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1

Smith, Alice M., Jürgen Agreiter e Vladimir E. Bondybey. "Laser-induced fluorescence of matrix-isolated HCCCCCN+ and HCCCCCCCN+". Chemical Physics Letters 244, n.º 5-6 (outubro de 1995): 379–87. http://dx.doi.org/10.1016/0009-2614(95)00915-q.

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2

Bartel, Christoph, Peter Botschwina, Hans Bürger, Antonio Guarnieri, Änne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak e El Bachir Mkadmi. "Cyanisocyanacetylen, N≡C−C≡C−N≡C". Angewandte Chemie 110, n.º 20 (16 de outubro de 1998): 3036–40. http://dx.doi.org/10.1002/(sici)1521-3757(19981016)110:20<3036::aid-ange3036>3.0.co;2-n.

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3

Bartel, Christoph, Peter Botschwina, Hans Bürger, Antonio Guarnieri, Änne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak e El Bachir Mkadmi. "Cyanoisocyanoacetylene, N≡C−C≡C−N≡C". Angewandte Chemie International Edition 37, n.º 20 (2 de novembro de 1998): 2879–82. http://dx.doi.org/10.1002/(sici)1521-3773(19981102)37:20<2879::aid-anie2879>3.0.co;2-0.

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4

Okabayashi, T., M. Tanimoto, K. Tanaka e E. Hirota. "Microwave spectroscopy of fluorocyanobutadiyne (F-CC-CC-CN)". Chemical Physics Letters 230, n.º 6 (dezembro de 1994): 530–35. http://dx.doi.org/10.1016/0009-2614(94)01205-9.

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5

Makovicky, Emil, e Sven Karup-Møller. "Exploratory studies of the Cu–Pd–Se system at 650°C, 550°C, 400°C, and 300°C". European Journal of Mineralogy 29, n.º 4 (10 de outubro de 2017): 645–52. http://dx.doi.org/10.1127/ejm/2017/0029-2651.

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6

Sinha, Narayan, Dorus Heijnen, Ben L. Feringa e Michael G. Organ. "Murahashi Cross‐Coupling at −78 °C: A One‐Pot Procedure for Sequential C−C/C−C, C−C/C−N, and C−C/C−S Cross‐Coupling of Bromo‐Chloro‐Arenes". Chemistry – A European Journal 25, n.º 39 (24 de junho de 2019): 9180–84. http://dx.doi.org/10.1002/chem.201901678.

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7

Bartel, Christoph, Peter Botschwina, Hans Buerger, Antonio Guarnieri, Aenne Heyl, Aiko Huckauf, Dieter Lentz, Tatjana Merzliak e El Bachir Mkadmi. "ChemInform Abstract: Cyanoisocyanoacetylene, NC-CC-NC." ChemInform 30, n.º 14 (16 de junho de 2010): no. http://dx.doi.org/10.1002/chin.199914088.

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8

Smith, Alice M., Günter Schallmoser, Anton Thoma e Vladimir E. Bondybey. "Infrared spectral evidence of N≡C–C≡C–N≡C: Photoisomerization of N≡C–C≡C–C≡N in an argon matrix". Journal of Chemical Physics 98, n.º 3 (fevereiro de 1993): 1776–85. http://dx.doi.org/10.1063/1.464266.

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9

A. Adrio, Luis, e King Kuok (Mimi) Hii. "Palladium-Catalyzed Heterofunctionalization of C-H, C=C and C≡ C Bonds". Current Organic Chemistry 15, n.º 18 (1 de setembro de 2011): 3337–61. http://dx.doi.org/10.2174/138527211797248003.

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10

Allen, Gregory W., Robert S. Armstrong, Manuel J. Aroney, Raymond K. Pierens e Alan J. Williams. "Polarisability anisotropies of C—H, C—C, C—Cl and C—Br bonds". J. Chem. Soc., Faraday Trans. 2 84, n.º 11 (1988): 1775–78. http://dx.doi.org/10.1039/f29888401775.

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11

TANABE, YASUHIRO, e EIICHI YASUDA. "C/C Composite". Sen'i Gakkaishi 44, n.º 11 (1988): P440—P443. http://dx.doi.org/10.2115/fiber.44.11_p440.

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12

Monnier, Florian, e Marc Taillefer. "Katalytische C-C-, C-N- und C-O-Ullmann-Kupplungen". Angewandte Chemie 121, n.º 38 (7 de setembro de 2009): 7088–105. http://dx.doi.org/10.1002/ange.200804497.

