Relevant bibliographies by topics / Group 13 / Journal articles

Journal articles on the topic 'Group 13'

To see the other types of publications on this topic, follow the link: Group 13.
Author: Grafiati
Published: 10 December 2022
Last updated: 28 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 'Group 13.'

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

Schulz, Stephan, Andreas Kuczkowski, Daniella Schuchmann, Ulrich Flörke, and Martin Nieger. "Group 13−Group 13 Donor−Acceptor Complexes." Organometallics 25, no. 22 (October 2006): 5487–91. http://dx.doi.org/10.1021/om0606946.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Atwood, David A. "Cationic group 13 complexes." Coordination Chemistry Reviews 176, no. 1 (September 1998): 407–30. http://dx.doi.org/10.1016/s0010-8545(98)00127-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Macdonald, Charles L. B., John D. Gorden, Andreas Voigt, Silvia Filipponi, and Alan H. Cowley. "Group 13 decamethylmetallocenium cations." Dalton Trans., no. 9 (2008): 1161–76. http://dx.doi.org/10.1039/b716220k.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Cowley, Alan H. "From group 13–group 13 donor–acceptor bonds to triple-decker cations." Chem. Commun., no. 21 (2004): 2369–75. http://dx.doi.org/10.1039/b409497m.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Cultrara, Nicholas D., Maxx Q. Arguilla, Shishi Jiang, Chuanchuan Sun, Michael R. Scudder, R. Dominic Ross, and Joshua E. Goldberger. "Group-13 and group-15 doping of germanane." Beilstein Journal of Nanotechnology 8 (August 9, 2017): 1642–48. http://dx.doi.org/10.3762/bjnano.8.164.

Full text
Abstract:
Germanane, a hydrogen-terminated graphane analogue of germanium has generated interest as a potential 2D electronic material. However, the incorporation and retention of extrinsic dopant atoms in the lattice, to tune the electronic properties, remains a significant challenge. Here, we show that the group-13 element Ga and the group-15 element As, can be successfully doped into a precursor CaGe2 phase, and remain intact in the lattice after the topotactic deintercalation, using HCl, to form GeH. After deintercalation, a maximum of 1.1% As and 2.3% Ga can be substituted into the germanium lattice. Electronic transport properties of single flakes show that incorporation of dopants leads to a reduction of resistance of more than three orders of magnitude in H2O-containing atmosphere after As doping. After doping with Ga, the reduction is more than six orders of magnitude, but with significant hysteretic behavior, indicative of water-activation of dopants on the surface. Only Ga-doped germanane remains activated under vacuum, and also exhibits minimal hysteretic behavior while the sheet resistance is reduced by more than four orders of magnitude. These Ga- and As-doped germanane materials start to oxidize after one to four days in ambient atmosphere. Overall, this work demonstrates that extrinsic doping with Ga is a viable pathway towards accessing stable electronic behavior in graphane analogues of germanium.
APA, Harvard, Vancouver, ISO, and other styles
6

Munoz-Hernandez, Miguel-Angel, Pingrong Wei, Shengming Liu, and David A. Atwood. "Tetrametallic Group 13 ‘Mitsubishi’ Molecules." Coordination Chemistry Reviews 210, no. 1 (December 2000): 1–10. http://dx.doi.org/10.1016/s0010-8545(00)00314-3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Roberson, Loriann, Benjamin M. Galvin, and Atira Cherise Charles. "13 When Group Identities Matter." Academy of Management Annals 1, no. 1 (December 2007): 617–50. http://dx.doi.org/10.5465/078559818.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Roberson, Loriann, Benjamin M. Galvin, and Atira Cherise Charles. "13 When Group Identities Matter." Academy of Management Annals 1, no. 1 (December 2007): 617–50. http://dx.doi.org/10.1080/078559818.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Chitsaz, Soheila, and Bernhard Neumüller. "BINOL Compounds of Group 13." Organometallics 20, no. 11 (May 2001): 2338–43. http://dx.doi.org/10.1021/om010042b.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Thomas, Florian, Stephan Schulz, Heidi Mansikkamäki, and Martin Nieger. "Unexpected Rearrangement Reaction of Lewis Base Stabilized Group 13/15 Compounds with Group 13 Trialkyls." Organometallics 22, no. 17 (August 2003): 3471–77. http://dx.doi.org/10.1021/om0303451.

