Log in

Relevant bibliographies by topics / Pnicogen bond / Journal articles

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

Journal articles on the topic 'Pnicogen bond'

Author: Grafiati

Published: 6 September 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 'Pnicogen bond.'

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

Xu, Hui-Ying, Wei Wang, Jian-Wei Zou та Xiao-Lu Xu. "Theoretical calculations of π-type pnicogen bonds in the triad intermolecular complexes". Journal of Theoretical and Computational Chemistry 13, № 08 (2014): 1450068. http://dx.doi.org/10.1142/s0219633614500680.

Full text

Abstract:

The pnicogen bonding interactions of PCl3and π-electron systems (acetylene, ethylene, benzene) were calculated by using MP2/aug-cc-pVDZ method and the effect of hydrogen bond on pnicogen bond systems were investigated. It has been indicated that the hydrogen bonding and the pnicogen bonding interactions have influence on each other and the positively cooperative effect has been detected. The interaction energies of pnicogen bonded supramolecular system were also calculated by using DFT method (M06-2X) and some simple comparisons with those by using MP2 method were made. It has been disclosed f

APA, Harvard, Vancouver, ISO, and other styles

2

Esrafili, Mehdi D., and Fariba Mohammadian-Sabet. "Cooperative effects in hydrogen bond and pnicogen bond: a comparative study." Canadian Journal of Chemistry 92, no. 12 (2014): 1151–56. http://dx.doi.org/10.1139/cjc-2014-0379.

Full text

Abstract:

A comparative study of the cooperative effects of hydrogen and pnicogen bonding on open-chain clusters of (PH2CN)n=2–7 and (HCN)n=2–7 is performed at the MP2/6-311++G(d,p) level of theory. These effects are studied in terms of geometric and energetic properties, electron density analysis, and 15N chemical shielding parameters of the clusters at the MP2/6-311++G** level. The intermolecular distances observed in the (HCN)n clusters exhibit quite larger bond contractions than those found in the (PH2CN)n clusters. Our results strongly suggest that cooperative effects induced by pnicogen and hydrog

APA, Harvard, Vancouver, ISO, and other styles

3

Chandra, Swaroop, B. Suryaprasad, N. Ramanathan та K. Sundararajan. "Nitrogen as a pnicogen?: evidence for π-hole driven novel pnicogen bonding interactions in nitromethane–ammonia aggregates using matrix isolation infrared spectroscopy and ab initio computations". Physical Chemistry Chemical Physics 23, № 10 (2021): 6286–97. http://dx.doi.org/10.1039/d0cp06273a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Alkorta, Ibon, Cristina Trujillo, Goar Sánchez-Sanz, and José Elguero. "Solvent and Substituent Effects on the Phosphine + CO2 Reaction." Inorganics 6, no. 4 (2018): 110. http://dx.doi.org/10.3390/inorganics6040110.

Full text

Abstract:

A theoretical study of the substituent and solvent effects on the reaction of phosphines with CO2 has been carried out by means of Møller-Plesset (MP2) computational level calculations and continuum polarizable method (PCM) solvent models. Three stationary points along the reaction coordinate have been characterized, a pre-transition state (TS) assembly in which a pnicogen bond or tetrel bond is established between the phosphine and the CO2 molecule, followed by a transition state, and leading finally to the adduct in which the P–C bond has been formed. The solvent effects on the stability and

APA, Harvard, Vancouver, ISO, and other styles

5

Grabowski, Sławomir J. "Classification of So-Called Non-Covalent Interactions Based on VSEPR Model." Molecules 26, no. 16 (2021): 4939. http://dx.doi.org/10.3390/molecules26164939.