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13

Chen, Tieqiao, e Li-Biao Han. "Nickelkatalysierte C-O/C-H-Kreuzkupplungen zur C-C-Bindungsbildung". Angewandte Chemie 127, n.º 30 (12 de junho de 2015): 8722–24. http://dx.doi.org/10.1002/ange.201503204.

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14

Monnier, Florian, e Marc Taillefer. "Katalytische C-C-, C-N- und C-O-Ullmann-Kupplungen". Angewandte Chemie 120, n.º 17 (14 de abril de 2008): 3140–43. http://dx.doi.org/10.1002/ange.200703209.

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15

Karamanis, Panaghiotis, e George Maroulis. "Single (C–C) and triple (CC) bond-length dependence of the static electric polarizability and hyperpolarizability of H–CC–CC–H". Chemical Physics Letters 376, n.º 3-4 (julho de 2003): 403–10. http://dx.doi.org/10.1016/s0009-2614(03)00784-x.

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16

SMITH, A. M., G. SCHALLMOSER, A. THOMA e V. E. BONDYBEY. "ChemInform Abstract: IR Spectral Evidence of NC-CC-NC: Photoisomerization of NC-CC-CN in an Argon Matrix." ChemInform 24, n.º 28 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199328112.

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17

Kulchat, Sirinan, Kamel Meguellati e Jean-Marie Lehn. "Organocatalyzed and Uncatalyzed CC/CC and CC/CN Exchange Processes betweenKnoevenageland Imine Compounds in Dynamic Covalent Chemistry". Helvetica Chimica Acta 97, n.º 9 (setembro de 2014): 1219–36. http://dx.doi.org/10.1002/hlca.201400187.

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18

Nguyen, Trang T., Jeffery A. Bertke, Danielle L. Gray e Kami L. Hull. "Facile C–H, C–F, C–Cl, and C–C Activation by Oxatitanacyclobutene Complexes". Organometallics 34, n.º 17 (26 de agosto de 2015): 4190–93. http://dx.doi.org/10.1021/acs.organomet.5b00470.

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19

Savitskiy, V. O., e D. V. Sidorov. "Incremental source code analysis for C/C++ languages". Proceedings of the Institute for System Programming of RAS 22 (2012): 119–30. http://dx.doi.org/10.15514/ispras-2012-22-8.

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20

Reed, Ishmael. "The C above C above High C". Antioch Review 57, n.º 3 (1999): 333. http://dx.doi.org/10.2307/4613883.

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21

Reed, Ishmael. "The C above C above High C". Antioch Review 59, n.º 2 (2001): 460. http://dx.doi.org/10.2307/4614179.

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22

Yeang, Calvin, Joseph L. Witztum e Sotirios Tsimikas. "‘LDL-C’ = LDL-C + Lp(a)-C". Current Opinion in Lipidology 26, n.º 3 (junho de 2015): 169–78. http://dx.doi.org/10.1097/mol.0000000000000171.

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23

Cataldo, F. "Structural relationships between dicopper diacetylide (Cu-C≡C-C≡C-Cu) and dicopper acetylide (Cu-C≡C-Cu)". European Journal of Solid State and Inorganic Chemistry 35, n.º 3 (março de 1998): 281–91. http://dx.doi.org/10.1016/s0992-4361(98)80009-x.

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24

Dembitsky, Valery M., Hijazi Abu Ali e Morris Srebnik. "Recent developments in bisdiborane chemistry: B?C?B, B?C?C?B, B?C?C?B and B?C?C?B compounds". Applied Organometallic Chemistry 17, n.º 6-7 (2003): 327–45. http://dx.doi.org/10.1002/aoc.430.

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25

Kulchat, Sirinan, Kamel Meguellati e Jean-Marie Lehn. "Erratum: Organocatalyzed and Uncatalyzed CC/CC and CC/CN Exchange Processes betweenKnoevenageland Imine Compounds in Dynamic Covalent Chemistry". Helvetica Chimica Acta 98, n.º 1 (janeiro de 2015): 153. http://dx.doi.org/10.1002/hlca.201590000.

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26

Yokota, Akira, Emiko Hiyama e Makoto Oka. "Possible Existence of $${(c\bar{c})}$$ ( c c ¯ ) –Nucleus Bound States". Few-Body Systems 55, n.º 8-10 (10 de maio de 2014): 761–65. http://dx.doi.org/10.1007/s00601-014-0895-2.

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27

Cataldo, F. "From dicopper diacetylide (Cu-C≡C-C≡C-Cu) to carbyne". European Journal of Solid State and Inorganic Chemistry 35, n.º 3 (março de 1998): 293–304. http://dx.doi.org/10.1016/s0992-4361(98)80018-0.