Full text
APA, Harvard, Vancouver, ISO, and other styles
11

GE, ShengBo, and JinKe HAI. "Normalizer property for integral group rings of nite groups." SCIENTIA SINICA Mathematica 45, no. 6 (June 1, 2015): 745–50. http://dx.doi.org/10.1360/012015-13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
12

N K Goswami, N. K. Goswami, and P. J. Handique P. J. Handique. "Explants Size Response to in Vitro Propagation of Musa (Aaa Group) ‘Amritsagar’ Musa (Aab Group) ‘Malbhog’ and Musa (Aab Group) ‘Chenichampa’ Banana." Indian Journal of Applied Research 3, no. 8 (October 1, 2011): 40–43. http://dx.doi.org/10.15373/2249555x/aug2013/13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
13

Gupta, Drishti, and Thomas R. Cundari. "Group 13 complexes for methane activation." Computational and Theoretical Chemistry 1214 (August 2022): 113788. http://dx.doi.org/10.1016/j.comptc.2022.113788.

Full text
APA, Harvard, Vancouver, ISO, and other styles
14

Vidovic, Dragoslav, and Simon Aldridge. "Coordination chemistry of group 13 monohalides." Chemical Science 2, no. 4 (2011): 601. http://dx.doi.org/10.1039/c0sc00508h.

Full text
APA, Harvard, Vancouver, ISO, and other styles
15

Hill, Michael, Jolin Jegier, Miguel-Angel Munoz-Hernandez, Drew Rutherford, Amy Singer, and David Atwood. "New Precursors to Group 13 Nitrides." Phosphorus, Sulfur, and Silicon and the Related Elements 124, no. 1 (January 1, 1997): 183–92. http://dx.doi.org/10.1080/10426509708545623.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

Pinkas, Jiri, Tieli Wang, Robert A. Jacobson, and John G. Verkade. "Group 13 Azatranes: Structure and Reactivity." Inorganic Chemistry 33, no. 23 (November 1994): 5244–53. http://dx.doi.org/10.1021/ic00101a016.

Full text
APA, Harvard, Vancouver, ISO, and other styles
17

Ong, Christopher M., and Douglas W. Stephan. "1,2-Cyclopentadienyl Diimine−Group 13 Complexes." Inorganic Chemistry 38, no. 22 (November 1999): 5189–91. http://dx.doi.org/10.1021/ic9903782.

Full text
APA, Harvard, Vancouver, ISO, and other styles
18

Atwood, David A., and Melanie J. Harvey. "Group 13 Compounds Incorporating Salen Ligands." Chemical Reviews 101, no. 1 (January 2001): 37–52. http://dx.doi.org/10.1021/cr990008v.

Full text
APA, Harvard, Vancouver, ISO, and other styles
19

Bhattacharjee, Hridaynath, and Jens Müller. "Metallocenophanes bridged by group 13 elements." Coordination Chemistry Reviews 314 (May 2016): 114–33. http://dx.doi.org/10.1016/j.ccr.2015.09.008.

Full text
APA, Harvard, Vancouver, ISO, and other styles
20

Atwood, David A. "ChemInform Abstract: Cationic Group 13 Complexes." ChemInform 30, no. 12 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199912269.

Full text
APA, Harvard, Vancouver, ISO, and other styles
21

Varns, Rebecca, and Paul Strange. "Super-atom properties of 13 atom clusters of group 13 elements." physica status solidi (b) 249, no. 11 (August 22, 2012): 2179–89. http://dx.doi.org/10.1002/pssb.201248199.

Full text
APA, Harvard, Vancouver, ISO, and other styles
22

Linton, David J., Paul Schooler, and Andrew E. H. Wheatley. "Group 12 and heavier Group 13 alkali metal 'ate complexes." Coordination Chemistry Reviews 223, no. 1 (December 2001): 53–115. http://dx.doi.org/10.1016/s0010-8545(01)00379-4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
23

Kumar, Dr Shakti. "Middle Income Group and Debt Fund." Indian Journal of Applied Research 2, no. 3 (October 1, 2011): 43. http://dx.doi.org/10.15373/2249555x/dec2012/13.