Full text

Abstract:

The variety of interactions have been analyzed in numerous studies. They are often compared with the hydrogen bond that is crucial in numerous chemical and biological processes. One can mention such interactions as the halogen bond, pnicogen bond, and others that may be classified as σ-hole bonds. However, not only σ-holes may act as Lewis acid centers. Numerous species are characterized by the occurrence of π-holes, which also may play a role of the electron acceptor. The situation is complicated since numerous interactions, such as the pnicogen bond or the chalcogen bond, for example, may be

APA, Harvard, Vancouver, ISO, and other styles

6

Alkorta, Ibon, Goar Sánchez-Sanz, José Elguero, and Janet E. Del Bene. "Influence of Hydrogen Bonds on the P···P Pnicogen Bond." Journal of Chemical Theory and Computation 8, no. 7 (2012): 2320–27. http://dx.doi.org/10.1021/ct300399y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Lo, Rabindranath, Petr Švec, Zdeňka Růžičková, Aleš Růžička та Pavel Hobza. "On the nature of the stabilisation of the E⋯π pnicogen bond in the SbCl3⋯toluene complex". Chemical Communications 52, № 17 (2016): 3500–3503. http://dx.doi.org/10.1039/c5cc10363k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Sánchez-Sanz, Goar, Cristina Trujillo, Ibon Alkorta, and José Elguero. "Intramolecular pnicogen interactions in phosphorus and arsenic analogues of proton sponges." Phys. Chem. Chem. Phys. 16, no. 30 (2014): 15900–15909. http://dx.doi.org/10.1039/c4cp01072h.

Full text

Abstract:

A computational study of the intramolecular pnicogen bond in 1,8-bis-substituted naphthalene derivatives (ZXH and ZX<sub>2</sub> with Z = P, As and X = H, F, Cl, and Br), structurally related to proton sponges, has been carried out.

APA, Harvard, Vancouver, ISO, and other styles

9

Zhu, Jian-Qing, Sheng-Wei Cao, Wei Wang, Xiao-Lu Xu та Hui-Ying Xu. "The Substituent Effects on π-type Pnicogen Bond Interaction". IOP Conference Series: Earth and Environmental Science 63 (травень 2017): 012027. http://dx.doi.org/10.1088/1755-1315/63/1/012027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Scheiner, Steve. "The Pnicogen Bond: Its Relation to Hydrogen, Halogen, and Other Noncovalent Bonds." Accounts of Chemical Research 46, no. 2 (2012): 280–88. http://dx.doi.org/10.1021/ar3001316.

Full text

APA, Harvard, Vancouver, ISO, and other styles

11

Scheiner, Steve. "Detailed comparison of the pnicogen bond with chalcogen, halogen, and hydrogen bonds." International Journal of Quantum Chemistry 113, no. 11 (2012): 1609–20. http://dx.doi.org/10.1002/qua.24357.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

Li, Qingzhong, Hongjie Zhu, Hongying Zhuo, Xin Yang, Wenzuo Li, and Jianbo Cheng. "Complexes between hypohalous acids and phosphine derivatives. Pnicogen bond versus halogen bond versus hydrogen bond." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 132 (November 2014): 271–77. http://dx.doi.org/10.1016/j.saa.2014.05.001.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Jiao, Yinchun, and Frank Weinhold. "What Is the Nature of Supramolecular Bonding? Comprehensive NBO/NRT Picture of Halogen and Pnicogen Bonding in RPH2···IF/FI Complexes (R = CH3, OH, CF3, CN, NO2)." Molecules 24, no. 11 (2019): 2090. http://dx.doi.org/10.3390/molecules24112090.

Full text

Abstract:

We employ a variety of natural bond orbital (NBO) and natural resonance theory (NRT) tools to comprehensively investigate the nature of halogen and pnicogen bonding interactions in RPH2···IF/FI binary complexes (R = CH3, OH, CF3, CN, and NO2) and the tuning effects of R-substituents. Though such interactions are commonly attributed to “sigma-hole”-type electrostatic effects, we show that they exhibit profound similarities and analogies to the resonance-type 3-center, 4-electron (3c/4e) donor-acceptor interactions of hydrogen bonding, where classical-type “electrostatics” are known to play only

APA, Harvard, Vancouver, ISO, and other styles

14

Grabowski, Sławomir J. "σ-Hole Bonds and the VSEPR Model—From the Tetrahedral Structure to the Trigonal Bipyramid". Sci 4, № 2 (2022): 17. http://dx.doi.org/10.3390/sci4020017.