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28

Okabayashi, Toshiaki, Noriko Yamashita, Yoshiko Sakai e Mitsutoshi Tanimoto. "Millimeter-Wave Spectrum of Fluorodiacetylene (HCCCCF)". Journal of Molecular Spectroscopy 193, n.º 2 (fevereiro de 1999): 273–76. http://dx.doi.org/10.1006/jmsp.1998.7738.

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29

Thomas, Phillip S., Nathan P. Bowling, Nicola J. Burrmann e Robert J. McMahon. "Dialkynyl Carbene Derivatives: Generation and Characterization of Triplettert-Butylpentadiynylidene (t-Bu−C≡C−C̈−C≡C−H) and Dimethylpentadiynylidene (Me−C≡C−C̈−C≡C−Me)". Journal of Organic Chemistry 75, n.º 19 (outubro de 2010): 6372–81. http://dx.doi.org/10.1021/jo101096n.

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30

Shaimov, A. Yu. "ORGANIZATION AND MAINTENANCE OF PROGRAM TIMERS IN C/C++". Vektor of development 1, n.º 12 (2023): 129–34. http://dx.doi.org/10.53852/2782-3962-2023-1-12-129-134.

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31

KOGO, Yasuo, Akihiro KIKKAWA, Wataru SAITO e Hiroshi HATTA. "Tensile properties of monofilament C/C composites". Proceedings of Conference of Kanto Branch 2004.10 (2004): 347–48. http://dx.doi.org/10.1299/jsmekanto.2004.10.347.

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32

Wang, Wen-Xue, Yoshihiro Takao e Terutake Matsubara. "Tensile strength and fracture toughness of C/C and metal infiltrated composites Si–C/C and Cu–C/C". Composites Part A: Applied Science and Manufacturing 39, n.º 2 (fevereiro de 2008): 231–42. http://dx.doi.org/10.1016/j.compositesa.2007.11.004.

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33

Bürger, Hans, Dieter Lentz, Britta Meisner, Natascha Nickelt, Dagmar Preugschat e Michael Senzlober. "Syntheses and1H-,13C- and15N-NMR Spectra of Ethynyl Isocyanide, H−C≡C−N≡C, D−C≡C−N≡C and Prop-1-ynyl Isocyanide, H3C−C≡C−N≡C, D3C−C≡C−N≡C: High Resolution Infrared Spectrum of Prop-1-ynyl Isocyanide". Chemistry - A European Journal 6, n.º 18 (15 de setembro de 2000): 3377–85. http://dx.doi.org/10.1002/1521-3765(20000915)6:18<3377::aid-chem3377>3.0.co;2-1.

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34

Lussier, L. S., C. Sandorfy, H. OA L E-Thanh e D. Vocelle. "THE EFFECT OF ACIDS ON THE INFRARED SPECTRA OF SCHIFF BASES—II. IMINES CONTAINING THE C=C-C=N AND C=C-C=C-C=N UNITS". Photochemistry and Photobiology 45, s1 (maio de 1987): 801–8. http://dx.doi.org/10.1111/j.1751-1097.1987.tb07886.x.

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35

Yam, Vivian Wing-Wah, Samuel Hung-Fai Chong, Chi-Chiu Ko e Kung-Kai Cheung. "Synthesis and Luminescence Behavior of Rhenium(I) Triynyl Complexes. X-ray Crystal Structures of [Re(CO)3(tBu2bpy)(C⋮C−C⋮C−C⋮CPh)] and [Re(CO)3(Me2bpy)(C⋮C−C⋮C−C⋮CSiMe3)]". Organometallics 19, n.º 24 (novembro de 2000): 5092–97. http://dx.doi.org/10.1021/om000725b.

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36

Nodelman, Vladimir. "OOP via C++, C#...?" ACM SIGCSE Bulletin 36, n.º 3 (setembro de 2004): 255. http://dx.doi.org/10.1145/1026487.1008087.

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37

RITTER, STEPHEN K. "EXTREME C–C BONDS". Chemical & Engineering News 87, n.º 19 (11 de maio de 2009): 32–33. http://dx.doi.org/10.1021/cen-v087n019.p032.

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38

Accardi, Luigi, Ameur Dhahri e Habib Rebei. "$$C^*$$ C ∗ -Quadratic Quantization". Journal of Statistical Physics 172, n.º 5 (23 de julho de 2018): 1187–209. http://dx.doi.org/10.1007/s10955-018-2085-y.