Full text
APA, Harvard, Vancouver, ISO, and other styles
24

Cui, Zhong-hua, Yu-qian Liu, Runfeng Huang, Meng-hui Wang, Bing Yan, and Lili Zhao. "Linear group 13 EE triple bonds." Physical Chemistry Chemical Physics 23, no. 20 (2021): 11611–15. http://dx.doi.org/10.1039/d1cp01035b.

Full text
Abstract:
The surrounding Na5 motifs suppress the nonbonded electron density of E atoms, effectively resulting in two degenerate π bonds and one multicenter σ bond in the unprecedented linear heavier group 13 EE triple bonds.
APA, Harvard, Vancouver, ISO, and other styles
25

Bridgeman, Adam J. "Structure and bonding of Group 13 monocarbonyls." Journal of the Chemical Society, Dalton Transactions, no. 8 (1997): 1323–30. http://dx.doi.org/10.1039/a606474d.

Full text
APA, Harvard, Vancouver, ISO, and other styles
26

Smith, Marion W., L. Gregory Lawton, and Jaime Checkoff. "Tetrapyridyl Porphyrin Derivatives of Group 13 Metals." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 23, no. 4 (April 1993): 639–51. http://dx.doi.org/10.1080/15533179308016663.

Full text
APA, Harvard, Vancouver, ISO, and other styles
27

Okazaki, Renji. "Cyclic Chalcogenides Containing Group 13–15 Elements." Phosphorus, Sulfur, and Silicon and the Related Elements 168, no. 1 (January 1, 2001): 41–50. http://dx.doi.org/10.1080/10426500108546529.

Full text
APA, Harvard, Vancouver, ISO, and other styles
28

Pauls, Jochen, Soheila Chitsaz, and Bernhard Neumüller. "Alkoxo and Amido Compounds of Group 13." Phosphorus, Sulfur, and Silicon and the Related Elements 168, no. 1 (January 1, 2001): 233–38. http://dx.doi.org/10.1080/10426500108546559.

Full text
APA, Harvard, Vancouver, ISO, and other styles
29

Ziemkowska, Wanda, and Romana Anulewicz-Ostrowska. "Sterically crowded diolates of group 13 metals." Journal of Organometallic Chemistry 689, no. 12 (June 2004): 2056–65. http://dx.doi.org/10.1016/j.jorganchem.2004.03.016.

Full text
APA, Harvard, Vancouver, ISO, and other styles
30

Jaśkowska, Eliza, Iwona Justyniak, Michał K. Cyrański, Agnieszka Adamczyk-Woźniak, Andrzej Sporzyński, Ewa Zygadło-Monikowska, and Wanda Ziemkowska. "Benzoxaborolate ligands in group 13 metal complexes." Journal of Organometallic Chemistry 732 (May 2013): 8–14. http://dx.doi.org/10.1016/j.jorganchem.2013.01.023.

Full text
APA, Harvard, Vancouver, ISO, and other styles
31

Atwood, David A., Alan H. Cowley, Rodney D. Schluter, Marcus R. Bond, and Carl J. Carrano. "Intramolecularly Base-Stabilized Group 13 Aryloxide Complexes." Inorganic Chemistry 34, no. 8 (April 1995): 2186–89. http://dx.doi.org/10.1021/ic00112a034.

Full text
APA, Harvard, Vancouver, ISO, and other styles
32

Müller, Jens. "Azides of the heavier Group 13 elements." Coordination Chemistry Reviews 235, no. 1-2 (December 2002): 105–19. http://dx.doi.org/10.1016/s0010-8545(02)00181-9.

Full text
APA, Harvard, Vancouver, ISO, and other styles
33

Barik, Ranjan Kumar, Ritesh Kumar, and Abhishek K. Singh. "Topological Phases in Hydrogenated Group 13 Monolayers." Journal of Physical Chemistry C 123, no. 42 (September 27, 2019): 25985–90. http://dx.doi.org/10.1021/acs.jpcc.9b07095.