Full text

Abstract:

Complexes linked by various interactions are analysed in this study. They are characterized by the tetrahedral configuration of the Lewis acid centre. Interactions, being a subject of this study, are classified as σ-hole bonds, such as the halogen, chalcogen, pnicogen, and tetrel bonds. In the case of strong interactions, the tetrahedral configuration of the Lewis acid centre changes into the trigonal bipyramid configuration. This change is in line with the Valence-Shell Electron-Pair Repulsion model, VSEPR, and this is supported here by the results of high-level ab initio calculations. The th

APA, Harvard, Vancouver, ISO, and other styles

15

Scheiner, Steve. "New ideas from an old concept: the hydrogen bond." Biochemist 41, no. 4 (2019): 6–9. http://dx.doi.org/10.1042/bio04104006.

Full text

Abstract:

Ongoing studies of the hydrogen bond (HB), in which a hydrogen (H) atom acts as a bridge between a pair of chemical groups, continues to offer new ideas about this interaction that have applications to biochemical processes. The ability of a proton to transfer within a HB can be controlled by conformational changes that cause small alterations to the HB geometry. The CH group, widely prevalent in biological systems, participates in HBs and contributes to the structure and stability of commonly occurring protein secondary structures such as the β-sheet. The concept of the HB has been extended t

APA, Harvard, Vancouver, ISO, and other styles

16

Zhuo, Hongying, Qingzhong Li, Wenzuo Li, and Jianbo Cheng. "The dual role of pnicogen as Lewis acid and base and the unexpected interplay between the pnicogen bond and coordination interaction in H3N⋯FH2X⋯MCN (X = P and As; M = Cu, Ag, and Au)." New Journal of Chemistry 39, no. 3 (2015): 2067–74. http://dx.doi.org/10.1039/c4nj02051k.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Lu, Jia, and Steve Scheiner. "Effects of Halogen, Chalcogen, Pnicogen, and Tetrel Bonds on IR and NMR Spectra." Molecules 24, no. 15 (2019): 2822. http://dx.doi.org/10.3390/molecules24152822.

Full text

Abstract:

Complexes were formed pairing FX, FHY, FH2Z, and FH3T (X = Cl, Br, I; Y = S, Se, Te; Z = P, As, Sb; T = Si, Ge, Sn) with NH3 in order to form an A⋯N noncovalent bond, where A refers to the central atom. Geometries, energetics, atomic charges, and spectroscopic characteristics of these complexes were evaluated via DFT calculations. In all cases, the A–F bond, which is located opposite the base and is responsible for the σ-hole on the A atom, elongates and its stretching frequency undergoes a shift to the red. This shift varies from 42 to 175 cm−1 and is largest for the halogen bonds, followed b

APA, Harvard, Vancouver, ISO, and other styles

18

Grabowski, Sławomir J. "Hydrogen Bond and Other Lewis Acid–Lewis Base Interactions as Preliminary Stages of Chemical Reactions." Molecules 25, no. 20 (2020): 4668. http://dx.doi.org/10.3390/molecules25204668.

Full text

Abstract:

Various Lewis acid–Lewis base interactions are discussed as initiating chemical reactions and processes. For example, the hydrogen bond is often a preliminary stage of the proton transfer process or the tetrel and pnicogen bonds lead sometimes to the SN2 reactions. There are numerous characteristics of interactions being first stages of reactions; one can observe a meaningful electron charge transfer from the Lewis base unit to the Lewis acid; such interactions possess at least partly covalent character, one can mention other features. The results of different methods and approaches that are a

APA, Harvard, Vancouver, ISO, and other styles

19

Michalczyk, Zierkiewicz, Wysokiński, and Scheiner. "Theoretical Studies of IR and NMR Spectral Changes Induced by Sigma-Hole Hydrogen, Halogen, Chalcogen, Pnicogen, and Tetrel Bonds in a Model Protein Environment." Molecules 24, no. 18 (2019): 3329. http://dx.doi.org/10.3390/molecules24183329.