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39

Kaupp, Gerd, e Jürgen Boy. "Überlange C-C-Einfachbindungen". Angewandte Chemie 109, n.º 1-2 (13 de janeiro de 1997): 48–50. http://dx.doi.org/10.1002/ange.19971090108.

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40

Huntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott e Roald Hoffmann. "Squeezing CC Bonds". Angewandte Chemie 117, n.º 46 (25 de novembro de 2005): 7721–25. http://dx.doi.org/10.1002/ange.200502721.

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41

Huntley, Deborah R., Georgios Markopoulos, Patrick M. Donovan, Lawrence T. Scott e Roald Hoffmann. "Squeezing CC Bonds". Angewandte Chemie International Edition 44, n.º 46 (25 de novembro de 2005): 7549–53. http://dx.doi.org/10.1002/anie.200502721.

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42

Liu, Liang, Hui Chen, Zhenqiang Yang, Junnian Wei e Zhenfeng Xi. "C,C- and C,N-Chelated Organocopper Compounds". Molecules 26, n.º 19 (25 de setembro de 2021): 5806. http://dx.doi.org/10.3390/molecules26195806.

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Resumo:
Copper-catalyzed and organocopper-involved reactions are of great significance in organic synthesis. To have a deep understanding of the reaction mechanisms, the structural characterizations of organocopper intermediates become indispensable. Meanwhile, the structure-function relationship of organocopper compounds could advance the rational design and development of new Cu-based reactions and organocopper reagents. Compared to the mono-carbonic ligand, the C,N- and C,C-bidentate ligands better stabilize unstable organocopper compounds. Bidentate ligands can chelate to the same copper atom via η2-mode, forming a mono-cupra-cyclic compounds with at least one acute C-Cu-C angle. When the bidentate ligands bind to two copper atoms via η1-mode at each coordinating site, the bimetallic macrocyclic compounds will form nearly linear C-Cu-C angles. The anionic coordinating sites of the bidentate ligand can also bridge two metals via μ2-mode, forming organocopper aggregates with Cu-Cu interactions and organocuprates with contact ion pair structures. The reaction chemistry of some selected organocopper compounds is highlighted, showing their unique structure–reactivity relationships.
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43

DePinto, Jeffrey T., Wendy A. deProphetis, Jessica L. Menke e Robert J. McMahon. "Triplet 1,3-Diphenylpropynylidene (Ph−C−C−C−Ph)". Journal of the American Chemical Society 129, n.º 8 (fevereiro de 2007): 2308–15. http://dx.doi.org/10.1021/ja066300j.

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44

Zheng, Qing-Zhong, e Ning Jiao. "Ag-catalyzed C–H/C–C bond functionalization". Chemical Society Reviews 45, n.º 16 (2016): 4590–627. http://dx.doi.org/10.1039/c6cs00107f.

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45

Smith, William B. "Publication is as easy as C-C-C". Communications in Statistics - Simulation and Computation 26, n.º 1 (janeiro de 1997): xi—xvi. http://dx.doi.org/10.1080/03610919708813363.

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46

Yiwen, Mou, e T. Y. Hsu (Xu Zuyao). "C-C interaction energy in FeC alloys". Acta Metallurgica 34, n.º 2 (fevereiro de 1986): 325–31. http://dx.doi.org/10.1016/0001-6160(86)90203-8.

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47

Majek, Michal, e Axel Jacobi von Wangelin. "Lichtvermittelte kupferkatalysierte C-C- und C-N-Bindungsknüpfung". Angewandte Chemie 125, n.º 23 (6 de maio de 2013): 6033–35. http://dx.doi.org/10.1002/ange.201301843.

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48

Goto, Akihiko. "射出成形 (C-101 ~ C-110, C-201 ~ C-214)". Seikei-Kakou 17, n.º 1 (20 de janeiro de 2005): 23. http://dx.doi.org/10.4325/seikeikakou.17.23.

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49

Etienne, Michel, e Andrew S. Weller. "Intramolecular C–C agostic complexes: C–C sigma interactions by another name". Chem. Soc. Rev. 43, n.º 1 (2014): 242–59. http://dx.doi.org/10.1039/c3cs60295h.

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50

Simić, Lj, e M. Kornicer. "Proton stopping inC+C,d+C,C+Ta,andd+Tacollisions at4.2AGeV/c". Physical Review C 58, n.º 4 (1 de outubro de 1998): 2585–87. http://dx.doi.org/10.1103/physrevc.58.2585.

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