Full text
APA, Harvard, Vancouver, ISO, and other styles
34

Tun, Zin-Min, Amy J. Heston, Matthew J. Panzner, Vincenzo Scionti, Doug A. Medvetz, Brian D. Wright, Nicholas A. Johnson, et al. "Group 13 Superacid Adducts of [PCl2N]3." Inorganic Chemistry 55, no. 7 (March 14, 2016): 3283–93. http://dx.doi.org/10.1021/acs.inorgchem.5b02341.

Full text
APA, Harvard, Vancouver, ISO, and other styles
35

Justyniak, Iwona, Daniel Prochowicz, Adam Tulewicz, Wojciech Bury, Piotr Goś, and Janusz Lewiński. "Structure investigations of group 13 organometallic carboxylates." Dalton Transactions 46, no. 3 (2017): 669–77. http://dx.doi.org/10.1039/c6dt03958h.

Full text
Abstract:
The effect of both the relative magnitude of electrophilicity of metal centres and the character of a Lewis base on the molecular structure of the electron-precise [R2M(μ-O2CPh)]2-type carboxylates and their Lewis acid–base adducts [(R2M)(μ-O2CPh)(py-Me)] is reported.
APA, Harvard, Vancouver, ISO, and other styles
36

Gjerlevsen Nielsen, Ida, Sanna Sommer, and Bo Brummerstedt Iversen. "Structures of the Group 13 prenucleation clusters." Acta Crystallographica Section A Foundations and Advances 75, a2 (August 18, 2019): e697-e697. http://dx.doi.org/10.1107/s2053273319088594.

Full text
APA, Harvard, Vancouver, ISO, and other styles
37

Erfjord, Ingvald, Götz Krummheuer, and Ema Mamede. "CERME7 Working Group 13: Early Years mathematics." Research in Mathematics Education 14, no. 2 (July 2012): 207–8. http://dx.doi.org/10.1080/14794802.2012.694293.

Full text
APA, Harvard, Vancouver, ISO, and other styles
38

Haiges, Ralf, Piyush Deokar, Monica Vasiliu, Trent H. Stein, David A. Dixon, and Karl O. Christe. "Preparation and Characterization of Group 13 Cyanides." Chemistry - A European Journal 23, no. 38 (May 24, 2017): 8991. http://dx.doi.org/10.1002/chem.201701749.

Full text
APA, Harvard, Vancouver, ISO, and other styles
39

Singh, Sanjay, and Herbert W. Roesky. "Fluorine functionalized compounds of group 13 elements." Journal of Fluorine Chemistry 128, no. 4 (April 2007): 369–77. http://dx.doi.org/10.1016/j.jfluchem.2006.07.018.

Full text
APA, Harvard, Vancouver, ISO, and other styles
40

Munoz-Hernandez, Miguel-Angel, Pingrong Wei, Shengming Liu, and David A. Atwood. "ChemInform Abstract: Tetrametallic Group 13 “Mitsubishi” Molecules." ChemInform 32, no. 7 (May 30, 2010): no. http://dx.doi.org/10.1002/chin.200107233.

Full text
APA, Harvard, Vancouver, ISO, and other styles
41

Haiges, Ralf, Piyush Deokar, Monica Vasiliu, Trent H. Stein, David A. Dixon, and Karl O. Christe. "Preparation and Characterization of Group 13 Cyanides." Chemistry - A European Journal 23, no. 38 (May 19, 2017): 9054–66. http://dx.doi.org/10.1002/chem.201700611.

Full text
APA, Harvard, Vancouver, ISO, and other styles
42

Spallone, Marco, and Pina Murè. "Strategic group lending for banks." Banks and Bank Systems 13, no. 1 (March 29, 2018): 115–27. http://dx.doi.org/10.21511/bbs.13(1).2018.11.

