime Yoshida, Masakazu Iwasaki, Masahiko Saburi, Meguru Tezuka, Teiji Chihara, and Yasuo Wakatsuki. "An Unprecedented Dimerization of 1,2,3-Butatriene Catalyzed by Palladium Complexes." Chemistry Letters 33, no. 11 (November 2004): 1466–67. http://dx.doi.org/10.1246/cl.2004.1466.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Wrobel, Roman, Wolfram Sander, Dieter Cremer, and Elfi Kraka. "Photochemistry of Butatriene − Spectroscopic Evidence for the Existence of Allenylcarbene†." Journal of Physical Chemistry A 104, no. 16 (April 2000): 3819–25. http://dx.doi.org/10.1021/jp9940147.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Onuma, Kaoru, Katsunori Suzuki, and Makoto Yamashita. "Dimesitylboryl- and Amino-substituted Acetylene Having Butatriene-type Resonance Contribution." Chemistry Letters 44, no. 3 (March 5, 2015): 405–7. http://dx.doi.org/10.1246/cl.141063.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Sakurai, Hideki, Muneo Kudo, Kenkichi Sakamoto, Yasuhiro Nakadaira, Mitsuo Kira, and Akira Sekiguchi. "A Facile Synthesis of Tetrakis(trimethylsilyl)butatriene Properties and Cycloadditions." Chemistry Letters 17, no. 8 (August 5, 1988): 1441–44. http://dx.doi.org/10.1246/cl.1988.1441.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Maercker, Adalbert, and Ralf Dujardin. "2,3-Dilithio-1,3-butadiene durch Addition von Lithium an Butatriene." Angewandte Chemie 97, no. 7 (July 1985): 612–13. http://dx.doi.org/10.1002/ange.19850970738.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Leroyer, Leo, Valerie Maraval, and Remi Chauvin. "ChemInform Abstract: Synthesis of the Butatriene C4Function: Methodology and Applications." ChemInform 43, no. 22 (May 3, 2012): no. http://dx.doi.org/10.1002/chin.201222222.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Schmidbaur, Hubert, Stefan Manhart, and Annette Schier. "New Organophosphorus Ligands: 1,1,4,4-Tetrakis(diphenylphosphanyl)butatriene and Its Tetrasulfide." Chemische Berichte 126, no. 11 (November 1993): 2389–91. http://dx.doi.org/10.1002/cber.19931261107.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Sayil, C. M., N. G. Deniz, and C. Ibis. "Crystal structure and properties of a tetrakis(tert-butylthio) butatriene compound." Acta Crystallographica Section A Foundations of Crystallography 61, a1 (August 23, 2005): c290. http://dx.doi.org/10.1107/s0108767305087647.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Liang, Congxin, Yaoming Xie, Henry F. Schaefer, Kwang S. Sim, and Ho Soon Kim. "Vibrational spectra of butatriene (C4H4) and pentatetraene (C5H4): is pentatetraene bent?" Journal of the American Chemical Society 113, no. 7 (March 1991): 2452–59. http://dx.doi.org/10.1021/ja00007a016.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Ando, Wataru, Hiroshi Hayakawa, and Norihiro Tokitoh. "A novel formation of 1,2,3-butatriene episulfides by thionation of methylenecyclopropanones." Tetrahedron Letters 28, no. 16 (January 1987): 1803–5. http://dx.doi.org/10.1016/s0040-4039(00)95426-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Maeda, Hajime, Shogo Nishioka, and Kazuhiko Mizuno. "Regioselective photoaddition of alcohols to 1,2,3-butatriene derivatives via photoinduced electron transfer." Tetrahedron Letters 44, no. 35 (August 2003): 6601–3. http://dx.doi.org/10.1016/s0040-4039(03)01668-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

SCHMIDBAUR, H., S. MANHART, and A. SCHIER. "ChemInform Abstract: New Organophosphorus Ligands: 1,1,4,4-Tetrakis(diphenylphosphanyl) butatriene and Its Tetrasulfide." ChemInform 25, no. 22 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199422194.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Kubozono, Y., T. Miyamoto, T. Shinmyozu, M. Aoyagi, Y. Gondo, H. Takemura, and M. Shiotani. "An ESR and MO study of the butatriene and tetramethylbutatriene radical cations." Spectrochimica Acta Part A: Molecular Spectroscopy 49, no. 8 (July 1993): 1187–90. http://dx.doi.org/10.1016/0584-8539(93)80078-o.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Araki, M., S. Uchida, N. Kondo, Y. Matsushita, K. Abe, K. Ito, and K. Tsukiyama. "Developments of Optical Spectrometers as Approaches to Diffuse Interstellar Bands." Proceedings of the International Astronomical Union 9, S297 (May 2013): 291–93. http://dx.doi.org/10.1017/s1743921313016013.

Full text

Abstract:

AbstractA discharge-emission spectrometer and a cavity ringdown spectrometer have been developed to aid in the solution to the diffuse interstellar band (DIB) problem. A hollow cathode was used to generate molecular ions in a discharge because it has been suggested that molecular ions are probable DIB candidates. The discharge was produced by a pulsed voltage of 1300–1500 V. A wide wavelength range of optical emission from the discharge was examined by a HORIBA Jobin Yvon iHR320 monochromator. The dispersed discharge emission was detected by a photomultiplier and was recorded via a lock-in amplifier. The 2B3u–X2B2g electronic transition of the butatriene cation H2CCCCH2+ was observed in the discharge emission of 2-butyne H3CCCCH3. The frequency of the electronic transition was measured to be 20381 cm−1, and a comparison study was made with known DIB spectra.The resolution of the discharge-emission spectrometer is insufficient to make precise comparisons between laboratory frequencies and astronomically observed DIB spectra. We therefore developed the cavity ringdown spectrometer using the same hollow cathode. The high sensitivity of this spectrometer was confirmed by the observation of the forbidden band of O2.