Full text

Abstract:

Various types of σ-hole bond complexes were formed with FX, HFY, H2FZ, and H3FT (X = Cl, Br, I; Y = S, Se, Te; Z = P, As, Sb; T = Si, Ge, Sn) as Lewis acid. In order to examine their interactions with a protein, N-methylacetamide (NMA), a model of the peptide linkage was used as the base. These noncovalent bonds were compared by computational means with H-bonds formed by NMA with XH molecules (X = F, Cl, Br, I). In all cases, the A–F bond, which lies opposite the base and is responsible for the σ-hole on the A atom (A refers to the bridging atom), elongates and its stretching frequency undergo

APA, Harvard, Vancouver, ISO, and other styles

20

Lu, Jia, and Steve Scheiner. "Relationships between Bond Strength and Spectroscopic Quantities in H-Bonds and Related Halogen, Chalcogen, and Pnicogen Bonds." Journal of Physical Chemistry A 124, no. 38 (2020): 7716–25. http://dx.doi.org/10.1021/acs.jpca.0c05936.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Scheiner, Steve. "On the Ability of Nitrogen to Serve as an Electron Acceptor in a Pnicogen Bond." Journal of Physical Chemistry A 125, no. 48 (2021): 10419–27. http://dx.doi.org/10.1021/acs.jpca.1c09213.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Setiawan, Dani, Elfi Kraka, and Dieter Cremer. "Strength of the Pnicogen Bond in Complexes Involving Group Va Elements N, P, and As." Journal of Physical Chemistry A 119, no. 9 (2014): 1642–56. http://dx.doi.org/10.1021/jp508270g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Esrafili, Mehdi D., Parvin Fatehi, and Mohammad Solimannejad. "Mutual interplay between pnicogen bond and dihydrogen bond in HMH⋯HCN⋯PH2X complexes (M=Be, Mg, Zn; X=H, F, Cl)." Computational and Theoretical Chemistry 1034 (April 2014): 1–6. http://dx.doi.org/10.1016/j.comptc.2014.02.003.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Dong, Wenbo, Yu Wang, Jianbo Cheng, Xin Yang та Qingzhong Li. "Competition between σ-hole pnicogen bond and π-hole tetrel bond in complexes of CF2=CFZH2 (Z = P, As, and Sb)". Molecular Physics 117, № 3 (2018): 251–59. http://dx.doi.org/10.1080/00268976.2018.1508782.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Scheiner, Steve. "Relative Strengths of a Pnicogen and a Tetrel Bond and Their Mutual Effects upon One Another." Journal of Physical Chemistry A 125, no. 12 (2021): 2631–41. http://dx.doi.org/10.1021/acs.jpca.1c01211.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

Michalczyk, Mariusz, Magdalena Malik, Wiktor Zierkiewicz, and Steve Scheiner. "Experimental and Theoretical Studies of Dimers Stabilized by Two Chalcogen Bonds in the Presence of a N···N Pnicogen Bond." Journal of Physical Chemistry A 125, no. 2 (2021): 657–68. http://dx.doi.org/10.1021/acs.jpca.0c10814.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Esrafili, Mehdi D., Fariba Mohammadian-Sabet та Mohammad Solimannejad. "Mutual influence between anion–π and pnicogen bond interactions: The enhancement of P⋯N and P⋯O interactions by an anion–π bond". Journal of Molecular Graphics and Modelling 57 (квітень 2015): 99–105. http://dx.doi.org/10.1016/j.jmgm.2015.01.010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Zabardasti, Abedien, Saeed Farhadi, and Aliyar Mahdizadeh. "Cooperative effect between pnicogen bond and hydrogen bond interactions in typical X…AsH2F…HF complexes (X = NR3, PR3 and OR2; R = CH3, H, F)." Phosphorus, Sulfur, and Silicon and the Related Elements 193, no. 11 (2018): 759–65. http://dx.doi.org/10.1080/10426507.2018.1513514.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Abroushan, Eslam, Abedien Zabaradsti, Saeed Farhadi, and Ahmad Abodolmaleki. "Pnicogen bond interaction between PF2Y (Y = –C☰N, –N☰C) with NH3, CH3OH, H2O, and HF molecules." Structural Chemistry 28, no. 6 (2017): 1843–51. http://dx.doi.org/10.1007/s11224-017-0968-1.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