Full text
Abstract:
Credit institutions often refuse to lend money to small firms. Usually, this happens because small firms are not able to provide collateral to lenders. Moreover, given the small amount of required loans, the relative cost of full monitoring is too high for lenders. Group lending contracts have been viewed as an effective solution to credit rationing of small firms in both developing and industrialized countries. The aim of this paper is to highlight the potential of group lending contracts in terms of credit risk management. In particular, this paper provides a theoretical explanation of the potential of group lending programs in screening good borrowers from bad ones to reduce the incidence of non-performing-loans (NPL). This paper shows that the success of firms involved in selected group lending programs is due to the fact that co-signature is an effective screening device: more precisely, if lenders make a proper use of co-signature to screen good firms from bad ones, then only firms that are good ex-ante enter group lending contracts. So, the main argument of this paper is that well designed group lending programs induce good firms to become jointly liable, at least partially, with other good firms and discourage other – bad-firms to do the same. Specifically, co-signature is proven to be a screening device only in the case of a perfectly competitive bank sector.
APA, Harvard, Vancouver, ISO, and other styles
43

Linton, David J., Paul Schooler, and Andrew E. H. Wheatley. "ChemInform Abstract: Group 12 and Heavier Group 13 Alkali Metal ′Ate Complexes." ChemInform 32, no. 51 (May 23, 2010): no. http://dx.doi.org/10.1002/chin.200151247.

Full text
APA, Harvard, Vancouver, ISO, and other styles
44

Ota, Kei, and Rei Kinjo. "Zero-valent species of group 13–15 elements." Chem 8, no. 2 (February 2022): 340–50. http://dx.doi.org/10.1016/j.chempr.2022.01.010.

Full text
APA, Harvard, Vancouver, ISO, and other styles
45

Lewiński, Janusz, Janusz Zachara, Kazimierz B. Starowieyski, Zbigniew Ochal, Iwona Justyniak, Tomasz Kopeć, Patryk Stolarzewicz, and Maciej Dranka. "Structure Investigations of Group 13 Derivatives ofN-Phenylsalicylideneimine." Organometallics 22, no. 18 (September 2003): 3773–80. http://dx.doi.org/10.1021/om030331v.

Full text
APA, Harvard, Vancouver, ISO, and other styles
46

Atwood, David A., and Drew Rutherford. "The Trimetallic Structural Motif in Group 13 Chemistry." Comments on Inorganic Chemistry 19, no. 1 (December 1996): 25–45. http://dx.doi.org/10.1080/02603599608032726.

Full text
APA, Harvard, Vancouver, ISO, and other styles
47

Rivard, Eric, Andrew R. McWilliams, Alan J. Lough, and Ian Manners. "REVERSIBLE SKELETAL SUBSTITUTION REACTIONS INVOLVING GROUP 13 HETEROPHOSPHAZENES." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 4-5 (April 1, 2004): 845–47. http://dx.doi.org/10.1080/10426500490427312.

Full text
APA, Harvard, Vancouver, ISO, and other styles
48

McWilliams, Andrew R., Eric Rivard, Alan J. Lough, and Ian Manners. "Reversible skeletal substitution reactions involving group 13 heterophosphazenes." Chemical Communications, no. 10 (April 23, 2002): 1102–3. http://dx.doi.org/10.1039/b201582j.

Full text
APA, Harvard, Vancouver, ISO, and other styles
49

Köster, Marcel, Annikka Kreher, and Carsten von Hänisch. "Synthesis of ternary group 13/15 chain compounds." Dalton Transactions 47, no. 24 (2018): 7875–78. http://dx.doi.org/10.1039/c8dt01119b.

Full text
Abstract:
A seven heteroatom chain molecule (see figure) of the composition HB{N(H)PtBu2BH3}2 was obtained from the reaction of tBu2PNH2 with H3B·SMe2.
APA, Harvard, Vancouver, ISO, and other styles
50

Ziemkowska, Wanda, Eliza Jaśkowska, Ewa Zygadło-Monikowska, and Michał K. Cyrański. "Reactions of group 13 metal trialkyls with oxamides." Journal of Organometallic Chemistry 696, no. 10 (May 2011): 2079–85. http://dx.doi.org/10.1016/j.jorganchem.2010.11.005.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the bibliographies on the topic 'Group 13' for other source types:
Dissertations / Theses Books
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!

To the bibliography