APA, Harvard, Vancouver, ISO, and other styles

37

Jing-cui, Peng. "The Butatriene-to-Acetylene Transition in Polydiacetylene Due to Thermal and Quantum Fluctuation." Communications in Theoretical Physics 8, no. 1 (July 1987): 119–26. http://dx.doi.org/10.1088/0253-6102/8/1/119.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Kusumoto, Tetsuo, and Tamejiro Hiyama. "Reduction and oxidation of carbon-carbon double bonds of 1,1,4,4-tetrakis(trimethylsilyl)butatriene." Tetrahedron Letters 28, no. 16 (January 1987): 1811–12. http://dx.doi.org/10.1016/s0040-4039(00)95428-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Carlson, Heather A., Geoffrey E. Quelch, and Henry F. Schaefer. "How stable is cyclobutyne? The activation energy for the unimolecular rearrangement to butatriene." Journal of the American Chemical Society 114, no. 13 (June 1992): 5344–48. http://dx.doi.org/10.1021/ja00039a053.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Katagiri, Hideki, Yukihiro Shimoi, and Shuji Abe. "A density functional study of backbone structures of polydiacetylene: destabilization of butatriene structure." Chemical Physics 306, no. 1-3 (November 2004): 191–200. http://dx.doi.org/10.1016/j.chemphys.2004.07.033.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Feldhaus, Philipp, Birgitta Schirmer, Birgit Wibbeling, Constantin G. Daniliuc, Roland Fröhlich, Stefan Grimme, Gerald Kehr, and Gerhard Erker. "Frustrated Lewis pair addition to conjugated diynes: Formation of zwitterionic 1,2,3-butatriene derivatives." Dalton Transactions 41, no. 30 (2012): 9135. http://dx.doi.org/10.1039/c2dt30321c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Osella, Domenico, Olimpia Gambino, Roberto Gobetto, Piero Zanello, Franco Laschi, Catherine E. Housecroft, and Steven M. Owen. "Investigation of the electrochemical behavior and electronic structure of (.mu.-butatriene)hexacarbonyldiiron complexes." Organometallics 9, no. 6 (June 1990): 1792–97. http://dx.doi.org/10.1021/om00156a017.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

LIANG, C., Y. XIE, H. F. III SCHAEFER, K. S. KIM, and H. S. KIM. "ChemInform Abstract: Vibrational Spectra of Butatriene (C4H4) and Pentatetraene (C5H4): Is Pentatetraene Bent?" ChemInform 22, no. 28 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199128032.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Awaji, Hiroshi, Toyonari Sugimoto, and Zen-Ichi Yoshida. "Ethenediylidene-2,2? -bis(1,3-dithiole) and butatriene-1,4-diylidene-2,2?-bis(1,3-dithiole)." Journal of Physical Organic Chemistry 1, no. 1 (January 1988): 47–51. http://dx.doi.org/10.1002/poc.610010108.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

van Loon, Jan-Dirk, Paul Seiler, and Fran�ois Diederich. "Tetrakis(trialkylsilylethynyl)butatriene and 1,1,4,4-Tetrakis(trialkylsilylethynyl)-1,3-butadiene: Novel Cross-Conjugated Chromophores." Angewandte Chemie International Edition in English 32, no. 8 (August 1993): 1187–89. http://dx.doi.org/10.1002/anie.199311871.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Yoshifuji, Masaaki, Kozo Toyota, Takahiko Uesugi, Ikuko Miyahara, and Ken Hirotsu. "X-Ray analysis of 1-phospha-1,2,3-butatriene as a ligand of carbonyltungsten complex." Journal of Organometallic Chemistry 461, no. 1-2 (November 1993): 81–84. http://dx.doi.org/10.1016/0022-328x(93)83277-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Connors, Robert E., Veeradej Chynwat, Christine H. Clifton, and Tracy L. Coffin. "Temperature dependence of aryl butatriene fluorescence: barrier to twisting on S1 for 1,1,4,4-tetraphenylbutatriene." Journal of Molecular Structure 443, no. 1-3 (February 1998): 107–13. http://dx.doi.org/10.1016/s0022-2860(97)00363-3.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Morimoto, Yoshihiro, Yoshiki Higuchi, Kuni Wakamatsu, Koichiro Oshima, Kiitiro Utimoto, and Noritake Yasuoka. "Structure of a Cumulene Bearing Bulky Substituents. X-Ray Study of 1,1,4,4-Tetrakis(trimethylsilyl)butatriene." Bulletin of the Chemical Society of Japan 62, no. 2 (February 1989): 639–41. http://dx.doi.org/10.1246/bcsj.62.639.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Filipkowski, Karol, Jan Fulara, and John P. Maier. "The C∼2B3u←X∼2B2g electronic absorption spectrum of butatriene cation in a neon matrix." Journal of Molecular Spectroscopy 310 (April 2015): 45–49. http://dx.doi.org/10.1016/j.jms.2015.01.009.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Eigemann, Sven-Eric, Walter Förtsch, Frank Hampel, and Rainer Schobert. "Novel Synthesis of (Butatriene)hexacarbonyldiiron Complexes. Stereochemical Aspects and an X-ray Crystal Structure Determination." Organometallics 15, no. 5 (January 1996): 1511–13. http://dx.doi.org/10.1021/om950679t.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!