LIU, YAN-ZHI, KUN YUAN, ZHAO YUAN, YUAN-CHENG ZHU, and XIANG ZHAO. "Theoretical exploration of pnicogen bond noncovalent interactions in HCHO⋯PH2X (X=CH3, H, C6H5, F, Cl, Br, and NO2) complexes." Journal of Chemical Sciences 127, no. 10 (2015): 1729–38. http://dx.doi.org/10.1007/s12039-015-0933-8.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Gholipour, Alireza. "Mutual interplay between pnicogen–π and tetrel bond in PF3⊥X–Pyr…SiH3CN complexes: NMR, SAPT, AIM, NBO, and MEP analysis". Structural Chemistry 29, № 5 (2018): 1255–63. http://dx.doi.org/10.1007/s11224-018-1106-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

32

Esrafili, Mehdi D., and Hossein Akhgarpour. "Anab initiostudy on competition between pnicogen and chalcogen bond interactions in binary XHS:PH2X complexes (X = F, Cl, CCH, COH, CH3, OH, OCH3and NH2)." Molecular Physics 114, no. 12 (2016): 1847–55. http://dx.doi.org/10.1080/00268976.2016.1158421.

Full text

APA, Harvard, Vancouver, ISO, and other styles

33

Ghafari Nikoo Jooneghani, Saber, та Alireza Gholipour. "Mutual cooperation of π-π stacking and pnicogen bond interactions of substituted monomeric Lawesson’s reagent and pyridine rings: Theoretical insight into Pyr||X-PhPS2⊥pyr complexes". Chemical Physics Letters 721 (квітень 2019): 91–98. http://dx.doi.org/10.1016/j.cplett.2019.02.027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

34

Shukla, Rahul, and Deepak Chopra. "“Pnicogen bonds” or “chalcogen bonds”: exploiting the effect of substitution on the formation of P⋯Se noncovalent bonds." Physical Chemistry Chemical Physics 18, no. 20 (2016): 13820–29. http://dx.doi.org/10.1039/c6cp01703g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Jing, Xinyue, Yanli Zeng, Xueying Zhang, Lingpeng Meng, and Xiaoyan Li. "Competition and conversion between pnicogen bonds and hydrogen bonds involving prototype organophosphorus compounds." Physical Chemistry Chemical Physics 23, no. 34 (2021): 18794–805. http://dx.doi.org/10.1039/d1cp00474c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

36

Shukla, Rahul, та Deepak Chopra. "Characterization of N⋯O non-covalent interactions involving σ-holes: “electrostatics” or “dispersion”". Physical Chemistry Chemical Physics 18, № 43 (2016): 29946–54. http://dx.doi.org/10.1039/c6cp05899j.

Full text

APA, Harvard, Vancouver, ISO, and other styles

37

Guan, Liangyu, and Yirong Mo. "Electron Transfer in Pnicogen Bonds." Journal of Physical Chemistry A 118, no. 39 (2014): 8911–21. http://dx.doi.org/10.1021/jp500775m.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Alkorta, Ibon, José Elguero, and Sławomir J. Grabowski. "Pnicogen and hydrogen bonds: complexes between PH3X+ and PH2X systems." Physical Chemistry Chemical Physics 17, no. 5 (2015): 3261–72. http://dx.doi.org/10.1039/c4cp04840g.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Roohi, Hossein, and Tahereh Tondro. "Exploring the pnicogen bond non-covalent interactions in 4-XPhNH 2 :PF n H 3-n complexes (n = 1–3, X = H, F, CN, CHO, NH 2 , CH 3 , NO 2 and OCH 3 )." Journal of Fluorine Chemistry 202 (October 2017): 19–33. http://dx.doi.org/10.1016/j.jfluchem.2017.08.009.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Alkorta, Ibon, Janet Del Bene, and Jose Elguero. "H2XP:OH2 Complexes: Hydrogen vs. Pnicogen Bonds." Crystals 6, no. 2 (2016): 19. http://dx.doi.org/10.3390/cryst6020019.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

Zahn, Stefan, René Frank, Eva Hey‐Hawkins, and Barbara Kirchner. "Pnicogen Bonds: A New Molecular Linker?" Chemistry – A European Journal 17, no. 22 (2011): 6034–38. http://dx.doi.org/10.1002/chem.201002146.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Del Bene, Janet E., Ibon Alkorta та José Elguero. "Can HNNH, FNNH, or HNCHOH bridge the σ-hole and the lone pair at P in binary complexes with H2XP, for X = F, Cl, NC, OH, CN, CCH, CH3, and H?" Physical Chemistry Chemical Physics 17, № 45 (2015): 30729–35. http://dx.doi.org/10.1039/c5cp05832e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Mohajeri, Afshan, K. Eskandari, and Saeedeh Amin Safaee. "Endohedral pnicogen and triel bonds in doped C60 fullerenes." New Journal of Chemistry 41, no. 19 (2017): 10619–26. http://dx.doi.org/10.1039/c7nj01477e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Scheiner, Steve. "Comparison of halide receptors based on H, halogen, chalcogen, pnicogen, and tetrel bonds." Faraday Discussions 203 (2017): 213–26. http://dx.doi.org/10.1039/c7fd00043j.

Full text

Abstract:

A series of halide receptors are constructed and the geometries and energetics of their binding to F<sup>−</sup>, Cl<sup>−</sup>, and Br<sup>−</sup>assessed by quantum calculations. The dicationic receptors are based on a pair of imidazolium units, connectedviaa benzene spacer. The imidazoliums each donate a proton to a halide in a pair of H-bonds. Replacement of the two bonding protons by Br leads to bindingviaa pair of halogen bonds. Likewise, chalcogen, pnicogen, and tetrel bonds occur when the protons are replaced, respectively, by Se, As, and Ge. Regardless of the binding group considered

APA, Harvard, Vancouver, ISO, and other styles

45

Lin, Hui, Lingpeng Meng, Xiaoyan Li, Yanli Zeng, and Xueying Zhang. "Comparison of pnicogen and tetrel bonds in complexes containing CX2 carbenes (X = F, Cl, Br, OH, OMe, NH2, and NMe2)." New Journal of Chemistry 43, no. 39 (2019): 15596–604. http://dx.doi.org/10.1039/c9nj03397a.

Full text

Abstract:

The similarities and differences of pnicogen and tetrel bonds formed by carbenes CX<sub>2</sub> with H<sub>3</sub>AsO and H<sub>3</sub>SiCN were investigated by carrying out ab initio calculations in association with topological analysis of electron density.

APA, Harvard, Vancouver, ISO, and other styles

46

Saha, Arijit, Ragima V. P. Veluthaparambath, and Binoy K. Saha. "Directionality of P⋯O pnicogen bonding in light of geometry corrected statistical analysis." New Journal of Chemistry 44, no. 23 (2020): 9607–10. http://dx.doi.org/10.1039/d0nj01683g.

Full text

Abstract:

Cone corrected statistical analysis suggests that the X–P⋯O angle prefers linearity which is more prominent in the case of X<sub>3</sub>P⋯O compared to X<sub>4</sub>P⋯O pnicogen bonds. This preference also increases with an increase in the electronegativity of X.

APA, Harvard, Vancouver, ISO, and other styles

47

Zahn, Stefan, René Frank, Evamarie Hey-Hawkins, and Barbara Kirchner. "Corrigendum: Pnicogen Bonds: A New Molecular Linker?" Chemistry - A European Journal 19, no. 5 (2013): 1526. http://dx.doi.org/10.1002/chem.201204538.

Full text

APA, Harvard, Vancouver, ISO, and other styles

48

Avens, Larry R., Leonard V. Cribbs, and Jerry L. Mills. "Exchange reactions of tetrakis(trifluoromethyl)diphosphine with pnicogen-pnicogen, phosphorus-hydrogen, and phosphorus-chlorine bonds." Inorganic Chemistry 28, no. 2 (1989): 211–14. http://dx.doi.org/10.1021/ic00301a011.

Full text

APA, Harvard, Vancouver, ISO, and other styles

49

Tripathi, Garima, Khalid Badi-uz-zama, and Gurunath Ramanathan. "N…N pnicogen bonds in Boc-DOPA-OMe." Chemical Physics Letters 653 (June 2016): 117–21. http://dx.doi.org/10.1016/j.cplett.2016.04.076.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Grabowski, Sławomir J. "Pnicogen and tetrel bonds—tetrahedral Lewis acid centres." Structural Chemistry 30, no. 4 (2019): 1141–52. http://dx.doi.org/10.1007/s11224-019-01358-1.

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!